WALA Compendium of Medicines

WALA Compendium of Medicines

Nature´s Treasures Transformed for You

31st Edition

31st Edition, September 2009

WALA

Compendium of Medicines

www.walaarzneimittel.de

Cat. No.: 410 000 136 / 1H

Medicines

WALA Compendium of Medicines

WALA Heilmittel GmbH 73085 Bad Boll/Eckwälden Germany Phone: +49 (0)7164 930-0 The WALA Compendium of Medicines

Fax: +49 (0)7164 930-297

is also available on CD.

www.walaarzneimittel.de

For ordering information, see page 17.

[email protected] 1

Table of Contents Introduction

The most important sections at a glance Medicines Substances Indications Abbreviations Contraindications during pregnancy and breastfeeding WALA medicinal products available by prescription WALA medicinal products for general sale

WALA Heilmittel GmbH – a synopsis

21 565 619 18

Anthroposophical Medicine

660 658 658

WALA Compendium of Medicines

WALA medicinal products – beginnings, processes, effects Bibliography List of abbreviations

General remarks Alphabetical list of WALA medicinal products

Index of Substances General remarks Alphabetical list of active ingredients used

Index of Indications General remarks Alphabetical index of indications

Preparation Overviews WALA medicinal products by dosage form WALA medicinal products available by prescription only WALA medicinal products for general sale WALA medicinal products contraindicated during pregnancy and breastfeeding WALA medicinal products contraindicated in children

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5 6 8 10 14 18 21 22 24 565 566 568 619 621 622 643 644 658 658 660 662

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Introduction WALA Heilmittel GmbH – a synopsis

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WALA Medicines

Dr.Hauschka Med

6 7 7

Anthroposophical Medicine

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Dr.Hauschka Skin Care

WALA medicinal products – beginnings, processes, Effects

Anthropological considerations

10 10 10 11 11 12 12 12 13

Bibliography

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List of abbreviations

18

History and background of the WALA medicinal products Processes and substances Primary manufacturing processes Basic substances (mother tinctures) from plants Medicinal products from the animal kingdom Substances of mineral origin Compositions

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WALA Heilmittel GmbH – a synopsis Since its inception more than 70 years ago, WALA Heilmittel GmbH of Bad Boll/Eckwälden, near Stuttgart, has developed around 900 medicinal products and more than 130 skin care products which benefit people, conserve natural resources and are holistically derived from nature. WALA medicinal products, Dr.Hauschka Skin Care and Dr.Hauschka Med products are sold in around 40 countries around the world. The company has been owned by the WALA Foundation since 1986 and has a current workforce of about 700. Following the tradition of its founder, Dr. Rudolf Hauschka (1891-1969), the company bases its research, development and production on the principles of anthroposophy – principles which also form part of the corporate culture. All WALA‘s products originate from a carefully thought-through process in harmony with nature; for example, from WALA‘s own biodynamically managed medicinal herb garden or from the various agricultural projects sponsored by the company around the world in countries such as Burkina Faso and Bulgaria.

WALA Medicines – Nature‘s Treasures Transformed for You

Dr.Hauschka Skin Care – Composed from Nature

Dr.Hauschka Med – Medicinal Care with the Knowledge of Nature

Anthroposophical medicine was founded nearly a hundred years ago by Dr. Rudolf Steiner (18611925) and Dr. Ita Wegman (1876-1943). The holistic and integrative medical system builds on conventional medicine. It uses modern diagnostic methods and treatments and complements them with medicinal products and methods that activate the self-healing powers of the human being. Its therapeutic tools include anthroposophical medicines such as the WALA medicinal products, artistic therapies, speech therapies, counselling and physical treatments.

The Viennese chemist Dr Rudolf Hauschka wanted to expand the WALA range to include exceptional skin care products which would match the company‘s philosophy. So, in 1962, he wrote to Elisabeth Sigmund, a cosmetologist, also of Viennese origin. Hauschka was so enamoured of her reply and her unusual ideas for new approaches to skin care that he invited her to Eckwälden. Elisabeth Sigmund did not hesitate long: shortly after receiving the invitation she packed her bags and left her then home in Stockholm for Eckwälden. In a phase of intense productivity a diverse mixture of people – pharmacists, chemists, anthroposophical physicians and Elisabeth Sigmund as cosmetologist – worked together to develop the ‘WALA’ skin care range. The new brand went on the market in 1967.

In 2009, the experience gained by WALA during more than 70 years of developing Dr.Hauschka Skin Care and WALA medicinal products gave birth to Dr.Hauschka Med, a range of medicinal personal care products derived from nature and tailored to particular needs. Through their protective and harmonising qualities the Dr.Hauschka Med products provide more than normal care and help to keep skin and teeth healthy. Substances from nature form the heart of these products: natural oils and medicinal plants which are combined in the company‘s research laboratories – using state-of-the art scientific expertise and in collaboration with dermatologists, dentists, estheticians, test institutes and universities – to produce precisely thought-out care formulas.

The natural world can be divided into three realms: mineral, plant and animal. In WALA medicinal products, materials from these three natural realms are combined in precisely formulated compositions. By rhythmisation, homoeopathic potentisation and other processes the individual components are prepared in such a way that they are brought closer to the human processes and acquire healing powers. The finished composition supports the body‘s self-healing powers and so contributes to the recovery of body, soul The core idea which led to the founding of WALA and spirit. Independent studies have demonstrated the effectiveness of anthroposophical is the rhythmic production process developed by medicines. Rudolf Hauschka, a special process in which the freshly harvested medicinal herbs are treated with At present WALA offers around 900 different medicinal products for acute and chronic diswater to obtain the vital constituents, producing eases, including remedies for self-treatment of the so-called mother tincture which forms the minor ailments such as gastrointestinal upsets, basis for the medicinal products. As a result of this special processing method, these mother tinc- eye and ear problems, coughs and colds, minor injuries and many more. tures remain stable without the use of alcohol.

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This avant-garde natural cosmetics company today produces a range of more than 130 preparations: from facial care products to body washes and bath essences, personal care products to lipsticks and make-up. What they all have in common is that they are composed of highquality natural ingredients and contain medicinal herbs that support the natural functions of the skin. They are free of synthetic chemical colours, fragrances and preservatives and carry the BDIH "Certified Natural Cosmetics" seal.

Further information www.walaarzneimittel.de www.fachkreise.walaarzneimittel.de (professionals) www.dr.hauschka.de www.dr.hauschka-med.de

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Anthroposophical Medicine: A Holistic Approach

The metabolic-limb system comprises all processes in the human body involving intense metabolic activity. An example is digestion. The characteristic features of this level of organisation are There are different ways to go about helping development of heat, breakdown and movement. someone who is ill. The therapist can describe It is symbolised by the element sulphur with its the symptom and develop a treatment for it. Or he/she can ask how the symptom has come about fiery quality. In contrast to this is the nerve-sense system and what it expresses. For this he/she has to see which is associated with the central nervous the person as a whole being and in the context of his/her environment. This is the approach used system. With its qualities of coolness, rest and reduced metabolic activity it enhances clarity of by anthroposophical practitioners, who attempt consciousness and is seen as the direct opposite to understand their patients in terms of the anthroposophical concept of the human being and pole of the metabolic-limb system. Salt (sal), with its attribute of coolness, is the fitting symuse this understanding as a basis for developing a holistic treatment consisting not only of medi- bol of this system. cation, but also including advice about modifica- Two polar systems in the same body need a metion of lifestyle, or simply creating space to listen diator. This role is carried out by the rhythmic system, which is associated with respiration and to the person seeking help. the cardiovascular system. The rhythmic system, symbolised by quicksilver (mercury), connects, transforms and harmonises the external and the The Threefold Human Being internal world, the metabolic-limb system and the nerve-sense system. Anthroposophy describes the human being not only in physical, anatomical terms but also according to functional considerations. The three functional systems distinguished are: > Metabolic-Limb System > Nerve-Sense System > Rhythmic System

The Fourfold Human Being The question of the forces which maintain the form of the human body leads to a second mode of description. All earthly matter eventually decays. What is it that reverses this process in the physical body? One way of looking at this is to divide the human being into the physical body and three additional constituent elements which permeate this body: > Physical body > Etheric (life) body > Astral (feeling) body > "I" (Ego) The physical body corresponds to the physically measurable body. The three constituent elements in which it is enclosed preserve its form and structure. The etheric body gives the strength for growth, preservation and renewal as well as healing. In the fully grown organism a part of its forces are freed for the power of thinking. The astral body enables the body to move and endows the human being with a soul. The "I", the spiritual core and thus the highest level of organisation, gives the human being purpose, meaning and guidance and is what constitutes the individual personality.

Illness as Expression of Imbalance Anthroposophy sees illness as a healthy process in the wrong place or at the wrong time. For example, in the case of inflammation of the eye there is misplaced activity of the metabolic-limb system in the nerve-sense system.

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Loss of the state of equilibrium between the four constituent elements also leads to disruption of normal processes. The intestine is a good illustration of this. The complex processes of intestinal peristalsis depend on the right balance between the higher constituent elements (astral body and ego organisation) and the lower ones (etheric body and physical body). A predominance of the higher constituent elements leads to intestinal hypertonicity. In this context, abdominal pain is a ‘process of consciousness’ in the wrong place, i.e. not in the free soul but attached to an abdominal organ. Conversely, insufficient engagement of the higher constituent elements in the lower elements results in atonicity.

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History and Background of the WALA Medicinal Products WALA medicinal products are preparations whose raw materials are taken from the three realms of nature: the mineral, plant and animal kingdoms. These medicinal products originated from a fundamental aspiration, namely the desire to find an appropriate process for creating preparations from living plant organisms without the use of alcohol. This meant diverging from conventional practice and travelling new paths.

Processes and substances

Primary manufacturing processes

The essential element of all primary WALA manufacturing processes is their underlying rhythmic order. All living processes display a rhythmically structured organisation. It thus seems appropriate to use rhythmically organised processes in the preparation of substances which were originally part of a living context.

The preparation of basic substances (mother tinctures) and their potentisation are referred to as primary processes. Special methods are used, depending on whether the medicinal substances come from the plant, animal or mineral kingdom. The processes used for preparation of the basic substances of plant and animal origin were developed when the WALA medicinal products first came into being. In 1978, these pharmaceutical processing steps were integrated in the General Methods of Production of the German Homoeopathic Pharmacopoeia. These methods, which form the basis of the regulatory status of WALA medicinal products, have been adapted to the nomenclature of the pharmacopoeia and adopted in the WALA Compendium of Medicines. This means that for plant preparations and preparations originating from the animal kingdom we have used the term mother tincture in place of the WALA term basic substance which was originally used. The mineral preparations are also based on the methods of the German Homoeopathic Pharmacopoeia. Another consequence of the formal alignment of the WALA medicinal products with the pharmacopoeial methods is that a number of shorthand terms indicating certain methods of production of the Homoeopathic Pharmacopoeia had to be incorporated in the official names of the medicinal products. These obligatory shorthand terms are used in the list of medicinal products; an overview of the terms can be found on page 18 and in the index of substances on page 565.

In addition to the specific substance-related rhythmic processes, potentising according to the rules of homoeopathy is used as general proceThe endeavours to prepare and stabilise such plant dure for further processing. The manual act of extracts go back to statements by Rudolf Steiner potentising, which transforms every substance and to the collaboration with Ita Wegman, chief into the dynamic state, is also based on rhythmic sequences. Expansion and contraction, together physician of the Clinical Therapeutic Institute in with the vortex formation which generates a Arlesheim, Switzerland (4)*. In 1929, at the sugstate of chaos while simultaneously opening the gestion of Ita Wegman, Rudolf Hauschka began way for an impulse to create a new order, are systematic development work with the aim of finding methods which would do justice to plants essential elements of the potentising process (2)*. The medicinal substances in the narrower sense as living organisms and which would make it (in formal terms the active ingredients), and the possible to preserve their healing powers effecvehicles with which they are processed, together tively over a long period of time (1)*. form a single unit. Water is the ideal vehicle; it is indifferent and does not add any effect of its This work was performed in the medical laboraown to the medicinal product. Moreover, water is tory of the Arlesheim Clinic. The subsequent extremely sensitive to rhythmic impulses. Organcollaboration with the doctors at the clinic ised life cannot exist without water (3)*. Water is led to suggestions for specific pharmaceutical formulations. Together with potentised prepara- of paramount significance for the manufacture of the WALA medicinal products. Apart from tions from minerals and from basic substances certain dosage forms for external use, which of animal origin this created the foundation for require the use of oils and fat-like substances, or the later WALA medicinal products. Therefore, the manufacturing processes and the application in certain cases ethanol, water is used particularly for preparing the basic substances (mother principles of these medicines were shaped from tinctures) from plants and also as the potentising the very beginning by the extended perception of nature and the art of healing derived from the medium. For further vehicles and excipients used in specific cases the principle is always followed spiritual science of Rudolf Steiner. that they must also be of direct natural origin or – as in the case of glycerol and ethanol for example – obtained indirectly from natural substances by a simple chemical reaction.

* see literature reference on page 14 ff

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Basic substances (mother tinctures) from plants The description of the process used for preparing plant mother tinctures presented here has an exemplifying character as the detailed description at the same time serves as an illustration of general working principles. The production process is based on the life rhythm of the plant (1)*. This is shaped essentially by the cosmic terrestrial phenomenon of the rising and setting of the sun; at these times of mercurial transition the vitality of the plant is at its greatest. The plants are harvested at sunrise. This is followed immediately by the manual processing of the plant parts which are carefully sorted, cleaned, finely chopped and mixed with distilled spring water. During the next seven days the mixture is repeatedly – again at sunrise and sunset – given a movement impulse and is at the same time cooled – by placing the vessel in an ice-water mixture – and exposed to the influence of the cosmos. In the intervening periods of rest during the day and night the mixture is warmed to 37°C in a protected place. In this way the plant mixture goes through a rhythm of rest and movement and cold and heat within a cosmically oriented light rhythm. Observations of the behaviour of the mixture are documented daily. Finally, a part of the ash of the residue after pressing is added to the filtrate. After this the preparation is usually left to stand for one year. During preparation and later at yearly intervals a number of quality tests are performed which are the prerequisite for the release of the mother tincture for potentising. The mother tinctures are prepared from biodynamically grown plants, in special cases from plants collected in the wild. The production process employed for mistletoe (Viscum album), when used for cancer treatment, is different from the usual method. The extracts prepared after the summer and winter harvests are mixed mechanically using a special process.

* see literature reference on page 14 ff

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The mother tinctures obtained in this way are potentised in vicesimal steps, i.e. in a dilution ratio of 1 to 20. The resulting potencies are referred to as 'strengths', strength A designating the highest level of dilution.

Medicinal products from the animal kingdom These include > potentised preparations from invertebrates (whole animals) and their secretions, or > potentised preparations from organs and tissues of mammals (slaughtered animals), mainly from young cattle. The mother tinctures are prepared with glycerol, as a medium appropriate for the animal protein organ substances, with the addition of an aqueous saline solution. According to the definition of the German Homoeopathic Pharmacopoeia these preparations are additionally labelled "Gl". On account of its hundredfold dilution the mother tincture corresponds to "D2" (Ø = D2). This means that in the case of the organ (or animal) monopreparations labelled Gl the lowest commercially available potency available is D4. In the case of the potentised organ preparations it is essential that the organ tissue for the preparation of the mother tinctures is processed immediately after slaughter. The animals themselves are reared on farms working according to biodynamic principles. Feeding with animal meal is not allowed.

Substances of mineral origin Mineral medicinal substances are either naturally occurring minerals or mineral-like or mineral secretions of animals, e.g. oyster shells (conchae). Metals are also treated as mineral substances. Water-soluble minerals are usually dissolved in

water in a ratio of 1:9 (Ø = D1) and further potentised in an aqueous milieu. Water-insoluble minerals and metals, on the other hand, must first be finely ground according to the pharmacopoeial requirements. They are then potentised by intensive trituration with lactose. Further potentisation of these triturations in an aqueous milieu is possible from D4 upwards at the lowest. Water-insoluble substances which cannot be triturated in lactose but are soluble in ethanol, e.g. phosphorus, as well as plant secretions and resins, constitute a special case. Potentisation is performed in ethanol as far as necessary and continued in water as soon as the solubility conditions permit.

Compositions The collaboration with medical practitioners has led to the development of a large number of typical composite medicinal products or compositions. Each of these compositions forms a therapeutic unit, a medicinal product organism. Compositions are produced by co-potentising of all components through several dilution steps. A particular group of compositions are the organ-metal combinations (see overview on page 648). For the treatment of illnesses of the large internal organs and the endocrine glands there are composition preparations available which contain a potentised metal preparation that specifically addresses the organ concerned. Incorporation of the metal component considerably enhances the action of the organ preparation.

Anthropological considerations

exceeds the extent which is physiologically appropriate at a certain site in the human body, the result is illness in the form of inflammation, The underlying basis of finding the drug, the development of the compositions and the under- proliferation. In the nerve-sense system, on the other hand, the feeling and ego organisation act standing of the indications of anthroposophical from the outside in effecting breakdown of submedicine is the extended understanding of hustance, devitalisation, death. They permit sensory man beings and nature based on the spiritual perception and waking consciousness. Pathologiscience of Rudolf Steiner. Here, health, illness cally increased intervention of these constituent and healing are judged not only according to physical laws but by taking into account equally elements in the nerve-sense system leads to increased breakdown, catabolism, degeneration the attributes of higher levels of organisation, the so-called constituent elements of the human and ultimately even cancer. The cardiovascular functions and respiration of the middle rhythmic being, and their interdependence. A person‘s system link the functioning of the two polar physical body is what gives him his solid framesystems, nerve-sense system and metabolic limb work, the object of anatomical investigation, which bears a material relationship to the exter- system, in an alternating, rhythmic fashion. Herein lies the balancing, fundamentally healing nal natural mineral kingdom. On the next funcproperty of the middle system. tional level we have the processes of nutrition, growth and reproduction. These are described by Any shift in the balance of the constituent physiology and are subject to the laws of the life elements of the human organism always corresponds to a particular unbalanced formation in body, which overcomes physical decay until our the natural kingdoms outside the human being. death and which we have in common with the It is this bridge between the internal and exterplant kingdom. The feeling organisation occurs nal natural worlds which permits a truly rational for the first time in the animal kingdom. It pertherapy. This is described in the book: Fundamenmits intrapsychic qualities which are expressed in polarities such as sympathy and antipathy. On tals of Therapy. An Extension of the Art of Healing the organic level the feeling organisation effects through Spiritual-Scientific Knowledge (5)* which breakdown and elimination. The only specifically maps out for the first time a methodological human level is the ego organisation. Overcoming path to the development of drug compositions for typical illnesses. the material level and being responsible for the individuality of each human being – it provides the basis for our waking self-awareness. The manifestation of these constituent elements is specific to each site in the human body so that this differentiated interaction of the formative principles leads to the specific organ gestalt, e.g. of the lungs, liver, kidneys, and heart. The functional interaction between the described organisational levels results in a fundamental tripartite organisation of the human organism which is the precondition for an extended understanding of illness. In the metabolic limb system, the higher constituent elements of the feeling and ego organisation are submerged in the metabolic processes and effect the building up of organic matter. If this anabolic process * see literature reference on page 14 ff

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Bibliography

Further Reading

Introductory works on anthroposophical (1) Hauschka R. medicine and pharmacy Heilmittellehre: Ein Beitrag zu einer Girke M. Innere Medizin: Grundlagen und therapeutische Konzepte der Anthroposophischen Medizin Berlin: Salumed 2010 Soldner G, Stellmann H. Individuelle Pädiatrie: Leibliche, seelische und geistige Aspekte in Diagnostik und Beratung. Anthroposophisch-homöopathische Therapie Stuttgart: Wissenschaftliche Verlagsgesellschaft 2007 Gesellschaft Anthroposophischer Ärzte in Deutschland, Medizinische Sektion der Freien Hochschule für Geisteswissenschaft Dornach, Schweiz (Hrsg) Vademecum - Anthroposophische Arzneimittel Stuttgart: Gesellschaft anthroposophischer Ärzte in Deutschland 2008, CD-Version 2010

zeitgemäßen Heilmittelerkenntnis Frankfurt: Klostermann 2004 Hauschka R. Substanzlehre – Zum Verständnis der Physik, der Chemie und therapeutischer Wirkungen der Stoffe Frankfurt: Klostermann 2007 Husemann F, Wolff O, translation by Luborsky P. The Anthroposophical Approach to Medicine, Vol. 1, 2, 3 Hudson, New York: Anthroposophic Press 1982/1987/2003 Medizinisches Seminar Bad Boll (Hrsg) Anthroposophische Medizin in der Praxis 1 Berlin: Salumed 1998

Medizinisches Seminar Bad Boll (Hrsg) Anthroposophische Medizin in der Praxis 2 Medical Section of the School of Spiritual Science, Berlin: Salumed 2002 Dornach, Switzerland International Federation of Anthroposophic Medical Assosiations (IVAA) Pelikan W, translation by Meuss A.R. Association of Anthroposophic Physicians in Healing Plants – Insights Through Spiritual Science Germany (GAÄD) Spring Valley, New York: Mercury Press 1997 Vademecum of Anthroposophic Medicines (available only on CD) Pelikan W, translation by Lebensart C. Stuttgart: Gesellschaft anthroposophischer Ärzte The secrets of metals Hudson, New York: Anthroposophic Press 1973 in Deutschland 2009 Vogel H-H, translation by McKibben, M. Finding Remedies. Spiritual Knowledge of Man and Nature. A Contribution towards understanding Anthroposophie Remedies, based on the Example of the Wala Remedy Compositions. 2 volumes. Berlin: Salumed 2000

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Bühler W, translation by Collis J. Living with Your Body. The Body as an Instrument of the Soul London: Publisher Rudolf Steiner Press 1979 Hauschka R. Ernährungslehre – Zum Verständnis der Physiologie der Verdauung und der ponderablen und imponderablen Qualitäten der Nahrungsstoffe Frankfurt: Klostermann 1999

Husemann F. Wie findet man die richtige Arzneimitteldosis? Der Merkurstab 1991; 44: 120-127 (2) Schaper LC, et al. Über das Potenzieren – Originalangaben bei R. Steiner – eine Übersicht Der Merkurstab 1992; 45: 110-120 (3) Schwenk T, translation by Collis J. Sensitive Chaos: The Creation of Flowing Forms in Water and Air London: Publisher Rudolf Steiner Press 2008 Vogel H-H. Die vier Hauptorgane Herz, Niere, Leber, Lunge. Anthroposophisch-menschenkundliche Gesichtspunkte zur Entwicklungsgeschichte, Pathologie, Psychosomatik und Therapie Berlin: Salumed 1995 Vogel H-H. Organe der Ich-Organisation. Ihre Wirksamkeit in Haut, Blut und Lymphe, Pankreas und Wirbelsäule. Das Problem der Allergie Berlin: Salumed 1996 Vogel H-H. Zur Krankheitsdisposition. Krankheit und Heilung – Neurasthenie und Hysterie – Das Altern – Die Immunität und der rheumatische Formenkreis Berlin: Salumed 1997

Historic reference material (4) Hauschka R. Ita Wegmans Forschungsauftrag Beiträge zu einer Erweiterung der Heilkunst 1956; 9: 209-215

Meyer U. „Studieren Sie den Rhythmus - Rhythmus trägt Leben” Das Gespräch Steiner/Hauschka im Kontext der Arnheimer Vorträge 1924 Der Merkurstab 2008; 61: 263-269 Selg P. Rudolf Hauschka am klinisch-therapeutischen Institut in Arlesheim 1929–1940 Arlesheim: Verlag des Ita Wegman Instituts 2010

Works by Rudolf Steiner (5) Steiner R, Wegman I, translation by van Tellingen C. Fundamentals of Therapy An Extension of the Art of Healing through Spiritual-Scientific Knowledge GA 27. Spring Valley, New York: Mercury Press 1999 Steiner R, translation by Creeger C. Introducing Anthroposophical Medicine (previously published as: Spiritual Science and Medicine) Twenty lectures, Dornach 21 March - 9 April 1920 GA 312. Great Barrington, MA: Steiner Books 2010 Steiner R, translation by Karnow G. Anthroposophical Spiritual Science and Medical Therapy. The second medical course. Dornach, April 11-18, 1921 GA 313. Spring Valley, New York: Mercury Press 1991 Steiner R, translation by Karnow G, Wulsin A. Physiology and Therapeutics. Four lectures, Dornach October 7-9, 1920 From GA 314. Spring Valley, New York: Mercury Press 1986

Hauschka R. Wetterleuchten einer Zeitenwende Autobiographie Berlin: Salumed 2007 15

Steiner R, translation by Stott A. Eurythmy Therapy. Eight lectures Dornach, April 1921 and October 1922 GA 315. London: Rudolf Steiner Press 2009 Steiner R, translation by Karnow G. Meditative contemplation and instructions for deepening the art of healing. Course for Young Doctors. GA 316. Spring Valley, New York: Mercury Press 1994 Steiner R, translation by Adams M. Education for Special Needs. The Curative Education Course. 12 lectures, Dornach 25 June to 7 July 1924 GA 317. London: Rudolf Steiner Press 1998

Periodicals Der Merkurstab – Beiträge zu einer Erweiterung der Heilkunst nach geisteswissenschaftlichen Erkenntnissen. Bimonthly journal. Publisher: Gesellschaft anthroposophischer Ärzte, Stuttgart www.merkurstab.de

WALA publications

Numerous further publications, information and downloads can be found on the DocCheck®password protected internet pages of

www.fachkreise.walaarzneimittel.de. To order the WALA publications and for further information on WALA medicinal products please contact our international customer service.

To order phone +49 (0)7164 930-0 or send an email to [email protected]

WALA Compendium of Medicinies Available as a CD Vademecum An introduction to select WALA Medicines for physicians and pharmacists

Steiner R, translation by Hahn G. Broken Vessels: The Spiritual Structure of Human Organpräparate Kompendium Frailty. Dornach, September 8-18, 1924 Eine Einführung mit topographischen Zeichnungen GA 318. Great Barrington, MA: Steiner Books 2004 Steiner R, translation by Creeger C. The Healing Process: Spirit, Nature & Our Bodies. Eleven lectures, various cities, August 28, 1923-August 29, 1924 GA 319. Great Barrington, MA: Steiner Books 2010 Steiner R. Individuelle Geistwesen und einheitlicher Weltengrund. In: Individuelle Geistwesen und ihr Wirken in der Seele des Menschen. GA 178. Dornach: Rudolf Steiner Publisher 1992: 170 ff

Iscucin® Kompendium Malignomtherapie mit den Mistelpräparaten der WALA Hebammen Kompendium Natürliche Behandlung und Pflege während Schwangerschaft, Geburt und Wochenbett Pflege Kompendium Einführung in die Erwachsenenpflege mit ausgewählten WALA Arzneimitteln WALA Med Special Issues Allergien, Augenerkrankungen, Klimakterium, Neurodermitis, Rheumatische Erkrankungen, Wirbelsäulenerkrankungen, Zyklusbedingte Störungen WALA Med Special Issue Rheumatic Disorders

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List of Abbreviations The WALA medicinal products are manufactured largely according to the General Production Methods set out in the German Homoeopathic Pharmacopoeia. This applies both to the manufacture of specific dosage forms such as liquid dilutions for injection, globuli velati and eye drops, and to the preparation of the individual medicinal substances. A large number of the Methods applicable here are based on what were originally in-house WALA manufacturing formulas which were subsequently incorporated in the German Homoeopathic Pharmacopoeia; this applies particularly to methods which, in departure from conventional methods, prescribe water or oil or more dilute alcohol as the vehicle. The unambiguous labelling of the preparations manufactured according to these Methods must comply with the relevant labelling regulations; for this purpose certain shorthand terms are specified which are usually appended as suffix to the product names (e.g. Arnica montana e planta tota ferm 33c). Translations or explanations of the Latin designations of the plant parts used can be found under the respective substances in the Index of Substances starting on page 565.

aquos.

LA 25%

Aqueous solutions: according to HAB, Method 5b or aqueous preparations made from triturations: according to HAB, Method 8b.

Tinctures for external use: according to HAB, Method 12o, aqueous-alcoholic extracts produced from fresh plants or plant parts.

Decoctum

LA 25% sicc.

Heat-treated aqueous mother tinctures and liquid dilutions thereof: according to HAB, Method 23a, preparations (decoctions) produced from dried plant parts.

Tinctures for external use: according to HAB, Method 12m, aqueous-alcoholic extracts produced from dried plants or plant parts.

Decoctum LA 10% Tinctures for external use: according to HAB, Method 12k, aqueous-alcoholic extracts (decoctions) produced from fresh plant parts.

Oils for external use: according to HAB, Method 12f or 12g, respectively, extracts produced (at 37°C) from dried plants or plant parts and olive or arachis oil.

ferm. (e.g. ferm 33a)

10% or 5%

Heat-treated and fermented aqueous mother tinctures and liquid dilutions thereof (potencies): according to HAB, Methods 33a-f, 34a-i, 35a-c, 36, 37a-b and 51.

W 10% or W 5%

Oils for external use: according to HAB, Method 12h or 12i, respectively, mixtures of an essential oil with a vegetable oil (usually olive oil).

GI (= Glycerol) Gl mother tinctures and liquid dilutions thereof: according to HAB, Methods 41a-d, preparations produced from organs and tissues of higher animals and preparations produced from invertebrates (whole animal) or their secretions.

Infusum Heat-treated aqueous mother tinctures and liquid dilutions thereof: according to HAB, Method 24a, preparations (infusions) produced from dried plant parts.

K Cold-treated aqueous mother tinctures and liquid dilutions thereof (strengths): according to HAB, Method 38, preparations produced from mistletoe plants using the Iscucin process. LA 20% Tinctures for external use: according to HAB, Method 12c, aqueous-alcoholic extracts produced from fresh plants or plant parts. 18

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WALA Compendium of Medicines

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General remarks

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Alphabetical List of WALA medicinal products

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General remarks Indications

Liquid dilution for injection

Composition of the serial packs

The indications given in the Compendium and any contraindications, side-effects or warnings for patients are formulated on the basis of the respective monographs of Commission C (Commission for Regulatory Assessment of Anthroposophical Medicinal Products at the Federal Institute of Drugs and Medical Devices in Germany) and of the licences granted. The indication consists of three parts: 1. the causal disturbance in the interaction of the constituent elements of the human being 2. the resulting pathological process, followed by 3. specific indications which can be regarded as useful examples

Method of administration We recommend that you always explain the injection technique to your patient. The sites usually used for the injections are the thigh, the upper arm or the abdomen or, if specifically stated, a site in the proximity of the disease focus.

Serial pack I (former designation: organ potency series D) 4 amps. D5, 4 amps. D6, 2 amps. D8

Warning concerning gluten intolerance The medicinal products from WALA Heilmittel GmbH are gluten-free unless it is explicitly stated that the product contains gluten. The following contain gluten: › Aurum/Apis regina comp., Globuli velati › Aurum/Apis regina comp., Flüssige Verdünnung zur Injektion › Avena comp., Globuli velati › Avena comp., Flüssige Verdünnung zur Injektion › Passiflora Kinderzäpfchen › Passiflora Zäpfchen › Passiflora Nerventonikum › Triticum comp. I, Globuli velati

Warning concerning lactose intolerance The medicinal products from WALA Heilmittel GmbH are lactose-free unless it is explicitly stated in the list of ingredients that the product contains lactose.

22

Excipients of the dosage form liquid dilution for injection Sodium chloride, sodium hydrogen carbonate, water for injections.

Serial pack II (former designation: organ potency series E) 2 amps. D8, 2 amps. D10, 3 amps. D12, 2 amps. D15, 1 amp. D30 Serial pack III (former designation: organ potency series D5-D30) 2 amps. D5, 2 amps. D6, 2 amps. D8, 1 amp. D10, 1 amp. D12, 1 amp. D15, 1 amp. D30 Serial pack (former designation: organ potency series R) 1 amp. D5, 2 amps. D6, 2 amps. D8, 2 amps. D12, 2 amps. D15, 1 amp. D30

D5 Serial pack I (degeneration)

D6

D8

D10

D12

D15

D30

4 amps. 4 amps. 2 amps.

Serial pack II (inflammation)

2 amps. 2 amps. 3 amps. 2 amps. 1 amp.

Serial pack III (entire spectrum)

2 amps. 2 amps. 2 amps. 1 amp.

1 amp.

Serial pack

1 amp.

2 amps. 2 amps. 1 amp.

2 amps. 2 amps.

1 amp.

1 amp.

Dosage Serial packs I and III and serial pack: Starting with the low potencies, thus in increasing potency. Serial pack II: Starting with the high potencies, thus in decreasing potency.

23

A

Abrotanum ex herba

Composition Liquid dilution for injection: 1 ml contains: achillea millefolium ferm 33d dil. D6 1 ml

Active ingredient: artemisia abrotanum ex herba ferm 33c Globuli velati Potency/Strength Package Size Size Category D3

20 g

Composition Globuli velati: 10 g contain: artemisia abrotanum ex herba ferm 33c dil. D3 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Abrotanum ex herba.

N1

PZN

Price Group

8783243

A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: agate water aquos. Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: agate water dil. D.. aquos. 1 ml (HAB, Method 5b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1

PZN 2421177 0436499 2421237 0436507

Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Active ingredient: achillea millefolium ferm 33d Liquid dilution for injection

24

10 x 1 ml

D3

20 g

Composition Globuli velati: 10 g contain: achillea millefolium ferm 33d dil. D3 1g Contains sucrose (saccharose/sugar).

N1

PZN 2883541

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Achillea ex herba.

N1

PZN 8783272

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection

Achillea ex herba

D6

Potency/Strength Package Size Size Category

Aconitum comp.

Contraindications None known.

Potency/Strength Package Size Size Category

Side-effects None known.

Active ingredient: achillea millefolium ferm 33d Globuli velati

Contraindications None known.

Potency/Strength Package Size Size Category

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Achillea ex herba

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Achatwasser

D10 D12 D15 D30

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

A

Contraindications None known.

Price Group 31

Status

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aconitum napellus e tubere ferm 33c dil. D29 0.1 g (HAB, Method 33c) atropa belladonna e radice ferm 33b dil. D29 0.1 g (HAB, Method 33b) toxicodendron quercifolium e foliis ferm 33d dil. D29 0.1 g (HAB, Method 33d)

N1 N2

PZN 1750499 2084573

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Nerve pain (neuralgia) and nerve inflammation (neuritis) caused by increased influence of the feeling organisation in the nerve-sense system, e.g. in shingles, febrile respiratory infections and radicular syndromes.

Pharmacy only

25

A

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above inject 1 ml subcutaneously 1 to 3 times weekly to once daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor.

Aconitum e tubere

Side-effects None known.

D4 D6 D10 D20 D30

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aconitum napellus e tubere ferm 33c dil. D29 0.1 g (HAB, Method 33c) atropa belladonna e radice ferm 33b dil. D29 0.1 g (HAB, Method 33b) toxicodendron quercifolium e foliis ferm 33d dil. D29 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Nerve pain (neuralgia) and nerve inflammation (neuritis) caused by increased influence of the feeling organisation in the nerve-sense system, e.g. in shingles and radicular syndromes. Contraindications None known.

N1

PZN 8783295

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aconitum comp. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment In acute situations treatment for up to two weeks is necessary. If the symptoms still persist after this time, treatment for a longer period is possible after consulting the treating physician. Side-effects None known.

Aconitum comp. Ohrentropfen see Aconit Ohrentropfen

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aconitum napellus e tubere ferm 33c dil. D.. 1 ml (HAB, Method 33c)

Aconitum comp.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1

PZN 2899826 2899849 2883564 2899884 2899909

Price Group 31 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously or intracutaneously as a wheal 1 to 3 times a week to once daily. Side-effects None known.

Aconitum e tubere

Active ingredient: aconitum napellus e tubere ferm 33c Globuli velati Potency/Strength Package Size Size Category D6 D10 D20 D30

20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: aconitum napellus e tubere ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aconitum e tubere.

26

A

Active ingredient: aconitum napellus e tubere ferm 33c Liquid dilution for injection

N1 N1 N1 N1

PZN 8783332 8783349 8783355 8783361

Price Group A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

27

A

Aconitum e tubere W 5%, Oleum

system, e.g. inflammation of the outer-ear canal (otitis externa) and inflammation of the middle ear (otitis media).

Active ingredient: aconitum napellus e tubere W 5% Oil Potency/Strength Package Size Size Category

50 ml

Composition 10 g (11 ml) contain: aconitum napellus e tubere W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Painful states, also where there is increased sensitivity to pain, e.g. trigeminal neuralgia, shingles pain (postherpetic neuralgia). Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above rub in 2 to 3 ml oil (depending on the part

N1

PZN 2088134

Price Group V4

Status Prescription only

of the body affected) 1 to 2 times daily, then wrap in a woollen cloth. For oil dispersion baths use 3 to 5 ml of oil (approx. 1 teaspoonful) for a bath tub (approx. 200 l water). The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects None known. Note: If the medicinal product is used as bath additive with an oil dispersion bath apparatus (Jungebad®), the manufacturer‘s instructions should be followed.

Aconit Nervenöl see Aconit Schmerzöl

Aconit Ohrentropfen Ear drops

Potency/Strength Package Size Size Category

10 ml

Composition 10 g (11 ml) contain: aconitum napellus e tubere ferm 33c dil. D9 oleos. (HAB, Method 33c and 12j, in refined arachis oil) 1,0 g D-camphor 0.1 g lavandulae aetheroleum 0.1 g

28

N1

PZN 1448553

Price Group B

Status Pharmacy only

quartz dil. D9 oleos. (HAB, Method 8a and 12j, in refined arachis oil) 1.0 g Excipient: refined arachis oil. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organism and integration of metabolic processes in painful, inflammatory disorders originating in the nerve-sense

Contraindications Aconit Ohrentropfen should not be used in the case of a torn (perforated) eardrum or hypersensitivity to camphor. Warnings and precautions for use In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis).

Dosage and method of administration Unless otherwise directed, instil 1 drop of oil (warmed to body temperature) into the ear 3 to 5 times daily. Duration of treatment In acute situations treatment for up to one week may be necessary. A doctor should be consulted before continuing treatment beyond this time. Side-effects Use of this medicinal product may very rarely cause mild skin irritation.

Aconit Schmerzöl (pain-relieving oil) Oily embrocation

Potency/Strength Package Size Size Category

50 ml 100 ml

Composition 10 g (11 ml) contain: aconitum napellus e tubere ferm 33c dil. D9 oleos. (HAB, Method 33c and 12j, in refined arachis oil) 1.0 g D-camphor 0.1 g lavandulae aetheroleum 0.1 g quartz dil. D9 oleos. (HAB, Method 8a and 12j, in refined arachis oil) 1.0 g Excipient: refined arachis oil. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organism and integration of metabolic processes in painful, inflammatory disorders originating in the nerve-sense system, nerve pain (e.g. neuralgia), nerve inflammation (neuritis), shingles (herpes zoster), rheumatic joint disease.

N1 N1

PZN 1448582 1448576

Price Group L L1

Status Pharmacy only Pharmacy only

Contraindications Aconit Schmerzöl should not be used in the case of hypersensitivity to camphor. Aconit Schmerzöl should not be used in children under 6 years. Warnings and precautions for use In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub Aconit Schmerzöl into the painful parts 1 to 3 times daily. Depending on the size of the affected area, use about 1 to 3 ml of oil per application. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In very rare cases use of this medicinal product may cause skin redness and rashes.

Aconitum/China comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8783378

Price Group A

Status Pharmacy only

29

A

A

Composition Globuli velati: 10 g contain: aconitum napellus e tubere ferm 33c dil. D3 0.1 g (HAB, Method 33c) bryonia cretica ferm 33b dil. D3 0.1 g cinchona succirubra e cortice ferm 35b dil. D2 0.1 g (HAB, Method 35b) eucalyptus globulus e foliis ferm 33d dil. D2 0.1 g (HAB, Method 33d) eupatorium cannabinum ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between ego organisation and feeling organisation in febrile, flu-like infections. Contraindications Do not use in the case of sensitivity to quinine or any of the other active ingredients.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 5 times daily, in the acute stage up to every 2 hours; children from 6 to under 12 years 5-7 globuli velati sublingually 3 to 5 times daily, in the acute stage up to every 2 hours; adults and children of 12 years and above 5-10 globuli velati sublingually 3 to 5 times daily, in the acute stage up to every 2 hours. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 to 3 days a doctor should be consulted. Side-effects In rare cases hypersensitivity reactions such as skin allergies or fever can occur after taking medicines containing quinine. In such cases a doctor should be seen. Note: Sensitisation to quinine or quinidine is possible.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aconitum/China comp.



10 x 2 g

N1

1880598

Price Group P

Status Pharmacy only

Composition 1 suppository (2 g) contains: aconitum napellus e tubere ferm 33c dil. D2 2 mg (HAB, Method 33c) bryonia cretica ferm 33b dil. D2 2 mg cinchona succirubra e cortice ferm 35b dil. D1 2 mg (HAB, Method 35b) eucalyptus globulus e foliis ferm 33d dil. D1 2 mg (HAB, Method 33d) eupatorium cannabinum ex herba ferm 33c dil. D1 2 mg (HAB, Method 33c) Excipients: hard fat, honey.

between ego organisation and feeling organisation in febrile, flu-like infections.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction

Side-effects None known.

30

Potency/Strength Package Size Size Category

10 x 1 g

N1

PZN 1880747

Composition 1 suppository (1 g) contains: aconitum napellus e tubere ferm 33c dil. D2 1 mg (HAB, Method 33c) bryonia cretica ferm 33b dil. D2 1 mg cinchona succirubra e cortice ferm 35b dil. D1 1 mg (HAB, Method 35b) eucalyptus globulus e foliis ferm 33d dil. D1 1 mg (HAB, Method 33d) eupatorium cannabinum ex herba ferm 33c dil. D1 1 mg (HAB, Method 33c) Excipients: hard fat, honey.

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between ego organisation and feeling organisation in febrile, flu-like infections.

Side-effects None known.

Price Group O

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum 1 to 2 times daily. Note: Aconitum/China Comp., Suppositorien für Kinder are paediatric suppositories intended for use in infants and children under 7 years. Duration of treatment Acute disorders should clear up within 2 weeks. If no improvement occurs within 2 to 3 days a doctor should be consulted.

Liquid dilution for injection

Suppositories

PZN

Paediatric suppositories

Adonis comp.

Aconitum/China comp., Suppositorien Potency/Strength Package Size Size Category

A

Aconitum/China comp., Suppositorien für Kinder

Contraindications None known. Dosage and method of administration Unless otherwise directed, children of 7 years and above and adults 1 suppository introduced into the rectum once to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If no improvement occurs within 2 to 3 days a doctor should be consulted.

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1750507 2084596

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: adonis vernalis ferm 33d dil. D2 0.1 g crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of cardiovascular functions, particularly in patients with age-related weak heart and beginning congestive heart failure.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications Do not use in the case of known hypersensitivity to any of the active ingredients.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Side-effects None known.

31

A

Adonis comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: adonis vernalis ferm 33d dil. D2 0.1 g crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of cardiovascular functions, particularly in patients with age-related weak heart and beginning congestive heart failure. Contraindications Do not use in the case of known hypersensitivity to any of the active ingredients.

N1

PZN 8783384

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Adonis comp. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 10 globuli velati sublingually 3 to 5 times daily. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Side-effects None known.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aesculus e semine.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Aesculus e semine W 5%, Oleum



Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: aesculus hippocastanum e semine ferm 34c dil. D6 1 ml (HAB, Method 34c)

Contraindications None known.

Potency/Strength Package Size Size Category

Active ingredient: aesculus hippocastanum e semine ferm 34c Liquid dilution for injection

10 x 1 ml

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Active ingredient: aesculus hippocastanum e semine W 5% Liquid bath additive

Aesculus e semine

D6

Composition Globuli velati: 10 g contain: aesculus hippocastanum e semine ferm 34c dil. D3 1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar).

N1

PZN 2900239

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Side-effects None known.

100 ml

Composition 10 g (11 ml) contain: aesculus hippocastanum e semine W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Structuring and toning of the fluid organism in disturbances of fluid distribution and in the lymphatic, capillary and venous circulation, e.g. in disorders of the veins, rheumatoid conditions, oedematous swelling. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Aesculus e semine

N1

PZN 2088186

Price Group N1

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, for adults and children of 12 years and above use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for an oil dispersion bath (about 200 l water). The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects None known. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Active ingredient: aesculus hippocastanum e semine ferm 34c Globuli velati Potency/Strength Package Size Size Category D3

32

20 g

N1

PZN 8783444

Price Group A

Status Pharmacy only

33

A

A

Aesculus-Essenz

Active ingredient: aesculus hippocastanum e semine LA 25% sicc. Tincture for external use Potency/Strength Package Size Size Category

100 ml

Composition 10 g (10.1 ml) contain: aesculus hippocastanum e semine LA 25% sicc. 10 g (HAB, Method 12m) Indications according to the anthroposophical understanding of human beings and nature. Structuring and toning of the fluid organism in disturbances of fluid distribution and in the lymphatic, capillary and venous circulation, e.g. in disorders of the veins, rheumatoid conditions, oedematous swelling. Contraindications None known.

N1

PZN 1753836

Price Group D

Status

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Contains 25% (v/v) alcohol.

Agropyron comp.

Dosage and method of administration Unless otherwise directed, for compresses add 1 to 2 teaspoonfuls of Aesculus-Essenz to about 250 ml boiled water, soak a compress with this solution and place on the affected skin area for about 15 minutes 1 to 2 times daily; for baths add 1 to 2 tablespoons of Aesculus-Essenz to a full bath tub (about 200 l water).

Liquid dilution for injection

Side-effects None known.

Tincture for external use

Potency/Strength Package Size Size Category 100 ml

Composition 10 g (10.2 ml) contain: aesculus hippocastanum e semine LA 25% sicc. 3.0 g (HAB, Method 12m) borago officinalis ex herba LA 20% 0.5 g (HAB, Method 12c) prunus spinosa e fructibus LA 25% 3.0 g (HAB, Method 12o) quercus robur/petraea e cortice, decoctum LA 10% 3.0 g (HAB, Method 12k) solidago virgaurea ex herba LA 20% 0.5 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. Invigoration and toning of the fluid organism in conditions where there is a weakness of the life organisation in the region of the peripheral circulation, e.g. pressure sores (decubital ulcers), superficial venous inflammation with development of thrombosis (peripheral thrombophlebitis), disorders associated with varicose veins (varicose symptom complex), accumulation of fluid in the

34

N1

PZN 1753842

Price Group D

Side-effects Hypersensitivity reactions (itching, skin rash) may very rarely occur. In this case use of the preparation should be stopped and a doctor consulted.

Pharmacy only

Aesculus/Prunus comp., Essenz



Duration of treatment Acute disorders should clear up within 2 weeks. If no improvement occurs within 2 to 3 days a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor.

Status Pharmacy only

tissues (oedema), feeling of heaviness in the legs. Contraindications Do not use in the case of hypersensitivity to horse chestnut, oak bark or goldenrod herb. Warnings and precautions for use In the event of sudden onset of increased pain, rapidly increasing swelling or bluish discoloration of the legs medical advice should be sought at once as these can be signs of deep vein thrombosis which requires rapid medical intervention. Other non-invasive treatments prescribed by the doctor, such as bandaging the legs, wearing compression stockings or hosing with cold water, should always be carried out. Contains 25% (v/v) alcohol. Dosage and method of administration Unless otherwise directed, for compresses add 1 tablespoonful of the essence to approx. 250 ml of luke warm water and use for compresses; for washings add 1 tablespoon of essence to 1 l of water; for rubbing in use the undiluted essence (only use on areas of unbroken skin).

see Agropyron Inject see Agropyron Globuli velati

Agropyron Inject

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: agropyron repens e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) kalium carbonicum e cinere fagi silvaticae dil. D9 aquos. 0.1 g (HAB, Method 5b) taraxacum officinale e planta tota ferm 34c dil. D4 0.1 g (HAB, Method 34c) cinnabar dil. D6 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Respiratory infections in the region of the head such as common cold, sinusitis, tonsillitis and flu-like infections.

N1 N2

PZN 0084853 0088331

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications You must not use the medicinal product if you are allergic to milk protein. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously into the upper arm 3 times a week to once daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously into the upper arm 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously between shoulder and neck once daily. In children under 12 years the subcutaneous injection is given on the outer side of the upper arm, in adults and children of 12 years and above in the region of the shoulder or back of the neck. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Agropyron Globuli velati Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: agropyron repens e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) kalium carbonicum e cinere fagi silvaticae dil. D9 aquos. 0.1 g (HAB, Method 5b).

N1

PZN 1447861

Price Group A

Status Pharmacy only

taraxacum officinale e planta tota ferm 34c dil. D4 0.1 g (HAB, Method 34c) cinnabar dil. D6 0.1 g Contains sucrose (saccharose/sugar) and lactose.

35

A

A

Indications according to the anthroposophical understanding of human beings and nature. Respiratory infections in the region of the head such as common cold, sinusitis, tonsillitis and flu-like infections. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Agropyron Globuli velati.

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 2 to 4 times daily, in the acute stage up to every 2 hours; children under 6 years 5-7 globuli velati sublingually 2 to 4 times daily, in the acute stage up to every 2 hours; children from 6 to 12 years 8-10 globuli velati sublingually 2 to 4 times daily, in the acute stage up to every 2 hours; adults and children of 12 years and above 10-15 globuli velati sublingually 2 to 4 times daily, in the acute stage up to every 2 hours. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Composition 10 g powder contain: placenta bovis Gl dil. D7 1.0 g (HAB, Method 41b) tropaeolum majus ex herba LA 20% 2.5 g (HAB, Method 12c) Excipients: medicinal clay, maize starch.

Side-effects None known.

Contraindications The medicinal product should not be used in the case of hypersensitivity to nasturtium (tropaeolum majus).

Akne-Gesichtsdampfbad (facial steam bath for treatment of acne) Mixture for external use

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (10.3 ml) contain: bellis perennis ex herba LA 20% 9.0 g (HAB, Method 12c) tropaeolum majus ex herba LA 20% 1.0 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the metabolic processes in the skin in circumscribed purulent, inflammatory conditions, e.g. acne (acne vulgaris), overactivity of the sebaceous glands (seborrhoea). Contraindications Do not use in the case of hypersensitivity to daisies or other plants of the Compositae family. Akne-Gesichtsdampfbad should not be used while pregnant or breastfeeding.

N1

PZN 1399949

Price Group R

Dosage and method of administration Unless otherwise directed, adults and children of 6 years and above add 2 tablespoons of the tincture to 500 ml of very hot water and use as facial steam bath 1 to 3 times a week, in special cases once daily. Increase the time gradually from 5 minutes at first to 10 minutes. After the steam bath, rinse the face with cold water and dry. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment must be discussed with the doctor. Side-effects None known.

Akne-Gesichtsmaske (facial mask for treatment of acne) Powder (for external use)

36

100 g

N1

PZN 1399955

Price Group R

Side-effects In rare cases mild local skin reactions may occur.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 6 years.

Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should



Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment must be discussed with the doctor.

Status

therefore not be used in children under 6 years. Contains 25% (v/v) alcohol.

Potency/Strength Package Size Size Category

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the skin in circumscribed purulent, inflammatory conditions, e.g. acne vulgaris, overactivity of the sebaceous glands (seborrhoea).

Dosage and method of administration Unless otherwise directed, use 1 to 3 times per week, in special cases once daily. Mix 5 teaspoonfuls of powder with at least 2 teaspoonfuls of water to make a smooth paste. Apply to the face and forehead – preferably with a flat brush, otherwise with the fingers – avoiding the area immediately surrounding the eyes. Leave the mask on the face for 15 minutes to take effect, then remove with warm water. Finish by rinsing with cold water.

Status

Akne-Kapseln (capsules for treatment of acne) Hard capsule

Potency/Strength Package Size Size Category  

100 capsules

Composition 1 hard capsule contains: amethyst 5,0 mg betula pendula ferm 34e Ø 0,05 mg carbo vegetabilis 5,0 mg carvi aetheroleum 0,25 mg cochlearia officinalis ex herba ferm 33b Ø 0.05 mg (HAB, Method 33b) foeniculi amari fructus aetheroleum 0,25 mg fucus vesiculosus e planta tota ferm 51 Ø 0.05 mg (HAB, Method 51) fumaria officinalis ex herba ferm 33c Ø 0.05 mg (HAB, Method 33c) graphites dil. D11 aquos. 0,05 mg juniperus communis e fructibus ferm 35a Ø 0.05 mg (HAB, Method 35a)

N1

PZN 1399961

Price Group C1

Status Pharmacy only

oxalis acetosella e planta tota ferm 34b Ø 0.05 mg (HAB, Method 34b) rhamnus frangula e cortice ferm 33e Ø 0.05 mg (HAB, Method 33e) rosa e floribus ferm cum ferro Ø 0.05 mg (HAB, Method 37a) tropaeolum majus ex herba ferm 33b Ø 0.05 mg (HAB, Method 33b) urtica dioica e planta tota ferm 33c Ø 0.05 mg (HAB, Method 33c) viola tricolor ex herba ferm 33e Ø 0.05 mg (HAB, Method 33e) Excipients: acacia (spray-dried), gelatine, glucose syrup (spray-dried), medicinal clay, maltodextrin, purified water. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the intermediate metabolism to relieve the skin from heightened metabolic activity, e.g. acne vulgaris, overactivity of the sebaceous glands (seborrhoea).

Pharmacy only

37

A

A

Contraindications Known hypersensitivity to formulations containing birch pollen, fennel, juniper, caraway, other plants of the Umbelliferae or Compositae families, or to any other ingredients of the medicinal product • Pregnancy and breastfeeding • Children under 10 years • Hypersensitivity to iodine; people with thyroid disorders should consult a doctor before using the medicinal product • Kidney diseases • Do not take together with laxatives. Warnings and precautions for use This medicinal product contains glucose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Akne-Kapseln.

Interactions with other agents On account of possible interactions, laxatives should not be used while taking Akne-Kapseln. Dosage and method of administration Unless otherwise directed, 1 hard capsule in the morning and 2 hard capsules in the evening taken with fluid. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Gastrointestinal complaints (nausea, vomiting, diarrhoea) and allergic reactions (skin rashes, swelling and itchiness) may very rarely occur. If side-effects occur, the preparation should be discontinued and a doctor consulted.

Akne-Wasser (lotion for the treatment of acne) Mixture for external use

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (10.2 ml) contain: aesculus hippocastanum e cortice, decoctum LA 10% 0.30 g (HAB, Method 12k) anthyllis vulneraria ex herba LA 20% 0.75 g (HAB, Method 12c) bellis perennis ex herba LA 20% 0.15 g (HAB, Method 12c) calendula officinalis e floribus LA 20% 0.75 g (HAB, Method 12c) cutis feti bovis Gl dil. D5 0.10 g (HAB, Method 41b) echinacea pallida ex herba LA 20% 0.25 g (HAB, Method 12c) funiculus umbilicalis bovis Gl dil. D5 0.10 g (HAB, Method 41b) glandulae suprarenales bovis Gl dil. D5 0.10 g (HAB, Method 41a) placenta bovis Gl dil. D5 0.10 g (HAB, Method 41b) tropaeolum majus ex herba LA 20% 0.50 g (HAB, Method 12c) Excipients: ethanol 96%, purified water, lactic acid, sodium chloride, sodium hydrogen carbonate.

38

N1

PZN 1399978

Price Group R

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the skin in circumscribed purulent, inflammatory conditions, e.g. acne vulgaris, overactivity of the sebaceous glands (seborrhoea). Contraindications The preparation should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. Out of fundamental considerations Akne-Wasser should not be used by patients with progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases directed against the tissues of the patient‘s own body). Warnings and precautions for use Contains 15 % (v/v) alcohol.

Dosage and method of administration Unless otherwise directed, apply undiluted with a cotton ball and allow to soak into the skin; use twice daily.

Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea).

Allium cepa e bulbo

Active ingredient: allium cepa ferm 34a Globuli velati Potency/Strength Package Size Size Category D3

20 g

Composition Globuli velati: 10 g contain: allium cepa ferm 34a dil. D3 1g Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Allium cepa e bulbo.

N1

PZN 8783527

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Amethyst

Active ingredient: amethyst aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D15

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: amethyst dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2900676

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

39

A

A

Ammi visnaga comp., Suppositorien Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: ammi visnaga e fructibus ferm 35b Ø 20 mg (HAB, Method 35b) atropa belladonna ex herba ferm 33a Ø 4 mg (HAB, Method 33a) chamomilla recutita e radice ferm 33c Ø 12 mg (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b Ø 4 mg (HAB, Method 33b) Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the dystopic influence of the feeling organisation in the case of cramps (spasms) of the smooth muscle, particularly in the gastrointestinal tract and the organs of the small pelvis. Contraindications Do not use in the case of known hypersensitivity to chamomile or other plants of the Compositae family, to belladonna (deadly nightshade), ammi visnaga (khella) or any of the other active ingredients or excipients.

N1

PZN 1880606

Price Group V2

Status Prescription only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 7 years. Dosage and method of administration Unless otherwise directed, adults and children of 7 years and above: for acute and chronic conditions insert 1 suppository well up into the rectum 1 to 3 times daily, after a bowel movement if possible. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Very rarely, children suffering from bronchial asthma and patients with Down‘s syndrome react sensitively to constituents of deadly nightshade (Atropa belladonna) and show a temporary change in respiratory rate or increased tiredness. In such cases treatment with the preparation should be discontinued and medical advice obtained.

Ammi visnaga comp., Suppositorien für Kinder Paediatric suppositories

Potency/Strength Package Size Size Category

10 x 1 g

Composition 1 suppository (1 g) contains: ammi visnaga e fructibus ferm 35b Ø 10 mg (HAB, Method 35b) atropa belladonna ex herba ferm 33a Ø 2 mg (HAB, Method 33a) chamomilla recutita e radice ferm 33c Ø 6 mg (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b Ø 2 mg (HAB, Method 33b) Excipients: hard fat, honey.

40

N1

PZN 1880753

Price Group V1

Status Prescription only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the dystopic influence of the feeling organisation in the case of cramps (spasms) of the smooth muscle, particularly in the gastrointestinal tract and the organs of the small pelvis.

Dosage and method of administration Unless otherwise directed, children from 1 year to under 7 years: for acute and chronic conditions insert 1 suppository well up into the rectum 1 to 3 times daily, after a bowel movement if possible. Note: Ammi visnaga comp., Suppositorien für Kinder are paediatric suppositories intended for use in children from 1 to 7 years. Duration of treatment Acute disorders should clear up within 2 weeks. If there

is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Very rarely, children suffering from bronchial asthma and patients with Down‘s syndrome react sensitively to constituents of deadly nightshade (Atropa belladonna) and show a temporary change in respiratory rate or increased tiredness. In such cases treatment with the preparation should be discontinued and medical advice obtained.

Amnion Gl

Active ingredient: amnion bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: amnion bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic drug for use in anthroposophical medicine, therefore without specification of a therapeutic indication. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N2 N1 N1 N1

PZN 3359196 3359204 3359121 3359138 3359144 3359150 2831432 2900788 0847400 0845393 2493001

Price Group 61 61 61 61 61 61 61 62 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously once a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously once a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications Do not use in: • children under 1 year • known hypersensitivity to chamomile or other plants of the Compositae family, to belladonna (deadly nightshade), ammi visnaga (khella) or any of the other active ingredients or excipients.

41

A

A

Anagallis comp.

Active ingredient: anus bovis Gl Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: anagallis arvensis e planta tota ferm 33b dil. D4 0.1 g (HAB, Method 33b) cichorium intybus e planta tota ferm 33c dil. D6 0.1 g (HAB, Method 33c) kalium carbonicum e cinere fagi silvaticae dil. D6 aquos. 0.1 g (HAB, Method 5b). silybum marianum e fructibus ferm 36 dil. D4 0.1 g (HAB, Method 36) taraxacum officinale e planta tota ferm 34c dil. D4 0.1 g (HAB, Method 34c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the metabolic functions in hepatic and biliary disorders (hepatochol-

N1 N2

PZN 1750536 2084610

Price Group 11 12

Status Pharmacy only Pharmacy only

ecystopathies) accompanied by lack of appetite, feeling of fullness, flatulence and itching of the skin; eczema. Contraindications None known. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 1 to 3 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously 1 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times a week to once daily. Note: Please discard any solution left in the ampoule after the injection. Side-effects None known.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: anagallis arvensis e planta tota ferm 33b dil. D2 0.1 g (HAB, Method 33b) cichorium intybus e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) kalium carbonicum e cinere fagi silvaticae dil. D5 aquos. 0.1 g (HAB, Method 5b). silybum marianum e fructibus ferm 36 dil. D2 0.1 g (HAB, Method 36) taraxacum officinale e planta tota ferm 34c dil. D2 0.1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the metabolic functions in hepatic and biliary disorders (hepatocholecystopathies) accompanied by lack of appetite, feeling of fullness, flatulence and itching of the skin; eczema.

42

N1

PZN 8783579

Price Group A

D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: anus bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic drug for use in anthroposophical medicine, therefore without specification of a therapeutic indication.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2900831 2900854 2900877 2900908 2900920 2900943 2900972 2493018

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Anagallis comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Potency/Strength Package Size Size Category

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Anagallis comp.



A

Anus Gl

Liquid dilution for injection

Aorta (tota) Gl

Active ingredient: aorta tota bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aorta tota bovis Gl dil. D.. 1 ml (HAB, Method 41c)

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2901434 2901457 2901486 2901500 2901523 2901552 2901575 2493107

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic drug for use in anthroposophical medicine, therefore without specification of a therapeutic indication.

43

A

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Apis/Arnica

Duration of treatment The duration of treatment should be discussed with the doctor.

Potency/Strength Package Size Size Category

Side-effects None known.

Active ingredient: apis mellifica ex animale toto Gl Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D.. 1 ml (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the warmth organism and structuring of the metabolic activity in localised inflammatory processes and disorders of the peripheral metabolic organisation, e.g. lacunar tonsillitis, adjuvant treatment of inflammation of the lymphatics (lymphangitis), inflammation of the uterine appendages (adnexitis); rheumatic disorders including acute inflammatory episodes; urticarial rashes. Contraindications The medicinal product should not be used in the case of hypersensitivity to bee venom. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reac-

44

N1 N1 N1 N1 N1 N1 N1 N2

PZN 4614667 2831780 4614696 3359233 3359256 3353265 2829381 2901658

Liquid dilution for injection



10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c) arnica montana e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c)

Apis ex animale Gl

D5 D6 D8 D12 D15 D20 D30 D30

A

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Price Group 61 61 61 61 61 61 61 62

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

tions is likely to be increased if the drug is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within two days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the warmth organism and stimulation of the formative powers in inflammatory and degenerative disorders, e.g. spinal syndromes, nerve pain (neuralgia), nerve inflammation (neuritis), shingles (herpes zoster), rheumatic joint diseases, muscular knots (myogelosis). Contraindications Do not use in the case of known hypersensitivity to bee venom, arnica or other members of the Compositae family. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

N1

PZN 1750559

Price Group 11

Status Pharmacy only

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In very rare cases hypersensitivity reactions may occur; in this case treatment with the medicinal product should be discontinued. In rare cases harmless redness around the injection site can occur. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the drug is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate.

Apis/Arnica Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c). arnica montana e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

N1

PZN 8783616

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the warmth organism and stimulation of the formative powers in inflammatory and degenerative disorders, e.g. spinal syndromes, nerve pain (neuralgia), rheumatic joint diseases, muscular knots (myogelosis); for adjunctive treatment of nerve inflammation (neuritis) and shingles (herpes zoster).

Side-effects None known.

45

A

Contraindications Do not use in the case of known hypersensitivity to bee venom, arnica or other members of the Compositae family. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 6 years. In children between 6 and 12 years medical advice should be sought before using the preparation and it should not be used in place of any other medication prescribed by the doctor. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Apis/Arnica.

Dosage and method of administration Unless otherwise directed, adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 5 times daily.

Apis Belladonna Globuli velati

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.



Side-effects Hypersensitivity reactions may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted.

Apis Belladonna Inject Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c). atropa belladonna e fructibus ferm 33a dil. D3 0.1 g (HAB, Method 33a) Indications according to the anthroposophical understanding of human beings and nature. Incipient and chronically recurrent inflammatory conditions with or without fever, particularly those of the oronasopharynx and the skin, e.g. cellulitis involving the superficial layers of the skin (erysipelas), inflammation of the breast (mastitis), inflammation of the lymphatics (lymphangitis), inflammation of the middle ear (otitis media). Contraindications Do not use in the case of known hypersensitivity to bee venom. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The

46

N1 N2

PZN 0084899 0088348

Price Group 11 12

Status Pharmacy only Pharmacy only

risk of such reactions is likely to be increased if the drug is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 2 to 3 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously 2 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week to once daily. Duration of treatment There is no evidence suggesting that prolonged use of the preparation may have negative effects. However, as treatment of the above conditions usually takes a maximum of two weeks, the preparation should only be used for longer periods if expressly ordered by the doctor. Side-effects Harmless redness may occur around the injection site after injection.

A

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c). atropa belladonna e fructibus ferm 33a dil. D3 0.1 g (HAB, Method 33a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Incipient and chronically recurrent inflammatory conditions with or without fever, particularly those of the oronasopharynx and the skin, e.g. cellulitis involving the superficial layers of the skin (erysipelas), inflammation of the breast (mastitis), inflammation of the lymphatics (lymphangitis), inflammation of the middle ear (otitis media). Contraindications Do not use in the case of known hypersensitivity to bee venom.

N1

PZN 0084882

Price Group A

Status Pharmacy only

consult your doctor before taking Apis Belladonna Globuli velati. Dosage and method of administration Unless otherwise directed, infants and children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, in the acute stage every 1 to 2 hours; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily, in acute cases every 1 to 2 hours. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment There is no evidence suggesting that prolonged use of the preparation may have negative effects. However, as treatment of the above conditions usually takes a maximum of two weeks, the preparation should only be used for longer periods if expressly ordered by the doctor. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should

Apis/Belladonna cum Mercurio Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c). atropa belladonna e fructibus ferm 33a dil. D3 0.1 g (HAB, Method 33a) mercurius solubilis Hahnemanni dil. D14 aquos. 0.1 g

N1 N2

PZN 0084899 0088348

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation and life organisation in locally circumscribed – also purulent and abscess-forming – inflammatory conditions, e.g. inflammation of the tonsils (tonsillitis), mouth ulcers (aphthous stomatitis), purulent skin conditions (pyoderma), boils (furunculosis).

47

A

Contraindications The preparation should not be used in the case of hypersensitivity to bee venom. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the drug is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 1 to 3 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously 1 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times a week to once daily. Duration of treatment The condition should have cleared up within two weeks. If there is no improvement within two days a doctor should be consulted. Side-effects Harmless redness around the injection site can occur after subcutaneous injection.

Apis/Belladonna cum Mercurio Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c). atropa belladonna e fructibus ferm 33a dil. D3 0.1 g (HAB, Method 33a) mercurius solubilis Hahnemanni dil. D14 aquos. 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation and life organisation in locally circumscribed – also purulent and abscess-forming – inflammatory conditions, e.g. inflammation of the tonsils (tonsillitis), mouth ulcers (aphthous stomatitis), purulent skin conditions (pyoderma), boils (furunculosis). Contraindications Do not use in the case of known hypersensitivity to bee venom.

48

N1

PZN 0084882

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Apis/Belladonna cum Mercurio. Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, in acute cases temporarily every 1 to 2 hours; children under 6 years 5-7 globuli velati sublingually 1 to 3 times daily, in acute cases temporarily every 1 to 2 hours; adults and children of 6 years and above 8-10 globuli velati sublingually 1 to 3 times daily, in acute cases temporarily every 1 to 2 hours. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted.

In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The possibility of allergic reactions, such as transient skin rashes or diarrhoea, being triggered in rare cases by the

bee venom (apis) contained in the medicinal product cannot be ruled out. In such cases treatment with Apis/ Belladonna cum Mercurio Globuli velati should be discontinued.

Apis/Bryonia

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c) bryonia cretica ferm 33b dil. D2 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between ego organisation and feeling organisation in painful inflammatory and degenerative disorders with swelling, particularly in the musculoskeletal system, e.g. rheumatic disorders of the joints and surrounding tissues; low back pain. Contraindications Do not use in the case of known hypersensitivity to bee venom. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product

N1 N2

PZN 1750588 2084685

Price Group 11 12

Status Pharmacy only Pharmacy only

has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the drug is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 2 to 3 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously 2 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week to once daily. Side-effects Harmless redness may occur around the injection site after injection.

Apis/Bryonia Globuli velati

Potency/Strength Package Size Size Category Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c)

20 g

N1

PZN 8783645

Price Group A

Status Pharmacy only

bryonia cretica ferm 33b dil. D2 0.1 g Contains sucrose (saccharose/sugar).

49

A

A

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between ego organisation and feeling organisation in painful inflammatory and degenerative disorders with swelling, particularly in the musculoskeletal system, e.g. rheumatic disorders of the joints and surrounding tissues; low back pain.

therefore not be used in children under 6 years. In children between 6 and 12 years medical advice should be sought before using the medicinal product and it should not be used in place of any other medication prescribed by the doctor. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Apis/Bryonia.

Contraindications Do not use in the case of known hypersensitivity to bee venom.

Dosage and method of administration Unless otherwise directed, adults and children of 6 years and above 5-10 globuli velati sublingually once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

Side-effects None known.

Apis/Levisticum I

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D3 0.1 g (HAB, Method 41c) levisticum officinale e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of ego organisation and feeling organisation in acute inflammatory, painful conditions of the nerve-sense system and the metabolic-limb system, e.g. inflammation of a nerve (neuritis), nerve pain (neuralgia), muscle pain (myalgia), inflammation of the middle ear (otitis media). Contraindications Do not use in the case of known hypersensitivity to bee venom. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The

50

N1

PZN 0447646

Price Group 11

Status Pharmacy only

risk of such reactions is likely to be increased if the drug is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously twice a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously twice a week to once daily; adults and children of 12 years and above 1 ml as subcutaneous or intramuscular injection twice a week to once daily. Duration of treatment Treatment for a period of not more than three weeks is usually sufficient. If treatment for a longer period is necessary please obtain your doctor‘s advice first. Side-effects Harmless redness may occur around the injection site after injection.

A

Apis/Levisticum I Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D3 0.1 g (HAB, Method 41c) levisticum officinale e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of ego organisation and feeling organisation in acute inflammatory, painful conditions of the nerve-sense system and the metabolic-limb system, e.g. inflammation of a nerve (neuritis), nerve pain (neuralgia), muscle pain (myalgia), inflammation of the middle ear (otitis media). Contraindications Do not use in the case of known hypersensitivity to bee venom. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Apis/Levisticum I.

N1

PZN 0271756

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 2 to 3 times daily, in the acute stage up to every 2 hours; children under 6 years 5-7 globuli velati sublingually 2 to 3 times daily, in the acute stage up to every 2 hours; children from 6 to under 12 years 8-10 globuli velati sublingually 2 to 3 times daily, in the acute stage up to every 2 hours; adults and children of 12 years and above 5-10 globuli velati sublingually 2 to 3 times daily, in the acute stage up to once an hour. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Treatment for a period of not more than three weeks is usually sufficient. If treatment for a longer period is necessary please obtain your doctor‘s advice first. Side-effects None known.

Apis/Levisticum II

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c) levisticum officinale e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of ego organisation and feeling organisation in acute inflammatory, painful conditions of the nerve-sense sys-

N1 N2

PZN 0447669 0447675

Price Group 11 12

Status Pharmacy only Pharmacy only

tem and the metabolic-limb system, e.g. inflammation of a nerve (neuritis), nerve pain (neuralgia), muscle pain (myalgia), inflammation of the middle ear (otitis media). Contraindications Do not use in the case of known hypersensitivity to bee venom. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic

51

A

reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the drug is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously twice a week to once daily; children

Apis regina Gl

Duration of treatment Treatment for a period of not more than three weeks is usually sufficient. If treatment for a longer period is necessary please obtain your doctor‘s advice first.

Potency/Strength Package Size Size Category

Side-effects Harmless redness may occur around the injection site after injection.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c) levisticum officinale e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of ego organisation and feeling organisation in acute inflammatory, painful conditions of the nerve-sense system and the metabolic-limb system, e.g. inflammation of a nerve (neuritis), nerve pain (neuralgia), muscle pain (myalgia), inflammation of the middle ear (otitis media). Contraindications Do not use in the case of hypersensitivity to bee venom. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Apis/Levisticum II.

Active ingredient: apis regina tota Gl Liquid dilution for injection

D5 D8 D12 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis regina tota Gl Dil. D.. 1 ml (HAB, Method 41c)

Apis/Levisticum II



N1

PZN 0271733

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 2 to 4 times daily, in the acute stage up to every 2 hours; children under 6 years 5-7 globuli velati sublingually 2 to 4 times daily, in the acute stage up to every 2 hours; children from 6 to under 12 years 8-10 globuli velati sublingually 2 to 4 times daily, in the acute stage up to every 2 hours; adults and children of 12 years and above 5-10 globuli velati sublingually 2 to 3 times daily, in the acute stage up to once an hour. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Treatment for a period of not more than three weeks is usually sufficient. If treatment for a longer period is necessary please obtain your doctor‘s advice first. Side-effects None known.

Indications Registered homeopathic drug for use in anthroposophical medicine, therefore without specification of a therapeutic indication. Contraindications Do not use in the case of known hypersensitivity to bee venom.

N1 N1 N1 N1 N1

PZN 4614710 4614733 4614762 4626104 2901724

Price Group 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Apis regina comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis regina tota Gl dil. D16 0.1 g (HAB, Method 41c) truncus cerebri bovis Gl dil. D7 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the vitalising and formative regenerative processes in the nervous system, e.g. in degenerative and traumatic changes. Contraindications Do not use in the case of known hypersensitivity to bee venom.

52

A

from 6 to under 12 years: 0.5-1 ml injected subcutaneously twice a week to once daily; adults and children of 12 years and above 1 ml as subcutaneous or intramuscular injection twice a week to once daily.

N1 N2

PZN 1750619 2084633

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for usee Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment The disorder should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

53

A

Apis regina comp.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apis regina tota Gl dil. D16 0.1 g (HAB, Method 41c) truncus cerebri bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the vitalising and formative regenerative processes in the nervous system, e.g. in degenerative and traumatic changes. Contraindications Do not use in the case of known hypersensitivity to bee venom.

N1

PZN 8783591

Price Group A

Status

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually once daily; adults and children of 6 years and above 5-10 globuli velati sublingually once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The disorder should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that

Appendix vermiformis Gl

Active ingredient: appendix vermiformis cuniculi GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: appendix vermiformis cuniculi Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic drug for use in anthroposophical medicine, therefore without specification of a therapeutic indication.

54

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2901836 2901859 2901871 2901894 2901919 2901931 2901954 2493113

Price Group 61 61 61 61 61 61 61 51

Side-effects None known.

Pharmacy only

you suffer from intolerance to certain sugars you should consult your doctor before taking Apis regina comp.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Duration of treatment The duration of treatment should be discussed with the doctor.

Aquilinum comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: chelidonium majus e floribus ferm 34b dil. D4 0.1 g (HAB, Method 34b) dryopteris filix-mas e radice ferm 33c dil. D4 0.1 g (HAB, Method 33c) phyllitis scolopendrium e foliis ferm 34h dil. D4 0.1 g (HAB, Method 34h) pteridium aquilinum e foliis ferm 34c dil. D4 0.1 g (HAB, Method 34c) solidago virgaurea ex herba ferm 33c dil. D4 0.1 g (HAB, Method 33c) taraxacum officinale e planta tota ferm 34c dil. D4 0.1 g (HAB, Method 34c) Indications according to the anthroposophical understanding of human beings and nature. Digestive weakness with impairment of motility and secretion in the gastrointestinal tract, e.g. abdominal gas (flatulence), diarrhoea, constipation, dysbiosis, tendency to worm infections; eczema. Contraindications Do not use in the case of known allergy to any of the ingredients. In the case of a history of liver disease and/ or concomitant use of substances that can damage the liver, Aquilinum comp. should only be used after consulting a doctor. Do not use while pregnant or breastfeeding.

N1 N2

PZN 1750625 2084722

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 to 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. If the medicinal product is used for more than 4 weeks liver function tests should be carried out (determination of transaminases). Side-effects Increases in liver function values (transaminases) and bilirubin, including drug-induced jaundice (toxic hepatitis), have very rarely been observed during treatment with medicinal products containing chelidonium (celandine) alkaloids. If such reactions occur, treatment with the medicinal product should be discontinued and a doctor consulted.

Aquilinum comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8783680

Price Group A

Status Pharmacy only

55

A

A

Composition Globuli velati: 10 g contain: chelidonium majus e floribus ferm 34b dil. D2 0.1 g (HAB, Method 34b) dryopteris filix-mas e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) phyllitis scolopendrium e foliis ferm 34h dil. D2 0.1 g (HAB, Method 34h) pteridium aquilinum e foliis ferm 34c dil. D2 0.1 g (HAB, Method 34c) solidago virgaurea ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) taraxacum officinale e planta tota ferm 34c dil. D2 0.1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Digestive weakness with impairment of motility and secretion in the gastrointestinal tract, e.g. abdominal gas (flatulence), diarrhoea, constipation, dysbiosis, tendency to worm infections; eczema. Contraindications Do not use in the case of known allergy to any of the ingredients. In the case of a history of liver disease and/or concomitant use of substances that can damage the liver, Aquilinum comp. should only be used after consulting a doctor. Do not use while pregnant or breastfeeding.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aquilinum comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 5 times daily; children from 6 to under 12 years 5-7 globuli velati sublingually 3 to 5 times daily; adults and children of 12 years and above 5-10 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 to 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. If the medicinal product is used for more than 4 weeks liver function tests should be carried out (determination of transaminases). Side-effects Increases in liver function values (transaminases) and bilirubin, including drug-induced jaundice (toxic hepatitis), have very rarely been observed during treatment with medicinal products containing chelidonium (celandine) alkaloids. If such reactions occur, treatment with the medicinal product should be discontinued and a doctor consulted.

Aranea ex animale Gl

D8 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aranea diadema ex animale toto Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic drug for use in anthroposophical medicine, therefore without specification of a therapeutic indication.

56

N1 N1 N1

A

Side-effects None known.

Duration of treatment The duration of treatment should be discussed with the doctor.

Archangelica comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: angelica archangelica e radice ferm 33c dil. D4 0.1 g (HAB, Method 33c) argentum nitricum dil. D14 aquos. 0.1 g (HAB, Method 5b). hyoscyamus niger ex herba ferm 33d dil. D6 0.1 g (HAB, Method 33d) pyrite dil. D6 0.1 g salvia officinalis e foliis ferm 33d dil. D2 0.1 g (HAB, Method 33d)

N1 N2

PZN 1750631 2084739

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of allergy to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Archangelica comp.

Active ingredient: aranea diadema ex animale toto Gl Liquid dilution for injection Potency/Strength Package Size Size Category

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Globuli velati PZN

4626127 2902209 4614822

Price Group 61 61 61

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only



Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

20 g

Composition Globuli velati: 10 g contain: angelica archangelica e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) argentum nitricum dil. D14 aquos. 0.1 g (HAB, Method 5b). hyoscyamus niger ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) pyrite trit. D2 0.5 g salvia officinalis e foliis ferm 33d Ø 0.25g (HAB, Method 33d) Contains sucrose (saccharose/sugar) and lactose.

N1

PZN 8783697

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Inflammatory conditions of the airways, e.g. inflammation of the vocal cords (laryngitis), inflammation of the windpipe (tracheitis), dry tickly cough. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Archangelica comp.

57

A

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Argentum nitricum comp.

Side-effects None known.

Potency/Strength Package Size Size Category

Liquid dilution for injection

Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum nitricum dil. D19 aquos. 0.1 g (HAB, Method 5b). chlorophyceae ferm 33e dil. D2 0.1 g (HAB, Method 33e) echinacea pallida e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) eucalyptus globulus e foliis ferm 33d Ø 0.05 g (HAB, Method 33d) thuja occidentalis e summitatibus ferm 33e dil. D2 0.1 g (HAB, Method 33e) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation and structuring of anabolic processes in infectious febrile to septic, also chronic recurrent inflammatory disorders, e.g. of the genitourinary system, in the head and neck region, of the skin. Contraindications Argentum nitricum comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to plants of the Compositae family. Do not use in children under 2 years. Out of fundamental considerations, Argentum nitricum comp. should not be used by patients with progressive systemic diseases such as tuberculosis, leukoses (leukaemia

N1 N2

PZN 1750648 2084745

Globuli velati



Argentum nitricum comp.



A

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Price Group 11 12

Status Pharmacy only Pharmacy only

or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases caused by a reaction of the individual‘s immune system against the organs or tissues of his or her own body). Dosage and method of administration Unless otherwise directed, children from 2 to under 6 years 0.5 ml by intramuscular injection 1 to 3 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml by intramuscular injection 1 to 3 times a week to once daily; adults and children of 12 years and above 1 ml by intramuscular injection 1 to 3 times a week to once daily. Duration of treatment Argentum nitricum comp. should not be used continuously for more than 2 weeks. In the case of chronic recurrent courses longer treatment is possible after consultation with the treating physician. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicine and see a doctor.

20 g

Composition Globuli velati: 10 g contain: argentum nitricum dil. D19 aquos. 0.1 g (HAB, Method 5b). chlorophyceae ferm 33e dil. D2 0.1 g (HAB, Method 33e) echinacea pallida e planta tota ferm 33c dil. D1 0.1 g (HAB, Method 33c) eucalyptus globulus e foliis ferm 33d Ø 0.5 g (HAB, Method 33d) thuja occidentalis e summitatibus ferm 33e dil. D2 0.1 g (HAB, Method 33e) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation and structuring of anabolic processes in infectious febrile to septic, also chronic recurrent inflammatory disorders, e.g. of the genitourinary system, in the head and neck region, of the skin. Contraindications Argentum nitricum comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. Out of fundamental considerations, Argentum nitricum comp. should not be used by patients with progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases

N1

Price Group A

Status Pharmacy only

caused by a reaction of the individual‘s immune system against the organs or tissues of his or her own body). Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Argentum nitricum comp. Dosage and method of administration Unless otherwise directed, infants and children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, in acute cases every 1 to 2 hours; in this treatment phase the daily dose can be up to 7 x 5 (35) globuli velati per day. Adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily, in acute cases every 1 to 2 hours; in this treatment phase the daily dose can be up to 7 x 10 (70) globuli velati per day. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Argentum nitricum comp. should not be used continuously for more than 2 weeks. In the case of chronic recurrent courses longer treatment is possible after consultation with the treating physician. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicine and see a doctor.

Argentum/Quarz

Liquid dilution for injection Potency/Strength Package Size Size Category

58

PZN 8783705

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1750654 2084751

Price Group 11 12

Status Pharmacy only Pharmacy only

59

A

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D19 aquos. 0.1 g quartz dil. D29 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Structuring of dystopic and heightened metabolic processes in local inflammatory conditions with a tendency towards suppuration and sepsis, e.g. inflammation of the paranasal sinuses (sinusitis), ear infections (otitis),

bacterial infection of the skin and underlying tissues (cellulitis), inflammation of the lymph glands (lymphadenitis). Contraindications None known. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously twice weekly, in the acute stage up to 3 times daily; adults and children of 6 years and above 1 ml injected subcutaneously twice weekly, in the acute stage up to 3 times daily. Side-effects None known.

Argentum/Quarz

Composition Globuli velati: 10 g contain: argentum metallicum dil. D19 aquos. 0.1 g quartz dil. D29 aquos. 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Structuring of dystopic and heightened metabolic processes in local inflammatory conditions with a tendency towards suppuration and sepsis, e.g. inflammation of the paranasal sinuses (sinusitis), ear infections (otitis), cellulitis, inflammation of the lymph glands (lymphadenitis). Contraindications None known.

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 1 to 3 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected sub-

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Contraindications Do not use in the case of allergy to milk protein.

cutaneously 1 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times a week to once daily.

Argentum/Rohrzucker

Globuli velati



Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation and vital upbuilding forces in states of exhaustion and shock sequelae as well as in susceptibility to seizures due to physical or psychological trauma.

N1

PZN 8783711

Price Group A

Status

Potency/Strength Package Size Size Category

Pharmacy only



Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Argentum/Quarz. Dosage and method of administration Unless otherwise directed, infants 3-5 globuli velati sublingually 3 to 5 times daily; children under 6 years 5-7 globuli velati sublingually 3 to 5 times daily; adults and children of 6 years and above 8-10 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D5 0.1 g saccharum sacchari dil. D9 aquos. 0.1 g (HAB, Method 5b). Contains sucrose (saccharose/sugar) and lactose.

N1

PZN 8783728

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Argentum/ Rohrzucker.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation and vital upbuilding forces in states of exhaustion and shock sequelae as well as in susceptibility to seizures due to physical or psychological trauma.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Contraindications None known.

Side-effects None known.

Arnica e floribus W 5%, Oleum

Active ingredient: arnica montana e floribus W 5% Liquid bath additive

Argentum/Rohrzucker Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D5 0.1 g

60

N1 N2

PZN 1750660 2084768

Price Group 11 12

saccharum sacchari dil. D9 aquos. 0.1 g (HAB, Method 5b).

Status Pharmacy only Pharmacy only

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: arnica montana e floribus W 5% (HAB, Method 12g with virgin olive oil) 10 g

PZN 2088217

Price Group N1

Status General sale

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of tissue and organ healing with particular emphasis on metabolic processes, e.g. blunt injuries such as pulled muscles or ligaments,

61

A

A

contusions, bruises, muscle soreness; myogelosis (muscular knots), subacute and chronic inflammatory joint disease; adjunctive treatment after concussion, stroke, palsies. Contraindications Do not use Arnica e floribus W 5%, Oleum • in the case of known hypersensitivity to formulations of arnica or other plants of the Compositae family such as chrysanthemum or yarrow, or to any other ingredient of the medicinal product • on damaged skin (e.g. injured or burned skin) • during pregnancy Warnings and precautions for use The medicinal product should not be used in children with subacute or chronic inflammatory joint disease or in patients with concussion, stroke or palsies without first obtaining medical advice and should not be used in place of any medication prescribed by the doctor.

Dosage and method of administration Unless otherwise directed, use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for an oil dispersion bath (about 200 l water). The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously twice a week; children from 6 to 12 years 0.5-1 ml injected subcutaneously twice a week; adults and children of 12 years and above 1 ml injected subcutaneously twice a week.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Duration of treatment Acute disorders should clear up within 2 weeks. If there

Side-effects Hypersensitivity reactions may occur in sensitised persons. In this case use of the medicinal product should be stopped and a doctor consulted. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Arnica e planta tota

Active ingredient: arnica montana e planta tota ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D2 D3 D3 D4 D6 D10 D12 D15 D20 D20 D30 D30

10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D.. 1 ml (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the metabolic and formative processes after tissue or organ damage, particularly after damage caused by extraneous mechanical forces or insufficient blood supply to the

62

N1 N1 N2 N1 N1 N1 N1 N1 N1 N2 N1 N2

PZN 3358009 3358015 2902416 3358021 2830415 3358038 3358044 3358050 2832644 2902474 2832667 2902480

Price Group 31 31 32 31 31 31 31 31 31 32 31 32

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

tissues (mechanical or ischaemic injury), e.g. restriction of voluntary movement, sore muscles, sprains and strains, bruises; follow-up treatment after heart attack, followup treatment after stroke (CVA), adjunctive treatment of angina pectoris, concussion; late effects of psychological shock experiences, adjunctive treatment of multiple sclerosis. Contraindications Do not use in the case of hypersensitivity to arnica or other plants of the Compositae family.

is no improvement within three days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted.

Arnica e planta tota

Active ingredient: arnica montana e planta tota ferm 33c Globuli velati Potency/Strength Package Size Size Category D2 D3 D4 D6 D10 D12 D15 D20 D30

20 g 20 g 20 g 20 g 20 g 20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the metabolic and formative processes after tissue or organ damage, particularly after damage caused by extraneous mechanical forces or insufficient blood supply to the tissues (mechanical or ischaemic injury), e.g. restriction of voluntary movement, sore muscles, sprains and strains, bruises; follow-up treatment after heart attack, follow-up treatment after stroke (CVA), concussion; late effects of psychological shock experiences. Contraindications D2, 3, 4, 6: Do not use in the case of hypersensitivity to arnica or other plants of the Compositae family. D10, 12, 15, 20, 30: None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Arnica e planta tota.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 8783763 8783786 8783792 8783800 8783817 8783823 8783846 8783852 8783869

Price Group A A A A A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration D2, D3, D4, D6: Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. D10, D12, D15, D20, D30: Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually once daily; adults and children of 6 years and above 5-10 globuli velati sublingually once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within three days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects D2, 3, 4, 6: Hypersensitivity reactions may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted. D10, 12, 15, 20, 30: None known.

63

A

A

Arnica/Aurum I

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 0454563

Price Group 11

Status

Potency/Strength Package Size Size Category

Pharmacy only



Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) aurum metallicum dil. D9 0.1 g

Contraindications Do not use in the case of allergy to milk protein.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic organisation for harmonisation of formative and metabolic processes in degenerative and congestive cardiovascular diseases, also in the presence of organic lesions, e.g. high blood pressure (hypertension), angina; follow-up treatment of stroke and myocardial infarction; accompanying agitation and anxiety states.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Arnica/Aurum I

N1 N2

PZN 0454617 0454646

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) aurum metallicum dil. D29 aquos. 0.1 g

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic organisation for harmonisation of formative and metabolic processes in degenerative and congestive cardiovascular diseases, also in the presence of organic lesions, e.g. high blood pressure (hypertension), angina; follow-up treatment of stroke and myocardial infarction; accompanying agitation and anxiety states.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Side-effects None known.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) aurum metallicum dil. D9 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic organisation for harmonisation of formative and metabolic processes in degenerative and congestive cardiovascular diseases, also in the presence of organic lesions, e.g. high blood pressure (hypertension), angina; follow-up treatment of stroke and myocardial infarction; accompanying agitation and anxiety states.

64

10 x 1 ml 50 x 1 ml

Arnica/Aurum II

Globuli velati



A

Arnica/Aurum II

Liquid dilution for injection

N1

PZN 0454592

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Arnica/ Aurum I. Dosage and method of administration Unless otherwise directed, infants and children under 6 years 3-5 globuli velati 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) aurum metallicum dil. D29 aquos. 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic organisation for harmonisation of formative and metabolic processes in degenerative and congestive cardiovascular diseases, also in the presence of organic lesions, e.g. high blood pressure (hypertension), angina; follow-up treatment of stroke and myocardial infarction; accompanying agitation and anxiety states.

N1

PZN 0454675

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Arnica/Aurum II. Dosage and method of administration Unless otherwise directed, infants and children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

65

A

Arnica/Plumbum comp. A Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D28 0.01 g (HAB, Method 33c) betula pendula e cortice, decoctum dil. D3 0.01 g (HAB, Method 23a) cerebellum bovis Gl dil. D15 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D15 0.01 g (HAB, Method 41a) hypophysis bovis Gl dil. D15 0.01 g (HAB, Method 41a) iris bovis Gl dil.D15 0.01 g (HAB, Method 41b) medulla oblongata bovis Gl dil. D15 0.01 g (HAB, Method 41a) nervus opticus bovis Gl dil. D15 0.01 g (HAB, Method 41a) plumbum mellitum dil. D28 aquos. 0.02 g (HAB, Method 8b) retina et chorioidea bovis Gl dil. D15 0.01 g (HAB, Method 41c) thalamus bovis Gl dil. D15 0.01 g (HAB, Method 41a)

N1 N2

PZN 1750708 2084840

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers through the ego organisation in sclerotic changes of the blood vessels of the brain and the eye, e.g. for adjunctive treatment of cerebral circulatory disorders, status post stroke and degenerative changes of the eye.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Arnica/Plumbum comp. A Globuli velati



20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D28 0.01 g (HAB, Method 33c) betula pendula e cortice, decoctum Ø 0.01 g (HAB, Method 23a) cerebellum bovis Gl dil. D15 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D15 0.01 g (HAB, Method 41a) hypophysis bovis Gl dil. D15 0.01 g (HAB, Method 41a)

66

N1

8783958

Contraindications None known.

Side-effects None known.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

Liquid dilution for injection

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

PZN

therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Arnica/Plumbum comp. A.

Arnica/Plumbum comp. B

Contraindications None known.

Potency/Strength Package Size Size Category

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers through the ego organisation in sclerotic changes of the blood vessels of the brain and the eye, e.g. in circulatory disorders of the brain, for follow-up treatment after stroke, degenerative changes of the eye.

Price Group A

iris bovis Gl dil. D15 0.01 g (HAB, Method 41b) medulla oblongata bovis Gl dil. D15 0.01 g (HAB, Method 41a) nervus opticus bovis Gl dil. D15 0.01 g (HAB, Method 41a) plumbum mellitum dil. D28 aquos. 0.02 g (HAB, Method 8b) retina et chorioidea bovis Gl dil. D15 0.01 g (HAB, Method 41c) thalamus bovis Gl dil. D15 0.01 g (HAB, Method 41a) Contains sucrose (saccharose/sugar).

Status Pharmacy only

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D28 0.01 g (HAB, Method 33c) betula pendula e cortice, decoctum dil. D3 0.01 g (HAB, Method 23a) cerebellum bovis Gl dil. D15 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D15 0.01 g (HAB, Method 41a) epiphysis bovis Gl dil. D15 0.01 g (HAB, Method 41a) labyrinthus bovis Gl dil. D15 0.01 g (HAB, Method 41a) medulla oblongata bovis Gl dil. D15 0.01 g (HAB, Method 41a) nervus statoacusticus bovis Gl dil. D15 0.01 g (HAB, Method 41a) plumbum mellitum dil. D28 aquos. 0.02 g (HAB, Method 8b)

N1 N2

PZN 1750714 2084857

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. For adjunctive treatment of circulatory disorders of the brain, for follow-up treatment post stroke, degenerative changes of the inner ear with dizziness, ringing in the ears and hearing loss. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

67

A

A

Arnica/Plumbum comp. B Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D28 0.01 g (HAB, Method 33c) betula pendula e cortice, decoctum Ø 0.01 g (HAB, Method 23a) cerebellum bovis Gl dil. D15 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D15 0.01 g (HAB, Method 41a) epiphysis bovis Gl dil. D15 0.01 g (HAB, Method 41a) labyrinthus bovis Gl dil. D15 0.01 g (HAB, Method 41a) medulla oblongata bovis Gl dil. D15 0.01 g (HAB, Method 41a) nervus statoacusticus bovis Gl dil. D15 0.01 g (HAB, Method 41a) plumbum mellitum dil. D28 aquos. 0.02 g (HAB, Method 8b) Contains sucrose (saccharose/sugar).

N1

PZN 8783964

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers through the ego organisation in sclerotic changes of the blood vessels of the brain and the inner ear, e.g. in circulatory disturbances of the brain (cerebral circulatory disorders), for follow-up treatment post stroke, degenerative changes of the inner ear with dizziness, ringing in the ears and hearing loss. Contraindications None known.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Side-effects None known.

Arnica/Plumbum mellitum Liquid dilution for injection



10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D29 0.1 g (HAB, Method 33c) plumbum mellitum dil. D29 aquos. 0.2 g (HAB, Method 8b)

N1 N2

PZN 1750720 2084811

68

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Reintegration of the ego organisation and feeling organisation in the vascular system in increased tendency to deposits and hardening, e.g. general vascular sclerosis, cerebral circulatory disorders. Contraindications None known.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week.

Arnica/Plumbum mellitum globuli velati are recommended for this age group. Duration of treatment Unless otherwise directed by the doctor, Arnica/Plumbum mellitum should not be taken continuously for more than 8 weeks. Side-effects None known.

Note: Arnica/Plumbum mellitum, liquid dilution for injection, is not suitable for use in children under 12 years.

Arnica/Plumbum mellitum Globuli velati

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Arnica/Plumbum comp. B.

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.



20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D29 0.1 g (HAB, Method 33c) plumbum mellitum dil. D29 aquos. 0.2 g (HAB, Method 8b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Reintegration of the ego organisation and feeling organisation in the vascular system in increased tendency to deposits and hardening, e.g. general vascular sclerosis, cerebral circulatory disorders.

N1

PZN 8783970

Price Group A

Status Pharmacy only

you suffer from intolerance to certain sugars you should consult your doctor before taking Arnica/Plumbum mellitum. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Contraindications None known.

Duration of treatment Unless otherwise directed by the doctor, Arnica/Plumbum mellitum should not be taken continuously for more than 8 weeks.

Warnings and precautions for use This medicinal product contains sucrose. If you know that

Side-effects None known.

Arnika Essenz

Active ingredient: arnica montana e floribus LA 20% Tincture for external use Potency/Strength Package Size Size Category Composition 10 g (10.2 ml) contain: arnica montana e floribus LA 20% 10 g (HAB, Method 12c)

100 ml

PZN 1753859

Price Group D

Status General sale

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of tissue and organ healing with particular emphasis on metabolic processes, e.g. blunt

69

A

A

injuries such as sprains and strains, contusions, bruises, muscle soreness; hardened areas in the muscles (myogelosis), subacute and chronic inflammatory joint disorders; following concussion, stroke, palsies. Contraindications Do not use Arnika-Essenz • in the case of known hypersensitivity to formulations of arnica or other plants of the Compositae family, e.g. chamomile flowers, calendula or yarrow, or to any other ingredient of the medicinal product • on damaged skin (e.g. injured or burned skin); • during pregnancy or breastfeeding. Warnings and precautions for use There is insufficient documented experience on the use of this medicinal product in children for the indications subacute and chronic inflammatory joint disease, status post concussion, stroke or paralysis. The medicinal product should therefore not be used for these indications in children under 12 years of age without first obtaining the advice of a doctor and should not be used in place of any medication prescribed by the doctor for these indications. Contains 25% (v/v) alcohol

Dosage and method of administration Unless otherwise directed: Compresses: add 1 tablespoon of tincture to approx. 250 ml of water and use for compresses. Airtight covering of the compress should be avoided. Baths: use 2 to 3 tablespoons of tincture for a full bath; use correspondingly less for partial baths. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Prolonged and frequent external use can produce skin reactions with swelling and blistering. This can be due to a hypersensitivity reaction of the skin or to direct tissue damage by Arnika-Essenz. Eczema may also occur with prolonged use. Skin reactions with tissue destruction may rarely occur.

Arnika Salbe Ointment

Potency/Strength Package Size Size Category

30 g 100 g

N1 N2

PZN 2198147 2198153

Price Group J J1

Status Pharmacy only Pharmacy only

Composition 10 g contain: arnica montana e planta tota ferm 33c Ø 0.5 g (HAB, Method 33c) formica rufa ex animale toto Gl Ø 0.01 g (HAB, Method 41c) symphytum officinale e radice ferm 34c Ø 0.2 g (HAB, Method 34c) Excipients: refined arachis oil, white soft paraffin, purified water, wool fat.

Contraindications Arnica Salbe should not be used in the case of allergy to • arnica and other plants of the Compositae family, e.g. chamomile flowers, • calendula or yarrow, • ant venom or peanuts or soy or any other ingredient of the medicinal product. Do not apply to damaged skin. The medicinal product should not be used in children under 1 year.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of tissue and organ healing after blunt injuries and in inflammatory and degenerative disorders of the musculoskeletal system.

Warnings and precautions for use In rare cases wool fat can cause local skin reactions (e.g. contact dermatitis).

Dosage and method of administration Unless otherwise directed, rub in the ointment 1 to 2 times daily or use as ointment dressing. Duration of treatment Acute disorders should clear up within 2 weeks. In the case of chronic conditions the duration of treatment should not exceed 6 weeks.

Side-effects In rare cases allergic skin reactions may occur in individuals with hypersensitivity to ingredients of Arnika Salbe, particularly to arnica and arachis oil. If the skin becomes red, with or without itching, treatment with Arnika Salbe should be discontinued and a doctor consulted.

Arnika Wundtuch (wet wipes for minor injuries) Active ingredient: arnica montana e floribus LA 20% Wet wipes Potency/Strength Package Size Size Category 5 wipes Composition 1 wet wipe contains: arnica montana e floribus LA 20% 4 g (HAB, Method 12c) Excipient: crepe paper.

Price Group D2

Status General sale

Contains 25% (v/v) alcohol. Because of the alcohol content of the medicinal product, frequent use on the skin may cause irritation or inflammation and may dry out the skin.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of tissue and organ healing with particular emphasis on metabolic processes, e.g. for first aid after blunt injuries such as sprains and strains, contusions, bruises. Contraindications Arnika Wundtuch should not be used • in the case of known hypersensitivity to formulations of arnica or other plants of the Compositae family, e.g. chrysanthemums or yarrow, • on damaged skin (e.g. injured or burned skin), • during pregnancy. Warnings and precautions for use As with all medicines, women who are breastfeeding should obtain medical advice before using Arnika Wundtuch. Women who are breastfeeding should not use Arnika Wundtuch in the region of the nipples.

Dosage and method of administration Unless otherwise directed, use Arnika Wundtuch as compresses for application to the skin. Tear open the sachet at the side, place the wipe on the affected site and moisten with a little water if necessary. Leave in place for about half an hour and then replace with a fresh wipe. Airtight covering of the compress should be avoided. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Side-effects Prolonged and frequent external use can often produce skin reactions with swelling and blistering. This can be due to a hypersensitivity reaction of the skin or to direct tissue damage by Arnika Wundtuch. Eczema may also occur with prolonged use. Skin reactions with tissue destruction may rarely occur.

Arsenicum album

Active ingredient: arsenicum album aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D12 D30

70

PZN 4495731

10 x 1 ml 10 x 1 ml

N1 N1

PZN 3358682 2832785

Price Group 31 31

Status Pharmacy only Pharmacy only

71

A

A

Composition Liquid dilution for injection: 1 ml contains: arsenicum album dil. D.. aquos. 1 ml (HAB, Method 5b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Potency D12: Unless otherwise directed, inject 1 ml subcutaneously 1 to 2 times weekly to once daily. Potency D30: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Arsenicum album

Active ingredient: arsenicum album aquos. Globuli velati Potency/Strength Package Size Size Category D6 D12 D30

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: arsenicum album dil. D.. aquos. 1 g (HAB, Method 5b) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Arsenicum album.

N1 N1 N1

PZN 8783987 8783993 8784001

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: arteriae bovis Gl (consisting of equal parts of a. basilaris, a. brachialis, a. coronaria, a. femoralis, a. mesenterica superior, a. pulmonalis, a. renalis) Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 4614874 2902729 4614897 4614911 0488800 2902764 2488856

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Composition Liquid dilution for injection: 1 ml contains: arteriae bovis Gl (consisting of equal parts of a. basilaris, a. brachialis, a. coronaria, a. femoralis, a. mesenterica superior, a. pulmonalis, a. renalis) dil. D.. 1 ml (HAB, Method 41c)

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Duration of treatment Acute disorders should clear up within 2 weeks. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Side-effects None known.

Arteria basilaris Gl

Active ingredient: arteria basilaris bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria basilaris bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

72

A

Arteriae Gl

N1 N1 N1 N1

PZN 2902824 2902876 2902913 2902965

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

73

A

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Arteria brachialis Gl

Active ingredient: arteria brachialis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria brachialis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 and D30: None known.

N1 N1 N1

PZN 2903025 2903114 2903166

Price Group 61 61 61

Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: arteria carotis communis et sinus caroticus bovis Gl Liquid dilution for injection

74

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2903232 2903255 2903278 2903290 2903315 2903338 2903350 2493194

Price Group 61 61 61 61 61 61 61 51

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Arteria cerebri media Gl

Active ingredient: arteria cerebri media bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria cerebri media bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Arteria carotis communis et sinus caroticus Gl

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Status

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: arteria carotis communis et sinus caroticus bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2903841 2903864 2903887 2903924 2903947 2903999 2488595

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

75

A

A

Arteria coronaria Gl

Composition Liquid dilution for injection: 1 ml contains: arteria femoralis bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Active ingredient: arteria coronaria bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria coronaria bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3359262 2829760 3359279 3359285 3359291 3359316 3359339 0847469 2493260

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

see Arteria ophthalmica Gl

Active ingredient: arteria femoralis bovis GI Liquid dilution for injection

76

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2904160 2904183 2904214 2904266 2904289 2904332 2488632

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Arteria ophthalmica Gl

Active ingredient: arteria ophthalmica bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Arteria femoralis Gl

D5 D6 D8 D12 D15 D30 Serial pack

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Composition Liquid dilution for injection: 1 ml contains: arteria ophthalmica bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Arteria et Vena ophthalmica GI

Potency/Strength Package Size Size Category

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 1491916 1491968 1492229 1492318 1492436 1492459 1492956 1493200

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

77

A

A

Arteria poplitea Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Active ingredient: arteria poplitea bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria poplitea bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2905047 2905076 2905099 2905142 2905165 2905188 2488750

Price Group 61 61 61 61 61 61 51

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: arteria pulmonalis bovis GI Liquid dilution for injection

D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria pulmonalis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

78

N1 N1 N1

PZN 3767216 3767274 3767334

Arteria renalis Gl

Active ingredient: arteria renalis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria renalis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Arteria pulmonalis Gl

Potency/Strength Package Size Size Category

Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2905248 2905260 2905283 2905314 2905337 2905366 2905403 2493403

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

79

A

A

Arteria vertebralis Gl

Composition Liquid dilution for injection: 1 ml contains: articulatio coxae bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Active ingredient: arteria vertebralis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria vertebralis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2905722 2905745 2905768 2905780 2905805 2905828 2905840 2493426

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Articulatio coxae Gl

Active ingredient: articulatio coxae bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

80

10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N2 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3359368 2829464 2905900 3359374 3359380 3359397 3359405 2830763 0847506 0845625 2493550

Price Group 61 61 62 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the organ-forming powers in degenerative and chronic inflammatory disorders of the hip joint. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Dosage and method of administration Potencies below D20: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potencies D20 and above: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Liquid dilution for injection D5, D6: Hypersensitivity reactions to the protein of the donor animal may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Articulatio cubiti Gl

Active ingredient: articulatio cubiti bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulatio cubiti bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2906012 2906035 2906058 2906093 2906118 2906130 2488997

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

81

A

A

Articulatio genus Gl

Potency/Strength Package Size Size Category

Active ingredient: articulatio genus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D5 D6 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 50 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulatio genus bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the organ-forming powers in degenerative and chronic inflammatory disorders of the knee joint. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this

N1 N2 N1 N2 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3353271 2906182 2829412 2906199 3353288 3353294 3353302 3353319 2831567 0847512 0845720 2493567

Price Group 61 62 61 62 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 12 years.

82

N1 N1 N1 N1 N1 N1

2906302 2906325 2906348 2906360 2906383 2906414

Price Group 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

61 51 51

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: articulatio radiocarpea bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulatio radiocarpea bovis Gl dil. D.. 1 ml (HAB, Method 41b) PZN

Price Group

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Potency/Strength Package Size Size Category

PZN 2906437 0847529 2493656

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Liquid dilution for injection D5, D6: Hypersensitivity reactions to the protein of the donor animal may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1

Composition Liquid dilution for injection: 1 ml contains: articulatio humeri bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Articulatio radiocarpea Gl

Active ingredient: articulatio humeri bovis GI Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

10 x 1 ml 10 x 1 ml 10 x 1 ml

Dosage and method of administration Potencies below D20: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potencies D20 and above: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Articulatio humeri Gl

D5 D6 D8 D10 D12 D15

D30 Serial pack I Serial pack III

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2907135 2907158 2907170 2907193 2907218 2907230 2907253 2493662

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

83

A

A

Articulatio sacroiliaca Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Active ingredient: articulatio sacroiliaca bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulatio sacroiliaca bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2907336 2907359 2907371 2907394 2907419 2907431 2907454 2493679

Price Group 61 61 61 61 61 61 61 51

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: articulatio subtalaris bovis GI Liquid dilution for injection

D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulatio subtalaris bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

84

N1 N1 N1 N1

Articulatio talocruralis Gl

Active ingredient: articulatio talocruralis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulatio talocruralis bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Articulatio subtalaris Gl

Potency/Strength Package Size Size Category

Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

PZN 2907520 2907572 2907626 2907661

Price Group 61 61 61 61

Status

Duration of treatment The duration of treatment should be discussed with the doctor.

N1 N1 N1 N1 N1 N1 N1

PZN 2907939 2907951 2907974 2908011 2908034 2908057 2489293

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

85

A

A

Articulatio talocruralis comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: allium cepa ferm 34a dil. D2 0.01 g arnica montana e planta tota ferm 33c dil. D4 0.01 g (HAB, Method 33c) articulatio subtalaris bovis Gl dil. D4 0.01 g (HAB, Method 41b) articulatio subtalaris bovis Gl dil. D8 0.01 g (HAB, Method 41b) articulatio talocruralis bovis Gl dil. D4 0.01 g (HAB, Method 41b) articulatio talocruralis bovis Gl dil. D8 0.01 g (HAB, Method 41b) nervus ischiadicus bovis Gl dil. D4 0.01 g (HAB, Method 41a) periosteum bovis Gl dil. D15 0.01 g (HAB, Method 41b) stannum metallicum dil. D13 aquos. 0.01 g symphytum officinale e radice ferm 34c dil. D1 0.01 g (HAB, Method 34c) tendo bovis Gl dil. D4 0.01 g (HAB, Method 41b)

N1

PZN 2084863

Price Group 11

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the regenerative and formative processes in degenerative/reactive inflammatory joint disorders, e.g. osteoarthritis (arthrosis deformans), particularly of the ankle joints. Contraindications Do not use in case of hypersensitivity to the protein of the donor animal. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly, in acute states once to twice daily. Duration of treatment The condition should have cleared up within 2 weeks. If acute inflammation does not improve within 2 days a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

Articulatio talocruralis comp.

symphytum officinale e radice ferm 34c dil. D1 0.01 g (HAB, Method 34c) tendo bovis Gl dil. D4 0.01 g (HAB, Method 41b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the regenerative and formative processes in degenerative/reactive inflammatory joint disorders, e.g. osteoarthritis (arthrosis deformans), particularly of the ankle joints. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Articulatio talocruralis comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 2 to 3 times daily. Duration of treatment The condition should have cleared up within 2 weeks. If acute inflammation does not improve within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Articulatio temporomandibularis Gl

Active ingredient: articulatio temporomandibularis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2908123 2908152 2908175 2908198 2908212 2908235 2908258 0847558 2493691

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: allium cepa ferm 34a dil. D2 0.01 g arnica montana e planta tota ferm 33c dil. D4 0.01 g (HAB, Method 33c) articulatio subtalaris bovis Gl dil. D4 0.01 g (HAB, Method 41b) articulatio subtalaris bovis Gl dil. D8 0.01 g (HAB, Method 41b)

86

N1

PZN 8784018

Price Group A

articulatio talocruralis bovis Gl dil. D4 0.01 g (HAB, Method 41b) articulatio talocruralis bovis Gl dil. D8 0.01 g (HAB, Method 41b) nervus ischiadicus bovis Gl dil. D4 0.01 g (HAB, Method 41a) periosteum bovis Gl dil. D15 0.01 g (HAB, Method 41b) stannum metallicum dil. D13 aquos. 0.01 g

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: articulatio temporomandibularis bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

87

A

A

Articulationes intercarpeae Gl

Active ingredient: articulationes intercarpeae bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulationes intercarpeae bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN

Price Group

2906503 2906532 2906555 2906590 2906615 2906638 2489821

61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: articulationes intervertebrales cervicales bovis Gl Liquid dilution for injection

D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulationes intervertebrales cervicales bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

88

N1 N1 N1 N1 N1 N1 N1

PZN 2906733 2906762 2906785 2906839 2906851 2906874 2489838

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Articulationes intervertebrales lumbales Gl

Active ingredient: articulationes intervertebrales lumbales bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulationes intervertebrales lumbales bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Articulationes intervertebrales cervicales Gl

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2906934 2906957 2906986 2907023 2907052 2907075 2489844

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Atlas Gl

Active ingredient: atlas bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1

PZN 2908318 2908407 2908459

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

89

A

A

Composition Liquid dilution for injection: 1 ml contains: atlas bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Atropa belladonna e fructibus, Einzeldosis-Augentropfen Atropa belladonna e radice

Active ingredient: atropa belladonna e radice ferm 33b Liquid dilution for injection Potency/Strength Package Size Size Category D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna e radice ferm 33b dil. D.. 1 ml (HAB, Method 33b)

Atropa belladonna ex herba, Einzeldosis-Augentropfen

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

see Belladonna ex herba Augentropfen

Atropa belladonna e fructibus

A

see Belladonna e fructibus Augentropfen

N1 N1 N1

PZN 3155536 3358127 3358156

Price Group 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once to twice a week. Side-effects None known.

Active ingredient: atropa belladonna e fructibus ferm 33a Globuli velati Potency/Strength Package Size Size Category D6 D20

20 g 20 g

N1 N1

PZN 8784047 8784053

Price Group A A

Status Pharmacy only Pharmacy only

Atropa belladonna e radice

Active ingredient: atropa belladonna e radice ferm 33b Globuli velati Potency/Strength Package Size Size Category

Composition Globuli velati: 10 g contain: atropa belladonna e fructibus ferm 33a dil. D.. 1 g (HAB, Method 33a) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Atropa belladonna e fructibus.

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

D3 D6 D10 D15 D20 D30

20 g 20 g 20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: atropa belladonna e radice ferm 33b dil. D.. 1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you

90

N1 N1 N1 N1 N1 N1

PZN 8784076 8784082 8784099 8784107 8784113 8784136

Price Group A A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

should consult your doctor before taking Atropa belladonna e radice. Dosage and method of administration Unless otherwise directed D3, D6 infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. D10, D15: infants 3 globuli velati sublingually once to twice daily, children up to 6 years 3-7 globuli velati sublingually once to twice daily, adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily. D20, D30: infants 3 globuli velati sublingually once daily, children up to 6 years 3-7 globuli velati sublingually once daily, adults and children of 6 years and above 5-10 globuli velati sublingually once daily.

91

A

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Side-effects None known.

D10, D15: infants 3 globuli velati sublingually once to twice daily, children up to 6 years 3-7 globuli velati sublingually once to twice daily, adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily. D20, D30: infants 3 globuli velati sublingually once daily, children up to 6 years 3-7 globuli velati sublingually once daily, adults and children of 6 years and above 5-10 globuli velati sublingually once daily.

Duration of treatment The duration of treatment should be discussed with the doctor.

Atropa belladonna ex herba

Active ingredient: atropa belladonna ex herba ferm 33a Liquid dilution for injection Potency/Strength Package Size Size Category D6 D10 D20 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna ex herba ferm 33a dil. D.. 1 ml (HAB, Method 33a) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1

PZN 3155513 3358191 3358179 3358185

Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once to twice a week. Side-effects None known.

Atropa belladonna ex herba

Active ingredient: atropa belladonna ex herba ferm 33a Globuli velati

D3 D6 D10 D15 D20 D30

20 g 20 g 20 g 20 g 20 g 20 g

N1 N1 N1 N1 N1 N1

PZN 8784142 8784159 8784165 8784171 8784188 8784194

Price Group A A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Globuli velati: 10 g contain: atropa belladonna ex herba ferm 33a dil. D.. 1 g (HAB, Method 33a) Contains sucrose (saccharose/sugar).

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Atropa belladonna ex herba.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed D3, D6 infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Contraindications None known.

92

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Aurum comp.

Contraindications None known.

Potency/Strength Package Size Size Category

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum trit. D6 0.01 g myrrha trit. D3 0.01 g (HAB, Method 6) olibanum trit. D3 0.01 g (HAB, Method 6) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation and stabilisation of the constituent elements of the human being in chronic degenerative or traumatic disorders of the central nervous system as well as for follow-up treatment of inflammatory disorders of the brain, for mental disorders, developmental and behavioural disorders and functional cardiovascular disorders. Contraindications Do not use in the case of allergy to milk protein.

N1 N2

PZN 1750737 2084892

Price Group 11 12

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 1 to 2 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously 1 to 2 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 1 to 2 times a week to once daily. Duration of treatment The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects In individual cases a temporary exacerbation of symptoms has been observed after use of Aurum comp. for postencephalitic hyperactivity; this was usually followed by marked improvement. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Aurum comp. Globuli velati

Potency/Strength Package Size Size Category Composition Globuli velati: 10 g contain: aurum metallicum trit. D7 0.1 g myrrha trit. D4 0.1 g (HAB, Method 6)

20 g

N1

PZN 8784202

Price Group A

Status Pharmacy only

olibanum trit. D4 0.1 g (HAB, Method 6) Contains sucrose (saccharose/sugar) and lactose.

93

A

A

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation and stabilisation of the constituent elements of the human being in chronic degenerative or traumatic disorders of the central nervous system as well as for follow-up treatment of inflammatory disorders of the brain, for mental disorders, developmental and behavioural disorders and functional cardiovascular disorders.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Contraindications None known.

Duration of treatment The duration of treatment of chronic conditions should be discussed with the doctor.

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum comp.

Side-effects In individual cases a temporary exacerbation of symptoms has been observed after use of Aurum comp. for postencephalitic hyperactivity; this was usually followed by marked improvement.

Aurum comp., Unguentum Ointment

Potency/Strength Package Size Size Category

30 g

Composition 10 g contain: aurum metallicum trit. D3 0.1 g myrrha 0.1 g olibanum 0.1 g Excipients: refined arachis oil, white soft paraffin, purified water, wool fat. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation and stabilisation of the constituent elements of the human being in disorders of the central nervous system of chronic degenerative or traumatic origin as well as for follow-up treatment of inflammatory diseases of the brain, for mental disorders, developmental and behavioural disorders, functional cardiovascular disorders. Contraindications Do not use in the case of hypersensitivity to components of the ointment base.

94

N1

PZN 2198176

Price Group D

Status Pharmacy only

Warnings and precautions for use In rare cases arachis (peanut) oil and wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, children under 6 years apply a ribbon of ointment about 0.5 cm long to the skin in the region of the heart once to twice daily or apply a ribbon of ointment about 1 cm long to a cotton cloth about the size of the palm of the hand and place this over the heart; children from 6 to 12 years apply a ribbon of ointment about 1 cm long to the skin in the region of the heart once to twice daily or apply a ribbon of ointment about 2.5 cm long to a cotton cloth about the size of the palm of the hand and place this over the heart; adults and children of 12 years and above apply a ribbon of ointment about 2 cm long to the skin in the region of the heart once to twice daily or apply a ribbon of ointment about 5 cm long to a cotton cloth about the size of the palm of the hand and place this over the heart. Note: Do not allow the ointment to come into contact with the eye or mucous membranes.

Side-effects Very rarely a temporary exacerbation of symptoms has been observed after use of Aurum comp. Unguentum for

postencephalitic hyperactivity; this was usually followed by marked improvement.

Aurum/Apis regina comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: acidum phosphoricum dil. D4 0.1 g apis regina tota Gl dil. D5 0.1 g (HAB, Method 41c) aurum chloratum dil. D6 aquos. 0.1 g (HAB, Method 5b) avena sativa ferm 33c dil. D2 0.1 g (HAB, Method 33c) hypericum perforatum ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) strychnos ignatii e semine ferm 35b dil. D4 0.1 g (HAB, Method 35b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the constituent elements of the human being in functional organic disorders of psychological origin manifesting as headaches, gastric symptoms, vertigo, low back pain etc. (neurasthenia, neurovegetative dysregulation), states of nervous exhaustion, menopausal mood swings, feelings of depression, poor concentration and memory.

N1 N2

PZN 1750743 2084900

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of known hypersensitivity to bee venom. Warnings and precautions for use Warning for people with gluten intolerance: Aurum/Apis regina comp. contains gluten. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 1 to 3 times a week to once daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously 1 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times a week to once daily. Duration of treatment Aurum/Apis regina comp. should not be used for more than 6 weeks without consulting a doctor. Side-effects The possibility that the bee venom (apis regina) contained in the medicinal product may rarely cause allergic reactions such as transient skin rashes or asthma-like symptoms, cannot be ruled out. If such symptoms occur, treatment with Aurum/Apis regina comp. should be discontinued immediately.

Aurum/Apis regina comp. Globuli velati

Potency/Strength Package Size Size Category Composition Globuli velati: 10 g contain: acidum phosphoricum dil. D4 0.1 g

20 g

N1

PZN 8784219

Price Group A

Status Pharmacy only

apis regina tota Gl dil. D5 0.1 g (HAB, Method 41c) aurum chloratum dil. D6 aquos. 0.1 g (HAB, Method 5b)

95

A

A

avena sativa ferm 33c dil. D2 0.1 g (HAB, Method 33c) hypericum perforatum ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) strychnos ignatii e semine ferm 35b dil. D4 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the constituent elements of the human being in functional organic disorders of psychological origin manifesting as headaches, gastric symptoms, vertigo, low back pain etc. (neurasthenia, neurovegetative dysregulation), states of nervous exhaustion, menopausal mood swings, feelings of depression, poor concentration and memory. Contraindications Do not use in the case of known hypersensitivity to bee venom. Warnings and precautions for use Warning for people with gluten intolerance: Aurum/Apis regina comp. contains gluten.

This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/Apis regina comp.

Aurum/Belladonna comp.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.



Duration of treatment Aurum/Apis regina comp. should not be used for more than 6 weeks without consulting a doctor. Side-effects The possibility that the bee venom (apis regina) contained in the medicinal product may rarely cause allergic reactions such as transient skin rashes or asthma-like symptoms, cannot be ruled out. If such symptoms occur, treatment with Aurum/Apis regina comp. should be discontinued immediately.

Aurum/Belladonna comp.

A

Globuli velati

Potency/Strength Package Size Size Category 20 g

N1

PZN 8784225

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: atropa belladonna ex herba ferm 33a dil. D9 0.1 g (HAB, Method 33a) aurum metallicum dil. D9 0.1 g plumbum mellitum dil. D11 aquos. 0.2 g (HAB, Method 8b) Contains sucrose (saccharose/sugar) and lactose.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/ Belladonna comp.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the rhythmic system in disorders with an increased tendency to deposits in and hardening of the blood vessels, e.g. beginning vascular sclerosis, impaired blood supply to the brain (cerebral circulatory disorders), high blood pressure (hypertension).

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Contraindications None known.

Side-effects None known.

Duration of treatment Unless otherwise directed by the doctor Aurum/Belladonna comp. should not be used continuously for longer than 8 weeks.

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna ex herba ferm 33a dil. D9 0.1 g (HAB, Method 33a) aurum metallicum dil. D9 0.1 g plumbum mellitum dil. D11 aquos. 0.2 g (HAB, Method 8b) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the rhythmic system in disorders with an increased tendency to deposits in and hardening of the blood vessels, e.g. beginning vascular sclerosis, impaired blood supply to the brain (cerebral circulatory disorders), high blood pressure (hypertension). Contraindications Do not use in the case of allergy to milk protein.

96

N1 N2

PZN 1750766 2084917

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week. Duration of treatment Unless otherwise directed by the doctor Aurum/Belladonna comp. should not be used continuously for longer than 8 weeks. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Aurum/Equisetum I Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 0426874

Price Group 11

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b)

Contraindications Do not use in the case of allergy to milk protein.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic system and the renal activity directed to the organism, e.g. for adjunctive treatment of beginning renal failure and heart failure.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Warnings and precautions for use There is no adequately documented experience of use of this medicinal product in children. It should therefore not be used in children under 12 years.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

97

A

Aurum/Equisetum I Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar) and lactose. Indications ion of the rhythmic system and the renal activity directed to the organism, e.g. for adjunctive treatment of beginning renal failure and heart failure.

N1

PZN 0459454

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/ Equisetum I. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 2 times daily. Side-effects None known.

Contraindications None known.

Composition Globuli velati: 10 g contain: aurum metallicum dil. D29 aquos. 0.1 g equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic system and the renal activity directed to the organism, e.g. for adjunctive treatment of beginning renal failure and heart failure.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/Equisetum II. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually once to twice daily. Side-effects None known.

Aurum/Prunus

Liquid dilution for injection Potency/Strength Package Size Size Category

Aurum/Equisetum II Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 0426897

Price Group 11

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D29 aquos. 0.1 g equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b)

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic system and the renal activity directed to the organism, e.g. for adjunctive treatment of beginning renal failure and heart failure.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Side-effects None known.

Aurum/Equisetum II

98

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g prunus spinosa e floribus et summitatibus ferm 33d dil. D5 0.1 g (HAB, Method 33d) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation and the rhythmic system, e.g. in states of exhaustion with symptoms of low blood pressure. Contraindications Do not use in the case of allergy to milk protein.

N1

PZN 1750795

Price Group 11

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment There is no evidence suggesting that prolonged use of the preparation may have negative effects. However, as the above conditions usually require treatment for a maximum of eight weeks a temporary switch to a different preparation or temporary interruption of the treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Globuli velati

Potency/Strength Package Size Size Category 20 g

10 x 1 ml

Aurum/Prunus

Globuli velati



A

Contraindications None known.

N1

PZN 0459448

Price Group A

Status

Potency/Strength Package Size Size Category

Pharmacy only



20 g

N1

PZN 8784254

Price Group A

Status Pharmacy only

99

A

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g prunus spinosa e floribus et summitatibus ferm 33d dil. D5 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation and the rhythmic system, e.g. in states of exhaustion with symptoms of low blood pressure. Contraindications None known.

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/Prunus. Dosage and method of administration Unless otherwise directed, infants and children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Aurum/Stibium/Hyoscyamus Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1750803 2084969

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g hyoscyamus niger ex herba ferm 33d dil. D4 0.1 g (HAB, Method 33d) stibium metallicum dil. D7 0.1 g

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation and stabilisation of the rhythmic system, e.g. functional heart complaints, ectopic beats, difficulty falling asleep; emotional disturbances which can manifest as various organic symptoms (psychovegetative disorders).

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor.

Contraindications Do not use • in the case of a particularly slow heart rate (bradycardia) • in the case of known hypersensitivity to gold (aurum metallicum) or to any of the other ingredients • in the case of hypersensitivity to milk protein

100

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above inject 1 ml subcutaneously 1 to 3 times weekly to once daily.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

A

Aurum/Stibium/Hyoscyamus Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g hyoscyamus niger ex herba ferm 33d dil. D4 0.1 g (HAB, Method 33d) stibium metallicum dil. D7 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation and stabilisation of the rhythmic system, e.g. functional heart complaints, ectopic beats, difficulty falling asleep; emotional disturbances which can manifest as various organic symptoms (psychovegetative disorders). Contraindications Do not use in the case of pronounced bradycardia.

N1

PZN 8784260

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/ Stibium/Hyoscyamus. Dosage and method of administration Unless otherwise directed, children under 6 years 5 globuli velati sublingually 2 to 3 times daily; children from 6 to under 12 years 10 globuli velati sublingually 3 to 4 times daily; adults and children of 12 years and above 10-15 globuli velati sublingually 2 to 4 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Aurum/Strophanthus Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1750826 2084975

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g strophanthus kombe e semine ferm 35b dil. D5 0.1 g (HAB, Method 35b)

Contraindications Do not use in the case of allergy to milk protein.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the metabolic activity to compensate degenerative processes in the heart and their sequelae; e.g. age-related heart weakness, latent heart failure, particularly also in the case of bradycardia.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

101

A

Aurum/Strophanthus Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g strophanthus kombe e semine ferm 35b dil. D5 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the metabolic activity to compensate degenerative processes in the heart and their sequelae; e.g. age-related heart weakness, latent heart failure, particularly also in the case of bradycardia. Contraindications None known.

N1

PZN 8784277

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/ Strophanthus. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Side-effects None known.

see Aurum Valeriana Inject see Aurum Valeriana Globuli velati

Aurum Valeriana Inject Liquid dilution for injection



10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g camphora dil. D3 aquos. 0.1 g (HAB, Method 5b) crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) selenicereus grandiflorus ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) strophanthus kombe e semine ferm 35b dil. D5 0.1 g (HAB, Method 35b) valeriana officinalis e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c)

102

N1 N2

PZN 0084907 0089342

Dosage and method of administration Unless otherwise directed, children from 2 to under 6 years 0.5 ml by subcutaneous injection 2 to 3 times a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously 2 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week to once daily.

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the rhythmic system in neurovegetative dysregulation, functional heart complaints (including those of degenerative origin), nausea and vertigo. If the patient experiences chest pain radiating into the arms, the upper abdomen or the neck, or if there is difficulty breathing, examination by a doctor is essential.

Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Aurum Valeriana Globuli velati Globuli velati

Potency/Strength Package Size Size Category

Aurum/Valeriana comp.

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 2 years.

20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D5 0.1 g camphora dil. D3 aquos. 0.1 g (HAB, Method 5b) crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) selenicereus grandiflorus ex herba ferm 33d dil. D2 0.1 g (HAB, Method 33d) strophanthus kombe e semine ferm 35b dil. D3 0.1 g (HAB, Method 35b) valeriana officinalis e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the rhythmic system in neurovegetative dysregulation, functional heart complaints (including those of degenerative origin), nausea and vertigo. If the patient experiences chest pain radiating into the arms, the upper abdomen or the neck, or if there is difficulty breathing, examination by a doctor is essential.

N1

PZN 0084936

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Aurum Valeriana globuli velati should not be used in children under 2 years as there is no adequately documented experience of use in this age group. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Aurum/ Valeriana Globuli velati. Dosage and method of administration Unless otherwise directed, children from 2 to 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. Note: Aurum Valeriana globuli velati should not be used in children under 2 years as insufficient experience has been obtained with this age group. Side-effects None known.

Contraindications Do not use in the case of allergy to milk protein.

103

A

A

Avena comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: avena sativa ferm 33c dil. D5 0.1 g (HAB, Method 33c) conchae dil. D6 0.1 g phosphorus Dil. D24 0.1 g sulfur dil. D24 aquos. 0.1 g valeriana officinalis e radice ferm 33c dil. D7 0.1 g (HAB, Method 33c)

N1

PZN 1750849

Price Group 11

Status

Contraindications Do not use in the case of allergy to milk protein. Warnings and precautions for use Warning for people with gluten intolerance: Avena comp., liquid dilution for injection contains gluten. Dosage and method of administration Unless otherwise directed, 1 ml injected subcutaneously 2 to 3 times a week to once daily in the evening. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Avena comp. Globuli velati

20 g

Composition Globuli velati: 10 g contain: avena sativa ferm 33c dil. D2 0.1 g (HAB, Method 33c) conchae dil. D6 0.1 g phosphorus Dil. D24 0.1 g sulfur dil. D24 aquos. 0.1 g valeriana officinalis e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Difficulty falling asleep and staying asleep, evening restlessness, particularly in patients with a neurasthenic constitution, hypersensitivity and nervousness.

104

Axis Gl

Active ingredient: axis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: axis bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Potency/Strength Package Size Size Category N1

PZN 8784308

Price Group A

A

Side-effects None known.

Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.



Duration of treatment The disorder should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted.

Status Pharmacy only

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 upwards: None known.

N1 N1 N1

PZN 2908637 2908732 2908778

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications None known. Warnings and precautions for use Warning for people with gluten intolerance: Avena comp., globuli velati contain gluten. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Avena comp. Dosage and method of administration Unless otherwise directed, infants and small children up to 6 years 3-5 globuli velati sublingually once daily, in the case of difficulty falling asleep and staying asleep 5-10 globuli velati sublingually ½ hour before bedtime; adults and children of 6 years and above 5-10 globuli velati sublingually once daily, in the case of difficulty falling asleep and staying asleep 10-30 globuli velati (children from 6 to 12 years up to 20 globuli velati) sublingually ½ hour before bedtime. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

105

Bambusa e nodo

Active ingredient: phyllostachys e nodo ferm 35c Liquid dilution for injection

B

Potency/Strength Package Size Size Category D3 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: phyllostachys e nodo ferm 35c dil. D.. 1 ml (HAB, Method 35c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 3358216 2832638

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously three times a week to once daily. Side-effects None known.

Composition Liquid dilution for injection: 1 ml contains: barium citricum dil. D9 0.1 g (HAB, Method 6) carbo vegetabilis dil. D5 0.1 g cichorium intybus e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) pancreas suis Gl dil. D7 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Digestive disturbances in pancreatic disorders.

Warnings and precautions for use Barium/Pancreas comp. should not be used in children under 12 years as there is no adequately documented experience of use in this age group. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications Do not use in the case of allergy to milk protein.

Bambusa e nodo

Active ingredient: phyllostachys e nodo ferm 35c Globuli velati Potency/Strength Package Size Size Category D3 D6

20 g 20 g

Composition Globuli velati: 10 g contain: phyllostachys e nodo ferm 35c dil. D.. 1 g (HAB, Method 35c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the organising and formative powers, particularly in degenerative spinal diseases and connective tissue weakness. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

N1 N1

Barium/Pancreas comp. PZN 8784314 8784320

Price Group A A

Status Pharmacy only Pharmacy only

therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bambusa e nodo. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

106



N1

PZN 1750855

20 g

Composition Globuli velati: 10 g contain: barium citricum dil. D9 0.1 g (HAB, Method 6) carbo vegetabilis dil. D5 0.1 g cichorium intybus e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) pancreas suis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose.

Contraindications None known.

Liquid dilution for injection

10 x 1 ml

Potency/Strength Package Size Size Category

Indications according to the anthroposophical understanding of human beings and nature. Digestive disturbances in pancreatic disorders.

Barium/Pancreas comp.



Globuli velati

Price Group 11

N1

PZN 8784366

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Barium/Pancreas comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The condition should have cleared up within 2 weeks. If there is no improvement within this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Status Pharmacy only

107

B

Belladonna

Contraindications The medicinal product should not be used in the case of allergic reactions to constituents of deadly nightshade (atropa belladonna). Do not use in the case of allergy to chamomile (chamomilla recutita) or other members of the Compositae family.

see Atropa belladonna e fructibus see Atropa belladonna e radice see Atropa belladonna ex herba

B

Belladonna comp., Suppositorien Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: atropa belladonna ex herba ferm 33a dil. D2 2 mg (HAB, Method 33a) chamomilla recutita e radice ferm 33c Ø 2 mg (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D4 2 mg (HAB, Method 33b) Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the balance between anabolic and catabolic processes in the smooth muscular organs of the abdominal cavity, e.g. cramping in the region of the digestive and genitourinary systems. Contraindications The medicinal product should not be used in the case of allergic reactions to constituents of deadly nightshade (atropa belladonna). Do not use in the case of allergy to chamomile (chamomilla recutita) or other plants of the Compositae family.

N1

PZN

Price Group

1880612

P

Status Pharmacy only

Warnings and precautions for use There is no adequately documented experience of use of this medicinal product in children. It should therefore not be used in children under 12 years.

Belladonna/Chamomilla

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Potency/Strength Package Size Size Category

Side-effects Very rarely, children suffering from bronchial asthma and patients with Down‘s syndrome react sensitively to constituents of deadly nightshade (atropa belladonna) and show a temporary change in respiratory rate or increased tiredness. In such cases treatment with the preparation should be discontinued and medical advice obtained.

Paediatric suppositories

Potency/Strength Package Size Size Category 10 x 1 g

Composition 1 suppository (1 g) contains: atropa belladonna ex herba ferm 33a dil. D2 1 mg (HAB, Method 33a) chamomilla recutita e radice ferm 33c Ø 1 mg (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D4 1 mg (HAB, Method 33b) Excipients: hard fat, honey.

108

Note: Belladonna comp., Suppositorien für Kinder are paediatric suppositories intended for use in infants and children under 7 years.

Side-effects Very rarely, newborn babies and infants up to 12 weeks, children suffering from bronchial asthma and patients with Down‘s syndrome react sensitively to constituents of deadly nightshade (atropa belladonna) which may cause a temporary change in respiratory rate or increased tiredness. In such cases treatment with the preparation should be discontinued and a doctor consulted.

Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum 1 to 3 times daily.

Belladonna comp., Suppositorien für Kinder



Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum 1 to 3 times daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

N1

PZN 1880776

Price Group O

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the balance between anabolic and catabolic processes in the smooth muscular organs of the abdominal cavity, e.g. cramping in the region of the digestive and genitourinary systems.

Liquid dilution for injection



10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna e radice ferm 33b dil. D5 0.1 g (HAB, Method 33b) chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Integration of the feeling organisation in the rhythmic functional processes of motility and secretion in the smooth-muscular hollow organs of the abdominal cavity, e.g. stomach/abdominal cramps (gastrointestinal spasms), indigestion (dyspepsia), painful periods (dysmenorrhoea). Contraindications Do not use in the case of known hypersensitivity to chamomile and other plants of the Compositae family or deadly nightshade.

N1 N2

PZN 1750861 2085012

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Belladonna/Chamomilla Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8784372

Price Group A

Status Pharmacy only

109

B

B

Composition Globuli velati: 10 g contain: atropa belladonna e radice ferm 33b dil. D5 0.1 g (HAB, Method 33b) chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Integration of the feeling organisation in the rhythmic functional processes of motility and secretion in the smooth-muscular hollow organs of the abdominal cavity, e.g. stomach/abdominal cramps (gastrointestinal spasms), indigestion (dyspepsia), painful periods (dysmenorrhoea). Contraindications Do not use in the case of known hypersensitivity to chamomile and other plants of the Compositae family or deadly nightshade.

consult your doctor before taking Belladonna/Chamomilla comp. Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. In acute cases the appropriate number of globuli velati should be taken sublingually every 1 to 2 hours. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should

Belladonna ex herba Augentropfen Eye drops

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: atropa belladonna ex herba ferm 33a dil. D5 0.05 g rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g Excipients: sodium chloride, sodium hydrogen carbonate and water for injections. Indications according to the anthroposophical understanding of human beings and nature. Disturbed relationship between anabolism and catabolism associated with congestion, sclerosis and deposits in the eye, e.g. cataracts. Contraindications None known.

N1 N2

PZN 1447915 1447909

Price Group C C1

B

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac 2 to 3 times weekly to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Belladonna e fructibus Augentropfen Eye drops

Berberis e fructibus

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: atropa belladonna e fructibus ferm 33a dil. D5 0.05 g (HAB, Method 33a) rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g Excipients: sodium chloride, sodium hydrogen carbonate and water for injections. Indications according to the anthroposophical understanding of human beings and nature. Disturbed relationship between anabolism and catabolism which is associated with congestion, sclerosis and deposits in the eye, e.g. accommodation disorders. Contraindications None known.

110

N1 N2

PZN 1447890 1447884

Price Group C C1

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac 2 to 3 times weekly to twice daily (see How to use/ Application of the drops). Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Active ingredient: berberis vulgaris e fructibus ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e fructibus ferm 33c dil. D.. 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2908815 2883788

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Side-effects None known.

Side-effects None known.

111

Berberis e fructibus

Berberis e fructibus comp.

Active ingredient: berberis vulgaris e fructibus ferm 33c Globuli velati

B

Potency/Strength Package Size Size Category D3 D6

20 g 20 g

Composition Globuli velati: 10 g contain: berberis vulgaris e fructibus ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis e fructibus.

N1 N1

PZN 8784395 8784426

Globuli velati Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e fructibus ferm 33c dil. D1 0.1 g (HAB, Method 33c) urtica dioica e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Integration of the feeling organisation in the life organisation in the region of the nasopharynx, e.g. inflammation of the paranasal sinuses (sinusitis), chronic inflammation or hypertrophy of the palatine or pharyngeal tonsils, mucosal hypertrophy; lymphatic constitution. Contraindications Do not use in the case of known allergy to any of the active ingredients.

112

20 g

Composition Globuli velati: 10 g contain: berberis vulgaris e fructibus ferm 33c Ø 0.1 g (HAB, Method 33c) urtica dioica e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Integration of the feeling organisation in the life organisation in the region of the nasopharynx, e.g. inflammation of the paranasal sinuses (sinusitis), chronic inflammation or hypertrophy of the palatine or pharyngeal tonsils, mucosal hypertrophy; lymphatic constitution.

N1

PZN 8784389

Price Group A

B

Status Pharmacy only

consult your doctor before taking Berberis e fructibus comp. Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 3 to 5 times daily; children under 6 years 3-7 globuli velati sublingually 3 to 5 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should

Liquid dilution for injection

10 x 1 ml



Contraindications Do not use in the case of known allergy to any of the active ingredients.

Berberis e fructibus comp.



Potency/Strength Package Size Size Category

N1

PZN 1750884

Price Group 11

Status Pharmacy only

Berberis e radice

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Active ingredient: berberis vulgaris e radice ferm 33d Liquid dilution for injection

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

D3 D6

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e radice ferm 33d dil. D.. 1 ml (HAB, Method 33d) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2908850 2883765

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

113

Berberis e radice

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 6 years.

Active ingredient: berberis vulgaris e radice ferm 33d Globuli velati

B

Potency/Strength Package Size Size Category D3

20 g

Composition Globuli velati: 10 g contain: berberis vulgaris e radice ferm 33d dil. D3 1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis e radice.

N1

PZN 8784432

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Berberis/Apis comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) atropa belladonna ex herba ferm 33a dil. D5 0.1 g (HAB, Method 33a) berberis vulgaris e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) terebinthina laricina dil. D7 0.1 g (HAB, Method 6) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organism and harmonisation of the interaction between feeling and life organisation in inflammation in the region of the lower urinary tract, e.g. in irritable bladder, cystitis.

114

N1

PZN 1750878

Price Group 11

Status Pharmacy only

Contraindications Do not use in the case of hypersensitivity to bee venom and milk protein. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the medicinal product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate.

Dosage and method of administration Unless otherwise directed, adults and children of 6 years and above 1 ml injected subcutaneously 1 to 3 times weekly to once daily.

Duration of treatment There is no evidence suggesting that prolonged use of the medicinal product might have negative effects. However, as the indications usually require treatment for a maximum of six weeks, the medicinal product should only be used for longer periods if expressly ordered by the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Berberis/Apis comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) atropa belladonna ex herba ferm 33a dil. D3 0.1 g (HAB, Method 33a) berberis vulgaris e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) terebinthina laricina trit. D2 0.1 g (HAB, Method 6) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organism and harmonisation of the interaction between feeling and life organisation in inflammation in the region of the lower urinary tract, e.g. in irritable bladder, cystitis. Contraindications Do not use in the case of known hypersensitivity to bee venom.

N1

PZN 8784449

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 6 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Apis comp. Dosage and method of administration Unless otherwise directed, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 4 times daily, in acute cases every 1 to 2 hours. Duration of treatment There is no evidence suggesting that prolonged use of the medicinal product might have negative effects. However, as the indications usually require treatment for a maximum of six weeks, the medicinal product should only be used for longer periods if expressly ordered by the doctor. Side-effects None known.

Berberis/Hypericum comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 1750890

Price Group 11

Status Pharmacy only

115

B

B

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) hypericum perforatum ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) kalium phosphoricum dil. D4 aquos. 0.1 g (HAB, Method 5b) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the feeling organisation in the pelvic region, e.g. bed wetting (enuresis nocturna), weak bladder; fluor albus. Contraindications Do not use in the case of known hypersensitivity to any of the active ingredients.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Berberis/Hypericum comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: berberis vulgaris e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) hypericum perforatum ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) kalium phosphoricum dil. D4 aquos. 0.1 g (HAB, Method 5b). Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the feeling organisation in the pelvic region, e.g. bed wetting (enuresis nocturna), weak bladder; fluor albus. Contraindications Do not use in the case of known hypersensitivity to any of the active ingredients. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Hypericum comp.

116

N1

PZN 8784455

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 2 to 4 times daily; children under 6 years 3-7 globuli velati sublingually 2 to 4 times daily; children of 6 to under 12 years 5-10 globuli velati sublingually 2 to 4 times daily; adults and children of 12 years and above 10 globuli velati sublingually 2 to 4 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Berberis/Nicotiana comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 1750909

Price Group 11

B

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e fructibus ferm 33c dil. D3 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) pulsatilla vulgaris e floribus ferm 33c dil. D5 0.1 g (HAB, Method 33c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in the anabolic metabolism where there is a tendency to spasms of the smooth muscle, particularly in the area of the reproductive organs, e.g. tendency to miscarriage, painful periods (dysmenorrhoea).

Duration of treatment There is no evidence suggesting that prolonged use of the medicinal product may have negative effects. However, as the indications for Berberis/Nicotiana comp. usually require treatment for a maximum of six weeks, the medicinal product should only be used for longer periods if expressly ordered by the doctor.

Contraindications None known.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to twice daily.

Side-effects None known.

Berberis/Nicotiana comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8784461

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: berberis vulgaris e fructibus ferm 33c dil. D3 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) pulsatilla vulgaris e floribus ferm 33c dil. D5 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in the anabolic metabolism where there is a tendency to spasms of the smooth muscle, particularly in the area of the reproductive organs, e.g. tendency to miscarriage, painful periods (dysmenorrhoea).

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 to 5 times daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Nicotiana comp.

Side-effects None known.

117

Berberis/Prostata comp. Liquid dilution for injection

B

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris ex herba ferm 33c (HAB, Method 33c) - berberis vulgaris e radice ferm 33d (HAB, Method 33d) (2:1) dil. D1 0.1 g granite dil. D9 0.1 g (HAB, Method 6) magnesium sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b). oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) prostata bovis Gl dil. D5 0.1 g (HAB, Method 41a) urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) viscum album (abietis) e planta tota ferm 34g dil. D3 0.1 g (HAB, Method 34g)

N1 N2

PZN 1750915 2085035

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers in prostatic adenomyomatosis. Contraindications Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Berberis/Prostata comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: berberis vulgaris e radice ferm 33d Ø 0.034 g (HAB, Method 33d) berberis vulgaris ex herba ferm 33c Ø 0.066 g (HAB, Method 33c) granite dil. D9 0.1 g (HAB, Method 6) magnesium sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b). oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) prostata bovis Gl dil. D5 0.1 g (HAB, Method 41a)

N1

PZN 8784478

Price Group A

Status Pharmacy only

urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) viscum album (abietis) e planta tota ferm 34g dil. D3 0.1 g (HAB, Method 34g) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers in enlargement of the prostate gland (prostatic adenomyomatosis). Contraindications None know.

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Prostata comp.

Dosage and method of administration Unless otherwise directed, 10-15 globuli velati sublingually three times daily. Side-effects None known.

Berberis/Pyrit comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c) berberis vulgaris e fructibus ferm 33c dil. D2 0.1 g (HAB, Method 33c) pyrite dil. D7 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in catarrhal inflammation of the upper airways, e.g. inflammation of the vocal cords (laryngitis), inflammation of the lining of the throat (pharyngitis), inflammation of the paranasal sinuses (sinusitis). Contraindications Do not use in the case of hypersensitivity to bee and wasp venom. Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to twice daily.

N1 N2

Price Group 11 12

Status Pharmacy only Pharmacy only

Duration of treatment Acute disorders should clear up within 2 weeks. If an acute inflammation of the upper airways does not improve within 2 days a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions. In patients with bee and wasp venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the medicinal product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. Harmless redness around the injection site can occur occasionally after subcutaneous injection.

Berberis/Quarz

Liquid dilution for injection Potency/Strength Package Size Size Category

118

PZN 1681195 2085041

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1750921 2085058

Price Group 11 12

Status Pharmacy only Pharmacy only

119

B

B

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e fructibus ferm 33c dil. D2 0.1 g (HAB, Method 33c) quartz dil. D19 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling and life organisation in the anabolic metabolism, particularly in the region of the head, e.g. constitutional, chronic and acute inflammatory swelling of the mucous membranes in the upper airways and sinuses, enlarged nasopharyngeal tonsils (adenoids).

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Contraindications None known.

Side-effects None known.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g berberis vulgaris e radice ferm 33d dil. D1 0.1 g (HAB, Method 33d) placenta bovis Gl dil. D7 0.1 g (HAB, Method 41b) sepia officinalis e volumine bursae rec. Gl dil. D6 0.1 g (HAB, Method 41c) urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Berberis/Quarz Globuli velati

Berberis/Sepia comp.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: berberis vulgaris e fructibus ferm 33c dil. D2 0.1 g (HAB, Method 33c) quartz dil. D19 aquos. 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling and life organisation in the anabolic metabolism, particularly in the region of the head, e.g. constitutional, chronic and acute inflammatory swelling of the mucous membranes in the upper airways and sinuses, enlarged nasopharyngeal tonsils (adenoids). Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that

N1

PZN 8784484

Price Group A

Status

Globuli velati

Pharmacy only

Potency/Strength Package Size Size Category

you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Quarz. Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.



20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g berberis vulgaris e radice ferm 33d Ø 0.1 g (HAB, Method 33d) placenta bovis Gl dil. D7 0.1 g (HAB, Method 41b) sepia officinalis e volumine bursae rec. Gl dil. D6 0.1 g (HAB, Method 41c) urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose. Indications Harmonisation of formative and regenerative processes in benign tumours of the uterine muscle (uterine fibroids) with abnormal bleeding; menopausal symptoms. Contraindications None known.

N1

PZN 8784509

Price Group A

Status Pharmacy only

Warnings and precautions for use As the indications of Berberis/Sepia comp. do not occur in children the medicinal product should not be used in children. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Sepia comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually three times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Berberis/Sepia comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

120

10 x 1 ml

N1

PZN 1750944

Price Group 11

Status Pharmacy only

121

B

Berberis/Uterus comp.

Berberis/Urtica urens

Liquid dilution for injection

Liquid dilution for injection

B

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1750950 2085101

Price Group 11 12

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only



Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e radice ferm 33d dil. D1 0.1 g (HAB, Method 33d) urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c)

Contraindications Do not use in the case of known allergy to any of the active ingredients.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the interaction between feeling and life organisation in weakened formative processes in the pelvic region, e.g. prolonged, heavy menstrual periods (menorrhagia), bleeding due to benign muscular growths in the womb (metrorrhagia due to uterine fibroids), difficulty passing water due to enlargement of the prostate (micturition problems in stage 1 to 2 prostatic adenoma).

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Side-effects None known.

Berberis/Urtica urens

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris ex herba ferm 33c (HAB, Method 33c) - berberis vulgaris e radice ferm 33d (HAB, Method 33d (2:1) dil. D1 0.1 g granite dil. D9 0.1 g (HAB, Method 6) magnesium sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b). ovaria bovis Gl dil. D5 0.1 g (HAB, Method 41a) oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) uterus bovis Gl dil. D5 0.1 g (HAB, Method 41c) viscum album (mali) e planta tota ferm 34i dil. D3 0.1 g (HAB, Method 34i)

N1 N2

PZN 1750973 2085118

Price Group 11 12

B

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in abnormalities of form in the uterus, e.g. benign growths in the wall of the uterus (uterine fibroids). Contraindications Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8784515

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: berberis vulgaris e radice ferm 33d Ø 0.1 g (HAB, Method 33d) urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

Contraindications Do not use in the case of known allergy to any of the active ingredients.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the interaction between feeling and life organisation in weakened formative processes in the pelvic region, e.g. prolonged, heavy menstrual periods (menorrhagia), bleeding due to benign muscular growths in the womb (metrorrhagia due to uterine fibroids), difficulty passing water due to enlargement of the prostate (micturition problems in stage 1 to 2 prostatic adenoma).

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually three times daily.

122

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Urtica urens.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Berberis/Uterus comp. Globuli velati

Potency/Strength Package Size Size Category Composition Globuli velati: 10 g contain: berberis vulgaris e radice ferm 33d Ø 0.034 g (HAB, Method 33d) berberis vulgaris ex herba ferm 33c Ø 0.066 g (HAB, Method 33c) granite dil. D9 0.1 g (HAB, Method 6) magnesium sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b) ovaria bovis Gl dil. D5 0.1 g (HAB, Method 41a)

20 g

N1

PZN 8784521

Price Group A

Status Pharmacy only

oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) uterus bovis Gl dil. D5 0.1 g (HAB, Method 41c) viscum album (mali) e planta tota ferm 34i dil. D3 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose.

Side-effects None known.

123

B

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in abnormalities of form in the uterus, e.g. benign growths in the wall of the uterus (uterine fibroids). Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Berberis/Uterus comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Side-effects None known.

Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor.

Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Betula/Arnica comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

Betula e foliis



Active ingredient: betula pendula ferm 34e Liquid dilution for injection Potency/Strength Package Size Size Category D4

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: betula pendula ferm 34e dil. D4 1 ml (HAB, Method 34e) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2908933

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Side-effects None known.

Betula e foliis W 5%, Oleum

Active ingredient: betula pendula/pubescens e foliis sicc. W 5% Liquid bath additive Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: betula pendula/pubescens e foliis W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Prevention and treatment of metabolic disorders leading to tissue deposits and degenerative changes, such as gout, rheumatism, sclerosis;

124

N1

PZN 2088252

Price Group N1

Status Pharmacy only

stimulation of the excretory function of the kidneys; eczema. Contraindications None known. Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths.

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D7 0.1 g arnica montana e planta tota ferm 33c dil. D14 0.1 g (HAB, Method 33c) betula pendula e cortice, decoctum dil. D4 0.1 g (HAB, Method 23a) betula pendula ferm 34e dil. D3 0.1 g formica rufa ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) sulfur dil. D5 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Inflammatory conditions of the joints (acute arthritides) of rheumatic or degenerative origin, muscular rheumatism, disorders of the tissues around the joints (periarthropathy).

N1 N2

PZN 1750996 2085124

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use There is no adequately documented experience of the use of Betula/Arnica comp. in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Betula/Arnica comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8784544

Price Group A

Status Pharmacy only

125

B

B

Composition Globuli velati: 10 g contain: argentum metallicum dil. D7 0.1 g arnica montana e planta tota ferm 33c dil. D14 0.1 g (HAB, Method 33c) betula pendula e cortice, decoctum Ø 0.2 g (HAB, Method 23a) betula pendula ferm 34e dil. D1 0.1 g formica rufa ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) sulfur dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose.

Warnings and precautions for use There is no adequately documented experience of use of this medicinal product in children under 6 years. It should therefore not be used in children under 6 years. In children between 6 and 12 years medical advice should be sought before using Betula/Arnica comp. and the medicinal product should not be used in place of any other treatment prescribed by the doctor. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Betula/Arnica comp.

Indications according to the anthroposophical understanding of human beings and nature. Acute inflammatory conditions of the joints (arthritides) of rheumatic or degenerative origin, muscular rheumatism, disorders of the tissues around the joints (periarthropathy).

Duration of treatment The condition should have cleared up within 2 weeks. If there is no improvement within this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor.

Contraindications None known.

Dosage and method of administration Unless otherwise directed, adults and children from 6 to under 12 years 5 to 10 globuli velati sublingually once to twice daily.

Side-effects None known.

Betula/Mandragora comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: betula pendula e cortice, decoctum dil. D3 0.1 g (HAB, Method 23a) filipendula ulmaria ferm 34c dil. D2 0.1 g galenite dil. D6 0.1 g mandragora officinarum e radice ferm 34d dil. D3 0.1 g (HAB, Method 34d) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in painful degenerative and chronic inflammatory disorders of the musculoskeletal system, e.g. inflammation of the joints (arthritis), degenerative joint disease (osteoarthritis), subacute muscular and articular rheumatism.

126

N1 N2

PZN 1751004 2085130

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of known allergy to birch or any of the other active ingredients. Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use There is no adequately documented experience of use of this medicinal product in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Harmless irritation at the site of injection may very rarely occur.

B

Betula/Mandragora comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: betula pendula e cortice, decoctum dil. D3 0.1 g (HAB, Method 23a) filipendula ulmaria ferm 34c dil. D2 0.1 g galenite dil. D6 0.1 g mandragora officinarum e radice ferm 34d dil. D3 0.1 g (HAB, Method 34d) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in painful degenerative and chronic inflammatory disorders of the musculoskeletal system, e.g. inflammation of the joints (arthritis), degenerative joint disease (osteoarthritis), subacute muscular and articular rheumatism.

N1

PZN 8784550

Price Group A

Status Pharmacy only

the other active ingredients. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Betula/ Mandragora comp. Dosage and method of administration Unless otherwise directed, children under 6 years 5-10 globuli velati sublingually 2 to 4 times daily; adults and children of 6 years and above 10-15 globuli velati sublingually 2 to 4 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications Do not use in the case of known allergy to birch or any of

Bindegewebe Gl

Active ingredient: textus connectivus bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2831366 3359575 2831142 3359581 3359598 3359606 3359612 3359629 0847564 2493716

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

127

B

Composition Liquid dilution for injection: 1 ml contains: textus connectivus bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use There is no adequately documented experience of use of this medicinal product in children. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Dosage and method of administration Unless otherwise directed, rub the oil into the affected joints and areas of muscle once to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be

Oily embrocation

Potency/Strength Package Size Size Category

Birken Rheumaöl mit Arnika (birch-based rheumatism oil with arnica) Oily embrocation



50 ml 100 ml

Composition 10 g (11 ml) contain: anisi stellati aetheroleum 0.035 g arctium lappa e radice W 5% (HAB, Method 12g with refined arachis oil) 2.45 g arnica montana e floribus W 5% (HAB, Method 12g with refined arachis oil) 2.45 g betula pendula/pubescens e foliis W 5% (HAB, Method 12g with refined arachis oil) 2.45 g oily extract of formica rufa rec. (10:1); extraction agent: refined arachis oil 0.01 g urtica dioica ex herba W 5% (HAB, Method 12g with refined arachis oil) 2.45 g Excipient: refined arachis oil.

N1 N1

PZN 1753606 1753701

Side-effects In rare cases hypersensitivity reactions may occur in the skin; in this case use of the preparation should be discontinued.

Birken Rheumaöl ohne Arnika (birch-based rheumatism oil without arnica)



Potency/Strength Package Size Size Category

consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Price Group L L1

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Painful, traumatic, inflammatory or rheumatic disorders of the muscles or joints. Contraindications Birken Rheumaöl mit Arnika should not be used for children under 2 years, for patients with known hypersensitivity to arnica or other plants of the Compositae family, to aniseed or anethol, birch pollen or to any of the other active ingredients. Do not apply to damaged skin. Warnings and precautions for use Birken Rheumaöl mit Arnika should not be used for children from 2 to 12 years of age without the advice of a doctor and should not be used in place of any other treatment prescribed by the doctor. In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis).

100 ml

Composition 10 g (11 ml) contain: anisi stellati aetheroleum 0.035 g arctium lappa e radice W 5% (HAB, Method 12g with refined arachis oil) 3.30 g betula pendula/pubescens e foliis W 5% (HAB, Method 12g with refined arachis oil) 3.30 g oily extract of formica rufa rec. (10:1); extraction agent: refined arachis oil 0.01 g urtica dioica ex herba W 5% (HAB, Method 12g with refined arachis oil) 3.30 g Excipient: refined arachis oil. Indications according to the anthroposophical understanding of human beings and nature. Painful traumatic, inflammatory or rheumatic disorders of the muscles or joints. Contraindications Birken Rheumaöl ohne Arnika should not be used for children under 2 years or for patients with known hypersen-

N1

PZN 1753718

Price Group L1

Status Pharmacy only

sitivity to aniseed or anethol, birch pollen or any of the other active ingredients. Warnings and precautions for use Birken Rheumaöl ohne Arnika should not be used in children from 2 to 12 years of age without the advice of a doctor and should not be used in place of any other treatment prescribed by the doctor. In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub the oil into the affected joints and areas of muscle once to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases hypersensitivity reactions may occur in the skin; in this case use of the preparation should be discontinued.

Bitter Elixier Syrup

Potency/Strength Package Size Size Category

128

18 ml 180 ml

PZN 4505990 1119022

Price Group T1 T

Status General sale General sale

129

B

B

Composition 10 g (8.5 ml) contain: aqueous whole extract with sugar from gentian root 0.2165 g from ginger root 0.133 g from calamus root 0.02 g from pepper fruits 0.004 g from aerial parts of wormwood 0.1665 g Excipient: sucrose (saccharose). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the peptic digestive activity by harmonisation of the motor and secretory processes, e.g. lack of appetite, feeling of fullness, nausea. Contraindications Bitter Elixier should not be used in the case of known hypersensitivity to ginger or pepper or in the case of gastrointestinal ulcers. Patients with gallstones should only use the medicinal product after consulting their doctor. Bitter Elixier should not be used while pregnant or breastfeeding.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in small children is not available. It should therefore not be used in children under 6 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bitter Elixier. 1 tablespoonful (15 ml) contains 7 g sucrose (sugar), equivalent to about 0.4 BE (1 BE [bread exchange] is equivalent to 10-12 g carbohydrates). If you are on a diabetes diet you must take this into account. Dosage and method of administration Unless otherwise directed, children from 6 to under 12 years take 1 teaspoonful of Bitter Elixier 1 to 3 times daily before meals, either undiluted or diluted with water; adults and children of 12 years and above take 1 tablespoonful of syrup, diluted with water if desired, 1 to 3 times daily before meals.

Side-effects None known.



Potency/Strength Package Size Size Category

Composition 10 g powder contain: acorus calamus e rhizoma ferm 33d Ø 0.01 g (HAB, Method 33d) anisi stellati aetheroleum 0.05 g arsenicum album dil. D4 aquos. 0.01 g (HAB, Method 5b) artemisia abrotanum ex herba ferm 33c Ø 0.01 g (HAB, Method 33c) carbo vegetabilis trit. D1 0.1 g carvi aetheroleum 0.05 g chamomilla recutita e planta tota ferm 33c Ø 0.01 g (HAB, Method 33c)

130

Dosage and method of administration Unless otherwise directed, children under 6 years 1/2 to 1 teaspoonful of Bolus alba comp. Pulver, adults and children of 6 years and above 1 to 2 teaspoonsful of Bolus alba comp. Pulver stirred into a cup of warm water and

Borago comp.

Powder

50 g

Warnings and precautions for use This medicinal product contains glucose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bolus alba comp. Pulver.

Duration of treatment The condition should have cleared up within 5 days. If no improvement occurs during this time a doctor should be consulted.

Bolus alba comp. Pulver



Contraindications The medicinal product should not be used in the case of known hypersensitivity to chamomile or other plants of the Compositae family, anise or anethol, umbellifers, caraway oil or to any of the excipients.

N1

PZN 1447938

Price Group Q

Status Pharmacy only

gentiana lutea e radice ferm 33c Ø 0.01 g (HAB, Method 33c) geum urbanum e radice ferm 33c Ø 0.01 g (HAB, Method 33c) kaolinum ponderosum 9.26 g Excipients: glucose syrup (spray dried), acacia (spray dried), maltodextrin. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the metabolic processes in the digestive system in disturbances of secretion and motility in the gastrointestinal tract, e.g. in diarrhoea, vomiting.

drunk in sips every two hours to hourly in the course of the day. Duration of treatment In the case of acute diarrhoea and vomiting the medicinal product should not be used for more than two days without obtaining medical advice. In the case of infants and small children a doctor should be seen after one day already. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects On account of the anise oil contained in the medicinal product, in rare cases allergic reactions of the skin, the airways or the gastrointestinal tract may occur; in such cases you should stop using the medicinal product and see a doctor.

Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aesculus hippocastanum e semine ferm 34c dil. D9 0.1 g (HAB, Method 34c) borago officinalis e foliis ferm 34b dil. D2 0.1 g (HAB, Method 34b) cnicus benedictus ex herba ferm 33d dil. D2 0.1 g (HAB, Method 33d) hamamelis virginiana e foliis ferm 33d dil. D2 0.1 g (HAB, Method 33d) nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) scorodite dil. D9 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative and rheological forces in inflammation of the veins with development of thrombosis (thrombophlebitis), thrombosis and varicose veins (varicose symptom complex).

N1 N2

PZN 1751010 2085147

Price Group 11 12

Status Pharmacy only Pharmacy only

positae family, or to any other ingredient of the medicinal product. Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications Do not use in the case of known hypersensitivity to holy thistle (cnicus benedictus) and other plants of the Com-

131

B

Borago comp. Globuli velati

B

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aesculus hippocastanum e semine ferm 34c dil. D9 0.1 g (HAB, Method 34c) borago officinalis e foliis ferm 34b dil. D2 0.1 g (HAB, Method 34b) cnicus benedictus ex herba ferm 33d dil. D2 0.1 g (HAB, Method 33d) hamamelis virginiana e foliis ferm 33d dil. D2 0.1 g (HAB, Method 33d) nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) scorodite dil. D9 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative and rheological forces in inflammation of the veins with development of thrombosis (thrombophlebitis), thrombosis and varicose veins (varicose symptom complex).

N1

PZN 8784567

Price Group A

Status Pharmacy only

Contraindications None known.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily, in the acute stage every 1 to 2 hours. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

Active ingredient: borago officinalis ex herba LA 20% Tincture for external use



100 ml

Composition 10 g (10.3 ml) contain: borago officinalis ex herba LA 20 % 10 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic and structuring forces, e.g. in disorders associated with varicose veins (varicose symptom complex) with venous congestion, inflammation of the veins with development of thrombosis (thrombophlebitis) and accompanying eczematous skin disorders.

132

N1

1681309

B

Tincture for external use

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (10.2 ml) contain: arnica montana e floribus LA 20% 1.5 g (HAB, Method 12c) calendula officinalis e floribus LA 20% 1.0 g (HAB, Method 12c) cantharis ex animale toto Gl dil. D6 1.0 g (HAB, Method 41c) symphytum officinalis ex herba LA 20 % 1.0 g (HAB, Method 12c) thuja occidentalis e summitatibus LA 20% 1.0 g (HAB, Method 12c) urtica urens ex herba LA 20 % 4.5 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. First and second degree burns and scalds, sunburn, allergic and hyperergic skin disorders (dermatoses), insect bites and stings, grazes and ulcers.

Borago-Essenz

PZN

Side-effects None known.

Brandessenz (burns lotion)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Borago comp.

Potency/Strength Package Size Size Category

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Price Group E

N1

PZN 1681315

Price Group E

Status Pharmacy only

Contraindications Brandessenz should not be used in the case of hypersensitivity to Arnica, other plants of the Compositae family or Thuja (arbor vitae). Warnings and precautions for use Contains 23% (v/v) alcohol. Dosage and method of administration Unless otherwise directed, add 1 tablespoonful of Brandessenz to approx. 250 ml of luke warm water and use for compresses. For treatment of insect bites and stings dab the affected areas with undiluted Brandessenz. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases allergic skin reactions may occur in people who are hypersensitive to arnica. In this case use of the preparation should be discontinued.

Status Pharmacy only

Contraindications Do not use in the case of known hypersensitivity to the active ingredient. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Contains 25% (v/v) alcohol. Dosage and method of administration Unless otherwise directed, add 5 to not more than 10 ml of tincture to approx. 125 ml of luke warm water and use once daily for compresses. The enclosed measuring cup should be used.

Bronchi Gl

Active ingredient: bronchi bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 3359658 3359664 3359670 3359687 3359693 3359701 2831194

Price Group 41 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

133

Potency/Strength Package Size Size Category D30 Serial pack II Serial pack III

B

10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1

PZN 3359718 0845803 2494012

Price Group 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: bronchi bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Bronchi/Plantago comp. see Bronchi Plantago Inject see Bronchi Plantago Globuli velati

Bronchi Plantago Inject Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bronchi bovis Gl dil. D16 0.1 g (HAB, Method 41b) bryonia cretica ferm 33b dil. D7 0.1 g eupatorium cannabinum ex herba ferm 33c dil. D7 0.1 g (HAB, Method 33c) larynx bovis Gl dil. D16 0.1 g (HAB, Method 41b) plantago lanceolata e foliis ferm 34c dil. D5 0.1 g (HAB, Method 34c) pyrite dil. D14 aquos. 0.1 g tunica mucosa nasi bovis Gl dil. D13 0.1 g (HAB, Method 41a)

134

N1 N2

PZN 0085060 0089690

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the engagement of the feeling organisation in the mucous membranes of the airways, e.g. in acute and chronic inflammation of the vocal cords (larynx) and bronchi. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times weekly to once daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If an acute inflammation of the upper airways does not improve within 2 days a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor.

Side-effects None known.

B

Bronchi Plantago Globuli velati Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: bronchi bovis Gl dil. D16 0.1 g (HAB, Method 41b) bryonia cretica ferm 33b dil. D7 0.1 g eupatorium cannabinum ex herba ferm 33c dil. D7 0.1 g (HAB, Method 33c) larynx bovis Gl dil. D16 0.1 g (HAB, Method 41b) plantago lanceolata e foliis ferm 34c dil. D5 0.1 g (HAB, Method 34c) pyrite dil. D14 aquos. 0.1 g tunica mucosa nasi bovis Gl dil. D13 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the engagement of the feeling organisation in the mucous membranes of the airways, e.g. in acute and chronic inflammation of the larynx (vocal cords) and bronchi.

N1

PZN 0085350

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bronchi/Plantago Globuli velati. Dosage and method of administration Unless otherwise directed, infants and small children under 6 years 3-5 globuli velati sublingually once to twice daily; adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If an acute inflammation of the upper airways does not improve within 2 days a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Bryonia comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) atropa belladonna e radice ferm 33b dil. D5 0.1 g (HAB, Method 33b)

N1

PZN 1751027

Price Group 11

Status Pharmacy only

bryonia cretica ferm 33b dil. D5 0.1 g pulsatilla vulgaris e floribus ferm 33c dil. D5 0.1 g (HAB, Method 33c)

135

B

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between the feeling and life organisation chiefly in the region of the reproductive organs, e.g. inflammation of the uterine appendages (adnexitis), ovarian cysts. Contraindications Do not use in the case of known hypersensitivity to bee venom. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the medicinal product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should

therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate.

Bryonia e radice

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

D3 D4 D8 D12 D30

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case the patient should see a doctor. Side-effects None known.

Bryonia comp.

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bryonia cretica ferm 33b dil. D.. 1 ml Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1

B PZN 2832779 3358222 3358239 3358245 2832704

Price Group 31 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Active ingredient: bryonia cretica ferm 33b Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c) atropa belladonna e radice ferm 33b dil. D3 0.1 g (HAB, Method 33b) bryonia cretica ferm 33b dil. D2 0.1 g pulsatilla vulgaris e floribus ferm 33c dil. D5 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between the feeling and life organisation chiefly in the region of the reproductive organs, e.g. inflammation of the uterine appendages (adnexitis), ovarian cysts. Contraindications Do not use in the case of known hypersensitivity to bee venom.

136

Potency/Strength Package Size Size Category

Bryonia e radice

Globuli velati



Active ingredient: bryonia cretica ferm 33b Liquid dilution for injection

N1

PZN 8784596

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of Bryonia comp. for the specified indications in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bryonia comp. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily to every 2 hours. Duration of treatment Acute disorders should clear up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

Potency/Strength Package Size Size Category D3 D4 D6 D12 D20

20g 20g 20g 20g 20g

Composition Globuli velati: 10 g contain: bryonia cretica ferm 33b dil. D.. 1g Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bryonia e radice.

N1 N1 N1 N1 N1

PZN 8784604 8784610 8784627 8784633 8784656

Price Group A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

137

Bryonia/Aconitum

Bryonia/Stannum

Liquid dilution for injection

B

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 2233866

Price Group 11

Status

Potency/Strength Package Size Size Category

Pharmacy only



Composition Liquid dilution for injection: 1 ml contains: aconitum napellus e tubere ferm 33c dil. D5 0.1 g (HAB, Method 33c) bryonia cretica ferm 33b dil. D7 0.1 g

medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the rhythmic relationship between life and feeling organisation in febrile illnesses with inflammation in the region of the airways.

Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications None known.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously once to twice daily.

Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bryonia cretica ferm 33b dil. D2 0.1 g stannum metallicum dil. D9 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Structuring of the fluid organism in conditions involving exudates or transudates of the serous membranes, e.g. adjunctive treatment of inflammation of the membrane covering the lungs (pleurisy) and inflammation of the lining of the abdominal cavity (peritonitis), joint inflammation (acute arthritis), inflammation of a bursa (bursitis). Contraindications Do not use in the case of hypersensitivity to milk protein. Do not use in children under 6 years.

Bryonia/Aconitum

N1 N2

PZN 1751033 2085207

Price Group 11 12

B

Status Pharmacy only Pharmacy only

Warnings and precautions for use In children from 6 to 12 years Bryonia/Stannum should only be used for the indications pleurisy and peritonitis after consulting a doctor. Dosage and method of administration Unless otherwise directed, children from 6 to under 12 years 0.5-1 ml injected subcutaneously once a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aconitum napellus e tubere ferm 33c dil. D5 0.1 g bryonia cretica ferm 33b dil. D7 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the rhythmic relationship between life and feeling organisation in febrile illnesses with inflammation in the region of the airways. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bryonia/Aconitum.

138

N1

PZN 8784662

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 4 times daily, children under 6 years 3-5 globuli velati sublingually 2 to 4 times daily and children from 6 years to under 12 years 5-7 globuli velati sublingually 2 to 4 times daily; adults and children of 12 years and above 5-10 globuli velati sublingually 2 to 4 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Bryonia/Stannum Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8784679

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: bryonia cretica ferm 33b dil. D2 0.1 g stannum metallicum dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose.

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Structuring of the fluid organism in conditions involving exudates or transudates of the serous membranes, e.g. joint inflammation (acute arthritis), inflammation of a bursa (bursitis), adjunctive treatment of inflammation of the membrane covering the lungs (pleurisy) and inflammation of the lining of the abdominal cavity (peritonitis).

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; children from 6 to under 12 years 5-7 globuli velati sublingually 1 to 3 times daily; adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bryonia/ Stannum.

139

B

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Bryophyllum comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Bryophyllum comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 2085213

Price Group 11

Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Indications according to the anthroposophical understanding of human beings and nature. Integration of metabolic processes that have become independent with hysteriform symptoms and dysphoric moods, e.g. states of anxiety and agitation, menopausal symptoms and premenstrual syndrome.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Bryophyllum comp. Globuli velati



20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D5 0.1 g kalanchoe daigremontiana/pinnata e foliis ferm 33b dil. D3 0.1 g (HAB, Method 33b) uterus bovis Gl dil. D5 0.1 g (HAB, Method 41c) Contains sucrose (saccharose/sugar) and lactose.

140

N1

PZN 8784685

Price Group A

Side-effects None known.

Bulbus olfactorius Gl

Active ingredient: bulbus olfactorius bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bulbus oflactorius bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Potency/Strength Package Size Size Category

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Status

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D5 0.1 g kalanchoe daigremontiana/pinnata e foliis ferm 33b dil. D3 0.1 g (HAB, Method 33b) uterus bovis Gl dil. D5 0.1 g (HAB, Method 41c)

Contraindications Do not use in the case of hypersensitivity to the donor animal protein or to milk protein.

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Status Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2909594 2909619 2909631 2909677 2909708 2909720 2490014

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Integration of metabolic processes that have become independent with hysteriform symptoms and dysphoric moods, e.g. states of anxiety and agitation, menopausal symptoms and premenstrual syndrome. Contraindications None known.

141

B

Bursae articulationis humeri-Komplex Gl

Cactus ex herba

Active ingredient: bursae artuculationis humeri complex bovis GI Liquid dilution for injection

B

Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bursae articulationis humeri complex bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 4616175 2910120 4616198 0488970 4626191 2910172 2490066

Active ingredient: selenicereus grandiflorus ex herba ferm 33d Liquid dilution for injection

Price Group 61 61 61 61 61 61 51

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

D2 D10

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: selenicereus grandiflorus ex herba ferm 33d dil. D.. 1 ml (HAB, Method 33d) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2910396 2883883

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Cactus ex herba

Active ingredient: selenicereus grandiflorus ex herba ferm 33d Globuli velati Potency/Strength Package Size Size Category D2 D4

20 g 20 g

Composition herba ferm 33d dil. D.. 1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cactus ex herba.

N1 N1

PZN 8784751 8784768

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Cactus comp. II

Liquid dilution for injection Potency/Strength Package Size Size Category

142

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1751062 2085259

Price Group 11 12

Status Pharmacy only Pharmacy only

143

C

C

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D14 0.1 g (HAB, Method 33c) cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) dil. D5 0.1 g (HAB, Method 6) crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) selenicereus grandiflorus ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the life organisation in the rhythmic system, e.g. in functional cardiac dysrhythmias, tightness in the chest (anginal pain), age-related heart weakness and after heart attack.

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times weekly to once daily. Cactus comp. II, liquid dilution for injection is not suitable for use in children under 12 years. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Cactus comp. II Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D14 0.1 g (HAB, Method 33c) cinis e fructibus avenae sativaecum magnesio phosphorico (1:1) trit. D2 0.5 g (HAB, Method 6) crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) selenicereus grandiflorus ex herba ferm 33d dil. D2 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the life organisation in the rhythmic system, e.g. in functional cardiac dysrhythmias, tightness in the chest (anginal pain), age-related heart weakness and after heart attack.

144

N1

PZN 8784745

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cactus comp. II. Dosage and method of administration Unless otherwise directed, infants and children up to under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, in acute cases every 1 to 2 hours; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily, in acute cases every 1 to 2 hours. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Duration of treatment If symptoms persist a doctor should be consulted.

Side-effects None known.

Calcea Wund- und Heilcreme (healing cream)

C

Cream

Potency/Strength Package Size Size Category

10 g 30 g 100 g

Composition 10 g contain: mixture of calendula ex herba flor. pressed juice and 96% ethanol (1:0.33) 1.0 g echinacea Ø 1.1 g Excipients: emulsifying cetylstearyl alcohol (type A), 96% ethanol, refined maize oil, yellow beeswax, purified water. Indications according to the anthroposophical understanding of human beings and nature. Topical treatment of wounds and superficial inflammatory conditions of the skin, prevention and treatment of pressure sores (decubital ulcers). Contraindications The medicinal product should not be used in the case of known hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. Warnings and precautions for use Cetylstearyl alcohol can cause local skin reactions (e.g. contact dermatitis).

N1 N1 N2

PZN 3932891 3932916 3932922

Price Group J2 J3 J4

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, apply the cream sparingly 2 to 3 times daily to the skin areas requiring protection, to affected skin areas or to wounds. Massage gently into intact skin. Duration of treatment Do not use for longer than eight weeks without obtaining medical advice. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using preparations containing formulations of purple cone flower (echinacea). There have been reports of local allergic reactions (inflammation of the skin). In such cases you should stop using the medicinal product and see a doctor. Because of the alcohol content, brief stinging may occur when the cream is applied to open wounds or mucous membranes.

Calcium carbonicum/Cortex Quercus see Calcium Quercus Inject see Calcium Quercus Inject 10 see Calcium Quercus Globuli velati

Calcium carbonicum cum Quercu

Active ingredient: quercus robur/petraea e cortice cum calcio carbonico aquos. Liquid dilution for injection Potenz/Stärke Packungsgröße Normgröße PZN D12

10 x 1 ml

N1

2910410

Preisgruppe 31

Status Pharmacy only

145

C

Composition Liquid dilution for injection: 1 ml contains: quercus robur/petraea e cortice cum calcio carbonico dil. sol.=D6 prepared by potentising quercus robur/petraea e cortice, decoctum Ø (HAB, Method 23a) five times with saturated aqueous solution of calcium carbonicum e cinere quercus) D12 aquos. 1 ml (HAB, Method 5b)

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Calcium Quercus Inject 10

Active ingredient: quercus robur/petraea e cortice cum calcio carbonico solution = D6 Liquid dilution for injection Potency/Strength Package Size Size Category

5 x 10 ml 20 x 10 ml

Composition Liquid dilution for injection: 10 ml contain: quercus robur/petraea e cortice cum calcio carbonico sol.=D6 [prepared from quercus robur/petraea e cortice, decoctum Ø (HAB, Method 23a) by potentising five times with saturated aqueous solution of calcium carbonicum e cinere quercus] 10 ml (HAB, Method 5b) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation in dystopic activity of the feeling organisation with disturbances of the anabolic metabolism, e.g. allergies, eczema, inflammatory skin conditions (dermatitis), excessive menstrual flow (menorrhagia).

N1 N2

PZN 0079898 0089885

Price Group 21 22

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, in acute cases 10 ml by intravenous or intramuscular injection once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: quercus robur/petraea e cortice cum calcio carbonico solution = D6 Liquid dilution for injection

10 x 1 ml 50 x 1 ml

N1 N2

PZN 0079757 0089879

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 2 to 3 times a week to once daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously 2 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Calcium Quercus Globuli velati

Active ingredient: quercus robur/petraea e cortice cum calcio carbonico solution = D6 Globuli velati



Calcium Quercus Inject



Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation in dystopic activity of the feeling organisation with disturbances of the anabolic metabolism, e.g. allergies, eczema, inflammatory skin conditions (dermatitis), excessive menstrual flow (menorrhagia).

Contraindications None known.

Potency/Strength Package Size Size Category

Contraindications None known.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: quercus robur/petraea e cortice cum calcio carbonico sol.=D6 [prepared from quercus robur/petraea e cortice, decoctum Ø (HAB, Method 23a) by potentising five times with saturated aqueous solution of calcium carbonicum e cinere quercus)] 1 ml (HAB, Method 5b)

Price Group 11 12

Status Pharmacy only Pharmacy only

20 g

Composition Globuli velati: 10 g contain: quercus robur/petraea e cortice cum calcio carbonico sol.=D6 [prepared from quercus robur/petraea e cortice, decoctum Ø (HAB, Method 23a) by potentising four times with saturated aqueous solution of calcium carbonicum e cinere quercus and subsequent potentising with sugar syrup prepared therefrom] 1 g (HAB, Method 5b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation in dystopic activity of the feeling organisation with disturbances of the anabolic metabolism, e.g. allergies, eczema, inflammatory skin conditions (dermatitis), excessive menstrual flow (menorrhagia). Contraindications None known.

N1

PZN 0081091

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Calcium Quercus Globuli velati. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Calendula e floribus W 10%, Oleum

Active ingredient: calendula officinalis e floribus W 10% Bath additive, liquid Potency/Strength Package Size Size Category

146

100 ml

PZN 2088312

Price Group N1

Status General sale

147

C

C

Composition 10 g (11 ml) contain: calendula officinalis e floribus W 10% (HAB, Method 12f with virgin olive oil) 10 g

full bath tub (about 200 l water) for oil dispersion baths. Measure out the correct amount using the measuring cup provided. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Indications according to the anthroposophical understanding of human beings and nature. Subacute inflammatory processes of the skin.

Duration of treatment If there is no marked improvement in the symptoms after using the medicinal product for one week please see a doctor.

Contraindications Do not use Calendula e floribus W 10%, Oleum, in the case of hypersensitivity to calendula or other plants of the Compositae family.

Side-effects None known.

Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive for a

Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: calendula officinalis ex herba ferm 33c dil. D3 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N2

PZN 2910433 2910456

Price Group 31 32

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Potency/Strength Package Size Size Category

Composition 10 g (10.3 ml) contain: calendula officinalis e floribus LA 20% 10 g (HAB, Method 12c) Indications according to the anthroposophical understanding of hu-

148

Potency/Strength Package Size Size Category D3

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: camphora dil. D3 aquos. 1 ml (HAB, Method 5b)) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2830421

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Active ingredient: camphora 5% Bath additive, liquid 100 ml

Active ingredient: calendula officinalis e floribus LA 20% Tincture

100 ml 500 ml

Side-effects Allergy to calendula (pot marigold) can occur. The frequency is not known.

Camphora 5%, Oleum

Calendula-Essenz



Dosage and method of administration Unless otherwise directed the following applies for adults and children of all age groups: Compresses: add 1 to 2 teaspoonsful of Calendula-Essenz to about 250 ml boiled water, soak a compress with this

Duration of treatment If no definite wound healing is observed after using the medicinal product for one week, a doctor should be consulted. Nevertheless, large wounds, particularly in areas with a poor blood supply (e.g. decubital ulcers), may require more long-term treatment with Calendula-Essenz.

Active ingredient: camphora aquos. Liquid dilution for injection

Active ingredient: calendula officinalis ex herba ferm 33c Liquid dilution for injection

10 x 1 ml 50 x 1 ml

Warnings and precautions for use In the case of pronounced redness of the wound edges, increasing pain, weeping wounds and suppuration (pus formation) treatment by a doctor is necessary. Mouthwashing in children should only be performed under adult supervision. Contains 25% (v/v) alcohol.

solution and place on the affected skin area for about 15 minutes once to twice daily. Mouthwashes: add 1 tablespoonful of Calendula-Essenz to about 125 ml warm water and rinse the oral cavity for about 2 to 3 minutes 1 to 3 times daily.

Camphora

Calendula ex herba

D3 D3

Contraindications Calendula-Essenz must not be used in the case of hypersensitivity to calendula or other plants of the Compositae family.

N1 N2

PZN 1681338 1948528

Potency/Strength Package Size Size Category Price Group D D1

Status Pharmacy only Pharmacy only

man beings and nature. Inflammatory conditions of the skin and underlying tissues in which there is a tendency to pus formation; wounds healing by secondary intention. Local treatment of wounds and superficial inflammation. Irrigation of wound cavities and inflamed mucous membranes.



100 ml

Composition 10 g (11 ml) contain: camphora 5% (HAB, Method 12i in virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Peripheral vascular disease, nerve pain (neuralgia), rheumatic pain, bronchitis.

N1

PZN 2088341

Price Group N1

Status Pharmacy only

Contraindications The medicinal product must not be used • in the case of known hypersensitivity to camphor, • in the case of high blood pressure (hypertension), • during pregnancy, breastfeeding or in children under two years because of the camphor content, • in damaged skin, e.g. in the case of burns.

149

C

C

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children from 2 to under 12 years after consulting a doctor. When using Camphora 5%, Oleum, do not allow the medicinal product to come into contact with the eyes. Dosage and method of administration Unless otherwise directed, for adults and children of 12 years and above use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects In the case of hypersensitivity to camphor contact eczema may occasionally occur; in this case use of the preparation should be discontinued. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Camphora/Hypericum, Unguentum Ointment

Potency/Strength Package Size Size Category

30 g

Composition 10 g contain: d-camphor 0.25 g oily extract of hypericum perforatum, herba rec. (4:1) Extraction agent: refined arachis oil 2.00 g Excipients: white soft paraffin, wool fat. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation in rheumatic disorders, degenerative joint disease, nerve pain, nervous angina. Contraindications The medicinal product must not be used in the case of known hypersensitivity to camphor or to any of the excipients (e.g. wool fat), on account of the camphor content during pregnancy and breastfeeding and in children under 7 years, in damaged skin, e.g. in the case of burns.

N1

PZN 2198182

Price Group J

Status Pharmacy only

Warnings and precautions for use There is no adequately documented experience of the use of Camphora/Hypericum, Unguentum in children. It should therefore not be used in children from 7-12 years either. In rare cases arachis (peanut) oil and wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in the ointment 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Photosensitisation or redness of the skin may very rarely occur; in such cases use of the medicinal product should be discontinued. Because of the camphor content the occurrence of contact dermatitis is possible.

Cantharis Blasen Inject (bladder remedy) Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: achillea millefolium ferm 33d dil. D3 0.1 g cantharis ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) equisetum arvense ex herba ferm 35b dil. D3 0.1 g (HAB, Method 35b) vesica urinaria bovis Gl dil. D7 0.1 g (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Harmonious integration of the feeling organisation in the region of the lower urinary tract in acute and subacute inflammatory conditions, e.g. inflammation of bladder, renal pelvis and kidney (cystopyelonephritis), irritable bladder. Contraindications The medicinal product should not be used in the case of

PZN 0081116 0090078

Price Group 11 12

Status Pharmacy only Pharmacy only

hypersensitivity to yarrow or other plants of the Compositae family. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. In such cases use of the medicinal product should be stopped and a doctor consulted.

Cantharis Blasen Globuli velati (bladder remedy) Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: achillea millefolium ferm 33d dil. D2 0.1 g cantharis ex animale toto Gl dil. D5 0.1 g (HAB, Method 41c) equisetum arvense ex herba ferm 35b dil. D2 0.1 g (HAB, Method 35b) vesica urinaria bovis Gl dil. D7 0.1 g (HAB, Method 41c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonious integration of the

150

N1 N2

N1

PZN 0081234

Price Group A

Status Pharmacy only

feeling organisation in the region of the lower urinary tract in acute and subacute inflammatory conditions, e.g. inflammation of bladder, renal pelvis and kidney (cystopyelonephritis), irritable bladder. Contraindications The medicinal product should not be used in the case of hypersensitivity to yarrow or other plants of the Compositae family. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cantharis Blasen Globuli velati.

151

C

C

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted.

Composition Liquid dilution for injection: 1 ml contains: cardia suis Gl dil. D.. 1 ml (HAB, Method 41c)

Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Cantharis comp.

see Cantharis Blasen Inject see Cantharis Blasen Globuli velati

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Cantharis ex animale Gl

Active ingredient: cantharis ex animale toto Gl Liquid dilution for injection Potency/Strength Package Size Size Category D8

10 x 1 ml

N1

Carduus marianus e fructibus PZN 4616241

Price Group 61

Status

Active ingredient: silybum marianum e fructibus ferm 36 Liquid dilution for injection

Pharmacy only Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: cantharis ex animale toto Gl dil. D8 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

D3

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: silybum marianum e fructibus ferm 36 dil. D3 1 ml (HAB, Method 36) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2910918

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Carduus marianus e fructibus

Active ingredient: silybum marianum e fructibus ferm 36 Globuli velati

Cardia Gl

Potency/Strength Package Size Size Category

Active ingredient: cardia suis GI Liquid dilution for injection

D3

Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

152

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2910769 2910781 2910806 2910841 2910864 2910887 2490072

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

20 g

Composition Globuli velati: 10 g contain: silybum marianum e fructibus ferm 36 dil. D3 1 g (HAB, Method 36) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 8784892

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Carduus marianus e fructibus. Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli

153

C

velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

C

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

you suffer from intolerance to certain sugars you should consult your doctor before taking Carduus marianus/Oxalis. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

C

Side-effects None known.

Carduus marianus/Oxalis Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) silybum marianum e fructibus ferm 36 dil. D2 0.1 g (HAB, Method 36) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolic activity in the hepatobiliary system, e.g. degenerative liver diseases, bile duct dyskinesia and tendency to stone formation; bowel sluggishness (constipation). Contraindications None known.

N1

PZN 1751091

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) silybum marianum e fructibus ferm 36 dil. D2 0.1 g (HAB, Method 36) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic meta-

154

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hepar bovis Gl dil. D7 0.1 g (HAB, Method 41a) silybum marianum e fructibus ferm 36 dil. D2 0.1 g (HAB, Method 36) viscum album (mali) e planta tota ferm 34i dil. D4 0.1 g (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in chronic inflammatory and sclerosing liver diseases, e.g. chronic inflammation of the liver (hepatitis), liver cirrhosis; adjunctive treatment of malignant diseases. Contraindications Do not use in the case of known allergy to mistletoe formulations.

Carduus marianus/Oxalis



Carduus marianus/Viscum Mali comp.

N1

PZN 8784900

Price Group A

Status Pharmacy only

bolic activity in the hepatobiliary system, e.g. degenerative liver diseases, bile duct dyskinesia and tendency to stone formation; bowel sluggishness (constipation). Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

N1

PZN 1751116

Price Group 11

Status Pharmacy only

therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment The disorder should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In very rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock, in which case treatment with the medicinal product must be discontinued immediately and medical assistance sought.

Carduus marianus/Viscum Mali comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8784917

Price Group A

Status Pharmacy only

155

C

Composition Globuli velati: 10 g contain: hepar bovis Gl dil. D7 0.1 g (HAB, Method 41a) silybum marianum e fructibus ferm 36 dil. D2 0.1 g (HAB, Method 36) viscum album (mali) e planta tota ferm 34i dil. D4 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in chronic inflammatory and sclerosing liver diseases, e.g. chronic inflammation of the liver (hepatitis), liver cirrhosis; adjunctive treatment of malignant diseases. Contraindications None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Carduus marianus/Viscum Mali comp.

Cartilago articularis (genus) Gl

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 2 to 4 times daily; children under 6 years 5-7 globuli velati sublingually 2 to 4 times daily; children from 6 to under 12 years 8-10 globuli velati sublingually 2 to 4 times daily; adults and children of 12 years and above 10-20 globuli velati sublingually 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I

Side-effects None known.

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cartilago articularis coxae bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

156

N1 N1 N1 N1 N1 N1 N1 N1 N1

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: cartilago articularis coxae bovis GI Liquid dilution for injection

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: cartilago articularis genus bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Cartilago articularis (coxae) Gl

Potency/Strength Package Size Size Category

Active ingredient: cartilago articularis genus bovis GI Liquid dilution for injection

PZN 2831484 3359428 2829895 3359434 3359440 3359457 3359463 2831596 0847587

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2831395 3359492 2830059 3359500 3359517 3359523 3359546 2831691 0847593

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Contraindications None known.

Cartilago comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: allium cepa ferm 34a dil. D14 0.1 g aurum metallicum dil. D9 0.1 g betula pendula ferm 34e dil. D4 0.1 g cartilago articularis bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D16 0.1 g (HAB, Method 41c) stannum metallicum dil. D7 0.1 g

N1 N2

PZN 1751122 2085302

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the anabolic and catabolic forces, particularly in degenerative but also in chronic inflammatory joint disease, e.g. osteoarthritis (Arthrosis deformans), inflammation of the joints (chronic arthritis). Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

157

C

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily particularly over the affected areas.

C

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions. Note: There has been one report of local irritation after subcutaneous injection. The reaction subsided rapidly when treatment with Cartilago comp. was discontinued. If redness or pain develops at the injection site after injection please stop using the medicinal product and consult your doctor before performing further injections.

Cartilago comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: allium cepa ferm 34a dil. D14 0.1 g aurum metallicum dil. D9 0.1 g betula pendula ferm 34e dil. D4 0.1 g cartilago articularis bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D16 0.1 g (HAB, Method 41c) stannum metallicum dil. D7 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the anabolic and catabolic forces, particularly in degenerative but also in chronic inflammatory joint disease, e.g. chronic degen-

N1

PZN 8784923

Price Group A

Status Pharmacy only

erative joint disease (osteoarthritis), chronic joint inflammation (chronic arthritis). Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cartilago comp.

Dosage and method of administration Unless otherwise directed, infants and children up to under 6 years 3-5 globuli velati sublingually 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Ointment

158

30 g 100 g

N1 N2

PZN 2198199 2198207

Contraindications None known. Warnings and precautions for use In rare cases arachis (peanut) oil and wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub the following amounts of ointment into the affected joints or the surrounding area once to twice daily depending on the size of the joint: a) a ribbon of ointment about 2 cm long for the large joints (e.g. knee, hip, ankle joint), b) a ribbon of ointment about 1/2 cm long for the small joints (e.g. finger or toe joints). Side-effects None known.

Cartilago comp., Suppositorien Suppositories



Cartilago comp., Unguentum



Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the anabolic

and catabolic forces, particularly in degenerative but also in chronic inflammatory joint disease, e.g. chronic degenerative joint disease (osteoarthritis), chronic joint inflammation (chronic arthritis).

Potency/Strength Package Size Size Category

Contraindications None known.

Potency/Strength Package Size Size Category

Composition Ointment: 10 g contain: allium cepa ferm 34a dil. D1 0.1 g aurum metallicum dil. D8 0.1 g betula pendula ferm 34e dil. D1 0.1 g cartilago articularis bovis Gl dil. D3 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D3 0.1 g (HAB, Method 41c) stannum metallicum dil. D6 0.1 g Excipients: refined arachis oil, sodium chloride, sodium hydrogen carbonate, white soft paraffin, purified water, wool fat.

Price Group J J1

Status Pharmacy only Pharmacy only

10 x 2 g

Composition 1 suppository (2 g) contains: allium cepa ferm 34a dil. D13 2 mg aurum metallicum dil. D8 2 mg betula pendula ferm 34e dil. D3 2 mg cartilago articularis bovis Gl dil. D6 2 mg (HAB, Method 41b) formica rufa ex animale toto Gl dil. D15 2 mg (HAB, Method 41c) stannum metallicum dil. D6 2 mg Excipients: hard fat, honey.

N1

PZN 1880635

Price Group P

Status Pharmacy only

in chronic inflammatory joint disease, e.g. chronic degenerative joint disease (osteoarthritis), chronic joint inflammation (arthritis). Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum 3 times a week to once daily. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the anabolic and catabolic forces, particularly in degenerative but also

159

C

Cartilago/Echinacea comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

C

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: articulatio interphalangea bovis Gl dil. D16 0.1 g (HAB, Method 41b) echinacea pallida e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) quartz dil. D29 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of formative and regenerative processes in inflammatory disorders of the small joints. Contraindications Cartilago/Echinacea comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to plants of the Compositae family. On the basis of fundamental considerations, Cartilago/ Echinacea comp. should not be used by patients with progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS

N1

PZN 2085319

Price Group 11

Status Pharmacy only

virus), chronic viral diseases or autoimmune diseases (diseases caused by a reaction of a person‘s immune system against the organs or tissues of his or her own body). Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Cartilago/Echinacea comp. should not be used continuously for more than 2 weeks. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Cartilago/Echinacea comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: articulatio interphalangea bovis Gl dil. D16 0.1 g (HAB, Method 41b) echinacea pallida e planta tota ferm 33c dil. D1 0.1 g (HAB, Method 33c) quartz dil. D29 aquos. 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of hu-

160

N1

PZN 8784946

Price Group A

Status Pharmacy only

man beings and nature. Stimulation and harmonisation of formative and regenerative processes in inflammatory disorders of the small joints. Contraindications Cartilago/Echinacea comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations, Cartilago/ Echinacea comp. should not be used by patients with progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases

(inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases caused by a reaction of a person‘s immune system against the organs or tissues of his or her own body).

Duration of treatment Cartilago/Echinacea comp. should not be taken continuously for more than 2 weeks. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cartilago/Echinacea comp.

Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually up to once daily.

Cartilago/Mandragora comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: antimonite dil. D5 0.1 g argentum metallicum dil. D7 0.1 g betula pendula ferm 34e dil. D4 0.1 g cartilago articularis bovis Gl dil. D7 0.1 g (HAB, Method 41b) mandragora officinarum e radice ferm 34d dil. D4 0.1 g (HAB, Method 34d) Indications according to the anthroposophical understanding of human beings and nature. Degenerative joint disease (osteoarthritis) in the inflammatory stage; primary chronic rheumatoid arthritis (polyarthritis). Contraindications Do not use in the case of hypersensitivity to milk protein.

N1 N2

PZN 1751139 2085331

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use The medicinal product Cartilago/Mandragora comp. should only be given to children under 12 years after consulting a doctor as there is to date no adequately documented experience available to permit a general recommendation for this age group. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously three times a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

161

C

Cartilago/Mandragora comp. Globuli velati

Potency/Strength Package Size Size Category

C

20 g

Composition Globuli velati: 10 g contain: antimonite dil. D5 0.1 g argentum metallicum dil. D7 0.1 g betula pendula ferm 34e dil. D4 0.1 g cartilago articularis bovis Gl dil. D7 0.1 g (HAB, Method 41b) mandragora officinarum e radice ferm 34d dil. D4 0.1 g (HAB, Method 34d) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Degenerative joint disease (osteoarthritis) in the inflammatory stage; primary chronic rheumatoid arthritis (polyarthritis).

N1

PZN 8784952

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cartilago/Mandragora comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Dosage and method of administration Unless otherwise directed, apply the following amounts of ointment, depending on the size of the joint, to the affected joints or the surrounding area once to twice daily: a) a ribbon of ointment about 2 cm long for the large joints (e.g. knee, hip, ankle joint), b) a ribbon of ointment about 0.5 cm long for the small joints (e.g. finger or toe joints). In children the amount of ointment should be appropriately reduced in relation to the child's height. Use as ointment dressing: Depending on the size of the joint, apply a ribbon of ointment 0.5 to 2 cm long to the skin and cover with a thin cloth. Secure the thin cloth with an (elastic) bandage or stocking depending on the joint.

Carum carvi comp., Suppositorien see Carum carvi Zäpfchen

Carum carvi comp., Suppositorien für Kinder see Carum carvi Kinderzäpfchen

Paediatric suppositories

Potency/Strength Package Size Size Category

Cartilago/Mandragora comp., Unguentum Ointment

Potency/Strength Package Size Size Category 30 g 100 g

Composition 10 g contain: antimonite trit. D4 0.1 g argentum metallicum dil. D6 0.1 g betula pendula ferm 34e dil. D1 0.1 g cartilago articularis bovis Gl dil. D3 0.1 g (HAB, Method 41b) mandragora officinarum e radice ferm 34d dil. D1 0.1 g (HAB, Method 34d) Excipients: refined arachis oil, sodium chloride, sodium hydrogen carbonate, white soft paraffin, purified water, wool fat.

162

Side-effects In the case of hypersensitivity to any of the ingredients of Cartilago/Mandragora comp., Unguentum - particularly to wool fat or peanut oil - allergic reactions may occur. If skin redness develops, with or without itching, you should stop using Cartilago/Mandragora comp., Unguentum and see a doctor if necessary.

Carum carvi Kinderzäpfchen

Contraindications None known.



Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

N1 N2

PZN 2198213 2198236

Price Group J J1

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Degenerative joint disease (osteoarthritis) in the inflammatory stage; primary chronic rheumatoid arthritis (polyarthritis). Contraindications Do not use in the case of hypersensitivity to any of the active ingredients or excipients. Do not apply to damaged skin. Warnings and precautions for use In rare cases arachis (peanut) oil and wool fat can cause local skin reactions (e.g. contact dermatitis).

10 x 1 g

Composition 1 suppository (1 g) contains: atropa belladonna ex herba ferm 33a dil. D2 1 mg (HAB, Method 33a) concentrated aqueous extract of carvi fructus sicc. (5:1); extraction agent: purified water, drug-extract ratio: 1.8:1 20 mg chamomilla recutita e radice ferm 33c Ø 1 mg (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D4 1 mg (HAB, Method 33b) Excipients: glycerol, hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the metabolic system in the case of digestive weakness with flatulence and a tendency to abdominal cramps as well as associated restlessness and sleep disturbances. Contraindications Do not use in the case of known hypersensitivity to chamomile or other plants of the Compositae family, caraway

N1

PZN 1448004

Price Group O

Status Pharmacy only

or other umbellifers, to deadly nightshade (atropa belladonna) or other active ingredients or excipients. Dosage and method of administration Unless otherwise directed, for infants introduce 1/2 suppository into the rectum 1 to 3 times daily. A suppository can be divided into two equal halves by carefully cutting lengthwise with a warmed knife. Children under 7 years, introduce 1 suppository into the rectum 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Very rarely, newborn babies and infants up to 12 weeks, children suffering from bronchial asthma and patients with Down‘s syndrome react sensitively to constituents of deadly nightshade (atropa belladonna) which may cause a temporary change in respiratory rate or increased tiredness. In such cases treatment with the preparation should be discontinued and a doctor consulted.

163

C

Carum carvi Zäpfchen Suppositories

Potency/Strength Package Size Size Category

C

10 x 2 g

Composition 1 suppository (2 g) contains: atropa belladonna ex herba ferm 33a dil. D2 2 mg (HAB, Method 33a) concentrated aqueous extract of carvi fructus sicc. (5:1); extraction agent: purified water; drug-extract ratio: 1.8:1 40 mg chamomilla recutita e radice ferm 33c Ø 2 mg (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D4 2 mg (HAB, Method 33b) Excipients: glycerol, hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the metabolic system in the case of digestive weakness with flatulence and a tendency to abdominal cramps as well as associated restlessness and sleep disturbances.

N1

PZN 1447973

Price Group P

Status Pharmacy only

or other umbellifers, to deadly nightshade (atropa belladonna) or other active ingredients or excipients. Dosage and method of administration Unless otherwise directed, adults and children of 7 years and above 1 suppository introduced into the rectum 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Very rarely, children suffering from bronchial asthma and patients with Down‘s syndrome react sensitively to constituents of deadly nightshade (atropa belladonna) and show a temporary change in respiratory rate or increased tiredness. In such cases treatment with the preparation should be discontinued and medical advice obtained.

Contraindications Do not use in the case of known hypersensitivity to chamomile or other plants of the Compositae family, caraway

Cavum tympani Gl

Active ingredient: cavum tympani bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cavum tympani bovis Gl dil. D.. 1 ml (HAB, Method 41b)

164

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2911415 2911438 2911450 2911473 2911504 2911527 2911556 0845849 2494383

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Cepa

see Allium cepa e bulbo

Cera/Aesculus comp., Unguentum Ointment

Potency/Strength Package Size Size Category

30 g 100 g

N1 N2

PZN 2198242 2198259

Price Group J J1

Status Pharmacy only Pharmacy only

Composition 10 g contain: aesculus hippocastanum e semine ferm 34c Ø 0.33 g (HAB, Method 34c) brassica nigra e semine W 10% (HAB, Method 12f with refined arachis oil) 2.00 g bryonia cretica ferm 33b Ø 0.01 g cera flava 1.17 g D-camphor 0.10 g equisetum arvense ex herba ferm 35b Ø 0.10 g (HAB, Method 35b) formica rufa ex animale toto Gl Ø 0.01 g (HAB, Method 41c) mel 0.20 g Excipients: refined arachis oil, glycerol, cacao butter, purified water, wool fat.

spinal disorders, degenerative disorders of the joints, capsules and ligaments, painful muscular tension.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the metabolic processes in the case of an increased tendency to deposits and hardening, particularly in degenerative

Side-effects None known.

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. In rare cases arachis (peanut) oil and wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in a ribbon of ointment about 0.5 to 3 cm long (depending on the size of the affected area) once to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

165

C

Cerebellum Gl

Contraindications Do not use in the case of hypersensitivity to milk protein.

Active ingredient: cerebellum bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

C

D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cerebellum bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3359730 3359747 3359753 3359776 3359782 3359799 3359807 2494408

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Cerebellum comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apatite dil. D6 0.1 g arnica montana e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) cerebellum bovis Gl dil. D7 0.1 g (HAB, Method 41a) conchae dil. D5 0.1 levisticum officinale e radice ferm 33c dil. D5 0.1 g (HAB, Method 33c)

166

N1 N2

PZN 1751145 2085348

Price Group 11 12

Status Pharmacy only Pharmacy only

natrium carbonicum dil. D5 aquos. 0.1 g (HAB, Method 5b) orchis e tubere, decoctum dil. D7 0.1 g (HAB, Method 23a) scorodite dil. D6 0.1 g

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously three times a week to once daily.

Duration of treatment The disorder should have cleared up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Cerebellum comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apatite dil. D6 0.1 g arnica montana e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) cerebellum bovis Gl dil. D5 0.1 g (HAB, Method 41a) conchae trit. D3 0.1 g levisticum officinale e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) natrium carbonicum dil. D4 aquos. 0.1 g (HAB, Method 5b) orchis e tubere, decoctum dil. D7 0.1 g (HAB, Method 23a) scorodite dil. D6 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Adjunctive treatment of concussion and its sequelae, vertigo of cerebral origin, ataxic and hyperkinetic disorders. Contraindications None known.

N1

PZN 8784969

Price Group A

Status Pharmacy only

Warnings and precautions for use Cerebellum comp. should only be given to children under 12 years after consulting a doctor as there is to date no adequately documented experience available to permit a general recommendation for this age group. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cerebellum comp. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily to every 2 hours. The dosage in children under 12 years should be determined by the doctor. For infants we recommend dissolving the prescribed number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Indications gaccording to the anthroposophical understanding of human beings and nature. Adjunctive treatment of concussion and its sequelae, vertigo of cerebral origin, ataxic and hyperkinetic disorders.

167

C

Cerebrum comp. A Liquid dilution for injection

Potency/Strength Package Size Size Category

C

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cerebellum bovis Gl dil. D8 0.1 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D8 0.1 g (HAB, Method 41a) hypophysis bovis Gl dil. D8 0.1 g (HAB, Method 41a) iris bovis Gl dil. D8 0.1 g (HAB, Method 41b) medulla oblongata bovis Gl dil. D8 0.1 g (HAB, Method 41a) nervus opticus bovis Gl dil. D8 0.1 g (HAB, Method 41a) retina et chorioidea bovis Gl dil. D8 0.1 g (HAB, Method 41c) thalamus bovis Gl dil. D8 0.1 g (HAB, Method 41a)

N1 N2

PZN 1751151 2085377

Price Group 11 12

Status Pharmacy only Pharmacy only

in degenerative processes of the nerve-sense system, e.g. degenerative eye disorders, poor vision. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Regeneration of visual function

Cerebrum comp. A Globuli velati

Potency/Strength Package Size Size Category Composition Globuli velati: 10 g contain: cerebellum bovis Gl dil. D8 0.1 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D8 0.1 g (HAB, Method 41a) hypophysis bovis Gl dil. D8 0.1 g (HAB, Method 41a) iris bovis Gl dil. D8 0.1 g (HAB, Method 41b) medulla oblongata bovis Gl dil. D8 0.1 g (HAB, Method 41a) nervus opticus bovis Gl dil. D8 0.1 g (HAB, Method 41a)

168

20 g

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cerebrum comp A.

N1

PZN 8784975

Price Group A

Status Pharmacy only

retina et chorioidea bovis Gl dil. D8 0.1 g (HAB, Method 41c) thalamus bovis Gl dil. D8 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Regeneration of visual function in degenerative processes of the nerve-sense system, e.g. degenerative eye disorders, poor vision.

Dosage and method of administration Unless otherwise directed, 10-15 globuli velati sublingually 1 to 3 times daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Cerebrum comp. A cum Auro comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum trit. D6 0.01 g cerebellum bovis Gl dil. D7 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D7 0.01 g (HAB, Method 41a) hypophysis bovis Gl dil. D7 0.01 g (HAB, Method 41a) iris bovis Gl dil. D7 0.01 g (HAB, Method 41b) medulla oblongata bovis Gl dil. D7 0.01 g (HAB, Method 41a) myrrha trit. D3 0.01 g (HAB, Method 6) nervus opticus bovis Gl dil. D7 0.01 g (HAB, Method 41a) olibanum trit. D3 0.01 g (HAB, Method 6) retina et chorioidea bovis Gl dil. D7 0.01 g (HAB, Method 41c) thalamus bovis Gl dil. D7 0.01 g (HAB, Method 41a)

N1 N2

PZN 1751174 2085354

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the functional components of the human organism in the case of degenerative changes and sequelae of inflammation in the central nervous system, particularly with involvement of the organ of vision. Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications None known.

169

C

Cerebrum comp. A cum Auro comp.

Contraindications None known.

Globuli velati

Potency/Strength Package Size Size Category

C

20 g

Composition Globuli velati: 10 g contain: aurum metallicum trit. D6 0.01 g cerebellum bovis Gl dil. D7 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D7 0.01 g (HAB, Method 41a) hypophysis bovis Gl dil. D7 0.01 g (HAB, Method 41a) iris bovis Gl dil. D7 0.01 g (HAB, Method 41b) medulla oblongata bovis Gl dil. D7 0.01 g (HAB, Method 41a) myrrha trit. D3 0.01 g (HAB, Method 6) nervus opticus bovis Gl dil. D7 0.01 g (HAB, Method 41a) olibanum trit. D3 0.01 g (HAB, Method 6) retina et chorioidea bovis Gl dil. D7 0.01 g (HAB, Method 41c) thalamus bovis Gl dil. D7 0.01 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose.

N1

PZN 8784981

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the functional components of the human organism in the case of degenerative changes and sequelae of inflammation in the central nervous system, particularly with involvement of the organ of vision. Contraindications None known.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Cerebrum comp. B Liquid dilution for injection



10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cerebellum bovis Gl dil. D8 0.1 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D8 0.1 g (HAB, Method 41a) epiphysis bovis Gl dil. D8 0.1 g (HAB, Method 41a) labyrinthus bovis Gl dil. D8 0.1 g (HAB, Method 41a)

170

N1 N2

PZN 1751180 2085383

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Cerebrum comp. B Globuli velati

Potency/Strength Package Size Size Category

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cerebrum comp A cum Auro.

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Price Group 11 12

Status Pharmacy only Pharmacy only



20 g

Composition Globuli velati: 10 g contain: cerebellum bovis Gl dil. D8 0.1 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D8 0.1 g (HAB, Method 41a) epiphysis bovis Gl dil. D8 0.1 g (HAB, Method 41a) labyrinthus bovis Gl dil. D8 0.1 g (HAB, Method 41a) medulla oblongata bovis Gl dil. D8 0.1 g (HAB, Method 41a) nervus statoacusticus bovis Gl dil. D8 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Regeneration of the hearing and equilibrium functions in degenerative processes in the nerve-sense system, e.g. in hyperacusis and Menière‘s syndrome.

N1

PZN 8784998

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cerebrum comp B. Dosage and method of administration Unless otherwise directed, 10-15 globuli velati sublingually 1 to 3 times daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

medulla oblongata bovis Gl dil. D8 0.1 g (HAB, Method 41a) nervus statoacusticus bovis Gl dil. D8 0.1 g (HAB, Method 41a)

Cerebrum comp. B cum Auro comp.

Indications according to the anthroposophical understanding of human beings and nature. Regeneration of the hearing and equilibrium functions in degenerative processes in the nerve-sense system, e.g. in hyperacusis and Menière‘s syndrome.



Liquid dilution for injection

Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

N1 N2

PZN 1751205 2085360

Price Group 11 12

Status Pharmacy only Pharmacy only

171

C

C

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum trit. D6 0.01 g cerebellum bovis Gl dil. D7 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D7 0.01 g (HAB, Method 41a) epiphysis bovis Gl dil. D7 0.01 g (HAB, Method 41a) labyrinthus bovis Gl dil. D7 0.01 g (HAB, Method 41a) medulla oblongata bovis Gl dil. D7 0.01 g (HAB, Method 41a) myrrha trit. D3 0.01 g (HAB, Method 6) nervus statoacusticus bovis Gl dil. D7 0.01 g (HAB, Method 41a) olibanum trit. D3 0.01 g (HAB, Method 6) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation

of the functional components of the human organism in the case of degenerative changes and sequelae of inflammation in the central nervous system, particularly with involvement of the organ of hearing and equilibrium. Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati



20 g

Composition Globuli velati: 10 g contain: aurum metallicum trit. D6 0.01 g cerebellum bovis Gl dil. D7 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D7 0.01 g (HAB, Method 41a) epiphysis bovis Gl dil. D7 0.01 g (HAB, Method 41a) labyrinthus bovis Gl dil. D7 0.01 g (HAB, Method 41a) medulla oblongata bovis Gl dil. D7 0.01 g (HAB, Method 41a) myrrha trit. D3 0.01 g (HAB, Method 6) nervus statoacusticus bovis Gl dil. D7 0.01 g (HAB, Method 41a) olibanum trit. D3 0.01 g (HAB, Method 6) Contains sucrose (saccharose/sugar) and lactose.

172

N1

PZN 8785006

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the functional components of the human organism in the case of degenerative changes and sequelae of inflammation in the central nervous system, particularly with involvement of the organ of hearing and equilibrium. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cerebrum comp B cum Auro comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Side-effects None known.

C

Cerebrum, regio motorica Gl

Active ingredient: cerebrum, regio motorica bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack I

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cerebrum, regio motorica bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Cerebrum comp. B cum Auro comp. Potency/Strength Package Size Size Category

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 3359836 3359842 4616465 4616488 3359865 3359871 0847624

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Cervix uteri Gl

Active ingredient: cervix uteri bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2911792 2911817 2911846 2911869 2911881 2911906 2911929 2494414

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

173

Composition Liquid dilution for injection: 1 ml contains: cervix uteri bovis Gl dil. D.. 1 ml (HAB, Method 41c)

C

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor.

Side-effects Hypersensitivity reactions may very rarely occur. In such cases use of Chamomilla e floribus W 10%, Oleum should be discontinued and a doctor consulted. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Chamomilla e planta tota

Active ingredient: chamomilla recutita e planta tota ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D30

Chalcedon

Active ingredient: chalcedony aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D15

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: chalcedony dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2911941

Price Group 31

Status Pharmacy only

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: chamomilla recutita e planta tota ferm 33c dil. D.. 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

N1 N1

PZN 2883989 2884055

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications D3: The medicinal product should not be used in the case of known hypersensitivity to chamomile or other plants of the Compositae family. D30: None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Side-effects None known.

Chamomilla e planta tota

Active ingredient: chamomilla recutita e planta tota ferm 33c Globuli velati

Chamomilla e floribus W 10%, Oleum Active ingredient: chamomilla recutita e floribus W 10% Bath additive, liquid Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: chamomilla recutita e floribus W 10% (HAB, Method 12f with virgin olive oil) 10 g Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

174

PZN 2088370

Potency/Strength Package Size Size Category Price Group N1

Status General sale

Contraindications Do not use in the case of hypersensitivity to chamomile and other plants of the Compositae family. Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

D3 D6 D12

20 g 20 g 20 g

N1 N1 N1

PZN 8785041 8785058 8785064

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Composition Globuli velati: 10 g contain: chamomilla recutita e planta tota ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Chamomilla e planta tota.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Contraindications None known.

175

C

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

C

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects None known.

C Chamomilla/Nicotiana

Chamomilla e radice

Liquid dilution for injection

Active ingredient: chamomilla recutita e radice ferm 33c Liquid dilution for injection

Potency/Strength Package Size Size Category Potency/Strength Package Size Size Category D6 D30

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: chamomilla recutita e radice ferm 33c dil. D.. 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications D6: The medicinal product should not be used in the case

N1 N1

PZN 2912024 2912047

Price Group 31 31

Status Pharmacy only Pharmacy only

of known hypersensitivity to chamomile or other plants of the Compositae family. D30: None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Side-effects None known.

Active ingredient: chamomilla recutita e radice ferm 33c Globuli velati

D3 D6 D20 D30

20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: chamomilla recutita e radice ferm 33c dil. D.. 1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Gastrointestinal and biliary complaints in functional disturbances of motility and secretion, as adjunctive treatment of gastric and duodenal ulcers, in tendency to flatulence and cramping, painful menstrual symptoms (dysmenorrhoea), metabolismrelated migraine-like headaches, teething symptoms, unstable blood pressure, facial neuralgia, sleep problems in small children.

176

N1 N1 N1 N1

PZN 8785070 8785087 8785093 8785101

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between life and feeling organisation in conditions involving cramps particularly of the smooth musculature, e.g. gastrointestinal cramps, painful periods (dysmenorrhoea). Contraindications Do not use in the case of known allergy to chamomile and other plants of the Compositae family.

Chamomilla e radice

Potency/Strength Package Size Size Category



Price Group A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Chamomilla e radice. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

N1

PZN 1751211

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Chamomilla/Nicotiana Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between life and feeling organisation in conditions invol-

N1

PZN 8785118

Price Group A

Status Pharmacy only

ving cramps particularly of the smooth musculature, e.g. gastrointestinal cramps, painful periods (dysmenorrhoea). Contraindications Do not use in the case of known allergy to chamomile or other plants of the Compositae family. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Chamomilla/Nicotiana comp.

177

C

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 5 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications D4: In the case of a history of liver disease and/or concomitant use of substances that can damage the liver, a doctor should be consulted before using Chelidonium e planta tota D4. D8: None known.

Chelidonium/Berberis comp. Kapseln see Chelidonium Kapseln

Chelidonium comp. Augentropfen Eye drops

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

N1 N2

PZN 1448027 1448010

Price Group C C1

Status Pharmacy only Pharmacy only

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the metabolic processes of the eye, e.g. in dry inflamed eyes, irritation and eye fatigue.

Note: Without preservatives.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection

178

D3 D6

20 g 20 g

Composition Globuli velati: 10 g contain: chelidonium majus e radice ferm 34b dil. D.. 0.33 g (HAB, Method 34b) chelidonium majus ex herba ferm 34b dil. D.. 0.66 g (HAB, Method 34b) Contains sucrose (saccharose/sugar).

Contraindications None known.

N1 N1

PZN 2884078 2884090

Side-effects D4: In very rare cases increases in liver function values (transaminases) and in bilirubin, sometimes with druginduced jaundice (toxic hepatitis), have been observed during treatment with preparations containing celandine. These reactions subsided and returned to normal after discontinuing the medication. In such cases treatment with the medicinal product should be discontinued and a doctor consulted. D8: None known.

Potency/Strength Package Size Size Category

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Chelidonium e planta tota

10 x 1 ml 10 x 1 ml

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. D4: If the medicinal product is used for more than 4 weeks liver function tests (transaminases) should be carried out.

Globuli velati

Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac 2 to 3 times per week, in acute cases up to twice daily.

Potency/Strength Package Size Size Category

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Chelidonium e planta tota

Composition 0.5 ml contain: chelidonium majus ex herba ferm 34b dil. D3 0.033 g (HAB, Method 34b) chelidonium majus e radice ferm 34b dil. D3 0.017 g (HAB, Method 34b) rosa e floribus ferm cum ferro dil. D3 0.05 g (HAB, Method 37a) ruta graveolens ex herba ferm 33c dil. D3 0.05 g (HAB, Method 33c) terebinthina laricina dil. D5 0.05 g (HAB, Method 6) Excipients: sodium chloride, sodium hydrogen carbonate and water for injections.

D4 D8

Composition Liquid dilution for injection: 1 ml contains: chelidonium majus e radice ferm 34b dil. D.. 0.33 g (HAB, Method 34b) chelidonium majus ex herba ferm 34b dil. D.. 0.66 g (HAB, Method 34b)

Price Group 31 31

Status

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Chelidonium e planta tota.

N1 N1

PZN 8785124 8785130

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Pharmacy only Pharmacy only

179

C

Chelidonium e radice

Active ingredient: chelidonium majus e radice ferm 34b Liquid dilution for injection Potency/Strength Package Size Size Category

C

D3 D30

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: chelidonium majus e radice ferm 34b dil. D.. 1 ml (HAB, Method 34b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications D3: In the case of a history of liver disease and/or concomitant use of substances that can damage the liver, a doctor should be consulted before using Chelidonium e radice D3. D30: None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

N1 N1

PZN 2912082 2884150

Price Group 31 31

Status Pharmacy only Pharmacy only

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. D3: If the medicinal product is used for more than 4 weeks liver function tests (transaminases) should be carried out. Side-effects D3: In very rare cases increases in liver function values (transaminases) and in bilirubin, sometimes with druginduced jaundice (toxic hepatitis), have been observed during treatment with medicinal products containing celandine. These reactions subsided and returned to normal after discontinuing the medication. In such cases treatment with the medicinal product should be discontinued and a doctor consulted. D30: None known.

Chelidonium/Colocynthis

Composition Liquid dilution for injection: 1 ml contains: chelidonium majus e radice ferm 34b dil. D2 0.033 g (HAB, Method 34b) chelidonium majus ex herba ferm 34b dil. D2 0.066 g (HAB, Method 34b) citrullus colocynthis e fructibus ferm 33a dil. D3 0.1 g (HAB, Method 33a) Indications Homeopathic medicinal product for use in anthroposoph-

N1

PZN 1751228

Price Group 11

Status Pharmacy only

ical medicine, therefore no therapeutic indication stated. Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Chelidonium/Colocynthis Globuli velati

Potency/Strength Package Size Size Category

180

20 g

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the metabolic system, particularly in the hepatobiliary system, e.g. biliary dyskinesia and colics, abdominal cramps.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. If the medicinal product is used for more than 4 weeks liver function tests (transaminases) should be carried out.

Contraindications Do not use in the case of known hypersensitivity to any of the active ingredients. In the case of a history of liver disease and/or concomitant use of substances that can damage the liver, a doctor should be consulted before taking Chelidonium/Colocynthis, Globuli velati. As the medicinal product contains celandine (Chelidonium) it should not be used during pregnancy or breastfeeding or in children under 2 years.

Dosage and method of administration Unless otherwise directed, children from 2 to 6 years 5-7 globuli velati sublingually 3 to 5 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 5 times daily.

Side-effects In very rare cases increases in liver function values (transaminases) and in bilirubin, sometimes with druginduced jaundice (toxic hepatitis), have been observed during treatment with medicinal products containing celandine. These reactions subsided and returned to normal after discontinuing the medication. In such cases treatment with the medicinal product should be discontinued and a doctor consulted.

Soft capsules

Potency/Strength Package Size Size Category 10 x 1 ml

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Chelidonium/Colocynthis.

Chelidonium Kapseln

Liquid dilution for injection



Composition Globuli velati: 10 g contain: chelidonium majus e radice ferm dil. D2 0.033 g (HAB, Method 34b) chelidonium majus ex herba ferm 34b dil. D2 0.066 g (HAB, Method 34b) citrullus colocynthis e fructibus ferm 33a dil. D3 0.1 g (HAB, Method 33a) Contains sucrose (saccharose/sugar).

N1

PZN 8785147

Price Group A

Status

Potency/Strength Package Size Size Category

30 capsules 90 capsules

Composition 1 soft capsule contains: anisi stellati aetheroleum 18.3 mg berberis vulgaris e radice W 10% (HAB, Method 12f with virgin olive oil) 54.9 mg carvi aetheroleum 9.15 mg chelidonium majus e radice ferm 34b Ø 0.0305 mg (HAB, Method 34b) chelidonium majus ex herba ferm 34b Ø 0.061 mg (HAB, Method 34b) cichorium intybus e planta tota ferm 33c Ø 0.0915 mg (HAB, Method 33c)

N1 N1

PZN 1448062 2482664

Price Group Q Q1

Status Pharmacy only Pharmacy only

citrullus colocynthis e fructibus ferm 33a Ø 0.0915 mg (HAB, Method 33a) Iecoris aselli oleum A 45.75 mg lini oleum virginale 457.5 mg menthae piperitae aetheroleum 9.15 mg ricini oleum virginale 45.75 mg tritici aestivi oleum raffinatum 83.0 mg Excipients: gelatin, glycerol 85%, cacao butter, virgin olive oil, purified water.

Pharmacy only

181

C

C

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth and feeling organisation in the metabolic system in digestive disorders, biliary dysfunction, constipation; wind (flatulence). Contraindications The medicinal product should not be used while pregnant or breastfeeding. The medicinal product should not be used in the case of known hypersensitivity to anise or anethol, caraway oil, chicory and other plants of the Compositae family or in case of cross-allergy to umbellifers. Warnings and precautions for use There is no adequately documented experience of use of Chelidonium Kapseln in children. It should therefore not be used in children under 12 years.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted; In the case of chronic conditions the duration of treatment should be discussed with the doctor. If the medicinal product is used for more than 4 weeks liver function tests (transaminases) should be carried out. Side-effects In rare cases stimulation of intestinal motility can cause upper abdominal symptoms and diarrhoea. In very rare cases increases in liver function values (transaminases) and in bilirubin, including drug-induced jaundice (toxic hepatitis), have been observed during treatment with medicinal products containing chelidonium. These reactions subsided after discontinuing the medication.

Dosage and method of administration Unless otherwise directed, 1 soft capsule taken with fluid with or after meals 2 to 3 times daily.

Potency/Strength Package Size Size Category 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: chrysoprase dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2912142

Price Group 31

Status Pharmacy only

Potency/Strength Package Size Size Category D3 D6

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cichorium e planta tota.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: cichorium intybus e planta tota ferm 33c dil. D4 1 ml (HAB, Method 33c)

8785213 8785236

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Cichorium e planta tota 5%

Active ingredient: cichorium intybus e planta tota ferm 33c Globuli velati Potency/Strength Package Size Size Category

Active ingredient: cichorium intybus e planta tota ferm 33c Liquid dilution for injection

10 x 1 ml

N1 N1

PZN

Contraindications None known.

Cichorium e planta tota

182

20 g 20 g

Composition Globuli velati: 10 g contain: cichorium intybus e planta tota ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

5%

D4

C

Active ingredient: cichorium intybus e planta tota ferm 33c Globuli velati

Contraindications None known.

Active ingredient: chrysopras aquos. Liquid dilution for injection

Side-effects None known.

Cichorium e planta tota

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Chrysopras

D15

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

N1

PZN 2912165

Price Group 31

Status Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

20 g

N1

PZN 8785207

Price Group A

Status Pharmacy only

Composition 10 g globuli velati contain: cichorium intybus e planta tota ferm 33c Ø 0.5 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cichorium e planta tota 5%.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Contraindications Cichorium e planta tota 5% should not be used by patients with known hypersensitivity to chicory and other plants of the Compositae family.

183

Duration of treatment The duration of treatment should be discussed with the doctor.

C

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Side-effects None known.

Cichorium/Pancreas comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cichorium intybus e planta tota ferm 33c dil. D3 0.1 g (HAB, Method 33c) pancreas suis Gl dil. D7 0.1 g (HAB, Method 41a) stibium metallicum dil. D5 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of peptic digestive activity in the case of weak digestion and inflammatory changes of the gastrointestinal tract. Contraindications Do not use in the case of hypersensitivity to milk protein.

N1 N2

PZN 1751240 2085437

Price Group 11 12

Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously, preferentially in the region of the upper abdomen, one to three times a week to once daily. Duration of treatment Acute disorders should clear up within 1 week. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

Cichorium/Pancreas comp. Globuli velati



20 g

Composition Globuli velati: 10 g contain: cichorium intybus e planta tota ferm 33c dil. D3 0.1 g (HAB, Method 33c) pancreas suis Gl dil. D4 0.1 g (HAB, Method 41a) stibium metallicum dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation

184

Circulus arteriosus cerebri Gl

Active ingredient: circulus arteriosus cerebri Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: circulus arteriosus cerebri bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 8785242

Price Group A

C

Side-effects None known.

Status

therefore only be used in children under 12 years after consulting a doctor.

Potency/Strength Package Size Size Category

Duration of treatment Acute disorders should clear up within 1 week. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Status

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN

Price Group

2912283 2912314 2912337 2912366 2912389 2912403 2912432 2494420

61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Pharmacy only

of peptic digestive activity in the case of weak digestion and inflammatory changes of the gastrointestinal tract. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cichorium/Pancreas.

Citrus e fructibus

Active ingredient: citrus medica ssp. limonum e fructibus ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D2

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: citrus medica ssp. limonum e fructibus ferm 33c dil. D2 1 ml (HAB, Method 33c)

N1

PZN 2912656

Price Group 31

Status Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

185

Contraindications The medicinal product should not be used in the case of hypersensitivity to citrus fruits.

C

Side-effects Signs of irritation (mild burning, redness) may occasionally occur at the injection site but are no cause for concern.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Side-effects Signs of irritation (mild burning, redness) may occasionally occur at the injection site but are no cause for concern.

C

Citrus, Oleum aethereum 10% Active ingredient: limonis aetheroleum 10% Bath additive, liquid

Citrus e fructibus

Potency/Strength Package Size Size Category

Active ingredient: citrus medica ssp. limonum e fructibus ferm 33c Globuli velati Potency/Strength Package Size Size Category D2

20 g

N1

PZN 8785271



Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: citrus medica ssp. limonum e fructibus ferm 33c dil. D2 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

you suffer from intolerance to certain sugars you should consult your doctor before taking Citrus e fructibus. Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Contraindications None known.

Duration of treatment The duration of treatment should be discussed with the doctor.

Warnings and precautions for use This medicinal product contains sucrose. If you know that

Side-effects None known.

Citrus e fructibus/Cydonia e fructibus



10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: citrus medica ssp. limonum e fructibus ferm 33c dil. D1 0.1 g (HAB, Method 33c) cydonia oblonga e fructibus ferm 33b dil. D1 0.1 g (HAB, Method 33b) Indications according to the anthroposophical understanding of human beings and nature. Treatment and prevention of allergic disorders, particularly of the airways (e.g. hay fever), exudative diathesis.

186

N1 N2

PZN 0426986 0426992

Composition 10 g (11 ml) contain: limonis aetheroleum 10% (HAB, Method 12h with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the toning and vitalising forces, e.g. in connective tissue weakness, prolapse, varicose veins, bronchial asthma. Contraindications The medicinal product should not be used in the case of hypersensitivity to citrus fruits. Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive (about 1/2 - 1 teaspoonful) for a full bath tub (about 200 l wa-

PZN 2088401

Price Group N1

Status General sale

ter) for oil dispersion baths. Use correspondingly less for partial baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may occur in sensitised persons; In this case use of the medicinal product should be stopped and a doctor consulted. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Cochlea Gl

Liquid dilution for injection

Potency/Strength Package Size Size Category

100 ml

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications The medicinal product should not be used in the case of hypersensitivity to citrus fruits. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 1 to 3 times a week to once daily; children under 12 years 0.5-1 ml injected subcutaneously 1 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times a week to once daily.

Active ingredient: cochlea bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2912768 2912780 2912805 2912828 2912840 2912863 2912917 0847653 0845884 2494437

Price Group 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

187

Composition Liquid dilution for injection: 1 ml contains: cochlea bovis Gl dil. D.. 1 ml (HAB, Method 41b)

C

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Cochlearia ex herba

Active ingredient: cochlearia officinalis ex herba ferm 33b Globuli velati Potency/Strength Package Size Size Category D3

20 g

Composition Globuli velati: 10 g contain: cochlearia officinalis ex herba ferm 33b dil. D3 1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cochlearia ex herba.

N1

PZN 8785319

Price Group A

Status

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Colchicum comp.

Liquid dilution for injection



188

10 x 1 ml

N1

PZN 1751257

Price Group V5

Indications according to the anthroposophical understanding of human beings and nature. These include various forms of goitre. Contraindications Do not use in the case of hypersensitivity to colchicine. In the case of a history of liver disease and/or concomitant use of substances that can damage the liver, Colchicum comp. should only be used after consulting a doctor. Colchicum comp. must not be used during pregnancy or while breastfeeding. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times a week. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. If the medicinal product is used for more than 4 weeks liver function tests (transaminases) should be carried out. Side-effects In very rare cases increases in liver function values (transaminases) and in bilirubin, sometimes with druginduced jaundice (toxic hepatitis), have been observed during treatment with medicinal products containing celandine. These reactions subsided and returned to normal after discontinuing the medication. In such cases treatment with the medicinal product should be discontinued and a doctor consulted.

Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: chelidonium majus e floribus ferm 34b dil. D2 0.1 g (HAB, Method 34b) colchicum autumnale e planta tota ferm 34c dil. D2 0.1 g (HAB, Method 34c)

Status Prescription only

Colchicum comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8785348

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: chelidonium majus e floribus ferm 34b dil. D2 0.1 g (HAB, Method 34b) colchicum autumnale e planta tota ferm 34c dil. D2 0.1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar).

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Colchicum comp.

Indications according to the anthroposophical understanding of human beings and nature. Various forms of goitre.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

Contraindications Do not use in the case of hypersensitivity to colchicine. In the case of a history of liver disease and/or concomitant use of substances that can damage the liver, Colchicum comp. should only be used after consulting a doctor. Colchicum comp. must not be used during pregnancy or while breastfeeding.

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. If the medicinal product is used for more than 4 weeks liver function tests (transaminases) should be carried out.

189

C

Side-effects In very rare cases increases in liver function values (transaminases) and in bilirubin, sometimes with druginduced jaundice (toxic hepatitis), have been observed during treatment with medicinal products containing cel-

andine. These reactions subsided and returned to normal after discontinuing the medication. In such cases treatment with the medicinal product should be discontinued and a doctor consulted.

Colchicum e planta tota

Active ingredient: colchicum autumnale e planta tota ferm 34c Liquid dilution for injection Potency/Strength Package Size Size Category

C

D8 D30

Colchicum comp., Unguentum Ointment

Potency/Strength Package Size Size Category

30 g

Composition 10 g contain: chelidonium majus e floribus ferm 34b Ø 0.1 g (HAB, Method 34b) colchicum autumnale e planta tota ferm 34c Ø 0.1 g (HAB, Method 34c) Excipients: refined arachis oil, white soft paraffin, purified water, wool fat. Indications according to the anthroposophical understanding of human beings and nature. These include various forms of goitre. Contraindications Colchicum comp. Unguentum must not be used in the case of hypersensitivity to any of the active ingredients, peanuts or soy or to any of the excipients. Do not use in the case of hypersensitivity to colchicine. In the case of a history of liver disease and/or concomitant use of substances that can damage the liver, Colchicum comp., Unguentum should only be used after consulting a doctor. Colchicum comp. Unguentum must not be used during pregnancy or while breastfeeding. During treatment with this medicinal product both sexes must ensure that effective contraception is used. Men should continue to use effective contraception for 3 months after termination of treatment with Colchicum comp., Unguentum. Women should use effective contraception up to the next period. Do not use in children under 12 years.

190

N1

PZN 2198265

Price Group V3

Status Prescription only

Warnings and precautions for use Colchicum comp., Unguentum contains wool fat which can cause allergies if used for prolonged periods. Therefore please pay particular attention to new occurrence or exacerbation of itching, redness and swelling in the treated area. If you notice any such signs, please stop using Colchicum comp., Unguentum and consult your doctor. Wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in the ointment daily in the region of the thyroid or use over night as ointment dressing. No more than a ribbon of ointment of 15 cm should be used. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. If the medicinal product is used for more than 4 weeks liver function tests (transaminases) should be carried out. Side-effects In rare cases arachis (peanut) oil can cause severe allergic reactions. On topical application allergic reactions to wool fat can occur. If you notice signs of such a reaction, e.g. skin redness, with or without itching, you should stop using Colchicum comp., Unguentum and see your doctor if necessary.

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: colchicum autumnale e planta tota ferm 34c dil. D.. 1 ml (HAB, Method 34c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2884256 3769155

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Side-effects None known.

Colchicum e planta tota

Active ingredient: colchicum autumnale e planta tota ferm 34c Globuli velati Potency/Strength Package Size Size Category D3 D6

20 g 20 g

Composition Globuli velati: 10 g contain: colchicum autumnale e planta tota ferm 34c dil. D.. 1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Colchicum e planta tota.

N1 N1

PZN 8785354 8785360

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

191

C

Colocynthis e fructibus

Colon Gl

Active ingredient: citrullus colocynthis e fructibus ferm 33a Liquid dilution for injection Potency/Strength Package Size Size Category

C

D4 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: citrullus colocynthis e fructibus ferm 33a dil. D.. 1 ml (HAB, Method 33a) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2832673 2884279

Active ingredient: colon suis GI Liquid dilution for injection Price Group 31 31

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only

D4 D5 D6 D8 D8 D10 D12 D15 D20 D30 Serial pack I Serial pack II Serial pack III

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Colocynthis e fructibus

Active ingredient: citrullus colocynthis e fructibus ferm 33a Globuli velati Potency/Strength Package Size Size Category D6

20 g

Composition Globuli velati: 10 g contain: citrullus colocynthis e fructibus ferm 33a dil. D6 1 g (HAB, Method 33a) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Colocynthis e fructibus.

192

N1

PZN 8785383

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: colon suis Gl dil. D.. 1 ml (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the organ-forming forces in inflammatory and degenerative diseases of the colon such as inflammation of the colon (colitis), diverticulosis, irritable colon. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N2 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2830728 3359888 2830013 3359894 2913259 3359902 3359919 2831202 3359925 3359931 0847682 0845890 2494443

Price Group 41 61 61 61 62 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Potencies below D20: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potencies D20 and above: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment There is no evidence suggesting that prolonged use of the preparation may have negative effects. In the case of acute inflammatory bowel diseases the treatment should not be continued for longer than one week without consulting a doctor. In the case of chronic degenerative bowel diseases treatment under the supervision of a doctor can require more prolonged use of the preparation. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

193

C

Colon sigmoideum Gl

Duration of treatment The duration of treatment should be discussed with the doctor.

Active ingredient: colon sigmoideum suis Gl Liquid dilution for injection Potency/Strength Package Size Size Category

C

D5 D6 D8 D10 D12 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: colon sigmoideum suis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2913377 2913408 2913420 2913443 2913472 2913495 2913526

Price Group 61 61 61 61 61 61 61

Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

C

Columna posterior Gl

Active ingredient: columna posterior bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D6 D8 D15

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: columna posterior bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 and D15: None known.

N1 N1 N1

PZN 2913934 4616809 4626245

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Columna anterior Gl

Active ingredient: columna anterior cervicalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D12

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: columna anterior cervicalis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the

194

N1 N1 N1

PZN 0489053 0489076 0489099

Conchae Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

donor animal protein. Liquid dilution for injection D12: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Active ingredient: conchae aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D8 D10 D20 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: conchae dil. D.. aquos. 1 ml Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1

PZN 2913957 2913986 2914000 2914023

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week.

Contraindications Do not use in the case of hypersensitivity to milk protein.

195

Duration of treatment The duration of treatment should be discussed with the doctor.

C

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Conchae comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: amanita muscaria e planta tota ferm 33b dil. D6 0.1 g (HAB, Method 33b) argentum metallicum dil. D4 0.1 g conchae dil. D4 0.1 g dryopteris filix-mas e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) phyllitis scolopendrium e foliis ferm 34h dil. D2 0.1 g (HAB, Method 34h) pteridium aquilinum e foliis ferm 34c dil. D2 0.1 g (HAB, Method 34c) Indications according to the anthroposophical understanding of human beings and nature. For stimulation and structuring of the anabolic metabolism as adjunctive treatment in the case of chronic purulent inflammation and necrosis and to encourage the processes of excretion.

N1

PZN 1751263

Price Group V5

Status Prescription only

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: amanita muscaria e planta tota ferm 33b dil. D6 0.1 g (HAB, Method 33b) argentum metallicum trit. D4 0.1 g conchae trit. D4 0.1 g dryopteris filix-mas e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c)

196

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years of age without first obtaining the advice of a doctor and should not be used in place of any medication prescribed by the doctor for these indications. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Conchae comp.

N1

PZN 8785408

Price Group A

Status Pharmacy only

phyllitis scolopendrium e foliis ferm 34h dil. D2 0.1 g (HAB, Method 34h) pteridium aquilinum e foliis ferm 34c dil. D2 0.1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar) and lactose.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Conjunctiva Gl

Active ingredient: conjunctiva bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: conjunctiva bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Conchae comp.



case of chronic purulent inflammation and necrosis and to encourage the processes of excretion.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3359960 3359977 3359983 3360006 3360012 2831030 3360029 2494816

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the anabolic metabolism as adjunctive treatment in the

197

C

Conjunctiva comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

C

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D29 aquos. 0.1 g atropa belladonna ex herba ferm 33a dil. D14 0.1 g (HAB, Method 33a) conjunctiva bovis Gl dil. D16 0.1 g (HAB, Method 41b) echinacea pallida e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) quartz dil. D19 aquos 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the body‘s defences and formative forces in acute and chronic conjunctivitis. Contraindications Conjunctiva comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations Conjunctiva comp. should not be used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemialike diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases

N1

PZN 2085472

Price Group 11

Status Pharmacy only

or autoimmune diseases (diseases in which the immune system attacks the body‘s own tissues). Warnings and precautions for use The medicinal product Conjunctiva comp. should only be given to children under 12 years after consulting a doctor as there is to date no adequately documented experience available to permit a general recommendation for this age group. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Conjunctiva comp. should not be used continuously for more than 2 weeks. Side-effects In very rare cases hypersensitivity reactions may occur; in this case treatment with the preparation should be discontinued. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea).

Conjunctiva comp.

Contraindications Conjunctiva comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations, Conjunctiva comp. should not be used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemialike diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own tissues or organs). Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Conjunctiva comp.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Conjunctiva comp. should not be used continuously for more than 2 weeks. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Cor Gl

Active ingredient: cor bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829820 3360041 2829926 3360058 3360064 3360070 3360087 3360093 0847713 2494851

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D29 aquos. 0.1 g atropa belladonna ex herba ferm 33a dil. D14 0.1 g (HAB, Method 33a) conjunctiva bovis Gl dil. D16 0.1 g (HAB, Method 41b) echinacea pallida e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c)

198

N1

PZN 8785443

Price Group A

Status Pharmacy only

quartz dil. D19 aquos 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the body‘s defences and formative forces in acute and chronic conjunctivitis.

Composition Liquid dilution for injection: 1 ml contains: cor bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the organ-forming powers in degenerative heart conditions such as agerelated heart weakness, also for adjunctive treatment of heart problems causing shortness of breath or ankle swelling (heart failure); for follow-up treatment after heart attacks.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

199

C

Dosage and method of administration Potencies below D20: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potencies D20 and above: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

C

Duration of treatment In the case of chronic conditions the duration of treat-

ment should be discussed with the doctor. Side-effects Liquid dilution for injection D4, D5, D6: Hypersensitivity reactions to the protein of the donor animal may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted. Liquid dilution for injection D8 upwards: None known.

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If an acute inflammation does not improve within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Cor/Aurum I

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g cor bovis Gl dil. D5 0.1 g (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the rhythmic organic processes of the heart in heart diseases, e.g. for adjunctive treatment of heart failure, age-related heart weakness. Contraindications Do not use in the case of hypersensitivity to milk protein or to the donor animal protein.

N1 N2

PZN 1223564 1223570

Price Group 11 12

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions. Hypersensitivity reactions to the protein of the donor animal may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Cornea Gl

Active ingredient: cornea bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack II

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cornea bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Cor/Aurum II

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2914520 2914543 2914572 2914595 2914626 2914649 2914661 0846079

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g cor bovis Gl dil. D16 0.1 g (HAB, Method 41c)

200

N1

PZN 1223707

Price Group 11

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the rhythmic organic processes of the heart in heart diseases, e.g. for adjunctive treatment of heart failure, inflammation of the heart muscle (myocarditis).

Cornea/Levisticum comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

N1 N2

PZN 2085532 2085549

Price Group 11 12

Status Pharmacy only Pharmacy only

201

C

C

Composition Liquid dilution for injection: 1 ml contains: cornea bovis Gl dil. D6 0.1 g (HAB, Method 41c) corpus vitreum bovis Gl dil. D6 0.1 g (HAB, Method 41b) lens cristallina bovis Gl dil. D6 0.1 g (HAB, Method 41b) levisticum officinale e radice ferm 33c dil. D5 0.1 g (HAB, Method 33c) nervus opticus bovis Gl dil. D5 0.1 g (HAB, Method 41a) quercus robur/petraea e cortice cum calcio carbonico dil. D12 aquos. (HAB, Method 5b; sol. = D6 prepared by potentising quercus robur/petraea e cortice, decoctum Ø (HAB, Method 23a) five times with saturated aqueous solution of calcium carbonicum e cinere quercus) 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Vitalisation of the metabolic

processes in clouding of the refractive media of the eye (cornea, lens and vitreous body). Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously into the region of the temples 3 times a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Eye drops



5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: cornea bovis Gl dil. D6 0.05 g (HAB, Method 41c) corpus vitreum bovis Gl dil. D6 0.05 g (HAB, Method 41b) lens cristallina bovis Gl dil. D6 0.05 g (HAB, Method 41b) levisticum officinale e radice ferm 33c dil. D5 0.05 g (HAB, Method 33c) nervus opticus bovis Gl dil. D5 0.05 g (HAB, Method 41a) quercus robur/petraea e cortice cum calcio carbonico dil. D12 aquos. (HAB, Method 5b; sol. = D6 prepared by potentising quercus robur/petraea e cortice, decoctum Ø (HAB, Method 23a) five times with saturated aqueous solution of calcium carbonicum e cinere quercus) 0.05 g rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g

202

N1 N2

PZN 1448116 1448091

Active ingredient: corpora quadrigemina bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: corpora quadrigemina bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Cornea Levisticum comp. Augentropfen Potency/Strength Package Size Size Category

Corpora quadrigemina Gl

Price Group C C1

Status

PZN 2914939 2914951 2914974 2915011 2915034 2915057 2490095

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Pharmacy only Pharmacy only

Excipients: sodium chloride, sodium hydrogen carbonate and water for injections. Indications according to the anthroposophical understanding of human beings and nature. Vitalisation of the metabolic processes in clouding of the refractive media (cornea, lens and vitreous body) in the eye. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac once to twice daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known. Note: Without preservatives.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

Corpus amygdaloideum Gl

Active ingredient: corpus amygdaloideum bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: corpus amygdaloideum bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1 N1 N1

PZN 2915123 2915152 2915175 2915212 2915235 2915258 2490103

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

203

C

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

C

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: corpus luteum bovis GI Liquid dilution for injection

D4 D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: corpus luteum bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3360118 3360124 3360130 3360147 3360176 3360182 3360199 2490221

Price Group 41 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: corpus striatum bovis GI Liquid dilution for injection

D5 D8 D30

204

10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1

PZN 4617097 4617111 2915471

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Price Group 61 61 61

Side-effects None known.

Corpus vitreum Gl

Active ingredient: corpus vitreum bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: corpus vitreum bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Corpus striatum Gl

Potency/Strength Package Size Size Category

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Corpus luteum Gl

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Composition Liquid dilution for injection: 1 ml contains: corpus striatum bovis Gl dil. D.. 1 ml (HAB, Method 41a)

N1 N1 N1 N1 N1 N1 N1

PZN 2915531 2915554 2915577 2915620 2915643 2915672 2490422

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only

205

C

Crataegus e foliis et fructibus

Crataegus/Cor comp.

Active ingredient: crataegus laevigata/monogyna e foliis et fructibus ferm 33d Liquid dilution for injection Potency/Strength Package Size Size Category

C

D2 D2 D3

10 x 1 ml 50 x 1 ml 10 x 1 ml

N1 N2 N1

PZN 2915896 2915904 2915910

Composition Liquid dilution for injection: 1 ml contains: crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D.. 1 ml (HAB, Method 33d)

Contraindications None known.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Side-effects None known.

Price Group 31 32 31

Liquid dilution for injection Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Crataegus e foliis et fructibus

Active ingredient: crataegus laevigata/monogyna e foliis et fructibus ferm 33d Globuli velati Potency/Strength Package Size Size Category D2 D3 D6

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D.. 1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Crataegus e foliis et fructibus.

206

N1 N1 N1

PZN 8785472 8785489 8785466

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cerite dil. D5 0.1 g (HAB, Method 6) cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) dil. D5 0.1 g (HAB, Method 6) cor bovis Gl dil. D7 0.1 g (HAB, Method 41c) crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling and life organisation in the heart, e.g. in age-related weak heart, "tightness in the chest" (angina), after infarction, in functional heart symptoms, during and after overexertion, heart rhythm disorders particularly those involving a slow heart beat (bradycardia).

N1 N2

PZN 1751286 2085555

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Crataegus/Cor comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: cerite dil. D5 0.1 g (HAB, Method 6) cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) dil. D5 0.1 g (HAB, Method 6) cor bovis Gl dil. D4 0.1 g (HAB, Method 41c) crataegus laevigata/monogyna e foliis et fructibus ferm 33d Ø 0.2 g (HAB, Method 33d)

N1

PZN 8785495

Price Group A

Status Pharmacy only

nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling and life organisation in the heart, e.g. in age-related weak heart, "tightness in the chest" (angina), after infarction, in functional heart symptoms, during and after overexertion, predominantly bradycardiac heart rhythm disorders (involving a slow heart beat).

207

C

Contraindications None known.

C

Warnings and precautions for use In children under 12 years the medicinal product should only be used for treatment of functional heart complaints. There is no adequately documented experience of use of the preparation in children under 12 years for treatment of other conditions. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Crataegus/Cor comp.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection

Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cuprum aceticum dil. D5 aquos. 0.1 g (HAB, Method 5b) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) renes bovis Gl dil. D5 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the dystopic activity of the feeling organisation in conditions involving a tendency to cramping of the smooth muscles, e.g. bronchial asthma (asthma bronchiale), spastic bronchitis, spasms of the small arterial vessels, bowel cramps (intestinal spasms). Contraindications The preparation should not be used in the case of hyper-

N1 N2

PZN 1751292 2085561

Price Group 11 12

Status Pharmacy only Pharmacy only

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Allergic reactions may occur in the case of hypersensitivity to any of the ingredients of Cuprum/Nicotiana, Unguentum - particularly to copper oxide or arachis (peanut) oil. If you experience reddening of the skin, with or without itching, please stop using Cuprum/Nicotiana, Unguentum and see your doctor if necessary.

Cuprum/Quarz comp., Unguentum

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 2 to 3 times a week to 2 to 3 times daily; adults and children of 6 years and above 0.5 -1 ml injected subcutaneously 2 to 3 times a week to 2 to 3 times daily.

Potency/Strength Package Size Size Category

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor. Side-effects Hypersensitivity reactions to the protein of the donor animal may occur in sensitised persons. In such cases use of the medicinal product should be stopped and a doctor consulted.

Potency/Strength Package Size Size Category

208

Dosage and method of administration Unless otherwise directed, rub in the ointment once to twice daily or use as ointment dressing.

Ointment

Ointment

30 g

Warnings and precautions for use In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis).

sensitivity to the donor animal protein.

Cuprum/Nicotiana, Unguentum



Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the dystopic activity of the feeling organisation, e.g. in bowel cramps (abdominal spasms), flatulence (meteorism), peripheral vascular disease and muscle pain. Contraindications None known.

Cuprum aceticum comp.



Composition 10 g contain: cuprum oxydulatum rubrum 0.04 g nicotiana tabacum e foliis ferm 33b dil. D1 0.0001 g (HAB, Method 33b) Excipients: refined arachis oil, cacao butter, white soft paraffin.

N1

PZN 2198271

Price Group J

Status Pharmacy only



30 g 100 g

Composition 10 g contain: cuprum metallicum (95%) 2.0 g quartz 0.4 g rosmarini aetheroleum 0.5 g Excipients: white soft paraffin, wool fat.

N1 N2

PZN 2198590 2198609

Price Group J J1

Status Pharmacy only Pharmacy only

• on damaged skin, e.g. on burns, wounds, skin rashes. On account of the cineole and camphor contained in Cuprum/Quarz comp., Unguentum (constituents of rosemary oil) the ointment must not be used during pregnancy or breastfeeding. Cuprum/Quarz comp., Unguentum must not be used in infants or small children under the age of 2 years.

Indications Stimulation of the warmth organisation for toning and vitalisation of the fluid organism, e.g. in lymphatic congestion, disturbances of venous and arterial circulation, trauma-induced swelling, rheumatic disorders.

Warnings and precautions for use In children between 2 and 12 years medical advice should be sought before using Cuprum/Quarz comp., Unguentum and the medicinal product should not be used in place of any other treatment prescribed by the doctor. In rare cases wool fat can cause local skin reactions (e.g. contact dermatitis).

Contraindications Do not use Cuprum/Quarz comp., Unguentum • in the case of known hypersensitivity to rosemary oil or copper or to any of the excipients (e.g. wool fat); • in the case of bronchial asthma, whooping cough or croup;

Dosage and method of administration Unless otherwise directed, use the ointment 2 to 3 times daily as ointment dressing. In children from 2 to 12 years apply once to twice daily depending on the body surface area. Please learn how to use the medicinal product from a person experienced in its use.

209

C

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

C

Side-effects In rare cases breathing in the essential oil can cause coughing and in very rare cases involuntary closure of the vocal cords (laryngospasm). Cramping of the respiratory muscles (bronchospasm) may be exacerbated.

Local allergic reactions may occur in the case of hypersensitivity to ingredients of Cuprum/Quarz comp., Unguentum, particularly to copper, rosemary or wool alcohols. If you experience skin redness, with or without itching, please stop using Cuprum/Quarz comp., Unguentum and see a doctor if necessary.

Active ingredient: cutis feti bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Active ingredient: cydonia oblonga e fructibus ferm 33b Liquid dilution for injection Potency/Strength Package Size Size Category D2

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cydonia oblonga e fructibus ferm 33b dil. D2 1 ml (HAB, Method 33b)

Cutis (feti) Gl

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

Cydonia e fructibus

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2830970 3357688 2831171 3357694 3357702 3357719 3357725 3357731 0846085 2495046

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Side-effects None known.

Potency/Strength Package Size Size Category D2

20 g

Composition Globuli velati: 10 g contain: cydonia oblonga e fructibus ferm 33b dil. D2 1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar).

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications None known.

210

Price Group

Active ingredient: cydonia oblonga e fructibus ferm 33b Globuli velati

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Side-effects None known.

PZN 2916430

Cydonia e fructibus

Composition Liquid dilution for injection: 1 ml contains: cutis feti bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1

N1

PZN 8785503

Price Group A

Status Pharmacy only

This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Cydonia e fructibus. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

211

C

Dens Gl

Liquid dilution for injection D8 upwards: None known.

Active ingredient: dens bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

D

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: dens bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2916594 2916619 2916631 2916677 2916708 2916720 2490451

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: diaphragma bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: diaphragma bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in an-

212

N1 N1 N1 N1 N1 N1 N1

PZN 2916795 2916826 2916849 2916884 2916909 2916921 2490468

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

D

Diaphragma pelvis Gl

Active ingredient: diaphragma pelvis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: diaphragma pelvis bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Diaphragma Gl

D5 D6 D8 D12 D15 D30 Serial pack

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2916996 2917010 2917033 2917085 2917116 2917139 2490681

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

throposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

213

Diencephalon Gl

Contraindications None known.

Active ingredient: diencephalon bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D20 D30 Serial pack III

D

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: diencephalon bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3357754 3357760 3357777 3357783 3357808 3357814 3357820 3357837 2495170

Price Group 61 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Disci comp. cum Aesculo Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aesculus hippocastanum e semine ferm 34c dil. D49 0.1 g (HAB, Method 34c) arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b)

214

N1 N2

PZN 1751300 2085578

Price Group 11 12

Status Pharmacy only Pharmacy only

formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously in the vicinity of the spine once a week to once daily.

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

D

Disci comp. cum Aesculo Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aesculus hippocastanum e semine ferm 34c dil. D49 0.1 g (HAB, Method 34c) arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in degenerative changes with acute pain and a tendency to venous congestion.

N1

PZN 8785561

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci comp. cum Aesculo. Dosage and method of administration Unless otherwise directed, infants and small children up to under 6 years 3-5 globuli velati sublingually once daily; adults and children of 6 years and above 5-10 globuli velati sublingually once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Contraindications Disci comp. cum Aesculo should not be used in the case of hypersensitivity to formic acid.

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in degenerative changes with acute pain and a tendency to venous congestion.

215

Disci comp. cum Aesculo, Gelatum Gel

Potency/Strength Package Size Size Category

D

30 g

Composition 10 g contain: aesculus hippocastanum e semine ferm 34c dil. D1 0.1 g (HAB, Method 34c) arnica montana e planta tota ferm 33c dil. D1 0.1 g (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D3 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D3 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D1 0.1 g (HAB, Method 35c) Excipients: 96 % alcohol, glycerol, guar, litsea fruit oil, sodium alginate, sodium chloride, sodium hydrogen carbonate, rosemary oil, Dalmatian sage oil, tea tree oil, thyme oil, purified water. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in degenerative changes with acute pain and a tendency to venous congestion.

N1

PZN 2198294

Price Group J

Status Pharmacy only

Contraindications Disci comp. cum Aesculo, Gelatum, must not be used in the case of known hypersensitivity to any of the active ingredients or excipients. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, rub in the gel once or twice daily along the spine. Duration of treatment The condition should have cleared up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In very rare cases allergic reactions can occur after using Disci comp. cum Aesculo, Gelatum. Redness and itching of the skin can occur and existing irritation can be exacerbated. Contact dermatitis and/or hypersensitivity reactions may also occur. In such cases use of the medicinal product should be discontinued and a doctor consulted.

Disci comp. cum Argento Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml 5 x 10 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D19 aquos. 0.1 g arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c)

216

N1 N2 N1

PZN 1751317 2085584 8510344

Price Group 11 12 21

Status Pharmacy only Pharmacy only Pharmacy only

disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c)

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in states of acute pain with an inflammatory component, e.g. radicular syndromes. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Dosage and method of administration 1 ml: Unless otherwise directed, inject 1 ml subcutaneously in the proximity of the spine 1 to 3 times a week to once daily. 10 ml: Unless otherwise directed, inject aliquots subcutaneously at several points in the painful area once a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Disci comp. cum Argento Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D19 aquos. 0.1 g arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in states of acute pain with an inflammatory component, e.g. radicular syndromes.

N1

PZN 8785578

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci comp. cum Argento. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 3-5 globuli velati sublingually once to twice daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Contraindications Disci comp. cum Argento should not be used in the case of hypersensitivity to formic acid.

217

D

Disci comp. cum Auro Liquid dilution for injection

Potency/Strength Package Size Size Category

D

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) aurum metallicum dil. D14 aquos. 0.1 g disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation with concomitant cardiovascular disorders and emotional instability.

N1

PZN 1751323

Price Group 11

Status Pharmacy only

Contraindications None known. Warnings and precautions for use There is no adequately documented experience of the use of Disci comp. cum Auro in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously in the vicinity of the thoracic spine 1 to 3 times a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If there is no improvement within this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Disci comp. cum Auro Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) aurum metallicum dil. D14 aquos. 0.1 g disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) Contains sucrose (saccharose/sugar).

N1

PZN 8785584

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation with concomitant cardiovascular disorders and emotional instability. Contraindications Disci comp. cum Auro should not be used in the case of hypersensitivity to formic acid. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci comp. cum Auro.

Dosage and method of administration Unless otherwise directed, infants and small children under 6 years 3-5 globuli velati sublingually once to twice daily; adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Side-effects None known.

D

Disci comp. cum Nicotiana Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) hypophysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D9 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in adolescence, e.g. postural weakness, paravertebral muscular tension, scoliosis, Scheuermann‘s disease.

N1 N2

PZN 1751346 2085609

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use There is no adequately documented experience of the use of Disci comp. cum Nicotiana in children. It should therefore not be used in children under 6 years. The medicinal product Disci comp. cum Nicotiana should only be given to children from 6 to 12 years after consulting a doctor as there is to date no adequately documented experience available to permit a general recommendation for this age group. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously in the vicinity of the thoracic spine 1 to 3 times a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Disci comp. cum Nicotiana Globuli velati

Potency/Strength Package Size Size Category

218

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor.

20 g

N1

PZN 8785590

Price Group A

Status Pharmacy only

219

D

Composition Globuli velati: 10 g contain: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) hypophysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D9 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in adolescence, e.g. postural weakness, paravertebral muscular tension, scoliosis, Scheuermann‘s disease.

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci comp. cum Nicotiana. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

Disci comp. cum Pulsatilla Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D5 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D3 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) pulsatilla vulgaris e floribus ferm 33c dil. D3 0.1 g (HAB,Method 33c) stannum metallicum dil. D5 0.1 g viscum album (mali) e planta tota ferm 34i dil. D2 0.1 g (HAB, Method 34i) vivianite dil. D5 0.1 g

220

N1 N2

PZN 1751352 2085615

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in the case of degenerative changes, in women particularly in the change of life (menopause) and in the case of a tendency to venous congestion in the pelvic region. Contraindications Do not use in the case of hypersensitivity to milk protein.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously in the proximity of the spine 1 to 3 times a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be con-

sulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

D Disci comp. cum Pulsatilla Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D5 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D3 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) pulsatilla vulgaris e floribus ferm 33c dil. D3 0.1 g (HAB, Method 33c) stannum metallicum dil. D5 0.1 g viscum album (mali) e planta tota ferm 34i dil. D2 0.1 g (HAB, Method 34i) vivianite dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in the case of degenerative changes, in women particularly in the change of life (menopause) and in the case of a tendency to venous congestion in the pelvic region.

N1

PZN 8785621

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci comp. cum Pulsatilla. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

221

Disci comp. cum Pulsatilla, Unguentum Ointment

Potency/Strength Package Size Size Category

D

30 g

N1

PZN 2198302

Price Group J

Status Pharmacy only

Composition 10 g contain: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D3 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D1 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D3 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D1 0.1 g (HAB, Method 35c) pulsatilla vulgaris e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) stannum metallicum trit. D4 0.1 g viscum album (mali) e planta tota ferm 34i dil. D1 0.1 g (HAB, Method 34i) vivianite trit. D4 0.1 g Excipients: refined arachis oil, sodium chloride, sodium hydrogen carbonate, white soft paraffin, purified water, wool fat.

tive changes, in women particularly in the change of life (menopause) and in the case of a tendency to venous congestion in the pelvic region.

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in the case of degenera-

Side-effects In rare cases arachis (peanut) oil can cause severe allergic reactions. If you experience skin redness, with or without itching, please stop using Disci comp. cum Pulsatilla and see your doctor if necessary.

Contraindications Disci comp. cum Pulsatilla must not be used in the case of hypersensitivity to any of the active ingredients, peanuts or soy or to any of the excipients. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. In rare cases wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in the ointment once to twice daily in the region of the spine. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Disci comp. cum Stanno Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml 5 x 10 ml

Composition Liquid dilution for injection: 1 ml contains: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D5 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b)

222

N1 N2 N1

PZN 1751369 2085621 8510367

Price Group 11 12 21

formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D5 0.1 g

Status Pharmacy only Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of man and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in degenerative changes with states of acute and chronic pain; adjunctive treatment of chronic, inflammatory and degenerative joint disorders.

Dosage and method of administration 1 ml: Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week to once daily in the vicinity of the spine or the affected joints. 10 ml: Unless otherwise directed, inject aliquots subcutaneously or intracutaneously along the spine 1 to 3 times a week.

Contraindications Do not use in the case of hypersensitivity to ant venom, milk protein or to the donor animal protein.

Duration of treatment The disorder should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Disci comp. cum Stanno Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D5 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in degenerative changes with states of acute and chronic pain; adjunctive treatment of chronic, inflammatory and degenerative joint disorders.

N1

PZN 8785609

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci comp. cum Stanno. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications None known.

223

D

Disci comp. cum Stibio Liquid dilution for injection

Potency/Strength Package Size Size Category

D

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stibium metallicum dil. D7 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal

N1 N2

PZN 1751375 2085638

Price Group 11 12

Status Pharmacy only Pharmacy only

column formation, e.g. postural weakness during adolescence, pain associated with chronic inflammatory disorders of the spine and with degenerative joint disease. Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously in the proximity of the spine 1 to 3 times a week to once daily. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D19 0.1 g (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D7 0.1 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stibium metallicum dil. D7 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes

224

N1

PZN 8785615

Price Group A

Status Pharmacy only

of erectness, movement and form of the entire spinal column formation, e.g. postural weakness during adolescence, pain associated with chronic inflammatory disorders of the spine and with degenerative joint disease.

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

D Disci intervertebrales (cervicales) Gl

Active ingredient: disci intervertebrales cervicales bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: disci intervertebrales cervicales bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Disci comp. cum Stibio



5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1 N1 N1 N1 N1

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Contraindications None known.

Contraindications None known.

Disci intervertebrales (feti) Gl

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci comp. cum Stibio.

Potency/Strength Package Size Size Category

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; children from 6 to under 12 years 5-7 globuli velati sublingually 1 to 3 times daily; adults and children of 12 years and above

PZN 3357872 2831604 3357889 3357895 3357903 3357926 3357932 0847765 2495187

Active ingredient: disci intervertebrales feti bovis Gl Liquid dilution for injection

D5 D6 D8

10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1

PZN 4617447 2917599 4617476

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

225

Composition Liquid dilution for injection: 1 ml contains: disci intervertebrales feti bovis Gl dil. D.. 1 ml (HAB, Method 41b)

D

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Disci intervertebrales (lumbales) Gl

Active ingredient: disci intervertebrales lumbales bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: disci intervertebrales lumbales bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

226

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3357990 2831283 3357949 3357955 3357961 3357978 3357375 0847771 2495342

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Disci/Pulsatilla comp. cum Stanno, Suppositorien Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D3 2 mg (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D1 2 mg (HAB, Method 35b) formica rufa ex animale toto Gl dil. D3 2 mg (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D1 2 mg (HAB, Method 35c) pulsatilla vulgaris e floribus ferm 33c dil. D2 2 mg (HAB, Method 33c) stannum metallicum trit. D4 2 mg viscum album (mali) e planta tota ferm 34i dil. D4 2 mg (HAB, Method 34i) Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal

N1

PZN 1880658

Price Group P

Status Pharmacy only

column formation, particularly in the case of degenerative changes associated with acute pain, e.g. radicular syndromes, low back pain (lumbago); and particularly in women during the change of life (menopause). Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein (bovine) or to formic acid. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum 3 times a week to once or twice daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Disci/Rhus toxicodendron comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml 5 x 10 ml 20 x 10 ml

Composition Liquid dilution for injection: 1 ml contains: aconitum napellus e tubere ferm 33 c dil. D4 0.01 g (HAB, Method 33c) argentum metallicum dil. D18 aquos. 0.01 g arnica montana e planta tota ferm 33c dil. D18 0.01 g (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D6 0.01 g (HAB, Method 41b) formica rufa ex animale toto Gl dil. D5 0.01 g (HAB, Method 41c)

N1 N2 N1 N2

PZN 2085644 2085650 8510350 2420634

Price Group 11 12 21 22

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

gelsemium sempervirens e rhizoma ferm 35b dil. D2 0.01 g (HAB, Method 35b) granite dil. D8 0.01 g (HAB, Method 6) leontopodium alpinum e planta tota ferm 36 dil. D2 0.01 g (HAB, Method 36) mandragora officinarum e radice ferm 34d dil. D4 0.01 g (HAB, Method 34d) phyllostachys e nodo ferm 35c dil. D4 0.01 g (HAB, Method 35c) toxicodendron quercifolium e foliis ferm 33d dil. D4 0.01 g (HAB, Method 33d)

227

D

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in acute pain associated with degenerative changes of the spine and in painful joint disorders; nerve pain (neuralgia).

D

Contraindications Do not use in the case of hypersensitivity to milk protein or the donor animal protein. The medicinal product should not be used in the case of known hypersensitivity to plants of the poison sumac family or to any of the other ingredients. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Dosage and method of administration Unless otherwise directed, 1 ml: inject 1 ml subcutaneously in the vicinity of the spine 1 to 3 times a week to once daily. 10 ml: inject aliquots subcutaneously at several points in the painful area 1 to 3 times a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Disci/Viscum comp. cum Argento, Suppositorien Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: argentum metallicum dil. D18 aquos. 2 mg arnica montana e planta tota ferm 33c dil. D1 2 mg (HAB, Method 33c) disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D3 2 mg (HAB, Method 41b) formica rufa ex animale toto Gl dil. D3 2 mg (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D1 2 mg (HAB, Method 35c) pulsatilla vulgaris e floribus ferm 33c dil. D2 2 mg (HAB, Method 33c) viscum album (mali) e planta tota ferm 34i dil. D4 2 mg (HAB, Method 34i) Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal col-

228

N1

PZN 1880664

Price Group P

Status Pharmacy only

umn formation, in both chronic inflammatory and degenerative changes and nerve pain (neuralgia), e.g. intercostal neuralgia, lumbago, sciatica, ankylosing spondylitis. Contraindications The medicinal product should not be used in the case of known hypersensitivity to arnica. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Disci/Viscum comp. cum Stanno Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D5 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D5 0.1 g viscum album (mali) e planta tota ferm 34i dil. D5 0.1 g (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in the case of degenerative changes with pronounced, especially hyperplastic deformities, and acute and chronic pain. Contraindications Do not use in the case of hypersensitivity to milk protein or the donor animal protein. Disci/Viscum comp. cum Stanno should not be used in case of known allergy to mistletoe formulations.

N1 N2

PZN 1751381 2085667

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously in the proximity of the spine 1 to 3 times a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If acute pain does not improve within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases, hypersensitivity to mistletoe may lead to local or systemic allergic or allergy-like reactions, such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum twice a week to once or twice daily.

Disci/Viscum comp. cum Stanno

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Potency/Strength Package Size Size Category

Globuli velati



20 g

N1

PZN 8785638

Price Group A

Status Pharmacy only

Side-effects None known.

229

D

D

Composition Globuli velati: 10 g contain: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D5 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D5 0.1 g viscum album (mali) e planta tota ferm 34i dil. D5 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in the case of degenerative changes with pronounced, especially hyperplastic deformities, and acute and chronic pain.

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Disci/Viscum comp. cum Stanno. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Side-effects None known.

D5 D6 D8 D10 D12 D15 D30 Serial pack II

Potency/Strength Package Size Size Category

Composition 10 g contain: disci intervertebrales cervicales, thoracici et lumbales bovis Gl dil. D3 0.1 g (HAB, Method 41b) equisetum arvense ex herba ferm 35b dil. D1 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D3 0.1 g (HAB, Method 41c) phyllostachys e nodo ferm 35c dil. D1 0.1 g (HAB, Method 35c) stannum metallicum trit. D4 0.1 g viscum album (mali) e planta tota ferm 34i dil. D1 0.1 g (HAB, Method 34i) Excipients: refined arachis (peanut) oil, sodium chloride, sodium hydrogen carbonate, white soft paraffin, water for injections and wool fat.

230

Side-effects Allergic reactions may occur in the case of hypersensitivity to ingredients of Disci/Viscum comp. cum Stanno, Unguentum, particularly to wool fat or arachis (peanut) oil.

Ductus choledochus Gl

Ointment

30 g 100 g

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Duration of treatment The condition should have cleared up within 2 weeks. If acute pain does not improve within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Disci/Viscum comp. cum Stanno, Unguentum



Dosage and method of administration Unless otherwise directed, rub in the ointment once or twice daily along the spine.

N1 N2

PZN 2198325 2198331

Price Group J J1

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of the processes of erectness, movement and form of the entire spinal column formation, particularly in the case of degenerative changes with pronounced, especially hyperplastic deformities, and acute and chronic pain. Contraindications Disci/Viscum comp. cum Stanno, Unguentum must not be used in the case of known hypersensitivity to any of the active ingredients or excipients and in the case of known allergy to mistletoe formulations.

If you experience skin redness, with or without itching, please stop using Disci/Viscum comp. cum Stanno, Unguentum and see your doctor if necessary. In rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought.

Active ingredient: ductus choledochus suis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ductus choledochus suis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2917984 2918009 2918021 2918044 2918067 2918096 2918110 0846145

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. In rare cases arachis (peanut) oil and wool fat can cause local skin reactions (e.g. contact dermatitis).

231

D

Ductus thoracicus Gl

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Active ingredient: ductus thoracicus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D15 D30

D

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ductus thoracicus bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1

PZN 2919026 2919061 2919121 2919144

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: duodenum suis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: duodenum suis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

232

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2919227 2919256 2919279 2919291 2919322 2919345 2919368 2919380 2495365

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Side-effects None known.

D Dura mater encephali Gl

Active ingredient: dura mater encephali bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: dura mater encephali bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Duodenum Gl

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack III

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Duration of treatment The duration of treatment should be discussed with the doctor.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2920236 2920259 2920271 2920294 2920319 2920331 2920354 2495371

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

233

Echinacea/Argentum Liquid dilution for injection

Potency/Strength Package Size Size Category

E

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D29 aquos. 0.1 g echinacea pallida e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the immune system in acute inflammatory, febrile to septic processes of all kinds. Contraindications Echinacea/Argentum should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to plants of the Compositae family. On the basis of fundamental considerations, Echinacea/ Argentum must not be used in the case of progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own organs or tissues).

N1 N2

PZN 1751398 2085673

Price Group 11 12

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 2 to 3 times a week to once to twice daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously 2 to 3 times a week to once to twice daily; adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week to once to twice daily. Duration of treatment Echinacea/Argentum should not be used continuously for more than 2 weeks. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor. Harmless signs of irritation around the injection site may occur rarely after subcutaneous injection of the medicinal product. In such cases the injection treatment should be discontinued and treatment continued with Echinacea/Argentum, Globuli velati if appropriate.

Echinacea/Argentum Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D29 aquos. 0.1 g echinacea pallida e radice ferm 33d dil. D1 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the immune sys-

234

N1

PZN 8785710

Price Group A

Status Pharmacy only

tem in acute inflammatory, febrile to septic processes of all kinds. Contraindications Echinacea/Argentum should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to plants of the Compositae family. On the basis of fundamental considerations, Echinacea/ Argentum must not be used in the case of progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (in-

flammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own organs or tissues). Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Echinacea/Argentum. Dosage and method of administration Unless otherwise directed, infants and children up to under 6 years 3-5 globuli velati sublingually 2 to 4 times daily to every two hours; adults and children of 6 years and above 5-10 globuli velati sublingually 2 to 4 times daily to

every two hours. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Echinacea/Argentum should not be taken continuously for more than 2 weeks. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the product and see a doctor.

Echinacea Augentropfen Eye drops

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: echinacea pallida e planta tota ferm 33c dil. D2 0.05 g (HAB, Method 33c) rosae aetheroleum dil. (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) D7 0.05 g Excipients: sodium chloride, sodium hydrogen carbonate and water for injections. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the involvement of the feeling organisation in acute inflammatory diseases of the eye and the surrounding area, e.g. inflammation of the conjunctiva (conjunctivitis), inflammation of the eyelids (blepharitis). Contraindications The preparation should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea Augentropfen must not be used in progressive systemic

N1 N2

PZN 1448139 1448122

Price Group C C1

Status Pharmacy only Pharmacy only

diseases such as tuberculosis, leukaemia or leukaemialike diseases, inflammatory diseases of the connective tissue (collagen disorders), multiple sclerosis, AIDS, HIV infections, chronic viral diseases or other autoimmune diseases. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac once to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

235

E

Echinacea e planta tota

Active ingredient: echinacea pallida e planta tota ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D2 D2 D3 D30

E

10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N2 N1 N1

PZN 2832590 2920377 2832584 3358280

Price Group 31 32 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: echinacea pallida e planta tota ferm 33c dil. D.. 1 ml (HAB, Method 33c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. For harmonisation of the feeling organisation in febrile, inflammatory circumscribed and systemic processes, e.g. furunculosis, poorly healing wounds, inflammation of the uterine appendages (adnexitis), inflammation of the pelvic connective tissue (parametritis), inflammation of the lining of the womb (endometritis), inflammation of the lymph nodes (lymphadenitis), flu-like infections.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times weekly to once daily.

Contraindications Liquid dilution for injection D2, D3: The medicinal product should not be used in the case of hypersensitivity to the active ingredient or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea e planta tota must not be used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus) or other autoimmune diseases (diseases in which the immune system attacks the body‘s own tissues). Liquid dilution for injection D30: None known.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Liquid dilution for injection D2, D3: Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor. Liquid dilution for injection D30: None known.

Echinacea e planta tota

Active ingredient: echinacea pallida e planta tota ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D6

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: echinacea pallida e planta tota ferm 33c dil. D6 1 ml (HAB, Method 33c)

236

N1

PZN 2884463

Price Group 31

Status Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Contraindications The medicinal product should not be used in the case of hypersensitivity to any of the active ingredients or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea e planta tota must not be used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus) or other autoimmune diseases (diseases in which the immune system attacks the body‘s own tissues). Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Echinacea e planta tota

Active ingredient: echinacea pallida e planta tota ferm 33c Globuli velati Potency/Strength Package Size Size Category D3

20 g

Composition Globuli velati: 10 g contain: echinacea pallida e planta tota ferm 33c dil. D3 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. For harmonisation of the feeling organisation in febrile, inflammatory circumscribed and systemic processes, e.g. furunculosis, poorly healing wounds, inflammation of the uterine appendages (adnexitis), inflammation of the pelvic connective tissue (parametritis), inflammation of the lining of the womb (endometritis), inflammation of the lymph nodes (lymphadenitis), flu-like infections. Contraindications The medicinal product should not be used in the case of hypersensitivity to the active ingredient or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea e planta tota D3 must not be used in progressive systemic diseases such as tuberculosis, leukaemia or leukaemialike diseases, inflammatory diseases of the connective

N1

PZN 8785696

Price Group A

Status Pharmacy only

tissue (collagen disorders), multiple sclerosis, AIDS, HIV infections, chronic viral diseases or other autoimmune diseases. Warnings and precautions for use There is no adequately documented experience of the use of Echinacea e planta tota D3 in children under 4 years. It should therefore not be used. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Echinacea e planta tota. Dosage and method of administration Unless otherwise directed, children from 4 to under 6 years 3-5 globuli velati sublingually 1 to 5 times daily; children from 6 to under 12 years 5-10 globuli velati sublingually 1 to 5 times daily; adults and children of 12 years and above 10-15 globuli velati sublingually 1 to 5 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

237

E

Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been

observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Echinacea e planta tota

Active ingredient: echinacea pallida e planta tota ferm 33c Globuli velati

E

Potency/Strength Package Size Size Category D6

20 g

Composition Globuli velati: 10 g contain: echinacea pallida e planta tota ferm 33c dil. D6 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications The medicinal product should not be used in the case of hypersensitivity to the active ingredient or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea e planta tota D6 must not be used in progressive systemic diseases such as tuberculosis, leukaemia or leukaemialike diseases, inflammatory diseases of the connective tissue (collagen disorders), multiple sclerosis, AIDS, HIV infections, chronic viral diseases or other autoimmune diseases. Warnings and precautions for use There is no adequately documented experience of the use of Echinacea e planta tota D6 in children under 4 years. It should therefore not be used.

N1

PZN 8785704

Price Group A

Status Pharmacy only

This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Echinacea e planta tota. Dosage and method of administration Unless otherwise directed, children from 4 to under 6 years 3-5 globuli velati sublingually 1 to 5 times daily; children from 6 to under 12 years 5-10 globuli velati sublingually 1 to 5 times daily; adults and children of 12 years and above 10-15 globuli velati sublingually 1 to 5 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Echinacea-Essenz

Active ingredient: echinacea pallida ex herba LA 20% Tincture for external use Potency/Strength Package Size Size Category

100 ml

N1

PZN 1948534

Price Group E

Status Pharmacy only

Warnings and precautions for use Contains 25% (v/v) alcohol.

Composition 10 g (10.2 ml) contain: echinacea pallida ex herba LA 20% 10 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. For harmonisation of the feeling organisation in febrile, inflammatory circumscribed and systemic processes, e.g. furunculosis, poorly healing wounds, inflammation of the uterine appendages (adnexitis), inflammation of the pelvic connective tissue (parametritis), inflammation of the lining of the womb (endometritis), inflammation of the lymph nodes (lymphadenitis), pyaemia, flu-like infections. Contraindications The medicinal product should not be used in the case of hypersensitivity to the active ingredient or to other plants of the Compositae family.

Dosage and method of administration Unless otherwise directed, add 1 to 2 teaspoons of tincture to approx. ¼ l water and use for compresses or for irrigation. Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Echinacea/Mercurius comp., Suppositorien Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: apis mellifica ex animale toto Gl dil. D3 2 mg (HAB, Method 41c) argentum metallicum dil. D18 aquos. 2 mg atropa belladonna e fructibus ferm 33a dil. D2 2 mg (HAB, Method 33a) echinacea pallida e radice ferm 33d Ø 2 mg (HAB, Method 33d) mercurius solubilis Hahnemanni dil. D13 aquos. 2 mg Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the body‘s defences in febrile, acute inflammatory processes of a more circumscribed nature, e.g. tonsillitis, tendency to abscess formation.

N1

PZN 1880670

Price Group P

Status Pharmacy only

or excipients or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea/ Mercurius comp., Suppositorien must not be used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own organs or tissues). Dosage and method of administration Unless otherwise directed, adults and children of 7 years and above 1 suppository introduced into the rectum 2 to 3 times daily. Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. The medicinal product should not be used for more than 8 weeks without seeking medical advice.

Contraindications The medicinal product should not be used in the case of known hypersensitivity to any of the active ingredients

238

239

E

Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been ob-

served after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Echinacea/Mercurius comp., Suppositorien für Kinder Paediatric suppositories

Potency/Strength Package Size Size Category

E



10 x 1 g

N1

PZN 1880799

Price Group O

Status Pharmacy only

Composition 1 suppository (1 g) contains: apis mellifica ex animale toto Gl dil. D3 1 mg (HAB, Method 41c) argentum metallicum dil. D18 aquos. 1 mg atropa belladonna e fructibus ferm 33a dil. D2 1 mg (HAB, Method 33a) echinacea pallida e radice ferm 33d Ø 1 mg (HAB, Method 33d) mercurius solubilis Hahnemanni dil. D13 aquos. 1 mg Excipients: hard fat, honey.

used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own organs or tissues).

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the body‘s defences in febrile, acute inflammatory processes of a more circumscribed nature, e.g. tonsillitis, tendency to abscess formation.

Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. The medicinal product should not be used for more than 8 weeks without seeking medical advice.

Contraindications The medicinal product should not be used in the case of known hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea/ Mercurius comp., Suppositorien für Kinder must not be

Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum 2 to 3 times daily. Note: Echinacea/Mercurius comp., Suppositorien für Kinder are intended for use in infants and children up to 7 years.

Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Composition 10 g spray for application to the oral cavity contain: argentum nitricum dil. D13 aquos. 0.1 g (HAB, Method 5b) calendula officinalis e floribus LA 20% 1.0 g (HAB, Method 12c) echinacea pallida ex herba LA 20% 1.0 g (HAB, Method 12c) eucalyptus globulus e foliis ferm 33d dil. D1 0.1 g (HAB, Method 33d) gingiva bovis Gl dil. D4 0.1 g (HAB, Method 41b) gingiva bovis Gl dil. D8 0.1 g (HAB, Method 41b) salvia officinalis e foliis LA 20% 1.0 g (HAB, Method 12c) tonsillae palatinae bovis Gl dil. D4 0.1 g (HAB, Method 41a) tonsillae palatinae bovis Gl dil. D8 0.1 g (HAB, Method 41a) Excipients: ethanol (96%), carbon dioxide as propellant, sodium chloride, sodium hydrogen carbonate, purified water. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the oropharyngeal region in acute and chronic inflammatory conditions of the mucous membranes and the tonsils and in the case of a lymphatic diathesis. Contraindications On the basis of fundamental considerations, Echinacea Mund- und Rachenspray must not be used in children under 4 years. On account of the sage contained in the product Echinacea Mund- und Rachenspray should not be used during pregnancy.

The medicinal product should not be used in the case of hypersensitivity to the donor protein, to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations, Echinacea Mund- und Rachenspray must not be used in the case of progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own organs or tissues). Warnings and precautions for use On account of the sage contained in the product women who are breastfeeding should only use Echinacea Mundund Rachenspray after consulting a doctor. Contains 18% (v/v) alcohol. Dosage and method of administration Unless otherwise directed, apply 2 to 3 short squirts of the spray to the gums, tonsils or lymphatic ring twice a week, in acute cases up to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted; Echinacea Mund- und Rachenspray should not be used for longer than 2 weeks. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Echinacea Quarz comp. Augentropfen Eye drops

Potency/Strength Package Size Size Category

Echinacea Mund- und Rachenspray (mouth and throat spray) Spray

Potency/Strength Package Size Size Category

240

50 ml

N1

PZN 1448613

Price Group L

Status Pharmacy only



5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: argentum metallicum dil. D29 aquos. 0.05 g atropa belladonna ex herba ferm 33a dil. D14 0.05 g (HAB, Method 33a) echinacea pallida e planta tota ferm 33c dil. D2 0.05 g (HAB, Method 33c)

N1 N2

PZN 1448151 1448145

Price Group C C1

Status Pharmacy only Pharmacy only

quartz dil. D19 aquos. 0.05 g rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g Excipients: sodium chloride, sodium hydrogen carbonate and water for injections.

241

E

Indications according to the anthroposophical understanding of human beings and nature. Superinfection of allergic conjunctivitis.

E

Contraindications The medicinal product should not be used in the case of hypersensitivity to any of the active ingredients or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea Quarz comp. Augentropfen must not be used in progressive systemic diseases such as tuberculosis, leukaemia or leukaemia-like diseases, inflammatory diseases of the connective tissue (collagen disorders), multiple sclerosis, AIDS, HIV infections, chronic viral diseases or other autoimmune diseases.

Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac once or twice daily to hourly. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Echinacea/Viscum comp., Gelatum Gel



30 g

Composition 10 g contain: argentum metallicum dil. D10 0.1 g calendula officinalis e floribus LA 20% 1.0 g (HAB, Method 12c) cuprum aceticum dil. D6 aquos. 0.1 g (HAB, Method 5b) cutis (feti bovis) Gl dil. D4 0.1 g (HAB, Method 41b) echinacea pallida ex herba LA 20% 2.5 g (HAB, Method 12c) funiculus umbilicalis bovis Gl dil. D4 0.1 g (HAB, Method 41b) placenta (bovis) Gl dil. D4 0.1 g (HAB, Method 41b) rosmarini aetheroleum 0.03 g terebinthina laricina 0.02 g viscum album (mali) e planta tota ferm 34i dil. D2 0.1 g (HAB, Method 34i) Excipients: glycerol, sodium alginate, sodium chloride, sodium hydrogen carbonate, aqueous colloidal silicium dioxide solution produced with citric acid monohydrate, thyme oil, water for injections and purified water.

242

N1

PZN 2198348

Price Group J

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

E Endocardium Gl

Active ingredient: endocardium bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

Note: Without preservatives.

Potency/Strength Package Size Size Category

Dosage and method of administration Unless otherwise directed, apply the gel once to twice daily to intact skin; in the case of skin defects apply a thick layer of gel (about the thickness of the back of a knife) and cover with a dressing.

Status Pharmacy only

D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the anabolic and catabolic forces of the skin in degenerative, atrophic, hyperplastic and inflammatory, ulcerous disorders, e.g. senile skin, scar complaints, keloid formation, leg ulcers (ulcera crurum), tears in the skin around the opening of the anus (anal fissures).

Composition Liquid dilution for injection: 1 ml contains: endocardium bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Contraindications The medicinal product should not be used in case of known hypersensitivity to thyme oil, rosemary oil or other essential oils, to any of the other active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations Echinacea/ Viscum comp., Gelatum should not be used in the case of progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own organs or tissues). In infants and small children under 2 years the gel should not be used on the face and particularly not in the region of the nose.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2920489 2920503 2920532 2920555 2920578 2920590 2920615 2495477

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Endometrium Gl

Active ingredient: endometrium bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1

PZN 2920673 2920727 2920791 2920822

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

243

Composition Liquid dilution for injection: 1 ml contains: endometrium bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

E

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Endometrium comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D29 aquos. 0.1 g echinacea pallida e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) endometrium bovis Gl dil. D16 0.1 g (HAB, Method 41c) quartz dil. D29 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the body‘s defences and formative forces in inflammation of the lining of the womb (endometritis). Contraindications Endometrium comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations Endometrium comp. should not be used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection

244

N1

PZN 2085696

Price Group 11

Status Pharmacy only

(infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own tissues). Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Endometrium comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D29 aquos. 0.1 g echinacea pallida e planta tota ferm 33c dil. D1 0.1 g (HAB, Method 33c) endometrium bovis Gl dil. D16 0.1 g (HAB, Method 41c) quartz dil. D29 aquos. 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the body‘s defences and formative forces in inflammation of the lining of the womb (endometritis). Contraindications Endometrium comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations, Endometrium comp. should not be used in progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases

N1

PZN

Price Group

8785727

A

Status Pharmacy only

in which the immune system attacks the body‘s own tissues or organs). Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Endometrium comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually up to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see a doctor.

Enzian Magentonikum (gentian stomach tonic) Liquid to be taken internally

Potency/Strength Package Size Size Category

18 ml 100 ml

Composition 10 g contain: 10 g aqueous whole extract of gentian root 0.3608 g ginger root 0.2215 g

PZN

Price Group

0117417 3062131

K1 K3

Status Pharmacy only Pharmacy only

calamus root 0.0333 g pepper fruits 0.0066 g wormwood (aerial parts) 0.2775 g

245

E

E

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the peptic digestive activity by harmonisation of the motor and secretory processes, e.g. lack of appetite, feeling of fullness, nausea.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1/2 to 1 teaspoonful of Enzian Magentonikum 1 to 3 times daily before meals, either undiluted or diluted with water.

Contraindications Do not use Gentian Magentonikum • in the case of known hypersensitivity to ginger or pepper, • in the case of gastrointestinal ulcers, • in children under 12 years, • during pregnancy or breastfeeding.

Duration of treatment The condition should have cleared up within 5 days. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

Active ingredient: epididymis (sinistra) bovis GI Liquid dilution for injection

D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: epididymis sinistra bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 and D30: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

N1 N1 N1

PZN 2921106 2921164 2921201

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

therefore only be used in children under 12 years after consulting a doctor. On account of its composition the medicinal product is only for use in male patients. In the case of hypersensitivity reactions to foreign protein the medicinal product should be discontinued immediately and a doctor consulted. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: epiphysis bovis GI Liquid dilution for injection

246

Composition Liquid dilution for injection: 1 ml contains: epiphysis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml

N1 N1 N1

PZN 3357458 2831811 3357381

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

N1 N1 N1 N1 N1

PZN 2831509 3357398 3357406 3357464 2495974

Price Group 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

injected subcutaneously twice a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously twice a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment The treatment of disorders of growth and development and adjunctive treatment of malignant systemic diseases requires the agreement of a doctor. Side-effects Liquid dilution for injection D5, D6: Hypersensitivity reactions to the protein of the donor animal may occur in sensitised persons. In this case use of the medicinal product should be stopped and a doctor consulted. Liquid dilution for injection D8 upwards: None known.

Epiphysis/Plumbum Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: epiphysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) plumbum metallicum dil. D29 aquos. 0.1 g

Contraindications None known.

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications according to the anthroposophical understanding of human beings and nature. For structuring of the disturbed warmth organisation, e.g. in disorders of bone formation.

Epiphysis Gl

D5 D6 D8

D10 D12 D15 D30 Serial pack III

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the functional constitution in disorders of growth and development and for adjunctive treatment of malignant systemic diseases.

Epididymis (sinistra) Gl

Potency/Strength Package Size Size Category

Potency/Strength Package Size Size Category

N1

PZN 1751406

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

247

E

Epiphysis/Plumbum

Equisetum ex herba

Globuli velati

Active ingredient: equisetum arvense ex herba ferm 35b Globuli velati

Potency/Strength Package Size Size Category

E

20 g

Composition Globuli velati: 10 g contain: epiphysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) plumbum metallicum dil. D29 aquos. 0.1 g Contains sucrose (saccharose/sugar).

N1

PZN 8785733

Price Group A

Status Pharmacy only

consult your doctor before taking Epiphysis/Plumbum. Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually once daily.

Indications according to the anthroposophical understanding of human beings and nature. For structuring of the disturbed warmth organisation, e.g. in disorders of bone formation.

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications None known.

Side-effects None known.

Potency/Strength Package Size Size Category D3 D6 D10 D15

20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: equisetum arvense ex herba ferm 35b dil. D.. 1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Equisetum ex herba.

N1 N1 N1 N1

PZN 8785756 8785762 8785779 8785785

Price Group A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Equisetum ex herba

Active ingredient: equisetum arvense ex herba ferm 35b Liquid dilution for injection Potency/Strength Package Size Size Category D6 D8 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: equisetum arvense ex herba ferm 35b dil. D.. 1 ml (HAB, Method 35b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

248

N1 N1 N1 N1

PZN 2921365 2921388 2921402 2921425

Equisetum ex herba W 5%, Oleum Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously several times a week. Side-effects None known.

Active ingredient: equisetum arvense ex herba W 5% Bath additive, liquid Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: equisetum arvense ex herba W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the renal activity directed towards the organism; metabolic disorders with a tendency to formation of deposits and stone formation. Delayed healing of inflammatory conditions of the skin, mucous membranes and connective tissue, chronic inflammatory and degenerative disorders of the joints and nerves, degenerative and chronifying inflammatory disorders of the kidneys.

PZN 2088430

Price Group N1

Status Pharmacy only

In children under 12 years only for the indication: delayed healing of inflammatory disorders of the skin, mucous membranes and connective tissue. Contraindications Do not use in the case of hypersensitivity to the active ingredient. Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

249

E

Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor.

Equisetum/Formica

Side-effects None known.

Liquid dilution for injection

Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Equisetum-Essenz

Active ingredient: equisetum arvense ex herba LA 20% Tincture for external use

E

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (10.3 ml) contain: equisetum arvense ex herba LA 20% 10 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the renal activity directed towards the organism; metabolic disorders with a tendency to formation of deposits and stone formation. Delayed healing of inflammatory disorders of the skin, mucous membranes and connective tissue, inflammatory disorders of the kidneys that are becoming chronic or are of a degenerative nature. Indication in children under 12 years: delayed healing of inflammatory disorders of the skin, mucous membranes and connective tissue. Contraindications None known. Warnings and precautions for use Contains 25% (v/v) alcohol. On account of the alcohol content frequent application to the skin can cause irritation or inflammation and dry skin.

N1

PZN 1681344

Price Group E

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, for compresses add 2 teaspoonfuls of Equisetum-Essenz to about 250 ml of luke warm water, soak a compress with this solution and place on the affected skin area for about 15 minutes once to twice daily. For kidney packs add 2 teaspoons of Equisetum-Essenz to about 250 ml warm water. Moisten a sufficiently large compress or cloth with the mixture and place on the skin in the area of the kidneys. Wrap a woollen cloth firmly around the body to hold the compress in place. The pack should be applied for about 15 to 20 minutes followed by resting for about half an hour. Baths: add 4 tablespoons of Equisetum-Essenz to a full bath tub (about 200 l water). Duration of treatment If no significant improvement is seen after one week a doctor should be consulted. Nonetheless, the specified indications may require more prolonged treatment. Side-effects None known.

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D11 0.1 g (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Metabolic disorders with a tendency towards deposits and circumscribed hardening, e.g. chronic inflammatory and degenerative disorders of the joints and surrounding tissues. Contraindications None known.

PZN 1751412 2085727

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Even anthroposophical medicines should not be taken for prolonged periods without obtaining the advice of a doctor. Side-effects None known.

Equisetum/Formica Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: equisetum arvense ex herba ferm 35b dil. D5 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Metabolic disorders with a tendency towards deposits and circumscribed hardening, e.g. chronic inflammatory and degenerative disorders of the joints and surrounding tissues. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children under 6 years is not available. It should therefore not be used in children under 6 years.

250

N1 N2

N1

PZN 8785791

Price Group A

Status Pharmacy only

In children between 6 and 12 years medical advice should be sought before using Equisetum/Formica and it should not be used in place of any other treatment prescribed by the doctor. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should therefore consult your doctor before taking Equisetum/ Formica. Dosage and method of administration Unless otherwise directed, adults and children of 6 years and above 5-10 globuli velati sublingually 3 times daily. Duration of treatment Even anthroposophical medicines should not be taken for prolonged periods without obtaining the advice of a doctor. Side-effects None known.

251

E

Equisetum/Stannum

Equisetum/Viscum

Liquid dilution for injection

Liquid dilution for injection

Potency/Strength Package Size Size Category

E

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1751429 2085733

Price Group 11 12

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only



Composition Liquid dilution for injection: 1 ml contains: equisetum arvense ex herba ferm 35b dil. D14 0.1 ml (HAB, Method 35b) stannum metallicum dil. D9 0.1 ml

medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Metabolic disorders with a tendency towards deposits and deformation, e.g. degenerative joint disease (osteoarthritis), also with joint effusion.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications Do not use in the case of hypersensitivity to milk protein.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Warnings and precautions for use Sufficiently documented experience for the use of this

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) stannum metallicum dil. D9 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Metabolic disorders with a tendency towards deposits and deformation, e.g. degenerative joint disease (osteoarthritis), also with joint effusion. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Equisetum/Stannum.

252

Composition Liquid dilution for injection: 1 ml contains: equisetum arvense ex herba ferm 35b dil. D5 0.1 ml (HAB, Method 35b) viscum album (mali) e planta tota ferm 34i dil. D5 0.1 ml (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling and life organisation in the renal system, e.g. in high blood pressure (hypertension), chronic inflammatory, degenerative kidney diseases, ureteral colic. Contraindications Do not use in the case of known allergy to mistletoe formulations. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Equisetum/Stannum



10 x 1 ml 50 x 1 ml

N1

PZN 8785816

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 5 times daily; children from 6 to under 12 years 5-10 globuli velati sublingually 3 to 5 times daily; adults and children of 12 years and above 10-15 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

N1 N2

PZN 1751435 2085756

Price Group 11 12

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought.

Equisetum/Viscum Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: equisetum arvense ex herba ferm 35b dil. D3 0.1 g (HAB, Method 35b) viscum album (mali) e planta tota ferm 34i dil. D3 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling and life organisation in the renal system, e.g. in high blood pressure (hypertension), chronic inflammatory, degenerative kidney diseases, ureteral colic.

N1

PZN 8785822

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Equisetum/Viscum. Dosage and method of administration Unless otherwise directed, 10-15 globuli velati sublingually three times daily.

253

E

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications Do not use in the case of known hypersensitivity to any of the active ingredients.

Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously once to twice daily.

Erythrocyten Gl

Active ingredient: erythrocyten equi GI Liquid dilution for injection

E

Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: erythrocyten equi Gl dil. D.. 1 ml (HAB, Method 41d) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3357487 3357493 3357501 3357518 3357524 3357530 3357547 2495980

Price Group 41 41 41 41 41 41 41 51

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

254

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: cuprum sulfuricum dil. D4 aquos. 0.1 g (HAB, Method 5b) eucalyptus globulus e foliis ferm 33d Ø 0.5 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Disturbed integration of the warmth organism in the metabolic system in febrile inflammatory diseases of the intestine, adjunctive treatment of intestinal parasites.

N1

PZN 8785839

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 5 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Eucalyptus comp.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: cuprum sulfuricum dil. D4 aquos. 0.1 g (HAB, Method 5b) eucalyptus globulus e foliis ferm 33d Ø 0.05 g (HAB, Method 33d)

E

Eucalyptus comp.

Contraindications Do not use in the case of known hypersensitivity to any of the active ingredients.

Liquid dilution for injection

10 x 1 ml

Side-effects None known after intramuscular administration. Harmless redness at the injection site can occur occasionally after subcutaneous injection.

Status

Eucalyptus comp.



Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor.

N1

PZN 1751441

Price Group 11

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Disturbed integration of the warmth organism in the metabolic system in febrile inflammatory diseases of the intestine, adjunctive treatment of intestinal parasites.

Eucalyptus, Oleum aethereum 10% Active ingredient: eucalypti aetheroleum 10% Bath additive, liquid

Potency/Strength Package Size Size Category

100 ml

PZN 2088476

Price Group N1

Status General sale

255

Composition 10 g (11 ml) contain: eucalypti aetheroleum 10% (HAB, Method 12h with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. E.g. acute inflammation of the airways.

E

Contraindications Do not use Eucalyptus, Oleum aethereum 10% • in the case of known hypersensitivity to eucalyptus oil or cineole, the main constituent of eucalyptus oil • in the case of eczema • in the case of whooping cough, croup or bronchial asthma because of marked hypersensitivity of the airways • in the case of other disorders of the airways in which there is a marked hypersensitivity of the airways as the inhalation of eucalyptus oil can lead to involuntary contraction of the bronchi • in infants and small children up to 2 years as respiratory arrest due to involuntary contraction of the vocal cords has occurred in rare cases after the inhalation of essential oils. Patients with skin injuries affecting larger areas, acute skin conditions of unclear origin, severe febrile and infectious diseases, weak heart or high blood pressure should obtain the advice of a doctor before taking a full bath of any kind, irrespective of the additive used. Warnings and precautions for use During breastfeeding: Do not breastfeed immediately after the bath. Clean the skin in the region of the breasts before breastfeeding.

Interactions with other agents Eucalyptus oil activates the enzyme system in the liver which breaks down foreign substances. Even when used as bath additive the possibility of effects of other medicinal products being weakened or shortened cannot be ruled out.

Contraindications None known.

sulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In sensitive persons application of the drops may cause a mild burning sensation which decreases as the inflammation subsides.

Dosage and method of administration Unless otherwise directed, for adults and children of 2 years and above use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Dosage and method of administration Unless otherwise directed, adults and children of all age groups 1 drop instilled into the conjunctival sac once to twice daily (see note on application). Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be con-

Note: Without preservatives.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The following side-effects can occur after inhalation of essential oils: • irritation of skin and mucous membranes • coughing and exacerbation of bronchospasm (involuntary contraction of the breathing muscles). Precipitation of contact allergy after use as bath additive cannot be ruled out. In such cases the treatment should be discontinued and a doctor consulted. In very rare cases hypersensitivity reactions with racing heart, suppression of respiratory drive and seizures have been reported, particularly in infants and small children, after use of concentrated essential oils. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

E Euphrasia e planta tota

Active ingredient: euphrasia ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D6

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: euphrasia ferm 33c dil. D6 1 ml Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Eye drops

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: euphrasia ferm 33c dil. D2 0.05 g rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g

256

N1 N2

PZN 1448174 1448168

Price Group C C1

Status Pharmacy only Pharmacy only

Excipients: sodium chloride, sodium hydrogen carbonate and water for injections. Indications according to the anthroposophical understanding of human beings and nature. Structuring of the fluid organism in the region of the eye, e.g. in catarrhal conjunctivitis.

PZN 2921572

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Side-effects None known.

Euphrasia e planta tota

Active ingredient: euphrasia ferm 33c Globuli velati Potency/Strength Package Size Size Category D4

Euphrasia Augentropfen

N1

20 g

Composition Globuli velati: 10 g contain: euphrasia ferm 33c dil. D4 1g Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Euphrasia e planta tota.

N1

PZN 8785845

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

257

Fasciculus atrioventricularis Gl

Contraindications None known.

Active ingredient: fasciculus atrioventricularis bovis Gl [consisting of truncus fasciculi atrioventricularis and rami subendocardiales] Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

F

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: fasciculus atrioventricularis bovis Gl [consisting of truncus fasciculi atrioventricularis and rami subendocardiales] dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3357553 2829955 3357576 3357582 2831573 3357599 3357607 2496034

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Femur Gl

Active ingredient: femur bovis Gl Liquid dilution for injection

F

Potency/Strength Package Size Size Category D5

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: femur bovis Gl dil. D5 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

N1

PZN 4618151

Price Group 61

Status Pharmacy only

medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this

Fasciculus opticus see Nervus opticus Gl

Ferrum silicicum comp. Liquid dilution for injection

Fel Gl

Active ingredient: fel tauri Gl Liquid dilution for injection

Potency/Strength Package Size Size Category

Potency/Strength Package Size Size Category D8 D30

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: fel tauri Gl dil. D.. 1 ml (HAB, Method 41a)

258

N1 N1

PZN 4618139 2875694

Price Group 61 61

10 x 1 ml

N1

PZN 1751458

Price Group 11

Status Pharmacy only

Status Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Composition Liquid dilution for injection: 1 ml contains: ferrum oxydulatum nigrum dil. D6 0.1 g (HAB, Method 6) nontronite dil. D6 0.1 g pimpinella anisum e fructibus, infusum dil. D4 0.1 g (HAB, Method 24a) urtica dioica e planta tota ferm 33c dil. D7 0.1 g (HAB, Method 33c)

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the iron metabolism for integration of the ego organisation in the blood, e.g. for adjunctive treatment of anaemia, convalescence. Contraindications Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

259

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati

Potency/Strength Package Size Size Category

F

20 g

Composition Globuli velati: 10 g contain: ferrum oxydulatum nigrum trit. D4 0.1 g (HAB, Method 6) nontronite trit. D4 0.1 g pimpinella anisum e fructibus, infusum Ø 0.8 g (HAB, Method 24a) urtica dioica e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the iron metabolism for integration of the ego organisation in the blood, e.g. for adjunctive treatment of anaemia, convalescence. Contraindications None known.

N1

PZN 8785851

Price Group A

Pharmacy only

sugars you should consult your doctor before taking Ferrum silicum comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

260

F

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: ferrum metallicum dil. D7 0.1 g quartz dil. D19 aquos. 0.1 g sulfur dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between nerve-sense, rhythmic and metabolic system in the head, e.g. in migraine, also with depressed mood.

N1

PZN 8785868

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually up to twice daily; adults and children of 6 years and above 5-10 globuli velati sublingually up to twice daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Ferrum/Sulfur comp.

Liquid dilution for injection

Composition Liquid dilution for injection: 1 ml contains: ferrum metallicum dil. D7 0.1 g quartz dil. D19 aquos. 0.1 g sulfur dil. D5 0.1 g

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Ferrum/Sulfur comp.

Contraindications None known.

Ferrum/Sulfur comp.

10 x 1 ml

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Status

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain



Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

Ferrum silicicum comp.



Contraindications Do not use in the case of hypersensitivity to milk protein.

N1

PZN 1751464

Price Group 11

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between nerve-sense, rhythmic and metabolic system in the head, e.g. in migraine, also with depressed mood.

261

Folliculi lymphatici aggregati Gl

Composition Liquid dilution for injection: 1 ml contains: formica rufa ex animale toto Gl dil. D.. 1 ml (HAB, Method 41c)

Active ingredient: folliculi lymphatici aggregati suis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

F

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2876386 2876400 2876423 2876452 2876475 2876498 2876512 0847860 0846323 2496040

Price Group 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: folliculi lymphatici aggregati suis Gl dil. D.. 1 ml (HAB, Method 41c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Formica ex animale Gl

Active ingredient: formica rufa ex animale toto GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D5 D8 D12 D15 D30 D40 D60

262

10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N2 N1 N1 N1 N1 N1 N1

PZN 4618300 4618317 4618323 3357636 3357642 2830651 2884492 4626280

Price Group 61 62 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. For stimulation and structuring of metabolic processes in conditions involving an increased tendency to deposits and hardening, e.g. chronic rheumatic disorders, gout, osteoarthritis, muscle hardening (myogeloses), nerve pain (neuralgia); eczema. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to ant venom. Liquid dilution for injection D8 upwards: None known.

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously once a week to once daily, children of 6 to under 12 years 0.5-1 ml injected subcutaneously once a week to once daily, adults and children of 12 years and above 1 ml injected subcutaneously once a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions to ant venom are possible in rare cases. In such cases use of the medicinal product should be stopped immediately and a doctor consulted.

Formica/Oxalis

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: formica rufa ex animale toto Gl dil. D4 0.1 g (HAB, Method 41c) oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of anabolic metabolic and elimination processes in conditions involving increased tendencies to deposits and hardening, e.g. rheumatic disorders. Contraindications Do not use in the case of known hypersensitivity to formic acid.

N1 N2

PZN 2085785 2233926

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Harmless redness around the injection site may very rarely occur.

263

F

Fucus vesiculosus e planta tota

Funiculus umbilicalis Gl

Active ingredient: fucus vesiculosus e planta tota ferm 51 Liquid dilution for injection Potency/Strength Package Size Size Category D3

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: fucus vesiculosus e planta tota ferm 51 dil. D3 1 ml (HAB, Method 51)

F

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2921750

Active ingredient: funiculus umbilicalis bovis GI Liquid dilution for injection Price Group 31

Status

Potency/Strength Package Size Size Category

Pharmacy only

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack III

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2831656 3357079 2830881 3357085 3357091 3357665 3357671 2831840 2496152

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Fucus vesiculosus e planta tota

Composition Liquid dilution for injection: 1 ml contains: funiculus umbilicalis bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Potency/Strength Package Size Size Category

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Active ingredient: fucus vesiculosus e planta tota ferm 51 Globuli velati

D2 D3 D6

20 g 20 g 20 g

N1 N1 N1

PZN 8785874 8785880 8785905

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Composition Globuli velati: 10 g contain: fucus vesiculosus e planta tota ferm 51 dil. D.. 1 g (HAB, Method 51) Contains sucrose (saccharose/sugar).

therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking fucus vesiculosus e planta tota.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Contraindications Hypersensitivity to iodine. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

264

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

265

F

Galea aponeurotica Gl

Galenit/Retina comp.

Active ingredient: galea aponeurotica bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D30

G

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1

Globuli velati PZN 4618381 2831018 4618406 0489515

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: galea aponeurotica bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

N1 N2

PZN 1751470 2085791

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: galenite dil. D19 aquos. 0.1 g retina et chorioidea bovis Gl dil. D11 0.1 g (HAB, Method 41c) secale cornutum e sklerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b) terebinthina laricina dil. D9 0.1 g (HAB, Method 6)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the fluid organism in degenerative tendencies in the retina and choroid of the eye.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

266

N1

PZN 8785911

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: galenite dil. D19 aquos. 0.1 g retina et chorioidea bovis Gl dil. D11 0.1 g (HAB, Method 41c) secale cornutum e sklerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b) terebinthina laricina dil. D9 0.1 g (HAB, Method 6) Contains sucrose (saccharose/sugar) and lactose.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Galenit/ Retina comp.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the fluid organism in degenerative tendencies in the retina and choroid of the eye.

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Side-effects None known.

Liquid dilution for injection

Potency/Strength Package Size Size Category

Contraindications Do not use in the case of hypersensitivity to milk protein.

20 g

Gelsemium comp.

Liquid dilution for injection

10 x 1 ml 50 x 1 ml



Contraindications None known.

Galenit/Retina comp.



Potency/Strength Package Size Size Category

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bryonia cretica ferm 33b dil. D2 0.1 g gelsemium sempervirens e rhizoma ferm 35b dil. D2 0.1 g (HAB, Method 35b) gelsemium sempervirens e rhizoma ferm 35b dil. D14 0.1 g (HAB, Method 35b) vivianite dil. D7 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Flu-like infections, particularly with involvement of the head; neuralgiform pain. Contraindications The medicinal product should not be used in the case of

N1 N2

PZN 1751487 2085816

Price Group V5 V6

Status Prescription only Prescription only

known allergy to any of the active ingredients or if you are hypersensitive to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 3 times a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

267

G

Gelsemium e radice

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Active ingredient: gelsemium sempervirens e rhizoma ferm 35b Globuli velati Potency/Strength Package Size Size Category D6 D12 D30

Gelsemium comp. Globuli velati

Potency/Strength Package Size Size Category

G

20 g

N1

PZN 8785928

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: bryonia cretica ferm 33b dil. D2 0.1 g gelsemium sempervirens e rhizoma ferm 35b dil. D2 0.1 g (HAB, Method 35b) gelsemium sempervirens e rhizoma ferm 35b dil. D14 0.1 g (HAB, Method 35b) vivianite dil. D7 0.1 g Contains sucrose (saccharose/sugar) and lactose.

you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Gelsemium comp.

Indications according to the anthroposophical understanding of human beings and nature. Flu-like infections, particularly with involvement of the head; neuralgiform pain.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually up to twice daily; adults and children of 6 years and above 5-10 globuli velati sublingually up to twice daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Side-effects None known.

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: gelsemium sempervirens e rhizoma ferm 35b dil. D.. 1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Gelsemium e radice.

N1 N1 N1

PZN 8785934 8785940 8785957

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Gentiana comp.

see Gentiana Magen Inject see Gentiana Magen Globuli velati

Gentiana lutea e radice

Active ingredient: gentiana lutea e radice ferm 33c Globuli velati

Gelsemium e radice

Potency/Strength Package Size Size Category

Active ingredient: gelsemium sempervirens e rhizoma ferm 35b Liquid dilution for injection Potency/Strength Package Size Size Category D4 D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: gelsemium sempervirens e rhizoma ferm 35b dil. D.. 1 ml (HAB, Method 35b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

268

N1 N1 N1 N1

PZN 2884517 2922778 2884546 2922790

5% Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known.

20 g

Composition Globuli velati: 10 g contain: gentiana lutea e radice ferm 33c Ø 0.5 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 8785986

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Gentiana lutea e radice.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

269

G

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of

water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Gentiana lutea e radice

D2 D4

G

20 g 20 g

Composition Globuli velati: 10 g contain: gentiana lutea e radice ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Gentiana lutea e radice.

N1 N1

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Gentiana Magen Globuli velati (stomach remedy)

Active ingredient: gentiana lutea e radice ferm 33c Globuli velati Potency/Strength Package Size Size Category

Contraindications Do not use Gentiana Magen Inject in the case of known hypersensitivity to artemisia absinthium.

Globuli velati PZN 8785992 8786000

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: artemisia absinthium ex herba, infusum Ø 0.45 g (HAB, Method 24a) gentiana lutea e radice, decoctum Ø 0.45 g (HAB, Method 23a) strychnos nux-vomica e semine ferm 35b dil. D4 0.10 g (HAB, Method 35b) taraxacum officinale e planta tota ferm 34c Ø 0.05 g (HAB, Method 34c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of motility and secretion in digestive disorders of the gastrointestinal tract, e.g. digestive weakness, nausea, vomiting, flatulence. Contraindications Do not use Gentiana Magen Globuli velati in the case of known hypersensitivity to artemisia absinthium.

N1

PZN 0081441

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Gentiana Magen Globuli. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily before meals. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Gentiana Magen Inject (stomach remedy) Liquid dilution for injection

Geum urbanum e radice

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: artemisia absinthium ex herba, infusum dil. D3 0.1 g (HAB, Method 24a) gentiana lutea e radice, decoctum dil. D3 0.1 g (HAB, Method 23a) strychnos nux-vomica e semine ferm 35b dil. D5 0.1 g (HAB, Method 35b)

270

N1 N2

PZN 0081398 0090084

Price Group 11 12

Status Pharmacy only Pharmacy only

taraxacum officinale e planta tota ferm 34c dil. D2 0.1 g (HAB, Method 34c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of motility and secretion in digestive disorders of the gastrointestinal tract, e.g. digestive weakness, nausea, vomiting, flatulence.

Active ingredient: geum urbanum e radice ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D3

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: geum urbanum e radice ferm 33c dil. D3 1 ml (HAB, Method 33c)

N1

PZN 2832756

Price Group 31

Status Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

271

G

Contraindications None known.

Composition Liquid dilution for injection: 1 ml contains: glandula lacrimalis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

twice a week to once daily.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously

Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Gingiva Gl

Active ingredient: gingiva bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

G

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2922933 2922962 2922985 2923016 2923039 2923051 2923097 2496376

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

G

Glandula parotis Gl

Active ingredient: glandula parotis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: gingiva bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: glandula lacrimalis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category

272

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: glandula parotis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Glandula lacrimalis Gl

D5 D6 D8 D12 D15 D30 Serial pack

D5 D6 D8 D12 D15 D30 Serial pack

N1 N1 N1 N1 N1 N1 N1

PZN 2923157 2923186 2923200 2923252 2923275 2923298 2490830

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2923476 2923499 2923513 2923565 2923588 2923602 2490847

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

273

Glandula suprarenalis (Cortex) Gl

Liquid dilution for injection D8 upwards: None known.

Active ingredient: glandula suprarenalis cortex bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30

G

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: glandula suprarenalis cortex bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829903 3357145 3357151 3357168 3357174 3357180 3357197 3357211

Price Group 41 61 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: glandula suprarenalis dextra bovis GI Liquid dilution for injection

D4 D5 D6 D8 D10 D12 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: glandula suprarenalis dextra bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in an-

274

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2877144 2877167 2877196 2877210 2877233 2877262 2877285 2877339

Price Group 41 61 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

throposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Glandula suprarenalis dextra cum Cupro Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cuprum metallicum dil. D5 0.1 g glandula suprarenalis dextra bovis Gl dil. D7 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Integration of the warmth organism into the metabolic system and energising of the anabolic processes in the water organism, e.g. digestive disturbances in disorders of the hepatobiliary system, low blood pressure (hypotension), lack of drive. Contraindications Do not use in the case of hypersensitivity to milk protein.

Glandula suprarenalis dextra Gl

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

N1

PZN 1751518

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Glandula suprarenalis dextra cum Cupro Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: cuprum metallicum dil. D5 0.1 g glandula suprarenalis dextra bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose.

N1

PZN 8786017

Price Group A

Status Pharmacy only

man beings and nature. Integration of the warmth organism into the metabolic system and energising of the anabolic processes in the water organism, e.g. digestive disturbances in disorders of the hepatobiliary system, low blood pressure (hypotension), lack of drive. Contraindications None known.

Indications according to the anthroposophical understanding of hu-

275

G

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Glandula suprarenalis dextra cum Cupro. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dis-

solving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

D5 D6 D8 D10 D12 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: glandula suprarenalis, medulla bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2877397 2877411 2877434 2877457 2877486 2877500 2877552

Price Group 61 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Glandula suprarenalis sinistra Gl

Active ingredient: glandula suprarenalis sinistra bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6

276

10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1

PZN 2877612 2877635 2877658

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: glandula suprarenalis medulla bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

D8 D10 D12 D15 D30

Composition Liquid dilution for injection: 1 ml contains: glandula suprarenalis sinistra bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Glandula suprarenalis (Medulla) Gl

G

Potency/Strength Package Size Size Category

Price Group 41 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

N1 N1 N1 N1 N1

PZN 2877670 2877693 2877718 2877730 2877782

Price Group 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. It should be noted that Glandula suprarenalis Gl D4 must not be used for longer than 3 months. Intermittent use over a period of more than three months is possible provided that the total number of daily doses does not exceed 99 per year. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Glandula suprarenalis sinistra cum Cupro Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cuprum metallicum dil. D5 0.1 g glandula suprarenalis sinistra bovis Gl dil. D7 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Integration of the warmth organism into the metabolic system and energising of the anabolic processes in the water organism, e.g. digestive disturbances in disorders of the pancreas, stomach or duodenum, low blood pressure (hypotension), lack of drive. Contraindications Do not use in the case of hypersensitivity to milk protein or the donor animal protein.

N1

PZN 1751524

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

277

G

Glandula suprarenalis sinistra cum Cupro

Glandula thymi

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: cuprum metallicum dil. D5 0.1 g glandula suprarenalis sinistra bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose.

G

Indications according to the anthroposophical understanding of human beings and nature. Integration of the warmth organism into the metabolic system and energising of the anabolic processes in the water organism, e.g. digestive disturbances in disorders of the pancreas, stomach or duodenum, low blood pressure (hypotension), lack of drive. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance

N1

PZN 8786023

see Thymus (Glandula) GI Price Group A

Status Pharmacy only

to certain sugars you should consult your doctor before taking Glandula suprarenalis sinistra cum Cupro. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.



10 x 1 ml

N1

1751530

Price Group 11

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: glandula suprarenalis sinistra bovis Gl dil. D7 0.1 g (HAB, Method 41a) mercurius vivus dil. D14 aquos. 0.1 g

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of absorption and anabolism in metabolic weakness, e.g. nutritional and anabolic disorders, chronic gastrointestinal diseases.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

278

Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D20 D30 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications according to the anthroposophical understanding of human beings and nature. Hormonal dysfunction of the thyroid gland, enlarged thyroid gland (goitre).

Liquid dilution for injection

PZN

Active ingredient: glandula thyreoidea bovis GI Liquid dilution for injection

Composition Liquid dilution for injection: 1 ml contains: glandula thyreoidea bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Glandula suprarenalis sinistra/Mercurius Potency/Strength Package Size Size Category

Glandula thyreoidea Gl

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of an overactive thyroid gland (hyperthyroidism) or hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N2 N1 N1 N1

PZN 2831076 3357234 2829961 3357240 2831892 3357257 3357263 3357286 2830071 2877919 0847943 0846429 2496436

Price Group 41 61 61 61 61 61 61 61 61 62 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case the patient should see a doctor. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In sensitised persons hypersensitivity reactions to the donor animal protein can occur (at low potencies up to D7). In this case use of the medicinal product should be stopped and a doctor consulted.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Side-effects None known.

279

G

Glandulae parathyreoideae Gl

Active ingredient: glandulae parathyreoideae bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

G

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: glandulae parathyreoideae bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3357300 3357317 3357323 2830817 3357352 3357369 2830214 2496442

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Glandulae suprarenales Gl

Active ingredient: glandulae suprarenales bovis GI Liquid dilution for injection

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

280

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829406 3356743 2829582 3356766 3356795 3356803 2831716 3356772 0847972 0846441 2496459

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the organ function of the adrenal gland in states of exhaustion and weakness, also when accompanied by hypotensive circulatory dysregulation.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. For potencies D15 and D30: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case the patient must see a doctor. Side-effects None known.

G

Glandulae suprarenales comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: fel tauri Gl dil. D7 0.1 g (HAB, Method 41a) glandulae suprarenales bovis Gl dil. D7 0.1 g (HAB, Method 41a) lien bovis Gl dil. D7 0.1 g (HAB, Method 41a)

Side-effects None known.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: glandulae suprarenales bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the feeling organisation in the metabolic system, e.g. in hypotensive circulatory dysregulation, states of exhaustion and weakness, digestive weakness, allergic diathesis.

N1 N2

PZN 1751501 2085845

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Glandulae suprarenales comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8786046

Price Group A

Status Pharmacy only

281

Composition Globuli velati: 10 g contain: fel tauri Gl dil. D5 0.1 g (HAB, Method 41a) glandulae suprarenales bovis Gl dil. D4 0.1 g (HAB, Method 41a) lien bovis Gl dil. D5 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the feeling organisation in the metabolic system, e.g. in hypotensive circulatory dysregulation, states of exhaustion and weakness, digestive weakness, allergic diathesis.

G

Contraindications None known.

you suffer from intolerance to certain sugars you should consult your doctor before taking Glandulae suprarenales comp.

Gnaphalium comp.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Potency/Strength Package Size Size Category

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that

Gnaphalium comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cerebellum bovis Gl dil. D15 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D15 0.01 g (HAB, Method 41a) epiphysis bovis Gl dil. D15 0.01 g (HAB, Method 41a) labyrinthus bovis Gl dil. D15 0.01 g (HAB, Method 41a) leontopodium alpinum e planta tota ferm 36 dil. D13 0.01 g (HAB, Method 36) medulla oblongata bovis Gl dil. D15 0.01 g (HAB, Method 41a) nervus statoacusticus bovis Gl dil. D15 0.01 g (HAB, Method 41a) onyx dil. D18 aquos. 0.01 g stannum metallicum dil. D18 aquos. 0.01 g

282

N1 N2

PZN 1751547 2085851

Price Group 11 12

Status Pharmacy only Pharmacy only

Globuli velati



Composition Globuli velati: 10 g contain: cerebellum bovis Gl dil. D15 0.01 g (HAB, Method 41a) corpora quadrigemina bovis Gl dil. D15 0.01 g (HAB, Method 41a) epiphysis bovis Gl dil. D15 0.01 g (HAB, Method 41a) labyrinthus bovis Gl dil. D15 0.01 g (HAB, Method 41a) leontopodium alpinum e planta tota ferm 36 dil. D13 0.01 g (HAB, Method 36) medulla oblongata bovis Gl dil. D15 0.01 g (HAB, Method 41a) nervus statoacusticus bovis Gl dil. D15 0.01 g (HAB, Method 41a) onyx dil. D18 aquos. 0.01 g stannum metallicum dil. D18 aquos. 0.01 g Contains sucrose (saccharose/sugar).

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation in the ear in the case of hardening of bone in the inner ear (otosclerosis) and Menière’s syndrome.

Granat

Contraindications None known.

D15

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

20 g

N1

PZN 8786052

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation in the ear in otosclerosis and Menière’s syndrome. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Gnaphalium comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 to 5 times daily. Side-effects None known.

Active ingredient: garnet aquos. Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: garnet dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2878132

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

283

G

Graphites

Hamamelis e foliis

Active ingredient: graphites aquos. Liquid dilution for injection

Active ingredient: hamamelis virginiana e foliis ferm 33d Globuli velati

Potency/Strength Package Size Size Category D8 D30

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: graphites dil. D.. 1 ml

G

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2878356 2878379

Price Group 31 31

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only

D6

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Active ingredient: gyrus cinguli bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: gyrus cinguli bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Hamamelis e foliis.

Gyrus cinguli Gl

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Globuli velati: 10 g contain: hamamelis virginiana e foliis ferm 33d dil. D6 1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar).

Contraindications None known.

Contraindications Do not use in the case of hypersensitivity to milk protein.

D5 D6 D8 D12 D15 D30

20 g

N1 N1 N1 N1 N1 N1

PZN 2878445 2878468 2878480 2878528 2878540 2878563

Price Group 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

PZN

Price Group

8786069

A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Hamamelis-Essenz

Active ingredient: hamamelis virginiana e cortice et foliis LA 20% Tincture for external use Potency/Strength Package Size Size Category

100 ml

Composition 10 g (10.2 ml) contain: hamamelis virginiana e cortice et foliis (1:9) LA 20% 10 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the healing processes in wounds and vascular deformities, e.g. haemorrhoids, mucosal tears in the region of the back passage (anal fissures), disorders associated with varicose veins (varicose symptom complex), leg ulcers (crural ulcers). Contraindications Do not use in the case of known hypersensitivity to hamamelis. Warnings and precautions for use The duration of treatment of haemorrhoid disorders with

284

N1

N1

PZN 1681350

Price Group E

Status Pharmacy only

Hamamelis-Essenz should not exceed 2 weeks. In the case of application in the region of the nipples women who are breastfeeding should carefully cleanse the skin before feeding. Hamamelis-Essenz should only be used in children under 12 years after consulting a doctor. Contains 25% (v/v) alcohol. Dosage and method of administration Unless otherwise directed, for compresses add 1 to 2 teaspoons of Hamamelis-Essenz to approx. 250 ml water and use for compresses; for sitzbaths, use 1 to 2 tablespoons of Hamamelis-Essenz for 1 sitzbath. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

285

H

Side-effects Like all medicinal products, Hamamelis-Essenz can have side-effects. In the case of topical application allergic reactions to medicinal products containing hamamelis can occur.

If you notice signs of such a reaction, e.g. skin redness, with or without itching, you should stop using Hamamelis-Essenz and see your doctor if necessary.

Hepar Gl

Active ingredient: hepar bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category

Helleborus niger e planta tota

Active ingredient: helleborus niger e planta tota ferm 34c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D3 D6 D12 D30

H

10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: helleborus niger e planta tota ferm 34c dil. D.. 1 ml (HAB, Method 34c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N2 N1 N1 N1

PZN 2878669 2878675 2878681 2884569 2884581

Price Group 31 32 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Active ingredient: helleborus niger e planta tota ferm 34c Globuli velati

D6 D12

20 g 20 g

Composition Globuli velati: 10 g contain: helleborus niger e planta tota ferm 34c dil. D.. 1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Helleborus niger e planta tota.

286

N1 N1

PZN 8786075 8786081

Price Group A A

Status

Composition Liquid dilution for injection: 1 ml contains: hepar bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Adjunctive treatment of chronic liver disorders and depressive mood.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829524 3356849 2829748 3356855 3356861 3356878 2830823 2829932 0847989 0846493 2496465

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Potencies below D20: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potencies D20 and above: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this

Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Helleborus niger e planta tota

Potency/Strength Package Size Size Category

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

Hepar/Stannum I

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hepar bovis Gl dil. D5 0.1 g (HAB, Method 41a) stannum metallicum dil. D9 0.1 g

N1 N2

PZN 1223587 1223601

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the exhausted life organisation and harmonisation of the engagement of the feeling organisation in degenerative and chronic inflammatory processes in the liver and their psychological side-effects, e.g. chronic inflammation of the liver (chronic hepatitis), liver cirrhosis, depression.

287

H

Contraindications You must not use the medicinal product if you are hypersensitive to • the donor animal protein • milk protein Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Contraindications Do not use in the case of hypersensitivity to milk protein or the donor animal protein.

Duration of treatment The duration of treatment of chronic conditions should be discussed with the doctor.

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 3 times a week to once or twice daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously 3 times a week to once or twice daily; adults and children of 12 years and above 1 ml injected subcutaneously 3 times a week to once or twice daily.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

sulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In the case of hypersensitivity reactions to foreign protein treatment with the medicinal product should be discontinued immediately and a doctor consulted. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be con-

Hepar/Stannum II

Liquid dilution for injection Potency/Strength Package Size Size Category

H

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hepar bovis Gl dil. D16 0.1 g (HAB, Method 41a) stannum metallicum dil. D19 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic balancing and formative processes in both inflammatory, dissolving and degenerative disorders of the liver and their psychological side-effects, e.g. acute and chronic inflammation of the liver (hepatitis). Contraindications None known.

N1 N2

PZN 1223653 1223676

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

Liquid dilution for injection

Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hepar sulfuris dil. D5 0.1 g membrana sinuum paranasalium bovis Gl dil. D5 0.1 g (HAB, Method 41a)

288

Active ingredient: hippocampus bovis GI Liquid dilution for injection

N1 N2

PZN 2085874 2233955

Price Group 11 12

Status Pharmacy only Pharmacy only

H

Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hippocampus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Hepar sulfuris comp.



Hippocampus Gl

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2878853 2878882 2878907 2878936 2878959 2878971 2878994 2496471

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Subacute and chronic recurrent inflammation of the mucous membranes of the paranasal sinuses.

289

Hirnstamm Gl

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Active ingredient: truncus cerebri bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

H

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: truncus cerebri bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3356909 3356915 3356921 3356938 3356944 3356950 3356967 2496488

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Hirudo comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aesculus hippocastanum e semine ferm 34c dil. D3 0.1 g (HAB, Method 34c) hamamelis virginiana e cortice ferm 33e dil. D3 0.1 g (HAB, Method 33e) hirudo medicinalis ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) mercurius vivus dil. D14 aquos. 0.1 g paeonia officinalis e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) pulsatilla vulgaris e floribus ferm 33c dil. D3 0.1 g (HAB, Method 33c)

290

N1 N2

PZN 1751576 2085928

Price Group 11 12

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Hirudo comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aesculus hippocastanum e semine ferm 34c dil. D2 0.1 g (HAB, Method 34c) hamamelis virginiana e cortice ferm 33e dil. D2 0.1 g (HAB, Method 33e) hirudo medicinalis ex animale toto Gl dil. D5 0.1 g (HAB, Method 41c) mercurius vivus dil. D14 aquos. 0.1 g paeonia officinalis e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) pulsatilla vulgaris e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in the venous system, e.g. haemorrhoids, varicose symptom complex, inflammation of venous blood vessels with thrombus formation (thrombophlebitis).

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in the venous system, e.g. haemorrhoids, conditions involving varicose veins (varicose symptom complex), venous inflammation with thrombotic occlusion (thrombophlebitis).

Hirudo ex animale Gl

Contraindications None known.

D5

N1

PZN 8786106

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Hirudo comp. Dosage and method of administration Unless otherwise directed, 10-15 globuli velati sublingually twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: hirudo medicinalis ex animale toto Gl Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml

N1

PZN 4618955

Price Group 61

Status Pharmacy only

291

H

Composition Liquid dilution for injection: 1 ml contains: hirudo medicinalis ex animale toto Gl dil. D5 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this

Hornerz/Cartilago comp. Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cartilago articularis bovis Gl dil. D11 0.1 g (HAB, Method 41b) horn silver dil. D5 0.1 g (HAB, Method 6) viscum album (mali) e planta tota ferm 34i dil. D4 0.1 g (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. As additional (adjuvant) therapy in the treatment of spinal disorders with Disci preparations (WALA); degenerative changes of the bone and cartilage (osteochondrosis), degenerative joint disorders (osteoarthritis). Contraindications The medicinal product must not be used • in the case of known allergy to mistletoe formulations • in the case of hypersensitivity to milk protein.

N1

PZN 1751582

Price Group 11

Pharmacy only

Eye drops

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.



Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Potency/Strength Package Size Size Category

292

Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

N1

PZN 8786112

Price Group A

H

Hornerz Corpus vitreum comp. Augentropfen

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week.

Globuli velati

20 g

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Status

Hornerz/Cartilago comp.



Indications according to the anthroposophical understanding of human beings and nature. As additional (adjuvant) therapy in the treatment of spinal disorders with Disci preparations (WALA); degenerative changes of the bone and cartilage (osteochondrosis), degenerative joint disorders (osteoarthritis).

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Hornerz/Cartilago comp.

Contraindications None known.

Liquid dilution for injection

H

Composition Globuli velati: 10 g contain: cartilago articularis bovis Gl dil. D11 0.1 g (HAB, Method 41b) horn silver dil. D5 0.1 g (HAB, Method 6) viscum album (mali) e planta tota ferm 34i dil. D2 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose.

Status

Potency/Strength Package Size Size Category 5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: corpus vitreum bovis Gl dil. D7 0.05 g (HAB, Method 41b) lens cristallina bovis Gl dil. D11 0.05 g (HAB, Method 41b) rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g horn silver dil. D5 0.05 g (HAB, Method 6) viscum album (mali) e planta tota ferm 34i dil. D5 0.05 g (HAB, Method 34i) Excipients: sodium chloride, sodium hydrogen carbonate and water for injections.

N1 N2

PZN 1448205 1448197

Price Group C C1

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac once to twice daily. Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known. Note: Without preservatives.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation in degenerative and ageing-related eye diseases, e.g. cataracts, vitreous clouding, poor vision.

Pharmacy only

293

Hornerz/Corpus vitreum comp.

Hyoscyamus ex herba

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: corpus vitreum bovis Gl dil. D7 0.1 g (HAB, Method 41b) lens cristallina bovis Gl dil. D11 0.1 g (HAB, Method 41b) horn silver dil. D5 0.1 g (HAB, Method 6) viscum album (mali) e planta tota ferm 34i dil. D5 0.1 g (HAB, Method 34i)

H

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation in degenerative and ageing-related eye diseases, e.g. cataracts, vitreous clouding, poor vision. Contraindications The medicinal product must not be used • in the case of known allergy to mistletoe formulations • in the case of hypersensitivity to milk protein.

N1

Active ingredient: hyoscyamus niger ex herba ferm 33d Liquid dilution for injection PZN 1751599

Price Group 11

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In very rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Hornerz/Corpus vitreum comp.

Potency/Strength Package Size Size Category D4 D6 D10 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hyoscyamus niger ex herba ferm 33d dil. D.. 1 ml (HAB, Method 33d) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1

PZN 2879189 2884664 2879203 2884701

Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Side-effects None known.

H

Hyoscyamus ex herba

Active ingredient: hyoscyamus niger ex herba ferm 33d Globuli velati Potency/Strength Package Size Size Category D3 D6 D10 D30

20 g 20 g 20 g 20 g

N1 N1 N1 N1

PZN 8786141 8786164 8786170 8786187

Price Group A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: corpus vitreum bovis Gl dil. D7 0.1 g (HAB, Method 41b) lens cristallina bovis Gl dil. D11 0.1 g (HAB, Method 41b) horn silver dil. D5 0.1 g (HAB, Method 6) viscum album (mali) e planta tota ferm 34i dil. D2 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation in degenerative and ageing-related eye diseases, e.g. cataracts, vitreous clouding, poor vision.

294

N1

PZN 8786129

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Hornerz/Corpus vitreum comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Composition Globuli velati: 10 g contain: hyoscyamus niger ex herba ferm 33d dil. D.. 1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Hyoscyamus ex herba. Dosage and method of administration Unless otherwise directed, D3, D6: infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually

1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. D10: infants 3 globuli velati sublingually once to twice daily, children up to 6 years 3-7 globuli velati sublingually once to twice daily, adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily. D30: infants 3 globuli velati sublingually once daily, children up to 6 years 3-7 globuli velati sublingually once daily, adults and children of 6 years and above 5-10 globuli velati sublingually once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

295

Hypericum ex herba

Hypericum ex herba 5%, Oleum

Active ingredient: hypericum perforatum ex herba ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hypericum perforatum ex herba ferm 33c dil. D.. 1 ml (HAB, Method 33c)

H

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1

PZN 2879278 2879290 2879350 2879404

Active ingredient: oily extract of hypericum perforatum, herba rec. Oily embrocation Price Group 31 31 31 31

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only Pharmacy only



Contraindications Hypericum ex herba should not be used in patients with known hypersensitivity to St. John's wort. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Active ingredient: hypericum perforatum ex herba ferm 33c Globuli velati

D2 D3 D6

20 g 20 g 20 g

Composition 10 g globuli velati contain: hypericum perforatum ex herba ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Hypericum ex herba should not be used in patients with known hypersensitivity to St. John‘s wort. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Hypericum ex herba.

296

N1 N1 N1

PZN 8786193 8786201 8786218

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Composition 10 g (11 ml) contain: oily extract of hypericum perforatum, herba rec. (4:1), extraction agent: refined arachis oil 2.0 g Excipient: refined arachis oil. Indications according to the anthroposophical understanding of human beings and nature. Back pain, radicular syndromes, muscular rheumatism. Contraindications None known.

Hypericum ex herba

Potency/Strength Package Size Size Category

50 ml 100 ml

Warnings and precautions for use In children between 6 and 12 years medical advice should be sought before using Hypericum ex herba 5%, Oleum, and it should not be used in place of any other treatment prescribed by the doctor. There is no adequately documented experience of the use

N1 N1

PZN 1753635 1753730

Price Group L L1

Status Pharmacy only Pharmacy only

of Hypericum ex herba 5% in children. It should therefore not be used in children under 6 years. In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, depending on the part of the body treated rub in 2 to 3 ml oil once to twice daily. Duration of treatment The disorder should have cleared up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Photosensitisation or redness of the skin may rarely occur; in such cases use of the medicinal product should be discontinued.

Hypophysis Gl

Active ingredient: hypophysis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hypophysis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3356996 2829493 3357004 2831159 3357010 2831277 2831449 0848049 2496494

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the functional constitution in the case of disturbances of growth and maturation and in states of exhaustion.

297

H

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use The medicinal product should not be used in children under 12 years without the advice of a doctor and should not be used in place of any other treatment prescribed by the doctor.

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously once a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously once a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously once a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Hypophysis/Stannum. Dosage and method of administration Unless otherwise directed, infants and children under 6 years 3-5 globuli velati sublingually once daily; adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily.

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Side-effects None known.

Hypothalamus Gl

Active ingredient: hypothalamus bovis GI Liquid dilution for injection

Hypophysis/Stannum Liquid dilution for injection

H

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hypophysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) stannum metallicum dil. D14 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the functional constitution in weakness of organ formation and developmental disorders. Contraindications None known.

N1 N2

PZN 1751607 2085957

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects None known.

Globuli velati

Composition Globuli velati: 10 g contain: hypophysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) stannum metallicum dil. D14 aquos. 0.1 g Contains sucrose (saccharose/sugar).

298

20 g

N1

PZN 8786224

D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: hypothalamus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Hypophysis/Stannum Potency/Strength Package Size Size Category

Potency/Strength Package Size Size Category

Price Group A

Status Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3357027 2830154 3357033 3356401 3356418 3356424 3356447 0848078 0846530 2496502

Price Group 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the functional constitution in weakness of organ formation and developmental disorders. Contraindications None known.

299

H

Ignatia comp.

Ignatia e semine

Liquid dilution for injection

Active ingredient: strychnos ignatii e semine ferm 35b Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: kalanchoe daigremontiana/pinnata e foliis ferm 33b dil. D2 0.1 g (HAB, Method 33b) lachesis dil. D11 aquos. 0.1 g (HAB, Method 5b) strychnos ignatii e semine ferm 35b dil. D3 0.1 g (HAB, Method 35b)

I

Indications according to the anthroposophical understanding of human beings and nature. Menopausal symptoms, particularly of a psychological nature, hysteriform syndromes and dysphoric mood states.

N1 N2

PZN 1751613 2085963

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case the patient should see a doctor. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category D30

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: strychnos ignatii e semine ferm 35b dil. D30 1 ml (HAB, Method 35b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: kalanchoe daigremontiana/pinnata e foliis ferm 33b dil. D2 0.1 g (HAB, Method 33b) lachesis dil. D11 aquos. 0.1 g (HAB, Method 5b) strychnos ignatii e semine ferm 35b dil. D3 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Menopausal symptoms, particularly of a psychological nature, hysteriform syndromes and dysphoric mood states. Contraindications None known.

300

N1

PZN 8786230

Price Group A

Status Pharmacy only

Warnings and precautions for use There is no adequately documented experience of use of Ignatia comp. in children. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Ignatia comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor.

31

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Side-effects None known.

Ignatia e semine

Active ingredient: strychnos ignatii e semine ferm 35b Globuli velati

D4 D12 D30

Globuli velati

Price Group

Contraindications None known.

Potency/Strength Package Size Size Category

Ignatia comp.

PZN 2884747

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: strychnos ignatii e semine ferm 35b dil. D.. 1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Ignatia e semine.

N1 N1 N1

PZN 8786247 8786253 8786276

Price Group A A A

I

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Side-effects None known.

301

Ileum Gl

Composition Liquid dilution for injection: 1 ml contains: iris bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Active ingredient: ileum suis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ileum suis Gl dil. D.. 1 ml (HAB, Method 41c)

I

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN

Price Group

2879775 2879798 2879812 2879835 2879858 2879870 2879893 2496519

61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Iris bovis comp., Einzeldosis-Augentropfen see Iris Lens comp. Augentropfen

Iris (bovis) Gl

Active ingredient: iris bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

302

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2879982 2880005 2880028 2880063 2880092 2880117 2490882

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Iris Lens comp. Augentropfen Eye drops

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: iris bovis Gl dil. D6 0.05 g (HAB, Method 41b) lens cristallina bovis Gl dil. D5 0.05 g (HAB, Method 41b) nervus oculomotorius bovis Gl dil. D5 0.05 g (HAB, Method 41a) nervus ophthalmicus bovis Gl dil. D5 0.05 g (HAB, Method 41a) rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g Excipients: sodium chloride, sodium hydrogen carbonate and water for injections. Indications according to the anthroposophical understanding of human beings and nature. Inflammatory and degenerative

N1 N2

PZN 2650162 2650179

Price Group C C1

Status Pharmacy only Pharmacy only

processes of the eye, weakness of the muscular parts of the eye. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac once to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

303

I

Iscucin®

The Iscucin® preparations are prepared from summer- and winter-harvested mistletoe plants (viscum album) without application of heat. The whole plant is used, i.e. haustoria (with the exception of Iscucin® Quercus, which contains no haustoria component), stems, leaves and ripe (winter) or immature fruits (summer). The formulations are potentised in a dilution ratio of 1 to 20. The individual potency is designated strength (HAB, Method 38). Strength

Dilution

Mother tincture/strength/dilution used for potentising (1:20)

H

1st

Mother tincture

G

2nd

H

F

3rd

G

E

4th

F

D

5th

E

C

6th

D

From strength C onwards the 7th and 9th dilutions are not kept in stock but potentised again in a ratio of 1:20:

I

B

8th

7th dilution

A

10th

9th dilution

The mistletoe plants from the following host trees are used: apple tree (Iscucin® Mali), oak (Iscucin® Quercus), pine (Iscucin® Pini), lime tree (Iscucin® Tiliae), poplar (Iscucin® Populi), fir (Iscucin® Abietis), willow (Iscucin® Salicis), hawthorn (Iscucin® Crataegi).

Iscucin® Abietis Stärke A, B, C, D, E, F, G, H Active ingredient: viscum album (abietis) e planta tota K Liquid dilution for injection Potency/Strength Package Size Size Category A 10 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml G 10 x 1 ml H 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 4428686 4428700 4428723 4428752 4428775 4428798 4428812 4428835 4428858 4428864

Price Group 71 71 71 71 71 71 71 71 71 71

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only



Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 3 ampoules of strength D, 3 ampoules of strength E, 2 ampoules of strength F, 2 ampoules of strength G

304

Composition Liquid dilution for injection: 1 ml contains: viscum album (abietis) e planta tota K dil. strength .. 1 ml (HAB, Method 38) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of formative and integrating forces for disintegration and reintegration of growth processes that have become autonomous, e.g.: • malignant and benign tumours • defined precancers • relapse prevention after tumour operations • chronic-inflammatory, boundary-crossing disorders, e.g. Crohn‘s disease, chronic joint disorders Contraindications Iscucin® Abietis must not be used in the case of: • known allergy to mistletoe preparations: The treatment can only be continued after successful desensitisation. • acute inflammatory or highly febrile diseases (body temperature over 38°C): The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism. Warnings and precautions for use • Primary tumours of the brain or spinal cord or intracranial metastases with danger of elevation of intracranial pressure: In these cases the preparations should only be used after carefully weighing up the benefits and risks and with close clinical monitoring. • No effects have been reported to date which indicate that Iscucin® Abietis should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Abietis should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks. • As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Preclinical and clinical studies on the use of mistletoe preparations in malignant lymphomas and leukaemia have shown no evidence of tumour enhancement. In view of the debate on the theoretical possibility of tumour enhancement and the lack of relevant data, the

medicinal product should only be used in these diseases after carefully weighing up the potential benefits and risks, with careful monitoring of the course of the disease and by doctors experienced in this field. • In patients with autoimmune diseases particularly cautious dosing and careful monitoring is required on account of the possibility of stimulation of inflammatory processes. • The ampoule should be briefly warmed in the hand as the formation of cold agglutinins has been described after injection of mistletoe injection solutions which were not at body temperature. Dosage and method of administration For subcutaneous injection. The dosage should always be determined individually as directed by the doctor. See also Patient Information Leaflet or WALA Iscucin® Compendium. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the event of fever of more than 38°C, fatigue, shivering, general malaise, headaches, brief attacks of dizziness or larger local reactions with a diameter of more than 5 cm, the next injection should only be given after these symptoms have subsided and in a reduced concentration and/or dose. The fever caused by Iscucin® injection should not be suppressed by antipyretic medicinal products. If there is fever persisting longer than three days the possibility of an infectious process or tumour fever should be considered. Excessive local reactions can be reduced by diluting the contents of the ampoule with physiological saline. In rare cases, local or systemic allergic or allergoid reactions such as generalised itching, hives (urticaria), skin rash, blistering, swelling of the skin and mucous membranes in the region of the face (Quincke's oedema), shaking chills, difficulty breathing, involuntary contraction of the airways (bronchospasm) or shock may occur, in which case treatment with the preparation must be discontinued and medical assistance sought immediately. In rare cases activation of inflammation may occur.

305

I

Iscucin® Crataegi Stärke A, B, C, D, E, F, G, H

Iscucin® Mali Stärke A, B, C, D, E, F, G, H

Active ingredient: viscum album (crataegi) e planta tota K Liquid dilution for injection Potency/Strength Package Size Size Category A 10 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml G 10 x 1 ml H 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml

I

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3083274 3083280 3083297 3083305 3083311 3083328 3083334 3083340 3083357 3083363

Price Group 71 71 71 71 71 71 71 71 71 71

Active ingredient: viscum album (mali) e planta tota K Liquid dilution for injection Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

A 10 x 1 ml A 50 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml G 10 x 1 ml H 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml



Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 3 ampoules of strength D, 3 ampoules of strength E, 2 ampoules of strength F, 2 ampoules of strength G

Composition Liquid dilution for injection: 1 ml contains: viscum album (crataegi) e planta tota K dil. strength .. 1 ml (HAB, Method 38) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Iscucin® Crataegi must not be used in the case of: • known allergy to mistletoe preparations. • acute inflammatory or highly febrile conditions: The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism. Warnings and precautions for use • No effects have been reported to date which indicate that Iscucin® Crataegi should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Crataegi should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks. • As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Attention should be paid to careful dose escalation. If the dose escalation is too fast, particularly if a dilution is omitted in the lower potencies (e.g. jumping from strength C to E) allergic reactions may occur.

306

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. To avoid hypersensitivity reactions gradual dose titration is necessary. Treatment should be started with strength A. During careful dose escalation up to once-daily administration and progression to the next higher strength the local inflammatory reaction at the injection site should each time not exceed a diameter of 5 cm. If a dilution is omitted in the lower potencies (e.g. in the case of a jump from strength C to E) allergic reactions requiring emergency intervention may occur. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the case of intolerance of mistletoe, local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling in the region of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock can occur, in which case treatment with the preparation must be discontinued and immediate medical assistance sought. There are no data on the frequency of such reactions.

N1 N2 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 4428870 4428887 4428893 4428918 4428930 4428953 4428982 4429007 4429036 4429059 4429065

Price Group 71 72 71 71 71 71 71 71 71 71 71

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only



Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 3 ampoules of strength D, 3 ampoules of strength E, 2 ampoules of strength F, 2 ampoules of strength G

Composition Liquid dilution for injection: 1 ml contains: viscum album (mali) e planta tota K dil. strength .. 1 ml (HAB, Method 38) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of formative and integrating forces for disintegration and reintegration of growth processes that have become autonomous, e.g.: • malignant and benign tumours • defined precancers • relapse prevention after tumour operations • chronic-inflammatory, boundary-crossing disorders, e.g. Crohn‘s disease, chronic joint disorders Contraindications Iscucin® Mali must not be used in the case of: • known allergy to mistletoe preparations: The treatment can only be continued after successful desensitisation. • acute inflammatory or highly febrile diseases (body temperature over 38°C): The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism. Warnings and precautions for use • Primary tumours of the brain or spinal cord or intracranial metastases with danger of elevation of intracranial pressure: In these cases the preparations should only be used after carefully weighing up the benefits and risks and with close clinical monitoring.

• No effects have been reported to date which indicate that Iscucin® Mali should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Mali should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks. • As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Preclinical and clinical studies on the use of mistletoe preparations in malignant lymphomas and leukaemia have shown no evidence of tumour enhancement. In view of the debate on the theoretical possibility of tumour enhancement and the lack of relevant data, the medicinal product should only be used in these diseases after carefully weighing up the potential benefits and risks, with careful monitoring of the course of the disease and by doctors experienced in this field. • In patients with autoimmune diseases particularly cautious dosing and careful monitoring is required on account of the possibility of stimulation of inflammatory processes. • The ampoule should be briefly warmed in the hand as the formation of cold agglutinins has been described after injection of mistletoe injection solutions which were not at body temperature.

307

I

Dosage and method of administration For subcutaneous injection. The dosage should always be determined individually as directed by the doctor. See also Patient Information Leaflet or WALA Iscucin® Compendium. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the event of fever of more than 38°C, fatigue, shivering, general malaise, headaches, brief attacks of dizziness or larger local reactions with a diameter of more than 5 cm, the next injection should only be given after these symptoms have subsided and in a reduced concentration and/or dose.

The fever caused by Iscucin® injection should not be suppressed by antipyretic medicinal products. If there is fever persisting longer than three days the possibility of an infectious process or tumour fever should be considered. Excessive local reactions can be reduced by diluting the contents of the ampoule with physiological saline. In rare cases, local or systemic allergic or allergoid reactions such as generalised itching, hives (urticaria), skin rash, blistering, swelling of the skin and mucous membranes in the region of the face (Quincke‘s oedema), shaking chills, difficulty breathing, involuntary contraction of the airways (bronchospasm) or shock may occur, in which case treatment with the preparation must be discontinued and medical assistance sought immediately. In rare cases activation of inflammation may occur.

Iscucin® Pini Stärke A, B, C, D, E, F, G, H Active ingredient: viscum album (pini) e planta tota K Liquid dilution for injection

I

Potency/Strength Package Size Size Category A 10 x 1 ml A 50 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml G 10 x 1 ml H 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml

N1 N2 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 4429071 4429088 4429094 4429119 4429131 4429154 4429177 4429208 4429220 4429243 4429266

Price Group 71 72 71 71 71 71 71 71 71 71 71

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only



Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 3 ampoules of strength D, 3 ampoules of strength E, 2 ampoules of strength F, 2 ampoules of strength G

308

Composition Liquid dilution for injection: 1 ml contains: viscum album (pini) e planta tota K dil. strength .. 1 ml (HAB, Method 38) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of formative and integrating forces for disintegration and reintegration of growth processes that have become autonomous, e.g.: • malignant and benign tumours • defined precancers • relapse prevention after tumour operations • chronic-inflammatory, boundary-crossing disorders, e.g. Crohn‘s disease, chronic joint disorders Contraindications Iscucin® Pini must not be used in the case of: • known allergy to mistletoe preparations: The treatment can only be continued after successful desensitisation. • acute inflammatory or highly febrile diseases (body temperature over 38°C): The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism. Warnings and precautions for use • Primary tumours of the brain or spinal cord or intracranial metastases with danger of elevation of intracranial pressure: In these cases the preparations should only be used after carefully weighing up the benefits and risks and with close clinical monitoring. • No effects have been reported to date which indicate that Iscucin® Pini should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Pini should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks. • As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Preclinical and clinical studies on the use of mistletoe preparations in malignant lymphomas and leukaemia have shown no evidence of tumour enhancement. In view of the debate on the theoretical possibility of tumour enhancement and the lack of relevant data, the

medicinal product should only be used in these diseases after carefully weighing up the potential benefits and risks, with careful monitoring of the course of the disease and by doctors experienced in this field. • In patients with autoimmune diseases particularly cautious dosing and careful monitoring is required on account of the possibility of stimulation of inflammatory processes. • The ampoule should be briefly warmed in the hand as the formation of cold agglutinins has been described after injection of mistletoe injection solutions which were not at body temperature. Dosage and method of administration For subcutaneous injection. The dosage should always be determined individually as directed by the doctor. See also Patient Information Leaflet or WALA Iscucin® Compendium. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the event of fever of more than 38 °C, fatigue, shivering, general malaise, headaches, brief attacks of dizziness or larger local reactions with a diameter of more than 5 cm, the next injection should only be given after these symptoms have subsided and in a reduced concentration and/or dose. The fever caused by Iscucin® injection should not be suppressed by antipyretic medicinal products. If there is fever persisting longer than three days the possibility of an infectious process or tumour fever should be considered. Excessive local reactions can be reduced by diluting the contents of the ampoule with physiological saline. In rare cases, local or systemic allergic or allergoid reactions such as generalised itching, hives (urticaria), skin rash, blistering, swelling of the skin and mucous membranes in the region of the face (Quincke‘s oedema), shaking chills, difficulty breathing, involuntary contraction of the airways (bronchospasm) or shock may occur, in which case treatment with the preparation must be discontinued and medical assistance sought immediately. In rare cases activation of inflammation may occur.

309

I

Iscucin® Populi Stärke A, B, C, D, E, F, G, H

Status

Dosage and method of administration For subcutaneous injection. The dosage should always be determined individually as directed by the doctor. See also Patient Information Leaflet or WALA Iscucin® Compendium.

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the event of fever of more than 38°C, fatigue, shivering, general malaise, headaches, brief attacks of dizziness or larger local reactions with a diameter of more than 5 cm, the next injection should only be given after these symptoms have subsided and in a reduced concentration and/or dose.

Active ingredient: viscum album (populi) e planta tota K Liquid dilution for injection Potency/Strength Package Size Size Category A 10 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml G 10 x 1 ml H 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml

I

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 4429272 4429295 4429326 4429349 4429361 4429384 4429409 4429421 4429444 4429450

Price Group 71 71 71 71 71 71 71 71 71 71



Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 3 ampoules of strength D, 3 ampoules of strength E, 2 ampoules of strength F, 2 ampoules of strength G

Composition Liquid dilution for injection: 1 ml contains: viscum album (populi) e planta tota K dil. strength .. 1 ml (HAB, Method 38) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of formative and integrating forces for disintegration and reintegration of growth processes that have become autonomous, e.g.: • malignant and benign tumours • defined precancers • relapse prevention after tumour operations • chronic-inflammatory, boundary-crossing disorders, e.g. Crohn‘s disease, chronic joint disorders Contraindications Iscucin® Populi must not be used in the case of: • known allergy to mistletoe preparations: The treatment can only be continued after successful desensitisation. • acute inflammatory or highly febrile diseases (body temperature over 38°C): The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism. Warnings and precautions for use • Primary tumours of the brain or spinal cord or intracranial metastases with danger of elevation of intracranial pressure: In these cases the preparations should only be used after carefully weighing up the benefits and risks and with close clinical monitoring.

310

• No effects have been reported to date which indicate that Iscucin® Populi should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Populi should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks. • As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Preclinical and clinical studies on the use of mistletoe preparations in malignant lymphomas and leukaemia have shown no evidence of tumour enhancement. In view of the debate on the theoretical possibility of tumour enhancement and the lack of relevant data, the medicinal product should only be used in these diseases after carefully weighing up the potential benefits and risks, with careful monitoring of the course of the disease and by doctors experienced in this field. • In patients with autoimmune diseases particularly cautious dosing and careful monitoring is required on account of the possibility of stimulation of inflammatory processes. • The ampoule should be briefly warmed in the hand as the formation of cold agglutinins has been described after injection of mistletoe injection solutions which were not at body temperature.

The fever caused by Iscucin® injection should not be suppressed by antipyretic medicinal products. If there is fever persisting longer than three days the possibility of an infectious process or tumour fever should be considered. Excessive local reactions can be reduced by diluting the contents of the ampoule with physiological saline. In rare cases, local or systemic allergic or allergoid reactions such as generalised itching, hives (urticaria), skin rash, blistering, swelling of the skin and mucous membranes in the region of the face (Quincke‘s oedema), shaking chills, difficulty breathing, involuntary contraction of the airways (bronchospasm) or shock may occur, in which case treatment with the preparation must be discontinued and medical assistance sought immediately. In rare cases activation of inflammation may occur.

Iscucin® Quercus Stärke A, B, C, D, E, F Active ingredient: viscum album (quercus) ex herba K Liquid dilution for injection Potency/Strength Package Size Size Category A 10 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

I PZN

3083386 3083392 3083400 3083417 3083423 3083446 3083475 3083481

Price Group 71 71 71 71 71 71 71 71

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only



Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 4 ampoules of strength D, 3 ampoules of strength E, 3 ampoules of strength F

Composition Liquid dilution for injection: 1 ml contains: viscum album (quercus) ex herba K dil. strength.. 1 ml (HAB, Method 38)

• acute inflammatory or highly febrile diseases (body temperature over 38°C): The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use • No effects have been reported to date which indicate that Iscucin® Quercus should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Quercus should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks.

Contraindications Iscucin® Quercus must not be used in the case of: • known allergy to mistletoe preparations.

311

• As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Attention should be paid to careful dose escalation. If the dose escalation is too fast, particularly if a dilution is omitted in the lower potencies (e.g. jumping from strength C to E) allergic reactions may occur. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. To avoid hypersensitivity reactions gradual dose titration is necessary. Treatment should be started with strength A. During careful dose escalation up to once-daily administration and progression to the next higher strength the local inflammatory reaction at the injection site should each time not exceed a diameter of 5 cm. If a dilution is omitted in the lower potencies (e.g. in the case of a jump from strength C to E) allergic reactions requiring emergency intervention may occur.

Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the case of intolerance of mistletoe, local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling in the region of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock can occur, in which case treatment with the preparation must be discontinued and immediate medical assistance sought. There are no data on the frequency of such reactions.

I

Contraindications Iscucin® Salicis must not be used in the case of: • known allergy to mistletoe preparations. • acute inflammatory or highly febrile conditions: The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism. Warnings and precautions for use • No effects have been reported to date which indicate that Iscucin® Salicis should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Salicis should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks. • As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Attention should be paid to careful dose escalation. If the dose escalation is too fast, particularly if a dilution is omitted in the lower potencies (e.g. jumping from strength C to E) allergic reactions may occur.

Iscucin® Salicis Stärke A, B, C, D, E, F, G, H Active ingredient: viscum album (salicis) e planta tota K Liquid dilution for injection Potency/Strength Package Size Size Category A 10 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml G 10 x 1 ml H 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3083498 3083506 3083512 3083529 3083535 3083541 3083558 3083564 3083570 3083587

Price Group 71 71 71 71 71 71 71 71 71 71

Iscucin® Tiliae Stärke A, B, C, D, E, F, G, H

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 3 ampoules of strength D, 3 ampoules of strength E, 2 ampoules of strength F, 2 ampoules of strength G

312

Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the case of intolerance of mistletoe, local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling in the region of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock can occur, in which case treatment with the preparation must be discontinued and immediate medical assistance sought. There are no data on the frequency of such reactions.

Status



Composition Liquid dilution for injection: 1 ml contains: viscum album (salicis) e planta tota K dil. strength .. 1 ml (HAB, Method 38)

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. To avoid hypersensitivity reactions gradual dose titration is necessary. Treatment should be started with strength A. During careful dose escalation up to once-daily administration and progression to the next higher strength the local inflammatory reaction at the injection site should each time not exceed a diameter of 5 cm. If a dilution is omitted in the lower potencies (e.g. in the case of a jump from strength C to E) allergic reactions requiring emergency intervention may occur.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: viscum album (tiliae) e planta tota K Liquid dilution for injection Potency/Strength Package Size Size Category A 10 x 1 ml B 10 x 1 ml C 10 x 1 ml D 10 x 1 ml E 10 x 1 ml F 10 x 1 ml G 10 x 1 ml H 10 x 1 ml Potency series I 10 x 1 ml Potency series II 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 4429467 4429496 4429510 4429533 4429562 4429585 4429616 4429639 4429651 4429668

Price Group 71 71 71 71 71 71 71 71 71 71

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only



Potency series I (pack of 10 assorted ampoules): 3 ampoules of strength A, 3 ampoules of strength B, 3 ampoules of strength C, 1 ampoule of strength D



Potency series II (pack of 10 assorted ampoules): 3 ampoules of strength D, 3 ampoules of strength E, 2 ampoules of strength F, 2 ampoules of strength G

313

I

Composition Liquid dilution for injection: 1 ml contains: viscum album (tiliae) e planta tota K dil. strength .. 1 ml (HAB, Method 38) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of formative and integrating forces for disintegration and reintegration of growth processes that have become autonomous, e.g.: • malignant and benign tumours • defined precancers • relapse prevention after tumour operations • chronic-inflammatory, boundary-crossing disorders, e.g. Crohn‘s disease, chronic joint disorders

I

Contraindications Iscucin® Tiliae must not be used in the case of: • known allergy to mistletoe preparations: The treatment can only be continued after successful desensitisation. • acute inflammatory or highly febrile diseases (body temperature over 38°C): The treatment should be interrupted until the signs of inflammation have subsided. • uncontrolled hyperthyroidism. Warnings and precautions for use • Primary tumours of the brain or spinal cord or intracranial metastases with danger of elevation of intracranial pressure: In these cases the preparations should only be used after carefully weighing up the benefits and risks and with close clinical monitoring. • No effects have been reported to date which indicate that Iscucin® Tiliae should not be used during pregnancy or breastfeeding. However, as a particular precaution, Iscucin® Tiliae should only be used during pregnancy and breastfeeding after carefully weighing up the potential benefits and risks. • As there are insufficient data available on use in children under 12 years of age, children of this age should only be treated by doctors with relevant experience in this area. • Preclinical and clinical studies on the use of mistletoe preparations in malignant lymphomas and leukaemia have shown no evidence of tumour enhancement. In view of the debate on the theoretical possibility of tumour enhancement and the lack of relevant data, the

314

medicinal product should only be used in these diseases after carefully weighing up the potential benefits and risks, with careful monitoring of the course of the disease and by doctors experienced in this field. • In patients with autoimmune diseases particularly cautious dosing and careful monitoring is required on account of the possibility of stimulation of inflammatory processes. • The ampoule should be briefly warmed in the hand as the formation of cold agglutinins has been described after injection of mistletoe injection solutions which were not at body temperature. Dosage and method of administration For subcutaneous injection. The dosage should always be determined individually as directed by the doctor. See also Patient Information Leaflet or WALA Iscucin® Compendium. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the event of fever of more than 38°C, fatigue, shivering, general malaise, headaches, brief attacks of dizziness or larger local reactions with a diameter of more than 5 cm, the next injection should only be given after these symptoms have subsided and in a reduced concentration and/or dose. The fever caused by Iscucin® injection should not be suppressed by antipyretic medicinal products. If there is fever persisting longer than three days the possibility of an infectious process or tumour fever should be considered. Excessive local reactions can be reduced by diluting the contents of the ampoule with physiological saline. In rare cases, local or systemic allergic or allergoid reactions such as generalised itching, hives (urticaria), skin rash, blistering, swelling of the skin and mucous membranes in the region of the face (Quincke‘s oedema), shaking chills, difficulty breathing, involuntary contraction of the airways (bronchospasm) or shock may occur, in which case treatment with the preparation must be discontinued and medical assistance sought immediately. In rare cases activation of inflammation may occur.

Juglans regia comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: juglans regia e foliis et fructibus ferm 33c dil. D6 0.1 g (HAB, Method 33c) kalium phosphoricum dil. D5 aquos. 0.1 g (HAB, Method 5b) stannum metallicum dil. D11 aquos. 0.1 g

N1

PZN 4387533

Price Group 11

Status Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Juniperus/Berberis comp., Kapseln Soft capsules

Potency/Strength Package Size Size Category

30 capsules 90 capsules

Composition 1 soft capsule contains: acorus calamus e rhizoma ferm 33d Ø 0.0915 mg (HAB, Method 33d) anisi stellati aetheroleum 9.15 mg berberis vulgaris e radice W 10% (HAB, Method 12f with virgin olive oil) 27.45 mg D-camphor 0.0915 mg eucalypti aetheroleum 18.3 mg foeniculi amari fructus aetheroleum 9.15 mg iecoris aselli oleum A 45.75 mg juniperi aetheroleum 9.15 mg lini oleum virginale 457.5 mg

N1 N1

PZN 1948706 2482687

Price Group Q Q1

Status Pharmacy only Pharmacy only

pini pumilionis aetheroleum 9.15 mg ricini oleum virginale 45.75 mg solidago virgaurea ex herba ferm 33c dil. D3 0.0915 mg (HAB, Method 33c) terebinthina laricina 0.0915 mg terebinthinae aetheroleum rectificatum 9.15 mg tritici aestivi oleum raffinatum 183.0 mg Excipients: gelatin, glycerol 85%, cacao butter, virgin olive oil, purified water. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the feeling and warmth organisation in the region of the kidneys in excretory weakness, e.g. kidney stones, gout; wind (flatulence).

315

J

Contraindications Juniperus/Berberis comp., Kapseln must not be used in the case of inflammatory kidney diseases or in the case of known hypersensitivity to formulations of juniper berries (juniperi aetheroleum), golden rod (solidago virgaurea), larch resin (terebinthina laricina), purified essential oil from the turpentine of pine species (terebinthina aetheroleum rectificatum), flax seed, cineole, anise, anethol, fennel or other umbellifers or to any of the excipients of the medicinal product. As the Juniperus/Berberis comp. capsules contain calamus root they should not be used during pregnancy or breastfeeding or in children under 12 years. Interactions with other drugs Eucalyptus oil causes induction of the enzyme system in the liver which breaks down foreign substances (increases the activity of body substances responsible, amongst other

things, for the breakdown of medicinal products). This means that the action of other medicinal products can be weakened and/or shortened.

Kampfer Johanniskrautöl (camphor-St. John‘s wort oil)

Dosage and method of administration Unless otherwise directed, 1 soft capsule 1 to 3 times daily after meals taken with plenty of fluid. Not more than 3 soft capsules should be taken daily.

Potency/Strength Package Size Size Category

Duration of treatment As the medicinal product contains fennel oil Juniperus/ Berberis comp. capsules should not be taken for several weeks without consulting a doctor. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Prolonged use or overdosage can lead to kidney damage.

Oily embrocation



100 ml

PZN 1753724

Price Group L1

Status Pharmacy only

Composition 10 g (11 ml) contain: D-camphor 0.25 g oily extract of hypericum perforatum, herba rec. (4:1), extraction agent: refined arachis oil 1.25 g Excipient: refined arachis oil.

Warnings and precautions for use The medicinal product Kampfer Johanniskrautöl should not be given to children from 2-12 years without first consulting a doctor as there is insufficient experience available to date to permit a general recommendation for this age group. In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis).

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation in rheumatic disorders, degenerative joint disease, nerve pain; nervous angina.

Dosage and method of administration Unless otherwise directed, rub in 2-3 ml of oil 1 to 3 times daily.

Contraindications The medicinal product should not be used by persons with known hypersensitivity to camphor. Do not use on damaged skin, e.g. on burns. Kampfer Johanniskrautöl must not be used in children under 2 years. In small children formulations containing camphor should not be applied in the region of the face, especially the nose. As Kampfer Johanniskrautöl contains camphor it must not be used during pregnancy or breastfeeding.

J

N1

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Photosensitisation or redness of the skin may very rarely occur; in such cases use of the medicinal product should be discontinued. Because of the ingredient camphor the occurrence of contact dermatitis is possible.

Karneol

Active ingredient: carneole aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D15

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: carneole dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

316

N1

PZN 2880324

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

317

K

Keloid-Gel

Lachesis comp.

Kupfer Salbe rot (red copper ointment)

Potency/Strength Package Size Size Category

see Narben Gel

Liquid dilution for injection

Active ingredient: cuprum oxydulatum rubrum Ointment

Potency/Strength Package Size Size Category

30 g 100 g

Composition 10 g contain: cuprum oxydulatum rubrum 0.04 g Excipients: liquid paraffin, white soft paraffin. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation in the case of disturbed integration of the warmth organism in the circulatory and metabolic-musculoskeletal system, e.g. in hypostatic disturbances of the peripheral venous system, spasms and cramps of the gastrointestinal tract, impaired renal function.

K

Contraindications None known.

N1 N2

PZN 2198360 2198377

Price Group J J1

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, rub in the ointment twice a week to once daily or use as ointment dressing. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Allergic reactions can occur in the case of hypersensitivity to ingredients of Kupfer Salbe rot, particularly to copper oxide. If you experience reddening of the skin, with or without itching, you should stop using Kupfer Salbe rot and see your doctor if necessary.

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna ex herba ferm 33a dil. D3 0.1 g (HAB, Method 33a) hepar sulfuris dil. D7 0.1 g lachesis dil. D11 aquos. 0.1 g (HAB, Method 5b) mercurialis perennis ferm 34c dil. D5 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Structuring of the anabolic metabolism in highly febrile, acute inflammatory, also circumscribed purulent processes, e.g. tonsillitis, inflammation of the breast (mastitis), inflammation of the uterine appendages (adnexitis) and other bacterial infections.

N1 N2

PZN 1751642 2085992

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously once to twice daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

L

Lachesis comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: atropa belladonna ex herba ferm 33a dil. D3 0.1 g (HAB, Method 33a) hepar sulfuris dil. D7 0.1 g lachesis dil. D11 aquos. 0.1 g (HAB, Method 5b) mercurialis perennis ferm 34c dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Structuring of the anabolic metabolism in highly febrile, acute inflammatory, also

318

N1

PZN 8786359

Price Group A

Status Pharmacy only

circumscribed purulent processes, e.g. tonsillitis, inflammation of the breast (mastitis), inflammation of the uterine appendages (adnexitis) and other bacterial infections. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children under 6 years is not available. It should therefore not be used in children under 6 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Lachesis comp.

319

Dosage and method of administration Unless otherwise directed, adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 6 times daily.

Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor.

Composition Liquid dilution for injection: 1 ml contains: larynx bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Lachesis e veneno

Active ingredient: lachesis aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1

PZN 3356453 2884799 2831024

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Larynx comp.

Liquid dilution for injection Composition Liquid dilution for injection: 1 ml contains: lachesis dil. D.. aquos. 1 ml (HAB, Method 5b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

L

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this

medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Lamina quadrigemina see Corpora quadrigemina GI

Larynx Gl

Active ingredient: larynx bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

320

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2880689 2880703 2880732 2880755 2880778 2880790 2880815 2496525

Price Group 61 61 61 61 61 61 61 51

Status

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: larynx bovis Gl dil. D5 0.1 g (HAB, Method 41b) levisticum officinale e radice ferm 33c dil. D5 0.1 g (HAB, Method 33c) nervus laryngeus recurrens bovis Gl dil. D5 0.1 g (HAB, Method 41a) nervus laryngeus superior bovis Gl dil. D5 0.1 g (HAB, Method 41a) nervus vagus bovis Gl dil. D5 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the speech organisation, e.g. vocal cord weakness, chronic inflammation of the vocal cords (laryngitis).

N1

PZN 2086000

Price Group 11

Status Pharmacy only

Contraindications Do not use in the case of hypersensitivity to animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

321

L

Larynx comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: larynx bovis Gl dil. D5 0.1 g (HAB, Method 41b) levisticum officinale e radice ferm 33c dil. D5 0.1 g (HAB, Method 33c) nervus laryngeus recurrens bovis Gl dil. D5 0.1 g (HAB, Method 41a) nervus laryngeus superior bovis Gl dil. D5 0.1 g (HAB, Method 41a) nervus vagus bovis Gl dil. D5 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the speech organisation, e.g. vocal cord weakness, chronic inflammation of the vocal cords (laryngitis).

N1

PZN 8786365

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Larynx comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 5 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Contraindications None known.

L

Larynx/Apis comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D16 0.1 g (HAB, Method 41c) bryonia cretica ferm 33b dil. D14 0.1 g larynx bovis Gl dil. D16 0.1 g (HAB, Method 41b) levisticum officinale e radice ferm 33c dil. D14 0.1 g (HAB, Method 33c) nervus laryngeus recurrens bovis Gl dil. D16 0.1 g (HAB, Method 41a) nervus laryngeus superior bovis Gl dil. D16 0.1 g (HAB, Method 41a) nervus vagus bovis Gl dil. D16 0.1 g (HAB, Method 41a)

322

N1 N2

PZN 2086023 2086046

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonious reintegration of the ego and feeling organisation into the fluid processes in the region of the pharynx and larynx, e.g. inflammation of the vocal cords (laryngitis); treatment between episodes of recurrent swelling of the vocal cords (laryngeal oedema).

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted; In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for

several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate.

Larynx/Apis comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D16 0.1 g (HAB, Method 41c) bryonia cretica ferm 33b dil. D14 0.1 g larynx bovis Gl dil. D16 0.1 g (HAB, Method 41b) levisticum officinale e radice ferm 33c dil. D14 0.1 g (HAB, Method 33c) nervus laryngeus recurrens bovis Gl dil. D16 0.1 g (HAB, Method 41a) nervus laryngeus superior bovis Gl dil. D16 0.1 g (HAB, Method 41a) nervus vagus bovis Gl dil. D16 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonious reintegration of the ego and feeling organisation into the fluid processes in the region of the pharynx and larynx, e.g. inflammation

N1

PZN 8786371

Price Group A

Status Pharmacy only

of the vocal cords (laryngitis); treatment between episodes of recurrent swelling of the vocal cords (laryngeal oedema). Contraindications The medicinal product should not be used in the case of known hypersensitivity to bee venom. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Larynx/Apis comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually up to twice daily, adults and children of 6 years and above 5-10 globuli velati sublingually up to twice daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Contraindications Do not use in the case of known hypersensitivity to bee venom. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once to twice daily.

323

L

Lavandula, Oleum aethereum 10% Active ingredient: lavandulae aetheroleum 10% Bath additive, liquid

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: lavandulae aetheroleum 10% (HAB, Method 12h with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Vegetative balance problems with nervous restlessness, difficulty falling asleep, muscular tension and cramps; functional cardiovascular disorders, wind (flatulence), period problems (menstrual disorders), nerve pain (neuralgia); degenerative nerve disorders. Contraindications The medicinal product should not be used in the case of eczema unless expressly ordered by the doctor.

L

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children with degenerative nerve disorders and neuralgia is not available. It should therefore not be used for treatment of these disorders in children under 12 years.

PZN

Price Group

2088507

N1

Status General sale

Dosage and method of administration Unless otherwise directed, use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths 2 to 3 times a week. The temperature of the bath water should be between 35° and 37°, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about 2 to 3 times a week over a period of 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects None known.

Lens cristallina Gl

Active ingredient: lens cristallina bovis GI Liquid dilution for injection

D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: lens cristallina bovis Gl dil. D.. 1 ml (HAB, Method 41b)

324

N1 N1 N1 N1 N1 N1 N1

PZN 2880927 2880956 2880979 2881022 2881045 2881068 2490899

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Lens cristallina/Viscum comp. cum Stanno see Lens Viscum comp. Augentropfen see Lens Viscum comp. Inject see Lens Viscum comp. Globuli velati

Lens Viscum comp. Augentropfen Eye drops

Potency/Strength Package Size Size Category

Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Potency/Strength Package Size Size Category

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only



5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: equisetum arvense ex herba ferm 35b dil. D14 0.05 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.05 g (HAB, Method 41c) lens cristallina bovis Gl dil. D7 0.05 g (HAB, Method 41b) phyllostachys e nodo ferm 35c dil. D5 0.05 g (HAB, Method 35c) stannum metallicum dil. D9 0.05 g viscum album (mali) e planta tota ferm 34i dil. D5 0.05 g (HAB, Method 34i) Excipients: sodium chloride, sodium hydrogen cabonate and water for injections.

N1 N2

PZN 1448263 1448240

Price Group C C1

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Vitreous clouding, cataracts. Contraindications None known. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known. Note: Without preservatives.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

325

L

Lens Viscum comp. Inject

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) lens cristallina bovis Gl dil. D7 0.1 g (HAB, Method 41b) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D5 0.1 g viscum album (mali) e planta tota ferm 34i dil. D5 0.1 g (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. Vitreous clouding, cataracts. Contraindications The medicinal product must not be used • in the case of known allergy to mistletoe formulations • in the case of hypersensitivity to milk protein.

N1

PZN 0081530

Price Group 11

Side-effects None known.

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, 1 ml injected subcutaneously 2 to 3 times a week in the neck-shoulder region. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In very rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke's oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Levico comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1751665 2086069

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: hypericum perforatum ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) Levico water "strong” dil. D2 aquos. 0.1 g (HAB, Method 5b) prunus spinosa e floribus et summitatibus ferm cum ferro dil. D3 0.1 g (HAB, Method 37a)

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism, e.g. in states of exhaustion, hypotensive dysregulation, latent iron deficiency.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor.

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 3 to 4 times a week, children from 6 to under 12 years 0.5-1 ml injected subcutaneously 3 to 4 times a week and adults and children of 12 years and above 1 ml injected subcutaneously 3 to 4 times a week.

Side-effects None known.

L

L

Lens Viscum comp. Globuli velati Globuli velati

Levico comp.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) formica rufa ex animale toto Gl dil. D6 0.1 g (HAB, Method 41c) lens cristallina bovis Gl dil. D7 0.1 g (HAB, Method 41b) phyllostachys e nodo ferm 35c dil. D5 0.1 g (HAB, Method 35c) stannum metallicum dil. D5 0.1 g viscum album (mali) e planta tota ferm 34i dil. D5 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose.

326

N1

PZN 0081547

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Vitreous clouding, cataracts. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Lens Viscum comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually once to twice daily.

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: hypericum perforatum ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) Levico water "strong" dil. D2 aquos. 0.1 g (HAB, Method 5b) prunus spinosa e floribus et summitatibus ferm cum ferro dil. D2 0.1 g (HAB, Method 37a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic

N1

PZN 8786419

Price Group A

Status Pharmacy only

metabolism, e.g. in states of exhaustion, hypotensive dysregulation, latent iron deficiency. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Levico comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily.

327

For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be con-

sulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

Active ingredient: levisticum officinale e radice W 5 % Bath additive, liquid

Active ingredient: levisticum officinale e radice ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: levisticum officinale e radice ferm 33c dil. D.. 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2881105 2881128

Potency/Strength Package Size Size Category Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Side-effects None known.

Levisticum e radice

L

Active ingredient: levisticum officinale e radice ferm 33c Globuli velati Potency/Strength Package Size Size Category D3 D4 D6 D10

20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: levisticum officinale e radice ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Malnutrition due to digestive weakness with nervous hypersensitivity; inflammation in the nerve-sense region, e.g. middle ear inflammation and sequelae. Contraindications None known.

328

Side-effects None known.

Levisticum e radice W 5%, Oleum

Levisticum e radice

D4 D6

Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

N1 N1 N1 N1

PZN 8786425 8786431 8786448 8786454

Price Group A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Levisticum e radice. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.



100 ml

PZN

Price Group

2088542

N1

Status General sale

Composition 10 g (11 ml) contain: levisticum officinale e radice W 5% (HAB, Method 12g with virgin olive oil) 10 g

years and above use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath (about 200 l water) for oil dispersion baths 2 to 3 times per week. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Indications according to the anthroposophical understanding of human beings and nature. Nerve inflammation (neuritis). Contraindications None known.

Duration of treatment The treatment should usually take no more than 2-3 weeks. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Side-effects None known.

Dosage and method of administration Unless otherwise directed, for adults and children of 12

Levisticum Ohrentropfen

Active ingredient: levisticum officinale e radice W 5% Ear drops Potency/Strength Package Size Size Category

10 ml

Composition 10 g (11 ml) contain: levisticum officinale e radice W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Inflammation of the middle ear (otitis media).

N1

PZN 1754089

Price Group B

Status Pharmacy only

Contraindications Do not use in the case of hypersensitivity to levisticum officinale (lovage). Warnings and precautions for use This medicinal product should not be used to treat children under 2 years without medical advice as middle ear inflammation in this age group requires close monitoring by a doctor.

329

L

Dosage and method of administration The drops should be warmed to body temperature before use. Unless otherwise directed, infants and children under 6 years 1 to 2 drops instilled into the ear 1 to 3 times daily, adults and children of 6 years and above 3 to 4 drops instilled into the ear twice daily; alternatively place a strip of

cotton wool soaked in the warmed drops in the ear several times daily. After use of the ear drops, close the bottle with the screw-on/dropper cap. Side-effects None known.

Lien Gl

Active ingredient: lien bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

L

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: lien bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2830125 3353236 2829889 3356507 3356513 3356536 3356542 3356565 0848115 0846576 2496548

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Composition Liquid dilution for injection: 1 ml contains: cichorium intybus e planta tota ferm 33c dil. D14 0.1 g (HAB, Method 33c) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) lien bovis Gl dil. D5 0.1 g (HAB, Method 41a) mesenchym bovis Gl dil. D5 0.1 g (HAB, Method 41b) renes bovis Gl dil. D5 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the mesenchymal functions, e.g. in general weakness of the immune system.

Contraindications Do not use in the case of hypersensitivity to animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case the patient should see a doctor. Side-effects None known.

Lien comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: cichorium intybus e planta tota ferm 33c dil. D14 0.1 g (HAB, Method 33c) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) lien bovis Gl dil. D5 0.1 g (HAB, Method 41a) mesenchym bovis Gl dil. D5 0.1 g (HAB, Method 41b) renes bovis Gl dil. D5 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the mesenchymal functions, e.g. in general weakness of the immune system.

N1

PZN 8786460

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Lien comp. Dosage and method of administration Unless otherwise directed, children under 6 years 5-10 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 10-15 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Lien comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

330

10 x 1 ml 50 x 1 ml

N1 N2

PZN 2086075 2086081

Price Group 11 12

Status Pharmacy only Pharmacy only

331

L

Lien/Plumbum

Ligamentum longitudinale posterius Gl

Liquid dilution for injection

Active ingredient: ligamentum longitudinale posterius bovis Gl Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 2086098

Price Group 11

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: lien bovis Gl dil. D5 0.1 g (HAB, Method 41a) plumbum metallicum dil. D29 aquos. 0.1 g

Contraindications Do not use in the case of hypersensitivity to animal protein.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the catabolic and boundary-forming functions of the spleen, e.g. adjunctive treatment in the case of pathological enlargement of the spleen (splenomegaly), erythrocytosis, leukaemia, plasma cell tumour (multiple myeloma), bone metastases.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Duration of treatment The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

Active ingredient: ligamentum longitudinale anterius bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ligamentum longitudinale anterius bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

332

N1 N1 N1 N1 N1 N1 N1

PZN 2881559 2881571 2881594 2881631 2881654 2881677 2490907

Price Group 61 61 61 61 61 61 51

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ligamentum longitudinale posterius bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1 N1 N1

PZN 2881743 2881772 2881795 2881849 2881861 2881884 2490913

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

L

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

D5 D6 D8 D12 D15 D30 Serial pack

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Ligamentum longitudinale anterius Gl

L

Potency/Strength Package Size Size Category

Ligamentum vocale Gl

Active ingredient: ligamentum vocale bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ligamentum vocale bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2881944 2881967 2881996 2882010 2882033 2882062 2882085 2496554

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

333

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Lingua Gl

Active ingredient: lingua bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: lingua bovis Gl dil. D.. 1 ml (HAB, Method 41c)

L

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 upwards: None known.

N1 N1 N1

PZN 2882240 2882346 2882406

Price Group 61 61 61

Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

334

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2882464 2882487 2882501 2882524 2882547 2882576 2882599 2496560

Price Group 61 61 61 61 61 61 61 51

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Lobus frontalis Gl

Active ingredient: lobus frontalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: lobus frontalis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: liquor cerebrospinalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Status

Liquor cerebrospinalis Gl

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Composition Liquid dilution for injection: 1 ml contains: liquor cerebrospinalis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 4626297 2882642 4619498 4626334 4626357 2882665 2490942

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

335

L

Lobus occipitalis Gl

Active ingredient: lobus occipitalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 4626417 2882688 4619512 4626469 4626481 2882702 2490988

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Composition Liquid dilution for injection: 1 ml contains: lobus occipitalis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Side-effects None known.

Lobus parietalis Gl

Active ingredient: lobus parietalis bovis GI Liquid dilution for injection

D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: lobus parietalis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

336

N1 N1 N1 N1 N1 N1 N1

PZN 4619535 2882748 4619558 4619570 4626535 4626558 2490994

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Lobus temporalis Gl

Active ingredient: lobus temporalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: lobus temporalis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

L

Potency/Strength Package Size Size Category

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 4619593 2882814 4619618 2882837 4626630 4626653 2491002

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

337

L

Lycopodium comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: berberis vulgaris e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) lycopodium clavatum e planta tota ferm 33e dil. D4 0.1 g (HAB, Method 33e) mercurius dulcis dil. D9 0.1 g natrium sulfuricum dil. D9 aquos. 0.1 g (HAB, Method 5b) silybum marianum e fructibus ferm 36 dil. D3 0.1 g (HAB, Method 36) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the digestive activity in disorders of the hepatobiliary system, e.g. weak metabolism, also for adjunctive treatment of malignant diseases; cholecystopathies (diseases of the gallbladder), constipation.

L

N1 N2

PZN 1751688 2086129

Price Group 11 12

Status Pharmacy only Pharmacy only

or other plants belonging to the Compositae family. Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications Lycopodium comp. should not be used in the case of known hypersensitivity to milk thistle (silybum marianum)

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Lycopodium comp.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Side-effects Because of the ingredient mercurius (quicksilver) allergic reactions can occasionally occur. In this case treatment with the medicinal product should be discontinued and a doctor consulted.

Lycopodium e planta tota

Active ingredient: lycopodium clavatum e planta tota ferm 33e Liquid dilution for injection Potency/Strength Package Size Size Category D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: lycopodium clavatum e planta tota ferm 33e dil. D.. 1 ml (HAB, Method 33e) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1

PZN 2890831 2890854 2882903

Price Group 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Lycopodium comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: berberis vulgaris e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) lycopodium clavatum e planta tota ferm 33e dil. D2 0.1 g (HAB, Method 33e) mercurius dulcis trit. D4 0.1 g natrium sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b) silybum marianum e fructibus ferm 36 Ø 0.02 g (HAB, Method 36) Contains sucrose (saccharose/sugar) and lactose.

338

N1

PZN 8786537

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the digestive activity in disorders of the hepatobiliary system, e.g. metabolic weakness, also for adjunctive treatment of malignant diseases; diseases of the gallbladder (cholecystopathies), constipation. Contraindications Lycopodium comp. should not be used in the case of known hypersensitivity to silybum marianum (milk thistle) or other plants belonging to the Compositae family.

339

L

Lycopodium e planta tota

Magnesit/Mamma comp.

Active ingredient: lycopodium clavatum e planta tota ferm 33e Globuli velati Potency/Strength Package Size Size Category D6 D12 D30

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: lycopodium clavatum e planta tota ferm 33e dil. D.. 1 g (HAB, Method 33e) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Lycopodium e planta tota.

N1 N1 N1

PZN 8786566 8786543 8786572

Liquid dilution for injection Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

PZN 1751694 2086135

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D5 0.1 g (HAB, Method 41c) funiculus umbilicalis bovis Gl dil. D5 0.1 g (HAB, Method 41b) hypophysis bovis Gl dil. D5 0.1 g (HAB, Method 41a) magnesite dil. D7 0.1 g mamma bovis Gl dil. D5 0.1 g (HAB, Method 41c) viscum album (mali) e planta tota ferm 34i dil. D4 0.1 g (HAB, Method 34i)

difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in structural abnormalities of the breast, e.g. fibrocystic disease.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Contraindications Do not use in the case of hypersensitivity to bee venom, the donor animal protein or milk protein. In patients with bee venom allergy administration of this medicinal product can lead to allergic reactions such as hives (urticaria),

L

N1 N2

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Magnesit/Mamma comp. Globuli velati

Potency/Strength Package Size Size Category Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D5 0.1 g (HAB, Method 41c) funiculus umbilicalis bovis Gl dil. D5 0.1 g (HAB, Method 41b) hypophysis bovis Gl dil. D5 0.1 g (HAB, Method 41a)

340

20 g

N1

PZN 8786589

Price Group A

Status Pharmacy only

magnesite dil. D7 0.1 g mamma bovis Gl dil. D5 0.1 g (HAB, Method 41c) viscum album (mali) e planta tota ferm 34i dil. D4 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose.

341

M

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in structural abnormalities of the breast, e.g. disorder of the breast with cyst formation (fibrocystic disease). Contraindications Do not use in the case of known hypersensitivity to bee venom. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sug-

ars you should consult your doctor before taking Magnesit/Mamma comp.

Magnesium phosphoricum comp.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily.

Potency/Strength Package Size Size Category

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Magnesium phosphoricum comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

M

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arnica montana e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) dil. D5 0.1 g (HAB, Method 6) formica rufa ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the fluid organism in conditions where there is painful hardening and formation of tissue deposits together with muscular tension, e.g. muscular knots (myogelosis), muscular cramps, anginal pain, soft tissue rheumatism. Contraindications Magnesium phosphoricum comp. should not be used in

342

N1 N2

PZN 1751702 2086141

Price Group 11 12

Status Pharmacy only Pharmacy only

the case of hypersensitivity to arnica or other plants of the Compositae family. Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Side-effects Very rarely, harmless redness may appear at the injection site and - in the case of hypersensitivity to arnica - allergic reactions may occur. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati



20 g

N1

PZN 8786632

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: arnica montana e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) dil. D5 0.1g (HAB, Method 6) formica rufa ex animale toto Gl dil. D7 0.1 g (HAB, Method 41c) Contains sucrose (saccharose/sugar) and lactose.

the case of hypersensitivity to arnica or other plants of the Compositae family.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the fluid organism in conditions where there is painful hardening and formation of tissue deposits together with muscular tension, e.g. muscular knots (myogelosis), muscular cramps, "tightness in the chest" (anginal pain), soft tissue rheumatism.

Dosage and method of administration Unless otherwise directed, adults and children from 2 years to under 6 years 3-5 globuli velati sublingually 1 to 3 times daily to every 2 hours; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily to every 2 hours.

Contraindications Magnesium phosphoricum comp. should not be used in

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 2 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Magnesium phosphoricum comp.

Side-effects Very rarely – in the case of hypersensitivity to arnica – allergic reactions can occur.

Magnesium phosphoricum cum cinere Avenae

M

Active ingredient: cinis e fructibus avenae sativae cum magnesio phosphorico aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D8

10 x 1 ml

N1

PZN 2832615

Price Group 31

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) dil. D8 aquos. 1 ml (HAB, Method 8b)

Contraindications Do not use in the case of hypersensitivity to milk protein.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily.

343

Magnesium phosphoricum cum cinere Avenae

Active ingredient: cinis e fructibus avenae sativae cum magnesio phosphorico aquos. Globuli velati Potency/Strength Package Size Size Category D6 D12

20 g 20 g

Composition Globuli velati: 10 g contain: cinis e fructibus avenae sativae cum magnesio phosphorico dil. D.. aquos. 1 g (HAB, Method 8b) Contains sucrose (saccharose/sugar) and lactose. Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Magnesium phosphoricum cum cinere Avenae.

N1 N1

PZN 8786595 8786603

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor.

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D3 0.01 g (HAB, Method 41c) arnica montana e planta tota ferm 33c dil. D1 0.01 g (HAB, Method 33c) bryonia cretica ferm 33b dil. D2 0.01 g funiculus umbilicalis bovis Gl dil. D4 0.01 g (HAB, Method 41b) hypophysis bovis Gl dil. D4 0.01 g (HAB, Method 41a) magnesium sulfuricum dil. D4 aquos. 0.01 g (HAB, Method 5b) ovaria bovis Gl dil. D4 0.01 g (HAB, Method 41a) stannum metallicum dil. D8 0.01 g

344

Side-effects In rare cases, intolerance of mistletoe or allergy to bee or wasp venom can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke's oedema), shaking chills, difficulty breathing or shock, in which case

Potency/Strength Package Size Size Category

Potency/Strength Package Size Size Category 10 x 1 ml

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted.

Globuli velati

Liquid dilution for injection



Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

treatment with the preparation must be discontinued immediately and medical assistance sought. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Magnesium sulfuricum/Ovaria comp.

Side-effects None known.

Magnesium sulfuricum/Ovaria comp.

M

Warnings and precautions for use Magnesium sulfuricum/Ovaria comp. should not be used in children under 12 years as there is no adequately documented experience on use in this age group.

N1

PZN 1751719

Price Group 11

Status Pharmacy only

vespa crabro ex animale toto Gl dil. D3 0.01 g (HAB, Method 41c) viscum album (mali) e planta tota ferm 34i dil. D4 0.01 g (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers in the ovaries, e.g. ovarian cysts. Contraindications The medicinal product must not be used in the case of hypersensitivity to arnica or other plants of the Compositae family, known allergy to mistletoe formulations, hypersensitivity to bee or wasp venom or allergy to the donor animal protein or to milk protein.

20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D3 0.01 g (HAB, Method 41c) arnica montana e planta tota ferm 33c dil. D1 0.01 g (HAB, Method 33c) bryonia cretica ferm 33b dil. D2 0.01 g funiculus umbilicalis bovis dil. Gl D4 0.01 g (HAB, Method 41b) hypophysis bovis Gl dil. D4 0.01 g (HAB, Method 41a) magnesium sulfuricum dil. D4 aquos. 0.01 g (HAB, Method 5b) ovaria bovis Gl dil. D4 0.01 g (HAB, Method 41a) stannum metallicum dil. D8 0.01 g vespa crabro ex animale toto Gl dil. D3 0.01 g (HAB, Method 41c) viscum album (mali) e planta tota ferm 34i dil. D4 0.01 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose.

N1

PZN 8786649

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers in the ovaries, e.g. ovarian cysts. Contraindications Magnesium sulfuricum/Ovaria comp. should not be used in the case of hypersensitivity to arnica or other plants of the Compositae family. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Magnesium sulfuricum/Ovaria comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

345

M

Majorana comp., Gelatum

Malvenöl (mallow oil)

Majorana Vaginalgel (vaginal gel)

Potency/Strength Package Size Size Category

see Majorana Vaginalgel

Oily embrocation

Gel

Potency/Strength Package Size Size Category

M

30 g 100 g

Composition 10 g contain: acidum lacticum 0.03 g argentum colloidale dil. D4 0.10 g calendula officinalis ex herba ferm 33c Ø 0.10 g (HAB, Method 33c) echinacea pallida e planta tota ferm 33c Ø 0.10 g (HAB, Method 33c) eucalypti aetheroleum 0.02 g kreosotum dil. D4 0.10 g lilium lancifolium ex herba ferm 33c dil. D1 0.10 g (HAB, Method 33c) origanum majorana ex herba ferm 33c Ø 0.10 g (HAB, Method 33c) rosmarini aetheroleum 0.01 g salviae officinalis aetheroleum 0.01 g thuja occidentalis e summitatibus ferm 33e dil. D1 0.10 g (HAB, Method 33e) thymi aetheroleum 0.01 g Excipients: glycerol, litsea fruit oil, aqueous colloid silicium dioxide solution produced with citric acid monohydrate, tea tree oil, purified water, xanthan gum. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the constituent elements of the human being in inflammatory conditions of the female reproductive organs, e.g. inflammation of the vagina (vaginitis), inflammation of the vulva (vulvitis), non-specific vaginal discharge. Contraindications The medicinal product should not be used • in infants, small children and children under 6 years in view of the insufficiently clarified risks of ointments containing marjoram herb, • in the case of hypersensitivity to rosemary, thyme or other plants of the Lamiaceae family (labiates), to birch,

346

N1 N2

PZN 1061280 1448292

Price Group A J1

Status Pharmacy only Pharmacy only

mugwort, celery, to any of the other active ingredients or excipients or to other plants of the Compositae family, • in the case of progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases directed against the tissues of the patient‘s own body), on the basis of fundamental considerations. Warnings and precautions for use Majorana Vaginalgel must not be used together with latex condoms as it can cause the condoms to tear or become porous and their contraceptive action is therefore no longer ensured. Dosage and method of administration Unless otherwise directed, use 2 to 3 times a week to once to twice daily; to apply, introduce the gel into the vagina with the help of the applicator provided while lying on the back. In children from 6 years to under 12 years Majorana Vaginalgel should only be used in the region of the external genitals. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. As the medicinal product contains marjoram herb it is not suitable for prolonged use. Side-effects Very rarely • hypersensitivity reactions can occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). • stinging can occur at the application site. In such cases you should stop using the medicinal product and see your doctor.



50 ml 100 ml

N1 N1

PZN 1753641 1753747

Price Group L L1

Status Pharmacy only Pharmacy only

Contraindications Malvenöl should not be used in the case of hypersensitivity to geranium oil or any other of the active ingredients or in the case of hypersensitivity to arachis oil.

Composition 10 g (11 ml) oily embrocation contain: geranii aetheroleum 0.04 g oily extract of hypericum perforatum, herba rec. (4:1), extraction agent: refined arachis oil 1.25 g malva arborea e floribus W 5% (HAB, Method 12g with refined arachis oil) 1.25 g prunus spinosa e floribus W 5% (HAB, Method 12g with refined arachis oil) 1.25 g sambucus nigra ex umbella W 5% (HAB, Method 12g with refined arachis oil) 1.25 g tilia platyphyllos/cordata e floribus W 5% (HAB, Method 12g with refined arachis oil) 1.25 g Excipient: refined arachis oil.

Warnings and precautions for use In rare cases arachis oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in 2 to 3 ml of oil once to twice daily or use for massages with an appropriately larger amount of oil depending on the size of the body. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Photosensitisation or redness of the skin may very rarely occur; in such cases use of the medicinal product should be discontinued. In rare cases arachis oil can cause severe allergic reactions.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in nervous exhaustion, e.g. during convalescence.

M

Mamma (dextra) Gl

Active ingredient: mamma dextra bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2883127 2883156 2883179 2883191 2883222 2883245 2883268 2883280 2496577

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

347

Composition Liquid dilution for injection: 1 ml contains: mamma dextra bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Mandibula (feti) Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: mamma sinistra bovis GI Liquid dilution for injection

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack III

M

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2883340 2883363 2883392 2883417 2883446 2883469 2883481 2883506 2496583

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: mamma sinistra bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

348

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: mandibula feti bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Mamma (sinistra) Gl

Potency/Strength Package Size Size Category

Active ingredient: mandibula feti bovis GI Liquid dilution for injection

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2934184 2934209 2934221 2934244 2934267 2934296 2934333 0846636 2496608

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

M

Mandragora officinarum e radice

Active ingredient: mandragora officinarum e radice ferm 34d Liquid dilution for injection Potency/Strength Package Size Size Category D2 D3 D6 D10 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1

PZN 3358311 2832609 2832578 3358328 3358340

Price Group V5 V5 31 31 31

Status Prescription only Prescription only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: mandragora officinarum e radice ferm 34d dil. D.. 1 ml (HAB, Method 34d)

matory disorders of the joints and ligaments, also in connection with systemic metabolic disorders such as gout; cramping in the region of the digestive organs, nervous anxiety.

Indications according to the anthroposophical understanding of human beings and nature. Painful, degenerative and inflam-

Contraindications None known.

349

Warnings and precautions for use There is no adequately documented experience of the use of Mandragora officinarum e radice D2 and D3 in children. It should therefore not be used in children under 12 years. Dosage and method of administration D2, D3: Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously once to twice a week. D6 upwards: Unless otherwise directed, infants and small children 0.5 ml injected subcutaneously once to twice a week; children of 6 years and above 0.5 to 1 ml injected subcutaneously once to twice a week; adults and children of 12 years and above 1 ml injected subcutaneously once to twice a week.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Liquid dilution for injection D2: Dry mouth, enlargement of the pupils and accelerated heartbeat can occur in rare cases on use of Mandragora officinarum e radice D2. In this case use of the medicinal product should be stopped and a doctor consulted. Fleeting, harmless signs of irritation can occur around the injection site after subcutaneous injection. Liquid dilution for injection D3 upwards: None known.

Active ingredient: mandragora officinarum e radice ferm 34d Globuli velati

D4 D6 D12

M

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: mandragora officinarum e radice ferm 34d dil. D.. 1 g (HAB, Method 34d) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Mandragora officinarum e radice.

350

N1 N1 N1

PZN 8786655 8786661 8786678

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: maxilla feti bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: maxilla feti bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Mandragora officinarum e radice

Potency/Strength Package Size Size Category

Maxilla (feti) Gl

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN

Price Group

2934474 2934497 2934511 2934534 2934557 2934586 2934623 0848173 0846642 2496614

61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

M Medulla oblongata (Ventriculus quartus) Gl Active ingredient: medulla oblongata bovis GI Liquid dilution for injection

Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3356660 3356677 3356683 3356708 3356714 3356097 3356105 0848204 0846659 2496620

Price Group 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

351

Composition Liquid dilution for injection: 1 ml contains: medulla oblongata bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Medulla spinalis (tota) Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

D5 D6 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Medulla ossium Gl

Active ingredient: medulla ossium rubra bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

M

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: medulla ossium rubra bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of bone marrow activity in disorders of haematopoiesis; adjunctive treatment of aplastic anaemias and malignant bone marrow disorders. Contraindications Liquid dilution for injection D4, D5, D6: Do not use in status post bone marrow transplantation. The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

352

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2831248 3356134 3356140 3356157 3356163 3356186 3356192 3356200 0848227 0846665 2496637

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Active ingredient: medulla spinalis tota bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: medulla spinalis tota bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N2 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3356217 3356223 2935686 3356246 3356252 3356269 3356275 3356298 0848233 0846671 2496643

Price Group 61 61 62 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

M

Liquid dilution for injection D8 upwards: Do not use in status post bone marrow transplantation. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

353

Melissa ex herba W 5%, Oleum

Melissa/Sepia comp.

Active ingredient: melissa officinalis ex herba W 5% Liquid bath additive Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: melissa officinalis ex herba W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of hypersensitivity to lemon balm. Dosage and method of administration Unless otherwise directed, use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35° and 37°, the bathing time about 20 minutes.

N1

Globuli velati PZN

Price Group

2088571

N1

Status General sale

Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects Hypersensitivity reactions may very rarely occur. In such cases use of Melissa ex herba W 5%, Oleum should be discontinued and a doctor consulted. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Melissa/Sepia comp.

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aconitum napellus e tubere ferm 33c dil. D9 0.1 g (HAB, Method 33c) chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) lachesis dil. D11 aquos. 0.1 g (HAB, Method 5b) melissa officinalis ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) sepia officinalis e volumine bursae rec. Gl dil. D7 0.1 g (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the ego and feeling organisation in menopausal symptoms, e.g.

354

20 g

N1

PZN 8786709

Price Group A

Status Pharmacy only

Contraindications Do not use in the case of hypersensitivity to chamomile or other plants of the Compositae family.

Composition Globuli velati: 10 g contain: aconitum napellus e tubere ferm 33c dil. D9 0.1 g (HAB, Method 33c) chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) lachesis dil. D11 aquos. 0.1 g (HAB, Method 5b) melissa officinalis ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) sepia officinalis e volumine bursae rec. Gl dil. D5 0.1 g (HAB, Method 41c) Contains sucrose (saccharose/sugar).

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Melissa/Sepia comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment Even anthroposophical medicines should not be taken for prolonged periods without obtaining the advice of a doctor.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the ego and feeling organisation in menopausal symptoms, e.g. hot flushes, exhaustion, dizziness, irritability, depressive mood.

Side-effects None known.

Oily embrocation

Potency/Strength Package Size Size Category



Melissenöl (lemon balm oil)

Liquid dilution for injection

M

Potency/Strength Package Size Size Category

N1 N2

PZN 1751731 2086170

Price Group 11 12

Status Pharmacy only Pharmacy only

hot flushes, exhaustion, dizziness, irritability, depressive mood. Contraindications Do not use in the case of hypersensitivity to chamomile or other plants of the Compositae family. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects None known.

Potency/Strength Package Size Size Category

50 ml 100 ml

Composition 10 g (11 ml) contain: carvi aetheroleum 0.03 g foeniculi amari fructus aetheroleum 0.03 g melissa officinalis ex herba W 5% (HAB, Method 12g with refined arachis oil) 4.90 g origanum majorana ex herba W 5% (HAB, Method 12g with refined arachis oil) 4.90 g Excipient: refined arachis oil.

N1 N1

PZN 1753658 1753753

Price Group L L1

M

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation in the region of the metabolic-limb system, e.g. wind (flatulence), abdominal cramps. Contraindications Do not use in the case of known hypersensitivity to fennel oil and anethol, caraway oil or other umbellifers, arachis oil. Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in infants and small children under 6 years.

355

Warnings and precautions for use In rare cases arachis oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in 2 to 3 ml of oil once to twice daily or use an appropriately larger amount for massages. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be

consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. As the medicinal product contains marjoram herb it is not suitable for prolonged use.

Membrana sinus maxillaris Gl

Side-effects Hypersensitivity reactions may very rarely occur; in this case use of the preparation should be discontinued and a doctor consulted.

Potency/Strength Package Size Size Category

Membrana sinus frontalis Gl

Active ingredient: membrana sinus frontalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

M

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: membrana sinus frontalis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

356

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3356364 3356370 3356387 3356393 3355778 3355784 2831308 0846688 2496689

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: membrana sinus maxillaris bovis GI Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: membrana sinus maxillaris bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3355790 2831946 3355809 3355815 3355821 3355838 2830875 0846694 2496695

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

M Membrana sinuum paranasalium Gl

Active ingredient: membrana sinuum paranasalium bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3355933 3355956 3355962 3355979 2831515 2830065 2830869 3355991 0846702 2496703

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

357

Composition Liquid dilution for injection: 1 ml contains: membrana sinuum paranasalium bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Membrana sinuum paranasalium Gl D4 must not be used for longer than 3 months. Intermittent use over a period of more than three months is possible provided that the total number of daily doses does not exceed 99 per year.

Warnings and precautions for use Sufficiently documented experience for the use of this

Side-effects None known.

Active ingredient: membrana synovialis bovis GI Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack II

M

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: membrana synovialis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

358

N1 N1 N1 N1 N1 N1 N1 N1

Active ingredient: meniscus articularis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: meniscus articularis bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Membrana synovialis Gl

Potency/Strength Package Size Size Category

Meniscus Gl

PZN 3356051 3356068 3356074 3356016 3356022 3356039 3356045 0846719

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2936421 2936444 2936467 2936496 2936510 2936533 2936562 0848291 2496732

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

M

Mercurialis Augentropfen Eye drops

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: mercurialis perennis ferm 34c dil. D3 0.05 g rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g Excipients: sodium chloride, sodium hydrogen carbonate and water for injections.

N1 N2

PZN 1448317 1448300

Price Group C C1

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the fluid organism in the region of the eye in dry conjunctivitis, dry eye. Contraindications None known. Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac 1 to 3 times daily to every 2 hours.

359

Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling organisation and life organisation in the skin and subcutis in chronic inflammatory processes, suppurating, poorly healing wounds, eczema.

Side-effects None known.

Contraindications Mercurialis Salbe should not be applied to fresh, open wounds.

Mercurialis comp., Suppositorien Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: allium cepa ferm 34a Ø 8 mg calendula officinalis ex herba ferm 33c Ø 16 mg (HAB, Method 33c) mercurialis perennis ferm 34c Ø 40 mg stibium metallicum trit. D3 20 mg Excipients: hard fat, honey.

M

Indications according to the anthroposophical understanding of human beings and nature. Inner structuring in painful, oedematous, weeping acute to chronic inflammatory changes in the anal region, e.g. haemorrhoids, inflammation of the area around the anus (anitis), skin tears in the anal region (anal fissures), inflammation of the connective tissue around the rectum and anus (periproctitis).

N1

PZN 1880687

Price Group P

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum once to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Ointment

Potency/Strength Package Size Size Category 30 g 100 g

Composition 10 g contain: allium cepa ferm 34a Ø 0,1 g calendula officinalis ex herba ferm 33c Ø 0,2 g (HAB, Vs. 33c)

360

Dosage and method of administration Unless otherwise directed, apply Mercurialis Salbe thinly 1 to 3 times daily. Depending on the size of the affected area, use a ribbon of ointment about 0.5 to 2 cm long.

N1 N2

PZN 1448346 1448323

Price Group J J1

Status Pharmacy only Pharmacy only

mercurialis perennis ferm 34c Ø 0,5 g Excipients refine arachis oil, white soft paraffin, purified water, wool fat.

Duration of treatment If no improvement is seen after one week a doctor should be consulted. Nonetheless, the described indications may require prolonged treatment with Mercurialis Salbe. Side-effects Skin irritation can occur in rare cases.

Mesencephalon Gl

Active ingredient: mesencephalon bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: mesencephalon bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Mercurialis Salbe



Warnings and precautions for use In rare cases arachis oil and wool fat can cause local skin reactions (e.g. contact dermatitis).

For an ointment dressing, apply a ribbon of Mercurialis Salbe about 2 to 5 cm long to a gauze dressing and cover the inflamed area with this for 24 hours (keep in place with sticking plaster or a loose gauze bandage). Renew the ointment dressing after 24 hours. Note: Do not apply the ointment to the eye or mucous membranes.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 3355459 3355465 3355471 3355494 3355502 3355519 2491019

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

361

M

Mesenchym Gl

Active ingredient: mesenchym bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

M

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829487 3355525 2829777 3355531 3355548 2830987 3355554 3355577 2485987 0846731 2496749

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: mesenchym bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of regeneration of the skeletal and connective tissue and the immune system; for adjunctive treatment of chronic inflammatory, degenerative and malignant disorders.

Dosage and method of administration Potencies below D20: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potencies D20 and above: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection



10 x 1 ml 50 x 1 ml 5 x 10 ml

N1 N2 N1

PZN 1751748 2086187 8510396

of an allergic diathesis (increased susceptibility to the development of allergies).

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of organ activity in disorders of protein metabolism, particularly in the case

Side-effects None known.

Price Group 11 12 21

Status Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use The medicinal product Mesenchym/Calcium carbonicum comp. should only be given to children under 12 years after consulting a doctor as there is insufficient experience available to give a general recommendation for this age group. Dosage and method of administration 1 ml: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once to twice daily. 10 ml: Unless otherwise directed, inject 10 ml intramuscularly once a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Liquid dilution for injection

Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ferrum sidereum dil. D11 aquos. 0.1 g phosphorus dil. D5 0.1 g quartz dil. D11 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Flu-like infections, prolonged convalescence, general exhaustion. Contraindications None known.

362

Contraindications Do not use in the case of known hypersensitivity to the donor animal protein.

Meteoreisen Inject



Mesenchym/Calcium carbonicum comp. Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: cor bovis Gl dil. D5 0.1 g (HAB, Method 41c) hepar bovis Gl dil. D5 0.1 g (HAB, Method 41a) mesenchym bovis Gl dil. D5 0.1 g (HAB, Method 41b) pancreas suis Gl dil. D5 0.1 g (HAB, Method 41a) pulmo bovis Gl dil. D5 0.1 g (HAB, Method 41a) quercus robur/petraea e cortice cum calcio carbonico dil. D12 aquos. (HAB, METHOD 5b; solution = D6 prepared by potentising quercus robur/petraea e cortice, decoctum Ø (HAB, Method 23a) five times with saturated aqueous solution of calcium carbonicum e cinere quercus) 0.1 g renes bovis Gl dil. D5 0.1 g (HAB, Method 41a)

N1 N2

PZN 0081553 0090196

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

363

M

Meteoreisen Globuli velati Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 1448352

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: ferrum sidereum dil. D11 aquos. 0.1 g phosphorus dil. D5 0.1 g quartz dil. D11 aquos. 0.1 g Contains sucrose (saccharose/sugar).

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; children from 6 to under 12 years 5-7 globuli velati sublingually 1 to 3 times daily; adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Indications according to the anthroposophical understanding of human beings and nature. Flu-like infections, prolonged convalescence, general exhaustion.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Meteoreisen Globuli velati.

Side-effects None known.

Meteoreisen/Phosphor/Quarz

M



Potency/Strength Package Size Size Category

364

Dosage and method of administration Unless otherwise directed, apply the gel to the mucous membranes and dental necks several times daily (particularly at bedtime) – after thoroughly cleaning the teeth. After application, breathe through the mouth for a short time. Do not rinse off! In the case of sores caused by dentures, apply the gel to the dentures before inserting them in the mouth. Duration of treatment Do not use for longer than 8 weeks without obtaining medical advice. Side-effects Mundbalsam can cause spasm of the vocal cords in infants and children up to 2 years resulting in severe breathing difficulty. In rare cases arachis oil can cause severe allergic reactions. Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see your doctor.

Potency/Strength Package Size Size Category

Gel

Composition 10 g contain: antimonite trit. D4 0.1 g argentum nitricum dil. D19 aquos. 0.1 g (HAB, Method 5b) atropa belladonna ex herba ferm 33a dil. D13 0.1 g (HAB, Method 33a) echinacea pallida e planta tota ferm 33c dil. D3 0.1 g (HAB, Method 33c)

Contraindications The medicinal product should not be used in the case of hypersensitivity (allergy) to any of the active ingredients, peanuts or soy or to any of the excipients or to other plants of the Compositae family. On the basis of theoretical considerations, a risk of deterioration of the following disorders as a result of the stimulating action of echinacea on the immune system cannot be ruled out: progressive systemic diseases such as tuberculosis, leukaemia or leukaemia-like diseases (leukoses); rheumatic connective tissue disorders (collagen disease), multiple sclerosis, AIDS, HIV infection and other auto-immune diseases as well as juvenile type I diabetes. Patients with any of these conditions should consult their doctor before using Mundbalsam. Mundbalsam must not be used • in infants and small children under 2 years (danger of spasm of the vocal cords) • in patients with bronchial asthma or other airway disorders associated with pronounced hypersensitivity of the airways. Inhalation of Mundbalsam can lead to difficulty breathing or precipitate an asthma attack.

M

Mixture

Mundbalsam (mouth balm)

10 g 30 g

Warnings and precautions for use This medicinal product contains lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before using Mundbalsam. Contains 2.5 % (v/v) alcohol.

Mundbalsam flüssig (mouth balm, liquid)

see Meteoreisen Inject see Meteoreisen Globuli velati



Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the anabolic and catabolic processes in acute and chronic recurrent inflammatory conditions of the oral mucous membranes.

N1 N1

PZN 1280013 1448369

Price Group J5 J

Status Pharmacy only Pharmacy only

quartz dil. D20 aquos. 0.1 g rosae aetheroleum 0.005 g Excipients: cassia oil, chlorophyll-copper complex, aqueous extract of marshmallow root, refined arachis oil, 96% ethanol, glycerol, ginger oil, potassium dihydrogen phosphate, marjoram oil, sodium alginate, sodium chloride, disodium phosphate dihydrate, clove oil, peppermint oil, Dalmatian sage oil, refined sunflower oil, tea tree oil, purified water.

50 ml

Composition 10 g (10.2 ml) contain: antimonite dil. D7 0.1 g argentum nitricum dil. D19 aquos. 0.1 g (HAB, Method 5b) atropa belladonna ex herba ferm 33a dil. D13 0.1 g (HAB, Method 33a) echinacea pallida e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) quartz dil. D20 aquos. 0.1 g rosae aetheroleum 0.001 g

N2

PZN 1181280

Price Group N

Status Pharmacy only

Excipients: lemon oil, citric acid monohydrate, 96% ethanol, ginger oil, sodium chloride, clove oil, purified water. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the anabolic and catabolic processes in acute and chronic recurrent inflammatory conditions of the oral mucous membranes. Contraindications Mundbalsam flüssig should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to plants of the Compositae family or by people with alcohol dependence.

365

mouth and press against the affected site. In the case of severe pain use the preparation hourly to begin with and then proceed as above when symptoms improve. For inflammation and ulcers covering large areas add the contents of one pipette to about 50 ml (1/4 glass) warm water. Rinse with this solution for about 2 minutes 3 times daily.

On the basis of fundamental considerations, Mundbalsam flüssig must not be used in the case of progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases in which the immune system attacks the body‘s own organs or tissues).

Duration of treatment Mundbalsam flüssig should not be used continuously for more than 2 weeks.

Warnings and precautions for use This medicinal product contains lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before using Mundbalsam. Contains 13.5 % (v/v) alcohol.

Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see your doctor.

Dosage and method of administration Unless otherwise directed, for acute symptoms apply 5 drops of undiluted Mundbalsam flüssig to the affected areas 3 times daily using the pipette or apply 5 drops of Mundbalsam flüssig to a small cotton ball, place in the

Active ingredient: musculi glutaei bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

M

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: musculi glutaei bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Active ingredient: musculus deltoideus-complex bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: musculus deltoideus-complex bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Musculi glutaei Gl

D5 D6 D8 D12 D15 D30 Serial pack

Musculus deltoideus-Komplex Gl

N1 N1 N1 N1 N1 N1 N1

PZN 2936875 2936898 2936912 2936958 2936970 2936993 2491025

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2937053 2937082 2937107 2937159 2937171 2937194 2491031

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Musculus rectus abdominis Gl

M

Active ingredient: musculus rectus abdominis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: musculus rectus abdominis bovis Gl dil. D5 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

N1

PZN 4620509

Price Group 61

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

366

367

Musculus soleus-Komplex Gl

the paranasal sinuses; please ask your doctor about administration of the product.

Active ingredient: musculus soleus-complex bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2937811 2937834 2937857 2937900 2937923 2937952 2491054

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: musculus soleus-complex bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

M

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum nitricum dil. D19 aquos. 0.1 g (HAB, Method 5b) kalium bichromicum dil. D5 aquos. 0.1 g (HAB, Method 5b) myristica sebifera, succus e cortice dil. [HAB, METHOD 5b; sol. D1 with 62% (m/m) ethanol] D3 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Inflammation of the paranasal sinuses (sinusitis), particularly purulent forms.

368

Duration of treatment Do not use for longer than 2 weeks.

Myristica sebifera comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum nitricum dil. D19 aquos. 0.1 g (HAB, Method 5b) kalium bichromicum dil. D5 aquos. 0.1 g (HAB, Method 5b) myristica sebifera, succus e cortice dil. D3 [HAB, Method 5b, sol. D1 with 62% (m/m) ethanol] 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Inflammation of the paranasal sinuses (sinusitis), particularly purulent forms. Contraindications The medicinal product should not be used in the case of known hypersensitivity to constituents of Myristica species, particularly in the case of hypersensitivity to nutmeg.

Myristica sebifera comp.

N1 N2

PZN 1751760 2086201

Price Group 11 12

Side-effects None known.

N1

PZN 8786721

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Myristica sebifera comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment The disorder should have cleared up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

M

Status Pharmacy only Pharmacy only

Contraindications The medicinal product should not be used in the case of known hypersensitivity to constituents of Myristica species, particularly in the case of hypersensitivity to nutmeg. Because of the ingredient kalium bichromicum do not use while pregnant or breastfeeding. Dosage and method of administration Unless otherwise directed, infants and children under 6 years 0.5 ml injected subcutaneously 1 to 3 times a week; adults and children of 6 years and above 0.5-1 ml injected subcutaneously 1 to 3 times a week to twice daily. The subcutaneous injection should be given in the region of

369

Narben Gel (scar-treatment gel)

of the life organisation, e.g. acute and chronic inflammation of the mucous membranes, tissue wasting (atrophy) as well as dryness and irritability.

Gel

Potency/Strength Package Size Size Category

30 g

Composition 10 g contain: allium cepa ferm 34a Ø 0.1 g barium citricum dil. D10 aquos. 0.1 g (HAB, Method 8b) cutis feti bovis Gl dil. D4 0.1 g (HAB, Method 41b) hirudo medicinalis ex animale toto Gl Ø 0.1 g (HAB, Method 41c) mesenchym bovis Gl dil. D4 0.1 g (HAB, Method 41b) polygonatum odoratum e radice ferm 33d dil. D2 0.1 g (HAB, Method 33d) rosmarini aetheroleum 0.05 g thuja occidentalis e summitatibus ferm 33e dil. D6 0.1 g (HAB, Method 33e) vespa crabro ex animale toto Gl dil. D3 0.1 g (HAB, Method 41c) Excipients: glycerol, guar, sodium alginate, sodium chloride, sodium hydrogen carbonate, aqueous colloidal silicium dioxide solution produced with citric acid monohydrate, thyme oil, water for injections, purified water.

N1

PZN 1448234

Price Group D

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the structuring anabolic forces in scar, granuloma (nodule-like changes) and keloid formation of the skin. Contraindications The medicinal product must not be used in the case of known hypersensitivity to any of the active ingredients or excipients. Dosage and method of administration Unless otherwise directed, apply the gel 1 to 2 times daily and rub in until dry, or use as ointment dressing. Duration of treatment The condition should have cleared up within 2 weeks. If there is no improvement within this time a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects In very rare cases skin redness and urticaria (hives) may occur. In this case use of the medicinal product should be stopped and a doctor consulted.

Nasenbalsam (nasal balm)

N

Ointment

Potency/Strength Package Size Size Category Composition 10 g contain: balsamum peruvianum 0.05 g berberis vulgaris e fructibus ferm 33c Ø 1.00 g (HAB, Method 33c) cajeputi aetheroleum 0.25 g eucalypti aetheroleum 0.25 g prunus spinosa e fructibus LA 25% 0.50 g (HAB, Method 12o)

370

10 g

N1

PZN 2198437

Price Group P

Status Pharmacy only

aqueous colloidal silicium dioxide solution (corresponding to silicea colloidalis 0.05 g) produced with citric acid monohydrate 1.25 g Excipients: ethanol 96%, lecithin, virgin olive oil, wool fat. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling organisation and life organisation in the region of the mucous membranes of the nasopharynx and the sinuses in conditions involving impaired boundary formation towards outside influences and weakness

Contraindications The medicinal product should not be used • in the case of known hypersensitivity to eucalyptus oil, cineole, Peru balm, cinnamon (cross allergy) or any of the other ingredients or in the case of a marked allergic disposition, • in the case of bronchial asthma, whooping cough or croup, • on damaged skin, • in infants and small children up to 2 years. Nasenbalsam für Kinder is available for this age group. Warnings and precautions for use In rare cases wool fat can cause local skin reactions (e.g. contact dermatitis).

Dosage and method of administration Unless otherwise directed, introduce the ointment into the nose several times a day, particularly in the evening and if necessary also at night and/or apply around the nostrils. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases an urge to cough can occur. Allergic reactions can occur in the case of hypersensitivity to ingredients of Nasenbalsam, particularly to wool fat. If there is reddening of the skin, with or without itching, please stop using Nasenbalsam and consult a doctor if necessary.

Nasenbalsam für Kinder (nasal balm for children) Ointment

Potency/Strength Package Size Size Category

10 g

Composition 10 g contain: balsamum peruvianum 0.05 g berberis vulgaris e fructibus ferm 33c Ø 1.00 g (HAB, Method 33c) prunus spinosa e fructibus LA 25% 0.50 g (HAB, Method 12o) aqueous colloidal silicium dioxide solution (corresponding to silicea colloidalis 0.05 g) produced with citric acid monohydrate 1.25 g Excipients: ethanol 96%, lecithin, virgin olive oil, wool fat. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling organisation and life organisation in the region of the mucous membranes of the nasopharynx and the sinuses in conditions involving impaired boundary formation towards outside influences and weakness of the life organisation, e.g. acute and chronic inflammatory conditions, particularly in infants and children and in the case of particular sensitivity of the mucous membranes or a tendency to tissue wasting (atrophy). Contraindications The medicinal product should not be used in the case of

N1

PZN 1448375

Price Group P

Status Pharmacy only

known hypersensitivity to Peru balsam, cinnamon (cross allergy) or any of the other ingredients or in the case of a marked allergic disposition. Do not apply to damaged skin. Warnings and precautions for use In rare cases wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, introduce the ointment into the nose several times a day, particularly in the evening and if necessary at night. In infants and small children apply the ointment around the nostrils. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In the case of hypersensitivity to any of the ingredients of Nasenbalsam für Kinder, particularly to wool fat or Peru balsam, allergic reactions may occur. If there is reddening of the skin, with or without itching, please stop using Nasenbalsam für Kinder and see your doctor.

371

N

Nasenbalsam mild

Nervi intercostales

see Nasenbalsam für Kinder

Active ingredient: nervi intercostales bovis Gl Liquid dilution for injection

Nervennahrung

Potency/Strength Package Size Size Category

Medicinal honey

Potency/Strength Package Size Size Category

N

240 g

Composition 10 g contain: apis regina tota Gl Ø 0.01 g (HAB, Method 41c) cichorium intybus e planta tota ferm 33c Ø 0.001 g (HAB, Method 33c) cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) 0.0001 g conchae 0.01 g extract of fragaria vesca, fructus rec. (fruits to extract - 1:5, extraction agent water, saccharose 1:1) 0.05 g fragariae vescae folium sicc. 0.0125 g kalium carbonicum e cinere fagi silvaticae 0.0001 g natrium carbonicum 0.0001 g oxalidis acetosellae herba sicc. 0.005 g pollen combs 0.1 g salviae officinalis folium 0.0125 g spinacia oleracea e radice ferm 34f Ø 0.001 g (HAB, Method 34f) urticae dioicae herba sicc. 0.0125 g vivianite 0.0001 g Excipients: honey, lactose monohydrate, purified water.

PZN 1448607

Price Group T2

Status General sale

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in nervous exhaustion and during convalescence. Contraindications The medicinal product should not be used in the case of known hypersensitivity to honeybee protein, chicory or other plants of the Compositae family, strawberries, pollen, sage, nettles or any of the other ingredients. Warnings and precautions for use This medicinal product contains lactose and a mixture of glucose and fructose (honey). If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Nervennahrung. 1 teaspoonful contains approx. 7 g of a mixture of glucose and fructose equivalent to approx. 0.6 BE (1 BE [bread exchange] - 10-12 g carbohydrate). If you are on a diabetes diet you must take this into account. Nervennahrung can be harmful to the teeth (tooth decay). Dosage and method of administration Unless otherwise directed, take 1 teaspoonful of Nervennahrung in luke warm fluid once to twice daily, preferably in the morning and evening. Duration of treatment The treatment should not take longer than 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

D6 D12 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervi intercostales bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12, D15 and D30: None known.

N1 N1 N1 N1

PZN 2938360 0489857 4626713 2938414

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus abducens Gl

Active ingredient: nervus abducens bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus abducens bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

N1 N1 N1

PZN 2938532 2938578 2938615

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

372

373

N

Nervus accessorius Gl

Active ingredient: nervus accessorius bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1

PZN 2938673 2938727 2938779 2938822

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: nervus accessorius bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus facialis Gl

Active ingredient: nervus facialis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

N

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus facialis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

374

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3355749 3355755 3355761 3355689 3355695 3355703 3355726 2486018 0846748 2496755

Price Group 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus femoralis Gl

Active ingredient: nervus femoralis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2939170 2939193 2939218 2939253 2939282 2939307 2491083

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: nervus femoralis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

375

N

Nervus glossopharyngeus Gl

Active ingredient: nervus glossopharyngeus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus glossopharyngeus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2939371 2939394 2939419 2939454 2939477 2939508 2491108

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus hypoglossus Gl

Active ingredient: nervus hypoglossus bovis GI Liquid dilution for injection

N

Potency/Strength Package Size Size Category D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus hypoglossus bovis Gl dil. D.. 1 ml (HAB, Method 41a)

376

N1 N1 N1 N1

PZN 2939572 2939626 2939661 2939709

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus ischiadicus Gl

Active ingredient: nervus ischiadicus bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus ischiadicus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Adjunctive treatment of low back pain/sciatic nerve pain. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this

N1 N1 N1 N1 N1 N1 N1 N2 N1 N1 N1

PZN 3355169 2830645 3355175 3355181 3355198 3355146 2829837 2939810 2486024 0846754 2496761

Price Group 61 61 61 61 61 61 61 62 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potency D30: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

377

N

Nervus laryngeus recurrens Gl

Active ingredient: nervus laryngeus recurrens bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus laryngeus recurrens bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2939879 2939891 2939922 2939968 2939980 2940003 2491120

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: nervus medianus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus medianus bovis Gl dil. D.. 1 ml (HAB, Method 41a)

378

N1 N1 N1 N1 N1 N1 N1

PZN 2940279 2940291 2940322 2940368 2940380 2940405 2491137

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus oculomotorius Gl

Active ingredient: nervus oculomotorius bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus oculomotorius bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Nervus medianus Gl

N

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2940463 2940492 2940517 2940569 2940581 2940606 2491143

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

379

N

Nervus opticus Gl

Indications according to the anthroposophical understanding of human beings and nature. Degenerative processes of the retina and optic nerve.

Active ingredient: nervus opticus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D6 D8 D10 D12 D15 D30 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus opticus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N2 N1 N1 N1 N1 N1 N2 N1 N1 N1

PZN 3355206 2831685 2940859 3355212 3355229 3355235 3355241 2831260 2940902 2486053 0846760 2496778

Price Group 61 61 62 61 61 61 61 61 62 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

N Nervus opticus comp. Augentropfen Eye drops

Potency/Strength Package Size Size Category

5 x 0,5 ml 30 x 0,5 ml

Composition 0.5 ml contain: arnica montana e planta tota ferm 33c dil. D14 0.05 g (HAB, Method 33c) corpora quadrigemina bovis Gl dil. D5 0.05 g (HAB, Method 41a) nervus oculomotorius bovis Gl dil. D5 0.05 g (HAB, Method 41a)

380

N1 N2

PZN 1448398 1448381

Price Group C C1

Status Pharmacy only Pharmacy only

Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Warnings and precautions for use

Dosage and method of administration Unless otherwise directed, instil 1 drop into the conjunctival sac once to twice daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

The eyes should be examined by an eye specialist before use of the medicinal product. In the case of severe pain in the region of the eyes or sudden deterioration of vision a doctor should be seen immediately.

Nervus peronaeus Gl

Active ingredient: nervus peronaeus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2940954 2940977 2941008 2941043 2941072 2941095 2491539

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: nervus peronaeus bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

nervus opticus bovis Gl dil. D5 0.05 g (HAB, Method 41a) retina et chorioidea bovis Gl dil. D5 0.05 g (HAB, Method 41c) rosae aetheroleum dil. D7 (HAB, Method 5a, sol. D1 with 94% (m/m) alcohol) 0.05 g Excipients: sodium chloride, sodium hydrogen carbonate and water for injections.

381

N

Nervus phrenicus Gl

Duration of treatment The duration of treatment should be discussed with the doctor.

Active ingredient: nervus phrenicus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D6 D30

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus phrenicus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D30 upwards: None known.

N1 N1

PZN 2941149 2941161

Price Group 61 61

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: nervus pudendus bovis GI Liquid dilution for injection

D5 D6 D8 D12 D15 D30 Serial pack

N

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus pudendus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the

382

N1 N1 N1 N1 N1 N1 N1

Nervus radialis Gl

Active ingredient: nervus radialis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus radialis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Nervus pudendus Gl

Potency/Strength Package Size Size Category

PZN 2941221 2941244 2941267 2941310 2941333 2941362 2491605

Price Group 61 61 61 61 61 61 51

Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2941439 2941451 2941474 2941511 2941534 2941557 2491611

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

N Nervus statoacusticus Gl

Active ingredient: nervus statoacusticus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2942019 2942031 2942054 2942077 2942108 2942120 2942143 2486082 2496784

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

383

Composition Liquid dilution for injection: 1 ml contains: nervus statoacusticus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Nervus trigeminus Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

D5 D6 D8 D10 D12 D15 D20 D30 Serial pack I Serial pack II Serial pack III

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus tibialis Gl

Active ingredient: nervus tibialis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

N

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus tibialis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2942226 2942249 2942261 2942309 2942321 2942344 2491686

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: nervus trigeminus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus trigeminus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Adjunctive treatment of trigeminal and facial nerve pain. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

PZN 3355264 2830160 3355301 3355318 3355270 3355287 3355293 2831099 2486113 0846783 2496790

Price Group 61 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potency D30: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this

N

Nervus trochlearis

Active ingredient: nervus trochlearis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus trochlearis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

384

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

N1 N1 N1

PZN 2942551 2942611 2942657

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

385

Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 and D30: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nervus ulnaris Gl

Active ingredient: nervus ulnaris bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nervus ulnaris bovis Gl dil. D.. 1 ml (HAB, Method 41a)

N

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 2942723 2942752 2942775 2942812 2942835 2942858 2491723

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Nervus vagus Gl

Active ingredient: nervus vagus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nicotiana comp.

Liquid dilution for injection

Duration of treatment The duration of treatment should be discussed with the doctor.



Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: carbo vegetabilis dil. D19 aquos. 0.1 g chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in conditions where there is a tendency

386

PZN 3355347 3355353 3355376 3355382 3355399 3355407 2830941 2496809

Composition Liquid dilution for injection: 1 ml contains: nervus vagus bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Side-effects None known.

N1 N1 N1 N1 N1 N1 N1 N1

N1 N2

PZN 1751777 2086218

Price Group 11 12

N

Status Pharmacy only Pharmacy only

towards spasms of the smooth muscle, e.g. wind (flatulence), gastrocardiac symptom complex, irritable bowel (spastic colon), bronchial asthma. Contraindications Do not use in the case of known allergy to chamomile or other plants of the Compositae family. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

387

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to twice daily.

is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Duration of treatment Acute disorders should clear up within 2 weeks. If there

Side-effects None known.

Potency/Strength Package Size Size Category

Composition Globuli velati: 10 g contain: carbo vegetabilis dil. D19 aquos. 0.1 g chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in conditions where there is a tendency towards spasms of the smooth muscle, e.g. wind (flatulence), gastrocardiac symptom complex, irritable bowel (spastic colon), bronchial asthma.

N

Contraindications Do not use in the case of known allergy to chamomile or other plants of the Compositae family.

N1

PZN 8786738

Price Group A

Potency/Strength Package Size Size Category

Pharmacy only

D6 D10 D20

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Nicotiana comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 6 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 to 6 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

388

Composition Globuli velati: 10 g contain: nicotiana tabacum e foliis ferm 33b dil. D.. 1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Nicotiana e foliis.

N1 N1 N1

PZN

Price Group

8786744 8786750 8786767

A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nierentonikum (kidney tonic)

Active ingredient: extract of betula, folium; juniperi pseudo-fructus Syrup

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains:

20 g 20 g 20 g

N

Active ingredient: nicotiana tabacum e foliis ferm 33b Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Side-effects None known.

Status

Nicotiana e foliis

D2 D6 D10 D20 D30

Contraindications None known.

Active ingredient: nicotiana tabacum e foliis ferm 33b Globuli velati

Globuli velati

20 g

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Nicotiana e foliis

Nicotiana comp.



Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1 N1 N1

PZN 2943591 2943622 2943645 2943668 2943680

Potency/Strength Package Size Size Category Price Group 31 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

nicotiana tabacum e foliis ferm 33b dil. D.. 1 ml (HAB, Method 33b)



180 ml 450 ml

Composition 10 g (12 ml) contain: extract (10:1.3) of betula, folium; juniperi pseudo-fructus (5:1.5) (extraction agent: purified water, sucrose, honey, citric acid monohydrate) 10 g

PZN 1181311 1443739

Price Group K6 K7

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the excretory function of the kidneys in urinary tract infections and in metabolic disorders leading to deposits and degenerative changes such as gout, rheumatism, sclerosis.

389

Contraindications Nierentonikum should not be used during pregnancy or by patients with existing renal damage or inflammatory kidney disease. Do not use in the case of hypersensitivity to birch pollen. Warnings and precautions for use Nierentonikum should not be used in children under 12 years without the advice of a doctor and should not be used in place of any other treatment prescribed by the doctor. This medicinal product contains sucrose and a mixture of glucose and fructose (honey). If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Nierentonikum. 1 teaspoonful (5 ml) contains approx. 2 g of a mixture of glucose and fructose equivalent to approx. 0.2 BE (1 BE [bread exchange] = 10-12 g carbohydrate). If you are on a diabetes diet you must take this into account. Nierentonikum can be harmful to the teeth (tooth decay).

Dosage and method of administration Unless otherwise directed, take 1 teaspoonful of syrup, undiluted or diluted with a little water, 2 to 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Prolonged use or overdosage can lead to kidney damage. On account of the ingredient betula pendula (birch leaves) allergic reactions (skin rash, swelling, itching) can occur. In this case use of the medicinal product should be stopped and a doctor consulted.

Potency/Strength Package Size Size Category

N

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nodi lymphatici bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity

390

Active ingredient: nucleus ruber bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: nodi lymphatici bovis GI Liquid dilution for injection

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2831389 3355442 2831053 2830289 2829688 3354810 3354827 2830958 2486194 2496815

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Side-effects None known.

Nucleus ruber

Composition Liquid dilution for injection: 1 ml contains: nucleus ruber bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Nodi lymphatici Gl

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 and D30: None known.

N1 N1 N1

PZN 2943935 2943970 2944053

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nux vomica e semine

Active ingredient: strychnos nux-vomica e semine ferm 35b Liquid dilution for injection Potency/Strength Package Size Size Category D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: strychnos nux-vomica e semine ferm 35b dil. D.. 1 ml (HAB, Method 35b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1

PZN 2944082 2890908 2944107

N Price Group 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Side-effects None known.

391

Nux vomica e semine

Active ingredient: strychnos nux-vomica e semine ferm 35b Globuli velati Potency/Strength Package Size Size Category D3 D4 D6 D12 D30

20 g 20 g 20 g 20 g 20 g

Composition 10 g globuli velati contain: strychnos nux-vomica e semine ferm 35b dil. D.. 1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Nux vomica e semine.

N1 N1 N1 N1 N1

PZN 8786773 8786796 8786804 8786810 8786827

Price Group A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Nux vomica/Nicotiana comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

N



10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: carbo vegetabilis dil. D19 aquos. 0.1 g chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) renes bovis Gl dil. D6 0.1 g (HAB, Method 41a) strychnos nux-vomica e semine ferm 35b dil. D7 0.1 g (HAB, Method 35b)

392

N1

PZN 2233984

Price Group 11

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the respiratory organisation in the region of the metabolism in conditions where there is a tendency to spasms of the smooth muscular hollow organs, e.g. colic, functional intestinal obstruction.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case a doctor should be consulted.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times daily.

Side-effects None known.

Nux vomica/Nicotiana comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: carbo vegetabilis dil. D19 aquos. 0.1 g chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) renes bovis Gl dil. D6 0.1 g (HAB, Method 41a) strychnos nux-vomica e semine ferm 35b dil. D7 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the respiratory organisation in the region of the metabolism in conditions where there is a tendency to spasms of the smooth muscular hollow organs, e.g. colic, functional intestinal obstruction. Contraindications Nux vomica/Nicotiana comp. should not be used in the case of known hypersensitivity to chamomile or other plants of the Compositae family.

N1

PZN 8786833

Price Group A

Status Pharmacy only

Warnings and precautions for use Nux vomica/Nicotiana comp. should not be used in children under 4 years without the advice of a doctor and should not be used in place of any other treatment prescribed by the doctor. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Nux vomica/Nicotiana comp. Dosage and method of administration Unless otherwise directed, Infants and small children up to under 6 years 3-5 globuli velati sublingually once to twice daily; adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If intestinal obstruction does not improve within 2 days a doctor should be consulted. Side-effects None known.

Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein, chamomile or other plants of the Compositae family.

393

N

Oesophagus Gl

Active ingredient: oesophagus suis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2944171 2944194 2944219 2944231 2944254 2944277 2944308 2496821

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: oesophagus suis Gl dil. D.. 1 ml (HAB, Method 41c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Side-effects None known.

Oleum camphoratum comp. Oily solution for injection

Potency/Strength Package Size Size Category

O



10 x 1 ml

N1

PZN 1751783

Price Group 11

Status Pharmacy only

Composition 1 ampoule contains: D-camphor 0.092 g eucalypti aetheroleum 0.0046 g pini aetheroleum 0.0046 g terebinthinae aetheroleum rectificatum 0.0046 g Excipient: refined arachis oil.

circulation, also in febrile, inflammatory disorders of the respiratory organs.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of breathing and

Warnings and precautions for use In rare cases arachis oil can cause severe allergic reactions.

394

Dosage and method of administration Unless otherwise directed, inject 1 ml intramuscularly once a week to once daily. Note: You should not inject the preparation intramuscularly yourself. Please ask your doctor to give you the injection. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be con-

sulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Painful irritation can occur occasionally at the injection site. In this case use of the medicinal product should be stopped and a doctor consulted. In rare cases arachis oil can cause severe allergic reactions.

Oleum Petrae comp. Oily embrocation

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: amygdalae oleum virginale 7.00 g cera flava 0.50 g D-camphor 0.40 g petroleum rectificatum 2.00 g phosphorus 0.001 g Excipient: refined arachis oil. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers via the warmth organisation in chronic deforming joint disorders, e.g. joint inflammation (non-acute arthritis), joint deformation (osteoarthritis).

N1

PZN 1753776

Price Group L1

Status Pharmacy only

Contraindications The medicinal product should not be used • in children under 12 years, • in the case of allergic reactions to the active ingredients, • in the case of damaged skin, e.g. on burns. Warnings and precautions for use In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in 2 to 3 ml of oil (depending on the part of the body affected) once daily, then wrap in a woollen cloth. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

O

Side-effects Contact eczema is possible.

Contraindications The medicinal product should not be used in children under 12 year. The medicinal product must not be used if you are hypersensitive (allergic) to arachis (peanut) oil, peanuts or soy or to any of other ingredients of Oleum camphoratum comp. Bronchial asthma can be negatively influenced through the increased warmth impulse of the medicinal product and the associated effect on the blood vessels.

395

Opal

Organum quadruplex

Active ingredient: opal aquos. Liquid dilution for injection

Globuli velati

Potency/Strength Package Size Size Category D8 D12 D15 D20 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: opal dil. D.. aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D8: Do not use in the case of hypersensitivity to milk protein. Liquid dilution for injection D12 upwards: None known.

N1 N1 N1 N1 N1

PZN 0436513 0436542 0436559 0436571 0436588

Price Group 31 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects Liquid dilution for injection D8: The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions. Liquid dilution for injection D12 upwards: None known.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: cor bovis Gl dil. D4 0.1 g (HAB, Method 41c) hepar bovis Gl dil. D4 0.1 g (HAB, Method 41a) pulmo bovis Gl dil. D4 0.1 g (HAB, Method 41a) renes bovis Gl dil. D4 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism, e.g. in states of weakness and exhaustion, impaired protein building, malnutrition; eczema. Contraindications None known.

N1

PZN 8786862

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Organum quadruplex. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment In acute cases administration of the contents of one pack will often be sufficient. If no improvement occurs a doctor should be consulted. Side-effects None known.

Organum quadruplex Liquid dilution for injection

Potency/Strength Package Size Size Category

O

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cor bovis Gl dil. D7 0.1 g (HAB, Method 41c) hepar bovis Gl dil. D7 0.1 g (HAB, Method 41a) pulmo bovis Gl dil. D7 0.1 g (HAB, Method 41a) renes bovis Gl dil. D7 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism, e.g. in states of weakness and exhaustion, impaired protein building, malnutrition; eczema. Contraindications None known.

396

N1 N2

PZN 1751808 2086247

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If no improvement occurs a doctor should be consulted. Side-effects None known.

Ossicula auditus Gl

Active ingredient: ossicula auditus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ossicula auditus bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the

N1 N1 N1 N1

PZN 2944567 2944610 2944662 2944716

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

397

O

Duration of treatment The duration of treatment should be discussed with the doctor.

Side-effects None known.

Composition Liquid dilution for injection: 1 ml contains: apis regina tota Gl dil. D5 0.1 g (HAB, Method 41c) argentum metallicum dil. D5 0.1 g ovaria bovis Gl dil. D7 0.1 g (HAB, Method 41a)

Ovaria Gl

Active ingredient: ovaria bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ovaria bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

O

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2831722 3354862 2830303 3354879 2831478 3354885 3354891 2830094 2486366 0846837 2496838

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Ovaria comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

398

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1751814 2086276

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the endocrine ovarian functions in hypogonadism, particularly during puberty and the climacteric, e.g. disturbances of menstrual frequency, painful menstrual periods (dysmenorrhoea), menopausal and premenopausal symptoms.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications Do not use in the case of hypersensitivity to bee venom or milk protein.

Ovaria comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: apis regina tota Gl dil. D4 0.1 g (HAB, Method 41c) argentum metallicum dil. D5 0.1 g ovaria bovis Gl dil. D4 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of the endocrine ovarian functions in hypogonadism, particularly during puberty and the climacteric, e.g. disturbances of menstrual frequency, painful menstrual periods (dysmenorrhoea), menopausal and premenopausal symptoms.

N1

PZN 8786879

Price Group A

Status Pharmacy only

Contraindications Do not use in the case of known hypersensitivity to bee venom. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Ovaria comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually twice a week to 1 to 5 times daily. Side-effects None known.

399

O

Ovaria/Argentum

Oxalis e planta tota

Liquid dilution for injection

Active ingredient: oxalis acetosella e planta tota ferm 34b Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 1751820

Price Group 11

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D5 0.1 g ovaria bovis Gl dil. D7 0.1 g (HAB, Method 41a)

Contraindications Do not use in the case of hypersensitivity to animal protein or milk protein.

Indications according to the anthroposophical understanding of human beings and nature. Underfunction of the ovaries, absence of menstruation (amenorrhoea), menopausal deficiency symptoms.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week.

Potency/Strength Package Size Size Category D3 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: oxalis acetosella e planta tota ferm 34b dil. D.. 1 ml (HAB, Method 34b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 2830349 2890920

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Oxalis e planta tota

Active ingredient: oxalis acetosella e planta tota ferm 34b Globuli velati

Ovaria/Argentum Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D5 0.1 g ovaria bovis Gl dil. D4 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose.

O

Indications according to the anthroposophical understanding of human beings and nature. Underfunction of the ovaries, absence of menstruation (amenorrhoea), menopausal deficiency symptoms. Contraindications None known.

N1

PZN 8786885

A

Status Pharmacy only

Warnings and precautions for use In the case of menstrual disorders a doctor should first be consulted for diagnostic evaluation and to rule out pregnancy. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Ovaria/ Argentum. Dosage and method of administration Unless otherwise directed, women 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

400

Price Group

Potency/Strength Package Size Size Category D3 D6

20 g 20 g

Composition Globuli velati: 10 g contain: oxalis acetosella e planta tota ferm 34b dil. D.. 1 g (HAB, Method 34b) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Oxalis e planta tota.

N1 N1

PZN 8786916 8786922

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

401

O

Oxalis e planta tota W 10%, Oleum

Pancreas Gl

Active ingredient: oxalis acetosella e planta tota W 10% Liquid bath additive Potency/Strength Package Size Size Category

100 ml

N1

PZN 2088631

Active ingredient: pancreas suis GI Liquid dilution for injection Price Group N1

Status

Potency/Strength Package Size Size Category

Pharmacy only

D4 D5 D6 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

Composition 10 g (11 ml) contain: oxalis acetosella e planta tota W 10% (HAB, Method 12f with virgin olive oil) 10 g

age groups use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of anabolic metabolic activity, e.g. in tendency to stasis, constipation and a tendency to deposits or stone formation; spasms of the smooth muscle, particularly in the abdominal region; sequelae of shock.

Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor.

Contraindications None known. Warnings and precautions for use During breastfeeding: Do not breastfeed immediately after the bath. Clean the skin in the region of the breasts before breastfeeding.

Side-effects Precipitation of contact allergy after use as bath additive cannot be ruled out. In such cases the treatment should be discontinued and a doctor consulted. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Dosage and method of administration Unless otherwise directed, for adults and children of all

Active ingredient: oxalis acetosella e planta tota LA 20% Tincture for external use



O

100 ml

Composition 10 g (10.3 ml) contain: oxalis acetosella e planta tota LA 20% 10 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of anabolic metabolic activity, e.g. in tendency to stasis, constipation and a tendency to deposits or stone formation; spasms of the smooth muscle, particularly in the abdominal region; sequelae of shock. Contraindications Oxalis-Essenz should not be used in the case of inflamed or injured skin.

402

N1

PZN 1681373

Composition Liquid dilution for injection: 1 ml contains: pancreas suis Gl dil. D.. 1 ml (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of pancreas functions, particularly protein digestion, e.g. disorders of the pancreas, digestive disorders (dyspepsias). Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Oxalis-Essenz

Potency/Strength Package Size Size Category

10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Price Group E

Status Pharmacy only

N1 N1 N1 N2 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829501 2829783 2829429 2945294 3354922 2831426 3354945 3354951 2830177 2486389 0846843 2496844

Price Group 41 61 61 62 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Liquid dilution for injection D4, D5, D6: Hypersensitivity reactions to the protein of the donor animal may occur in sensitised persons. In this case use of the medicinal product should be stopped and a doctor consulted. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Warnings and precautions for use Contains 25% (v/v) alcohol. Dosage and method of administration Unless otherwise directed: Compresses: add 1 tablespoon of Oxalis-Essenz to approx. 250 ml of water and use for compresses. Baths: use 2 to 3 tablespoons of Oxalis-Essenz for 1 full bath. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

P

403

Pancreas/Argentum

Pancreas/Equisetum

Liquid dilution for injection

Globuli velati

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D19 aquos. 0.1 g pancreas suis Gl dil. D16 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Structuring of the metabolic processes in inflammatory disorders of the pancreas with digestive weakness. Contraindications None known.

N1 N2

PZN 2086313 2086336

Price Group 11 12

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only



Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

20 g

N1

PZN 8786939

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: equisetum arvense ex herba ferm 35b dil. D5 0.1 g (HAB, Method 35b) pancreas suis Gl dil. D4 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar).

Dosage and method of administration Unless otherwise directed, children under 6 years 5-10 globuli velati sublingually 3 times daily; adults and children of 6 years and above 10-15 globuli velati sublingually 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Indications according to the anthroposophical understanding of human beings and nature. Structuring of the protein metabolism, particularly in eczema.

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted.

Contraindications None known.

Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Pancreas/Equisetum.

Pancreas/Equisetum Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: equisetum arvense ex herba ferm 35b dil. D5 0.1 g (HAB, Method 35b) pancreas suis Gl dil. D4 0.1 g (HAB, Method 41a)

P

Indications according to the anthroposophical understanding of human beings and nature. Structuring of the protein metabolism, particularly in eczema. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

N1

PZN 1751843

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Side-effects In the case of hypersensitivity reactions to foreign protein treatment with the medicinal product should be discontinued immediately and a doctor consulted.

Pancreas/Meteoreisen Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ferrum sidereum dil. D19 aquos. 0.1 g pancreas suis Gl dil. D5 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego and feeling organisation in the metabolic system, e.g. digestive disorders (dyspepsias), disturbances of protein breakdown, symptoms caused by intestinal gas (flatulence, bloating), malabsorption, disorders of the pancreas. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

404

N1 N2

PZN 2086299 2086307

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case the patient should see a doctor. Side-effects None known.

405

P

Papillae duodeni Gl

Parametrium/Echinacea comp.

Active ingredient: papillae duodeni suis GI Liquid dilution for injection

Liquid dilution for injection

Potency/Strength Package Size Size Category D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: papillae duodeni suis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1

PZN 2945437 2945489 2945532 2945578

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Parametrium (dextrum) Gl

Active ingredient: parametrium dextrum bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D30

P

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: parametrium dextrum bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

406

N1 N1 N1

PZN 2945638 2945673 2945779

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: antimonite dil. D7 0.1 g echinacea pallida e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) ovaria bovis Gl dil. D5 0.1 g (HAB, Method 41a) ovaria bovis Gl dil. D11 0.1 g (HAB, Method 41a) parametrium bovis Gl dil. D5 0.1 g (HAB, Method 41b) parametrium bovis Gl dil. D11 0.1 g (HAB, Method 41b) tuba uterina bovis Gl dil. D5 0.1 g (HAB, Method 41b) tuba uterina bovis Gl dil. D11 0.1 g (HAB, Method 41b) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the body‘s defences and formative forces in pelvic inflammatory disorders, e.g. inflammation of the uterine appendages (adnexitis) and inflammation of the pelvic connective tissue (parametritis). Contraindications Parametrium/Echinacea comp. should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to plants of the Compositae family. Do

N1

PZN 1681226

Price Group 11

Status Pharmacy only

not use in the case of hypersensitivity to animal protein or milk protein. On the basis of fundamental considerations Parametrium/ Echinacea comp. must not be used in progressive systemic diseases such as tuberculosis, leukaemia or leukaemialike diseases, inflammatory diseases of the connective tissue (collagen disorders), multiple sclerosis, AIDS, HIV infections, chronic viral diseases or autoimmune diseases. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Parametrium/Echinacea comp. should not be taken continuously for more than 2 weeks. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions. Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see your doctor.

P

Parathyreoidea comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: glandulae parathyreoideae bovis Gl dil. D7 0.1 g (HAB, Method 41a)

N1

PZN 1751866

Price Group 11

Status Pharmacy only

saccharum sacchari dil. D9 aquos. 0.1 g (HAB, Method 5b) scorodite dil. D5 0.1 g

407

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the functional relationships between the metabolic-limb system and the nerve-sense system in tetaniform states which are not of organic origin.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week to 1 to 3 times daily.

Parathyreoidea/Aurum Potency/Strength Package Size Size Category

Contraindications Do not use in the case of hypersensitivity to milk protein.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Parathyreoidea comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: glandulae parathyreoideae bovis Gl dil. D7 0.1 g (HAB, Method 41a) saccharum sacchari dil. D9 aquos. 0.1 g (HAB, Method 5b) scorodite dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the functional relationships between the metabolic-limb system and the nerve-sense system in cramp-like (tetaniform) states which are not of organic origin.

P

Contraindications None known. Warnings and precautions for use In view of the indication the medicinal product should only be used in children under 12 years after consulting a doctor.

N1

PZN 8786951

Price Group A

Status Pharmacy only

This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Parathyreoidea comp. Dosage and method of administration Unless otherwise directed, children up to 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection



10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g glandulae parathyreoideae bovis Gl dil. D7 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation and harmonisation of the rhythmic system in the case of a tendency to cramps, e.g. cramp-like states, neurovegetative dysregulation. Contraindications Do not use in the case of hypersensitivity to milk protein.

N1

PZN 1751872

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to twice daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Parathyreoidea/Aurum Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g glandulae parathyreoideae bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation and harmonisation of the rhythmic system in the case of a tendency to cramps, e.g. cramp-like (tetaniform) states, neurovegetative dysregulation. Contraindications None known.

N1

PZN 8786968

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Parathyreoidea/Aurum. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 to 5 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects None known.

408

409

P

Pars pallida Gl

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Active ingredient: pars pallida bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D6 D8 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pars pallida bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1

PZN 2946201 4621940 2946224

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Passiflora/Avena comp., Suppositorien see Passiflora Zäpfchen

see Passiflora Kinderzäpfchen

Passiflora comp.

Potency/Strength Package Size Size Category

P

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) passiflora caerulea ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) salix alba ssp. vitellina e cortice et foliis ferm 33d dil. D2 0.1 g (HAB, Method 33d)

410

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) passiflora caerulea ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) salix alba ssp. vitellina e cortice et foliis ferm 33d dil. D2 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar).

Contraindications Do not use in the case of hypersensitivity to willow bark.

Liquid dilution for injection

N1

PZN 1751889

Price Group 11

Status Pharmacy only

Side-effects Hypersensitivity reactions may occur in sensitised persons. In this case use of the medicinal product should be stopped and a doctor consulted.

Passiflora comp.

Indications according to the anthroposophical understanding of human beings and nature. Sleep disturbances, nervous anxiety, cardiophobia.

Passiflora/Avena comp., Suppositorien für Kinder



Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily, to promote sleep 1 ml injected subcutaneously in the evening.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Passiflora comp.

N1

PZN 8786974

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 times daily. To promote sleep, depending on age 5-20 globuli velati sublingually in the evening. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may occur in sensitised persons. In this case use of the medicinal product should be stopped and a doctor consulted.

P

Indications according to the anthroposophical understanding of human beings and nature. Sleep disturbances, nervous anxiety, cardiophobia. Contraindications Do not use in the case of hypersensitivity to willow bark.

411

Passiflora Nerventonikum (nerve tonic)

Passiflora Kinderzäpfchen

Syrup

Potency/Strength Package Size Size Category

90 ml 180 ml

Composition 10 g contain: hypericum perforatum ex herba ferm 33c dil. D2 0.05 g (HAB, Method 33c) salix alba ssp. vitellina e cortice et foliis ferm 33d dil. D2 0.0167 g (HAB, Method 33d) salix purpurea e cortice et foliis ferm 33d dil. D2 0.0167 g (HAB, Method 33d) salix viminalis e cortice et foliis ferm 33d dil. D2 0.0167 g (HAB, Method 33d) aqueous extract with sugar of avena sativa, herba rec. (plant : water : sugar = 2 : 3.5 : 4.5) 4.00 g aqueous extract with sugar and citric acid of crataegus laevigata/monogyna, fructus rec. (plant : water : sugar : citric acid = 3 : 4.87 : 2.08 : 0.05) 2.00 g aqueous extract with sugar of humulus lupulus, herba et fructus rec. (plant : water : sugar = 2 : 3.5 : 4.5) 1.50 g aqueous extract with sugar of passiflora caerulea, herba rec. (plant : water : sugar = 2 : 3.5 : 4.5) 0.50 g aqueous extract with sugar of valeriana officinalis, radix rec. (plant : water : sugar = 2 : 3.5 : 4.5) 1.50 g Excipient: purified water.

P

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the life organisation and harmonisation of its interaction with the feeling organisation in the case of lack of vitality or nervous weakness, e.g. sleep disturbances and states of anxiety or agitation. Contraindications The medicinal product should not be used in the case of known hypersensitivity to oats, hops or valerian or any of

PZN 1119967 1443745

Paediatric suppositories Price Group K4 K5

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only



the other ingredients. Do not use Passiflora Nerventonikum if you suffer from the rare hereditary fructose intolerance, from glucosegalactose malabsorption or from sucrase-isomaltase deficiency. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Passiflora Nerventonikum. 1 teaspoonful (5 ml) of syrup is equivalent to 0.2 BE (1 BE [bread exchange] = 10 – 12 g carbohydrate). If you are on a diabetes diet you must take this into account. Passiflora Nerventonikum can be harmful to the teeth (tooth decay). Warning for people with gluten intolerance: Passiflora Nerventonikum contains gluten. Dosage and method of administration Unless otherwise directed: For sleep disorders: 1 to 3 teaspoonfuls of syrup in a little warm water taken in small sips at bedtime. For nervous restlessness: 2 teaspoonfuls of syrup, undiluted or diluted with a little water, 3 times daily. Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. As children under two years have often not yet developed a stable sleep/waking rhythm, difficulty falling asleep or waking during the night are not necessarily pathological symptoms requiring treatment. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may occur in rare cases.

10 x 1 g

Composition 1 suppository (1 g) contains: avena sativa ferm 33c Ø 10 mg (HAB, Method 33c) humulus lupulus ex herba et fructibus ferm 34d Ø 10 mg (HAB, Method 34d) passiflora caerulea ex herba ferm 33c Ø 2 mg (HAB, Method 33c) valeriana officinalis e radice ferm 33c Ø 10 mg (HAB, Method 33c) Ingredients 1 to 4 are concentrated to 10 mg. Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Sleep disturbances and anxiety states. Contraindications None known.

PZN 1448429

Price Group O

Status Pharmacy only

Warnings and precautions for use Warning for people with gluten intolerance: Passiflora Kinderzäpfchen contain gluten. Dosage and method of administration Unless otherwise directed, 1 suppository introduced into the rectum in the evening. Note: Passiflora Kinderzäpfchen are paediatric suppositories intended for use in infants and children up to 7 years. Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. As children under two years have often not yet developed a stable sleep/waking rhythm, difficulty falling asleep or waking during the night are not necessarily pathological symptoms requiring treatment. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Passiflora Zäpfchen Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: avena sativa ferm 33c Ø 20 mg (HAB, Method 33c) humulus lupulus ex herba et fructibus ferm 34d Ø 20 mg (HAB, Method 34d) passiflora caerulea ex herba ferm 33c Ø 4 mg (HAB, Method 33c) valeriana officinalis e radice ferm 33c Ø 20 mg (HAB, Method 33c) Ingredients 1 to 4 are concentrated to 20 mg. Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Sleep disturbances and states of anxiety.

412

N1

N1

PZN 1448406

Price Group P

Status Pharmacy only

Contraindications None known. What should you know if you are pregnant or breastfeeding? Because of the valepotriates contained in valerian (valeriana officinalis), Passiflora Zäpfchen should not be used during pregnancy or while breastfeeding. Warnings and precautions for use Warning for people with gluten intolerance: Passiflora Zäpfchen contain gluten. Dosage and method of administration Unless otherwise directed, 1 suppository introduced into the rectum in the evening. Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within 2 to 3 days a doctor should

413

P

be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects None known.

Duration of treatment The duration of treatment should be discussed with the doctor.

Patella Gl

Pericardium Gl

Active ingredient: patella bovis GI Liquid dilution for injection

Active ingredient: pericardium bovis GI Liquid dilution for injection

Potency/Strength Package Size Size Category D5 D8

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: patella bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8: None known.

N1 N1

PZN 4621963 4621992

Price Group 61 61

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Active ingredient: penis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

P

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: penis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

414

N1 N1 N1

PZN 2946589 2946632 2946715

Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pericardium bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Side-effects None known.

Penis Gl

D5 D8 D30

Side-effects None known.

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. On account of its composition the medicinal product is only for use in male patients. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2946773 2946804 2946827 2946856 2946879 2946891 2946922 2496867

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Periodontium Gl

Active ingredient: periodontium bovis GI Liquid dilution for injection

P

Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2946980 2947005 2947028 2947040 2947063 2947092 2947146 2496873

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

415

Composition Liquid dilution for injection: 1 ml contains: periodontium bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Chiefly inflammatory disorder of the supporting structures of the teeth (periodontitis), particularly after acute inflammation has subsided.

Periodontium/Silicea comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

P

10 x 1 ml 50 x 1 ml

N1 N2

PZN 2086394 2086402

Price Group 11 12

Pharmacy only Pharmacy only

man beings and nature. Chiefly inflammatory disorder of the supporting structures of the teeth (periodontitis) in the reactive inflammatory stage.

Indications according to the anthroposophical understanding of hu-

Side-effects None known.

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, 1 ml twice a week to once daily by subcutaneous or submucosal injection into the recess between the cheek and gums. You should not inject the medicinal product yourself. Please ask your doctor to give you the injection.

Liquid dilution for injection

416

10 x 1 ml 50 x 1 ml

N1 N2

PZN 2086419 2086425

Price Group 11 12

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, 1 ml twice a week to once daily by subcutaneous or submucosal injection into the recess between the cheek and gums. You should not inject the medicinal product yourself. Please ask your doctor to give you the injection. Side-effects None known.

Periosteum Gl

Active ingredient: periosteum bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: periosteum bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Periodontium/Stannum comp. Potency/Strength Package Size Size Category

Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein.

Status

Composition Liquid dilution for injection: 1 ml contains: argentum nitricum dil. D20 aquos. 0.1 g (HAB, Method 5b) atropa belladonna ex herba ferm 33a dil. D14 0.1 g (HAB, Method 33a) gingiva bovis Gl dil. D16 0.1 g (HAB, Method 41b) mandibula feti bovis Gl dil. D16 0.1 g (HAB, Method 41b) maxilla feti bovis Gl dil. D16 0.1 g (HAB, Method 41b) peridontium bovis Gl dil. D16 0.1 g (HAB, Method 41b) quartz dil. D21 aquos. 0.1 g



Composition Liquid dilution for injection: 1 ml contains: gingiva bovis Gl dil. D5 0.1 g (HAB, Method 41b) hypophysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) mandibula feti bovis Gl dil. D5 0.1 g (HAB, Method 41b) maxilla feti bovis Gl dil. D5 0.1 g (HAB, Method 41b) periodontium bovis Gl dil. D5 0.1 g (HAB, Method 41b) stannum metallicum dil. D14 aquos. 0.1 g

Status Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3354974 2830042 3354980 3354997 2831768 2829470 3354968 2496896

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

417

P

Peritonaeum Gl

Petasites comp.

Active ingredient: peritonaeum bovis GI Liquid dilution for injection

Globuli velati

Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2947301 2947324 2947347 2947376 2947399 2947413 2947442 2496904

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: peritonaeum bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

P

Composition Liquid dilution for injection: 1 ml contains: abies alba e summitatibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) petasites hybridus e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) plantago lanceolata e foliis ferm 34c dil. D2 0.1 g (HAB, Method 34c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the respiratory system, for adjuvant treatment of bronchitis and pneumonia (bronchopneumonia).

418

20 g

N1

PZN 8786980

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: abies alba e summitatibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) petasites hybridus e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) plantago lanceolata e foliis ferm 34c dil. D2 0.1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar).

Dosage and method of administration Unless otherwise directed, infants and children under 6 years 3-5 globuli velati sublingually 3 to 6 times daily; children from 6 to under 12 years 5-7 globuli velati sublingually 3 to 6 times daily; adults and children of 12 years and above 5-10 globuli velati sublingually 3 to 6 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in the respiratory system, for adjuvant treatment of bronchitis and pneumonia (bronchopneumonia).

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications None known.

Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Petasites comp.

Active ingredient: pharynx bovis GI Liquid dilution for injection

Liquid dilution for injection

10 x 1 ml 50 x 1 ml



Pharynx Gl

Petasites comp.



Potency/Strength Package Size Size Category

N1 N2

PZN 1751895 2086431

Price Group 11 12

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only

D5 D6 D8 D10 D12 D15 D30 Serial pack II

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to twice daily.

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2947502 2947525 2947548 2947560 2947583 2947614 2947637 0846932

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. Side-effects None known.

419

P

Composition Liquid dilution for injection: 1 ml contains: pharynx bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Composition 10 globuli velati contain: phosphorus dil. D.. 1g Contains sucrose (saccharose/sugar).

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Phosphorus. Dosage and method of administration D8: Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and

Phosphorus

Active ingredient: phosphorus Liquid dilution for injection Potency/Strength Package Size Size Category D8 D12 D15 D20 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Contraindications None known.

N1 N1 N1 N1 N1

PZN 2948275 2948298 2948312 2948335 2948358

Price Group 31 31 31 31 31

children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. D12: Unless otherwise directed, infants 3 globuli velati sublingually once to twice daily, children up to 6 years 3-7 globuli velati sublingually once to twice daily, adults and children of 6 years and above 5-10 globuli velati sublingually once to twice daily. D30: Unless otherwise directed, infants 3 globuli velati sublingually once daily, children up to 6 years 3-7 globuli velati sublingually once daily, adults and children of 6 years and above 5-10 globuli velati sublingually once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Pia mater encephali Gl

Active ingredient: pia mater encephali bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: phosphorus dil. D.. 1 ml Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

P

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this

medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: phosphorus Globuli velati Potency/Strength Package Size Size Category

420

20 g 20 g 20 g

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pia mater encephali bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Phosphorus

D8 D12 D30

D5 D6 D8 D10 D12 D15 D30 Serial pack II

N1 N1 N1

PZN 8787011 8787028 8787034

Price Group A A A

Status

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2948418 2948430 2948453 2948482 2948507 2948536 2948559 0846949

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Pharmacy only Pharmacy only Pharmacy only

421

P

Duration of treatment The duration of treatment should be discussed with the doctor.

Composition Liquid dilution for injection: 1 ml contains: placenta bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Pinus pumilio, Oleum aethereum 10% Active ingredient: pini pumilionis aetheroleum 10% Liquid bath additive Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: pini pumilionis aetheroleum 10% (HAB, Method 12h with virgin olive oil) 10 g Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of hypersensitivity to pine needle oil or in the case of bronchial asthma, whooping cough or other airway diseases associated with pronounced hypersensitivity of the airways. Dosage and method of administration Unless otherwise directed, use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths.

PZN

Price Group

2088660

N1

Status General sale

The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects Increased irritation of skin and mucous membranes can very rarely occur. In such cases use of Pinus pumilio, Oleum aethereum 10% should be discontinued and a doctor consulted. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Placenta (bovis) Gl

Active ingredient: placenta bovis GI Liquid dilution for injection

P

Potency/Strength Package Size Size Category D5 D5 D6 D6 D8 D8 D12 D15 D30 D30 Serial pack

422

10 x 1 ml 50 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N2 N1 N2 N1 N2 N1 N1 N1 N2 N1

PZN 3353331 2948594 3353348 2948602 3353354 2948619 3353377 3353383 3353408 2948654 2491870

Price Group 61 62 61 62 61 62 61 61 61 62 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Plantago Bronchialbalsam (bronchial balm) Ointment

Potency/Strength Package Size Size Category

30 g 100 g

Composition 10 g contain: cera flava 1.5 g D-camphor 0.2 g drosera e planta tota ferm 33c dil. D3 0.1 g (HAB, Method 33c) eucalypti aetheroleum 0.05 g petasites hybridus e radice ferm 33c dil. D1 0.1 g (HAB, Method 33c) plantago lanceolata e foliis ferm 34c dil. D1 0.1 g (HAB, Method 34c) terebinthina laricina 0.5 g thymi aetheroleum 0.05 g Excipients: refined arachis (peanut) oil, ethanol (96%), purified water, wool fat. Indications according to the anthroposophical understanding of human beings and nature. Catarrhal, inflammatory disorders of the airways.

N1 N2

PZN 2198466 2198472

Price Group J J1

Status Pharmacy only Pharmacy only

Contraindications Do not use • in children under 2 years • in the case of hypersensitivity to eucalyptus oil, cineole, thyme or other labiates (plants of the lamiaceae family), birch, mugwort, celery or any of the other active ingredients. • if you are hypersensitive (allergic) to peanuts or soy or to any of the other ingredients • in the case of bronchial asthma or other airway disorders associated with pronounced hypersensitivity of the airways. The medicinal product must not be applied to diseased skin, open wounds or damaged skin. Warnings and precautions for use Breastfeeding mothers should not apply the medicinal product in the region of the breasts. Wool fat can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub the ointment into the chest and back once to twice daily; in the case of chronic bronchitis use at least twice a week.

423

P

Duration of treatment The condition should have cleared up within 2 weeks. If acute inflammation does not improve within 2 days a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor.

Side-effects Eczema, skin rashes, skin redness, exanthems, contact dermatitis and allergies may very rarely occur when using the medicinal product. Skin irritation or hypersensitivity reactions of the skin may rarely occur. In rare cases arachis oil can cause severe allergic reactions. In such cases treatment with the medicinal product must be discontinued and a doctor consulted.

Plantago Hustensaft (cough mixture) Syrup

Potency/Strength Package Size Size Category

90 ml

Composition 10 g (8.5 ml) contain: petasites hybridus e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) aqueous extract with sugar (1:1) of 0.3 g picea abies, summitates rec. (4:1) 1.5 g aqueous extract with sugar (1:1) of 0.7 g plantago lanceolata, folium rec. (4:1) 3.5 g Excipients: sucrose, purified water. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of respiratory and mucus-forming processes in catarrhal, inflammatory disorders of the airways and to promote coughing up of phlegm (expectoration), e.g. in bronchitis, pneumonia (bronchopneumonia), bronchial asthma.

P

Contraindications As a general precaution, anyone allergic to plantain pollen should not take Plantago Hustensaft. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should

N1

PZN 1448435

Price Group J

Status Pharmacy only

consult your doctor before taking Plantago Hustensaft. If you are on a diabetes diet you must take the following into account: 1 tablespoonful (15 ml = 17.7g) of syrup is equivalent to 0.6 BE (= 7.1 g sugar). 1 teaspoonful (5 ml = 5.9 g) of syrup is equivalent to 0.2 BE (= 2.4 g sugar). Plantago Hustensaft can be harmful to the teeth (tooth decay). Dosage and method of administration Unless otherwise directed, infants and small children under 6 years 1 teaspoonful (5 ml) of syrup in warm water 3 to 4 times daily; adults and children of 6 years and above 1 tablespoonful (15 ml) of syrup in warm water 3 times daily, in acute cases 1 teaspoonful (5 ml) of syrup in warm water every 2 hours. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

424

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1751932 2086448

Price Group 11 12

Contraindications Do not use in the case of hypersensitivity to milk protein or platinum. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times weekly to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Platinum chloratum/Pancreas comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: carbo vegetabilis dil. D5 0.1 g cichorium intybus e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) pancreas suis Gl dil. D7 0.1 g (HAB, Method 41a) platinum chloratum dil. D5 aquos. 0.1 g (HAB, Method 5b) Contains sucrose (saccharose/sugar) and lactose.

Contraindications None known.

Liquid dilution for injection



Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the digestive and intermediate digestive activity in weakness of the pancreas.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the digestive and intermediate digestive activity in weakness of the pancreas.

Platinum chloratum/Pancreas comp. Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: carbo vegetabilis dil. D5 0.1 g cichorium intybus e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) oxalis acetosella e planta tota ferm 34b dil. D2 0.1 g (HAB, Method 34b) pancreas suis Gl dil. D7 0.1 g (HAB, Method 41a) platinum chloratum dil. D5 aquos. 0.1 g (HAB, Method 5b)

N1

PZN 8787057

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Platinum chloratum/Pancreas comp. Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually twice a week to 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 4 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Status Pharmacy only Pharmacy only

425

P

Platinum metallicum

therefore only be used in children under 12 years after consulting a doctor.

Active ingredient: platinum metallicum aquos. Globuli velati Potency/Strength Package Size Size Category D6 D30

20 g 20 g

Composition Globuli velati: 10 g contain: platinum metallicum dil. D.. aquos. 1g Contains sucrose (saccharose/sugar) and lactose. Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Platinum metallicum.

N1 N1

PZN 8787063 8787092

Price Group A A

Status

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

P

Composition Liquid dilution for injection: 1 ml contains: pleura bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

426

Active ingredient: plexus brachialis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: pleura bovis Gl Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Plexus brachialis Gl

Composition Liquid dilution for injection: 1 ml contains: plexus brachialis bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Potency/Strength Package Size Size Category N1 N1 N1 N1 N1 N1 N1 N1

PZN 2948789 2948803 2948832 2948855 2948878 2948890 2948915 2496933

Price Group 61 61 61 61 61 61 61 51

Side-effects None known.

Pharmacy only Pharmacy only

Pleura Gl

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Duration of treatment The duration of treatment should be discussed with the doctor.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3355028 3355034 3355040 3355057 3355063 3355086 3355100 2496979

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

P

Plexus cardiacus Gl

Active ingredient: plexus cardiacus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2949524 2949547 2949576 2949613 2949642 2949665 2491887

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

427

Composition Liquid dilution for injection: 1 ml contains: plexus cardiacus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Plexus gastricus Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

D5 D6 D8 D12 D15 D30 Serial pack

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: plexus coeliacus bovis GI Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack III

P

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: plexus gastricus bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Plexus coeliacus Gl

Potency/Strength Package Size Size Category

Active ingredient: plexus gastricus bovis GI Liquid dilution for injection

PZN 2949725 2949748 2949760 2949783 2949814 2949837 2949866 2496985

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Active ingredient: plexus rectalis bovis GI Liquid dilution for injection

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

D5 D6 D12 D30

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: plexus rectalis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the

428

PZN 4626848 4626860 4626883 4626937 4626966 4626989 2491901

Plexus haemorrhoidalis Gl

Composition Liquid dilution for injection: 1 ml contains: plexus coeliacus bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

N1 N1 N1 N1

PZN 0490808 0490814 0490837 0490866

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

donor animal protein. Liquid dilution for injection D12 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

429

P

Duration of treatment The duration of treatment should be discussed with the doctor.

Composition Liquid dilution for injection: 1 ml contains: plexus pelvinus bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Plexus lumbalis Gl

Active ingredient: plexus lumbalis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2951113 2951142 2951165 2951188 2951202 2951225 2951248 2496991

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Composition Liquid dilution for injection: 1 ml contains: plexus lumbalis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Side-effects None known.

Active ingredient: plexus pelvinus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

430

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2951917 2951946 2951969 2952006 2952029 2952041 2492013

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Plexus pulmonalis (Nervus vagus) Gl

Active ingredient: plexus pulmonalis, nervus vagus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: plexus pulmonalis, nervus vagus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Plexus pelvinus Gl

P

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 2952302 2952325 2952348 2952360 2952383 2952414 2952437 2497016

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

431

P

Plexus rectalis GI

Composition Liquid dilution for injection: 1 ml contains: pons bovis Gl dil. D.. 1 ml (HAB, Method 41a)

see Plexus haemorrhoidalis GI

Plexus sacralis Gl

Active ingredient: plexus sacralis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: plexus sacralis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 4622537 2952905 2952928 2952963 4626742 2952992 2492214

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Pons Gl

Active ingredient: pons bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

P

D5 D6 D8 D12 D15 D30 Serial pack

432

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 2953655 2953678 2953690 2953738 2953750 2953773 2492243

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Primula comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: conchae dil. D9 0.1 g hyoscyamus niger ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) onopordum acanthium e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) primula veris e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Disturbances of autonomic rhythms and their coordination, e.g. orthostatic dysregulation, functional heart complaints and symptoms related to low blood pressure. Contraindications Do not use in the case of hypersensitivity to milk protein, primulas, thistles or other plants of the Compositae family.

N1 N2

PZN 1751949 2086454

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use There is no adequately documented experience of use Primula comp. in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions. Hypersensitivity reactions may occur in sensitised persons. In this case use of the medicinal product should be stopped and a doctor consulted.

433

P

Primula comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: conchae dil. D9 0.1 g hyoscyamus niger ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) onopordum acanthium e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) primula veris e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of autonomic rhythms and their coordination, e.g. orthostatic dysregulation, functional heart complaints and symptoms related to low blood pressure. Contraindications Do not use in the case of hypersensitivity to primulas, thistles and other plants of the Compositae family. Warnings and precautions for use Sufficiently documented experience for the use of this

N1

PZN 8787117

Price Group A

Status Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 1 year. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Primula comp. Dosage and method of administration Unless otherwise directed, children from 1 to 6 years 3-5 globuli velati sublingually 3 times daily; children from 6 to 12 years 5-7 globuli velati sublingually 3 times daily; adults and children of 12 years and above 5-10 globuli velati sublingually 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Hypersensitivity reactions may occur in sensitised persons. In this case use of the medicinal product should be stopped and a doctor consulted.

Primula/Convallaria comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

P

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: conchae dil. D9 0.1 g convallaria majalis e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) cor bovis Gl dil. D7 0.1 g (HAB, Method 41c) hyoscyamus niger ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) onopordum acanthium e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c)

434

N1

PZN 1751955

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Primula/Convallaria comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: conchae dil. D9 0.1 g convallaria majalis e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) cor bovis Gl dil. D7 0.1 g (HAB, Method 41c) hyoscyamus niger ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) onopordum acanthium e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) primula veris e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) urginea maritima var. rubra e bulbo ferm 33b dil. D2 0.1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar) and lactose.

N1

PZN 8787146

Price Group A

Status Pharmacy only

Contraindications The medicinal product should not be used in the case of hypersensitivity to primula flowers (cowslip flowers). Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Primula/ Convallaria comp. Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 2 to 5 times daily. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of cardiac activity, e.g. beginning decline in cardiac performance (heart failure), functional rhythm disturbances.

P

primula veris e floribus ferm 33c dil. D2 0.1 g (HAB, Method 33c) urginea maritima var. rubra e bulbo ferm 33b dil. D2 0.1 g (HAB, Method 33b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of cardiac activity, e.g. beginning heart failure, functional rhythm disturbances. Contraindications Do not use in the case of hypersensitivity to milk protein or to primula flowers.

435

Primula Muskelnähröl (muscle oil) Oily embrocation

Potency/Strength Package Size Size Category

100 ml

Composition 110 g (11 ml) contain: hyoscyamus niger ex herba ferm 33d Ø 0.1 mg (HAB, Method 33d) myocardium bovis Gl dil. D7 0.1 mg (HAB, Method 41c) oily extract of hypericum perforatum, herba rec. (4:1), extraction agent: refined arachis oil 1.0 g primula veris e floribus W 5% (HAB, Method 12g with refined arachis oil) 4.5 g quartz 0.001 mg rosmarini aetheroleum 0.03 g Excipients: refined arachis oil, cacao butter. Indications according to the anthroposophical understanding of human beings and nature. Simulation of metabolic processes in muscular weakness and muscle wasting as a result of neurological and primarily muscular disorders as well as after prolonged immobilisation.

N1

PZN 1753782

Price Group L1

Status Pharmacy only

Contraindications Do not apply the oil to wounds, acutely inflamed or eczematous skin. In the case of hypersensitivity to cowslip (primula veris) the medicinal product should only be used after consulting a doctor. Warnings and precautions for use Primula Muskelnähröl should not be used without the advice of a doctor and should not be used in place of any other treatment prescribed by the doctor. In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in 2 to 3 ml of oil 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Photosensitisation or redness of the skin may very rarely occur; in such cases use of the medicinal product should be discontinued. In rare cases arachis oil can cause severe allergic reactions.

Prostata Gl

Active ingredient: prostata bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

P

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3355123 3354483 2830237 3354508 3354514 2831521 3354520 3354537 0847009 2497022

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: prostata bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. On account of its composition the medicinal product is only for use in male patients. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Prunus-Essenz

Active ingredient: prunus spinosa e fructibus LA 25% Tincture for external use Potency/Strength Package Size Size Category

100 ml

Composition 10 g (10.2 ml) contain: prunus spinosa e fructibus LA 25% 10 g (HAB, Method 12o) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism, particularly in states of exhaustion and prolonged convalescence, sclerosing diseases as an expression of weakness of the metabolic limb system. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Contains 25% (v/v) alcohol.

N1

Price Group J

Status Pharmacy only

Dosage and method of administration Unless otherwise directed: Compresses: add 1 to 2 teaspoons of Prunus-Essenz to approx. 125 ml water and use for compresses. Sitzbaths: use 1 to 2 tablespoons of Prunus-Essenz for 1 sitzbath. Full baths: use 2 to 3 tablespoons of Prunus-Essenz for 1 full bath. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Prunus spinosa e floribus et summitatibus

Active ingredient: prunus spinosa e floribus et summitatibus ferm 33d Ø Liquid dilution for injection Potency/Strength Package Size Size Category 5%

436

PZN 1753977

10 x 1 ml

N1

PZN 3358392

Price Group 31

Status Pharmacy only

437

P

Composition Liquid dilution for injection: 1 ml contains: prunus spinosa e floribus et summitatibus ferm 33d Ø 0.05 g (HAB, Method 33d) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily.

Composition Globuli velati: 10 g contain: prunus spinosa e floribus et summitatibus ferm 33d dil. D.. 1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar).

Duration of treatment The duration of treatment should be discussed with the doctor.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Side-effects None known.

Contraindications None known.

medicinal product in children is not available. It should therefore not be used in children under 12 years.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Prunus spinosa e floribus et summitatibus.

Prunus spinosa e floribus et summitatibus

Active ingredient: prunus spinosa e floribus et summitatibus ferm 33d Liquid dilution for injection Potency/Strength Package Size Size Category D2 D3 D6

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: prunus spinosa e floribus et summitatibus ferm 33d dil. D.. 1 ml (HAB, Method 33d) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

N1 N1 N1

PZN 3358363 3358386 2830355

Price Group 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this

P

Active ingredient: prunus spinosa e floribus et summitatibus ferm 33d Globuli velati Potency/Strength Package Size Size Category D2 D3 D6

438

20 g 20 g 20 g

N1 N1 N1

PZN 8787152 8787169 8787175

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Prunus spinosa e floribus W 5%, Oleum Active ingredient: prunus spinosa e floribus W 5% Liquid bath additive

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: prunus spinosa e floribus W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism, particularly in nervous exhaustion, neurovegetative dysregulation, tendency to colds, asthenia. Contraindications None known.

Prunus spinosa e floribus et summitatibus

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Warnings and precautions for use During breastfeeding: Do not breastfeed immediately after the bath. Cleanse the skin in the region of the breasts before breastfeeding.

PZN

Price Group

2088708

N1

Status General Sale

Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive (about 1/2-1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. Use correspondingly less for partial baths. The temperature of the bath water should be between 35° and 37°, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly, in acute conditions daily baths may, however, also be beneficial; acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

439

P

Prunuseisen

Pulmo Gl

Active ingredient: prunus spinosa e floribus et summitatibus ferm cum ferro Liquid dilution for injection Potency/Strength Package Size Size Category D6

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: prunus spinosa e floribus et summitatibus ferm cum ferro dil. D6 1 ml (HAB, Method 37a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation in the anabolic metabolism, e.g. in conditions of weakness or exhaustion, convalescence, low blood pressure (hypotension), for adjunctive treatment of anaemia.

N1

PZN 1751961

Price Group 11

Active ingredient: pulmo bovis GI Liquid dilution for injection Status

Potency/Strength Package Size Size Category

Pharmacy only

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously twice a week to once daily; children from 6 to under 12 years: 0.5-1 ml injected subcutaneously twice a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment For treatment of acute conditions administration of the contents of one pack is often sufficient. If this is not the case a doctor should be consulted. Side-effects None known.

Contraindications None known.

Active ingredient: prunus spinosa e floribus et summitatibus ferm cum ferro dil. D3 Globuli velati

D3

20 g

Composition Globuli velati: 10 g contain: prunus spinosa e floribus et summitatibus ferm cum ferro dil. D3 1 g (HAB, Method 37a) Contains sucrose (saccharose/sugar).

P

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation in the anabolic metabolism, e.g. in conditions of weakness or exhaustion, convalescence, anaemia, low blood pressure (hypotension). Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Prunuseisen.

N1

PZN 8787181

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati 3 times daily, children of 6 to under 12 years 5-10 globuli velati 3 times daily, adults and children of 12 years and above 10-15 globuli velati 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

Composition Liquid dilution for injection: 1 ml contains: pulmo bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Prunuseisen

Potency/Strength Package Size Size Category

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3354626 3354632 2830846 3354649 3354572 3354589 3354595 3354603 2487259 0847015 2497039

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Pulmo/Ferrum

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ferrum metallicum dil. D7 0.1 g pulmo bovis Gl dil. D16 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of form and function in the region of the lungs, e.g. pneumonia, bronchitis.

N1 N2

PZN 2086483 2086508

Price Group 11 12

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, children up to 6 years 0.5 ml injected subcutaneously 2 to 3 times a week to once daily; children up to 12 years 0.5-1 ml injected subcutaneously 2 to 3 times a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week to once daily. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications Do not use in the case of hypersensitivity to milk protein.

440

441

P

Pulmo/Mercurius

Pulmo/Tartarus stibiatus II

Liquid dilution for injection

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: mercurius vivus dil. D14 aquos. 0.1 g pulmo bovis Gl dil. D5 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the reorganisation of the organ lung in inflammatory processes, particularly in phases of increased production of secretions and tissue proliferation, e.g. bronchitis, pneumonia (bronchopneumonia) and sequelae such as over-inflation of the air sacs in the lungs (emphysema).

N1 N2

PZN 2086514 2086520

Price Group 11 12

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only



Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pulmo bovis Gl dil. D16 0.1 g (HAB, Method 41a) tartarus stibiatus dil. D7 aquos. 0.1 g (HAB, Method 5b) Indications according to the anthroposophical understanding of human beings and nature. Structuring and reorganisation of the anabolic metabolism in inflammatory disorders of the airways, e.g. acute forms of bronchitis, pneumonia (bronchopneumonia).

N1 N2

PZN 1223630 1223647

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously once to twice daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously once to twice daily; adults and children of 12 years and above 1 ml injected subcutaneously once to twice daily. Side-effects None known.

Pulmo/Vivianit comp. Liquid dilution for injection

Pulmo/Tartarus stibiatus I Liquid dilution for injection

Potency/Strength Package Size Size Category

Potency/Strength Package Size Size Category





10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pulmo bovis Gl dil. D5 0.1 g (HAB, Method 41a) tartarus stibiatus dil. D7 aquos. 0.1 g (HAB, Method 5b)

P

Indications according to the anthroposophical understanding of human beings and nature. Structuring and reorganisation of the anabolic metabolism in inflammatory disorders of the airways, e.g. chronic bronchitis, also with over-inflation of the air sacs in the lungs (emphysema).

N1 N2

PZN 1223618 1223624

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to animal protein. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously twice a week to once daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously twice a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Side-effects None known.

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bryonia cretica ferm 33b dil. D5 0.1 g pulmo bovis Gl dil. D16 0.1 g (HAB, Method 41a) tartarus stibiatus dil. D7 aquos. 0.1 g (HAB, Method 5b) vivianite dil. D7 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the ego organisation for harmonisation of metabolic processes, particularly for reorganisation of protein processes and fluid distribution in the lungs, e.g. pneumonia, bronchitis.

N1 N2

PZN 2422194 2420373

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 3 times a week to twice daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously 3 times a week to twice daily; adults and children of 12 years and above 1 ml injected subcutaneously 3 times a week to twice daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Pulmonium-Hustensaft N see Plantago Hustensaft

442

443

P

Pulpa dentis Gl

Pulsatilla e floribus

Active ingredient: pulpa dentis bovis GI Liquid dilution for injection

Active ingredient: pulsatilla vulgaris e floribus ferm 33c Globuli velati

Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D20 D30 D30 Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pulpa dentis bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N2 N1 N1

PZN 3354678 3354684 3354690 3354709 3354715 2830786 3354721 2831490 2955298 0847021 2497045

Price Group 61 61 61 61 61 61 61 61 62 51 51

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

D4 D6 D30

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

P

D4

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pulsatilla vulgaris e floribus ferm 33c dil. D4 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

444

N1

2955306

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Side-effects None known.

PZN 8787206 8787212 8787229

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Composition 10 g globuli velati contain: pulsatilla vulgaris e floribus ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar).

you suffer from intolerance to certain sugars you should consult your doctor before taking Pulsatilla e floribus.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications None known.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that

Pylorus Gl

Active ingredient: pylorus suis GI Liquid dilution for injection

D5 D8 D12 D30

Active ingredient: pulsatilla vulgaris e floribus ferm 33c Liquid dilution for injection PZN

N1 N1 N1

Potency/Strength Package Size Size Category

Pulsatilla e floribus

Potency/Strength Package Size Size Category

20 g 20 g 20 g

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: pylorus suis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1

PZN 2955364 2955401 2955447 2955499

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

445

P

Quarz

Contraindications None known.

Active ingredient: quartz aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D8 D12 D20 D20 D30 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml 10 x 1 ml 50 x 1 ml

N1 N1 N1 N2 N1 N2

PZN 2832791 2830450 2832822 2955542 2830444 2955559

Price Group 31 31 31 32 31 32

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: quartz dil. D.. aquos. 1 ml

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Impaired dissociation from outside influences, such as acute and chronic inflammation of the sensory organs, the skin and mucous membranes, e.g. adjunctive treatment of inflammation of the middle ear (otitis media), furunculosis, eczema, fistula formation; digestive weakness, intestinal parasites, adjunctive treatment of chronic inflammatory bowel disease, diarrhoea (summer diarrhoea), disturbances of integrative organ regulation such as migraine; cerebral degeneration associated with ageing, fibrosis, osteoarthritis, chronic rheumatic processes; developmental disorders in children.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week.

Contraindications Liquid dilution for injection D8: The medicinal product should not be used in the case of hypersensitivity to milk protein. Liquid dilution for injection D12 upwards: None known.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Liquid dilution for injection D8: The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions. Liquid dilution for injection D12 upwards: None known.

Composition Globuli velati: 10 g contain: quartz dil. D.. aquos. 1g Contains sucrose (saccharose/sugar).

446

Side-effects None known.

Quarz/Nicotiana Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) quartz dil. D9 0.1 g Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of structuring processes in disturbances of the boundary function of the skin, e.g. leg ulcers (ulcus cruris), varicose veins (varicosis).

N1

PZN 8787264

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Quarz/ Nicotiana. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection

Potency/Strength Package Size Size Category 20 g 20 g 20 g

Duration of treatment The duration of treatment should be discussed with the doctor.

Quarz/Oxalis comp.

Active ingredient: quartz aquos. Globuli velati

D12 D20 D30

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children

Contraindications None known.

Quarz

Q

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Quarz.

of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

N1 N1 N1

PZN 8787235 8787241 8787258

Price Group A A A

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only



Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nicotiana tabacum e foliis ferm 33b dil. D29 0.1 g (HAB, Method 33b) oxalis acetosella e planta tota ferm 34b dil. D29 0.1 g (HAB, Method 34b) quartz dil. D29 aquos. 0.1 g

N1

PZN 1751984

Price Group 11

Q

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in shock sequelae, particularly with abdominal pain.

447

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Quercus-Essenz

Side-effects None known.



Globuli velati

Potency/Strength Package Size Size Category 20 g

N1

Composition Globuli velati: 10 g contain: nicotiana tabacum e foliis ferm 33b dil. D29 0.1 g (HAB, Method 33b) oxalis acetosella e planta tota ferm 34b dil. D29 0.1 g (HAB, Method 34b) quartz dil. D29 aquos. 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction of feeling and life organisation in shock sequelae, particularly with abdominal pain. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that

Quercus comp., Unguentum

Q

see Quercus Salbe

Potency/Strength Package Size Size Category 100 ml

Composition 10 g (10.3 ml) contain: quercus robur/petraea e cortice, decoctum LA 10% 10 g (HAB, Method 12k)

Quarz/Oxalis comp.



Active ingredient: quercus robur/petraea e cortice, decoctum LA 10% Tincture for external use

PZN 8787270

Price Group A

Status Pharmacy only

you suffer from intolerance to certain sugars you should consult your doctor before taking Quarz/Oxalis comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually up to once daily; adults and children of 6 years and above 5-10 globuli velati sublingually up to once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the formative powers in the region of the connective tissue, impaired boundary formation with exudative inflammatory processes, e.g. disorders associated with varicose veins (varicose symptom complex), haemorrhoids; tears of the skin or mucous membranes (fissures), cracks in the skin (rhagades), dry and weeping eczema, allergic disposition of the body (allergic diathesis). Contraindications Do not use in the case of known hypersensitivity to the active ingredient.

PZN 1681404

Price Group E

Status Pharmacy only

Warnings and precautions for use Contains 25% (v/v) alcohol. Dosage and method of administration Unless otherwise directed: Compresses: add 1 tablespoon of Quercus-Essenz to approx. 250 ml of water and use for compresses. Baths: use 2 to 3 tablespoons of Quercus-Essenz for a full bath; use correspondingly less for partial baths. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Quercus Hämorrhoidalzäpfchen (haemorrhoid suppositories) Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

Composition 1 suppository (2 g) contains: aesculus hippocastanum e semine ferm 34c Ø 10 mg (HAB, Method 34c) borago officinalis e foliis ferm 34b Ø 10 mg (HAB, Method 34b) hamamelis virginiana e foliis ferm 33d Ø 10 mg (HAB, Method 33d) silybum marianum e fructibus ferm 36 Ø 10 mg (HAB, Method 36) Ingredients 1-4 concentrated to 20 mg. quercus robur/petraea e cortice, decoctum Ø 200 mg (HAB, Method 23a) (concentrated to 20 mg) Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic and structuring forces in deforming and chronic inflammatory

448

N1

N1

PZN 1880701

Price Group P

Status Pharmacy only

changes in the anal region, e.g. haemorrhoids, inflammation of the area around the anus (anitis). Contraindications None known. Warnings and precautions for use There is no adequately documented experience of use of the medicinal product in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum once to twice daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs within 2 to 3 days a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

449

Q

Quercus Salbe

Rectum Gl

Ointment

Active ingredient: rectum suis GI Liquid dilution for injection

Potency/Strength Package Size Size Category

30 g 100 g

Composition 10 g contain: borago officinalis e foliis ferm 34b Ø 0.05 g (HAB, Method 34b) hamamelis virginiana e foliis ferm 33d Ø 0.05 g (HAB, Method 33d) quercus robur/petraea e cortice, decoctum Ø 2.00 g (HAB, Method 23a) Excipients: refined arachis oil, white soft paraffin, wool fat. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic and structuring forces in deforming, chronic inflammatory changes of the mucous membranes, skin and subcutis, particularly where there are signs of congestion or stasis, e.g. haemorrhoids, disorders associated with varicose veins (varicose symptom complex), stasis dermatitis. Contraindications Quercus Salbe must not be used in the case of hypersensitivity to any of the active ingredients, peanuts or soy or to any of the other ingredients. Wool fat can cause local skin irritation (e.g. contact dermatitis).

N1 N2

PZN 1448458 1448441

Price Group J J1

Status Pharmacy only Pharmacy only

Warnings and precautions for use There is no adequately documented experience of use of Quercus Salbe in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, in adults and children of 12 years and above apply the ointment 1 to 3 times daily or use as ointment dressing. When treating haemorrhoids with Quercus Salbe the vaseline contained in the ointment can cause latex condoms to tear and thus reduce their safety. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In the case of hypersensitivity to any of the ingredients of Quercus Salbe, particularly to wool alcohols, allergic reactions may occur. If there is reddening of the skin, with or without itching, please stop using Quercus Salbe and consult a doctor if necessary.

Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2956027 2956056 2956079 2956091 2956122 2956145 2956168 2956180 0847038 2497051

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: rectum suis Gl dil. D.. 1 ml (HAB, Method 41c)

Warnings and precautions for use There is no adequately documented experience of use of the medicinal product in children. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Side-effects None known.

Regio substantiae nigrae Gl

Active ingredient: regio substantiae nigrae bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

Q

450

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 4623028 2956240 4623040 4623063 0491156 2956292 2492562

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

451

R

Composition Liquid dilution for injection: 1 ml contains: regio substantiae nigrae bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Renes, regio pyelorenalis Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: renes bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: renes, regio pyelorenalis pelvis et medulla bovis GI dil. D.. 1 ml (HAB, Method 41a)

Renes Gl

D4 D5 D6 D8 D10 D12 D15 D20 D30 Serial pack I Serial pack II Serial pack III

Active ingredient: renes, regio pyelorenalis pelvis et medulla bovis GI Liquid dilution for injection

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829599 3354744 2829530 3354750 2831923 3354767 2830935 3354773 2830036 2487331 0847044 2497074

Price Group 41 61 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

R

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of incretory and excretory kidney functions, adjunctive treatment of kidney disorders and bronchial asthma.

Dosage and method of administration Potencies below D20: Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Potencies D20 and above: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted.

452

Side-effects None known.

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Renes/Argentum nitricum Liquid dilution for injection

Potency/Strength Package Size Size Category Composition Liquid dilution for injection: 1 ml contains: renes bovis Gl dil. D.. 1 ml (HAB, Method 41a)

PZN 3354796 3354804 3354170 3354193 3354201 3354218 3354230 2497128



10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum nitricum dil. D19 aquos. 0.1 g (HAB, Method 5b) renes bovis Gl dil. D16 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Structuring of the lytic metabolic processes in acute and subacute inflammation of the kidneys and lower urinary tract, e.g. bacterial inflammation of the renal pelvis (pyelonephritis). Contraindications None known.

N1

PZN 2086595

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within two days a doctor should be consulted. The duration of treatment of chronic conditions should be discussed with the doctor. Side-effects None known.

453

R

Renes/Borago comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: borago officinalis e foliis ferm 34b dil. D5 0.1 g (HAB, Method 34b) cuprum aceticum dil. D5 aquos. 0.1 g (HAB, Method 5b) ductus thoracicus bovis Gl dil. D5 0.1 g (HAB, Method 41c) funiculus umbilicalis bovis Gl dil. D5 0.1 g (HAB, Method 41b) mesenchym bovis Gl dil. D5 0.1 g (HAB, Method 41b) renes bovis Gl dil. D5 0.1 g (HAB, Method 41a) textus connectivus bovis Gl dil. D5 0.1 g (HAB, Method 41b) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the fluid organism in the periphery of the body and in

N1 N2

PZN 2086626 2086632

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once to twice weekly to twice daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects None known.

Globuli velati

Potency/Strength Package Size Size Category

R

20 g

Composition Globuli velati: 10 g contain: borago officinalis e foliis ferm 34b dil. D5 0.1 g (HAB, Method 34b) cuprum aceticum dil. D5 aquos. 0.1 g (HAB, Method 5b) ductus thoracicus bovis Gl dil. D5 0.1 g (HAB, Method 41c) funiculus umbilicalis bovis Gl dil. D5 0.1 g (HAB, Method 41b) mesenchym bovis Gl dil. D5 0.1 g (HAB, Method 41b)

454

N1

PZN 8787330

Price Group A

Status Pharmacy only

renes bovis Gl dil. D5 0.1 g (HAB, Method 41a) textus connectivus bovis Gl dil. D5 0.1 g (HAB, Method 41b) Contains sucrose (saccharose/sugar).

Dosage and method of administration Unless otherwise directed, 10-15 globuli velati sublingually 2 to 3 times daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects None known.

the kidney functions directed towards the organism, e.g. in lymphoedema.

Renes/Borago comp.



Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Renes/Borago comp.

Renes/Cuprum

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: cuprum metallicum dil. D7 0.1 g renes bovis Gl dil. D5 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Stimulation and harmonisation of warmth and air organisation in the renal system, e.g. adjunctive treatment of inflammation of the kidney, also when associated with impaired renal function (glomerulonephritis with nephrotic syndrome); adjunctive treatment of inflammation of the renal pelvis (pyelonephritis), in impaired renal function (renal failure) and in bronchial asthma; inner anxiety.

N1 N2

PZN 2086649 2086655

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications Do not use in the case of hypersensitivity to the donor animal protein or milk protein.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the fluid organism in the periphery of the body and in the kidney functions directed towards the organism, e.g. in lymphoedema.

R

Contraindications None known.

455

Renes/Equisetum comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis mellifica ex animale toto Gl dil. D31 0.1 g (HAB, Method 41c) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) renes bovis Gl dil. D6 0.1 g (HAB, Method 41a) veratrum album e radice ferm 33c dil. D5 0.1 g (HAB, Method 33c) viscum album (mali) e planta tota ferm 34i dil. D14 0.1 g (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of renal activity in acute and chronic excretory disturbances. Contraindications The medicinal product must not be used • in the case of known allergy to mistletoe formulations • in the case of allergy to bee or wasp venom • in the case of hypersensitivity to the donor animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this

N1 N2

PZN 2086661 2086678

Price Group 11 12

Status Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If an acute excretory disorder does not improve within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. Rarely, intolerance of mistletoe or allergy to bee or wasp venom can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke's oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought.

Renes/Equisetum comp. Globuli velati

Potency/Strength Package Size Size Category

R

20 g

Composition Globuli velati: 10 g contain: apis mellifica ex animale toto Gl dil. D31 0.1 g (HAB, Method 41c) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) renes bovis Gl dil. D6 0.1 g (HAB, Method 41a) veratrum album e radice ferm 33c dil. D5 0.1 g (HAB, Method 33c)

456

N1

PZN 8787347

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Renes/Equisetum comp.

children of 6 years and above 5-10 globuli velati sublingually 2 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 2 to 5 times daily, adults and

Side-effects None known.

Resina laricis-Bademilch (bath milk) Active ingredient: terebinthina laricina Liquid for external use

Potency/Strength Package Size Size Category

100 ml

Composition 10 g contain: terebinthina laricina 2.0 g Excipients: potassium hydroxide, oleic acid, purified water. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth- and light-related organisational functions in the case of a tendency to hardening and deposits. Contraindications The medicinal product should not be used • in children under 6 years • for topical treatment of acute inflammatory disorders in the region of the eyes • in the case of hypersensitivity to essential oils. Dosage and method of administration Unless otherwise directed: Compresses: add 3 to 5 ml of liquid (approx. 1 teaspoonful) to approx. 250 ml water

PZN 1754008

Price Group D

Status Pharmacy only

and use for compresses; wet packs: add 10 ml of liquid (approx. 2 teaspoonsful) to approx. 250 ml water and use for wet packs; baths: add 30 ml of liquid (approx. 1 to 2 tablespoons) to 1 full bath. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment The medicinal product is usually used for two to three weeks in acute conditions, once daily if used for compresses or wet packs, 2 to 3 times a week if used as bath additive. The treatment may be continued for a longer period if permitted by the doctor. If an acute condition shows no improvement within 2 to 5 days a doctor should be consulted. Side-effects In rare cases urticarial skin reactions can occur which subside rapidly when use of the medicinal product is discontinued.

viscum album (mali) e planta tota ferm 34i dil. D14 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar).

R

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of renal activity in acute and chronic excretory disturbances. Contraindications Do not use in the case of known hypersensitivity to bee venom.

457

Reticuloendotheliales System Gl

Potency/Strength Package Size Size Category

Active ingredient: reticuloendothelial system bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: reticuloendothelial system bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2831610 2831745 2829731 3354276 3354282 3354299 3354247 3354253 2487526 0847067 2497134

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. It should be noted that Reticuloendotheliales System Gl D4 must not be used for longer than 3 months. Intermittent use over a period of more than three months is possible provided that the total number of daily doses does not exceed 99 per year. Side-effects None known.

Active ingredient: retina et chorioidea bovis GI Liquid dilution for injection

D4 D5 D6 D8 D10 D12

R

458

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1

PZN 2829458 3354313 3354336 3354342 3354359 3354365

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: retina et chorioidea bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Price Group 41 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

N1 N1 N1 N1 N1

PZN 3354371 2830119 2487532 0847073 2497140

Price Group 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Retina comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: galenite dil. D19 aquos. 0.1 g retina et chorioidea bovis Gl dil. D11 0.1 g (HAB, Method 41c) terebinthina laricina dil. D9 0.1 g (HAB, Method 6)

Retina et Chorioidea Gl

Potency/Strength Package Size Size Category

D15 D30 Serial pack I Serial pack II Serial pack III

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the metabolic processes in degenerative alteration of the retina. Contraindications Do not use in the case of hypersensitivity to milk protein.

N1 N2

PZN 2086684 2086690

Price Group 11 12

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, 1 ml injected subcutaneously in the region of the temples or the back of the neck 1 to 3 times a week to once daily. The injections should be given by a doctor or other experienced person as you cannot administer injections at these sites yourself. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

459

R

Rheuma-Badeöl (rheumatism bath oil) Bath additive, liquid

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: anisi stellati aetheroleum 0.035 g arctium lappa e radice W 5% (HAB, Method 12g with refined arachis oil) 2.45 g arnica montana e floribus W 5% (HAB, Method 12g with virgin olive oil) 2.45 g betula pendula/pubescens e foliis W 5% (HAB, Method 12g with virgin olive oil) 2.45 g oily extract of formica rufa rec. (10:1); extraction agent: refined arachis oil 0.01 g urtica dioica ex herba W 5% (HAB, Method 12g with virgin olive oil) 2.45 g Excipient: virgin olive oil. Indications according to the anthroposophical understanding of human beings and nature. Painful, traumatic, inflammatory or rheumatic disorders of the muscles or joints. Contraindications Rheuma Badeöl should not be used in the case of hypersensitivity to arnica or other plants of the Compositae family, hypersensitivity to anise or anethol, allergy to birch pollen or any of the other active ingredients.

N1

PZN

Price Group

2088737

N1

Status General Sale

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. In rare cases arachis (peanut) oil can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, for adults and children of 12 years and above use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects In rare cases hypersensitivity reactions may occur in the skin; in this case use of the preparation should be discontinued. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Rhus toxicodendron comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

R

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aconitum napellus e tubere ferm 33c dil. D5 0.1 g (HAB, Method 33c) gelsemium sempervirens e rhizoma ferm 35b dil. D3 0.1 g (HAB, Method 35b) granite dil. D9

460

N1 N2

PZN 1751990 2086709

Price Group 11 12

Status Pharmacy only Pharmacy only

0.1 g (HAB, Method 6) leontopodium alpinum e planta tota ferm 36 dil. D3 0.1 g (HAB, Method 36) mandragora officinarum e radice ferm 34d dil. D5 0.1 g (HAB, Method 34d) toxicodendron quercifolium e foliis ferm 33d dil. D5 0.1 g (HAB, Method 33d)

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in painful disorders of the musculoskeletal system, e.g. nerve pain (neuralgia), nerve inflammation (neuritis), muscle pain (myalgia).

medicinal product in children is not available. It should therefore not be used in children under 12 years.

Contraindications Do not use in the case of known allergy to birch, plants of the poison sumac family, edelweiss or other plants belonging to the Compositae family or the other active ingredients. Do not use in the case of hypersensitivity to milk protein.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Warnings and precautions for use Sufficiently documented experience for the use of this

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to twice daily.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Rhus toxicodendron comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition 10 g globuli velati contain: aconitum napellus e tubere ferm 33c dil. D3 0.1 g (HAB, Method 33c) gelsemium sempervirens e rhizoma ferm 35b dil. D2 0.1 g (HAB, Method 35b) granite dil. D9 0.1 g (HAB, Method 6) leontopodium alpinum e planta tota ferm 36 dil. D3 0.1 g (HAB, Method 36) mandragora officinarum e radice ferm 34d dil. D3 0.1 g (HAB, Method 34d) toxicodendron quercifolium e foliis ferm 33d dil. D3 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the feeling organisation in painful disorders of the musculoskeletal system, e.g. nerve pain (neuralgia), nerve inflammation (neuritis), muscle pain (myalgia). Contraindications Do not use in the case of known allergy to plants of the poison sumac family.

N1

PZN 8787407

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Rhus toxicodendron comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 6 times daily; children from 6 to under 12 years 5-7 globuli velati sublingually 3 to 6 times daily; adults and children of 12 years and above 5-10 globuli velati sublingually 3 to 6 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

461

R

Rhus toxicodendron e foliis

Rhus toxicodendron Salbe

Active ingredient: toxicodendron quercifolium e foliis ferm 33d Liquid dilution for injection Potency/Strength Package Size Size Category D6 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: toxicodendron quercifolium e foliis ferm 33d dil. D.. 1 ml (HAB, Method 33d) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1 N1

PZN 2832696 2890972 2832710

Active ingredient: toxicodendron quercifolium e foliis ferm 33d Ø Ointment Price Group 31 31 31

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only



Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Side-effects None known.

Rhus toxicodendron e foliis

Active ingredient: toxicodendron quercifolium e foliis ferm 33d Globuli velati Potency/Strength Package Size Size Category D6 D12 D30

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: toxicodendron quercifolium e foliis ferm 33d dil. D.. 1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

R

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Rhus toxicodendron e foliis.

462

N1 N1 N1

PZN 8787376 8787382 8787399

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

30 g

N1

PZN 1451383

Price Group J

Status Pharmacy only

Composition 10 g contain: toxicodendron quercifolium e foliis ferm 33d Ø 0.1 g (HAB, Method 33d) Excipients: refined arachis oil, white soft paraffin, purified water, wool fat.

Warnings and precautions for use Wool fat can cause local skin reactions (e.g. contact dermatitis).

Indications according to the anthroposophical understanding of human beings and nature. Painful disorders of the musculoskeletal system, e.g. joint inflammation (arthritis), also of the spine; muscle pain (myalgia), nerve pain (neuralgia) and nerve inflammation (neuritis); herpetiform skin disorders.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications Rhus toxicodendron Salbe must not be used in the case of hypersensitivity (allergy) to Rhus toxicodendron, peanuts or soy or to any of the other ingredients. Do not use in the case of known allergy to plants of the poison sumac family or to any of the excipients.

Dosage and method of administration Unless otherwise directed, rub in the ointment once to twice daily or use as ointment dressing.

Side-effects In the case of hypersensitivity to any of the ingredients of Rhus toxicodendron Salbe, particularly to wool alcohols, allergic reactions may occur. If there is reddening of the skin, with or without itching, please stop using Rhus toxicodendron Salbe and consult a doctor if necessary. In rare cases arachis oil can cause severe allergic reactions.

Robinia comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum nitricum dil. D5 aquos. 0.1 g (HAB, Method 5b) natrium phosphoricum dil. D9 aquos. 0.1 g (HAB, Method 5b) nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) robinia pseudoacacia e cortice ferm 33e dil. D3 0.1 g (HAB, Method 33e) strychnos nux-vomica e semine ferm 35b dil. D9 0.1 g (HAB, Method 35b)

N1 N2

PZN 1752009 2086715

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of secretion and motility in the upper digestive tract, e.g. in heartburn, excessive acidity of the gastric juice (hyperacidity), ulcers in the digestive tract (peptic ulcers).

R

Contraindications None known. Warnings and precautions for use There is no adequately documented experience of use of Robinia comp. in children. It should therefore not be used in children under 12 years.

463

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

is no improvement within this time a doctor should be consulted. Side-effects None known.

Duration of treatment Acute disorders should clear up within 2 weeks. If there

Contraindications None known. Warnings and precautions for use During breastfeeding: Do not breastfeed immediately after the bath. Cleanse the skin in the region of the breasts before breastfeeding.

Robinia comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum nitricum dil. D5 aquos. 0.1 g (HAB, Method 5b) natrium phosphoricum dil. D9 aquos. 0.1 g (HAB, Method 5b) nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) robinia pseudoacacia e cortice ferm 33e dil. D3 0.1 g (HAB, Method 33e) strychnos nux-vomica e semine ferm 35b dil. D9 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of secretion and motility in the upper digestive tract, e.g. in heartburn, excessive acidity of the gastric juice (hyperacidity), ulcers in the digestive tract (peptic ulcers).

N1

PZN 8787413

Price Group A

Status Pharmacy only

Warnings and precautions for use There is no adequately documented experience of use of Robinia comp. in children. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Robinia comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 to 6 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications None known.

Rosa e floribus 10%, Oleum Liquid bath additive

Potency/Strength Package Size Size Category

R



100 ml

Composition 10 g (11 ml) contain: rosa damascena/centifolia e floribus W 10% (HAB, Method 12f with virgin olive oil) 9.8 g

464

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in states of weakness and exhaustion, convalescence, failure to thrive.

PZN

Price Group

2088772

J1

Status General Sale

rosae aetheroleum 10% (HAB, Method 12h with virgin olive oil) 0.2 g

Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. The temperature of the bath water

should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Rosatum Heilsalbe (healing ointment) Ointment

Potency/Strength Package Size Size Category

30 g 100 g

Composition 10 g contain: geranii aetheroleum 0.025 g rosae aetheroleum 0.005 g aqueous colloidal silicium dioxide solution (corresponding to silicea colloidalis 0.1 g) produced with citric acid monohydrate 2.8 g Excipients: liquid paraffin, white soft paraffin, wool fat. Indications according to the anthroposophical understanding of human beings and nature. Disturbances of boundary formation with regard to external influences and shifts in inner processes of the skin, e.g. inflammation of the skin (dermatitis), atopic dermatitis, eczema, itching, superficial skin defects, tendency to fungal infections. Contraindications Rosatum Heilsalbe should not be used in the case of hypersensitivity to geranium oil.

N1 N2

PZN 1448547 1448530

Price Group J J1

Status Pharmacy only Pharmacy only

Warnings and precautions for use Wool fat can cause local skin reactions (e.g. contact dermatitis). If the ointment is used during breastfeeding any ointment residue should be removed from the breast before feeding. Dosage and method of administration Unless otherwise directed, rub in the ointment 2 to 3 times daily or use as ointment dressing. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Allergic skin reactions can occur in rare cases. In this case use of the medicinal product should be stopped and a doctor consulted.

465

R

Roseneisen

Roseneisen/Graphit

Active ingredient: rosa e floribus ferm cum ferro dil. D3 Globuli velati Potency/Strength Package Size Size Category

20 g

Composition 10 g globuli velati contain: rosa e floribus ferm cum ferro dil. D3 1 g (HAB, Method 37a) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Roseneisen.

N1

PZN 8787436

Globuli velati Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

R

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in states of exhaustion and weakness, particularly during childhood and recovery from illness (convalescence); inflammatory bronchopulmonary disorders.

466

Composition Globuli velati: 10 g contain: graphites dil. D14 aquos. 0.1 g rosa e floribus ferm cum ferro dil. D2 0.1 g (HAB, Method 37a) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism in states of exhaustion and weakness, particularly in children and during convalescence; inflammatory bronchopulmonary disorders.

N1

PZN 8787442

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Roseneisen/Graphit. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 2 to 4 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 2 to 4 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Side-effects None known.

Active ingredient: rose quartz aquos. Liquid dilution for injection

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: graphites dil. D14 aquos. 0.1 g rosa e floribus ferm cum ferro dil. D5 0.1 g (HAB, Method 37a)

20 g

Rosenquarz

Liquid dilution for injection

10 x 1 ml 50 x 1 ml



Contraindications None known.

Roseneisen/Graphit



Potency/Strength Package Size Size Category

N1 N2

PZN 1752021 2086721

Price Group 11 12

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only

D15

Contraindications None known. Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously 2 to 3 times a week to once daily, children of 6 to under 12 years 0.5-1 ml injected subcutaneously 2 to 3 times a week to once daily, adults and children of 12 years and above 1 ml injected subcutaneously 2 to 3 times a week to once daily.

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: rose quartz dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 3656758

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Side-effects None known.

R

467

Rosmarinus, Oleum aethereum 10% Active ingredient: rosmarini aetheroleum 10% Liquid bath additive

Potency/Strength Package Size Size Category

100 ml

Composition 10 g (11 ml) contain: rosmarini aetheroleum 10% (HAB, Method 12h with virgin olive oil) 10 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organism in metabolic weakness, disturbances of tissue nutrition and perfusion, rheumatic disorders, a general tendency to feel cold, morning tiredness; toning of the circulation. Contraindications Do not use in the case of known allergy to essential oils. Dosage and method of administration Unless otherwise directed, use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l

N1

PZN 2088803

Price Group N1

Status Pharmacy only

water) for oil dispersion baths. The temperature of the bath water should be between 35° and 37°, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects In rare cases use of the medicinal product can lead to local allergic reactions (contact dermatitis or itching). Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Potency/Strength Package Size Size Category

R

Composition 10 g contain: anus bovis Gl dil. D4 0.1 g (HAB, Method 41c) anus bovis Gl dil. D8 0.1 g (HAB, Method 41c) conchae dil. D8 0.1 g cutis feti feminini bovis Gl dil. D4 0.1 g (HAB, Method 41b) cutis feti feminini bovis Gl dil. D8 0.1 g (HAB, Method 41b) funiculus umbilicalis bovis Gl dil. D4 0.1 g (HAB, Method 41b) lavandulae aetheroleum 0.0425 g

468

Contraindications The medicinal product should not be used in case of known hypersensitivity • to the essential oils contained in the product (lavender oil, sage oil, rosemary oil) • to the donor animal protein (bovine)

N1

PZN 2198526

Price Group J

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children over 12 years apply the gel thinly 1 to 3 times daily and rub in without applying pressure. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases mild skin redness and burning may occur.

Rubin

Active ingredient: ruby aquos. Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ruby dil. D12 aquos. 1 ml (HAB, Method 8b)

Gel

30 g

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the regenerative processes in chronic inflammatory and dystrophic changes in the genital and anal region; pruritus (itching).

D12

Rosmarinus/Prunus comp., Gelatum



Excipients: argentum colloidale, lemon oil, geranium oil, glycerol, aqueous potassium hydroxide solution 10% (m/v), aqueous colloidal silicium dioxide solution produced with citric acid monohydrate, sodium alginate, thyme oil, purified water.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 3656853

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

pars fetalis, placenta bovis Gl dil. D4 0.1 g (HAB, Method 41b) prunus spinosa e fructibus LA 25% 1.5 g (HAB, Method 12o) pudendum femininum bovis Gl dil. D4 0.1 g (HAB, Method 41b) pudendum femininum bovis Gl dil. D8 0.1 g (HAB, Method 41b) rosmarini aetheroleum 0.085 g salviae officinalis aetheroleum 0.0136 g stannum metallicum dil. D8 0.1 g urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c)

R

469

Salix/Rhus comp.

Salix/Rhus comp.

Liquid dilution for injection

Globuli velati

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aconitum napellus e tubere ferm 33 c dil. D4 0.01 g (HAB, Method 33c) atropa belladonna e fructibus ferm 33a dil. D4 0.01 g (HAB, Method 33a) bryonia cretica ferm 33b dil. D3 0.01 g dryopteris filix-mas e radice ferm 33c dil. D3 0.01 g (HAB, Method 33c) phyllitis scolopendrium e foliis ferm 34h dil. D3 0.01 g (HAB, Method 34h) pteridium aquilinum e foliis ferm 34c dil. D3 0.01 g (HAB, Method 34c) salix alba ssp. vitellina e cortice et foliis ferm 33d dil. D3 0.0033 g (HAB, Method 33d) salix purpurea e cortice et foliis ferm 33d dil. D3 0.0033 g (HAB, Method 33d) salix viminalis e cortice et foliis ferm 33d dil. D3 0.0033 g (HAB, Method 33d) stibium metallicum dil. D6 0.01 g strychnos nux-vomica e semine ferm 35b dil. D4 0.01 g (HAB, Method 35b) toxicodendron quercifolium e foliis ferm 33d dil. D4 0.01 g (HAB, Method 33d)

N1

PZN 1752050

Price Group 11

Status

Potency/Strength Package Size Size Category

Pharmacy only



Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of hypersensitivity to poison sumac, in children under 4 years or during pregnancy or breastfeeding. Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

20 g

Composition Globuli velati: 10 g contain: aconitum napellus e tubere ferm 33 c dil. D4 0.01 g (HAB, Method 33c) atropa belladonna e fructibus ferm 33a dil. D4 0.01 g (HAB, Method 33a) bryonia cretica ferm 33b dil. D3 0.01 g dryopteris filix-mas e radice ferm 33c dil. D1 0.01 g (HAB, Method 33c) phyllitis scolopendrium e foliis ferm 34h dil. D1 0.01 g (HAB, Method 34h) pteridium aquilinum e foliis ferm 34c dil. D1 0.01 g (HAB, Method 34c) salix alba ssp. vitellina e cortice et foliis ferm 33d dil. D1 0.0033 g (HAB, Method 33d) salix purpurea e cortice et foliis ferm 33d dil. D1 0.0033 g (HAB, Method 33d) salix viminalis e cortice et foliis ferm 33d dil. D1 0.0033 g (HAB, Method 33d) stibium metallicum dil. D6 0.01 g strychnos nux-vomica e semine ferm 35b dil. D4 0.01 g (HAB, Method 35b) toxicodendron quercifolium e foliis ferm 33d dil. D4 0.01 g (HAB, Method 33d) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic har-

N1

PZN 8787548

Price Group A

Status Pharmacy only

monising processes in disorders of secretion and motility in the digestive tract, e.g. diarrhoea, digestive disorders, infections of the digestive tract (gastrointestinal infections). Contraindications Do not use in the case of hypersensitivity to plants of the poison sumac family, in children under 4 years or during pregnancy or breastfeeding. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children of 4 to 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Salix/ Rhus comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 to 5 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Salvia e foliis

Active ingredient: salvia officinalis e foliis ferm 33d Liquid dilution for injection Potency/Strength Package Size Size Category D6

S

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: salvia officinalis e foliis ferm 33d dil. D6 1 ml (HAB, Method 33d)

470

N1

PZN 3656936

Price Group 31

Status Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

471

S

Contraindications None known.

Side-effects None known.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: sambucus nigra e medulla ferm 35a dil. D5 0.1 g (HAB, Method 35a) sambucus nigra ex umbella ferm 33c dil. D5 0.1 g (HAB, Method 33c) terebinthina laricina dil. D7 0.1 g (HAB, Method 6) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be

Side-effects None known.

Active ingredient: saphir aquos. Liquid dilution for injection

Liquid dilution for injection

10 x 1 ml 50 x 1 ml

consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Saphir

Sambucus comp.



globuli velati in a small amount of water or unsweetened tea before administration.

N1 N2

PZN 1752067 2086773

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to twice daily. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Potency/Strength Package Size Size Category D15

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: sapphire dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 3657077

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Sarothamnus comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

Sambucus comp.



Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: sambucus nigra e medulla ferm 35a dil. D3 0.1 g (HAB, Method 35a) sambucus nigra ex umbella ferm 33c dil. D2 0.1 g (HAB, Method 33c) terebinthina laricina dil. D4 0.1 g (HAB, Method 6) Contains sucrose (saccharose/sugar) and lactose.

S

Indications according to the anthroposophical understanding of human beings and nature. Structuring of the fluid organism, e.g. in climacteric symptoms with hot flushes and excessive sweating, also at night; catarrhal and allergic disorders of the upper airways.

472

N1

PZN 8787554

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Sambucus comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily to every two hours; children from 6 to under 12 years 5-7 globuli velati sublingually 1 to 3 times daily to every two hours; adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily to every two hours. For infants we recommend dissolving the specified number of

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D14 aquos. 0.1 g camphora dil. D3 aquos. 0.1 g (HAB, Method 5b) cytisus scoparius ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) selenicereus grandiflorus ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the rhythmic system, adjunctive treatment of cardiac rhythm disorders. Contraindications None known.

N1 N2

PZN 1752096 2086804

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

S

473

Sarothamnus comp.

Scilla comp.

Globuli velati

Liquid dilution for injection

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D14 aquos. 0.1 g camphora dil. D3 aquos. 0.1 g (HAB, Method 5b) cytisus scoparius ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) selenicereus grandiflorus ex herba ferm 33d dil. D3 0.1 g (HAB, Method 33d) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the rhythmic system, adjunctive treatment of cardiac rhythm disorders. Contraindications None known.

N1

PZN 8787620

Price Group A

Status

Potency/Strength Package Size Size Category

Pharmacy only



Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Sarothamnus comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily to every 2 hours. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: adonis vernalis ferm 33d dil. D2 0.1 g convallaria majalis e planta tota ferm 33c dil. D3 0.1 g (HAB, Method 33c) crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) urginea maritima var. rubra e bulbo ferm 33b dil. D3 0.1 g (HAB, Method 33b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between feeling organisation and life organisation in beginning weakness of the heart muscle (congestive heart failure) particularly in the elderly.

N1 N2

PZN 1752104 2086810

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Scilla e bulbo

Active ingredient: urginea maritima var. rubra e bulbo ferm 33b Liquid dilution for injection Potency/Strength Package Size Size Category D2

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: urginea maritima var. rubra e bulbo ferm 33b dil. D2 1 ml (HAB, Method 33b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

S

N1

PZN 3657108

Scilla comp. Globuli velati Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: adonis vernalis ferm 33d dil. D2 0.1 g convallaria majalis e planta tota ferm 33c dil. D2 0.1 g (HAB, Method 33c) crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) urginea maritima var. rubra e bulbo ferm 33b dil. D1 0.1 g (HAB, Method 33b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction

474

N1

PZN 8787637

Price Group A

Status Pharmacy only

between feeling organisation and life organisation in beginning weakness of the heart muscle (congestive heart failure) particularly in the elderly. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Scilla comp.

475

S

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 10-15 globuli velati sublingually 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be

consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

D6 D12

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: sclera bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 and D30: None known.

N1 N1 N1

PZN 3657172 3657261 3657309

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

S

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: secale cornutum e sclerotio ferm 35b dil. D.. 1 ml (HAB, Method 35b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

476

N1 N1 N1

PZN 3657321 2891167 3663540

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Secale cornutum e grano.

Price Group 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

N1 N1

PZN 8787643 8787666

Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Secale/Argentum

Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D7 0.1 g secale cornutum e sclerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b)

Active ingredient: secale cornutum e sclerotio ferm 35b Liquid dilution for injection

D6 D12 D30

Contraindications None known.



Secale cornutum e grano

Potency/Strength Package Size Size Category

20 g 20 g

Composition 10 g globuli velati contain: secale cornutum e sclerotio ferm 35b dil. D.. 1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar).

Active ingredient: sclera bovis GI Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml

Active ingredient: secale cornutum e sclerotio ferm 35b Globuli velati Potency/Strength Package Size Size Category

Sclera Gl

D5 D12 D30

Secale cornutum e grano

Indications according to the anthroposophical understanding of human beings and nature. Stimulation and structuring of the anabolic metabolic processes in menstrual disorders, e.g. painful periods (dysmenorrhoea), absence of periods (amenorrhoea), forms of migraine associated with these disorders. Contraindications Do not use in the case of hypersensitivity to milk protein.

N1

PZN 1752110

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Side-effects None known.

477

S

Secale/Bleiglanz comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arteria poplitea bovis Gl dil. D7 0.1 g (HAB, Method 41c) betula pendula e cortice, decoctum dil. D4 0.1 g (HAB, Method 23a) galenite dil. D7 0.1 g nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) secale cornutum e sclerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between ego organisation and feeling organisation in functional peripheral circulatory disorders and arteriosclerotic or endangiitic vascular disorders, e.g. intermittent claudication, circulatory disorders of the hands and feet (Raynaud‘s syndrome).

N1 N2

PZN 1752127 2086833

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Side-effects None known.

Secale/Quarz

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 8787689

Price Group A

1752133

Price Group 11

Status Pharmacy only

medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Migraine and cerebral circulatory disturbances.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Warnings and precautions for use Sufficiently documented experience for the use of this

Potency/Strength Package Size Size Category

N1

PZN

Composition Liquid dilution for injection: 1 ml contains: quartz dil. D29 aquos. 0.1 g secale cornutum e sclerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b)

Contraindications None known.

Globuli velati

20 g

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Contraindications Do not use in the case of hypersensitivity to milk protein.

Secale/Bleiglanz comp.



Warnings and precautions for use There is insufficient experience of use of this medicinal product in children. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Secale/ Bleiglanz comp.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

Side-effects None known.

Status Pharmacy only

Secale/Quarz Globuli velati

S

Composition Globuli velati: 10 g contain: arteria poplitea bovis Gl dil. D7 0.1 g (HAB, Method 41c) betula pendula e cortice, decoctum Ø 0.2 g (HAB, Method 23a) galenite dil. D7 0.1 g nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) secale cornutum e sclerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar) and lactose.

478

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the interaction between ego organisation and feeling organisation in functional peripheral circulatory disorders and arteriosclerotic or endangiitic vascular disorders, e.g. intermittent claudication, circulatory disturbances of the hands and feet (Raynaud‘s syndrome). Contraindications None known.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: quartz dil. D29 aquos. 0.1 g secale cornutum e sclerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Migraine and cerebral circulatory disturbances.

N1

PZN 8787695

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Secale/Quarz. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 to 5 times daily; children from 6 to under 12 years 5-7 globuli velati sublingually 3 to 5

479

S

times daily; adults and children of 12 years and above 10 globuli velati sublingually 3 to 5 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there

is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications None known.

Secale/Retina comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: betula pendula e cortice, decoctum dil. D4 0.1 g (HAB, Method 23a) galenite dil. D7 0.1 g nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b) retina et chorioidea bovis Gl dil. D7 0.1 g (HAB, Method 41c) secale cornutum e sclerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b) Indications according to the anthroposophical understanding of human beings and nature. Degenerative changes and circulatory disturbances of the retina.

N1 N2

PZN 1752156 2086862

Price Group 11 12

Status

Warnings and precautions for use There is no adequately documented experience of use of the medicinal product in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Secale/Retina comp. Globuli velati



S

20 g

Composition Globuli velati: 10 g contain: betula pendula e cortice, decoctum dil. D2 0.1 g (HAB, Method 23a) galenite dil. D7 0.1 g nicotiana tabacum e foliis ferm 33b dil. D5 0.1 g (HAB, Method 33b)

480

N1

PZN 8787703

Price Group A

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Secale/ Retina comp.

Dosage and method of administration Unless otherwise directed, 10 globuli velati sublingually 2 to 4 times daily. Duration of treatment Even anthroposophical medicines should not be used for prolonged periods without obtaining the advice of a doctor. Side-effects None known.

Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein.

Potency/Strength Package Size Size Category

Indications according to the anthroposophical understanding of human beings and nature. Degenerative changes and circulatory disturbances of the retina.

Status Pharmacy only

Senecio comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: olivenite dil. D5 0.1 g senecio jacobaea ex herba ferm 33d dil. D2 0.1 g (HAB, Method 33d) spinacia oleracea e radice ferm 34f dil. D2 0.1 g (HAB, Method 34f) stannum metallicum dil. D7 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Vitalising and toning of connective tissue and smooth muscle in the metabolic-limb region, e.g. prolapse symptoms, connective tissue weakness, irritable bladder, venous congestion.

N1

PZN 1752162

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If acute inflammation does not improve within 2 days a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Contraindications Do not use in the case of hypersensitivity to milk protein.

retina et chorioidea bovis Gl dil. D7 0.1 g (HAB, Method 41c) secale cornutum e sclerotio ferm 35b dil. D5 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar) and lactose.

S

481

Senecio comp.

doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8787726

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: olivenite dil. D5 0.1 g senecio jacobaea ex herba ferm 33d dil. D2 0.1 g (HAB, Method 33d) spinacia oleracea e radice ferm 34f dil. D2 0.1 g (HAB, Method 34f) stannum metallicum dil. D7 0.1 g Contains sucrose (saccharose/sugar) and lactose.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Senecio comp.

Indications according to the anthroposophical understanding of human beings and nature. Vitalising and toning of connective tissue and smooth muscle in the metabolic-limb region, e.g. prolapse symptoms, connective tissue weakness, irritable bladder, venous congestion.

Duration of treatment The condition should have cleared up within 2 weeks. If acute inflammation does not improve within 2 days a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor.

Contraindications None known.

Side-effects None known.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily.

Side-effects None known.

Sepia e secreto Gl

Active ingredient: sepia officinalis e volumine bursae rec. GI Liquid dilution for injection Potency/Strength Package Size Size Category D8 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: sepia officinalis e volumine bursae rec. GI dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

N1 N1 N1

PZN 4623318 4626765 3663563

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

Senecio comp., Suppositorien Suppositories

Potency/Strength Package Size Size Category

S

10 x 2 g

Composition 1 suppository (2 g) contains: olivenite trit. D5 20 mg senecio jacobaea ex herba ferm 33d dil. D1 2 mg (HAB, Method 33d) spinacia oleracea e radice ferm 34f dil. D1 2 mg (HAB, Method 34f) stannum metallicum dil. D6 2 mg Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Vitalising and toning of connective tissue and smooth muscle in the metabolic-limb

482

N1

PZN 1880718

Price Group P

Status Pharmacy only

region, e.g. prolapse symptoms, connective tissue weakness, irritable bladder, venous congestion. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum 3 times a week to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If acute inflammation does not improve within two days a

Silicea see Quarz

Silicea colloidalis comp., Gelatum Gel

Potency/Strength Package Size Size Category

30 g

Composition 10 g contain: limonis aetheroleum 0.1 g aqueous colloidal silicium dioxide solution (corresponding to silicea colloidalis 0.25 g) produced with citric acid monohydrate 4.0 g Excipients: 96% ethyl alcohol, glycerol, guar, litsea fruit oil, sodium alginate, sorbitol, tea tree oil, purified water.

N1

PZN 2198532

Price Group J

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Disturbances of boundary formation with regard to external influences and shifts in inner processes of the skin, e.g. inflammatory skin conditions (dermatitis), weeping eczema, tendency to fungal infections. Contraindications The medicinal product should not be used in the case of known hypersensitivity to citrus fruits and should not be applied to mucous membranes or open wounds.

483

S

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, apply the gel several times a day according to the size of the affected skin area and cover overnight. For application to the soles of the feet, apply thinly at night and allow to dry.

Duration of treatment Acute disorders should clear up within 2 weeks. If no improvement occurs within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases skin reddening can occur in the case of hypersensitivity to lemon oil.

Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: argentum nitricum dil. D20 aquos. 0.1 g (HAB, Method 5b) atropa belladonna ex herba ferm 33a dil. D14 0.1 g (HAB, Method 33a) quartz dil. D21 aquos. 0.1 g Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of heightened metabolic processes, particularly in the region of the head, e.g. inflammation of the sinuses, the ear, the eye, the periodontium. Contraindications None known.

N1 N2

PZN 1752179 2086885

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Silicea comp. Globuli velati

Potency/Strength Package Size Size Category

S

20 g

Composition Globuli velati: 10 g contain: argentum nitricum dil. D20 aquos. 0.1 g (HAB, Method 5b) atropa belladonna ex herba ferm 33a dil. D14 0.1 g (HAB, Method 33a)

484

2 to under 6 years 3-7 globuli velati sublingually up to once daily; adults and children of 6 years and above 5-10 globuli velati sublingually up to once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Contraindications None known.

Duration of treatment Acute disorders should clear up within 1 week. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Silicea comp.

Silicea comp.



Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of heightened metabolic processes, particularly in the region of the head, e.g. inflammation of the sinuses, the ear, the eye, the periodontium.

N1

PZN 8787732

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, children under 2 years 3 globuli velati sublingually up to once daily; children from

Side-effects None known.

Silicea comp., Suppositorien Suppositories

Potency/Strength Package Size Size Category

10 x 2 g

N1

PZN 1880724

Price Group P

Status Pharmacy only

Composition 1 suppository (2 g) contains: argentum nitricum dil. D19 aquos. 2 mg (HAB, Method 5b) atropa belladonna ex herba ferm 33a dil. D13 2 mg (HAB, Method 33a) quartz dil. D20 aquos. 2 mg Excipients: hard fat, honey.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 7 years after consulting a doctor.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of heightened metabolic processes, particularly in the region of the head, e.g. inflammation of the sinuses, the ear, the eye, the periodontium.

Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted;

Contraindications The medicinal product should not be used in the case of allergic reactions to constituents of deadly nightshade (atropa belladonna).

Dosage and method of administration Unless otherwise directed, adults and children of 7 years and above 1 suppository introduced into the rectum once daily.

Side-effects None known.

quartz dil. D21 aquos. 0.1 g Contains sucrose (saccharose/sugar).

S

485

Silicea comp., Suppositorien für Kinder Paediatric suppositories

Potency/Strength Package Size Size Category

10 x 1 g

Composition 1 suppository (1 g) contains: argentum nitricum dil. D19 aquos. 1 mg (HAB, Method 5b) atropa belladonna ex herba ferm 33a dil. D13 1 mg (HAB, Method 33a) quartz dil. D20 aquos. 1 mg Excipients: hard fat, honey. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of heightened metabolic processes, particularly in the region of the head, e.g. inflammation of the sinuses, the ear, the eye, the periodontium.

N1

PZN 1880813

Price Group O

Status Pharmacy only

Contraindications The medicinal product should not be used in the case of allergic reactions to constituents of deadly nightshade (atropa belladonna). Dosage and method of administration Unless otherwise directed, introduce 1 suppository into the rectum once daily. Note: Silicea Comp., Suppositorien für Kinder are paediatric suppositories intended for use in infants and children under 7 years. Duration of treatment The treatment should not take longer than 2 weeks. If there is no improvement within 2 to 3 days a doctor should be consulted.

Sinus cavernosus-Komplex Gl

Active ingredient: sinus cavernosus complex bovis GI Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack III

S

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: sinus cavernosus complex bovis Gl [sinus cavernosus with parts of nervus opticus, nervus oculomotorius, nervus trochlearis, nervus trigeminus, nervus abducens, arteria carotis communis] dil. D.. 1 ml (HAB, Method 41a)

486

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3657611 3657634 3657657 3657686 3657700 3657723 3657752 2497559

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Skorodit comp.

see Skorodit Kreislauf Inject see Skorodit Kreislauf Globuli velati

Skorodit Kreislauf Inject (circulatory system remedy) Liquid dilution for injection

Potency/Strength Package Size Size Category

Side-effects None known.

Potency/Strength Package Size Size Category

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: camphora dil. D3 aquos. 0.1 g (HAB, Method 5b) hypophysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) prunus spinosa e floribus et summitatibus ferm 33d dil. D5 0.1 g (HAB, Method 33d) scorodite dil. D5 0.1 g veratrum album e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the interaction between the different constituent elements of the human being, e.g. in hypotensive circulatory dysregulation, states of exhaustion, phases of recovery from illness (convalescence), psychasthenia.

N1 N2

PZN 0084391 0090351

Price Group 11 12

Status Pharmacy only Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once to twice weekly to once daily. Duration of treatment The condition should have cleared up within 2 weeks. If no improvement occurs during this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

S

487

Skorodit Kreislauf Globuli velati (circulatory system remedy) Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 0084439

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: camphora dil. D3 aquos. 0.1 g (HAB, Method 5b) hypophysis bovis Gl dil. D7 0.1 g (HAB, Method 41a) prunus spinosa e floribus et summitatibus ferm 33d dil. D5 0.1 g (HAB, Method 33d) scorodite dil. D5 0.1 g veratrum album e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose.

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Skorodit Kreislauf Globuli velati.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the interaction between the different constituent elements of the human being, e.g. in hypotensive circulatory dysregulation, states of exhaustion, convalescence, psychasthenia.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications None known.

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Side-effects None known.

Solidago virgaurea ex herba

Active ingredient: solidago virgaurea ex herba ferm 33c Globuli velati Potency/Strength Package Size Size Category D3 D4 D6

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: solidago virgaurea ex herba ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Solidago virgaurea ex herba.

N1 N1 N1

PZN 8787755 8787761 8787778

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Solum Badezusatz Bath additive, liquid

Solidago virgaurea ex herba

Potency/Strength Package Size Size Category

Active ingredient: solidago virgaurea ex herba ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: solidago virgaurea ex herba ferm 33c dil. D.. 1 ml (HAB, Method 33c)

S

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

488

N1 N1

PZN 2891210 3657953

Price Group 31 31

N1 N3

PZN 1448470 1448487

Price Group D D1

Status Pharmacy only Pharmacy only

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

100 ml 500 ml

Composition 10 g contain: aesculus hippocastanum e semine LA 25% sicc. 0.1 g (HAB, Method 12m) equisetum arvense ex herba LA 20% 0.1 g (HAB, Method 12c) solum uliginosum, aqueous extract (peat extract) (drug to extraction agent = 1:5) 9.8 g Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and harmonisation of the feeling organisation, e.g. in rheumatic disorders, sensitivity to changes in the weather, spinal syndromes and nerve pain (neuralgia).

Contraindications As Solum Badezusatz contains peat extract it should not be used during pregnancy. Warnings and precautions for use Solum Badezusatz should not be used for children under 12 years without the advice of a doctor and should not be used in place of any other treatment prescribed by the doctor. Dosage and method of administration Unless otherwise directed, take a bath 2 to 3 times a week. Use 2 tablespoonfuls (approx. 30 ml) of bath additive for a full bath, one tablespoonful (approx. 15 ml) for a sitzbath. The temperature of the bath water should be between 35° and 37°, the bathing time about 20 minutes.

489

S

Duration of treatment In acute illness the medicinal product is usually used 2 to 3 times a week for 2 to 3 weeks. In chronic conditions the treatment may be continued for a longer period if permitted by the doctor.

Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily.

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Solum Inject 10

Liquid dilution for injection Potency/Strength Package Size Size Category

5 x 10 ml 20 x 10 ml

N1 N2

PZN 0084758 0090500

Price Group 21 22

Status Pharmacy only Pharmacy only

Solum Globuli velati Globuli velati

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 10 ml contain: aesculus hippocastanum e semine ferm 34c dil. D11 1.0 g (HAB, Method 34c) equisetum arvense ex herba ferm 35b dil. D11 1.0 g (HAB, Method 35b) solum uliginosum dil. D11 aquos. [HAB, Method 5b, D1 solution of aqueous extract (1 : 5) of solum uliginosum] 1.0 g

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and harmonisation of the feeling organisation, e.g. in rheumatic disorders, sensitivity to changes in the weather, spinal syndromes and nerve pain (neuralgia).

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Dosage and method of administration Unless otherwise directed, in painful states inject 10 ml intravenously once daily. You cannot perform the intravenous injection of the medicinal product yourself. Please ask your doctor to give you the injection.

Side-effects None known.

Contraindications None known.

Solum Inject

Liquid dilution for injection Potency/Strength Package Size Size Category

S

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aesculus hippocastanum e semine ferm 34c dil. D11 0.1 g (HAB, Method 34c) equisetum arvense ex herba ferm 35b dil. D11 0.1 g (HAB, Method 35b) solum uliginosum dil. D11 aquos. [HAB, Method 5b, D1 solution of aqueous extract (1 : 5) of solum uliginosum] 0.1 g

490

N1 N2

PZN 0084741 0090492

Price Group 11 12

Status

20 g

Composition Globuli velati: 10 g contain: aesculus hippocastanum e semine ferm 34c dil. D2 0.1 g (HAB, Method 34c) aesculus hippocastanum e semine ferm 34c dil. D4 0.1 g (HAB, Method 34c) equisetum arvense ex herba ferm 35b dil. D2 (HAB, Method 35b) equisetum arvense ex herba ferm 35b dil. D14 0.1 g (HAB, Method 35b) solum uliginosum dil. D14 aquos. [HAB, Method 5b, D1 solution of aqueous extract (1 : 5) of solum uliginosum] 0.1 g solum uliginosum dil. D2 aquos. [HAB, Method 5b, D1 solution of aqueous extract (1 : 5) of solum uliginosum] 0.1 g Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and harmonisation of the feeling organisation, e.g. in sensitivity to changes in the weather, nerve pain (neuralgia), adjunctive treatment of spinal complaints.

N1

PZN 0084824

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 6 years after consulting a doctor. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Solum Globuli velati. Dosage and method of administration Unless otherwise directed, children from 6 to under 12 years 5-10 globuli velati sublingually 1 to 3 times daily, in the case of acute pain 15 globuli velati sublingually up to 5 times; adults and children of 12 years and above 5-10 globuli velati daily sublingually 1 to 3 times daily, in the case of acute pain 30 globuli velati sublingually up to 5 times. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and harmonisation of the feeling organisation, e.g. in rheumatic disorders, sensitivity to changes in the weather, spinal syndromes and nerve pain (neuralgia).

S

Contraindications None known.

491

Solum Öl

Oily embrocation 50 ml (N1), 100 ml (N2), 500 ml (N3) Potency/Strength Package Size Size Category

50 ml 100 ml 500 ml

Composition 10 g (11 ml) contain: aesculus hippocastanum e semine LA 25% sicc. 0.02 g (HAB, Method 12m) equisetum arvense ex herba LA 20% 0.02 g (HAB, Method 12c) lavandulae aetheroleum 0.5 g solum uliginosum, aqueous extract (peat extract) (drug to extraction agent - 1:5) 1.96 g Excipients: virgin olive oil, wool alcohol ointment (cetyl stearyl alcohol, wool alcohols and white soft paraffin). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and harmonisation of the feeling organisation, e.g. in rheumatic disorders, sensitivity to changes in the weather, spinal syndromes and nerve pain (neuralgia).

N1 N1 N3

PZN 1448501 1448493 1448518

Price Group L L1 L2

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications Solum Öl should not be used on inflamed or damaged skin or in the case of hypersensitivity to any of the ingredients. Warnings and precautions for use Cetyl stearyl alcohol and wool alcohols can cause local skin reactions (e.g. contact dermatitis). Dosage and method of administration Unless otherwise directed, rub in 2 to 3 ml oil (depending on the part of the body affected) once to twice daily, then wrap in a woollen cloth. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Allergic skin reactions can occur in rare cases. In this case use of the medicinal product should be stopped and a doctor consulted.

Solum Salbe Ointment

Potency/Strength Package Size Size Category

S

30 g

Composition 10 g contain: aesculus hippocastanum e semine LA 25% sicc. 0.02 g (HAB, Method 12m) equisetum arvense ex herba LA 20% 0.02 g (HAB, Method 12c) solum uliginosum, aqueous extract (peat extract) (drug to extraction agent = 1:5) 1.96 g Excipients: refined arachis oil, white soft paraffin, wool fat.

492

N1

PZN 1448524

Price Group J

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and harmonisation of the feeling organisation, e.g. in rheumatic disorders, sensitivity to changes in the weather, spinal syndromes and nerve pain (neuralgia).

Warnings and precautions for use There is no adequately documented experience of use of the medicinal product in children. Solum Salbe should therefore not be used in children under 12 years. In rare cases arachis oil and wool fat can cause local skin reactions (e.g. contact dermatitis).

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Dosage and method of administration Unless otherwise directed, rub in the ointment locally once to twice daily.

Solum uliginosum comp. see Solum Badezusatz see Solum Globuli velati see Solum Inject see Solum Inject 10 see Solum Öl see Solum Salbe

Spongia comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8787790

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: euspongia officinalis 0.1 g saccharum candidum trit. D5 0.1 g (HAB, Method 6) testa ovorum trit. D5 0.1 g (HAB, Method 6) Contains sucrose (saccharose/sugar) and lactose.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. 10 globuli velati of the medicinal product contain approx. 20 µg iodine. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Spongia comp.

Indications according to the anthroposophical understanding of human beings and nature. For supporting treatment in the case of an enlarged thyroid gland with normal levels of thyroid hormone (euthyroid goitre).

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily.

Contraindications Do not use in the case of latent or manifest hyperthyroidism (overactive thyroid gland).

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Contraindications Solum Salbe should not be used on inflamed or damaged skin or in the case of hypersensitivity to any of the ingredients.

S

493

Spongia tosta

Spongia/Aurum/Pulsatilla comp.

Active ingredient: euspongia officinalis aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D6 D15

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: euspongia officinalis dil. D.. aquos. 1 ml (HAB, Method 6) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of hypersensitivity to milk protein.

N1 N1

Globuli velati PZN 3657982 3658007

Price Group 61 61

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g euspongia officinalis dil. D9 0.1 g (HAB, Method 6) pulsatilla vulgaris e floribus ferm 33c dil. D4 0.1 g (HAB, Method 33c) saccharum candidum dil. D9 0.1 g (HAB, Method 6) sepia officinalis e volumine bursae rec. Gl dil. D6 0.1 g (HAB, Method 41c) testa ovorum dil. D9 0.1 g (HAB, Method 6) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Symptoms associated with the change of life (menopausal symptoms), particularly with disturbances of thyroid function.

Spongia/Aurum/Pulsatilla comp.

N1

PZN 8787809

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Spongia/Aurum/Pulsatilla comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment If the symptoms persist for more than 3 months patients are advised to consult their doctor again. Side-effects None known.

Liquid dilution for injection

Potency/Strength Package Size Size Category

S

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g euspongia officinalis dil. D9 0.1 g (HAB, Method 6) pulsatilla vulgaris e floribus ferm 33c dil. D4 0.1 g (HAB, Method 33c) saccharum candidum dil. D9 0.1 g (HAB, Method 6) sepia officinalis e volumine bursae rec. Gl dil. D7 0.1 g (HAB, Method 41c) testa ovorum dil. D9 0.1 g (HAB, Method 6) Indications according to the anthroposophical understanding of human beings and nature. Symptoms associated with the

494

N1

PZN 1752222

Price Group 11

Status Pharmacy only

change of life (menopausal symptoms), particularly with disturbances of thyroid function. Contraindications Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment If the symptoms persist for more than 3 months patients are advised to consult their doctor again. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Stomachus

see Ventriculus GI

Strophanthus comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: aurum metallicum dil. D9 0.1 g stibium metallicum dil. D7 0.1 g strophanthus kombe e semine ferm 35b dil. D4 0.1 g (HAB, Method 35b) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of a weakened

N1 N2

PZN 1752239 2086945

Price Group 11 12

Status Pharmacy only Pharmacy only

cardiovascular system with disturbed rhythm, particularly after infectious diseases or in the case of mental and emotional stress. Contraindications Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

495

S

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there

is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Strophanthus comp. Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: aurum metallicum dil. D9 0.1 g stibium metallicum dil. D7 0.1 g strophanthus kombe e semine ferm 35b dil. D2 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of a weakened cardiovascular system with disturbed rhythm, particularly after infectious diseases or in the case of mental and emotional stress. Contraindications None known.

N1

PZN 8787838

Price Group A

Status Pharmacy only

Potency/Strength Package Size Size Category

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: strophanthus kombe e semine ferm 35b Globuli velati

D3 D6

20 g 20 g

Composition Globuli velati: 10 g contain: strophanthus kombe e semine ferm 35b dil. D.. 1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Potency/Strength Package Size Size Category

496

Side-effects None known.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 3 times daily.

Contraindications None known.

Active ingredient: strophanthus kombe e semine ferm 35b Liquid dilution for injection

S

Duration of treatment Acute disorders should clear up within 2 weeks. If no improvement occurs within 2 days a doctor should be consulted. In the case of chronic conditions the treatment must be given continuously or in the form of courses of treatment. This should be discussed with the doctor.

Strophanthus kombe e semine

Strophanthus kombe e semine

10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Dosage and method of administration Unless otherwise directed: Liquid dilution for injection D30: 1 ml by intramuscular injection 2 to 3 times a week. You should not perform the intramuscular injection of the medicinal product yourself. Please ask your doctor to give you the injection. Liquid dilution for injection D4 upwards: 1 ml by subcutaneous injection 2 to 3 times a week to once daily.

therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Strophanthus comp.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

D3 D3 D4 D6 D10

Indications according to the anthroposophical understanding of human beings and nature. Mild to moderately severe forms of heart failure on a degenerative basis, anginal complaints, states of anxiety and exhaustion. Contraindications None known.

Globuli velati



Composition Liquid dilution for injection: 1 ml contains: strophanthus kombe e semine ferm 35b dil. D.. 1 ml (HAB, Method 35b)

N1 N2 N1 N1 N1

PZN 3658243 3769190 3658266 3658303 2891262

Price Group V5 V6 31 31 31

Status

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

N1 N1

PZN 8787844 8787850

Price Group A A

Status Pharmacy only Pharmacy only

This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Strophanthus kombe e semine. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Prescription only Prescription only Pharmacy only Pharmacy only Pharmacy only

S

497

Strophanthus/Nicotiana comp.

sulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) plumbum mellitum dil. D14 aquos. 0.2 g (HAB, Method 8b) strophanthus kombe e semine ferm 35b dil. D5 0.1 g (HAB, Method 35b) Indications according to the anthroposophical understanding of human beings and nature. Harmonious integration of the feeling organisation in heart conditions of degenerative origin, e.g. impaired cardiac function associated with aging (presbycardia), "tightness in the chest" (stenocardia), angina pectoris, slow heartbeat (bradycardia).

N1 N2

PZN 1752245 2086951

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

20 g

Composition Globuli velati: 10 g contain: nicotiana tabacum e foliis ferm 33b dil. D9 0.1 g (HAB, Method 33b) plumbum mellitum dil. D14 aquos. 0.2 g (HAB, Method 8b) strophanthus kombe e semine ferm 35b dil. D5 0.1 g (HAB, Method 35b) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonious integration of the feeling organisation in heart conditions of degenerative origin, e.g. impaired cardiac function associated with aging (presbycardia), "tightness in the chest" (stenocardia), angina pectoris, slow heartbeat (bradycardia).

498

Potency/Strength Package Size Size Category D8 D12 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: sulfur dil. D.. aquos. 1 ml Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

N1 N1 N1 N1

PZN 3658450 2891285 3658473 3658504

Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

hypersensitivity to milk protein. Liquid dilution for injection D12 upwards: None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Active ingredient: sulfur aquos. Globuli velati

Globuli velati

S

Active ingredient: sulfur aquos. Liquid dilution for injection

Sulfur

Strophanthus/Nicotiana comp.



Sulfur

Contraindications Liquid dilution for injection D8: Do not use in the case of

Contraindications None known.

Potency/Strength Package Size Size Category

Side-effects None known.

PZN 8787867

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Strophanthus/Nicotiana comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily, in acute cases up to every 2 hours. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be con-

Potency/Strength Package Size Size Category D6 D12 D30

20 g 20 g 20 g

Composition Globuli velati: 10 g contain: sulfur dil. D.. aquos. 1g Contains sucrose (saccharose/sugar) and lactose. Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sug-

N1 N1 N1

PZN 8787873 8787896 8787904

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

ars you should consult your doctor before taking Sulfur. Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

499

S

Sympathicus Gl

hypersensitivity to arnica or other plants of the Compositae family or to any of the other ingredients.

Active ingredient: truncus sympathicus bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: truncus sympathicus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3658579 3658591 3658622 3658645 3658668 3658680 3658705 2497565

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

the medicinal product in children. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

Warnings and precautions for use There is no adequately documented experience of use of

Symphytum comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

S

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: allium cepa ferm 34a dil. D3 0.1 g arnica montana e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) stannum metallicum dil. D14 aquos. 0.1 g symphytum officinale e radice ferm 34c dil. D2 0.1 g (HAB, Method 34c)

500

N1 N2

PZN 1752251 2086968

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the structuring and form-giving processes in traumatic and inflammatory conditions of the bone and surrounding tissues, e.g. fractures, Sudeck's atrophy, inflammation of the outer layer of the bone (periostitis), tennis elbow (epicondylitis), repetitive strain injury (tendovaginitis).

Dosage and method of administration Unless otherwise directed, children under 6 years 0.5 ml injected subcutaneously twice a week to once daily; children from 6 to under 12 years 0.5-1 ml injected subcutaneously twice a week to once daily; adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

Symphytum comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: allium cepa ferm 34a dil. D3 0.1 g arnica montana e planta tota ferm 33c dil. D3 0.1 g (HAB, Method 33c) stannum metallicum dil. D9 0.1 g symphytum officinale e radice ferm 34c dil. D2 0.1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the structuring and form-giving processes in traumatic and inflammatory conditions of the bone and surrounding tissues, e.g. fractures, Sudeck‘s atrophy, inflammation of the outer layer of the bone (periostitis), tennis elbow (epicondylitis), repetitive strain injury (tendovaginitis). Contraindications The medicinal product should not be used in the case of hypersensitivity to arnica or other plants of the Compositae family or to any of the other ingredients.

N1

PZN 8787910

Price Group A

Status Pharmacy only

Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Symphytum comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Side-effects None known.

S

Contraindications The medicinal product should not be used in the case of

501

Symphytum e radice

Tabacum

Active ingredient: symphytum officinale e radice ferm 34c Liquid dilution for injection Potency/Strength Package Size Size Category D2 D3 D6

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: symphytum officinale e radice ferm 34c dil. D.. 1 ml (HAB, Method 34c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D2: Do not use during pregnancy or while breastfeeding. Liquid dilution for injection D3 and D6: None known.

N1 N1 N1

PZN 3358417 3358446 2832762

see Nicotiana tabacum e foliis Price Group 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Duration of treatment Do not use for longer than 6 weeks per year. Side-effects None known.

Potency/Strength Package Size Size Category

Composition Globuli velati: 10 g contain: symphytum officinale e radice ferm 34c dil. 1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known.

S

Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Symphytum e radice.

502

Potency/Strength Package Size Size Category D3 D3 D6 D8

10 x 1 ml 50 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: taraxacum officinale e planta tota ferm 34c dil. D.. 1 ml (HAB, Method 34c)

N1 N1

PZN 8787927 8787933

PZN 2891339 2891345 3769209 2891351

Price Group 31 32 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Active ingredient: taraxacum officinale e planta tota ferm 34c Globuli velati Price Group A A

Status Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

N1 N2 N1 N1

Taraxacum e planta tota

Active ingredient: symphytum officinale e radice ferm 34c Globuli velati

20 g 20 g

Active ingredient: taraxacum officinale e planta tota ferm 34c Liquid dilution for injection

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Symphytum e radice

D3 D6

Taraxacum e planta tota

Potency/Strength Package Size Size Category D3 D4 D6 D8 D30

20 g 20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: taraxacum officinale e planta tota ferm 34c dil. D.. 1 g (HAB, Method 34c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Taraxacum e planta tota.

N1 N1 N1 N1 N1

PZN 8787956 8787962 8787979 8787985 8787991

Price Group A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

T

503

Taraxacum e radice (autumnale)

Composition Liquid dilution for injection: 1 ml contains: tendo bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Active ingredient: taraxacum officinale e radice (autumnale) ferm 34c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: taraxacum officinale e radice (autumnale) ferm 34c dil. D.. 1 ml (HAB, Method 34c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN

Price Group

3658763 3658792

31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Tendo/Allium cepa comp. Liquid dilution for injection

Taraxacum e radice (vernale)

Potency/Strength Package Size Size Category

Active ingredient: taraxacum officinale e radice (vernale) ferm 34c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: taraxacum officinale e radice (vernale) ferm 34c dil. D.. 1 ml (HAB, Method 34c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 3658817 3658846



Price Group 31 31

Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Tendo Gl

Active ingredient: tendo bovis GI Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack III

T

504

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3658906 3658929 3658941 3658964 3658987 3659001 3659024 2497571

Price Group 61 61 61 61 61 61 61 51

N1 N2

PZN 2086974 2086980

Price Group 11 12

Status Pharmacy only Pharmacy only

Status

Contraindications None known.

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: allium cepa ferm 34a dil. D7 0.1 g arnica montana e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) periosteum bovis Gl dil. D16 0.1 g (HAB, Method 41b) stannum metallicum dil. D14 aquos. 0.1 g symphytum officinale e radice ferm 34c dil. D5 0.1 g (HAB, Method 34c) tendo bovis Gl dil. D16 0.1 g (HAB, Method 41b) vaginae synoviales tendinum bovis Gl dil. D16 0.1 g (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the processes of regeneration in conditions involving reactive inflamma-

tory changes of boundary-forming bradytrophic tissues of the musculoskeletal system, e.g. repetitive strain injury (tendovaginitis), inflammation of the outer layer of the bone (periostitis), tennis elbow (epicondylitis). Contraindications Tendo/Allium cepa comp. should not be used in the case of hypersensitivity to arnica or other plants of the Compositae family. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously in the vicinity of the affected region once to twice weekly, in acute states once to twice daily. Side-effects None known.

T

505

Tendo/Allium cepa comp.

Testes Gl

Globuli velati

Active ingredient: testes bovis GI Liquid dilution for injection

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: allium cepa ferm 34a dil. D7 0.1 g arnica montana e planta tota ferm 33c dil. D5 0.1 g (HAB, Method 33c) periosteum bovis Gl dil. D16 0.1 g (HAB, Method 41b) stannum metallicum dil. D14 aquos. 0.1 g symphytum officinale e radice ferm 34c dil. D5 0.1 g (HAB, Method 34c) tendo bovis Gl dil. D16 0.1 g (HAB, Method 41b) vaginae synoviales tendinum bovis Gl dil. D16 0.1 g (HAB, Method 41c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the processes of regeneration in conditions involving reactive inflammatory changes of boundary-forming bradytrophic tissues of the musculoskeletal system, e.g. repetitive strain injury (tendovaginitis), inflammation of the outer layer of the bone (periostitis), tennis elbow (epicondylitis).

N1

PZN 8788016

Price Group A

Status Pharmacy only

Contraindications Do not use in the case of hypersensitivity to arnica or other plants of the Compositae family. Warnings and precautions for use There is no adequately documented experience of use of Tendo/Allium cepa comp. in children under 2 years. It should therefore not be used in children under 2 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Tendo/ Allium cepa comp. Dosage and method of administration Unless otherwise directed, adults and children of 2 years and above 3-5 globuli velati sublingually up to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: terebinthina laricina dil. D.. 1 ml (HAB, Method 6)

T

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

506

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: testes bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3354394 3354402 3354419 3354425 2831254 3354431 3354448 3354454 2497654

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. On account of its composition the medicinal product is only for use in male patients. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Testes comp.

Liquid dilution for injection

Active ingredient: terebinthina laricina aquos. Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack III

Warnings and precautions for use Sufficiently documented experience for the use of this

Terebinthina laricina

D8 D12 D30

Potency/Strength Package Size Size Category

N1 N1 N1

Potency/Strength Package Size Size Category PZN 2891374 3659047 2891411

Price Group 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week.



10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: apis regina tota Gl dil. D5 0.1 g (HAB, Method 41c) argentum metallicum dil. D5 0.1 g testes bovis Gl dil. D7 0.1 g (HAB, Method 41a)

N1 N2

PZN 1752268 2086997

Price Group 11 12

Status Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of hypersensitivity to bee venom or milk protein.

Side-effects None known.

507

T

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. On account of its composition the medicinal product is only for use in male patients. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects In very rare cases hypersensitivity reactions may occur; in this case treatment with the medicinal product should be discontinued. In patients with bee venom allergy ad-

ministration of this medicinal product can lead to allergic reactions such as hives (urticaria), difficulty breathing (bronchospasm) and in extreme cases anaphylactic shock with cardiovascular arrest. Although the medicinal product has been used for several decades without any reports of severe systemic allergic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Testes/Argentum

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

11

Status Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Globuli velati

Potency/Strength Package Size Size Category 20 g

Composition Globuli velati: 10 g contain: apis regina tota Gl dil. D4 0.1 g (HAB, Method 41c) argentum metallicum dil. D5 0.1 g testes bovis Gl dil. D4 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose. Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of known hypersensitivity to bee venom.

N1

PZN 8788022

Price Group A

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Testes comp. On account of its composition the medicinal product is only for use in male patients. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Testes/Argentum Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: argentum metallicum dil. D5 0.1 g testes bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose. Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

508

Price Group

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. On account of its composition the medicinal product is only for use in male patients.

Testes comp.

T

PZN 1752274

Composition Liquid dilution for injection: 1 ml contains: argentum metallicum dil. D5 0.1 g testes bovis Gl dil. D7 0.1 g (HAB, Method 41a)

Contraindications Do not use in the case of hypersensitivity to milk protein.



N1

N1

PZN 8788039

Price Group A

Status Pharmacy only

This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Testes/ Argentum. On account of its composition the medicinal product is only for use in male patients. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

T

509

Thalamus Gl

Composition Liquid dilution for injection: 1 ml contains: thrombocytes equi Gl dil. D.. 1 ml (HAB, Method 41d)

Active ingredient: thalamus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: thalamus bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3659248 3659260 3659283 3659314 3659337 3659366 3659389 2497660

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3353868 3353874 3353880 3353897 3353905 3353911 3354460 0847162 2497677

Price Group 41 41 41 41 41 41 41 41 41

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Thuja e summitatibus

Active ingredient: thuja occidentalis e summitatibus ferm 33e Liquid dilution for injection Potency/Strength Package Size Size Category D3 D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: thrombocytes equi GI Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Composition Liquid dilution for injection: 1 ml contains: thuja occidentalis e summitatibus ferm 33e dil. D.. 1 ml (HAB, Method 33e)

Thrombocyten Gl

D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

N1 N1 N1 N1

PZN 3358452 3358469 2891434 3358475

Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Thuja e summitatibus

Active ingredient: thuja occidentalis e summitatibus ferm 33e Globuli velati Potency/Strength Package Size Size Category D3 D4 D6 D12 D15 D30

20 g 20 g 20 g 20 g 20 g 20 g

N1 N1 N1 N1 N1 N1

PZN 8788068 8788074 8788080 8788097 8788105 8788111

Price Group A A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

T

T

510

511

Composition Globuli velati: 10 g contain: thuja occidentalis e summitatibus ferm 33e dil. D.. 1 g (HAB, Method 33e) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the feeling organisation in digestive weakness with impaired internal uptake of nutrients and predominance of the unformed metabolic processes in the region of the head and in the region of the skin, e.g. inflammation of the ear (otitis), inflammation of the lining of the mouth (stomatitis), eczema; warts and other growths of the skin and mucous membranes. Contraindications None known.

you suffer from intolerance to certain sugars you should consult your doctor before taking Thuja e summitatibus. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use This medicinal product contains sucrose. If you know that

Potency/Strength Package Size Size Category

Composition 10 g (10.3 ml) contain: thuja occidentalis e summitatibus LA 20% 10 g (HAB, Method 12c) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the feeling organisation in digestive weakness with impaired internal uptake of nutrients and predominance of the unformed metabolic processes in the region of the head and in the region of the skin, e.g. adjunctive treatment of inflammation of the ear (otitis), inflammation of the lining of the mouth (stomatitis), eczema; warts and other growths of the skin and mucous membranes.

T

Contraindications Do not use in the case of known hypersensitivity to the active ingredient. As Thuja-Essenz contains thujone it must not be applied to mucous membranes during pregnancy or breastfeeding. As Thuja-Essenz contains thujone it must not be applied to mucous membranes of children under 12 years.

512

Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: thuja occidentalis e summitatibus LA 20% Tincture for external use

100 ml

Active ingredient: glandula thymi bovis Gl Liquid dilution for injection

Composition Liquid dilution for injection: 1 ml contains: glandula thymi bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Thuja-Essenz



Thymus (Glandula) Gl

N1

PZN 1681433

Price Group E

Status Pharmacy only

Warnings and precautions for use Contains 25% (v/v) alcohol. Dosage and method of administration Unless otherwise directed: Compresses; rinses: add 1 to 2 teaspoons of tincture to approx. 250 ml water and use for compresses or rinses. Baths: add 2 to 3 tablespoons of tincture to 1 full bath. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. Treatment of chronic conditions must be discussed with the doctor. Thuja-Essenz should not be used for rinses of mucous membranes for longer than 2 weeks without consulting a doctor. Side-effects Hypersensitivity reactions may occur in sensitised persons; in this case use of the medicinal product should be stopped and a doctor consulted.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2829441 2830266 2829576 3353928 3353934 3353940 3353957 3353986 2487733 0847179 2497944

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Thymus/Mercurius Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

N1

PZN 1752280

Price Group 11

Status Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: glandula thymi bovis Gl dil. D7 0.1 g (HAB, Method 41a) mercurius vivus dil. D14 aquos. 0.1 g

Contraindications None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

513

T

Duration of treatment The duration of treatment should be discussed with the doctor.

Side-effects None known.

(about 1 teaspoonful) for a full bath (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes.

Thymus/Mercurius Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: glandula thymi bovis Gl dil. D7 0.1 g (HAB, Method 41a) mercurius vivus dil. D14 aquos. 0.1 g Contains sucrose (saccharose/sugar).

N1

PZN 8788128

Price Group A

Status

Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Contraindications None known.

Duration of treatment The duration of treatment should be discussed with the doctor.

Warnings and precautions for use This medicinal product contains sucrose. If you know that

Side-effects None known.

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna ex herba ferm 33a dil. D14 0.1 g (HAB, Method 33a) chalkosine dil. D5 0.1 g conchae dil. D6 0.1 g glandula thyreoidea bovis Gl dil. D7 0.1 g (HAB, Method 41a)

Potency/Strength Package Size Size Category

Contraindications Do not use in the case of hypersensitivity to milk protein.

100 ml

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation in acute respiratory infections and chronic hardening processes, e.g. acute and spastic bronchitis, adjunctive treatment of Sudeck‘s atrophy and rickets. Contraindications Thymus, Oleum aethereum 5% should not be used in the

514

Liquid dilution for injection

Active ingredient: thymi aetheroleum 5% Liquid bath additive

Composition 10 g (11 ml) contain: thymi aetheroleum 5% (HAB, Method 12i with virgin olive oil) 10 g

T

Thyreoidea comp.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of thyroid function in overactivity of the thyroid gland (hyperthyroidism).

Thymus, Oleum aethereum 5%



PZN

Price Group

2088849

N1

Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Pharmacy only

you suffer from intolerance to certain sugars you should consult your doctor before taking Thymus/Mercurius.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects None known.

Status General Sale

case of known hypersensitivity to thyme or other plants of the Lamiaceae family (labiates). Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. During breastfeeding: Do not breastfeed immediately after the bath. Cleanse the skin in the region of the breasts before breastfeeding. Dosage and method of administration Unless otherwise directed, for adults and children of 12 years and above use 3 to 5 ml of liquid bath additive

N1 N2

PZN 1752297 2087028

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Duration of treatment The disorder should have cleared up within 2 weeks. If there is no improvement within three days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Thyreoidea comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: atropa belladonna ex herba ferm 33a dil. D14 0.1 g (HAB, Method 33a) chalkosine dil. D5 0.1 g

N1

PZN 8788134

Price Group A

Status Pharmacy only

conchae dil. D6 0.1 g glandula thyreoidea bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose.

T

515

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of thyroid function in overactivity of the thyroid gland (hyperthyroidism). Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain

sugars you should consult your doctor before taking Thyreoidea comp. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 3 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Thyreoidea/Ferrum.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily. Side-effects None known.

Thyreoidea/Thymus comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

Thyreoidea/Ferrum Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ferrum metallicum dil. D9 0.1 g glandula thyreoidea bovis Gl dil. D7 0.1 g (HAB, Method 41a) Indications according to the anthroposophical understanding of human beings and nature. Adjunctive treatment of mild forms of thyroid dysfunction. Contraindications Do not use in the case of hypersensitivity to milk protein.

N1 N2

PZN 1752305 2087034

Price Group 11 12

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times a week. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: arsenicum album dil. D5 aquos. 0.1 g (HAB, Method 5b) cuprum sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b) glandula thymi bovis Gl dil. D4 0.1 g (HAB, Method 41a) glandula thyreoidea bovis Gl dil. D31 0.1 g (HAB, Method 41a) hypophysis bovis Gl dil. D21 0.1 g (HAB, Method 41a) lycopus virginicus e planta tota ferm 33d dil. D2 0.1 g (HAB, Method 33d) melissa officinalis ex herba ferm 33c dil. D3 0.1 g (HAB, Method 33c) vespa crabro ex animale toto Gl dil. D5 0.1 g (HAB, Method 41c)

N1

PZN 1752311

Price Group 11

Status Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Thyreoidea/Ferrum Globuli velati

Thyreoidea/Thymus comp.

Potency/Strength Package Size Size Category

T

20 g

Composition Globuli velati: 10 g contain: ferrum metallicum dil. D9 0.1 g glandula thyreoidea bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar) and lactose.

516

N1

PZN 8788140

Price Group A

Status Pharmacy only

Indications according to the anthroposophical understanding of human beings and nature. Adjunctive treatment of mild forms of thyroid dysfunction. Contraindications None known.

Globuli velati

Potency/Strength Package Size Size Category Composition Globuli velati: 10 g contain: arsenicum album dil. D5 aquos. 0.1 g (HAB, Method 5b) cuprum sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b)

20 g

N1

PZN 8788157

Price Group A

Status Pharmacy only

glandula thymi bovis Gl dil. D4 0.1 g (HAB, Method 41a) glandula thyreoidea bovis Gl dil. D31 0.1 g (HAB, Method 41a) hypophysis bovis Gl dil. D21 0.1 g (HAB, Method 41a)

T

517

lycopus virginicus e planta tota ferm 33d dil. D2 0.1 g (HAB, Method 33d) melissa officinalis ex herba ferm 33c dil. D3 0.1 g (HAB, Method 33c) vespa crabro ex animale toto Gl dil. D5 0.1 g (HAB, Method 41c) Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should

therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Thyreoidea/Thymus comp.

Tonsilla pharyngea Gl

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually once a week to once daily.

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: tonsillae palatinae bovis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

T

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

518

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Active ingredient: tonsillae palatinae bovis GI Liquid dilution for injection

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: tonsilla pharyngea bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Tonsillae palatinae Gl

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

Active ingredient: tonsilla pharyngea bovis GI Liquid dilution for injection

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3354023 3354046 3354052 3354069 3354075 3354081 3354098 3354017 0847191 2498004

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3660470 3660493 3660518 3660530 3660553 3660582 3660607 2497950

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Topas

Active ingredient: topaz aquos. Liquid dilution for injection Potency/Strength Package Size Size Category D15

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: topaz dil. D15 aquos. 1 ml (HAB, Method 8b) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 3660820

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Side-effects None known.

T

519

Tormentilla comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1752328 2087057

Price Group 11 12

Status Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: cochlearia officinalis ex herba ferm 33b dil. D2 0.1 g (HAB, Method 33b) potentilla erecta e radice ferm 34d dil. D2 0.1 g (HAB, Method 34d) stibium metallicum dil. D5 0.1 g

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Structuring of the life organisation and forming of the blood-protein processes by the ego organisation in non-traumatic bleeding, e.g. excessive menstrual flow (menorrhagia), bleeding in the gastrointestinal tract.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications Do not use in the case of hypersensitivity to milk protein.

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously 3 times a week to twice daily.

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects None known.

Tormentilla e radice

Active ingredient: potentilla tormentilla e radice ferm 34d Liquid dilution for injection Potency/Strength Package Size Size Category D30

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: potentilla erecta e radice ferm 34d dil. D30 1 ml (HAB, Method 34d) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 3660843

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Tormentilla e radice

Active ingredient: potentilla tormentilla e radice ferm 34d Globuli velati

Tormentilla comp. Globuli velati

Potency/Strength Package Size Size Category

Potency/Strength Package Size Size Category

D6



20 g

Composition Globuli velati: 10 g contain: cochlearia officinalis ex herba ferm 33b dil. D2 0.1 g (HAB, Method 33b) potentilla erecta e radice ferm 34d dil. D2 0.1 g (HAB, Method 34d) stibium metallicum dil. D5 0.1 g Contains sucrose (saccharose/sugar) and lactose.

T

Indications according to the anthroposophical understanding of human beings and nature. Structuring of the life organisation and forming of the blood-protein processes by the ego organisation in non-traumatic bleeding, e.g. excessive menstrual flow (menorrhagia), bleeding in the gastrointestinal tract.

520

N1

PZN 8788163

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Tormentilla comp. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 5-10 globuli velati sublingually 3 times daily.

20 g

Composition Globuli velati: 10 g contain: potentilla erecta e radice ferm 34d dil. D6 1 g (HAB, Method 34d) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Tormentilla e radice.

N1

PZN 8788192

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

T

521

Trachea Gl

Composition Liquid dilution for injection: 1 ml contains: trigonum vesicae et musculus sphincter bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Active ingredient: trachea bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN

Price Group

3660926 3660949 3660961 3660984 3661009 3661021 3661044 2498085

61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: trachea bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: trigonum vesicae et musculus sphincter bovis Gl Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3661110 3661133 3661162 3661185 3661216 3661239 3661251 2487905 2498205

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

522

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: triticum aestivum e fructibus germinatis ferm 33d dil. D19 0.1 g (HAB, Method 33d) truncus cerebri bovis Gl dil. D7 0.1 g (HAB, Method 41a)

Contraindications None known.

N1

PZN 1752334

Price Group 11

Status Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 3 times a week. Duration of treatment Degenerative disorders require continuous treatment or courses of treatment. The duration of treatment should be discussed with the doctor. Side-effects None known.

Triticum comp. I Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: triticum aestivum e fructibus germinatis ferm 33d dil. D2 0.1 g (HAB, Method 33d)

T

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Triticum comp. I

Indications according to the anthroposophical understanding of human beings and nature. Reorganisation of the integrative structures of the nervous system in the interaction between life organisation and physical organisation, e.g. in degenerative central processes.

Trigonum vesicae et Musculus sphincter Gl

Potency/Strength Package Size Size Category

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

N1

PZN 8788200

Price Group A

Status Pharmacy only

truncus cerebri bovis Gl dil. D7 0.1 g (HAB, Method 41a) Contains sucrose (saccharose/sugar).

T

523

Indications according to the anthroposophical understanding of human beings and nature. Reorganisation of the integrative structures of the nervous system in the interaction between life organisation and physical organisation, e.g. in degenerative central processes. Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that

you suffer from intolerance to certain sugars you should consult your doctor before taking Triticum comp. I. Warning for people with gluten intolerance: Triticum comp. I globuli velati contain gluten.

Tuba auditiva Gl

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually once daily.

Potency/Strength Package Size Size Category

Duration of treatment Degenerative disorders require continuous treatment or courses of treatment. The duration of treatment should be discussed with the doctor. Side-effects None known.

Truncus coeliacus Gl

Active ingredient: truncus coeliacus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D6 D15

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: truncus coeliacus bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D15: None known.

Truncus sympathicus Gl see Sympathicus GI

N1 N1

PZN 3785970 3786053

Price Group 61 61

Status Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: tuba auditiva bovis GI Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

524

PZN 3354129 3354135 2830007 3354141 3354158 3354164 3353549 2498228

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: tuba auditiva bovis Gl dil. D.. 1 ml (HAB, Method 41b)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Tuba uterina Gl

Active ingredient: tuba uterina bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: tuba uterina bovis Gl dil. D.. 1 ml (HAB, Method 41b) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

T

N1 N1 N1 N1 N1 N1 N1 N1

N1 N1 N1 N1

PZN 3786840 3786892 3786946 3786981

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

525

T

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Side-effects None known.

Duration of treatment The duration of treatment should be discussed with the doctor.

Duration of treatment The duration of treatment should be discussed with the doctor.

Tulipa e planta tota

Tunica mucosa nasi Gl

Active ingredient: tulipa silvestris e planta tota ferm 33a Liquid dilution for injection Potency/Strength Package Size Size Category D6

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: tulipa silvestris e planta tota ferm 33a dil. D6 1 ml (HAB, Method 33a) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 2830378

Active ingredient: tunica mucosa nasi bovis GI Liquid dilution for injection Price Group 31

Status

Potency/Strength Package Size Size Category

Pharmacy only

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

see Colon GI

Tunica mucosa intestini tenuis Gl

Active ingredient: tunica mucosa intestini tenuis suis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: tunica mucosa intestini tenuis suis Gl dil. D.. 1 ml (HAB, Method 41a)

T

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

526

N1 N1 N1 N1 N1 N1 N1

PZN 3787549 3787561 3787584 3787621 3787644 3787667 2492591

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: tunica mucosa nasi bovis Gl dil. D.. 1 ml (HAB, Method 41a)

Tunica mucosa coli GI

D5 D6 D8 D12 D15 D30 Serial pack

Side-effects None known.

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3353555 3353561 3353584 3353590 3353609 2830852 3353615 2498234

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Tunica mucosa recti Gl

Active ingredient: tunica mucosa recti suis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 3787845 3787868 3787880 3787928 3787940 3787963 2492622

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

527

T

Composition Liquid dilution for injection: 1 ml contains: tunica mucosa recti suis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Ureter Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

D5 D6 D8 D10 D12 D15 D30 Serial pack III

Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Side-effects None known.

Active ingredient: tunica mucosa ventriculi suis GI Liquid dilution for injection

D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: tunica mucosa ventriculi suis Gl dil. D.. 1 ml (HAB, Method 41a) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1 N1

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ureter bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Tunica mucosa ventriculi Gl

Potency/Strength Package Size Size Category

Active ingredient: ureter bovis GI Liquid dilution for injection

PZN 3788046 3788069 3788081 3788106 3788129 3788141 3788164 2487986 0847274

Price Group 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3788448 3788460 3788483 3788514 3788537 3788566 3788589 2498292

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Urethra feminina Gl

Active ingredient: urethra feminina bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: urethra feminina bovis Gl dil. D.. 1 ml (HAB, Method 41c)

N1 N1 N1 N1 N1 N1 N1

PZN 3788655 3788678 3788690 3788738 3788750 3788773 2492639

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

T U 528

529

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Urethra masculina Gl

Active ingredient: urethra masculina anterior bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: urethra masculina anterior bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1 N1

Composition Liquid dilution for injection: 1 ml contains: conchae dil. D6 0.1 g stannum metallicum dil. D9 0.1 g urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic balance between anabolic and catabolic processes in exudative and allergic diathesis of the skin, e.g. eczema, inflammatory skin conditions (dermatitis), itching.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Contraindications Do not use in the case of hypersensitivity to milk protein. PZN

0491311 0491328 0491334 0491340 0491357 0491363 0491386 2498300

Price Group 61 61 61 61 61 61 61 51

Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Urtica comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: conchae trit. D2 0.5 g stannum metallicum dil. D9 0.1 g urtica urens ex herba ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the rhythmic balance between anabolic and catabolic processes in exudative and allergic diathesis of the skin, e.g. eczema, inflammatory skin conditions (dermatitis), itching. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If

Urtica comp.

Liquid dilution for injection



10 x 1 ml

N1

PZN 1752357

Price Group 11

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Status

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Potency/Strength Package Size Size Category

Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to once daily.

N1

PZN 8788223

Price Group A

Status Pharmacy only

you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Urtica comp. Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 2 to 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Status Pharmacy only

U

U 530

531

Urtica dioica e planta tota

Active ingredient: urtica dioica e planta tota ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D3 D6

10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: urtica dioica e planta tota ferm 33c dil. D.. 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1 N1

PZN 3789206 2891486

Price Group 31 31

Status Pharmacy only Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 2 to 3 times weekly to once daily. Side-effects None known.

Urtica dioica e planta tota

D3 D6

20 g 20 g

Composition Globuli velati: 10 g contain: urtica dioica e planta tota ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Urtica dioica e planta tota.

N1 N1

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Dosage and method of administration Unless otherwise directed, for adults and children of all age groups use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath tub (about 200 l water) for oil dispersion baths. The temperature of the bath water

should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for two to three weeks; in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects Hypersensitivity reactions may very rarely occur. In such cases use of Urtica dioica ex herba W 5%, Oleum should be discontinued and a doctor consulted. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Urtica urens ex herba

Active ingredient: urtica dioica e planta tota ferm 33c Globuli velati Potency/Strength Package Size Size Category

Composition 10 g (11 ml) contain: urtica dioica ex herba W 5% (HAB, Method 12g with virgin olive oil) 10 g

Active ingredient: urtica urens ex herba ferm 33c Liquid dilution for injection PZN

8788252 8788275

Price Group A A

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only

D6

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: urtica urens ex herba ferm 33c dil. D6 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Urtica urens ex herba

Active ingredient: urtica urens ex herba ferm 33c Globuli velati Potency/Strength Package Size Size Category D2 D4 D6

Urtica dioica ex herba W 5%, Oleum

PZN 2891500

20 g 20 g 20 g

N1 N1 N1

PZN 8788281 8788298 8788306

Price Group A A A

Status Pharmacy only Pharmacy only Pharmacy only

Active ingredient: urtica dioica ex herba W 5% Bath additive, liquid

Potency/Strength Package Size Size Category

100 ml

N1

PZN

Price Group

2088878

N1

Status General Sale

U

U 532

533

Composition Globuli velati: 10 g contain: urtica urens ex herba ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Urtica urens ex herba.

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily; children under 6 years 3-7 globuli velati sublingually 1 to 3 times daily; adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: uterus bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: uterus bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Active ingredient: vagina bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vagina bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Uterus Gl

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

Vagina Gl

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3789287 3789301 3789324 3789347 3789376 3789399 3789413 3789442 2488069 0847305 2498369

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

534

PZN 3789502 3789525 3789548 3789560 3789583 3789614 3789637 2498375

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Vaginae synoviales tendinum Gl

Active ingredient: vaginae synoviales tendinum bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vaginae synoviales tendinum bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the

U

N1 N1 N1 N1 N1 N1 N1 N1

N1 N1 N1

PZN 4624358 4624370 3789703

Price Group 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only

donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

535

V

Duration of treatment The duration of treatment should be discussed with the doctor.

Side-effects None known.

and above 5-10 globuli velati sublingually once daily; in the case of difficulty getting to sleep the dose should be taken in the late afternoon, no later than 1/2 hour before bedtime. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration.

Valeriana comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: conchae dil. D6 0.1 g phosphorus dil. D24 0.1 g sulfur dil. D24 aquos. 0.1 g valeriana officinalis e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 1752363

Price Group 11

Pharmacy only

Contraindications Do not use in the case of hypersensitivity to milk protein. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once to twice daily; in the case of difficulty getting to sleep the injection should be performed in the late afternoon, at the latest 1/2 hour before bedtime. Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the anabolic metabolism to relieve the nerve-sense-system, e.g. in difficulty falling asleep, states of restlessness.

V

536

Active ingredient: valeriana officinalis e radice ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D3

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: valeriana officinalis e radice ferm 33c dil. D3 1 ml (HAB, Method 33c) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

N1

PZN 3789778

Price Group 31

Status Pharmacy only

Contraindications None known. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Side-effects None known.

Active ingredient: valeriana officinalis e radice ferm 33c Globuli velati

Potency/Strength Package Size Size Category

Composition Globuli velati: 10 g contain: conchae dil. D6 0.1 g phosphorus dil. D24 0.1 g sulfur dil. D24 aquos. 0.1 g valeriana officinalis e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose.

Valeriana e radice

Valeriana e radice

Globuli velati

20 g

Side-effects None known.

Status

Valeriana comp.



Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 5 days a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

N1

PZN 8788312

Price Group A

Status

Potency/Strength Package Size Size Category

Pharmacy only

D4

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Valeriana comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually once daily; in the case of difficulty getting to sleep the dose should be taken in the late afternoon, no later than 1/2 hour before bedtime; children of 6 to under 12 years 5-7 globuli velati sublingually once daily; in the case of difficulty getting to sleep the dose should be taken in the late afternoon, no later than 1/2 hour before bedtime; adults and children 12 years

20 g

Composition Globuli velati: 10 g contain: valeriana officinalis e radice ferm 33c dil. D4 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Valeriana e radice.

N1

PZN 8788364

Price Group A

Status Pharmacy only

Dosage and method of administration Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7 globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

537

V

Valva trunci pulmonalis Gl

Duration of treatment The duration of treatment should be discussed with the doctor.

Active ingredient: valva trunci pulmonalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1

PZN 3789838 3789873 3789927 3789979

Price Group 61 61 61 61

Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Valvula mitralis Gl

Active ingredient: valvula mitralis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: valva trunci pulmonalis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: valvula aortae bovis GI Liquid dilution for injection

D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1

PZN 3790037 3790066 3790089 3790132 3790155 3790178 2492786

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: valvula mitralis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Valvula aortae Gl

Potency/Strength Package Size Size Category

D5 D6 D8 D12 D15 D30 Serial pack

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product

V

538

should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Valvula tricuspidalis Gl

Active ingredient: valvula tricuspidalis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

Composition Liquid dilution for injection: 1 ml contains: valvula aortae bovis Gl dil. D.. 1 ml (HAB, Method 41c)

PZN 3790238 3790250 3790273 3790327 3790356 3790379 2492800

D5 D8 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: valvula tricuspidalis bovis Gl dil. D.. 1 ml (HAB, Method 41c)

N1 N1 N1 N1

PZN 3790445 3790480 3790528 3790563

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

539

V

Contraindications Liquid dilution for injection D5: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Composition Liquid dilution for injection: 1 ml contains: vena femoralis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Vena cava Gl

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: vena cava bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8

10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vena cava bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8: None known.

N1 N1 N1

PZN 3790824 3790847 3790876

Price Group 61 61 61

Status

Vena portae Gl

Pharmacy only Pharmacy only Pharmacy only

Potency/Strength Package Size Size Category

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: vena femoralis bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category

V

540

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

D5 D6 D8 D12 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vena portae bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Vena femoralis Gl

D5 D6 D8 D12 D15 D30 Serial pack

Active ingredient: vena portae bovis GI Liquid dilution for injection

N1 N1 N1 N1 N1 N1 N1

PZN 3769994 3791025 3791048 3791083 3791114 3791137 2492875

Price Group 61 61 61 61 61 61 51

N1 N1 N1 N1 N1 N1

PZN 3791999 3792013 3792042 3792088 3792102 3792125

Price Group 61 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

541

V

Vena saphena magna Gl

Active ingredient: vena saphena magna bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3792390 3792415 3792438 3792450 3792473 3792504 3792527 2498429

Price Group 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: vena saphena magna bovis Gl dil. D.. 1 ml (HAB, Method 41c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Ventriculus Gl

Active ingredient: ventriculus suis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack I Serial pack II Serial pack III

V

542

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3353650 3353667 2831188 3353673 2831627 3353696 2831834 3353621 2488224 0847357 2498487

Price Group 41 61 61 61 61 61 61 61 51 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: ventriculus suis Gl Dil. D.. 1 ml (HAB, Method 41c)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Veratrum comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna ex herba ferm 33a dil. D2 0.1 g (HAB, Method 33a) chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) cinis e fructibus avenae sativae cum magnesio phosphorico (1:1) dil. D5 0.1 g (HAB, Method 6) cuprum sulfuricum dil. D5 aquos. 0.1 g (HAB, Method 5b) stibium metallicum dil. D5 0.1 g veratrum album e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the blood and nerve processes in varying physical symptoms not of organic origin, e.g. neurovegetative dysregulation, particularly with circulatory dysregulation. Contraindications The medicinal product should not be used in the case of known allergy to chamomile or other plants of the Compositae family, or known allergy to deadly nightshade or to the other active ingredients. It should also not be used

N1 N2

PZN 1752386 2234044

Price Group V5 V6

Status Prescription only Prescription only

in the case of raised intraocular pressure (glaucoma), enlargement of the prostate gland (prostatic adenoma) with incomplete bladder emptying, or cardiac rhythm disorders with accelerated heart beat. Do not use in the case of hypersensitivity to milk protein. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, adults and children of 12 years and above 1 ml injected subcutaneously twice a week to twice daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases dry mouth, facial flush, enlarged pupils, agitation or accelerated heart beat can occur on use of the medicinal product. In this case use of the medicinal product should be stopped and a doctor consulted. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

543

V

Veratrum comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: atropa belladonna ex herba ferm 33a dil. D2 0.1 g (HAB, Method 33a) chamomilla recutita e radice ferm 33c dil. D2 0.1 g (HAB, Method 33c) cinis e fructibus avenae sativaecum magnesio phosphorico (1:1) dil. D5 0.1 g (HAB, Method 6) cuprum sulfuricum dil. D3 aquos. 0.1 g (HAB, Method 5b) stibium metallicum dil. D5 0.1 g veratrum album e radice ferm 33c dil. D3 0.1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar) and lactose. Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the blood and nerve processes in varying physical symptoms not of organic origin, e.g. neurovegetative dysregulation, particularly with circulatory dysregulation. Contraindications The medicinal product should not be used in the case of known allergy to chamomile or other plants of the Compositae family, or known allergy to deadly nightshade or to the other active ingredients. It should also not be used in the case of raised intraocular pressure (glaucoma), en-

N1

PZN 8788387

Price Group A

Status Pharmacy only

largement of the prostate gland (prostatic adenoma) with incomplete bladder emptying, or cardiac rhythm disorders with accelerated heart beat. Warnings and precautions for use This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Veratrum comp. Dosage and method of administration Unless otherwise directed, children under 6 years 3-5 globuli velati sublingually 1 to 3 times daily, children of 6 to under 12 years 5-7 globuli velati sublingually 1 to 3 times daily, adults and children of 12 years and above 5-10 globuli velati sublingually 1 to 3 times daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases dry mouth, facial flush, enlarged pupils, agitation or accelerated heart beat can occur on use of the medicinal product. In this case use of the medicinal product should be stopped and a doctor consulted.

Veratrum e radice

Active ingredient: veratrum album e radice ferm 33c Liquid dilution for injection Potency/Strength Package Size Size Category D4 D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: veratrum album e radice ferm 33c dil. D.. 1 ml (HAB, Method 33c)

V

544

N1 N1 N1 N1

PZN 2832621 3358481 2891612 3358506

Price Group 31 31 31 31

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Contraindications D4: The medicinal product should not be used while pregnant or breastfeeding. Do not use in children under 6 years. D6, D12, D30: None known. Warnings and precautions for use D4: Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children between 6 and 12 years.

D6, D12, D30: Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Like all medicines, Veratrum e radice D6, D12 and D30 should only be used during pregnancy or breastfeeding after consultation of a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Side-effects None known.

Veratrum e radice

Active ingredient: veratrum album e radice ferm 33c Globuli velati Potency/Strength Package Size Size Category D3 D4 D6 D12 D30

20 g 20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: veratrum album e radice ferm 33c dil. D.. 1 g (HAB, Method 33c) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Acute circulatory weakness of mainly metabolic origin with a tendency to centralisation of the circulation and underactivity of the kidneys, particularly in connection with acute gastrointestinal disorders, poisoning and infectious diseases. Contraindications D3: The medicinal product should not be used while pregnant or breastfeeding. Do not use in children under 6 years. D4: The medicinal product should not be used while pregnant or breastfeeding. D6, D12 and D30: None known.

N1 N1 N1 N1 N1

PZN 8788393 8788401 8788418 8788424 8788430

Price Group A A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

D4, D6, D12 and D30: Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Veratrum e radice. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. D30: Unless otherwise directed, 5-10 globuli velati sublingually up to once daily. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within 1 day a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Warnings and precautions for use D3: Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children between 6 and 12 years.

545

V

Vertebra cervicalis Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily.

Active ingredient: vertebra cervicalis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vertebra cervicalis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 3793550 3793573 3793604 3793656 3793679 3793691 2492912

Price Group 61 61 61 61 61 61 51

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: vertebra coccygea bovis Gl Liquid dilution for injection

D5 D6 D12 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vertebra coccygea bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product

V

546

N1 N1 N1 N1

PZN 3793768 3793780 3793840 3793892

Vertebra lumbalis Gl

Active ingredient: vertebra lumbalis bovis Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D12 D15 D30 Serial pack

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vertebra lumbalis bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Vertebra coccygea Gl

Potency/Strength Package Size Size Category

Side-effects None known.

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Price Group 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D12 upwards: None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

Duration of treatment The duration of treatment should be discussed with the doctor.

Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

N1 N1 N1 N1 N1 N1 N1

PZN 3793969 3793981 3794006 3794041 3794064 3794087 2492964

Price Group 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Vesica fellea Gl

Active ingredient: vesica fellea bovis GI Liquid dilution for injection Potency/Strength Package Size Size Category D4 D5 D6 D8 D10 D12 D15 D30 Serial pack III

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 3353704 3353710 3353727 3353733 3353756 3353762 3353779 3353785 2498518

Price Group 41 61 61 61 61 61 61 61 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

547

V

Composition Liquid dilution for injection: 1 ml contains: vesica fellea bovis Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Vesica fellea/Ferrum I Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: ferrum metallicum dil. D7 0.1 g vesica fellea bovis Gl dil. D5 0.1 g (HAB, Method 41c) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of degenerative/ hardening and inflammatory/dissolving processes in the region of the biliary tract, e.g. stone formation (cholelithiasis), functional disturbances in the biliary tract. Contraindications Do not use in the case of hypersensitivity to milk protein or animal protein.

N1

PZN 1223736

Price Group 11

Vesica fellea/Ferrum II Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Price Group 11

Status Pharmacy only

Contraindications None known.

Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of degenerative/ hardening and inflammatory/dissolving processes in the region of the biliary tract, e.g. inflammation of the gallbladder (cholecystitis).

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Side-effects None known.

Status Pharmacy only

Vesica urinaria Gl

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Active ingredient: vesica urinaria bovis GI Liquid dilution for injection

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

D4 D5 D6 D8 D10 D12 D15 D30 Serial pack II Serial pack III

Side-effects The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D4, D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein. Liquid dilution for injection D8 upwards: None known.

548

PZN 1223682

Composition Liquid dilution for injection: 1 ml contains: ferrum metallicum dil. D19 aquos. 0.1 g vesica fellea bovis Gl dil. D16 0.1 g (HAB, Method 41c)

Composition Liquid dilution for injection: 1 ml contains: vesica urinaria bovis Gl dil. D.. 1 ml (HAB, Method 41c)

V

N1

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2830148 3353791 2831337 3353816 3353822 3353839 3353845 2830183 0847392 2498694

Price Group 41 61 61 61 61 61 61 61 51 51

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

549

V

Vespa Crabro ex animale Gl

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week.

Active ingredient: vespa crabro ex animale toto Gl Liquid dilution for injection Potency/Strength Package Size Size Category D5 D6 D8 D15 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: vespa crabro ex animale toto Gl dil. D.. 1 ml (HAB, Method 41c) Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Liquid dilution for injection D5, D6: The medicinal product should not be used in the case of hypersensitivity to the donor animal protein or hypersensitivity to bee venom. Liquid dilution for injection D8 upwards: The medicinal product should not be used in the case of hypersensitivity to bee venom.

N1 N1 N1 N1 N1

PZN 4625240 3794963 4625263 4626788 3794992

Price Group 61 61 61 61 61

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Dilution D20 upwards: Unless otherwise directed, inject 1 ml subcutaneously once a week to once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Active ingredient: viscum album (abietis) e planta tota ferm 34g Liquid dilution for injection

D2 D3 D6 D10 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: viscum album (abietis) e planta tota ferm 34g dil. D.. 1 ml (HAB, Method 34g) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

V

550

N1 N1 N1 N1 N1

PZN 3795046 3795069 3795106 3795141 3795201

Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous

Viscum comp.

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml 50 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: atropa belladonna e radice ferm 33b dil. D11 0.1 g (HAB, Method 33b) viscum album (populi) e planta tota ferm 33f dil. D5 0.1 g (HAB, Method 33f) Indications according to the anthroposophical understanding of human beings and nature. Harmonious integration of the feeling organisation in the metabolic and rhythmic systems, e.g. in mild forms of high blood pressure (hypertension), weakness of the heart associated with aging (presbycardia), follow-up treatment after stroke (CVA).

Viscum Abietis e planta tota

Potency/Strength Package Size Size Category

Duration of treatment The duration of treatment should be discussed with the doctor.

Price Group 41 41 41 41 41

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Contraindications Do not use in the case of known allergy to mistletoe formulations.

injection and temporary mild swelling of regional lymphnodes are no cause for concern. In very rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as: generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke‘s oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought.

Contraindications Do not use in the case of known allergy to mistletoe formulations. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily.

N1 N2

PZN 1752392 2234050

Price Group 11 12

Status Pharmacy only Pharmacy only

Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases, hypersensitivity to mistletoe may lead to local or systemic allergic or allergoid reactions, such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke's oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought. Although the medicinal product has been used for several decades without any reports of severe systemic reactions, such reactions cannot be ruled out. The risk of such reactions is likely to be increased if the product is inadvertently injected into a vein. The instructions on injection technique given under "Dosage and method of administration" should therefore be carefully observed. If itching, difficulty breathing, dizziness or other worrying symptoms occur during or after administration the injection should be interrupted and a doctor notified immediately. The patient should lie down flat, with the legs raised if appropriate.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

551

V

Viscum comp.

Duration of treatment The duration of treatment should be discussed with the doctor.

Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: atropa belladonna e radice ferm 33b dil. D9 0.1 g (HAB, Method 33b) viscum album (populi) e planta tota ferm 33f dil. D2 0.1 g (HAB, Method 33f) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonious integration of the feeling organisation in the metabolic and rhythmic systems, e.g. in mild forms of high blood pressure (hypertension), weakness of the heart associated with aging (presbycardia), follow-up treatment after stroke (CVA).

N1

PZN 8788447

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Viscum comp. Dosage and method of administration Unless otherwise directed, 10-15 globuli velati sublingually 1 to 3 times daily. Side-effects None known.

Viscum Mali e planta tota

Active ingredient: viscum album (mali) e planta tota ferm 34i Liquid dilution for injection Potency/Strength Package Size Size Category 2% 3% 5%

10 x 1 ml 10 x 1 ml 10 x 1 ml

PZN 3358564 3358570 3358587

Price Group 41 41 41

Status Pharmacy only Pharmacy only Pharmacy only

Composition Liquid dilution for injection: 1 ml contains: (in the respective medicinal product):

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

viscum mali e planta tota 2%: viscum album (mali) e planta tota ferm 34i Ø 0.02 g (HAB, Method 34i)

Contraindications Do not use in the case of known allergy to mistletoe formulations. The treatment can only be continued after desensitisation.

viscum mali e planta tota 3%: viscum album (mali) e planta tota ferm 34i Ø 0.03 g (HAB, Method 34i) viscum mali e planta tota 5%: viscum album (mali) e planta tota ferm 34i Ø 0.05 g (HAB, Method 34i)

V

N1 N1 N1

552

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week.

Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph

nodes are no cause for concern. In the case of intolerance of mistletoe, local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling in the region of the face (Quincke's oedema), shaking chills, difficulty breathing or shock can occur, in which case treatment with the preparation must be discontinued and immediate medical assistance sought. There are no data on the frequency of such reactions.

Viscum Mali e planta tota

Active ingredient: viscum album (mali) e planta tota ferm 34i Liquid dilution for injection Potency/Strength Package Size Size Category D2 D3 D4 D6 D8 D10 D12 D15 D30 D40 D60

10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: viscum album (mali) e planta tota ferm 34i D.. 1 ml (HAB, Method 34i). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of known allergy to mistletoe formulations. The treatment can only be continued after desensitisation. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

N1 N1 N1 N1 N1 N1 N1 N1 N1 N1 N1

PZN 2830390 2830384 2830409 2832733 3358512 3358529 3358541 3358558 2830361 0085539 0085640

Price Group 41 41 41 41 41 41 41 41 41 41 41

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the case of intolerance of mistletoe, local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling in the region of the face (Quincke's oedema), shaking chills, difficulty breathing or shock can occur, in which case treatment with the preparation must be discontinued and immediate medical assistance sought. There are no data on the frequency of such reactions.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week.

553

V

Viscum Mali e planta tota

Viscum Mali ex herba W 5%, Oleum

Active ingredient: viscum album (mali) e planta tota ferm 34i Globuli velati Potency/Strength Package Size Size Category D2 D4 D6 D30

20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: viscum album (mali) e planta tota ferm 34i dil. D.. 1 g (HAB, Method 34i). Contains sucrose (saccharose/sugar). Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should

N1 N1 N1 N1

PZN

Active ingredient: viscum album (mali) ex herba W 5% Liquid bath additive Price Group

8788476 8788499 8788507 8788513

A A A A

Status

Potency/Strength Package Size Size Category

Pharmacy only Pharmacy only Pharmacy only Pharmacy only



consult your doctor before taking Viscum Mali e planta tota. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 1 to 3 times daily. D30: Unless otherwise directed, 5-10 globuli velati sublingually once daily. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Viscum Mali e planta tota 3%, Unguentum



30 g

Composition 10 g contain: viscum album (mali) e planta tota ferm 34i Ø 0.3 g (HAB, Method 34i) Excipients: refined arachis oil, white soft paraffin, purified water, wool fat. Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications You must not use Viscum Mali e planta tota 3%, Unguentum if you know that you have had a hypersensitivity (allergic) reaction to mistletoe, peanut (arachis) oil or soy or to any of the other excipients of the preparation.

V

554

N1

PZN 2198578

Composition 10 g (11 ml) liquid bath additive contain: viscum album (mali) ex herba W 5% (HAB, Method 12g with virgin olive oil) 10 g Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications The medicinal product must not be used in the case of known hypersensitivity to the ingredient. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore only be used in children under 12 years after consulting a doctor.

PZN 2088909

Price Group J1

Status General Sale

Dosage and method of administration Unless otherwise directed, for adults and children of 12 years and above use 3 to 5 ml of liquid bath additive (about 1 teaspoonful) for a full bath (about 200 l water) for oil dispersion baths. The temperature of the bath water should be between 35°C and 37°C, the bathing time about 20 minutes. Duration of treatment Oil dispersion baths are usually used about twice weekly for 2 to 3 weeks, in acute conditions daily baths may, however, also be beneficial. For adjunctive treatment of chronic conditions oil dispersion baths may also be used for longer periods if permitted by the doctor. Side-effects None known. Note: When using the bath additive with an oil dispersion bath apparatus (Jungebad®) the manufacturer‘s instructions should be followed.

Viscum Mali, Senker

Active ingredient: viscum album (mali) e planta tota ferm 34i Ointment Potency/Strength Package Size Size Category

100 ml

Price Group D

Status Pharmacy only

Warnings and precautions for use Wool fat can cause local skin reactions (e.g. contact dermatitis).

Active ingredient: viscum album (mali) haustoria ferm 33e Liquid dilution for injection Potency/Strength Package Size Size Category D4 D6 D30 D30

10 x 1 ml 10 x 1 ml 10 x 1 ml 50 x 1 ml

N1 N1 N1 N2

PZN 3358593 3358601 2832650 3795684

Price Group 41 41 41 42

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Dosage and method of administration Unless otherwise directed, apply a ribbon of ointment of about 2 cm to the affected area once to twice daily. When the symptoms improve the frequency of use should be reduced.

Composition Liquid dilution for injection: 1 ml contains: viscum album (mali) haustoria ferm 33e dil. D.. 1 ml (HAB, Method 33e)

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years.

Duration of treatment The duration of treatment should be discussed with the doctor.

Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week.

Side-effects In rare cases arachis oil can cause severe allergic reactions. If the skin becomes red, with or without itching, please stop using the ointment and see a doctor if necessary.

Contraindications Do not use in the case of known allergy to mistletoe formulations. The treatment can only be continued after desensitisation.

Duration of treatment The duration of treatment should be discussed with the doctor.

555

V

Side-effects In the case of intolerance of mistletoe, local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling in the region of the face (Quincke's oedema), shaking chills, difficulty breathing or

shock can occur, in which case treatment with the preparation must be discontinued and immediate medical assistance sought. There are no data on the frequency of such reactions.

D6 D12 D20 D30

Active ingredient: viscum album (pini) e planta tota ferm 34g Liquid dilution for injection Potency/Strength Package Size Size Category 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml 10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: viscum album (pini) e planta tota ferm 34g dil. D.. 1 ml (HAB, Method 34g) Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of known allergy to mistletoe formulations. Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously 1 to 3 times a week.

V

556

Active ingredient: viscum album (pini) e planta tota ferm 34g Globuli velati Potency/Strength Package Size Size Category

Viscum Pini e planta tota

D2 D4 D6 D8 D15 D30 D40 D60

Viscum Pini e planta tota

N1 N1 N1 N1 N1 N1 N1 N1

PZN 3358653 3358630 3358618 3358624 3358647 2832727 0086970 0087432

Price Group 41 41 41 41 41 41 41 41

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only Pharmacy only

Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In very rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as: generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke's oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought.

20 g 20 g 20 g 20 g

Composition Globuli velati: 10 g contain: viscum album (pini) e planta tota ferm 34g dil. D.. 1 g (HAB, Method 34g) Contains sucrose (saccharose/sugar). Indications Homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Viscum Pini e planta tota. Dosage and method of administration D6, D12: Unless otherwise directed, infants 3 globuli velati sublingually 1 to 3 times daily, children up to 6 years 3-7

N1 N1 N1 N1

PZN 8788536 8788565 8788571 8788559

Price Group A A A A

Status Pharmacy only Pharmacy only Pharmacy only Pharmacy only

globuli velati sublingually 1 to 3 times daily, adults and children of 6 years and above 5-10 globuli velati sublingually 1 to 3 times daily. D20, D30: Unless otherwise directed, infants 3 globuli velati sublingually once daily, children up to 6 years 3-7 globuli velati sublingually once daily, adults and children of 6 years and above 5-10 globuli velati sublingually once daily. For infants we recommend dissolving the specified number of globuli velati in a small amount of water or unsweetened tea before administration. Duration of treatment The duration of treatment should be discussed with the doctor. Side-effects None known.

Viscum/Bryonia comp. Liquid dilution for injection

Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: bryonia cretica ferm 33b dil. D3 0.1 g peritonaeum bovis Gl dil. D5 0.1 g (HAB, Method 41b) stannum metallicum dil. D9 0.1 g viscum album (mali) e planta tota ferm 34i dil. D2 0.1 g (HAB, Method 34i)

N1

PZN 2420491

Price Group 11

Status Pharmacy only

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated. Contraindications Do not use in the case of hypersensitivity to milk protein or the donor animal protein or in the case of known hypersensitivity to mistletoe formulations.

557

V

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment The disorder should have cleared up within 2 weeks. If there is no improvement within this time a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor.

Side-effects In rare cases, intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke's oedema), shaking chills, difficulty breathing or shock, in which case treatment with the medicinal product must be discontinued immediately and medical assistance sought. The medicinal product contains small amounts of milk protein and can therefore trigger allergic reactions.

Viscum/Bryonia comp. Globuli velati

Potency/Strength Package Size Size Category

20 g

N1

PZN 8788588

Price Group A

Status Pharmacy only

Composition Globuli velati: 10 g contain: bryonia cretica ferm 33b dil. D3 0.1 g peritonaeum bovis Gl dil. D5 0.1 g (HAB, Method 41b) stannum metallicum dil. D9 0.1 g viscum album (mali) e planta tota ferm 34i dil. D2 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar) and lactose.

Warnings and precautions for use Sufficiently documented experience for the use of this medicinal product in children is not available. It should therefore not be used in children under 12 years. This medicinal product contains sucrose and lactose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Viscum/ Bryonia comp.

Indications Registered homeopathic medicinal product for use in anthroposophical medicine, therefore no therapeutic indication stated.

Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within this time a doctor should be consulted. The duration of treatment of chronic conditions must be discussed with the doctor.

Contraindications None known.

Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 to 5 times daily.

Side-effects None known.

Viscum/Crataegus

Liquid dilution for injection Potency/Strength Package Size Size Category

V

558

10 x 1 ml 50 x 1 ml

N1 N2

PZN 1752400 2234067

Price Group 11 12

Composition Liquid dilution for injection: 1 ml contains: crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) viscum album (tiliae) e planta tota ferm 33f dil. D5 0.1 g (HAB, Method 33f) Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the rhythmic interaction between feeling organisation and life organisation in the cardiovascular system, e.g. weakness of the heart associated with aging (presbycardia), hardening of the blood vessels supplying the heart muscle (coronary sclerosis). Contraindications Do not use in the case of known allergy to mistletoe formulations. Warnings and precautions for use Sufficiently documented experience for the use of this

medicinal product in children is not available. It should therefore not be used in children under 12 years. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. Intolerance of mistletoe can lead to local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), skin rash, swelling of the face (Quincke's oedema), shaking chills, difficulty breathing or shock, in which case treatment with the preparation must be discontinued immediately and medical assistance sought.

Viscum/Crataegus Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: crataegus laevigata/monogyna e foliis et fructibus ferm 33d dil. D2 0.1 g (HAB, Method 33d) viscum album (tiliae) e planta tota ferm 33f dil. D3 0.1 g (HAB, Method 33f) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Harmonisation of the rhythmic interaction between feeling organisation and life organisation in the cardiovascular system, e.g. weakness of the heart associated with aging (presbycardia), hardening of the blood vessels supplying the heart muscle (coronary sclerosis).

N1

PZN 8788594

Price Group A

Status Pharmacy only

Contraindications None known. Warnings and precautions for use This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Viscum/Crataegus. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 to 5 times daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects None known.

Status Pharmacy only Pharmacy only

559

V

Viscum/Echinacea

Liquid dilution for injection Potency/Strength Package Size Size Category

10 x 1 ml

Composition Liquid dilution for injection: 1 ml contains: echinacea pallida e planta tota ferm 33c dil. D1 0.1 g (HAB, Method 33c) viscum album (mali) e planta tota ferm 34i dil. D1 0.1 g (HAB, Method 34i) Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and the body‘s defences in general weakness of resistance and for adjunctive treatment of malignant diseases; adjunctive treatment of weakness of the immune system after radiation therapy. Contraindications Viscum/Echinacea must not be used in the following cases: • Malignant diseases of the blood-forming organs • Immunogenic tumours, e.g. hypernephroma and malignant melanoma • Acute inflammatory or highly febrile conditions: In this case the treatment should be interrupted until the signs of inflammation have subsided • Chronic granulomatous diseases and autoimmune diseases • Known allergy to mistletoe formulations: In this case the treatment can only be continued after desensitisation • Hypersensitivity to any of the other active ingredients or excipients or to other plants of the Compositae family • Uncontrolled hyperthyroidism • Progressive systemic diseases such as tuberculosis, collagen disorders (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infections (infection with the AIDS virus) and chronic viral infections See also "Precautions for use and warnings". Warnings and precautions for use Primary tumours of the brain or spinal cord or intracranial metastases with danger of elevation of intracranial pressure: In these cases the preparations should only be used after carefully weighing up the benefits and risks and with close clinical monitoring. The medicinal product should not be used without the advice of a doctor and should not be used in place of any other medication or other treatment prescribed by the

V

560

N1

PZN 1752417

Price Group 11

Status Pharmacy only

doctor. In the event of fever, tiredness and fatigue, physical weakness, lack of appetite, weight loss and/or pain a doctor should be consulted. Interactions with other agents There are no studies on interactions with other immunomodulating substances (e.g. thymus extracts). If such preparations are used in close temporal proximity, cautious dosing and monitoring of appropriate immune parameters are advised. Dosage and method of administration Unless otherwise directed, inject 1 ml subcutaneously twice a week to once daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Viscum/Echinacea should not be used for longer than 2 weeks. Side-effects Mild elevation of body temperature, local inflammatory reactions at the skin puncture site of the subcutaneous injection and temporary mild swelling of regional lymph nodes are no cause for concern. In the event of fever of more than 38 °C (possibly accompanied by fatigue, shivering, general malaise, headaches, brief attacks of dizziness) or larger local reactions with a diameter of more than 5 cm, the next injection should only be given after these symptoms have subsided and in a reduced concentration and/or dose. The fever caused by Viscum injection should not be suppressed by antipyretic agents. In the case of fever persisting longer than three days the possibility of an infectious process or tumour fever should be considered. Excessive local reactions can be reduced by diluting the contents of the ampoule with physiological saline. In rare cases, local or systemic allergic or allergoid reactions such as generalised itching, urticaria (hives), exanthems (skin rash), Quincke's oedema (swelling of the face), shaking chills, difficulty breathing or shock can occur, in which case treatment with the preparation must be discontinued immediately and medical assistance sought. In rare cases activation of inflammatory processes can occur (e.g. chronic sinusitis, periapical granulomas). Occasionally the veins can react with signs of inflammatory irritation. In this case temporary interruption of the treatment is necessary.

The occurrence of chronic granulomatous inflammatory disorders (sarcoidosis and erythema nodosum) has been very rarely reported. Autoimmune diseases (StevensJohnson syndrome and cold agglutinin disease) have occurred very rarely. Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of

breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see your doctor. An immunosuppressant effect of higher dosages cannot be ruled out. There are no systematic studies available on this.

Viscum/Echinacea Globuli velati

Potency/Strength Package Size Size Category

20 g

Composition Globuli velati: 10 g contain: echinacea pallida e planta tota ferm 33c Ø 0.1 g (HAB, Method 33c) viscum album (mali) e planta tota ferm 34i dil. D1 0.1 g (HAB, Method 34i) Contains sucrose (saccharose/sugar). Indications according to the anthroposophical understanding of human beings and nature. Stimulation of the warmth organisation and the body‘s defences in general weakness of resistance and for adjunctive treatment of malignant diseases; adjunctive treatment of weakness of the immune system after radiation therapy. Contraindications The medicinal product should not be used in the case of hypersensitivity to any of the active ingredients or excipients or to other plants of the Compositae family. On the basis of fundamental considerations, Viscum/Echinacea must not be used in the case of progressive systemic diseases such as tuberculosis, leukoses (leukaemia or leukaemia-like diseases), collagen diseases (inflammatory diseases of the connective tissue), multiple sclerosis, AIDS, HIV infection (infection with the AIDS virus), chronic viral diseases or autoimmune diseases (diseases caused by a reaction of an individual‘s immune system against the organs or tissues of his or her own body). Warnings and precautions for use Sufficiently documented experience for the use of this

N1

PZN 8788602

Price Group A

Status Pharmacy only

medicinal product in children is not available. In children under 12 years it should therefore only be used for stimulation of the warmth organisation and for treatment of weakness of the immune system after radiation therapy and should only be used after consulting a doctor. This medicinal product contains sucrose. If you know that you suffer from intolerance to certain sugars you should consult your doctor before taking Viscum/Echinacea. The medicinal product should not be used without the advice of a doctor and should not be used in place of any other medication or other treatment prescribed by the doctor. In the event of fever, tiredness and fatigue, physical weakness, lack of appetite, weight loss and/or pain a doctor should be consulted. Dosage and method of administration Unless otherwise directed, 5-10 globuli velati sublingually 3 times daily. Duration of treatment In the case of chronic conditions the duration of treatment should be discussed with the doctor. Viscum/Echinacea should not be used for longer than 2 weeks. Side-effects Hypersensitivity reactions may very rarely occur. Skin rashes, itching, rarely swelling of the face, shortness of breath, dizziness and fall in blood pressure have been observed after using medicinal products containing formulations of purple cone flower (echinacea). In such cases you should stop using the medicinal product and see your doctor.

561

V

Wund- und Brandgel (wounds and burns gel) Gel

Potency/Strength Package Size Size Category

30 g

Composition 10 g contain: argentum colloidale dil. D5 0.1 g arnica montana e floribus LA 20% 0.15 g (HAB, Method 12c) calendula officinalis e floribus LA 20% 0.1 g (HAB, Method 12c) cantharis ex animale toto Gl dil. D5 0.1 g (HAB, Method 41c) symphytum officinalis ex herba LA 20 % 0.1 g (HAB, Method 12c) thuja occidentalis e summitatibus LA 20% 0.1 g (HAB, Method 12c) urtica urens ex herba LA 20 % 0.45 g (HAB, Method 12c) Excipients: glycerol, potassium dihydrogen phosphate, sodium chloride, sodium hydrogen carbonate, disodium phosphate dihydrate, silver sulfate, thyme oil, traganth, purified water, water for injections, xanthan gum. Indications according to the anthroposophical understanding of human beings and nature. First and second degree burns

W

562

N1

PZN 2198584

Price Group J

Status Pharmacy only

and scalds, sunburn, allergic and hyperergic skin disorders (dermatoses), insect bites and stings, grazes and ulcers. Contraindications The medicinal product should not be used in the case of hypersensitivity to arnica or other plants of the Compositae family or to thuja (arbor vitae). Dosage and method of administration Unless otherwise directed, for burns immediately apply a thick layer of gel and keep moist with diluted Brandessenz. For other wounds, e.g. grazes, apply the gel and allow to dry. Duration of treatment Acute disorders should clear up within 2 weeks. If there is no improvement within one week a doctor should be consulted. In the case of chronic conditions the duration of treatment should be discussed with the doctor. Side-effects In rare cases – in the case of hypersensitivity to arnica – allergic skin reactions may occur. In this case treatment with the medicinal product should be discontinued.

563

Index of substances General remarks Alphabetical List of active ingredients Used

564

566 568

565

General remarks The following pages contain an alphabetical list of all active ingredients mentioned in the Compendium of Medicines. The medicinal products containing the respective substance or preparation are usually listed under the Latin name of the active ingredient. However, to make searching easier, commonly used English or Latin synonyms have also been included in the list. The preparations are based on plant, animal or mineral base materials which are given by their English and scientific names. In the case of plants, the part of the plant used is also given. Unless specified otherwise, fresh plants or parts of plants are always used. Animal base materials (organs, parts of organs or invertebrates – whole animal) are processed immediately after slaughter (organs, organ parts) or after euthanasia by carbon dioxide (invertebrates – whole animal).

According to the labelling requirements of the LA 20 % German Homoeopathic Pharmacopoeia (HAB), Tinctures for external use: according to HAB, the labelling of various preparations must contain Method 12c, aqueous-alcoholic extracts produced certain additional terms which permit precise al- from fresh plants or plant parts. location to the respective Methods of Production of the HAB. These additional terms are: LA 25 % Tinctures for external use: according to HAB, Decoctum Method 12o, aqueous-alcoholic extracts produced Heat-treated aqueous mother tinctures and liquid from fresh plants or plant parts. dilutions thereof: according to HAB, Method 23a, preparations (decoctions) produced from dried LA 25 % sicc. plant parts. Tinctures for external use: according to HAB, Method 12m, aqueous-alcoholic extracts proDecoctum LA 10 % duced from dried plants or plant parts. Tinctures for external use: according to HAB, Method 12k, aqueous-alcoholic extracts (decoc- W 10 % or W 5 % tions) produced from fresh plant parts. Oils for external use: according to HAB, Method 12f or 12g, respectively, extracts produced (at ferm... (e.g. ferm 33a) 37°C) from dried plants or plant parts and olive Heat-treated and fermented aqueous mother or arachis oil. tinctures and liquid dilutions thereof (potencies): according to HAB, Methods 33a-f, 34a-i, 35a-c, 10 % or 5 % 36, 37a-b and 51 Oils for external use: according to HAB, Method 12h or 12i, respectively, mixtures of an essential oil with a vegetable oil (usually olive oil). GI (= Glycerol) Gl mother tinctures and liquid dilutions thereof: according to HAB, Methods 41a-d, preparations produced from organs and tissues of vertebrates and preparations produced from invertebrates (whole animal) or their secretions.

Infusum

Heat-treated aqueous mother tinctures and liquid dilutions thereof: according to HAB, Method 24a, preparations (infusions) produced from dried plant parts.

K

Cold-treated aqueous mother tinctures and liquid dilutions thereof (strengths): according to HAB, Method 38, preparations produced from mistletoe plants using the Iscucin process.

566

567

Abies alba e summitatibus ferm 33d Silver fir – shoot tips (Abies alba Mill.) Petasites comp.

Abrotanum ex herba ferm 33c

see Artemisia abrotanum ex herba ferm 33c

Acori calami rhizoma

aqueous extract Sweet Flag, Calamus – underground parts (dried) Enzian Magentonikum

Acori calami rhizoma

Absinthium

aqueous extract with sugar Sweet Flag, Calamus – underground parts (dried) Bitter Elixier

Acacia, False

Acorus calamus e rhizoma ferm 33d

see Artemisa absinthium see Robinia pseudoacacia e cortice ferm 33e

Achillea ex herba ferm 33d

Yarrow – aerial parts of flowering plants (Achillea millefolium L.) Achillea ex herba D.. Cantharis Blasen Inject Cantharis Blasen Globuli velati

Acidum lacticum Lactic acid Majorana Vaginalgel

Acidum phosphoricum Ortho-phosphoric acid Aurum/Apis regina comp.

Aconite

see Aconitum napellus e tubere ferm 33c see Aconitum napellus e tubere W 5 %

Aconitum napellus e tubere ferm 33c

Monkshood, Aconite – underground parts (Aconitum napellus L.) Aconit Schmerzöl Aconitum e tubere D.. Aconitum comp. Aconit Ohrentropfen Aconitum/China comp. Aconitum/China comp., Suppositorien Aconitum/China comp., Suppositorien für Kinder Bryonia/Aconitum Disci/Rhus toxicodendron comp. Melissa/Sepia comp. Rhus toxicodendron comp. Salix/Rhus comp.

Aconitum napellus e tubere W 5%

Monkshood, Aconite – underground parts (dried) Aconitum e tubere W 5%, Oleum

Sweet Flag, Calamus – underground parts Bolus alba comp. Pulver Juniperus/Berberis comp., Kapseln

Adonis ex herba ferm 33d

False Hellebore, Yellow Pheasant‘s Eye – aerial parts of flowering plants (Adonis vernalis L.) Adonis comp. Scilla comp.

Aesculus hippocastanum e cortice, Decoctum LA 10% Horse Chestnut – bark of branches Akne-Wasser

Aesculus hippocastanum e semine ferm 34c Horse Chestnut - seeds Aesculus e semine D.. Borago comp. Cera/Aesculus comp., Unguentum Disci comp. cum Aesculo Disci comp. cum Aesculo, Gelatum Hirudo comp. Quercus Hämorrhoidalzäpfchen Solum Inject 10 Solum Inject Solum Globuli velati

Aesculus hippocastanum e semine LA 25% sicc. Horse Chestnut - seeds Aesculus-Essenz Aesculus/Prunus comp., Essenz Solum Badezusatz, Öl, Salbe

Aesculus hippocastanum e semine W 5% Horse Chestnut - seeds Aesculus e semine W 5 %, Oleum

Agaricus e planta tota ferm 33b

see Amanita muscaria e planta tota ferm 33b

Agate water

Naturally occurring water from intact agate geodes Achatwasser D..

Agropyron repens e radice ferm 33c Couch Grass – underground parts (Agropyron repens (L.) P. Beauv.) Agropyron Inject Agropyron Globuli velati

Alder Buckthorn

see Rhamnus frangula e cortice ferm 33e

Allium cepa ferm 34a

Onion – ripe bulb (Allium cepa L.) Allium cepa e bulbo D.. Articulatio talocruralis comp. Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Mercurialis comp., Suppositorien Mercurialis Salbe Narbengel Symphytum comp. Tendo/Allium cepa comp.

Almond oil, fatty

see Amygdalae oleum

Amanita muscaria e planta tota ferm 33b Fly Agaric – fruiting body (Amanita muscaria) Conchae comp.

Amethyst

Almond oil, fatty oil from sweet almonds (Prunus dulcis (Mill.) D. A. Webb) Oleum Petrae comp.

Anagallis arvensis e planta tota ferm 33b Scarlet Pimpernel – whole flowering plant (Anagallis arvensis L.) Anagallis comp.

Angelica

see Angelica archangelica e radice ferm 33c

Angelica archangelica e radice ferm 33c Angelica – roots (Angelica archangelica L.) Archangelica comp.

Anise

see Pimpinella anisum e fructibus, Infusum

Anise essential oil

see Anisi stellati aetheroleum

Anisi stellati aetheroleum (= Oleum Anisi)

Essential oil from star anise fruits (anise oil) (Illicium verum Hook. f.) Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Bolus alba comp. Pulver Chelidonium Kapseln Juniperus/Berberis comp., Kapseln Rheuma-Badeöl

Anisum e fructibus, Infusum

see Pimpinella anisum e fructibus, Infusum

Natural silicic anhydride with traces of manganese and iron Akne-Kapseln Amethyst D..

Anthyllis vulneraria ex herba LA 20%

Ammi visnaga e fructibus ferm 35b

Antimonite

Khella, Visnaga - fruits (Ammi visnaga (L.) Lam.) Ammi visnaga comp., Suppositorien Ammi visnaga comp., Suppositorien für Kinder

Amnion bovis Gl Amniotic membrane Amnion Gl D..

A

Amygdalae oleum

Kidney Vetch – aerial parts at flowering time (Anthyllis vulneraria L.) Akne-Wasser

Antimony glance, natural antimony(III) sulfide Cartilago/Mandragora comp. Cartilago/Mandragora comp., Unguentum Mundbalsam flüssig Mundbalsam Parametrium/Echinacea comp.

Antimonium crudum see Antimonite

568

569

Antimonium metallicum see Stibium metallicum

Antimony

see Stibium metallicum

Antimony glance see Antimonite

Antimony(III) sulfide, nat. see Antimonite

Anus bovis Gl

Anus Anus Gl D.. Rosmarinus/Prunus comp., Gelatum

Aorta tota bovis Gl Aorta Aorta (tota) Gl D..

Apatite

Natural calcium fluorophosphate Cerebellum comp.

Apis mellifica ex animale toto Gl

Honeybee – whole animal (Apis mellifica L.) Apis ex animale Gl D.. Apis/Arnica Apis Belladonna Inject Apis Belladonna Globuli velati Apis/Belladonna cum Mercurio Apis/Bryonia Apis/Levisticum I Apis/Levisticum II Berberis/Apis comp. Berberis/Pyrit comp. Bryonia comp. Echinacea/Mercurius comp., Suppositorien Echinacea/Mercurius comp., Suppositorien für Kinder Larynx/Apis comp. Magnesit/Mamma comp. Magnesium sulfuricum/Ovaria comp. Renes/Equisetum comp.

Apis regina Gl

Queen bee cell, with larva and royal jelly (Apis mellifica L.) Apis regina Gl D.. Apis regina comp. Aurum/Apis regina comp. Nervennahrung Ovaria comp.

570

Testes comp.

Appendix vermiformis cuniculi Gl Vermiform appendix Appendix vermiformis Gl D..

Apple mistletoe

see Viscum album (Mali) e planta tota ferm 34i see Viscum album (Mali) e planta tota K see Viscum album (Mali) ex herba W 5% see Viscum album (Mali), sinker ferm 33e

Aquilinum

see Pteridium aquilinum e foliis ferm 34c

Aranea ex animale Gl

Garden spider – whole animal (Araneus diadematus) Aranea ex animale Gl D..

Arborvitae

see Thuja occidentalis e summitatibus ferm 33e see Thuja occidentalis e summitatibus LA 20%

Archangelica e radice ferm 33c

see Angelica archangelica e radice ferm 33c

Arctium lappa e radice W 5%

Echinacea/Mercurius comp., Suppositorien für Kinder Echinacea Quarz comp. Augentropfen Echinacea/Viscum comp., Gelatum Endometrium comp. Ovaria comp. Ovaria/Argentum Pancreas/Argentum Secale/Argentum Testes comp. Testes/Argentum

Argentum nitricum

Silver nitrate Archangelica comp. Argentum nitricum comp. Echinacea Mund- und Rachenspray Mundbalsam flüssig Mundbalsam Myristica sebifera comp. Periodontium/Silicea comp. Renes/Argentum nitricum Robinia comp. Silicea comp. Silicea comp., Suppositorien Silicea comp., Suppositorien für Kinder

Burdock – underground parts (dried) (Arctium lappa L.) Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Rheuma-Badeöl

Arnica

Argentum colloidale

Arnica – inflorescences (Arnica montana L.) Arnika Essenz Arnika Wundtuch Brandessenz Wund- und Brandgel

Colloidal silver Majorana Vaginalgel Wund- und Brandgel

Argentum metallicum

Silver Argentum/Quarz Argentum/Rohrzucker Betula/Arnica comp. Bryophyllum comp. Cartilago/Mandragora comp. Cartilago/Mandragora comp., Unguentum Conchae comp. Conjunctiva comp. Disci comp. cum Argento Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Argento, Suppositorien Echinacea/Argentum Echinacea/Mercurius comp., Suppositorien

see Arnica montana e floribus LA 20% see Arnica montana e floribus W 5% see Arnica montana e planta tota ferm 33c

Arnica montana e floribus LA 20%

Arnica montana e floribus W 5% Arnica – inflorescences (dried) Arnica e floribus W 5 %, Oleum Birken Rheumaöl mit Arnika Rheuma-Badeöl

Arnica montana e planta tota ferm 33c Arnica – whole flowering plant Apis/Arnica Arnica e planta tota D.. Arnica/Aurum I Arnica/Aurum II Arnica/Plumbum comp. A Arnica/Plumbum comp. B

A

Arnica/Plumbum mellitum Arnika Salbe Articulatio talocruralis comp. Betula/Arnica comp. Cactus comp. II Cerebellum comp. Disci comp. cum Aesculo Disci comp. cum Aesculo, Gelatum Disci comp. cum Argento Disci comp. cum Auro Disci comp. cum Stibio Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Argento, Suppositorien Magnesium phosphoricum comp. Magnesium sulfuricum/Ovaria comp. Nervus opticus comp. Augentropfen Symphytum comp. Tendo/Allium cepa comp.

Arsenic, Arsenic(III) oxide see Arsenicum album

Arsenic(III) oxide, Arsenic see Arsenicum album

Arsenicum album

Arsenic, Arsenic(III) oxide Arsenicum album D.. Bolus alba comp. Pulver Thyreoidea/Thymus comp.

Artemisia abrotanum ex herba ferm 33c Southernwood – young shoots and leaves (Artemisia abrotanum L.) Abrotanum ex herba D.. Bolus alba comp. Pulver

Artemisia absinthium ex herba, Infusum Wormwood – tops and leaves at flowering time (dried) Gentiana Magen Inject Gentiana Magen Globuli velati

Artemisiae absinthii herba

aqueous extract Wormwood – tops and leaves at flowering time (dried) (Artemisia absinthium L.) Enzian Magentonikum

Artemisiae absinthii herba

aqueous extract with sugar Wormwood – tops and leaves at flowering time (dried) Bitter Elixier

571

Arteria basilaris bovis Gl

Basilar artery (at the base of the skull) Arteria basilaris Gl D..

Arteria brachialis bovis Gl Brachial artery Arteria brachialis Gl D..

Arteria carotis communis et sinus caroticus bovis Gl

Common carotid artery and carotid sinus Arteria carotis communis et sinus caroticus Gl D..

Arteria cerebri media bovis Gl Middle cerebral artery Arteria cerebri media Gl D..

Arteria coeliaca

see Truncus coeliacus bovis Gl

Arteria coronaria bovis Gl Coronary artery Arteria coronaria Gl D..

Arteria et Vena ophthalmica bovis Gl see Arteria ophthalmica bovis GI

Arteria femoralis bovis Gl Femoral artery Arteria femoralis Gl D..

Arteria ophthalmica bovis GI Ophthalmic artery Arteria ophtalmica GI D..

Arteria poplitea bovis Gl Popliteal artery Arteria poplitea Gl D.. Secale/Bleiglanz comp.

Arteria pulmonalis bovis Gl

Arteriae bovis Gl

Arteries (a. basilaris, a. brachialis, a. coronaria, a. femoralis, a. mesenterica superior, a. pulmonalis, a. renalis) – mixed in equal parts Arteriae Gl D..

Articulatio coxae bovis Gl Hip joint Articulatio coxae Gl D..

Articulatio cubiti bovis Gl Elbow joint Articulatio cubiti Gl D..

Articulatio genus bovis Gl Knee joint Articulatio genus Gl D..

Articulatio humeri bovis Gl Shoulder joint Articulatio humeri Gl D..

Articulatio interphalangea bovis GI

Interphalangeal joint of the fore and hind limbs Cartilago/Echinacea

Articulatio radiocarpea bovis Gl Wrist joint Articulatio radiocarpea Gl D..

Articulatio sacroiliaca bovis Gl Sacroiliac joint Articulatio sacroiliaca Gl D..

Articulatio subtalaris bovis Gl Subtalar joint (posterior portion) Articulatio subtalaris Gl D.. Articulatio talocruralis comp.

Articulatio talocruralis bovis Gl

(= Truncus pulmonalis) pulmonary artery Arteria pulmonalis Gl D..

Ankle joint Articulatio talocruralis Gl D.. Articulatio talocruralis comp.

Arteria renalis bovis Gl

Articulatio temporomandibularis bovis Gl

Arteria vertebralis bovis Gl

Articulationes intercarpeae bovis Gl

Renal artery Arteria renalis Gl D..

Vertebral artery Arteria vertebralis Gl D..

572

Temporomandibular joint Articulatio temporomandibularis Gl D.. Intercarpal joints Articulationes intercarpeae Gl D..

Articulationes intervertebrales cervicales bovis Gl

Intervertebral joints of the cervical spine including joint surfaces, capsules and ligaments Articulationes intervertebrales cervicales Gl D..

Articulationes intervertebrales lumbales bovis Gl

Intervertebral joints of the lumbar spine including joint surfaces, capsules and ligaments Articulationes intervertebrales lumbales Gl D..

Aurum chloratum

Atlas bovis Gl

Aurum metallicum

First cervical vertebra Atlas Gl D..

Atropa belladonna e fructibus ferm 33a Deadly Nightshade – fruits (Atropa belladonna L.) Apis Belladonna Inject Apis Belladonna Globuli velati Apis/Belladonna cum Mercurio Atropa belladonna e fructibus D.. Belladonna e fructibus Augentropfen Echinacea/Mercurius comp., Suppositorien Echinacea/Mercurius comp., Suppositorien für Kinder Salix/Rhus comp.

Atropa belladonna e radice ferm 33b Deadly Nightshade – underground parts Aconitum comp. Atropa belladonna e radice D.. Belladonna/Chamomilla Bryonia comp. Viscum comp.

Atropa belladonna ex herba ferm 33a

Deadly Nightshade – aerial parts of flowering plants Ammi visnaga comp., Suppositorien Ammi visnaga comp., Suppositorien für Kinder Atropa belladonna ex herba D.. Aurum/Belladonna comp. Belladonna ex herba Augentropfen Belladonna comp., Suppositorien Belladonna comp., Suppositorien für Kinder Berberis/Apis comp. Carum carvi Zäpfchen Carum carvi Kinderzäpfchen Conjunctiva comp. Echinacea Quarz comp. Augentropfen Lachesis comp. Mundbalsam flüssig

A

Mundbalsam Periodontium/Silicea comp. Silicea comp. Silicea comp., Suppositorien Silicea comp., Suppositorien für Kinder Thyreoidea comp. Veratrum comp. Tetrachlorogold(III) acid Aurum/Apis regina comp. Metallic gold Arnica/Aurum I Arnica/Aurum II Aurum comp. Aurum comp., Unguentum Aurum/Belladonna comp. Aurum/Equisetum I Aurum/Equisetum II Aurum/Prunus Aurum/Stibium/Hyoscyamus Aurum/Strophanthus Aurum Valeriana Inject Aurum Valeriana Globuli velati Berberis/Sepia comp. Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Cerebrum comp. A cum Auro comp. Cerebrum comp. B cum Auro comp. Cor/Aurum I Cor/Aurum II Disci comp. cum Auro Parathyreoidea/Aurum Sarothamnus comp. Spongia/Aurum/Pulsatilla comp. Strophanthus comp.

Avena e planta tota ferm 33c

Oats – whole plant at the milk ripeness stage Aurum/Apis regina comp. Avena comp. Passiflora Zäpfchen Passiflora Kinderzäpfchen

Avena sativa, Herba rec.

aqueous extract with sugar Oats - stalks, leaves and ears at the milk ripeness stage (Avena sativa L.) Passiflora Nerventonikum

573

Avens

see Geum urbanum e radice ferm 33c

Axis bovis Gl

(= Epistropheus) second cervical vertebra Axis Gl D..

Balsamum peruvianum

Peru balsam – resin from the trunk of Myroxylon balsamum Nasenbalsam Nasenbalsam für Kinder

Bamboo

see Phyllostachys e nodo ferm 35c

Bambusa e nodo ferm 35c

see Phyllostachys e nodo ferm 35c

Barberry

see Berberis vulgaris e fructibus ferm 33c see Berberis vulgaris e radice ferm 33d see Berberis vulgaris e radice W 10% see Berberis vulgaris ex herba ferm 33c

Barium citrate

see Barium citricum

Barium citricum

Barium citrate Barium/Pancreas comp. Narben Gel

Basal ganglia

see Corpus striatum bovis Gl see Hypothalamus bovis Gl see Nucleus ruber bovis Gl see Pars pallida bovis Gl see Regio substantiae nigrae bovis Gl

Basket Willow

see Salix purpurea e cortice et foliis ferm 33d

Bee

see Apis mellifica ex animale toto Gl

Beechwood tar distillate see Creosotum

Beeswax, yellow see Cera flava

574

Belladonna

see Atropa belladonna e fructibus ferm 33a see Atropa belladonna e radice ferm 33b see Atropa belladonna ex herba ferm 33a

Bellis perennis ex herba LA 20%

Daisy – aerial parts at flowering time (Bellis perennis L.) Akne-Gesichtsdampfbad Akne-Wasser

Berberis vulgaris e fructibus ferm 33c Barberry – berries (Berberis vulgaris L.) Berberis e fructibus D.. Berberis e fructibus comp. Berberis/Nicotiana comp. Berberis/Pyrit comp. Berberis/Quarz Nasenbalsam Nasenbalsam für Kinder

Berberis vulgaris e radice ferm 33d Barberry – underground parts Berberis e radice D.. Berberis/Apis comp. Berberis/Hypericum comp. Berberis/Prostata comp. Berberis/Sepia comp. Berberis/Urtica urens Berberis/Uterus comp. Lycopodium comp.

Berberis vulgaris e radice W 10%

Betula pendula e cortice sicc.,Decoctum Silver birch – bark (dried) Arnica/Plumbum comp. A Arnica/Plumbum comp. B Betula/Arnica comp. Betula/Mandragora comp. Secale/Bleiglanz comp. Secale/Retina comp.

Betula pendula, Folium rec. aqueous extract with sugar Silver birch - leaves Nierentonikum

Betula pendula/pubescens e foliis W 5% Silver birch – leaves (dried) Betula e foliis W 5%, Oleum Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Rheuma-Badeöl

Birch

see Betula e foliis ferm 34e see Betula pendula e cortice sicc., Decoctum see Betula pendula, Folium rec. – aqueous extract with sugar see Betula pendula/pubescens e foliis W 5%

Birch charcoal

see Carbo vegetabilis

Bitter Fennel, essential oil of

see Foeniculi amari fructus aetheroleum

Barberry – underground parts (dried) Chelidonium Kapseln Juniperus/Berberis comp., Kapseln

Bitter Gourd

Berberis vulgaris ex herba ferm 33c

Blackthorn

Barberry – aerial parts of flowering plants Berberis/Prostata comp. Berberis/Uterus comp.

Betula e foliis ferm 34e

Silver birch - leaves Akne-Kapseln Betula e foliis D.. Betula/Arnica comp. Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Cartilago/Mandragora comp. Cartilago/Mandragora comp., Unguentum

see Citrullus colocynthis e fructibus ferm 33a see Prunus spinosa e floribus et summitatibus ferm 33d see Prunus spinosa e floribus W 5% see Prunus spinosa ferm cum Ferro see Prunus spinosa, e fructibus LA 25%

Black Locust

see Robinia pseudoacacia e cortice ferm 33e

Black Mustard

see Brassica nigra e semine W 10%

Black Pepper

see Piperis nigri fructus – aqueous extract with sugar

A B

see Piperis nigri fructus – aqueous extract

Bladder Wrack

see Fucus vesiculosus e planta tota ferm 51

Blood cells, red

see Erythrozyten equi Gl

Bolus alba

see Kaolinum ponderosum

Borage

see Borago officinalis e foliis ferm 34b see Borago officinalis ex herba LA 20%

Borago officinalis e foliis ferm 34b Borage - leaves (Borago officinalis L.) Borago comp. Quercus Salbe Quercus Hämorrhoidalzäpfchen Renes/Borago comp.

Borago officinalis ex herba LA 20% Borage – aerial parts at flowering time Aesculus/Prunus comp., Essenz Borago-Essenz

Bracken

see Pteridium aquilinum e foliis ferm 34c

Brainstem

see Truncus cerebri bovis Gl

Brassica nigra e semine W 10% Black mustard – seeds (Brassica nigra (L.) W. D. J. Koch) Cera/Aesculus comp., Unguentum

Bronchi bovis Gl

Bronchial tubes that carry air to and from the lungs Bronchi Gl D.. Bronchi Plantago Inject Bronchi Plantago Globuli velati

Bryonia e radice ferm 33b

White Bryony – roots harvested before sprouting (Bryonia cretica L. ssp. dioica) Aconitum/China comp. Aconitum/China comp., Suppositorien Aconitum/China comp., Suppositorien für Kinder Apis/Bryonia Bronchi Plantago Inject Bronchi Plantago Globuli velati

575

Berberis e radice D.. Bryonia comp. Bryonia/Aconitum Bryonia/Stannum Cera/Aesculus comp., Unguentum Gelsemium comp. Larynx/Apis comp. Magnesium sulfuricum/Ovaria comp. Pulmo/Vivianit comp. Salix/Rhus comp. Viscum/Bryonia comp.

Calcium carbonate from eggshell

Bryophyllum

Calcium carbonicum e testa ovorum

see Kalanchoe daigremontiana/pinnata

Bryophyllum e foliis ferm 33b

see Kalanchoe daigremontiana/pinnata e foliis ferm 33b

Bugleweed

see Lycopus virginicus e planta tota ferm 33d

Bulbus olfactorius bovis Gl

Olfactory bulb (part of the olfactory tract in the brain) Bulbus olfactorius Gl D..

Burdock

see Arctium lappa e radice W 5%

Bursae articulationis humeri-Komplex bovis Gl Synovial sac in the region of the shoulder joint Bursae articulationis humeri-Komplex Gl D..

Butterbur

see Petasites hybridus e radice ferm 33c

Cajeputi aetheroleum rectificatum (= Oleum Cajeputi)

Essential oil from leaves and branch tips of various Melaleuca species such as Melaleuca leucadendra (L.) L. (cajeput oil) Nasenbalsam

Cajeput essential oil

see Cajeputi aetheroleum rectificatum

Calamus

see Acori calami rhizoma – aqueous extract see Acori calami rhizoma – aqueous extract with sugar see Acorus calamus e rhizoma ferm 33d

576

see Testa ovorum

Calcium carbonate from oyster shells see Conchae

Calcium carbonicum cum Quercu

see Quercus e cortice cum Calcio carbonico

Calcium carbonicum e cinere Quercus see Quercus e cortice cum Calcio carbonico see Testa ovorum

Calcium fluorophosphate, natural see Apatite

Calendula ex herba flor. – pressed juice Pot Marigold – aerial parts at flowering time Calcea Wund- und Heilcreme

Calendula officinalis e floribus LA 20%

Pot marigold – inflorescences (Calendula officinalis L.) Akne-Wasser Brandessenz Echinacea/Viscum comp., Gelatum Wund- und Brandgel Calendula-Essenz Echinacea Mund- und Rachenspray

Calendula officinalis e floribus W 10% Pot Marigold – inflorescences (dried) Calendula e floribus W 10%, Oleum

Calendula officinalis ex herba ferm 33c Pot Marigold – aerial parts at flowering time Calendula ex herba D.. Majorana Vaginalgel Mercurialis comp., Suppositorien Mercurialis Salbe

Camphor

see Camphora see Camphora 5%

Camphora

Camphor – from the wood of Cinnamomum camphora (L.) J.S. Presl Aconit Ohrentropfen Aconit Schmerzöl Aurum Valeriana Inject

Aurum Valeriana Globuli velati Camphora D.. Camphora/Hypericum, Unguentum Cera/Aesculus comp., Unguentum Juniperus/Berberis comp., Kapseln Kampfer Johanniskrautöl Oleum camphoratum comp. Oleum Petrae comp. Plantago Bronchialbalsam Sarothamnus comp. Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati

Carnelian

Camphora 5%

Cartilago articularis coxae bovis Gl

Camphor, in olive oil Camphora 5%, Oleum

Cane sugar

see Saccharum Sacchari

Cantharis ex animale Gl

Cartilago articularis bovis Gl

Joint cartilage Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Cartilago/Mandragora comp. Cartilago/Mandragora comp., Unguentum Hornerz/Cartilago comp. Cartilage (hip joint) Cartilago articularis (coxae) Gl D..

Cartilago articularis genus bovis Gl Cartilage (knee joint) Cartilago articularis (genus) Gl D..

Spanish Fly (Lytta vesicatoria Fabricius) Brandessenz Cantharis ex animale Gl D.. Cantharis Blasen Inject Cantharis Blasen Globuli velati Wund- und Brandgel

Carvi aetheroleum (= Oleum Carvi)

Caraway

Carvi fructus

see Carvi fructus – aqueous extract

Essential oil from caraway fruits (caraway oil) Akne-Kapseln Bolus alba comp. Pulver Chelidonium Kapseln Melissenöl

Caraway, essential oil of

aqueous extract Caraway – fruits (Carum carvi L.) Carum carvi Zäpfchen Carum carvi Kinderzäpfchen

Carbo vegetabilis

Castor oil

see Carvi aetheroleum

Birch charcoal from the wood of Betula pendula Roth Akne-Kapseln Barium/Pancreas comp. Bolus alba comp. Pulver Nicotiana comp. Nux vomica/Nicotiana comp. Platinum chloratum/Pancreas comp.

Cardia suis Gl

(= Ostium cardiacum) opening into the stomach Cardia Gl D..

Carduus benedictus ex herba ferm 33d see Cnicus benedictus ex herba ferm 33d

Carduus marianus e fructibus ferm 36 see Silybum marianum e fructibus ferm 36

B C

Iron-containing red variety of chalcedony Karneol D..

see Ricini oleum

Cavum tympani bovis Gl

Tympanic cavity in the middle ear Cavum tympani Gl D..

Celandine

see Chelidonium majus e floribus ferm 34b see Chelidonium majus e radice ferm 34b see Chelidonium majus ex herba cum radice ferm see Chelidonium majus ex herba ferm 34b

Cepa

see Allium cepa e bulbo ferm 34a

Cera flava

Yellow beeswax

577

Cera/Aesculus comp., Unguentum Oleum Petrae comp. Plantago Bronchialbalsam

Cerebellum bovis Gl

Chamomile

see Chamomilla recutita e floribus W 10% see Chamomilla recutita e planta tota ferm 33c see Chamomilla recutita e radice ferm 33c

Cerebellum Arnica/Plumbum comp. A Arnica/Plumbum comp. B Cerebellum Gl D.. Cerebellum comp. Cerebrum comp. A Cerebrum comp. A cum Auro comp. Cerebrum comp. B Cerebrum comp. B cum Auro comp. Gnaphalium comp.

Chamomilla recutita e floribus W 10%

Cerebrum

Chamomile – underground parts Ammi visnaga comp., Suppositorien Ammi visnaga comp., Suppositorien für Kinder Belladonna comp., Suppositorien Belladonna comp., Suppositorien für Kinder Belladonna/Chamomilla Carum carvi Zäpfchen Carum carvi Kinderzäpfchen Chamomilla e radice D.. Chamomilla/Nicotiana Melissa/Sepia comp. Nicotiana comp. Nux vomica/Nicotiana comp. Veratrum comp.

see Diencephalon bovis Gl see Gyrus cinguli bovis Gl see Lobus frontalis bovis Gl see Lobus occipitalis bovis Gl see Lobus parietalis bovis Gl see Lobus temporalis bovis Gl see Medulla oblongata bovis Gl see Mesencephalon bovis Gl see also Basal ganglia see also Limbic system

Cerebrum bovis, regio motorica Gl (= Gyrus praecentralis)

Precentral gyrus – the primary motor area of the brain Cerebrum, regio motorica Gl D..

Cerite

Natural cerium calcium iron silicate Crataegus/Cor comp.

Cervix uteri bovis Gl Uterine cervix Cervix uteri Gl D..

Chalcedony

Natural silicate with fibrous inclusions usually containing magnesium Chalcedon D..

Chalcedony, green variety containing nickel-silicate see Chrysopras

Chalkosine

Natural copper sulfide Thyreoidea comp.

578

Chamomile – flowerheads (dried) Chamomilla e floribus W 10%, Oleum

Chamomilla recutita e planta tota ferm 33c

Chamomile – whole plant at flowering time Bolus alba comp. Pulver Chamomilla e planta tota D..

Chamomilla recutita e radice ferm 33c

Charcoal from birch wood see Carbo vegetabilis

Chelidonium majus e floribus ferm 34b Celandine – flowers (Chelidonium majus L.) Aquilinum comp. Colchicum comp. Colchicum comp., Unguentum

Chelidonium majus e radice ferm 34b Celandine – underground parts Chelidonium e radice D.. Chelidonium Kapseln Chelidonium Augentropfen

Chelidonium majus ex herba cum radice ferm

Celandine – aerial parts of flowering plants and underground parts Chelidonium e planta tota D.. Chelidonium/Colocynthis

Chelidonium majus ex herba ferm 34b Celandine – aerial parts of flowering plants Chelidonium Augentropfen Chelidonium Kapseln

Cichorium intybus e planta tota ferm 33c Chicory – whole flowering plant (Cichorium intybus L.) Anagallis comp. Barium/Pancreas comp. Chelidonium Kapseln Cichorium e planta tota D.. Cichorium/Pancreas comp. Lien comp. Nervennahrung Platinum chloratum/Pancreas comp.

Chicory

see Cichorium intybus e planta tota ferm 33c

China e cortice ferm 35b

see Cinchona succirubra e cortice ferm 35b

Chlorargyrite, Horn Silver

Nat. silver chloride Hornerz/Cartilago comp. Hornerz/Corpus vitreum comp. Hornerz Corpus vitreum comp. Augentropfen

Chlorophyceae ferm 33e

Green algae (from the Chlorophyceae family) Argentum nitricum comp.

Chorioidea

see Retina et Chorioidea bovis Gl

Christmas rose

see Helleborus niger e planta tota ferm 34c

Chrysopras

Cinis e fructibus Avenae sativae cum Magnesio phosphorico

Magnesium monohydrogen phosphate with ash of oat grain Cactus comp. II Crataegus/Cor comp. Magnesium phosphoricum comp. Magnesium phosphoricum cum cinere Avenae D.. Nervennahrung Veratrum comp.

Cinnabar

Nat. mercury (II) sulfide Agropyron Inject Agropyron Globuli velati

Cinnabaris

see Cinnabar

Circulus arteriosus cerebri bovis Gl Circle of arteries at the base of the brain Circulus arteriosus cerebri Gl D..

Citrullus colocynthis e fructibus ferm 33a Bitter gourd – flesh (peeled fruit without seeds) (Citrullus colocynthis (L.) Schrad.) Chelidonium Kapseln Chelidonium/Colocynthis Colocynthis e fructibus D..

Citrus limon e fructibus ferm 33c Lemon – fruit (Citrus limon (L.) Burm. f.) Citrus e fructibus D.. Citrus e fructibus/Cydonia e fructibus

Citrus, Oleum aethereum 10% see Limonis aetheroleum 10%

Clay, white

see Kaolinum ponderosum

Green, nickel-silicate-containing variety of chalcedony Chrysopras D..

Club Moss

Cinchona succirubra e cortice ferm 35b

Cnicus benedictus ex herba ferm 33d

Peruvian bark - bark (dried) of Cinchona succiruba (Cinchona pubescens Vahl) Aconitum/China comp. Aconitum/China comp., Suppositorien Aconitum/China comp., Suppositorien für Kinder

see Lycopodium clavatum e planta tota ferm 33e

Holy Thistle – aerial parts of the flowering plant (Cnicus benedictus L.) Borago comp.

Cochlea bovis Gl

Cochlea – snail-like structure of the inner ear Cochlea Gl D..

579

C

Cochlearia officinalis ex herba ferm 33b Scurvy Grass – aerial parts of flowering plants (Cochlearia officinalis L.) Akne-Kapseln Cochlearia ex herba D.. Tormentilla comp.

Cod liver oil

see Iecoris aselli oleum A

Colchicum autumnale e planta tota ferm 34c

Meadow Saffron – whole flowering plant (Colchicum autumnale L.) Colchicum e planta tota D.. Colchicum comp. Colchicum comp., Unguentum

Colloidal silicic acid see Silicea colloidalis

Conchae

Oyster shells (Ostrea edulis) (nat. calcium carbonate) Avena comp. Cerebellum comp. Conchae D.. Conchae comp. Nervennahrung Primula comp. Primula/Convallaria comp. Rosmarinus/Prunus comp., Gelatum Thyreoidea comp. Urtica comp. Valeriana comp.

Conduction system

see Fasciculus atrioventricularis bovis Gl

Conjunctiva bovis Gl

Colloidal silver

(= Tunica conjunctiva) Conjunctival membrane of the eye Conjunctiva Gl D.. Conjunctiva comp.

Colocynthis e fructibus ferm 33a

Connective tissue

Colon, Ansa distalis

Convallaria majalis e planta tota ferm 33c

see Argentum colloidale see Citrullus colocynthis e fructibus ferm 33a see Colon sigmoideum suis Gl

Colon sigmoideum suis GI

Sigmoid colon – S-shaped portion of the large intestine Colon sigmoideum Gl D..

Colon suis Gl

see Textus connectivus bovis Gl

Lily of the Valley – whole flowering plant (Convallaria majalis L.) Primula/Convallaria comp. Scilla comp.

Copper

see Cuprum metallicum

Large intestine Colon Gl D..

Copper(I) oxide

Columna anterior cervicalis bovis Gl

Copper(II) acetate

Anterior column of the cervical spinal cord Columna anterior Gl D..

Columna posterior bovis Gl Posterior column (spinal cord) Columna posterior Gl D..

Comfrey

see Symphytum officinale e radice ferm 34c see Symphytum officinale ex herba LA 20%

Common Ragwort

see Senecio jacobaea ex herba ferm 33d

580

see Cuprum oxydulatum rubrum see Cuprum aceticum

Cor Gl D.. Cor/Aurum I Cor/Aurum II Crataegus/Cor comp. Mesenchym/Calcium carbonicum comp. Organum quadruplex Primula/Convallaria comp. see also Arteria coronaria bovis Gl see also Endocardium bovis Gl see also Fasciculus atrioventricularis bovis Gl see also Pericardium bovis Gl see also Valva trunci pulmonalis bovis Gl see also Valvula aortae bovis Gl see also Valvula mitralis bovis Gl see also Valvula tricuspidalis bovis Gl

Corpus vitreum Gl D.. Hornerz/Corpus vitreum comp. Hornerz Corpus vitreum comp. Augentropfen

Cornea bovis Gl

Hawthorn – leaves and fruit (Crataegus laevigata (Poir.) DC. und Cr. monogyna Jacq.) Adonis comp. Aurum Valeriana Inject Aurum Valeriana Globuli velati Cactus comp. II Crataegus e foliis et fructibus D.. Crataegus/Cor comp. Passiflora comp. Scilla comp. Viscum/Crataegus

Cornea – outermost layer of the eye Cornea Gl D.. Cornea/Levisticum comp. Cornea Augentropfen

Corpora quadrigemina bovis Gl

(Lamina tecti) Four colliculi in the brain Arnica/Plumbum comp. A Arnica/Plumbum comp. B Cerebrum comp. A Cerebrum comp. A cum Auro comp. Cerebrum comp. B Cerebrum comp. B cum Auro comp. Corpora quadrigemina Gl D.. Gnaphalium comp. Nervus opticus comp. Augentropfen

Corpus striatum bovis Gl

see Chalkosine

Cor bovis Gl Heart

Cowslip

see Primula veris e floribus ferm 33c see Primula veris e floribus W 5%

Crataegus laevigata/monogyna e foliis et fructibus ferm 33d

Crataegus laevigata/monogyna, Fructus rec. aqueous extract with sugar Hawthorn – fruit Passiflora Nerventonikum

Cross spider

Luteal body Corpus luteum Gl D..

Copper arsenate, nat. Copper sulfide, nat.

see Agropyron repens e radice ferm 33c

Corpus luteum bovis Gl

Corpus pineale

see Olivenite

Couch Grass

Creosotum, Kreosotum, Creosote

Copper(II) sulfate

see Cuprum sulfuricum

see Onopordum acanthium e floribus ferm 33c

Corpus amygdaloideum bovis Gl Almond-shaped structure in the brain Corpus amygdaloideum Gl D..

see Epiphysis bovis Gl

Basal ganglia (part of the telencephalon) Corpus striatum Gl D..

Corpus vitreum bovis Gl

Vitreous body of the eye Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen

C

Cotton Thistle

Beechwood tar distillate Majorana Vaginalgel

see Aranea ex animale Gl

Cuprum aceticum

Copper(II) acetate Cuprum aceticum comp. Echinacea/Viscum comp., Gelatum Renes/Borago comp.

Cuprum metallicum

Copper Cuprum/Quarz comp., Unguentum Glandula suprarenalis dextra cum Cupro Glandula suprarenalis sinistra cum Cupro Renes/Cuprum

581

Cuprum oxydulatum rubrum Copper(I) oxide Cuprum/Nicotiana, Unguentum Kupfer Salbe rot

Cuprum sulfuricum

Copper(II) sulfate Eucalyptus comp. Thyreoidea/Thymus comp. Veratrum comp.

Cutis feti bovis Gl

Skin (embryonic) Akne-Wasser Cutis feti Gl D.. Echinacea/Viscum comp., Gelatum Narben Gel

Cutis feti feminini bovis GI

Skin (embryonic, female) Rosmarinus/Prunus comp., Gelatum

Cuttlefish, secretion of

see Sepia officinalis e volumine bursae rec. Gl

Cydonia oblonga e fructibus ferm 33b Quince – fruit (Cydonia oblonga Mill.) Citrus e fructibus/Cydonia e fructibus Cydonia e fructibus D..

Cytisus scoparius ex herba ferm 33c

Broom – aerial parts of flowering plants (Cytisus scoparius L.) Sarothamnus comp.

Daisy

see Bellis perennis ex herba LA 20%

Dandelion

see Taraxacum officinale e planta tota ferm 34c see Taraxacum officinale e radice autumnale ferm 34c see Taraxacum officinale e radice vernale ferm 34c

Deadly Nightshade

see Atropa belladonna e fructibus ferm 33a see Atropa belladonna e radice ferm 33b see Atropa belladonna ex herba ferm 33a

Dens bovis Gl Tooth Dens Gl D..

582

Diaphragma bovis Gl Diaphragm Diaphragma Gl D..

Diaphragma pelvis bovis Gl Pelvic floor Diaphragma pelvis Gl D..

Diencephalon bovis Gl

Diencephalon (interbrain) Diencephalon Gl D.. see also Epiphysis bovis Gl see also Hypophysis bovis Gl

Disci intervertebrales cervicales bovis Gl Intervertebral disc (cervical spine) Disci intervertebrales (cervicales) Gl D..

Disci intervertebrales cervicales, thoracici et lumbales bovis Gl

Dryopteris filix-mas e radice ferm 33c Male fern – underground parts (Dryopteris filix-mas (L.) Schott) Aquilinum comp. Conchae comp. Salix/Rhus comp.

Ductus choledochus suis Gl Bile duct Ductus choledochus Gl D..

Duodenum suis Gl

Edelweiss

Duodenum Duodenum Gl D..

Disci intervertebrales feti bovis Gl

Pale purple cone flower – flowering plant (Echinacea pallida) Argentum nitricum comp. Cartilago/Echinacea comp. Conjunctiva comp. Echinacea e planta tota D.. Echinacea Augentropfen Echinacea Quarz comp. Augentropfen Endometrium comp. Majorana Vaginalgel Mundbalsam flüssig Mundbalsam Parametrium/Echinacea comp. Viscum/Echinacea

Intervertebral disk (lumbar spine) Disci intervertebrales (lumbales) Gl D..

Dog‘s Mercury

see Mercurialis ex herba ferm 34c

Drosera e planta tota ferm 33c

Sundew – whole plant at the beginning of flowering time (Drosera rotundifolia L. and Drosera anglica Huds.) Plantago Bronchialbalsam

Echinacea pallida ex herba LA 20% (Echinacea pallida, Herba rec . LA 20 %)

Thoracic duct Ductus thoracicus Gl D.. Renes/Borago comp.

Ductus thoracicus bovis Gl

Dura mater encephali bovis Gl

Disci intervertebrales lumbales bovis Gl

Pale purple cone flower – underground parts Echinacea/Argentum Echinacea/Mercurius comp., Suppositorien Echinacea/Mercurius comp., Suppositorien für Kinder

Pale purple cone flower – aerial parts at flowering time Akne-Wasser Echinacea/Viscum comp., Gelatum Echinacea-Essenz Echinacea Mund- und Rachenspray

Intervertebral discs of the cervical, thoracic and lumbar spine Disci comp. cum Aesculo Disci comp. cum Aesculo, Gelatum Disci comp. cum Argento Disci comp. cum Auro Disci comp. cum Nicotiana Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci comp. cum Stanno Disci comp. cum Stibio Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Argento, Suppositorien Disci/Viscum comp. cum Stanno Disci/Viscum comp, cum Stanno, Unguentum Intervertebral disk (embryonic) Disci intervertebrales (feti) Gl D..

Echinacea pallida e radice ferm 33d

Dura mater – outermost, fibrous membrane covering the brain Dura mater encephali Gl D..

Dwarf mountain pine, essential oil of see Pini pumilionis aetheroleum

Dwarf Nettle

see Urtica urens ex herba ferm 33c see Urtica urens ex herba LA 20%

Echinacea Ø

Pale purple cone flower (Echinacea pallida) Calcea Wund- und Heilcreme

Echinacea pallida e planta tota ferm 33c

see Leontopodium alpinum e planta tota ferm 36

Elder

see Sambucus nigra e medulla ferm 35a see Sambucus nigra ex umbella ferm 33c see Sambucus nigra ex umbella W 5%

Endocardium bovis Gl

Endocardium - membrane lining the inside of the heart Endocardium Gl D..

Endometrium bovis Gl

(= Tunica mucosa uteri) Mucous membrane lining the womb Endometrium Gl D.. Endometrium comp.

Epididymis sinistra bovis Gl Epididymis, left Epididymis (sinistra) Gl D..

Epiphysis bovis Gl

(= Corpus pineale) Pineal body Arnica/Plumbum comp. B Cerebrum comp. B Cerebrum comp. B cum Auro comp. Epiphysis Gl D.. Epiphysis/Plumbum Gnaphalium comp.

Epistropheus

see Axis bovis G

583

C D E

Equisetum arvense ex herba ferm 35b

Horsetail – green sterile shoot (dried) (Equisetum arvense L.) Aurum/Equisetum I Aurum/Equisetum II Cantharis Blasen Inject Cantharis Blasen Globuli velati Cera/Aesculus comp., Unguentum Disci comp. cum Nicotiana Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci comp. cum Stanno Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Viscum comp. cum Stanno Disci/Viscum comp, cum Stanno, Unguentum Equisetum ex herba D.. Equisetum/Formica Equisetum/Stannum Equisetum/Viscum Lens Viscum comp. Inject Lens Viscum comp. Globuli velati Lens Viscum comp. Augentropfen Lien comp. Pancreas/Equisetum Renes/Equisetum comp. Solum Inject Solum Inject 10 Solum Globuli velati

Equisetum arvense ex herba LA 20%

Essential oil of cajeput

Eucalypti aetheroleum 10%

Fel tauri Gl

Eucalyptus comp.

Femur bovis Gl

Essential oil of eucalyptus

Eucalyptus, essential oil of

Fennel, essential oil of

Essential oil of geranium

Eucalyptus globulus e foliis ferm 33d

Fern

see Cajeputi aetheroleum rectificatum

Essential oil of caraway see Carvi aetheroleum

Essential oil of dwarf mountain pine see Pini pumilionis aetheroleum see Eucalypti aetheroleum see Geranii aetheroleum

Essential oil from eucalyptus leaves (eucalyptus oil), in olive oil Eucalyptus, Oleum aethereum 10% Eucalyptus see Eucalyptus globulus e foliis ferm 33d see Eucalypti aetheroleum

Essential oil of lavender

Eucalyptus – leaves (Eucalyptus globulus Labill.) Aconitum/China comp. Aconitum/China comp., Suppositorien Aconitum/China comp., Suppositorien für Kinder Argentum nitricum comp. Echinacea Mund- und Rachenspray

Essential oil of lemon

Eupatorium cannabinum ex herba ferm 33c

Essential oil of juniper see Juniperi aetheroleum

see Lavandulae aetheroleum see Limonis aetheroleum

Essential oil of peppermint

see Menthae piperitae aetheroleum

Essential oil of pine see Pini aetheroleum

Hemp Agrimony – aerial parts of flowering plants (Eupatorium cannabinum L.) Aconitum/China comp. Aconitum/China comp., Suppositorien Aconitum/China comp., Suppositorien für Kinder Bronchi Plantago Inject Bronchi Plantago Globuli velati

see Foeniculi amari fructus aetheroleum see Dryopteris filix-mas e radice ferm 33c

Ferrum metallicum Iron Ferrum/Sulfur comp. Pulmo/Ferrum Thyreoidea/Ferrum Vesica fellea/Ferrum I Vesica fellea/Ferrum II

Ferrum oxydulatum nigrum (= Ferrum ustum; magnetite) Ferrum silicicum comp.

Ferrum sidereum see Meteoric iron

Essential oil of rose Essential oil of rosemary

Eyebright – whole flowering plant (Euphrasia rostkoviana Hayne) Euphrasia e planta tota D.. Euphrasia Augentropfen

Equisetum arvense ex herba W 5%

Essential oil of sage

Eyebright

Filix-mas e radice ferm 33c

Essential oil of thyme

False Acacia

Fir (silver)

Essential oil of turpentine

False Hellebore

Fir mistletoe

Eucalypti aetheroleum (= Oleum Eucalypti)

Fasciculus atrioventricularis bovis Gl

Horsetail – green, sterile shoot (dried) Equisetum ex herba W 5%, Oleum

Ergot

see Secale cornutum e sklerotio ferm 35b

Erythrocyten equi Gl Red blood cells Erythrocyten Gl D..

Essential oil of anise

see Anisi stellati aetheroleum

Essential oil of bitter fennel

see Foeniculi amari fructus aetheroleum

584

see Rosmarini aetheroleum

see Salviae officinalis aetheroleum see Thymi aetheroleum

see Terebinthinae aetheroleum rectificatum

Essential oil from eucalyptus leaves (eucalyptus oil) Juniperus/Berberis comp., Kapseln Majorana Vaginalgel Nasenbalsam Oleum camphoratum comp. Plantago Brochialbalsam

see Euphrasia e planta tota ferm 33c see Robinia pseudoacacia e cortice ferm 33e see Adonis ex herba ferm 33d

Ferrum silicicum see Nontronite

Ferrum ustum

see Ferrum oxydulatum nigrum see Dryopteris filix-mas e radice ferm 33c see Abies alba e summitatibus ferm 33d see Viscum album (Abietis) e planta tota ferm 34g see Viscum album (Abietis) e planta tota K

Conduction system of the heart Fasciculus atrioventricularis Gl D..

Fly Agaric

Fasciculus opticus

Fly, Spanish

see Nervus opticus bovis Gl

E F

Thigh bone Femur Gl D..

Horsetail – green, sterile shoot Equisetum-Essenz Solum Badezusatz Solum Öl Solum Salbe

see Rosae aetheroleum

Euphrasia e planta tota ferm 33c

Bile Fel Gl D.. Glandulae suprarenales comp.

see Amanita muscaria e planta tota ferm 33b see Cantharis ex animale Gl

585

Foeniculi amari fructus aetheroleum (= Oleum Foeniculi) Essential oil from fennel fruits (bitter fennel oil) (Foeniculum vulgare Mill.) Akne-Kapseln Juniperus/Berberis comp., Kapseln Melissenöl

Folliculi lymphatici aggregati suis Gl (Peyer‘s patches) Folliculi lymphatici aggregati Gl D..

Formica rufa

Oily extract Red wood ant – whole animal Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Rheuma-Badeöl

Formica rufa ex animale toto Gl

Red wood ant – whole animal (Formica rufa L.) Arnika Salbe Betula/Arnica comp. Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Cera/Aesculus comp., Unguentum Disci comp. cum Aesculo Disci comp. cum Aesculo, Gelatum Disci comp. cum Argento Disci comp. cum Auro Disci comp. cum Nicotiana Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci comp. cum Stanno Disci comp. cum Stibio Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Argento, Suppositorien Disci/Viscum comp. cum Stanno Disci/Viscum comp, cum Stanno, Unguentum Equisetum/Formica Formica ex animale Gl D.. Formica/Oxalis Lens Viscum comp. Inject Lens Viscum comp. Globuli velati Lens Viscum comp. Augentropfen Magnesium phosphoricum comp.

Fragaria vesca, Fructus rec. aqueous extract with sugar Wild strawberry - fruits Nervennahrung

586

Fragariae vescae folium

Wild strawberry – leaves (Fragaria vesca L.) Nervennahrung

Frangula e cortice ferm 33e

see Rhamnus frangula e cortice ferm 33e

Frankincense see Olibanum

Fucus vesiculosus e planta tota ferm 51 Bladder Wrack, thallus (Fucus vesiculosus L.) Akne-Kapseln Fucus vesiculosus e planta tota D..

Fumaria officinalis ex herba ferm 33c Fumitory – aerial parts of flowering plants (Fumaria officinalis L.) Akne-Kapseln

Fumitory

see Fumaria officinalis ex herba ferm 33c

Funiculus umbilicalis bovis Gl Umbilical cord Akne-Wasser Echinacea/Viscum comp., Gelatum

Funiculus umbilicalis Gl D..

Magnesit/Mamma comp. Magnesium sulfuricum/Ovaria comp. Renes/Borago comp. Rosmarinus/Prunus comp., Gelatum

Galea aponeurotica bovis Gl

Sheath of fibrous tissue covering the upper part of the cranium Galea aponeurotica Gl D..

Galenite

Lead glance – nat. lead sulfide Betula/Mandragora comp. Galenit/Retina comp. Retina comp. Secale/Bleiglanz comp. Secale/Retina comp.

Garden spider

see Aranea ex animale Gl

Garnet

Nat. silicate gemstone Granat D..

Gelsemium sempervirens e rhizoma ferm 35b Yellow Jasmine – underground parts (dried) (Gelsemium sempervirens (L.) Jaume St. Hil.) Disci/Rhus toxicodendron comp. Gelsemium e radice D.. Gelsemium comp. Rhus toxicodendron comp.

Gentian, yellow

see Gentiana lutea e radice ferm 33c see Gentiana lutea e radice, Decoctum see Gentianae luteae radix – aqueous extract siehe Gentianae luteae radix – aqueous extract with sugar

Gentiana lutea e radice, Decoctum

Echinacea Mund- und Rachenspray Gingiva Gl D.. Periodontium/Silicea comp. Periodontium/Stannum comp.

Glandula lacrimalis bovis Gl Tear gland Glandula lacrimalis Gl D..

F G

Glandula parotis bovis Gl Parotid gland Glandula parotis Gl D..

Glandula suprarenalis, Cortex bovis Gl Adrenal cortex Glandula suprarenalis (Cortex) Gl D..

Yellow Gentian – underground parts (Gentiana lutea L.) Gentiana Magen Inject Gentiana Magen Globuli velati

Glandula suprarenalis dextra bovis Gl

Gentianae luteae radix

Glandula suprarenalis, Medulla bovis Gl

Adrenal gland, right Glandula suprarenalis dextra Gl D.. Glandula suprarenalis dextra cum Cupro

aqueous extract Yellow Gentian – underground parts (dried) Enzian Magentonikum

Adrenal medulla Glandula suprarenalis (Medulla) Gl D..

Gentianae luteae radix

aqueous extract with sugar Yellow Gentian – underground parts (dried) Bitter Elixier

Adrenal gland, left Glandula suprarenalis sinistra Gl D.. Glandula suprarenalis sinistra cum Cupro Glandula suprarenalis sinistra/Mercurius

Geranii aetheroleum (= Oleum Geranii)

Glandula thymi bovis Gl

Essential oil from the aerial parts of the Pelargonium species (Geraniaceae) Malvenöl Rosatum Heilsalbe

Thymus gland Thymus (Glandula) Gl D.. Thymus/Mercurius Thyreoidea/Thymus comp.

Geranium essential oil

Glandula thyreoidea bovis Gl

see Geranii aetheroleum

Geum urbanum e radice ferm 33c

Avens – underground parts (Geum urbanum L.) Bolus alba comp. Pulver Geum urbanum e radice D..

Ginger

see Zingiberis rhizoma – aqueous extract see Zingiberis rhizoma – aqueous extract with sugar

Gingiva bovis Gl Gums

Glandula suprarenalis sinistra bovis Gl

Thyroid gland Glandula thyreoidea Gl D.. Thyreoidea comp. Thyreoidea/Ferrum Thyreoidea/Thymus comp.

Glandulae parathyreoideae bovis Gl Parathyroid glands Glandulae parathyreoideae Gl D.. Parathyreoidea comp. Parathyreoidea/Aurum

Glandulae suprarenales bovis Gl Adrenal glands

587

Akne-Wasser Glandulae suprarenales Gl D.. Glandulae suprarenales comp.

Globus pallidus

see Pars pallida bovis Gl

Gnaphalium leontopodium e planta tota ferm 36

see Leontopodium alpinum e planta tota ferm 36

Gold

see Aurum metallicum

Goldenrod

see Solidago virgaurea ex herba ferm 33c see Solidago virgaurea ex herba LA 20%

Golden Willow

see Salix alba ssp. vitellina e cortice et foliis ferm 33d

Granite

Primitive rock containing quartz, feldspar and mica Berberis/Prostata comp. Berberis/Uterus comp. Disci/Rhus toxicodendron comp. Rhus toxicodendron comp.

Graphite

see Graphites

Graphites

Graphite – flaky, crystalline carbon Akne-Kapseln Graphites D.. Roseneisen/Graphit

Greater Celandine

see Chelidonium majus e floribus ferm 34b see Chelidonium majus e radice ferm 34b see Chelidonium majus ex herba cum radice ferm see Chelidonium majus ex herba ferm 34b

Green algae

see Chlorophyceae ferm 33e

Gyrus cinguli bovis Gl

Cingulate gyrus – curved convolution of the brain arched over the corpus callosum Gyrus cinguli Gl D..

Gyrus praecentralis

588

see Cerebrum bovis, regio motorica Gl

Hamamelis

see Hamamelis virginiana e cortice et foliis LA 20% see Hamamelis virginiana e cortice ferm 33e see Hamamelis virginiana e foliis ferm 33d

Hamamelis virginiana e cortice et foliis LA 20% Witch Hazel – bark and leaves Hamamelis-Essenz

Hamamelis virginiana e cortice ferm 33e Witch Hazel – bark (Hamamelis virginiana L.) Hirudo comp.

Hamamelis virginiana e foliis ferm 33d Witch Hazel - leaves Borago comp. Hamamelis e foliis D.. Quercus Salbe Quercus Hämorrhoidalzäpfchen

Hart‘s Tongue

see Phyllitis scolopendrium e foliis ferm 34h

Hawthorn

see Crataegus laevigata/monogyna e foliis et fructibus ferm 33d see Crataegus laevigata/monogyna, Fructus rec. - aqueous extract with sugar

Hawthorn mistletoe

see Viscum album (Crataegi) e planta tota K

Hellebore, false

see Adonis ex herba ferm 33d

Hellebore, white false Helleborus niger e planta tota ferm 34c

Christmas Rose – flowering plant (Helleborus niger L.) Helleborus niger e planta tota D..

Hematite

Red iron ore, nat. iron(III) oxide Prunuseisen (Prunus spinosa ferm cum Ferro) Roseneisen (Rosa ferm cum Ferro) Roseneisen/Graphit Akne Kapseln Chelidonium comp. Augentropfen Levico comp. see Veratrum album e radice ferm 33c

Hemp agrimony

Hops

Henbane

Hornet

Hepar bovis Gl

Horn silver

see Eupatorium cannabinum ex herba ferm 33c see Hyoscyamus niger ex herba ferm 33d

Liver Carduus marianus/Viscum Mali comp. Hepar Gl D.. Hepar/Stannum I Hepar/Stannum II Mesenchym/Calcium carbonicum comp. Organum quadruplex

Hepar sulfuris

Liver of sulfur, calcium sulfide (crude) Hepar sulfuris comp. Lachesis comp.

Hexachloroplatinic acid see Platinum chloratum

High-moor peat

see Solum uliginosum – aqueous extract

Hirudo medicinalis ex animale toto Gl Leech – whole animal (Hirudo medicinalis L.) Hirudo ex animale toto Gl D.. Hirudo comp. Narben Gel

Hippocampus bovis Gl

see Humulus lupulus ex herba et fructibus ferm 34d see Vespa crabro ex animale Gl see Chlorargyrite see Equisetum arvense ex herba ferm 35b see Equisetum arvense ex herba LA 20% see Equisetum arvense ex herba W 5%

Horse Chestnut

see Aesculus hippocastanum e cortice, Decoctum LA 10 % see Aesculus hippocastanum e semine ferm 34c see Aesculus hippocastanum e semine LA 25% sicc. see Aesculus hippocastanum e semine W 5%

Humulus lupulus ex herba et fructibus ferm 34d Hops – bines with leaves and strobiles (Humulus lupulus L.) Passiflora Zäpfchen Passiflora Kinderzäpfchen

Humulus lupulus, Herba et Fructus rec. aqueous extract with sugar Hops – bines with leaves and strobiles Passiflora Nerventonikum

Structure adjacent to the inferior horn of the lateral ventricle in the brain (rhinencephalon) Hippocampus Gl D..

Hybrid tea rose

Hollyhock

Hyoscyamus niger ex herba ferm 33d

see Malva e floribus W 5%

Holy Thistle

see Cnicus benedictus ex herba ferm 33d

Honey

see Mel

Honeybee

see Apis mellifica ex animale toto Gl

Honeycomb

see Pollen comb

G H

Horsetail

see Rosa e floribus W 10% see Rosa e floribus ferm cum Ferro

Henbane – aerial parts of flowering plants (Hyoscyamus niger L.) Archangelica comp. Aurum/Stibium/Hyoscyamus Hyoscyamus ex herba D.. Primula comp. Primula/Convallaria comp. Primula Muskelnähröl

Hypericum perforatum ex herba ferm 33c St. John‘s Wort – aerial parts of flowering plants (Hypericum perforatum L.) Aurum/Apis regina comp. Berberis/Hypericum comp.

589

Hypericum ex herba D.. Levico comp. Passiflora Nerventonikum

Cerebrum comp. A cum Auro comp. Iris (bovis) Gl D.. Iris Lens comp. Augentropfen

Juniperus communis e fructibus ferm 35a

Hypericum perforatum, Herba rec.

Iron

Kalanchoe daigremontiana/pinnata e foliis ferm 33b

Oily extract St. John‘s Wort – aerial parts at flowering time Camphora/Hypericum, Unguentum Hypericum ex herba 5 %, Oleum Kampfer Johanniskrautöl Malvenöl Primula Muskelnähröl

Hypophysis bovis Gl

Pituitary gland Arnica/Plumbum comp. A Cerebrum comp. A Cerebrum comp. A cum Auro comp. Disci comp. cum Nicotiana Hypophysis Gl D.. Hypophysis/Stannum Magnesit/Mamma comp. Magnesium sulfuricum/Ovaria comp. Periodontium/Stannum comp. Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati Thyreoidea/Thymus comp.

Hypothalamus bovis Gl

Part of the diencephalon (under the thalamus) Hypothalamus Gl D..

Iecoris aselli oleum A

Cod liver oil, fatty oil from cod liver (Gadus morrhua L. and other species) Chelidonium Kapseln Juniperus/Berberis comp., Kapseln

Ignatia e semine ferm 35b

see Strychnos ignatii e semine ferm 35b

Ignatius bean

see Strychnos ignatii e semine ferm 35b

Ileum suis Gl

Ileum – part of the small intestine Ileum Gl D..

Iris bovis Gl

Iris (bovine) – coloured part of the eye Arnica/Plumbum comp. A Cerebrum comp. A

590

see Ferrum metallicum

Iron arsenate, nat. see Scorodite

Iron from meteorites (containing cobalt and nickel) see Meteoric iron

Iron sulfide, nat. see Pyrite

Iron(II) phosphate, nat. see Vivianite

Iron(III) oxide, nat. see Hematite

Jasmine, yellow

see Gelsemium sempervirens e rhizoma ferm 35b

Juniper – ripe cones Akne-Kapseln

Bryophyllum – leaf with plantlets (Kalanchoe daigremontiana Hamet et Perr. de la Bâthie) Bryophyllum comp. Ignatia comp.

Kalium bichromicum

(Lachesis muta L.) Ignatia comp. Lachesis e veneno D.. Lachesis comp. Melissa/Sepia comp.

Lactic acid

see Acidum lacticum

Lamina quadrigemina

see Corpora quadrigemina bovis Gl

Potassium dichromate Myristica sebifera comp.

Lamina tecti

Kalium carbonicum e cinere Fagi silvaticae

Lappa e radice W 5%

Potassium carbonate from beechwood ash Agropyron Inject Agropyron Globuli velati Anagallis comp. Nervennahrung

Kalium phosphoricum

Potassium dihydrogen phosphate Berberis/Hypericum comp.

see Corpora quadrigemina bovis Gl see Arctium lappa e radice W 5%

Larch resin

see Terebinthina laricina

Large-leaved lime

see Tilia platyphyllos/cordata e floribus W 5%

Larynx bovis Gl

Walnut – leaves and fruits Juglans regia comp.

Kerargyrite

Larynx – voice box Bronchi Plantago Inject Bronchi Plantago Globuli velati Larynx Gl D.. Larynx/Apis comp. see also Ligamentum vocale bovis Gl see also Nervus laryngeus recurrens bovis GI

Juniper

Khella

Lavandulae aetheroleum (= Oleum Lavandulae)

Jecoris Oleum

see Iecoris aselli oleum A

Juglans regia e foliis et fructibus ferm 33c

see Juniperi communis fructus – aqueous extract with sugar see Juniperus communis e fructibus ferm 35a

Juniper oil, essential

see Juniperi aetheroleum

Juniperi aetheroleum (= Oleum Juniperi)

Essential oil of juniper berries (juniper oil) Juniperus/Berberis comp., Kapseln

Juniperi communis fructus aqueous extract with sugar Juniper – ripe cones (dried) (Juniperus communis L.) Nierentonikum

Kaolinum ponderosum White clay Bolus alba comp. Pulver see Chlorargyrite see Ammi visnaga e fructibus ferm 35b

Kidney vetch

see Anthyllis vulneraria ex herba LA 20%

Labia majora et minora

see Pudendum femininum bovis GI

Labyrinthus bovis GI

(= L. Membranaceus et osseus) Inner ear Arnica/Plumbum comp. B Cerebrum comp. B Cerebrum comp. B cum Auro comp. Gnaphalium comp.

Lachesis

Venom of the Bushmaster (pit viper)

H I J K L

Essential oil from lavender flowers (lavender oil) Aconit Schmerzöl Aconit Ohrentropfen Rosmarinus/Prunus comp., Gelatum Solum Öl

Lavandulae aetheroleum 10%

Essential oil from lavender flowers (lavender oil), in olive oil Lavandula, Oleum aethereum 10%

Lavender, essential oil of see Lavandulae aetheroleum

Lead

see Plumbum metallicum see Plumbum mellitum

591

Lead glance see Galenite

Lemon

see Citrus limon e fructibus ferm 33c

Lemon oil, essential

see Limonis aetheroleum

Leech

see Hirudo medicinalis ex animale toto Gl

Lemon balm

see Melissa officinalis ex herba ferm 33c see Melissa officinalis ex herba W 5%

Lens cristallina bovis Gl

Lens of the eye Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen Hornerz/Corpus vitreum comp. Hornerz Corpus vitreum comp. Augentropfen Iris Lens comp. Augentropfen Lens cristallina Gl D.. Lens Viscum comp. Inject Lens Viscum comp. Globuli velati Lens Viscum comp. Augentropfen

Leontopodium alpinum e planta tota ferm 36 Edelweiss – plant with flowers (dried) (Leontopodium alpinum Cass.) Disci/Rhus toxicodendron comp. Gnaphalium comp. Rhus toxicodendron comp.

Levico water "strong"

Naturally occurring mineral containing (particularly iron(III), copper, sulfur and arsenic) spring water from Levico-Vetriolo (Trento/Northern Italy) Levico comp.

Levisticum officinale e radice ferm 33c Lovage – underground parts (Levisticum officinale W. D. J. Koch) Apis/Levisticum I Apis/Levisticum II Cerebellum comp. Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen Larynx comp. Larynx/Apis comp. Levisticum e radice D..

592

Levisticum officinale e radice W 5% Lovage – underground parts Levisticum e radice W 5%, Oleum Levisticum Ohrentropfen

Lien bovis Gl

Spleen Glandulae suprarenales comp. Lien Gl D.. Lien comp. Lien/Plumbum

Ligamentum longitudinale anterius bovis Gl Anterior longitudinal ligament of the spine Ligamentum longitudinale anterius Gl D..

Ligamentum longitudinale posterius bovis Gl Posterior longitudinal ligament of the spine Ligamentum longitudinale posterius Gl D..

Ligamentum vocale bovis Gl Vocal cords Ligamentum vocale Gl D..

Lilium lancifolium ex herba ferm 33c

Tiger Lily – aerial parts of flowering plants with bulblets (Lilium lancifolium Thunb.) Majorana Vaginalgel

Lilium tigrinum ex herba ferm 33c see Lilium lancifolium ex herba ferm 33c

Lily of the Valley

see Convallaria majalis e planta tota ferm 33c

Limbic System

see Corpus amygdaloideum bovis Gl see Gyrus cinguli bovis Gl see Hippocampus bovis Gl see Lobus frontalis bovis GI see Lobus temporalis bovis GI see Mesencephalon bovis GI see Thalamus bovis GI

Lime mistletoe

see Viscum album (Tiliae) e planta tota ferm 33f see Viscum album (Tiliae) e planta tota K

Lime tree

see Tilia platyphyllos/cordata e floribus W 5%

Limonis aetheroleum (= Oleum Citri) Essential oil from lemon peel (lemon oil) from Citrus limon L. Silicea colloidalis comp., Gelatum

Limonis aetheroleum 10% Essential oil from lemon peel (lemon oil), in olive oil Citrus, Oleum aethereum 10%

Lingua bovis Gl Tongue Lingua Gl D..

Lini oleum

Linseed oil, fatty oil from flax seeds (Linum usitatissimum L.) Chelidonium Kapseln Juniperus/Berberis comp., Kapseln

Linseed oil

see Lini oleum

Liquor cerebrospinalis bovis Gl

Cerebrospinal fluid – fluid circulating around the brain and spinal cord Liquor cerebrospinalis Gl D..

Lobus frontalis bovis Gl

Lycopodium clavatum e planta tota ferm 33e Club Moss – spore-bearing plant (Lycopodium clavatum L.) Lycopodium e planta tota D.. Lycopodium comp.

Lycopus virginicus e planta tota ferm 33d Bugleweed – whole flowering plant (Lycopus virginicus L.) Thyreoidea/Thymus comp.

Magnesite

Nat. magnesium carbonate Magnesit/Mamma comp.

Magnesium carbonate, nat. see Magnesite

Magnesium monohydrogen phosphate with ash of oat grain see Cinis e fructibus Avenae sativae cum Magnesio phosphorico

Magnesium phosphoricum cum cinere Avenae

see Cinis e fructibus Avenae sativae cum Magnesio phosphorico

Frontal lobe (brain) Lobus frontalis Gl D..

Magnesium sulfate

Lobus occipitalis bovis Gl

Magnesium sulfuricum

Occiptal lobe (brain) Lobus occipitalis Gl D..

Lobus parietalis bovis Gl Parietal lobe (brain) Lobus parietalis Gl D..

Lobus temporalis bovis Gl Temporal lobe (brain) Lobus temporalis Gl D..

Lovage

see Levisticum officinale e radice ferm 33c see Levisticum officinale e radice W 5%

Lupulus

see Humulus ex herba et fructibus ferm 34d see Humulus, Herba et Fructus rec. - aqueous extract with sugar

see Magnesium sulfuricum

Magnesium sulfate Berberis/Prostata comp. Berberis/Uterus comp. Magnesium sulfuricum/Ovaria comp.

Magnetite

see Ferrum oxydulatum nigrum

Marjoram

see Origanum majorana ex herba ferm 33c see Origanum majorana ex herba W 5%

Majorana ex herba ferm 33c

see Origanum majorana ex herba ferm 33c

Majorana ex herba W 5%

see Origanum majorana ex herba W 5%

Male fern

see Dryopteris filix-mas e radice ferm 33c

593

L M

Malva e floribus W 5%

Hollyhock – flowers (Alcea rosea L.) Malvenöl

Mamma bovis Gl

Mammary gland Magnesit/Mamma comp.

Mamma dextra bovis Gl Right breast Mamma (dextra) Gl D..

Mamma sinistra bovis Gl Left breast Mamma (sinistra) Gl D..

Mandibula feti bovis Gl

Lower jaw, embryonic Mandibula (feti) Gl D.. Periodontium/Silicea comp. Periodontium/Stannum comp.

Mandragora officinarum e radice ferm 34d

Mandrake – root (Mandragora officinarum L.) Betula/Mandragora comp. Cartilago/Mandragora comp. Cartilago/Mandragora comp, Unguentum Disci/Rhus toxicodendron comp. Mandragora officinarum e radice D.. Rhus toxicodendron comp.

Mandrake

see Mandragora officinarum e radice ferm 34d

Marigold, Pot

see Calendula ex herba flor. – pressed juice see Calendula officinalis e floribus LA 20% see Calendula officinalis e floribus W 10% see Calendula officinalis ex herba ferm 33c

Marine sponge

see Spongia tosta

Maxilla feti bovis Gl

Upper jaw, embryonic Maxilla (feti) Gl D.. Periodontium/Silicea comp. Periodontium/Stannum comp.

Meadow Saffron

see Colchicum autumnale e planta tota ferm 34c

594

Meadowsweet

see Spiraea ulmaria ex herba ferm 34c

Medicinal clay

see Terra medicinalis

Medulla oblongata bovis Gl

Medulla oblongata – lowest part of the brainstem, continuous with the spinal cord Arnica/Plumbum comp. A Arnica/Plumbum comp. B Cerebrum comp. A Cerebrum comp. A cum Auro comp. Cerebrum comp. B Cerebrum comp. B cum Auro comp. Gnaphalium comp. Medulla oblongata (Ventriculus quartus) Gl D.. see also Corpora quadrigemina bovis Gl see also Pons bovis Gl see also Truncus cerebri bovis Gl

Medulla oblongata Ventriculus quartus GI see Medulla oblongata bovis GI

Medulla ossium rubra bovis Gl Bone marrow, red Medulla ossium Gl D..

Medulla spinalis tota bovis Gl

Spinal cord Medulla spinalis (tota) Gl D.. see also Columna anterior cervicalis bovis Gl see also Columna posterior bovis Gl

Mel

Honey Cera/Aesculus comp., Unguentum

Melaleuca

see Cajeputi aetheroleum rectificatum

Melissa officinalis ex herba ferm 33c

Lemon Balm – aerial parts (Melissa officinalis L.) Melissa/Sepia comp. Thyreoidea/Thymus comp.

Melissa officinalis ex herba W 5% Lemon Balm – aerial parts (dried) Melissa ex herba W 5%, Oleum Melissenöl

Membrana sinus frontalis bovis Gl (= Tunica mucosa sinus frontalis) Mucosal lining of the frontal sinus Membrana sinus frontalis Gl D..

Membrana sinus maxillaris bovis Gl

Hirudo comp. Pulmo/Mercurius Thymus/Mercurius

Mercury (quicksilver) see Mercurius vivus

(= Tunica mucosa sinus maxillaris) Mucosal lining of the maxillary sinus Membrana sinus maxillaris Gl D..

Mercury amidonitrate (crude)

Membrana sinuum paranasalium bovis Gl

Mercury(I) chloride

see Mercurius solubilis Hahnemanni see Mercurius dulcis

(= Tunica mucosa sinuum paranasalium) Mucosa of the paranasal sinuses Hepar sulfuris comp. Membrana sinuum paranasalium Gl D..

Mercury(II) sulfide, nat.

Membrana synovialis bovis Gl

Mesencephalon bovis Gl

Synovial membrane Membrana synovialis Gl D..

Meniscus bovis Gl

(= Meniscus medialis) Meniscus – cartilage structure in the knee joint Meniscus Gl D..

see Cinnabar

Midbrain Mesencephalon Gl D.. see also Corpora quadrigemina bovis Gl see also Nucleus ruber bovis Gl see also Regio substantiae nigrae bovis Gl

Mesenchym bovis Gl

(= Oleum Menthae piperitae) Essential oil from leaves and flowering tips of peppermint (Mentha piperita L.) (peppermint oil) Chelidonium Kapseln

Connective tissue, embryonic Narben Gel Lien comp. Mesenchym Gl D.. Mesenchym/Calcium carbonicum comp. Renes/Borago comp.

Mercurialis ex herba ferm 34c

Mesenterium

Menthae piperitae aetheroleum

Dog‘s Mercury – aerial parts of flowering plants (Mercurialis perennis L.) Lachesis comp. Mercurialis comp., Suppositorien Mercurialis Augentropfen Mercurialis Salbe

Mercurius dulcis Mercury(I) chloride Lycopodium comp.

Mercurius solubilis Hahnemanni

Mercury amidonitrate (crude) Apis/Belladonna cum Mercurio Echinacea/Mercurius comp., Suppositorien Echinacea/Mercurius comp., Suppositorien für Kinder

Mercurius vivus

Mercury, quicksilver Glandula suprarenalis sinistra/Mercurius

M

see Radix mesenterii bovis GI

Meteoric iron

(= Ferrum sidereum), cobalt- and nickel-containing iron from meteorites Meteoreisen Inject Meteoreisen Globuli velati Pancreas/Meteoreisen

Milk Thistle

see Silybum marianum e fructibus ferm 36

Millefolium

see Achillea ex herba ferm 33d

Mistletoe from apple trees

see Viscum album (Mali) e planta tota ferm 34i see Viscum album (Mali) e planta tota K see Viscum album (Mali) ex herba W 5% see Viscum album (Mali), Senker ferm 33e

595

Mistletoe from fir trees

see Viscum album (Abietis) e planta tota ferm 34g see Viscum album (Abietis) e planta tota K

Mistletoe from hawthorn

see Viscum album (Crataegi) e planta tota K

Mistletoe from lime trees

see Viscum album (Tiliae) e planta tota ferm 33f see Viscum album (Tiliae) e planta tota K

Mistletoe from oak trees

see Viscum album (Quercus) ex herba K

Mistletoe from pine trees

see Viscum album (Pini) e planta tota ferm 34g see Viscum album (Pini) e planta tota K

Mistletoe from poplar trees

see Viscum album (Populi) e planta tota ferm 33f see Viscum album (Populi) e planta tota K

Mistletoe from willow trees

see Viscum album (Salicis) e planta tota K

Monkshood

see Aconitum napellus e tubere ferm 33c see Aconitum napellus e tubere W 5 %

Mother-of-Thousands

see Kalanchoe daigremontiana/pinnata

Musculi glutaei bovis Gl Gluteal muscles Musculi glutaei Gl D..

Musculus deltoideus-Komplex bovis Gl

Musculus sphincter

see Trigonum vesicae et Musculus sphincter bovis Gl

Mustard, black

see Brassica nigra e semine W 10%

Myocardium bovis GI Cardiac muscle Primula Muskelnähröl

Myristica sebifera, succus e cortice Sap from the bark of Virola sebifera Myristica sebifera comp.

Myrrh - resin see Myrrha

Myrrha

Myrrh – resin (Commiphora molmol Engl.) Aurum comp. Aurum comp., Unguentum Cerebrum comp. A cum Auro comp. Cerebrum comp. B cum Auro comp.

Nasturtium

see Tropaeolum majus ex herba ferm 33b see Tropaeolum majus ex herba LA 20%

Natrium carbonicum

Sodium carbonate monohydrate Cerebellum comp. Nervennahrung

Natrium phosphoricum

Sodium monohydrogen phosphate Robinia comp.

Shoulder-upper arm muscle complex (deltoid muscle, infraspinatus muscle, supraspinatus muscle, biceps muscle, triceps muscle) Musculus deltoideus-Komplex Gl D..

Natrium sulfuricum

Musculus erector spinae

Sodium sulfate Lycopodium comp.

Nervus facialis bovis Gl

Seventh cranial nerve (facial nerve) Nervus facialis Gl D..

Nervus femoralis bovis Gl Femoral nerve Nervus femoralis Gl D..

Nervus glossopharyngeus bovis Gl

Ninth cranial nerve (nerve supplying the tongue and the throat) Nervus glossopharyngeus Gl D..

Nervus hypoglossus bovis Gl

Twelfth cranial nerve (nerve supplying the tongue) Nervus hypoglossus Gl D..

Nervus ischiadicus bovis Gl Sciatic nerve Articulatio talocruralis comp. Nervus ischiadicus Gl D..

Nervus laryngeus recurrens bovis Gl

Recurrent laryngeal nerve (nerve supplying the voice box) Larynx comp. Larynx/Apis comp. Nervus laryngeus recurrens Gl D..

Nervus laryngeus superior bovis GI Superior laryngeal nerve Larynx comp. Larynx/Apis comp.

Nervus medianus bovis Gl Median nerve of the arm Nervus medianus Gl D..

Nervus oculomotorius bovis Gl

Nervi intercostales bovis Gl

(= Rami ventrales) intercostal nerves Nervi intercostales Gl D..

Third cranial nerve (nerve controlling the eye muscles) Iris Lens comp. Augentropfen Nervus oculomotorius Gl D.. Nervus opticus comp. Augentropfen

Musculus rectus abdominis bovis Gl

Nervus abducens bovis Gl

Nervus olfactorius

Musculus soleus-Komplex bovis Gl

Nervus accessorius bovis Gl

see Musculus sacrospinalis bovis Gl

Rectus muscle of the abdomen Musculus rectus abdominis Gl D..

Calf muscle complex (soleus muscle, peronaeus longus muscle, gastrocnemius muscle) Musculus soleus-Komplex Gl D..

596

Sixth cranial nerve Nervus abducens Gl D..

Eleventh cranial nerve Nervus accessorius Gl D..

see Bulbus olfactorius bovis Gl

Nervus ophthalmicus bovis Gl

Ophthalmic nerve (sensory branch of the trigeminal nerve) Iris Lens comp. Augentropfen see also Nervus trigeminus bovis GI

Nervus opticus bovis Gl

Second cranial nerve (optic nerve) Arnica/Plumbum comp. A Cerebrum comp. A Cerebrum comp. A cum Auro comp. Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen Nervus opticus Gl D.. Nervus opticus comp. Augentropfen

Nervus peronaeus bovis Gl

(= Nervus peronaeus communis) Fibular nerve Nervus peronaeus Gl D..

Nervus phrenicus bovis Gl Nerve supplying the diaphragm Nervus phrenicus Gl D..

Nervus pudendus bovis Gl

Pudendal nerve – nerve carrying sensations from the external genitals Nervus pudendus Gl D..

Nervus radialis bovis Gl Radial nerve Nervus radialis Gl D..

Nervus statoacusticus bovis Gl

(= N. vestibulocochlearis) Eighth cranial nerve (hearing and balance nerve) Arnica/Plumbum comp. B Cerebrum comp. B Cerebrum comp. B cum Auro comp. Gnaphalium comp. Nervus statoacusticus Gl D..

Nervus tibialis bovis Gl Tibial nerve Nervus tibialis Gl D..

Nervus trigeminus bovis Gl Fifth cranial nerve Nervus trigeminus Gl D..

Nervus trochlearis bovis Gl Fourth cranial nerve Nervus trochlearis Gl D..

Nervus ulnaris bovis Gl Ulnar nerve Nervus ulnaris Gl D..

597

M N

Nervus vagus bovis Gl Tenth cranial nerve Larynx comp. Larynx/Apis comp. Nervus vagus Gl D..

Nervus vestibulocochlearis

see Nervus statoacusticus bovis Gl

Nettle, Common/Stinging

see Urtica dioica e planta tota ferm 33c see Urtica dioica ex herba W 5% see Urticae dioicae herba

Nettle, Dwarf

see Urtica urens ex herba ferm 33c see Urtica urens ex herba LA 20%

Nettle, Small

see Urtica urens ex herba ferm 33c see Urtica urens ex herba LA 20%

Nicotiana tabacum e foliis ferm 33b

Tobacco – leaves (Nicotiana tabacum L.) Ammi visnaga comp., Suppositorien Ammi visnaga comp., Suppositorien für Kinder Belladonna comp., Suppositorien Belladonna comp., Suppositorien für Kinder Berberis/Nicotiana comp. Borago comp. Carum carvi Zäpfchen Carum carvi Kinderzäpfchen Chamomilla/Nicotiana Crataegus/Cor comp. Cuprum aceticum comp. Cuprum/Nicotiana, Unguentum Disci comp. cum Nicotiana Nicotiana e foliis D.. Nicotiana comp. Nux vomica/Nicotiana comp. Quarz/Nicotiana, Globuli velati Quarz/Oxalis comp. Robinia comp. Secale/Bleiglanz comp. Secale/Retina comp. Strophanthus/Nicotiana comp.

Night-Blooming Cereus

see Selenicereus grandiflorus ex herba ferm 33d

Nodi lymphatici bovis Gl Lymph nodes Nodi lymphatici Gl D..

598

Nontronite

Nat. iron (II, III) silicate Ferrum silicicum comp.

Nucleus ruber bovis Gl Red nucleus of the midbrain Nucleus ruber Gl D..

Nux Vomica

see Strychnos nux-vomica e semine ferm 35b

Nux vomica e semine ferm 35b

see Strychnos nux-vomica e semine ferm 35b

Oak

see Quercus robur/petraea e cortice cum Calcio carbonico (Ø = D6) see Quercus robur/petraea e cortice, Decoctum see Quercus robur/petraea e cortice, Decoctum LA 10%

Oak mistletoe

see Viscum album (Quercus) ex herba K

Oats

see Avena e planta tota ferm 33c see Avena sativa, Herba rec. - aqueous extract with sugar

Oesophagus suis Gl Gullet Oesophagus Gl D..

Oleum Amygdalarum dulce see Amygdalae oleum

Oleum Anisi

see Anisi stellati aetheroleum

Oleum Carvi

see Carvi aetheroleum

Oleum Citri

see Limonis aetheroleum

Oleum Jecoris

see Iecoris asseli oleum A

Oleum Lini

see Lini oleum

Oleum Menthae piperitae

see Menthae piperitae aetheroleum

Oleum Petrae

see Petroleum rectificatum

Oleum Pini pumilionis

see Pini pumilionis aetheroleum

Oleum Ricini

see Ricini oleum

Oleum Rosae

see Rosae aetheroleum

Orchis e tubere, Decoctum Orchids – daughter bulbs (dried) (Orchis species) Cerebellum comp.

Origanum majorana ex herba ferm 33c

Sweet Marjoram – above-ground flowering plants (Majorana hortensis L.) Majorana Vaginalgel

Origanum majorana ex herba W 5%

Oleum Salviae

Sweet Marjoram – aerial parts dried (Majorana hortensis L.) Melissenöl

Oleum Terebinthinae rectificatum

Osier Willow

Olibanum

Ossicula auditus bovis Gl

see Salviae aetheroleum see Terebinthinae aetheroleum rectificatum

Frankincense, gum resin from the tree Boswellia sacra Flueckiger Aurum comp. Aurum comp., Unguentum Cerebrum comp. A cum Auro comp. Cerebrum comp. B cum Auro comp.

Olivenite

Nat. copper arsenate Senecio comp. Senecio comp., Suppositorien

Onion

see Allium cepa ferm 34°

Onopordum acanthium e floribus ferm 33c

see Salix viminalis e cortice et foliis ferm 33d

(= Ossicula tympani), auditory ossicles (bones in the middle ear) Ossicula auditus Gl D..

N O

Ostium cardiacum see Cardia suis Gl

Ovaria bovis Gl

Ovaries Berberis/Uterus comp. Magnesium sulfuricum/Ovaria comp. Ovaria Gl D.. Ovaria comp. Ovaria/Argentum Parametrium/Echinacea comp. see also Corpus luteum bovis Gl

Cotton Thistle – flowerheads (Onopordum acanthium L.) Primula comp. Primula/Convallaria comp.

Oxalidis acetosellae herba

Onyx

Oxalis acetosella e planta tota ferm 34b

Nat. silicic acid with traces of iron oxide and carbon Gnaphalium comp.

Opal

Multicolored colloidal silica mineral with varying water content Opal D..

Orchids

see Orchis e tubere, Decoctum

Wood Sorrel – aerial parts (dried) (Oxalis acetosella L.) Nervennahrung Wood Sorrel – whole plant at flowering time Akne-Kapseln Barium/Pancreas comp. Berberis/Prostata comp. Berberis/Uterus comp. Carduus marianus/Oxalis Formica/Oxalis Oxalis e planta tota D.. Platinum chloratum/Pancreas comp. Quarz/Oxalis comp.

599

Oxalis acetosella e planta tota LA 20% Wood Sorrel – whole plant at flowering time Oxalis-Essenz

Oxalis acetosella e planta tota W 10% Wood Sorrel – whole plant at flowering time (dried) Oxalis e planta tota W 10%, Oleum

Oyster shells see Conchae

Paeonia officinalis e radice ferm 33c Peony – underground parts (Paeonia officinalis L.) Hirudo comp.

Pale Purple Cone Flower

see Echinacea Ø see Echinacea pallida e planta tota ferm 33c see Echinacea pallida e radice ferm 33d

Pallidum

see Pars pallida bovis GI

Pancreas suis Gl

Pancreas Barium/Pancreas comp. Cichorium/Pancreas comp. Mesenchym/Calcium carbonicum comp. Pancreas Gl D.. Pancreas/Argentum Pancreas/Equisetum Pancreas/Meteoreisen Platinum chloratum/Pancreas comp.

Pansy

see Viola tricolor ex herba ferm 33e

Papillae duodeni suis Gl

Papilla of Vater (point of opening of bile duct and pancreatic duct into the duodenum) Papillae duodeni Gl D..

Parametrium bovis Gl

Uterine connective tissue Parametrium/Echinacea comp.

Parametrium dextrum bovis Gl Uterine connective tissue, right Parametrium (dextrum) Gl D..

Parasympathicus

see Nervus vagus bovis Gl (nerve plexuses and ganglia of the autonomic nervous system are contained in various preparations designated "Plexus…. Gl")

Pars fetalis Placenta bovis Gl Placenta, fetal part Rosmarinus/Prunus comp., Gelatum

Pars pallida bovis Gl

(= Globus pallidus) Pale-appearing spherical structure in the brain, component of the basal ganglia Pars pallida Gl D..

see Piperis nigri fructus – aqueous extract see Piperis nigri fructus – aqueous extract with sugar

Peppermint, essential oil of

see Menthae piperitae aetheroleum

Pericardium bovis Gl

Pericardium – fibrous sac surrounding the heart Pericardium Gl D..

Periodontium bovis Gl

Pars uterina Placenta bovis Placenta, uterine part see Placenta bovis Gl

Periodontium – tissue surrounding and supporting the teeth Periodontium Gl D.. Periodontium/Silicea comp. Periodontium/Stannum comp.

Passiflora caerulea ex herba ferm 33c

Periosteum bovis Gl

Passion Flower – aerial parts of flowering plants (Passiflora caerulea L.) Passiflora comp. Passiflora Zäpfchen Passiflora Kinderzäpfchen

Passiflora caerulea, Herba rec.

Periosteum – fibrous membrane covering the bone Articulatio talocruralis comp. Periosteum Gl D.. Tendo/Allium cepa comp.

Peritonaeum bovis Gl

aqueous extract with sugar Passion Flower – aerial parts of flowering plants Passiflora Nerventonikum

Peritoneum – membrane lining the abdominal cavity and covering the abdominal organs Peritonaeum Gl D.. Viscum/Bryonia comp.

Passion Flower

Peru balsam

see Passiflora caerulea ex herba ferm 33c see Passiflora caerulea, Herba rec. – aqueous extract with sugar

Patella bovis Gl Patella of the knee Patella Gl D..

Pasque Flower

see Pulsatilla vulgaris e floribus ferm 33c

Peat Extract

see Solum uliginosum – aqueous extract

Penis bovis Gl

Male reproductive organ Penis Gl D..

Peony

see Paeonia officinalis e radice ferm 33c

600

Pepper, black

see Balsamum peruvianum

Peruvian bark

see Cinchona succirubra

Petasites hybridus e radice ferm 33c

Butterbur – underground parts (Petasites hybridus (L.) Ph. Gärtn., B. Mey. et Scherb.) Petasites comp. Plantago Bronchialbalsam Plantago Hustensaft

Petroleum

see Petroleum rectificatum (= Oleum Petrae)

Petroleum rectificatum (= Oleum Petrae) Petroleum Oleum Petrae comp.

Peyer‘s patches

see Folliculi lymphatici aggregati suis GI

Pharynx bovis Gl

(Pars laryngea et pars oralis) Throat Pharynx Gl D..

Pharynx, Pars laryngea

Throat, part lying behind the voice box see Pharynx bovis Gl

Pharynx, Pars oralis

Throat, part lying behind the oral cavity see Pharynx bovis Gl

Pheasant‘s Eye, Yellow

see Adonis ex herba ferm 33d

Phosphoric acid

see Acidum phosphoricum

Phosphorus

O P

Yellow phosphorus Avena comp. Meteoreisen Inject Meteoreisen Globuli velati Oleum Petrae comp. Phosphorus D.. Valeriana comp.

Phosphorus, yellow see Phosphorus

Phyllitis scolopendrium e foliis ferm 34h Hart‘s Tongue – leaves of spore-bearing plants (Phyllitis scolopendrium L.) Aquilinum comp. Conchae comp. Salix/Rhus comp.

Phyllostachys e nodo ferm 35c

Bamboo – stem nodes (Phyllostachys species) Bambusa e nodo D.. Disci comp. cum Aesculo Disci comp. cum Aesculo, Gelatum Disci comp. cum Argento Disci comp. cum Auro Disci comp. cum Nicotiana Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci comp. cum Stanno Disci comp. cum Stibio

601

Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Argento, Suppositorien Disci/Viscum comp. cum Stanno Disci/Viscum comp, cum Stanno, Unguentum Lens Viscum comp. Inject Lens Viscum comp. Globuli velati Lens Viscum comp. Augentropfen

Piperis nigri fructus

Plexus cardiacus bovis Gl

Pit viper (Bushmaster), venom of

Plexus coeliacus bovis Gl

Pia mater encephali bovis Gl

Placenta (bovine) Akne-Gesichtsmaske Akne-Wasser Berberis/Sepia comp. Echinacea/Viscum comp., Gelatum Placenta bovis Gl D..

Pia mater – fine vascular membrane enveloping the brain Pia mater encephali Gl D..

Picea abies, Summitates rec. aqueous extract with sugar Spruce – shoot tips (Picea abies L.) Plantago Hustensaft

Pimpinella anisum e fructibus, Infusum Anise fruits (dried) (Pimpinella anisum L.) Ferrum silicicum comp.

Pine essential oil

see Pini aetheroleum

Pine mistletoe

see Viscum album (Pini) e planta tota ferm 34g see Viscum album (Pini) e planta tota K

Pini aetheroleum (= Oleum Pini sylvestris)

Essential oil from fresh needles and branch tips or fresh branches with needles and branch tips of a pine species (Pinus silvestris L.) Oleum camphoratum comp.

Pini pumilionis aetheroleum (= Oleum Pini pumilionis)

Essential oil from fresh needles and branches of the Dwarf Mountain Pine (Pinus mugo Turra) Juniperus/Berberis comp., Kapseln

Pini pumilionis aetheroleum 10%

Essential oil from fresh needles and branches of the Dwarf Mountain Pine, in olive oil Pinus pumilio, Oleum aethereum 10%

Piperis nigri fructus

aqueous extract Black Pepper – fruits (dried) Enzian Magentonikum

602

aqueous extract with sugar Black Pepper – fruits (dried) Bitter Elixier see Lachesis

Placenta bovis Gl

Network of nerves controlling the heart (symp. and parasymp., around aortic arch and pulmonary trunk) Plexus cardiacus Gl D.. Solar plexus (network of autonomic nerves at the origin of the coeliac trunk) Plexus coeliacus Gl D..

Plexus gastricus bovis Gl

Network of autonomic nerves supplying the stomach Plexus gastricus Gl D..

Plexus haemorrhoidalis bovis GI

Placenta, Pars fetalis

(= Plexus venosus rectalis) Network of veins around the rectum Plexus haemorrhoidalis GI D...

Placenta, Pars uterina

Plexus lumbalis bovis Gl

see Pars fetalis Placenta bovis Gl see Pars uterina Placenta bovis Gl

Plantago lanceolata e foliis ferm 34c

Network of nerves of the lumbar spine Plexus lumbalis Gl D..

Ribwort Plaintain – leaves (Plantago lanceolata L.) Bronchi Plantago Inject Bronchi Plantago Globuli velati Petasites comp. Plantago Bronchialbalsam

Plexus pelvinus bovis Gl

Plantago lanceolata, Folium rec.

Network of autonomic nerves of the lungs Plexus pulmonalis (Nervus vagus) Gl D..

aqueous extract with sugar Ribwort Plantain - leaves Plantago Hustensaft

Platinum

see Platinum metallicum

Platinum chloratum

Hexachloroplatinic acid Platinum chloratum/Pancreas comp.

Platinum metallicum Platinum Platinum metallicum D..

Pleura bovis Gl

Pleural membrane - membrane covering the lungs. Pleura Gl D..

Plexus brachialis bovis Gl

Network of nerves controlling the arm Plexus brachialis Gl D..

Network of autonomic nerves of the pelvis, inferior part Plexus pelvinus Gl D..

Plexus pulmonalis Nervus vagus bovis Gl

Plexus rectalis bovis Gl

see Plexus haemorrhoidalis bovis Gl

Plexus sacralis bovis Gl

Plumbum metallicum Lead Epiphysis/Plumbum

Poison sumach

see Toxicodendron quercifolium e foliis ferm 33d

Pollen combs

Honeycombs containing flower pollen Nervennahrung

Polygonatum odoratum e radice ferm 33d Solomon‘s Seal – underground parts (Polygonatum odoratum (Mill.) Druce) Narben Gel

Pons bovis Gl

Pons – part of the brain stem Pons Gl D..

Poplar mistletoe

see Viscum album (Populi) e planta tota ferm 33f see Viscum album (Populi) e planta tota K

P

Pot Marigold, Calendula

see Calendula ex herba flor. – pressed juice see Calendula officinalis e floribus LA 20% see Calendula officinalis e floribus W 10% see Calendula officinalis ex herba ferm 33c

Potassium antimonyl tartrate see Tartarus stibiatus

Potassium carbonate from beechwood ash see Kalium carbonicum e cinere Fagi silvaticae

Network of spinal nerves supplying the legs Plexus sacralis Gl D..

Potassium dichromate

Plexus solaris

Potassium dihydrogen phosphate

Plumbum mellitum

Potentilla tormentilla e radice ferm 34d

see Plexus coeliacus bovis Gl

Lead with honey and cane sugar in a special preparation Arnica/Plumbum comp. A Arnica/Plumbum comp. B Arnica/Plumbum mellitum Aurum/Belladonna comp. Strophanthus/Nicotiana comp.

see Kalium bichromicum

see Kalium phosphoricum

Tormentil – rootstock (Potentilla erecta L.) Tormentilla comp. Tormentilla e radice D..

Primula veris e floribus ferm 33c Cowslip – flowers (Primula veris L.) Primula comp. Primula/Convallaria comp.

603

Primula veris e floribus W 5% Cowslip – flowers (dried) Primula Muskelnähröl

Prostata bovis Gl

Prostate gland Berberis/Prostata comp. Prostata Gl D..

Prunus spinosa e floribus et summitatibus ferm 33d

Blackthorn – flowers and young shoot tips Aurum/Prunus Prunus spinosa e floribus et summitatibus D.. Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati

Prunus spinosa e floribus W 5% Blackthorn – flowers (dried) Malvenöl Prunus spinosa e floribus W 5%, Oleum

Prunus spinosa, e fructibus LA 25% Blackthorn - fruits Aesculus/Prunus comp., Essenz Nasenbalsam Nasenbalsam für Kinder Prunus-Essenz Rosmarinus/Prunus comp., Gelatum

Prunus spinosa ferm cum Ferro

Blackthorn – flowers and shoot tips (Prunus spinosa L.) – extract prepared in the presence of hematite Levico comp. Prunuseisen

Prunuseisen

see Prunus spinosa ferm cum Ferro

Pteridium aquilinum e foliis ferm 34c Bracken – leaves (Pteridium aquilinum L.) Aquilinum comp. Conchae comp. Salix/Rhus comp.

Pudendum femininum bovis Gl Female genitals Rosmarinus/Prunus comp., Gelatum

Pulmo bovis Gl

Lung Mesenchym/Calcium carbonicum comp. Organum quadruplex

604

Pulmo Gl D.. Pulmo/Ferrum Pulmo/Mercurius Pulmo/Tartarus stibiatus I Pulmo/Tartarus stibiatus II Pulmo/Vivianit comp. Dental pulp Pulpa dentis Gl D..

Mundbalsam Periodontium/Silicea comp. Primula Muskelnähröl Quarz D.. Quarz/Nicotiana, Globuli velati Quarz/Oxalis comp. Secale/Quarz Silicea comp. Silicea comp., Suppositorien Silicea comp., Suppositorien für Kinder

Pulsatilla vulgaris e floribus ferm 33c

Queen bee

Pulpa dentis bovis Gl

Pasque Flower – flowers with bracts (Pulsatilla vulgaris Mill.) Berberis/Nicotiana comp. Bryonia comp. Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Viscum comp. cum Argento, Suppositorien Hirudo comp. Pulsatilla e floribus D.. Spongia/Aurum/Pulsatilla comp.

Purple Osier

see Salix purpurea e cortice et foliis ferm 33d

Pylorus suis Gl

Pylorus – outlet of the stomach Pylorus Gl D..

Pyrite

Nat. iron sulfide Archangelica comp. Berberis/Pyrit comp. Bronchi Plantago Inject Bronchi Plantago Globuli velati

Quartz

Rock crystal – nat. silicic acid, crystallised Aconit Ohrentropfen Aconit Schmerzöl Argentum/Quarz Berberis/Quarz Cartilago/Echinacea comp. Conjunctiva comp. Cuprum/Quarz comp., Unguentum Echinacea Quarz comp. Augentropfen Endometrium comp. Ferrum/Sulfur comp. Meteoreisen Inject Meteoreisen Globuli velati Mundbalsam flüssig

see Apis regina Gl

Queen of the Night

see Selenicereus grandiflorus ex herba ferm 33d

Quercus robur/petraea e cortice cum Calcio carbonico (Ø = D6) Oak bark decoction, potentised in a saturated solution of purified oak bark ash Calcium Quercus Inject Calcium Quercus Inject 10 Calcium Quercus Globuli velati Calcium carbonicum cum Quercu D.. Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen Mesenchym/Calcium carbonicum comp.

Quercus robur/petraea e cortice, Decoctum Oak – bark of young branches and root-collar shoots (dried) Quercus Hämorrhoidalzäpfchen Quercus Salbe see also Quercus e cortice cum Calcio carbonico

Rectum Gl D..

Red blood cells

see Erythrocyten equi Gl

Red iron ore see Hematite

Red wood ant

see Formica rufa – oily extract see Formica rufa ex animale toto Gl

Regio substantiae nigrae bovis Gl

Substantia nigra – small area of cells in the midbrain (mesencephalon) Regio substantiae nigrae Gl D..

Renes bovis Gl

Kidneys Cuprum aceticum comp. Lien comp. Mesenchym/Calcium carbonicum comp. Nux vomica/Nicotiana comp. Organum quadruplex Renes Gl D.. Renes/Argentum nitricum Renes/Borago comp. Renes/Cuprum Renes/Equisetum comp.

Renes bovis, regio pyelorenalis Gl Renal pelvis and renal medulla Renes, regio pyelorenalis Gl D..

Resina laricis

see Terebinthina laricina

Quercus robur/petraea e cortice, Decoctum LA 10%

Reticuloendotheliales System bovis Gl

Quicksilver

Retina et Chorioidea bovis Gl

Oak – bark of young branches and root-collar shoots Aesculus/Prunus comp., Essenz Quercus-Essenz see Mercurius vivus

Quince

see Cydonia oblonga e fructibus ferm 33b

Rami ventrales

see Nervi intercostales bovis Gl

Rectum suis Gl

P Q R

Connective tissue from thymus, lymph nodes, bone marrow, spleen, liver Reticuloendotheliales System Gl D.. Retina and choroid membrane of the eye Arnica/Plumbum comp. A Cerebrum comp. A Cerebrum comp. A cum Auro comp. Galenit/Retina comp. Nervus opticus comp. Augentropfen Retina et Chorioidea Gl D.. Retina comp. Secale/Retina comp.

Rectum

605

Rhamnus frangula e cortice ferm 33e

Alder Buckthorn – bark of the trunk and branches (Rhamnus frangula L.) Akne-Kapseln

Rhus toxicodendron e foliis ferm 33d

see Toxicodendron quercifolium e foliis ferm 33d

Ribwort Plantain

see Plantago lanceolata e foliis ferm 34c see Plantago lanceolata, Folium rec. - aqueous extract with sugar

Ricini oleum

Mercurialis Augentropfen Mundbalsam flüssig Mundbalsam Nervus opticus comp. Augentropfen Rosatum Heilsalbe

Rosae aetheroleum 10%

Essential oil from rose flowers (rose oil), in olive oil Rosa e floribus 10%, Oleum

Rose

see Rosa e floribus W 10%

Rose, essential oil of see Rosae aetheroleum

Fatty oil from seeds of the Castor Bean Plant (Ricinius communis L.) Chelidonium Kapseln Juniperus/Berberis comp., Kapseln

Rose iron

Robinia pseudoacacia e cortice ferm 33e

Rose quartz

see Rosa e floribus ferm cum Ferro

Black Locust (False Acacia) – bark of young branches (Robinia pseudoacacia L.) Robinia comp.

Quartz with a rose-pink colour due to traces of manganese Rosenquarz D..

Rock crystal

Rosmarini aetheroleum (= Oleum Rosmarini)

see Quartz

Rosa e floribus ferm cum Ferro

Red tea rose – flowers (suitable species of the genus Rosa L., particularly dark red hybrid tea roses) – extract prepared in the presence of hematite Akne-Kapseln Chelidonium comp. Augentropfen Roseneisen Roseneisen/Graphit

Rosa e floribus W 10%

Tea rose – petals (dried) (suitable species of the genus Rosa L., part. Rosa centifolia L., Rosa damascena Mill., Rosa gallica L. and hybrid tea roses) Rosa e floribus 10%, Oleum

Rosae aetheroleum

(= Oleum Rosae) Essential oil from rose flowers (suitable species of the genus Rosa L.) (rose oil) Belladonna e fructibus Augentropfen Belladonna ex herba Augentropfen Cornea Levisticum comp. Augentropfen Echinacea Augentropfen Echinacea Quarz comp. Augentropfen Euphrasia Augentropfen Hornerz Corpus vitreum comp. Augentropfen Iris Lens comp. Augentropfen

606

time (Ruta graveolens L.) Chelidonium comp. Augentropfen

Saccharose

see Saccharum candidum see Saccharum Sacchari

Saccharum candidum

Sucrose (saccharose) – crystallised (rock sugar) Spongia comp., Globuli velati Spongia/Aurum/Pulsatilla comp.

Saccharum Sacchari

Red corundum containing traces of iron and chromium (nat. aluminium oxide) Rubin D..

Rue

see Ruta graveolens ex herba ferm 33c

Ruta graveolens ex herba ferm 33c

Rue – aerial parts at the beginning of flowering

Sambucus nigra e floribus

see Sambucus nigra ex umbella ferm 33c

Elder – inflorescences Sambucus comp.

see Salvia officinalis e foliis ferm 33d see Salvia officinalis e foliis LA 20% see Salviae folium

Sage essential oil

see Salviae aetheroleum

Purple Osier (S. purpurea L., (L.) Arcang.) Salix/Rhus comp. Passiflora Nerventonikum

Ruby

Essential oil from sage leaves and stems (sage oil) Majorana Vaginalgel Rosmarinus/Prunus comp., Gelatum

Sage

Rosmarini aetheroleum 10%

see Rosmarini aetheroleum

Salviae officinalis aetheroleum (= Oleum Salviae)

Sambucus nigra e medulla ferm 35a

Salix alba ssp. vitellina e cortice et foliis ferm 33d

Rosemary essential oil

Sage – leaves (dried) Nervennahrung

Cane sugar (sucrose, saccharose) (Saccharum officinarum L.) Argentum/Rohrzucker Parathyreoidea comp.

Essential oil from rosemary leaves and stems (rosemary oil) (Rosmarinus officinalis L.) Cuprum/Quarz comp., Unguentum Echinacea/Viscum comp., Gelatum Narben Gel Majorana Vaginalgel Primula Muskelnähröl Rosmarinus/Prunus comp., Gelatum Essential oil from rosemary leaves and stems (rosemary oil), in olive oil (Rosmarinus officinalis L.) Rosmarinus, Oleum aethereum 10%

Salviae folium

Golden Willow – bark and leaves (Salix alba L. ssp. vitellina (L.) Arcang.) Passiflora comp. Salix/Rhus comp. Passiflora Nerventonikum

Salix purpurea e cortice et foliis ferm 33d

Salix viminalis e cortice et foliis ferm 33d Osier Willow (Salix viminalis L., (L.) Arcang.) Salix/Rhus comp. Passiflora Nerventonikum

Salvia officinalis e foliis ferm 33d Sage - leaves (Salvia officinalis L.) Archangelica comp. Salvia e foliis D..

Salvia officinalis e foliis LA 20% Sage – leaves Echinacea Mund- und Rachenspray

Elder – pith from the branches (Sambucus nigra L.) Sambucus comp.

Sambucus nigra ex umbella ferm 33c

Sambucus nigra ex umbella W 5% Elder – cymes with flowers (dried) Malvenöl

Sapphire

Blue corundum containing traces of iron and titanium (nat. aluminium oxide) Saphir D..

R S

Sarothamnus ex herba ferm 33c

see Cytisus scoparius ex herba ferm 33c

Scarlet Pimpernel

see Anagallis arvensis e planta tota ferm 33b

Sclera bovis Gl

Sclera – the white of the eye Sclera Gl D..

Scilla e bulbo ferm 33b

see Urginea maritima var. rubra e bulbo ferm 33b

Scolopendrium e foliis ferm 34h

see Phyllitis scolopendrium e foliis ferm 34h

Scorodite

Nat. iron arsenate Borago comp. Cerebellum comp. Parathyreoidea comp. Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati

607

Scurvy Grass

see Cochlearia officinalis ex herba ferm 33b

Sea onion

see Urginea maritima var. rubra e bulbo ferm 33b

Secale cornutum e sklerotio ferm 35b

Silver birch

see Betula e foliis ferm 34e see Betula pendula e cortice sicc., Decoctum see Betula pendula, Folium rec. – aqueous extract with sugar see Betula pendula/pubescens e foliis W 5%

Ergot sclerotium - dried (Claviceps purpurea (Fries) Tulasne) Galenit/Retina comp. Secale cornutum e grano D.. Secale/Argentum Secale/Bleiglanz comp. Secale/Quarz Secale/Retina comp.

Silver chloride, nat.

Selenicereus grandiflorus ex herba ferm 33d

Silybum marianum e fructibus ferm 36

Night-blooming Cereus (Queen of the Night) – young stems and flowers (Selenicereus grandiflorus (L.) Britt. et Rose) Aurum Valeriana Inject Aurum Valeriana Globuli velati Cactus ex herba D.. Cactus comp. II Sarothamnus comp.

Senecio jacobaea ex herba ferm 33d

Common Ragwort (Tansy) – aerial parts of flowering plants (Senecio jacobaea L.) Senecio comp. Senecio comp., Suppositorien

Sepia officinalis e volumine bursae rec. Gl Secretion of the cuttlefish (Sepia officinalis L.) Berberis/Sepia comp. Melissa/Sepia comp. Sepia e secreto Gl D.. Spongia/Aurum/Pulsatilla comp.

Silicea

see Quartz

Silicea colloidalis

Colloidal silicic acid Nasenbalsam Nasenbalsam für Kinder Silicea colloidalis comp., Gelatum Rosatum Heilsalbe

Silver

see Argentum metallicum

608

see Chlorargyrite

Silver fir

see Abies alba e summitatibus ferm 33d

Silver nitrate

see Argentum nitricum

Milk Thistle - fruits (Silybum marianum (L.) Gaertn.) Anagallis comp. Carduus marianus e fructibus D.. Carduus marianus/Oxalis Carduus marianus/Viscum Mali comp. Lycopodium comp. Quercus Hämorrhoidalzäpfchen

Sinus cavernosus-Komplex bovis Gl

Venous sinus in the region of the sphenoid bone with nerves (parts of optic nerve, oculomotor nerve, trochlear nerve, trigeminal nerve, abducens nerve) Sinus cavernosus-Komplex Gl D..

Snake venom see Lachesis

Sodium carbonate monohydrate see Natrium carbonicum

Sodium monohydrogen phosphate see Natrium phosphoricum

Sodium sulfate

see Natrium sulfuricum

Solidago virgaurea ex herba ferm 33c

Goldenrod – aerial parts of flowering plants (Solidago virgaurea L.) Aquilinum comp. Juniperus/Berberis comp., Kapseln Solidago virgaurea ex herba D..

Solidago virgaurea ex herba LA 20% Goldenrod – aerial parts of flowering plants Aesculus/Prunus comp., Essenz

Solomon‘s Seal

see Polygonatum odoratum e radice ferm 33d

Solum uliginosum – aqueous extract High-moor peat – aqueous extract Solum Inject Solum Inject 10 Solum Globuli velati Solum Badezusatz Solum Öl Solum Salbe

Southernwood

see Artemisia abrotanum ex herba ferm 33c

Spanish Fly

see Cantharis ex animale Gl

Spider

see Aranea ex animale Gl

Spinach

see Spinacia oleracea e radice ferm 34f

Spinacia oleracea e radice ferm 34f

Spinach – underground parts (Spinacia oleracea L.) Nervennahrung Senecio comp. Senecio comp., Suppositorien

Spiraea ulmaria ex herba ferm 34c

Meadowsweet – aerial parts of flowering plants (Filipendula ulmaria L.) Betula/Mandragora comp.

Spongia tosta

Bryonia/Stannum Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Disci comp. cum Nicotiana Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci comp. cum Stanno Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Viscum comp. cum Stanno Disci/Viscum comp, cum Stanno, Unguentum Equisetum/Stannum Gnaphalium comp. Hepar/Stannum I Hepar/Stannum II Hypophysis/Stannum Lens Viscum comp. Inject Lens Viscum comp. Globuli velati Lens Viscum comp. Augentropfen Magnesium sulfuricum/Ovaria comp. Periodontium/Stannum comp. Rosmarinus/Prunus comp., Gelatum Senecio comp. Senecio comp., Suppositorien Symphytum comp. Tendo/Allium cepa comp. Urtica comp. Viscum/Bryonia comp.

Stibium metallicum

Antimony Aurum/Stibium/Hyoscyamus Cichorium/Pancreas comp. Disci comp. cum Stibio Mercurialis comp., Suppositorien Salix/Rhus comp. Strophanthus comp. Tormentilla comp. Veratrum comp.

Toasted marine sponge (Euspongia officinalis L.) Spongia tosta D.. Spongia comp., Globuli velati Spongia/Aurum/Pulsatilla comp.

Stinging Nettle

Spruce

Stomachus

see Picea abies, Summitates rec. aqueous extract with sugar

Stannum metallicum

Metallic tin Articulatio talocruralis comp.

see Urtica dioica e planta tota ferm 33c see Urtica dioica ex herba W 5% siehe Urticae dioicae herba see Ventriculus suis Gl

Strawberry, Wild

see Fragaria vesca, Fructus rec. - aqueous extract with sugar see Fragariae vescae folium

609

S

Strophanthus

see Strophanthus kombe e semine ferm 35b

Strophanthus kombe e semine ferm 35b Strophanthus – seeds (dried) (Strophanthus kombe Oliv.) Aurum/Strophanthus Aurum Valeriana Inject Aurum Valeriana Globuli velati Strophanthus kombe e semine D.. Strophanthus comp. Strophanthus/Nicotiana comp.

Strychnos ignatii e semine ferm 35b Ignatius bean – seeds (dried) (Strychnos ignatii Bergius) Aurum/Apis regina comp. Ignatia e semine D.. Ignatia comp.

Strychnos nux-vomica e semine ferm 35b Nux vomica – seeds (dried) (Strychnos nux vomica L.) Gentiana Magen Inject Gentiana Magen Globuli velati Nux vomica e semine D.. Nux vomica/Nicotiana comp. Robinia comp. Salix/Rhus comp.

St. John‘s Wort

see Hypericum perforatum ex herba ferm 33c see Hypericum perforatum, Herba rec. – oily extract

Substantia nigra

see Regio substantiae nigrae bovis Gl

Sucrose

see Saccharum candidum see Saccharum Sacchari

Sulfur

Sulphur Avena comp. Betula/Arnica comp. Ferrum/Sulfur comp. Sulfur D.. Valeriana comp.

Sulphur

see Sulfur

610

Sundew

see Drosera e planta tota ferm 33c

Sweet Flag

see Acori calami rhizoma – aqueous extract see Acori calami rhizoma – aqueous extract with sugar see Acorus calamus e rhizoma ferm 33d

Sweet Marjoram

see Origanum majorana ex herba ferm 33c see Origanum majorana ex herba W 5%

Sympathicus bovis Gl

(Truncus sympathicus) Main trunk of the sympathetic nervous system Sympathicus Gl D..

Symphytum officinale e radice ferm 34c Comfrey – underground parts before sprouting (Symphytum officinale L.) Arnika Salbe (arnica ointment) Articulatio talocruralis comp. Symphytum e radice D.. Symphytum comp. Tendo/Allium cepa comp.

Symphytum officinale ex herba LA 20% Comfrey – aerial parts at flowering time Brandessenz Wund- und Brandgel

Tabacum

see Nicotiana tabacum e foliis ferm 33b

Tansy

see Senecio jacobaea ex herba ferm 33d

Taraxacum officinale e planta tota ferm 34c Dandelion – flowering plant (Taraxacum officinale Wiggers) Agropyron Inject Agropyron Globuli velati Anagallis comp. Aquilinum comp. Gentiana Magen Inject Gentiana Magen Globuli velati Taraxacum e planta tota D..

Taraxacum officinale e radice autumnale ferm 34c

Testes bovis Gl

Taraxacum officinale e radice vernale ferm 34c

Tetrachlorogold(III) acid

Dandelion – underground parts (autumn form) Taraxacum e radice (autumnale) D..

Dandelion – underground parts (spring form) Taraxacum e radice (vernale) D..

Tartarus stibiatus

Potassium antimonyl tartrate Pulmo/Tartarus stibiatus I Pulmo/Tartarus stibiatus II Pulmo/Vivianit comp.

Tendo bovis Gl

Tendon Articulatio talocruralis comp. Tendo Gl D.. Tendo/Allium cepa comp.

Terebinthinae aetheroleum rectificatum Purified essential oil from the turpentine of pine species Juniperus/Berberis comp., Kapseln Oleum camphoratum comp.

Terebinthina laricina

(= Resina laricis) Larch resin (Larix decidua Mill.) Berberis/Apis comp. Chelidonium comp. Augentropfen Echinacea/Viscum comp., Gelatum Galenit/Retina comp. Juniperus/Berberis comp., Kapseln Plantago Bronchialbalsam Resina laricis-Bademilch Retina comp. Sambucus comp. Terebinthina laricina D..

Terra medicinalis

Testicles Testes Gl D.. Testes comp. Testes/Argentum

see Aurum chloratum

Textus connectivus bovis Gl Connective tissue Renes/Borago Bindegewebe GI D4

Thalamus bovis Gl

Thalamus Arnica/Plumbum comp. A Cerebrum comp. A Cerebrum comp. A cum Auro comp. Thalamus Gl D..

Thrombocyten equi Gl Thrombocytes (platelets) Thrombocyten Gl D..

Thrombocytes

see Thrombozyten equi Gl

Thuja occidentalis e summitatibus ferm 33e

Arborvitae – shoot tips of one-year branches with leaves (Thuja occidentalis L.) Argentum nitricum comp. Majorana Vaginalgel Narben Gel Thuja e summitatibus D..

Thuja occidentalis e summitatibus LA 20% Arborvitae – shoot tips of one-year branches with leaves Brandessenz Wund- und Brandgel Thuja-Essenz

Medicinal clay Akne-Gesichtsmaske Akne-Kapseln

Thyme oil, essential

Testa ovorum

Thymi aetheroleum (= Oleum Thymi)

Calcium carbonate from eggshell Spongia comp., Globuli velati Spongia/Aurum/Pulsatilla comp.

see Thymi aetheroleum

Essential oil of thyme (thyme oil) (Thymus vulgaris L.) Majorana Vaginalgel Plantago Bronchialbalsam

611

S T

Thymi aetheroleum 5%

Trachea bovis Gl

Tuba uterina bovis Gl

Thymus Glandula bovis Gl

Trigonum vesicae et Musculus sphincter bovis Gl

Tulip

Essential oil of thyme, in olive oil Thymus, Oleum aethereum 5% see Glandula thymi bovis Gl

Windpipe Trachea Gl D..

Tiger Lily

Bladder sphincter with mucous membrane Trigonum vesicae et Musculus sphincter Gl D..

Tilia platyphyllos/cordata e floribus W 5%

Triticum aestivum e fructibus germinatum ferm 33d

see Lilium lancifolium ex herba ferm 33c

Summer and winter lime - inflorescences (Tilia platyphyllos Scop. u. Tilia cordata Mill.) Malvenöl

Tin

see Stannum metallicum

Tobacco

see Nicotiana tabacum e foliis ferm 33b

Tonsilla pharyngea bovis Gl Pharyngeal tonsils Tonsilla pharyngea Gl D..

Tonsillae palatinae bovis Gl

Palatine tonsils Echinacea Mund- und Rachenspray Tonsillae palatinae Gl D..

Topaz

Silica gemstone of various colours containing traces of chromium, iron or vanadium Topas D..

Wheat – fruits (germinated) Triticum comp. I

Triticum repens

see Agropyron repens e radice ferm 33c

Tropaeolum majus ex herba ferm 33b

Fallopian tube Parametrium/Echinacea comp. Tuba uterina Gl D.. see Tulipa silvestris e planta tota ferm 33a

Tulipa silvestris e planta tota ferm 33a Tulip – flowering plant (Tulipa silvestris L.) Tulipa e planta tota D..

Tunica conjunctiva

see Conjunctiva bovis Gl

Tunica mucosa (Endometrium) see Endometrium bovis Gl

Urginea maritima var. rubra e bulbo ferm 33b Sea onion – bulb scales (Urginea maritima L.) Primula/Convallaria comp. Scilla e bulbo D.. Scilla comp.

Urticae dioicae herba

Stinging nettle – aerial parts shortly before flowering (dried) (Urtica dioica L.) Nervennahrung

Tunica mucosa nasi bovis Gl Nasal mucosa Bronchi Plantago Inject Bronchi Plantago Globuli velati Tunica mucosa nasi Gl D..

Stinging nettle – whole flowering plant Akne-Kapseln Berberis e fructibus comp. Ferrum silicicum comp. Urtica dioica e planta tota D..

Truncus cerebri bovis Gl

Tunica mucosa recti suis Gl

Urtica dioica ex herba W 5%

Nasturtium – aerial parts at flowering time Akne-Gesichtsdampfbad Akne-Gesichtsmaske Akne-Wasser Apis regina comp. Hirnstamm GI D.. Triticum comp. I

Truncus coeliacus bovis Gl

Lining of the rectum Tunica mucosa recti Gl D..

Tunica mucosa sinus frontalis

see Membrana sinus frontalis bovis Gl

Tormentilla e radice ferm 34d

Truncus pulmonalis bovis

Tunica mucosa sinuum paranasalium

Toxicodendron quercifolium e foliis ferm 33d

Truncus sympathicus bovis

Tunica mucosa ventriculi suis Gl

612

Urethra, male, anterior portion Urethra masculina Gl D..

Tropaeolum majus ex herba LA 20%

Mucous membrane from the entire small intestine Tunica mucosa intestini tenuis Gl D..

Tunica mucosa sinus maxillaris

Poison sumach - leaves (Toxicodendron quercifolium (Michx.) Greene) Aconitum comp. Disci/Rhus toxicodendron comp. Rhus toxicodendron comp. Rhus toxicodendron e foliis D.. Rhus toxicodendron Salbe Salix/Rhus comp.

Urethra masculina anterior bovis Gl

Tunica mucosa intestini tenuis suis Gl

Tormentil

see Potentilla tormentilla e radice ferm 34d

Female urethra Urethra feminina Gl D..

Nasturtium – aerial parts of flowering plants (Tropaeolum majus L.) Akne-Kapseln

Coeliac trunk – arterial trunk arising from the abdominal aorta Truncus coeliacus Gl D..

see Potentilla tormentilla e radice ferm 34d

Urethra feminina bovis Gl

see Arteria pulmonalis bovis Gl see Sympathicus bovis Gl

Truncus sympathicus, Pars pelvina

see Membrana sinus maxillaris bovis Gl see Membrana sinuum paranasalium bovis Gl

Lining of the stomach Tunica mucosa ventriculi Gl D..

Sympathetic trunk of the autonomic nervous system, pelvic portion see Plexus pelvinus bovis Gl

Turpentine oil, essential oil of

Tuba auditiva bovis Gl

Ureter Ureter Gl D..

Eustachian tube Tuba auditiva Gl D..

see Terebinthinae aetheroleum rectificatum

Ureter bovis Gl

Urtica dioica e planta tota ferm 33c

Stinging nettle – aerial parts shortly before flowering (dried) (Urtica urens L.) Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Rheuma-Badeöl Urtica dioica ex herba W 5%, Oleum

T U

Urtica urens ex herba ferm 33c

Dwarf nettle – aerial parts at flowering time Berberis/Prostata comp. Berberis/Sepia comp. Berberis/Urtica urens Berberis/Uterus comp. Rosmarinus/Prunus comp., Gelatum Urtica comp. Urtica urens ex herba D..

Urtica urens ex herba LA 20%

Dwarf nettle – aerial parts at flowering time Brandessenz Wund- und Brandgel

613

Uterus bovis Gl

Uterus (womb) Berberis/Uterus comp. Bryophyllum comp. Uterus Gl D.. see also Cervix uteri bovis Gl see also Endometrium bovis Gl see also Parametrium bovis Gl

Vagina bovis Gl Vagina Vagina Gl D..

Vaginae synoviales tendinum bovis Gl (= Vaginae synoviales tendinum digitorum) Tendon sheaths of the fingers and toes Tendo/Allium cepa comp. Vaginae synoviales tendinum Gl D..

Valerian

see Valeriana officinalis e radice ferm 33c see Valeriana officinalis, Radix rec. – aqueous extract with sugar

Valvula pulmonalis

see Valva trunci pulmonalis bovis Gl

Valvula tricuspidalis bovis Gl

(= Valva atrioventricularis dextra) Valve between the right atrium and ventricle of the heart Valvula tricuspidalis Gl D..

Vena cava bovis Gl Vena cava Vena cava Gl D..

Valvula aortae bovis Gl (= Valva aortae) aortic valve Valvula aortae Gl D..

Valvula mitralis bovis Gl

(= Valvula bicuspidalis, Valva atrioventricularis sinistra) valve between the left atrium and ventricle of the heart Valvula mitralis Gl D..

614

Vertebra lumbalis bovis Gl

Vena ophthalmica

Vesica fellea bovis Gl

see Arteria et Vena ophthalmica bovis Gl

Vena portae bovis Gl Portal vein Vena portae Gl D..

Venom of the pit viper (Bushmaster)

Valve of the pulmonary trunk Valva trunci pulmonalis Gl D..

Coccygeal (tailbone) vertebra Vertebra coccygea Gl D..

Femoral vein (thigh vein) Vena femoralis Gl D..

Valeriana officinalis e radice ferm 33c

Valva trunci pulmonalis bovis Gl

Vertebra coccygea bovis Gl

Vena femoralis bovis Gl

Vena saphena magna bovis Gl

Valerian – underground parts (Valeriana officinalis L.) Aurum Valeriana Inject Aurum Valeriana Globuli velati Avena comp. Passiflora Zäpfchen Passiflora Kinderzäpfchen Valeriana comp. Valeriana e radice D..

Cervical vertebra Vertebra cervicalis Gl D.. see also Articulationes intervertebrales cervicales Gl see also Disci intervertebrales cervicales Gl

Lumbar vertebra Vertebra lumbalis Gl D.. see also Articulationes intervertebrales lumbales bovis Gl see also Disci intervertebrales lumbales bovis Gl

Valeriana officinalis, Radix rec. aqueous extract with sugar Valerian – underground parts Passiflora Nerventonikum

Vertebra cervicalis bovis Gl

Great saphenous vein (vein running up the medial side of the leg) Vena saphena magna Gl D.. see Lachesis

Ventriculus quartus

see Medulla oblongata bovis Gl

Ventriculus suis Gl

(= Ventriculus [Gaster]) Stomach Ventriculus Gl D.. see also Cardia suis Gl see also Pylorus suis Gl see also Tunica mucosa ventriculi suis GI

Veratrum album e radice ferm 33c White hellebore – underground parts (Veratrum album L.) Renes/Equisetum comp. Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati Veratrum e radice D.. Veratrum comp.

Viscum album (abietis) e planta tota K Mistletoe from fir trees – fruiting plant with haustorium (dried) Iscucin Abietis Stärke..

Viscum album (crataegi) e planta tota K Mistletoe from hawthorn – fruiting plant with haustorium (dried) Iscucin Crataegi Stärke..

Viscum album (mali) e planta tota ferm 34i

Hornet – whole animal (Vespa crabro L.) Magnesium sulfuricum/Ovaria comp. Narben Gel Thyreoidea/Thymus comp. Vespa Crabro ex animale Gl D..

Mistletoe from apple trees – fruiting plant with haustorium Berberis/Uterus comp. Carduus marianus/Viscum Mali comp. Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Viscum comp. cum Argento, Suppositorien Disci/Viscum comp. cum Stanno Disci/Viscum comp, cum Stanno, Unguentum Echinacea/Viscum comp., Gelatum Equisetum/Viscum Hornerz/Cartilago comp. Hornerz/Corpus vitreum comp. Hornerz Corpus vitreum Augentropfen Lens Viscum comp. Inject Lens Viscum comp. Globuli velati Lens Viscum comp. Augentropfen Magnesit/Mamma comp. Magnesium sulfuricum/Ovaria comp. Renes/Equisetum comp. Viscum/Bryonia comp. Viscum/Echinacea Viscum Mali e planta tota D.. Viscum Mali e planta tota 3%, Unguentum

Viola tricolor ex herba ferm 33e

Viscum album (mali) e planta tota K

Virola sebifera

Viscum album (mali) ex herba W 5%

Gallbladder Vesica fellea Gl D.. Vesica fellea/Ferrum I Vesica fellea/Ferrum II

Vesica urinaria bovis Gl

Urinary bladder Cantharis Blasen Inject Cantharis Blasen Globuli velati Vesica urinaria Gl D.. see also Trigonum vesicae et Musculus sphincter bovis Gl

Vespa crabro ex animale Gl

Pansy – aerial parts of flowering plants (Viola tricolor L.) Akne-Kapseln

see Myristica sebifera, succus e cortice

Viscum album (abietis) e planta tota ferm 34g Mistletoe from fir trees – fruiting plant with haustorium (Viscum album L.) Berberis/Prostata comp. Viscum Abietis e planta tota D..

U V

Mistletoe from apple trees – fruiting plant with haustorium (dried) Iscucin Mali Stärke.. Mistletoe from apple trees – branches with leaves, flowers and fruits (dried) Viscum Mali ex herba W 5%, Oleum

Viscum album (Mali), Senker ferm 33e Mistletoe from apple trees – haustorium Viscum Mali, Senker D..

615

Viscum album (Pini) e planta tota ferm 34g

Mistletoe from pine trees – fruiting plant with haustorium Viscum Pini e planta tota D..

Viscum album (Pini) e planta tota K

Mistletoe from pine trees – fruiting plant with haustorium (dried) Iscucin Pini Stärke..

Viscum album (Populi) e planta tota ferm 33f

Mistletoe from poplar trees – fruiting plant with haustorium Viscum comp.

Viscum album (Populi) e planta tota K

Mistletoe from poplar trees – fruiting plant with haustorium (dried) Iscucin Populi Stärke..

Viscum album (Quercus) ex herba K

Mistletoe from oak trees – fruiting plant without haustorium (dried) Iscucin Quercus Stärke..

Viscum album (Salicis) e planta tota K

Mistletoe from willow trees – fruiting plant with haustorium (dried) Iscucin Salicis Stärke..

Viscum album (Tiliae) e planta tota ferm 33f

Mistletoe from lime trees – fruiting plant with haustorium Viscum/Crataegus

Viscum album (Tiliae) e planta tota K Mistletoe from lime trees – fruiting plant with haustorium (dried) Iscucin Tiliae e planta tota Stärke..

Visnaga

see Ammi visnaga e fructibus ferm 35b

Vivianite

Nat. iron (II) phosphate Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Gelsemium comp. Nervennahrung Pulmo/Vivianit comp.

616

Walnut

see Juglans regia e foliis et fructibus ferm 33c

Wheat

see Triticum aestivum e fructibus germinatum ferm 33d

Wheat germ oil

Fatty oil from wheat germ (Triticum L.) Chelidonium Kapseln Juniperus/Berberis comp., Kapseln

White bryony

see Bryonia e radice ferm 33b

White clay

see Kaolinum ponderosum

White hellebore

see Veratrum album e radice ferm 33c

Wild strawberry

see Fragaria vesca, Fructus rec. - aqueous extract with sugar see Fragariae vescae folium

Willow, Basket

see Salix purpurea e cortice et foliis ferm 33d

Willow mistletoe

see Viscum album (Salicis) e planta tota K

Winter lime

see Tilia platyphyllos/cordata e floribus W 5%

Witch hazel

see Artemisiae absinthii herba – aqueous extract with sugar

Yarrow

see Achillea ex herba ferm 33d

Yellow beeswax see Cera flava

Yellow Gentian

see Gentiana lutea e radice ferm 33c see Gentiana lutea e radice, Decoctum see Gentianae luteae radix – aqueous extract see Gentianae luteae radix – aqueous extract with sugar

Yellow jasmine

see Gelsemium sempervirens e rhizoma ferm 35b

Yellow Pheasant‘s Eye

see Adonis ex herba ferm 33d

Yellow phosphorus see Phosphorus

Zingiberis rhizoma

aqueous extract Ginger – rootstock (dried) (Zingiber officinale Rosc.) Enzian Magentonikum

Zingiberis rhizoma

aqueous extract with sugar Ginger – rootstock (dried) Bitter Elixier

V W Y Z

see Hamamelis virginiana e cortice et foliis LA 20% see Hamamelis virginiana e cortice ferm 33e see Hamamelis virginiana e foliis ferm 33d

Wood ant, red

see Formica rufa – oily extract see Formica rufa ex animale toto Gl

Wood Sorrel

see Oxalidis acetosellae herba see Oxalis acetosella e planta tota ferm 34b see Oxalis acetosella e planta tota LA 20% see Oxalis acetosella e planta tota W 10%

Wormwood

see Artemisia absinthium ex herba, Infusum see Artemisiae absinthii herba – aqueous extract

617

Index of Indications General Remarks Alphabetical Index of Indications

618

621 622

619

General Remarks The index of indications has been used successfully by doctors in their practical work for decades. It has now been revised on the basis of the monographs of Commission C of the Federal Institute of Drugs and Medical Devices and the reported experience evaluated in these monographs. The listed indications are seen as suggestions intended to help the practitioner select a suitable medicinal product. They lay no claim to completeness and are not a substitute for any conventional medical treatments necessary. The index terms include clinical indications but also general states, such as "weakness of the immune system" or "states of exhaustion", which require diagnostic investigation. It is the task of the treating practitioner to select from amongst the medicinal products listed the ones which are most suitable for the individual case in question. Other medicines not listed here might be necessary. The basis for the choice of medicinal product is the study of the interrelationship between the human being and nature. Increasing immersion in the anthroposophical view of the world and the human being and increasing experience in the treatment of patients will make the practitioner more and more independent of a list and will become therapeutic intuition.

620

For easier orientation when selecting a medicinal product the following classification, based on the therapeutic experience of the WALA Physicians Group, has been used: Medicinal products which have proved particularly reliable for treatment of the indication named are printed in RED. Medicinal products which have proved therapeutically effective for the indication named are printed in BOLD black type. Medicinal products which have often proved useful as adjunctive treatment – also in addition to conventional medical treatment – are printed in BLACK. However, in individual cases these medicines may in fact be the treatment of choice.

(Organ preparation) This indicates the possibility of supplementary treatment with homologous potentised organ preparations.

621

Abdominal colics

see Colicky pain in the region of the abdomen

Abscesses

Apis/Belladonna cum Mercurio Calendula-Essenz Echinacea/Mercurius comp., Suppositorien Echinacea/Mercurius comp., Suppositorien für Kinder Lachesis comp. Mercurialis Salbe

Absorption disorders of the bowel Glandula suprarenalis sinistra/Mercurius

Accommodation disorders

Belladonna e fructibus Augentropfen

Acne

Akne-Gesichtsdampfbad Akne-Gesichtsmaske Akne-Kapseln Akne-Wasser Quarz D..

Acrodermatitis atrophicans Echinacea/Viscum comp., Gelatum (Organ preparation)

Adenoids

Berberis e fructibus comp. Berberis/Quarz

Adnexitis

Apis ex animale Gl D.. Bryonia comp. Echinacea e planta tota D.. Echinacea-Essenz Lachesis comp. Parametrium/Echinacea comp. (Organ preparation)

Allergic diathesis

Apis ex animale Gl D.. Calcium Quercus Inject Calcium Quercus Inject 10 Calcium Quercus Globuli velati Glandulae suprarenales comp. Mesenchym/Calcium carbonicum comp. Quercus-Essenz (Organ preparation)

622

Allergic disorders of the airways Apis ex animale Gl D.. Citrus e fructibus/Cydonia e fructibus Sambucus comp.

Allergic skin disorders

see Dermatitis see Pruritus Apis ex animale Gl D.. Brandessenz Wund- und Brandgel

Amenorrhoea

see Hypogonadism Ovaria/Argentum

Anaemia

Ferrum silicicum comp. (adjunctive treatment) Levico comp. Medulla ossium Gl D.. Prunuseisen

Anal fissures

Echinacea/Viscum comp., Gelatum Hamamelis-Essenz Mercurialis comp., Suppositorien Quarz D.. Quercus-Essenz Quercus Hämorrhoidalzäpfchen Quercus Salbe

Angina pectoris

see Coronary sclerosis see Chest pain, anginal Crataegus/Cor comp. Magnesium phosphoricum comp. Strophanthus kombe e semine D.. Strophanthus/Nicotiana comp. (Organ preparation)

Ankylosing spondylitis

Bambusa e nodo D.. Disci comp. cum Stibio Disci/Viscum comp. cum Argento, Suppositorien (Organ preparation)

Anuria

see Renal failure, acute

Anxiety states

see Nervous tension see Neurovegetative dysregulation Strophanthus kombe e semine D..

Appetite, lack of

Bitter Elixier Enzian Magentonikum

Arterial occlusive disease Arnica/Plumbum comp. A Arnica/Plumbum comp. B Arnica/Plumbum mellitum Aurum/Belladonna comp. Secale/Bleiglanz comp. Secale/Quarz (Organ preparation)

Arthritis

see Hip disorders see Knee disorders Apis ex animale Gl D.. Betula/Arnica comp. Bryonia/Stannum Cartilago/Echinacea comp. Mandragora officinarum e radice D.. Rhus toxicodendron Salbe (Organ preparation)

Arthritis, chronic

Ataxia

see Movement disorders, ataxic and hyperkinetic

Atopic dermatitis see Eczema

Backbone disorders

see Spinal cord disorders, degenerative see Spinal disorders

Back pain

see Intervertebral disc disorders, degenerative see Intervertebral disc disorders, inflammatory see Lumbago see Myalgia, myogelosis see Spinal complaints

Bedwetting

Berberis/Hypericum comp.

Biliary colic

Chelidonium Kapseln Chelidonium/Colocynthis

Bladder, inflammation of

see Hip disorders see Knee disorders Apis ex animale Gl D.. Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Equisetum/Formica Mandragora officinarum e radice D.. Oleum Petrae comp. (Organ preparation)

see Urinary tract infections Berberis/Apis comp. Cantharis Blasen Inject Cantharis Blasen Globuli velati

Asthenia

see Menorrhagia Tormentilla comp.

see Neurasthenia see Neurovegetative dysregulation Prunus spinosa e floribus W 5%, Oleum

Asthma, bronchial

Citrus, Oleum aethereum 10% Cuprum aceticum comp. Nicotiana comp. Plantago Hustensaft Renes/Cuprum

Asthma, cardiac see Heart failure

Bladder weakness

see Irritable bladder see Prolapse complaints Berberis/Hypericum comp.

Bleeding in the gastrointestinal tract

Blepharitis

Echinacea Augentropfen

Bloated feeling

see Wind Bitter Elixier Enzian Magentonikum Gentiana Magen Inject Gentiana Magen Globuli velati

Blood pressure regulation, disturbances of see Hypertension see Hypotension

623

A B

Bradycardia

see Cardiac rhythm disorders Aurum/Strophanthus Crataegus/Cor comp. Strophanthus/Nicotiana comp. (Organ preparation)

Bronchial asthma

see Asthma, bronchial

Bronchitis

see Cough, dry Archangelica comp. Bronchi Plantago Inject Bronchi Plantago Globuli velati Bryonia/Aconitum Camphora 5%, Oleum Eucalyptus, Oleum aethereum 10% Petasites comp. Plantago Bronchialbalsam Plantago Hustensaft Pulmo/Tartarus stibiatus II Roseneisen/Graphit Thymus, Oleum aethereum 5% (Organ preparation)

Bronchitis, chronic

Bronchi Plantago Inject Bronchi Plantago Globuli velati Petasites comp. Plantago Hustensaft Pulmo/Tartarus stibiatus I Roseneisen/Graphit (Organ preparation)

Bronchitis, spastic

see Asthma, bronchial Cuprum aceticum comp.

Bruise

see Haematoma

Burns, scalds

Brandessenz Wund- und Brandgel

Bursitis

Bryonia/Stannum (Organ preparation)

Cachexia

see Weight loss see Convalescence

624

Cancer

Cerebrovascular accident

Cardiac neurosis

Chest pain, anginal

see p. 304 ff (Iscucins)

see Heart symptoms, functional Cor GI D.. Primula comp. Strophanthus kombe e semine D..

Cardiac rhythm disorders

see Bradycardia see Tachycardia Aurum/Stibium/Hyoscyamus Cactus comp. II Primula/Convallaria comp. Sarothamnus comp. (Organ preparation)

Cardiovascular weaknesss

see Stimulation of breathing and circulation Primula comp. Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati Strophanthus comp.

Cataract

Belladonna ex herba Augentropfen Hornerz/Corpus vitreum comp. Hornerz Corpus vitreum comp. Augentropfen Lens Viscum comp. Augentropfen Lens Viscum comp. Inject Lens Viscum comp. Globuli velati

Catarrhal disorders of the upper airways

see Stroke

Cold, general feeling of

Chest tightness, nervous

Colicky pain in the region of the abdomen

see Angina pectoris see Cardiac neurosis Camphora/Hypericum, Unguentum Kampfer Johanniskrautöl Strophanthus kombe e semine D..

Cholecystitis

Vesica fellea/Ferrum II

Cholecystopathy

Anagallis comp. Carduus marianus/Oxalis Chamomilla e radice D.. Chelidonium Kapseln Chelidonium/Colocynthis Lycopodium comp. Vesica fellea/Ferrum I

Cholelithiasis

see Cholecystopathy see Stones Carduus marianus/Oxalis

Circulatory disorders, arterial see Arterial occlusive disease

Circulatory disorders, cerebral

Cellulitis

see Varicose symptom complex Kupfer Salbe rot

Cerebral sclerosis

see Arterial occlusive disease

B C

see Degenerative changes in the CNS see Inflammation sequelae in the CNS

see Angina pectoris Cactus comp. II

Agropyron Inject Agropyron Globuli velati Archangelica comp. Berberis/Pyrit comp. Berberis/Quarz Nasenbalsam Nasenbalsam für Kinder Sambucus comp. (Organ preparation)

see Abscesses Argentum/Quarz Echinacea e planta tota D..

CNS

see Dizziness see Arterial occlusive disease

Circulatory disorders, peripheral

Rosmarinus, Oleum aethereum 10% see Dysmenorrhoea see Biliary colic see Wind Ammi visnaga comp., Suppositorien Ammi visnaga comp., Suppositorien für Kinder Belladonna comp., Suppositorien Belladonna comp., Suppositorien für Kinder Belladonna/Chamomilla Chamomilla e radice D.. Chamomilla/Nicotiana Cuprum aceticum comp. Cuprum/Nicotiana, Unguentum Kupfer Salbe rot Mandragora officinarum e radice D.. Melissenöl Nicotiana comp. Nux vomica/Nicotiana comp. Oxalis e planta tota W 10%, Oleum Oxalis-Essenz

Colitis (mucosa, ulcerosa)

see Absorption disorders of the bowel Colon Gl D.. Quarz D.. Tormentilla comp. (Organ preparation)

Colon spasticum, irritable bowel Colon Gl D.. Nicotiana comp.

Camphora 5%, Oleum Cuprum/Nicotiana, Unguentum Kupfer Salbe rot

Commotio cerebri

Circulatory disorders, venous

Aurum/Apis regina comp.

Cirrhosis of the liver

see Liver disorders Carduus marianus/Viscum Mali comp. Hepar GI D.. Hepar/Stannum I

see Concussion

Concentration, lack of Concussion

see Shock, sequelae of Arnica e floribus W 5%, Oleum Arnica e planta tota D.. Arnika Essenz F Cerebellum comp.1

625

Congestive heart failure see Heart failure

Conjunctivitis

Conjunctiva comp. Echinacea Augentropfen Echinacea Quarz comp. Augentropfen Euphrasia Augentropfen Silicea comp., Suppositorien Silicea comp., Suppositorien für Kinder

Connective tissue disorders, degenerative see Rheumatic disorders

Connective tissue weakness Senecio comp. Mesenchym GI D..

Connective tissue weakness in the pelvic region see Prolapse complaints

Constipation

see Colicky pain in the region of the abdomen Aquilinum comp. Carduus marianus/Oxalis Chelidonium Kapseln Lycopodium comp. Oxalis e planta tota W 10%, Oleum Oxalis-Essenz

Contusions

see Haematoma see Wounds Arnica e floribus W 5%, Oleum Arnica e planta tota D.. Arnika-Essenz Arnika Salbe Arnika Wundtuch

Convalescence

see Exhaustion, states of Ferrum silicicum comp. Malvenöl Meteoreisen Inject Meteoreisen Globuli velati Nervennahrung Prunus-Essenz Prunuseisen Rosa e floribus 10%, Oleum Roseneisen/Graphit Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati

626

Corneal disorders

see Eye disorders, degenerative Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen

Aurum comp., Unguentum Epiphysis Gl D.. Hypophysis GI D.. Hypophysis/Stannum

Coronary heart disease

Diabetes mellitus, adjunctive treatment

Coronary sclerosis

Diarrhoea

see Angina pectoris

see Angina pectoris see Arterial occlusive disease Viscum/Crataegus

Cystitis

see Bladder, inflammation of

Cystopyelonephritis

see Urinary tract infections

Degenerative changes in the CNS Apis regina comp. Aurum comp. Aurum comp., Unguentum Cerebrum comp. A cum Auro comp. Cerebrum comp. B cum Auro comp. (Organ preparation)

Depressive mood

Aurum/Apis regina comp. Hepar GI D.. Melissa/Sepia comp.

Dermatitis

Calcea Wund- und Heilcreme Calcium Quercus Inject Calcium Quercus Inject 10 Calcium Quercus Globuli velati Equisetum ex herba W 5%, Oleum Equisetum-Essenz Rosatum Heilsalbe Silicea colloidalis comp., Gelatum Urtica comp.

Dermatitis, purulent

see Cellulitis Calendula e floribus W 10%, Oleum Calendula-Essenz

Descensus uteri

see Prolapse complaints

Developmental disorders, somatic Aurum comp.

see Pancreas disorders

see Enteritis Aquilinum comp. Bolus alba comp. Pulver Quarz D.. Salix/Rhus comp. Veratrum e radice D..

Digestive disorders

see Appetite, lack of see Dyspepsia see Constipation see Pancreas disorders Gentiana Magen Inject Gentiana Magen Globuli velati Glandula suprarenalis dextra cum Cupro Glandula suprarenalis sinistra cum Cupro Glandula suprarenalis sinistra/Mercurius Levisticum e radice D.. Pancreas GI D.. Quarz D..

Disc disorders

see Intervertebral disc disorders, degenerative see Intervertebral disc disorders, inflammatory

Diverticulosis Colon Gl D.. Senecio comp.

Dizziness

see Arterial occlusive disease Arnica/Plumbum comp. B Aurum Valeriana Inject Aurum Valeriana Globuli velati Cerebellum comp. Melissa/Sepia comp.

Dry cough

see Bronchitis Archangelica comp.

Dry eye

see Keratoconjunctivitis sicca (Organ preparation)

Dysmenorrhoea

see Menstrual disorders see Spasms of the organs in the small pelvis Belladonna/Chamomilla Chamomilla e radice D.. Chamomilla/Nicotiana Ovaria comp. Secale/Argentum

C D E

Dyspepsia

Belladonna/Chamomilla Cichorium/Pancreas comp. Glandulae suprarenales comp. Levisticum e radice D.. Pancreas GI D.. Pancreas/Meteoreisen Salix/Rhus comp. (Organ preparation)

Ectopic beats

see Cardiac rhythm disorders Aurum/Stibium/Hyoscyamus (Organ preparation)

Eczema

Anagallis comp. Aquilinum comp. Betula e foliis W 5%, Oleum Calcium Quercus Inject Calcium Quercus Inject 10 Calcium Quercus Globuli velati Formica ex animale Gl D.. Mercurialis Salbe Organum quadruplex Pancreas/Equisetum Quarz D.. Quercus-Essenz Quercus Salbe Rosatum Heilsalbe Silicea colloidalis comp., Gelatum Thuja e summitatibus D.. Urtica comp. (Organ preparation)

Emphysema

Pulmo/Mercurius Pulmo/Tartarus stibiatus I (Organ preparation)

Endometritis

Echinacea e planta tota D.. Echinacea-Essenz

627

Endometrium comp. (Organ preparation)

Enteritis

Bolus alba comp. Pulver Eucalyptus comp. Quarz D.. Veratrum e radice D..

Enuresis nocturna see Bedwetting

Epicondylitis

Symphytum comp. Tendo/Allium cepa comp. (Organ preparation)

Erysipelas

see Abscesses Apis Belladonna Inject Apis Belladonna Globuli velati

Exhaustion, states of

Argentum/Rohrzucker Aurum/Apis regina comp. Aurum/Prunus Glandulae suprarenales Gl D.. Glandulae suprarenales comp. Hypophysis GI D.. Levico comp. Melissa/Sepia comp. Meteoreisen Inject Meteoreisen Globuli velati Nervennahrung Organum quadruplex Prunus-Essenz Prunus spinosa e floribus W 5%, Oleum Rosa e floribus 10%, Oleum Roseneisen/Graphit Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati Strophanthus kombe e semine D..

Eye disorders, degenerative

see Vitreous clouding see Corneal disorders see Cataracts see Retinal disorders, degenerative see Optic nerve atrophy Cerebrum comp. A Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen Iris Lens comp. Augentropfen

628

Failure to thrive (in children)

see Anaemia Rosa e floribus 10%, Oleum Roseneisen/Graphit

Fatigue

see Exhaustion, states of

Fatty liver

see Liver disorders

Fibrocystic disease

Magnesit/Mamma comp.

Fissura ani

see Anal fissures

Fistulas Quarz D..

Flatulence see Wind

Flu-like infections

Mercurialis Salbe Quarz D..

Gallbladder disorders see Cholecystopathy

Gallbladder inflammation see Cholecystitis

Gallstones

see Cholelithiasis

Gastrocardiac symptom complex Nicotiana comp.

Gastroenteritis see Diarrhoea see Enteritis

Gastrointestinal motility, disturbances of see Diarrhoea see Colicky pain in the region of the abdomen see Wind

Gingivitis

Nierentonikum

Graves disease

see Hyperthyroidism

Growth disturbances

Haematoma

Arnica e floribus W 5%, Oleum Arnica e planta tota D.. Arnika-Essenz Arnika Salbe Arnika Wundtuch Cuprum/Quarz comp., Unguentum

Haemorrhoids

Hamamelis-Essenz Hirudo comp. Mercurialis comp., Suppositorien Quercus-Essenz Quercus Hämorrhoidalzäpfchen Quercus Salbe

see Catarrhal disorders of the upper airways Aconitum/China comp. Aconitum/China Comp., Suppositorien Aconitum/China comp., Suppositorien für Kinder Agropyron Inject Agropyron Globuli velati Echinacea e planta tota D.. Gelsemium comp. Meteoreisen Inject Meteoreisen Globuli velati

see Nephritis see Pyelonephritis Renes/Cuprum (adjunctive treatment)

Glue ear

Levisticum e radice D..

Arnica e planta tota D.. Arnica/Aurum I Arnica/Aurum II Cor GI D..

Food intolerance

Goitre

Heartburn

see Digestive disorders

Fractures

Symphytum comp. (Organ preparation)

Fungal infections of the skin see Mycoses of the skin

Furunculosis

see Acne Apis/Belladonna cum Mercurio Calendula-Essenz Echinacea e planta tota D.. Echinacea-Essenz Lachesis comp.

see Stomatitis

Glomerulonephritis

see Hyperthyroidism see Hypothyroidism Colchicum comp. Colchicum comp., Unguentum Glandula thyreoidea Gl D.. Spongia comp., Globuli velati

Gonads, underfunction of see Hypogonadism

Gout

see Arthritis see Arthritis, chronic Betula e foliis W 5%, Oleum Formica ex animale Gl D.. Juniperus/Berberis comp., Kapseln Mandragora officinarum e radice D..

E F G H

Epiphysis Gl D.. Hypophysis GI D..

Hay fever

see Allergic disorders of the airways Citrus e fructibus/Cydonia e fructibus

Heart attacks, follow-up treatment

Robinia comp.

Heart failure, adjunctive treatment

see Presbycardia (senile heart disease) Aurum/Equisetum I Aurum/Equisetum II Cor/Aurum I Primula/Convallaria comp. Scilla comp. Strophanthus kombe e semine D..   (Organ preparation)

Heart symptoms, functional

see Cardiac neurosis Aurum comp. Aurum comp., Unguentum Aurum/Stibium/Hyoscyamus

629

Aurum Valeriana Inject Aurum Valeriana Globuli velati Crataegus/Cor comp.

Hyperuricaemia

Hepatitis

Ovaria comp. Ovaria/Argentum Testes comp. Testes/Argentum (Organ preparation)

Carduus marianus/Viscum Mali comp. Hepar GI D.. Hepar/Stannum I Hepar/Stannum II (Organ preparation)

Herpes zoster

Aconit Schmerzöl Aconitum comp. (Organ preparation)

Herpes zoster, neuralgia following Aconitum e tubere W 5%, Oleum Apis/Arnica Rhus toxicodendron Salbe (Organ preparation)

Hip disorders

see Gout

Hypogonadism

Hypothyroidism

Intervertebral disc disorders, inflammatory

Hives

Hysteriform syndromes Bryophyllum comp. Ignatia comp.

Immune system, weakness of

see Menopausal symptoms Melissa/Sepia comp. Sambucus comp.

see Weakness of the immune system Mesenchym GI D..

Housemaid‘s knee

Incontinence

see Bursitis

Hyperacidity of the stomach

see Bedwetting see Prolapse complaints

see Peptic ulcer disease Bolus alba comp. Pulver Robinia comp. (Organ preparation)

Infections, bacterial

Hypertension

Inflammation of the skin

Arnica/Aurum I Arnica/Aurum II Aurum/Belladonna comp. Equisetum/Viscum Viscum comp.

Hyperthyroidism

Glandula thyreoidea Gl D.. Thyreoidea comp. Thyreoidea/Ferrum

630

Intervertebral disc disorders, degenerative

Glandulae suprarenales Gl D.. Glandulae suprarenales comp. Glandula suprarenalis dextra cum Cupro Glandula suprarenalis sinistra cum Cupro Levico comp. Rosmarinus, Oleum aethereum 10% Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati Veratrum e radice D..

Hypotension

Glandula thyreoidea Gl D.. Thyreoidea/Ferrum

Hot flashes

see Arterial occlusive disease Secale/Bleiglanz comp. (Organ preparation)

see Spinal disorders Bambusa e nodo D.. Cera/Aesculus comp., Unguentum Disci comp. cum Pulsatilla Disci comp. cum Stanno Disci/Viscum comp. cum Stanno Solum Badezusatz Solum Inject Solum Inject 10 Solum Globuli velati Solum Öl Solum Salbe Viscum Mali e planta tota 3%, Unguentum (Organ preparation)

Articulatio coxae Gl D.. see Pruritus

Intermittent claudication

Argentum/Quarz Echinacea/Argentum Lachesis comp. see Dermatitis

Inflammation sequelae in the CNS Cerebrum comp. A cum Auro comp. Cerebrum comp. B cum Auro comp.

Insect bites and stings Arnika Wundtuch Brandessenz Wund- und Brandgel

Disci comp. cum Argento (Organ preparation)

Irritable bladder

see Bladder, inflammation of Berberis/Apis comp. Cantharis Blasen Inject Cantharis Blasen Globuli velati Senecio comp. Senecio comp., Suppositorien (Organ preparation)

Iron deficiency see Anaemia

Itching

see Pruritus

Jaundice, infectious see Hepatitis

Joint disorders

see Arthritis see Arthritis, chronic see Osteoarthritis see Periarthropathy see Rheumatic disorders

Joint inflammation see Arthritis

Keloid

Echinacea/Viscum comp., Gelatum Narben Gel

Keratoconjunctivitis sicca

Chelidonium comp. Augentropfen Mercurialis Augentropfen

Kidney disorders, degenerative Aurum/Equisetum I Equisetum ex herba W 5%, Oleum Equisetum-Essenz Equisetum/Viscum (Organ preparation)

H I J K L

Kidney disorders, inflammatory see Nephritis see Pyelonephritis

Kidney stones

see Nephrolithiasis

Knee disorders

Articulatio genus Gl D.. Mandragora officinarum e radice D..

Lack of drive

Glandula suprarenalis dextra cum Cupro Glandula suprarenalis sinistra cum Cupro

Laryngitis

see Laryngeal oedema Archangelica comp. Berberis/Pyrit comp. Bronchi Plantago Inject Bronchi Plantago Globuli velati (Organ preparation)

Laryngeal oedema Larynx/Apis comp.

Leg ulcers

see Varicose symptom complex Echinacea/Viscum comp., Gelatum Hamamelis-Essenz Quarz/Nicotiana, Globuli velati Wund- und Brandgel (Organ preparation)

Liver congestion

see Liver disorders see Heart failure Carduus marianus/Oxalis

631

Liver disorders

see Cirrhosis of the liver Anagallis comp. Hepar GI D.. Hepar/Stannum I (Organ preparation)

Low back pain

see Neuralgia see Nerve root disorders Disci/Viscum comp. cum Argento, Suppositorien

Lumbago

see Myalgia, myogelosis see Nerve root disorders Apis/Bryonia Bambusa e nodo D.. Disci/Pulsatilla comp. cum Stanno, Suppositorien

Lymphadenitis

Argentum/Quarz Echinacea e planta tota D.. (Organ preparation)

Lymphangitis

Apis ex animale Gl D.. (adjunctive treatment) Apis Belladonna Inject Apis Belladonna Globuli velati Echinacea e planta tota D..

Lymphatic diathesis

see Allergic diathesis Berberis e fructibus comp. Echinacea Mund- und Rachenspray

Lymphoedema, lymphatic congestion Cuprum/Quarz comp., Unguentum Renes/Borago comp.

Macular degeneration

see Retinal disorders, degenerative

Maldigestion see Dyspepsia

Mastitis

Apis Belladonna Inject Apis Belladonna Globuli velati Calendula-Essenz Lachesis comp.

632

Menière‘s symptom complex Cerebrum comp. B Gnaphalium comp.

Menopausal symptoms

Aurum/Apis regina comp. Berberis/Sepia comp. Bryophyllum comp. Ignatia comp. Melissa/Sepia comp. Ovaria comp. Ovaria/Argentum Sambucus comp. Spongia/Aurum/Pulsatilla comp.

Menorrhagia

Berberis/Urtica urens Calcium Quercus Inject Calcium Quercus Inject 10 Calcium Quercus Globuli velati Tormentilla comp.

Menstrual disorders see Amenorrhoea see Dysmenorrhoea

Migraine

Chamomilla e radice D.. Ferrum/Sulfur comp. Quarz D.. Secale/Quarz

Movement disorders, ataxic and hyperkinetic Cerebellum comp. (Organ preparation)

Muscle disorders

see Myalgia, myogelosis

Muscle soreness

see Myalgia, myogelosis Arnica e planta tota D..

Myalgia, myogelosis

Apis ex animale Gl D.. Apis/Levisticum I Apis/Levisticum II Arnica e floribus W 5%, Oleum Arnika-Essenz Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Cera/Aesculus comp., Unguentum Formica ex animale Gl D.. Magnesium phosphoricum comp. Rhus toxicodendron Salbe Rhus toxicodendron comp.

Mycoses of the skin

see Degenerative changes in the CNS see Spinal cord disorders, degenerative Lavandula, Oleum aethereum 10%

Nerve root disorders

see Spinal disorders Aconitum comp. Bambusa e nodo D.. Disci comp. cum Argento Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Rhus toxicodendron comp. Hypericum ex herba 5% Oleum Nervus ischiadicus Gl D.. (Organ preparation)

see Digestive disorders Silicea colloidalis comp., Gelatum (Organ preparation)

Nervousness

Myocarditis

Nervous tension

Cor/Aurum II

Myomatosis uteri see Uterine fibroids

Nausea

Aurum Valeriana Inject Aurum Valeriana Globuli velati Bitter Elixier Enzian Magentonikum Gentiana Magen Inject Gentiana Magen Globuli velati

Nephritis

see Urinary tract infections see Pyelonephritis Renes/Argentum nitricum (Organ preparation)

Nephrolithiasis

Juniperus/Berberis comp., Kapseln

Nephrosclerosis

Muscle weakness Primula Muskelnähröl

see Hypertension Viscum/Crataegus (Organ preparation)

Muscular tension

Nephrotic syndrome

see Myalgia, myogelosis see Spinal disorders see Nerve root disorders Lavandula, Oleum aethereum 10%

Nerve disorders, degenerative

see Protein breakdown disorders see Protein metabolism disorders Renes/Cuprum

L M N

see Nervous tension

see Menopausal symptoms see Neurovegetative dysregulation Arnica/Aurum I Arnica/Aurum II Avena comp. Bryophyllum comp. Mandragora officinarum e radice D.. Passiflora Nerventonikum Passiflora Zäpfchen Passiflora Kinderzäpfchen Valeriana comp.

Neuralgia

Aconit Schmerzöl Aconitum comp. Aconitum e tubere W 5%, Oleum Apis/Levisticum I Apis/Levisticum II Camphora/Hypericum, Unguentum Chamomilla e radice D.. Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Argento, Suppositorien Formica ex animale Gl D.. Gelsemium comp.   Kampfer Johanniskrautöl Lavandula, Oleum aethereum 10% Levisticum e radice D.. Nervus trigeminus Gl D.. Rhus toxicodendron Salbe Rhus toxicodendron comp. Solum Badezusatz Solum Inject

633

Solum Inject 10 Solum Globuli velati Solum Öl Solum Salbe (Organ preparation) see Asthenia see Neurovegetative dysregulation Aurum/Apis regina comp.

Disci comp. cum Stanno Equisetum/Stannum Formica ex animale Gl D.. Hornerz/Cartilago comp. Kampfer Johanniskrautöl Mandragora officinarum e radice D.. Oleum Petrae comp. Quarz D.. Viscum Mali e planta tota W 5%, Oleum (Organ preparation)

Neuritis, adjunctive treatment of

Osteochondrosis

Neurasthenia

Apis/Arnica Levisticum e radice W 5%, Oleum (Organ preparation)

see Spinal disorders see Nerve root disorders Hornerz/Cartilago comp.

Neurovegetative dysregulation

Otitis media

see Exhaustion, states of see Cardiac neurosis see Tetaniform states Aurum/Apis regina comp. Aurum Valeriana Inject Aurum Valeriana Globuli velati Parathyreoidea/Aurum Prunus spinosa e floribus W 5%, Oleum Veratrum comp.

Noise, sensitivity to Cerebrum comp. B

Oedema

see Heart failure see Lymphoedema, lymphatic congestion see Kidney disorders, degenerative see Varicose symptom complex

Optic nerve atrophy

see Eye disorders, degenerative Nervus opticus comp. Augentropfen (Organ preparation)

Osteoarthritis

see Hip disorders see Knee disorders Apis ex animale Gl D.. Articulatio talocruralis comp. Betula/Mandragora comp. Camphora/Hypericum, Unguentum Cartilago comp. Cartilago comp., Suppositorien Cartilago comp., Unguentum Cartilago/Mandragora comp. Cartilago/Mandragora comp., Unguentum

634

Aconit Ohrentropfen Apis Belladonna Inject Apis Belladonna Globuli velati Apis/Levisticum I Apis/Levisticum II Argentum/Quarz Levisticum e radice D.. Levisticum Ohrentropfen Quarz D.. Silicea comp. Silicea comp., Suppositorien Silicea comp., Suppositorien für Kinder Thuja e summitatibus D.. (Organ preparation)

Otosclerosis

Gnaphalium comp. (Organ preparation)

Barium/Pancreas comp. Pancreas GI D.. Pancreas/Meteoreisen Platinum chloratum/Pancreas comp.

Pancreatitis

Pancreas GI D.. Pancreas/Argentum

Parametritis

Echinacea e planta tota D.. Echinacea-Essenz Parametrium/Echinacea comp.

Paranasal sinuses, inflammation of see Sinusitis

Parasitic intestinal diseases, follow-up treatment Eucalyptus comp. Quarz D..

Peptic ulcer disease Chamomilla e radice D.. Robinia comp. (Organ preparation)

Periarthropathy

see Myalgia, myogelosis Betula/Arnica comp. Formica ex animale Gl D.. (Organ preparation)

Periodontitis

Levisticum e radice D..

see Stomatitis Periodontium/Silicea comp. Periodontium/Stannum comp. Silicea comp.

Ovarian cysts

Period pains

Otitis media with effusion

Bryonia comp. Magnesium sulfuricum/Ovaria comp.

Ovarian underfunction see Hypogonadism

Pain, chronic

see Neuralgia see Rheumatic disorders see Nerve root disorders

Pancreas disorders see Dyspepsia

see Dysmenorrhoea

Periostitis

Pink eye

see Conjunctivitis see Keratoconjunctivitis sicca

Pleurisy

see Pleuritis

Pleuritis, adjunctive treatment Bryonia/Stannum (Organ preparation)

Pneumonia

see Stimulation of breathing and circulation Petasites comp. Plantago Hustensaft Pulmo/Ferrum Pulmo/Mercurius Pulmo/Tartarus stibiatus II Pulmo/Vivianit comp. (Organ preparation) see Hay fever

Polyarthritis

see Arthritis see Rheumatic disorders Cartilago/Mandragora comp. Cartilago/Mandragora comp., Unguentum Viscum Mali e planta tota W 5%, Oleum

Polyps

see Adenoids

Poor vision

Cerebrum comp. A Chelidonium comp. Augentropfen Hornerz/Corpus vitreum comp. Hornerz Corpus vitreum comp. Augentropfen

Postherpetic neuralgia

see Herpes zoster, neuralgia following

Symphytum comp. Tendo/Allium cepa comp. (Organ preparation)

Postural weakness, adolescent

Periproctitis

Presbycardia (senile heart disease)

see Anal fissures

Pharyngitis

Berberis/Pyrit comp. Echinacea Mund- und Rachenspray

N O P

Pollinosis

Bambusa e nodo D.. Disci comp. cum Nicotiana see Angina pectoris see Heart failure Adonis comp. Cactus comp. II

635

Crataegus/Cor comp. Strophanthus/Nicotiana comp. Viscum comp. Viscum/Crataegus (Organ preparation)

Presbyopia

see Age-related long-sightedness

Pressure sores

Renes/Cuprum (adjunctive treatment) Renes/Argentum nitricum (Organ preparation)

Pyoderma

see Furunculosis see Cellulitis Apis/Belladonna cum Mercurio Echinacea e planta tota D..

see Skin, disturbance of trophism and blood supply see Skin defects, superficial see Wounds Aesculus/Prunus comp., Essenz Calcea Wund- und Heilcreme Mercurialis Salbe

Radiculopathy

Proctitis

Radiotherapy

see Anal fissures

Prolapse symptoms

see Menopausal symptoms Citrus, Oleum aethereum 10% Senecio comp. Senecio comp., Suppositorien (Organ preparation)

Prostatic hypertrophy

see Nerve roor disorders

Radiation sequelae

see Skin, disturbance of trophism and blood supply see Weather, sensitivity to changes in see (adjunctive treatment of weakness of the immune system after radiation therapy)

Raynaud‘s disease

Cuprum aceticum comp. Secale/Bleiglanz comp.

Recurrent nerve palsy see Vocal cord weakness

see Urination problems due to prostate adenoma Berberis/Prostata comp. (Organ preparation)

Renal failure, acute

Protein breakdown disorders

Kupfer Salbe rot

Pancreas GI D.. Pancreas/Meteoreisen

Protein metabolism disorders

Mesenchym/Calcium carbonicum comp. Organum quadruplex Pancreas GI D.. Pancreas/Equisetum

Pruritus

Renes/Equisetum comp.

Renal function, impaired Renal pelvis, inflammation of see Pyelonephritis

Repetitive strain injury see Tendovaginitis

Respiratory tract infections, febrile see Flu-like infections

see Allergic skin disorders see Senile skin see Dermatitis see Mycoses of the skin Rosatum Heilsalbe Rosmarinus/Prunus comp., Gelatum Urtica comp.

Retinal disorders, degenerative

Pyelonephritis

see Anal fissures Quercus-Essenz

Argentum nitricum comp.

636

Galenit/Retina comp. Nervus opticus comp. Augentropfen Retina comp. Secale/Retina comp. (Organ preparation)

Rhagades

Rheumatic disorders

see Arthritis see Arthritis, chronic see Osteoarthritis see Myalgia, myogelosis see Neuralgia see Periarthropathy Apis ex animale Gl D.. Apis/Bryonia Betula e foliis W 5%, Oleum Betula/Arnica comp. Betula/Mandragora comp. Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Camphora 5%, Oleum Camphora/Hypericum, Unguentum Formica ex animale Gl D.. Formica/Oxalis Hypericum ex herba 5% Oleum Kampfer Johanniskrautöl Magnesium phosphoricum comp. Mandragora officinarum e radice D.. Nierentonikum Quarz D.. Rheuma-Badeöl Rosmarinus, Oleum aethereum 10% Solum Badezusatz Solum Inject Solum Inject 10 Solum Globuli velati Solum Öl Solum Salbe

Rhinitis

see Catarrhal disorders of the upper airways

Scar problems

Akne-Gesichtsmaske Akne-Kapseln Akne-Wasser

Senile skin

Echinacea/Viscum comp., Gelatum (Organ preparation)

Shingles

see Herpes zoster

Shock, sequelae of

Argentum/Rohrzucker Arnica e planta tota D.. Oxalis e planta tota W 10%, Oleum Oxalis-Essenz Quarz/Oxalis comp.

Sickness, feeling of see Nausea

Sinusitis

Agropyron Inject Agropyron Globuli velati Argentum/Quarz Berberis e fructibus comp. Berberis/Quarz Hepar sulfuris comp. Lachesis comp. Myristica sebifera comp. Silicea comp. Silicea comp., Suppositorien Silicea comp., Suppositorien für Kinder (Organ preparation)

Skin defects, superficial

Scheuermann‘s disease

see Pressure sores see Wounds Calcea Wund- und Heilcreme Rosatum Heilsalbe

Sciatica

Skin, disturbance of trophism and blood supply

see Nerve root disorders Nervus ischiadicus GI

Echinacea/Viscum comp., Gelatum Resina laricis-Bademilch

Scoliosis

Skin rashes

see Keloid

Disci comp. cum Nicotiana

see Spinal disorders Bambusa e nodo D.. Disci comp. cum Nicotiana

Seborrhoea

Akne-Gesichtsdampfbad

P R S

see Dermatitis

Sleep disturbances

Aurum/Stibium/Hyoscyamus Avena comp. Chamomilla e radice D..

637

Lavandula, Oleum aethereum 10% Passiflora comp. Passiflora Nerventonikum Passiflora Kinderzäpfchen Passiflora Zäpfchen Valeriana comp.

Sore throat

see Pharyngitis

Spasms, intestinal

see Colicky pain in the region of the abdomen Chamomilla e radice D..

Spasms of the organs in the small pelvis

see Dysmenorrhoea Ammi visnaga comp., Suppositorien Ammi visnaga comp., Suppositorien für Kinder Chamomilla e radice D..

Spasms of the small arterial blood vessels see Raynaud‘s disease

Spinal disorders

see Intervertebral disc disorders, degenerative see Ankylosing spondylitis see Postural weakness, adolescent see Lumbago see Osteochondrosis see Scheuermann‘s disease see Scoliosis see Nerve root disorders Bambusa e nodo D.. Cera/Aesculus comp., Unguentum Disci comp. cum Aesculo Disci comp. cum Aesculo, Gelatum Disci comp. cum Argento Disci comp. cum Auro Disci comp. cum Nicotiana Disci comp. cum Pulsatilla Disci comp. cum Pulsatilla, Unguentum Disci comp. cum Stanno Disci comp. cum Stibio Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Argento, Suppositorien Disci/Viscum comp. cum Stanno Disci/Viscum comp, cum Stanno, Unguentum Solum Badezusatz Solum Inject Solum Inject 10 Solum Globuli velati Solum Öl

638

Solum Salbe (Organ preparation)

Sprains

Arnica e planta tota D.. Arnica e floribus W 5%, Oleum Arnika-Essenz Arnika Salbe Arnika Wundtuch (Organ preparation)

Stimulation of breathing and circulation

see Cardiovascular weakness Oleum camphoratum comp.

Stomatitis

see Periodontitis Apis/Belladonna cum Mercurio Berberis/Apis comp. Echinacea Mund- und Rachenspray Mundbalsam Mundbalsam flüssig Thuja e summitatibus D.. Thuja-Essenz

Stones

see Cholelithiasis see Nephrolithiasis Equisetum ex herba W 5%, Oleum Equisetum-Essenz Oxalis e planta tota W 10%, Oleum Oxalis-Essenz

Stroke, follow-up or adjunctive treatment Arnica e planta tota D.. Arnica/Aurum I Arnica/Aurum II Arnica/Plumbum comp. A Arnica/Plumbum comp. B Viscum comp. (Organ preparation)

Sudeck‘s syndrome

Symphytum comp. Thymus, Oleum aethereum 5% (Organ preparation)

Sunburn

Brandessenz Wund- und Brandgel

Suppuration, chronic

Conchae comp. (adjunctive treatment)

Susceptibility to colds

see Flu-like infections Echinacea e planta tota D.. Prunus spinosa e floribus W 5%, Oleum

Tachycardia

see Cardiac rhythm disorders Adonis comp.

Teething problems

Chamomilla e radice D..

Tendovaginitis

Symphytum comp. Tendo/Allium cepa comp. (Organ preparation)

Tennis ellbow

see Epicondylitis

Tetaniform states Parathyreoidea comp.

Thrombophlebitis

Aesculus/Prunus comp., Essenz Borago comp. Borago-Essenz Hirudo comp.

Thrombosis

see Varicose symptom complex Borago comp. (Organ preparation)

Thyroid gland, enlarged see Goitre

Thyroid, hyperactivity of see Hyperthyroidism

Thyroid, underfunction of see Hypothyroidism

Tonsillitis

Agropyron Inject Agropyron Globuli velati Apis ex animale Gl D.. Apis/Belladonna cum Mercurio Echinacea Mund- und Rachenspray Echinacea/Mercurius comp., Suppositorien Echinacea/Mercurius comp., Suppositorien für Kinder Lachesis comp.

Tonsils, inflamed see Tonsillitis

Trauma

see Haematoma see Burns, scalds see Wounds see Sprains Arnica e planta tota D..

Twists

see Sprains (Organ preparation)

Ulcers

see Pressure sores see Leg ulcers

Undernourishment

see Protein metabolism disorders Organum quadruplex

Urinary tract infections

see Bladder, inflammation of see Pyelonephritis Argentum nitricum comp. Cantharis Blasen Inject Cantharis Blasen Globuli velati Nierentonikum

S T U V

Urination problems due to prostate adenoma

see Prostatic hypertrophy Berberis/Urtica urens

Urticaria

see Allergic diathesis see Allergic skin disorders see Pruritus

Uterine fibroids

Berberis/Sepia comp. Berberis/Urtica urens Berberis/Uterus comp. (Organ preparation)

Vagina, inflammation of see Vaginitis

Vaginal discharge, unspecific Berberis/Hypericum comp. Majorana Vaginalgel

639

Vaginitis

Majorana Vaginalgel

Varicose symptom complex Aesculus e semine W 5%, Oleum Aesculus-Essenz Aesculus/Prunus comp., Essenz Borago comp. Borago-Essenz Citrus, Oleum aethereum 10% Hamamelis-Essenz Hirudo comp. Quarz/Nicotiana, Globuli velati Quercus-Essenz Quercus Salbe Senecio comp. Senecio comp., Suppositorien (Organ preparation)

Varicose veins

see Varicose symptom complex

Vascular sclerosis

see Arterial occlusive disease

Vertigo

see Dizziness see Arterial occlusive disease

Vitreous clouding

Cornea/Levisticum comp. Cornea Levisticum comp. Augentropfen Hornerz/Corpus vitreum comp. Hornerz Corpus vitreum comp. Augentropfen Lens Viscum comp. Augentropfen Lens Viscum comp. Inject Lens Viscum comp. Globuli velati

Vocal cord weakness Larynx comp.

Voice box, inflammation of see Laryngitis

Vomiting

see Nausea Gentiana Magen Inject Gentiana Magen Globuli velati

Vulvitis

see Vaginitis Majorana Vaginalgel Rosmarinus/Prunus comp., Gelatum

640

Warts

Thuja e summitatibus D.. Thuja-Essenz

Weak resistance, general Viscum/Echinacea

Weakness of the immune system Echinacea/Argentum Lien comp. Thymus (Glandula) GI D..

Weather, sensitivity to changes in Solum Badezusatz Solum Inject Solum Inject 10 Solum Globuli velati Solum Öl Solum Salbe

Weight loss

Levisticum e radice D.

Wind

see Dyspepsia Aquilinum comp. Carum carvi Kinderzäpfchen Carum carvi Zäpfchen Chamomilla e radice D.. Chelidonium Kapseln Cuprum/Nicotiana, Unguentum Gentiana Magen Inject Gentiana Magen Globuli velati Juniperus/Berberis comp., Kapseln Lavandula, Oleum aethereum 10% Melissenöl Nicotiana comp. Pancreas/Meteoreisen (Organ preparation)

V W Z

Worm infections Aquilinum comp. Eucalyptus comp.

Wounds

Arnica e planta tota D.. Brandessenz Calcea Wund- und Heilcreme Calendula-Essenz Echinacea e planta tota D.. Echinacea-Essenz Mercurialis Salbe Wund- und Brandgel

641

Preparation Overviews WALA Medicinal Products by Dosage Form Liquid dilutions for injection/globuli velati Compositions Organ-metal combinations Mineral, plant and animal monopreparations Potentised organ preparations Further preparations for internal use Eye drops Ear drops Suppositories Paediatric suppositories Ointments Gels

Preparations for compresses, lavages and baths

656 657 657

WALA medicinal products Available by Prescription Only

658

WALA Medicinal Products for General Sale

658

WALA Medicinal Products Contraindicated During Pregnancy and Breastfeeding

660

WALA Medicinal Products Contraindicated in Children

662

Oils for embrocations and massages Dispersion bath oils

642

644 644 644 648 648 650 654 654 654 655 655 655 656

643

WALA Medicinal Products by Dosage Form

Preparation

Liquid Dilutions for Injection/Globuli Velati Package sizes: Liquid dilution for injection: 10 ampoules (N1), 50 ampoules (N2) x 1 ml in exceptional cases: 5 ampoules (N1), 20 ampoules (N2) x 10 ml Globuli velati: 20 g (N1)

Compositions Preparation Aconitum comp. Aconitum/China comp. Adonis comp. Agropyron Inject Agropyron Globuli velati Anagallis comp. Apis/Arnica Apis Belladonna Inject Apis Belladonna Globuli velati Apis/Belladonna cum Mercurio Apis/Bryonia Apis/Levisticum I Apis/Levisticum II Apis regina comp. Aquilinum comp. Archangelica comp. Argentum nitricum comp. Argentum/Quarz Argentum/Rohrzucker Arnica/Aurum I Arnica/Aurum II 644

Liqu. dil. for Globuli injection velati x x x x x x

x x x x x x x

x

x

x x x x x x x

x x x x x x x

x x x x

x x x x

Liqu. dil. for Globuli injection velati

Arnica/Plumbum comp. A

x

x

Arnica/Plumbum comp. B Arnica/Plumbum mellitum Articulatio talocruralis comp. Aurum comp. Aurum/Apis regina comp. Aurum/Belladonna comp. Aurum/Equisetum I Aurum/Equisetum II Aurum/Prunus Aurum/Stibium/ Hyoscyamus Aurum/Strophanthus Aurum Valeriana Inject Aurum Valeriana Globuli velati Avena comp.

x x

x x

x

x

x x

x x

x

x

x x x x

x x x x

x x

x

x

x

Barium/Pancreas comp. Belladonna/Chamomilla Berberis e fructibus comp. Berberis/Apis comp. Berberis/Hypericum comp. Berberis/Nicotiana comp. Berberis/Prostata comp. Berberis/Pyrit comp. Berberis/Quarz Berberis/Sepia comp. Berberis/Urtica urens Berberis/Uterus comp. Betula/Arnica comp. Betula/Mandragora comp. Borago comp. Bronchi Plantago Inject

x x x

x x x

x x

x x

x

x

x x x x x x x x x x

x

x

x x x x x x x

Preparation Bronchi Plantago Globuli velati Bryonia comp. Bryonia/Aconitum Bryonia/Stannum Bryophyllum comp. Cactus comp. II Calcium Quercus Inject Calcium Quercus Globuli velati Cantharis Inject Cantharis Globuli velati Carduus marianus/Oxalis Carduus marianus/ Viscum Mali comp. Cartilago comp. Cartilago/Echinacea comp. Cartilago/Mandragora comp. Cerebellum comp. Cerebrum comp. A Cerebrum comp. A cum Auro comp. Cerebrum comp. B Cerebrum comp. B cum Auro comp. Chamomilla/Nicotiana Chelidonium/Colocynthis Cichorium/Pancreas comp. Citrus e fructibus/ Cydonia e fructibus Colchicum comp. Conchae comp. Conjunctiva comp. Cor/Aurum I Cor/Aurum II Cornea/Levisticum comp.

Liqu. dil. for Globuli injection velati x x x x x

x x x x

x x

x x

x x x

x x x

x x

x x

x

x

x x x

x x x

x x

x x

x x

x x

x

x

x x x x x x x

x x x

Preparation

Liqu. dil. for Globuli injection velati

Crataegus/Cor comp. Cuprum aceticum comp.

x x

x

Disci comp. cum Aesculo Disci comp. cum Argento Disci comp. cum Auro Disci comp. cum Nicotiana Disci comp. cum Pulsatilla Disci comp. cum Stanno Disci comp. cum Stibio Disci/Rhus toxicodendron comp. Disci/Viscum comp. cum Stanno

x x

x x

x x

x x

x

x

x x x

x x

x

x

Echinacea/Argentum Endometrium comp. Epiphysis/Plumbum Equisetum/Formica Equisetum/Stannum Equisetum/Viscum Eucalyptus comp.

x x x x x x x

x x x x x x x

Ferrum silicicum comp. Ferrum/Sulfur comp. Formica/Oxalis

x x x

x x

Galenit/Retina comp. Gelsemium comp. Gentiana Magen Inject Gentiana Magen Globuli velati Glandulae suprarenales comp. Glandula suprarenalis dextra cum Cupro Glandula suprarenalis sinistra cum Cupro Glandula suprarenalis sinistra/Mercurius

x x x

x x x

x

x

x

x

x

x

x

645

Preparation

Liqu. dil. for Globuli injection velati

Gnaphalium comp.

x

Hepar/Stannum I Hepar/Stannum II Hepar sulfuris comp. Hirudo comp. Hornerz/Cartilago comp. Hornerz/Corpus vitreum comp. Hypophysis/Stannum

x x x x x x

x x x

x

x

Ignatia comp.

x

x

Juglans regia comp.

x

Lachesis comp. Larynx comp. Larynx/Apis comp. Lens Viscum comp. Inject Lens Viscum comp. Globuli velati Levico comp. Lien comp. Lien/Plumbum Lycopodium comp.

x x x x

x x x x

x x

Magnesit/Mamma comp. Magnesium phosphoricum comp. Magnesium sulfuricum/ Ovaria comp. Melissa/Sepia comp. Mesenchym/Calcium carbonicum comp. Meteoreisen Inject Meteoreisen Globuli velati Myristica sebifera comp.

x

x

646

x

x x x

x

x

x

x

x

x

x x

x

x x x

x

Preparation

Liqu. dil. for Globuli injection velati

Nicotiana comp. Nux vomica/Nicotiana comp.

x x

Oleum camphoratum comp. Organum quadruplex Ovaria/Argentum Ovaria comp.

x

Pancreas/Argentum Pancreas/Equisetum Pancreas/Meteoreisen Parametrium/Echinacea comp. Parathyreoidea/Aurum Parathyreoidea comp. Passiflora comp. Periodontium/Silicea comp. Periodontium/Stannum comp. Petasites comp. Platinum chloratum/ Pancreas comp. Primula comp. Primula/Convallaria comp. Pulmo/Ferrum Pulmo/Mercurius Pulmo/Tartarus stibiatus I Pulmo/Tartarus stibiatus II Pulmo/Vivianit comp.

x x x x

x x x

x x x x

x x

x x x x

x x x

x x x

x x

x x

x x

x x x x x

Quarz/Nicotiana Quarz/Oxalis comp.

x

Renes/Argentum nitricum Renes/Borago comp. Renes/Cuprum Renes/Equisetum comp. Retina comp.

x x x x x

x x x

Preparation

Liqu. dil. for Globuli injection velati

Rhus toxicodendron comp. Robinia comp. Roseneisen/Graphit

x

x

x x

x x

Salix/Rhus comp. Sambucus comp. Sarothamnus comp. Scilla comp. Secale/Argentum Secale/Bleiglanz comp. Secale/Quarz Secale/Retina comp. Senecio comp. Silicea comp. Skorodit Kreislauf Inject Skorodit Kreislauf Globuli velati Solum Inject Solum Globuli velati Spongia comp. Spongia/Aurum/ Pulsatilla comp. Strophanthus comp. Strophanthus/Nicotiana comp. Symphytum comp.

x x x x x x x x x x x

x x x x

Preparation Valeriana comp. Veratrum comp. Vesica fellea/Ferrum I Vesica fellea/Ferrum II Viscum comp. Viscum/Bryonia comp. Viscum/Crataegus Viscum/Echinacea

Liqu. dil. for Globuli injection velati x x x x x x x x

x x

x x x x

x x x x x x

x

x

x x x

x x

x x

x

x

Tendo/Allium cepa comp. Testes/Argentum Testes comp. Thymus/Mercurius Thyreoidea comp. Thyreoidea/Ferrum Thyreoidea/Thymus comp. Tormentilla comp. Triticum comp. I

x

x

x x x x x x

x x x x x x

x x

x x

Urtica comp.

x

x

x

647

Organ-Metal Combinations

Mineral, Plant and Animal Monopreparations

Preparation

By main organ Preparation Cor/Aurum I Cor/Aurum II Hepar/Stannum I Hepar/Stannum II Lien/Plumbum Pulmo/Ferrum Pulmo/Mercurius Pulmo/Tartarus stibiatus I Pulmo/Tartarus stibiatus II Renes/Argentum nitricum Renes/Cuprum Vesica fellea/Ferrum I Vesica fellea/Ferrum II

Liqu. dil. for Globuli injection velati

Abrotanum ex herba Achatwasser Achillea ex herba Aconitum e tubere Aesculus e semine Allium cepa e bulbo Amethyst Apis ex animale Gl Apis regina Gl Aranea ex animale Gl Arnica e planta tota Arsenicum album Atropa belladonna e fructibus Atropa belladonna e radice Atropa belladonna ex herba

x x x x x x x x x x x x x

By endocrine organ Epiphysis/Plumbum Glandula suprarenalis dextra cum Cupro Glandula suprarenalis sinistra cum Cupro Glandula suprarenalis sinistra/Mercurius Hypophysis/Stannum Ovaria/Argentum Pancreas/Argentum Pancreas/Meteoreisen Parathyreoidea/Aurum Testes/Argentum Thymus/Mercurius Thyreoidea/Ferrum

648

x x

x x

x

x

x x x x x x x x x

Preparation

x x

x x x x

Liqu. dil. for Globuli injection velati x x x x x x x x x x x

x x x x

x x x

x

x

x

x

Bambusa e nodo Berberis e fructibus Berberis e radice Betula e foliis Bryonia e radice

x x x x x

x x x

Cactus ex herba Calcium carbonicum cum Quercu Calendula ex herba Camphora Cantharis ex animale Gl Carduus marianus e fructibus Chalcedon Chamomilla e planta tota Chamomilla e radice

x x

x

x

x x x x

x

x x

x

x

x

Liqu. dil. for Globuli injection velati

Chelidonium e planta tota Chelidonium e radice Chrysopras Cichorium e planta tota Citrus e fructibus Cochlearia ex herba Colchicum e planta tota Colocynthis e fructibus Conchae Crataegus e foliis et fructibus Cydonia e fructibus

x

x

x

Echinacea e planta tota Equisetum ex herba Euphrasia e planta tota

x x x

x x x

Formica ex animale Gl Fucus vesiculosus e planta tota

x x

x

Gelsemium e radice Gentiana lutea e radice Geum urbanum e radice Granat Graphites

x

Hamamelis e foliis Helleborus niger e planta tota Hirudo ex animale Gl Hyoscyamus ex herba Hypericum ex herba Ignatia e semine Iscucin Abietis Iscucin Crataegi Iscucin Mali Iscucin Pini Iscucin Populi

x x x x x x x x

x x x x x x x x x

Liqu. dil. for Globuli injection velati

x

Iscucin Quercus Iscucin Salicis Iscucin Tiliae

x x x

x x x x x

Karneol

x

Lachesis e veneno Levisticum e radice Lycopodium e planta tota

x x x

x x

Magnesium phosphoricum cum cinere Avenae Mandragora officinarum e radice

x

x

x

x

Nicotiana e foliis Nux vomica e semine

x x

x x

Opal Oxalis e planta tota

x x

x

Phosphorus Platinum metallicum Prunus spinosa e floribus et summitatibus Prunuseisen Pulsatilla e floribus

x

x

x x

x x x x

Preparation

x x

x x x

x

x x x

x x

x x

Quarz

x

x

Rhus toxicodendron e foliis Roseneisen Rosenquarz Rubin

x

x

Salvia e foliis Saphir Scilla e bulbo Secale cornutum e grano Sepia e secreto Gl

x x x x

x x x

x

x

649

Preparation

Liqu. dil. for Globuli injection velati

Solidago virgaurea ex herba Spongia tosta Strophanthus kombe e semine Sulfur Symphytum e radice

x

x

x x

x

x x

x x

Taraxacum e planta tota Taraxacum e radice (autumnale) Taraxacum e radice (vernale) Terebinthina laricina Thuja e summitatibus Topas Tormentilla e radice Tulipa e planta tota

x x

x

Urtica dioica e planta tota Urtica urens ex herba

x

x

x

x

Valeriana e radice Veratrum e radice Vespa Crabro ex animale Gl Viscum Abietis e planta tota Viscum Mali e planta tota Viscum Mali, Senker Viscum Pini e planta tota

x x x

x x

650

x x x x x x

x x

x x x x

x

x

Potentised Organ Preparations

Preparation

Preparation

Bindegewebe Gl Bronchi Gl Bulbus olfactorius Gl Bursae articulationis humeri-Komplex Gl

x x x x

Cardia Gl Cartilago articularis (coxae) Gl Cartilago articularis (genus) Gl Cavum tympani Gl Cerebellum Gl Cerebrum, regio motorica Gl Cervix uteri Gl Circulus arteriosus cerebri Gl Cochlea Gl Colon Gl Colon sigmoideum Gl Columna anterior Gl Columna posterior Gl Conjunctiva Gl Cor Gl Cornea Gl Corpora quadrigemina Gl Corpus amygdaloideum Gl Corpus luteum Gl Corpus striatum Gl Corpus vitreum Gl Cutis (feti) Gl

x x

Dens Gl Diaphragma Gl Diaphragma pelvis Gl Diencephalon Gl Disci intervertebrales (cervicales) Gl

x x x x x

Amnion Gl Anus Gl Aorta (tota) Gl Appendix vermiformis Gl Arteria basilaris Gl Arteria brachialis Gl Arteria carotis communis et sinus caroticus Gl Arteria cerebri media Gl Arteria coronaria Gl Arteria femoralis Gl Arteria ophthalmica Gl Arteria poplitea Gl Arteria pulmonalis Gl Arteria renalis Gl Arteria vertebralis Gl Arteriae Gl Articulatio coxae Gl Articulatio cubiti Gl Articulatio genus Gl Articulatio humeri Gl Articulatio radiocarpea Gl Articulatio sacroiliaca Gl Articulatio subtalaris Gl Articulatio talocruralis Gl Articulatio temporomandibularis Gl Articulationes intercarpeae Gl Articulationes intervertebrales cervicales Gl Articulationes intervertebrales lumbales Gl Atlas Gl Axis Gl

Liqu. dil. for injection x x x x x x x x x x x x x x x x x x x x x x x x x x x x x x

Liqu. dil. for injection

x x x x x x x x x x x x x x x x x x x x

Preparation

Liqu. dil. for injection

Disci intervertebrales (feti) Gl Disci intervertebrales (lumbales) Gl Ductus choledochus Gl Ductus thoracicus Gl Duodenum Gl Dura mater encephali Gl

x

Endocardium Gl Endometrium Gl Epididymis (sinistra) Gl Epiphysis Gl Erythrocyten Gl

x x x x x

Fasciculus atrioventricularis Gl Fel Gl Femur Gl Folliculi lymphatici aggregati Gl Funiculus umbilicalis Gl

x

Galea aponeurotica Gl Gingiva Gl Glandula lacrimalis Gl Glandula parotis Gl Glandula suprarenalis (Cortex) Gl Glandula suprarenalis (Medulla) Gl Glandula suprarenalis dextra Gl Glandula suprarenalis sinistra Gl Glandula thyreoidea Gl Glandulae parathyreoideae Gl Glandulae suprarenales Gl Gyrus cinguli Gl

x x x x x

x x x x x

x x x x

x x x x x x x

651

Preparation

Liqu. dil. for injection

Hepar Gl Hippocampus Gl Hirnstamm Gl Hypophysis Gl Hypothalamus Gl

x x x x x

Ileum Gl Iris (bovis) Gl

x x

Larynx Gl Lens cristallina Gl Lien Gl Ligamentum longitudinale anterius Gl Ligamentum longitudinale posterius Gl Ligamentum vocale Gl Lingua Gl Liquor cerebrospinalis Gl Lobus frontalis Gl Lobus occipitalis Gl Lobus parietalis Gl Lobus temporalis Gl

x x x x

Mamma (dextra) Gl Mamma (sinistra) Gl Mandibula (feti) Gl Maxilla (feti) Gl Medulla oblongata (Ventriculus quartus) Gl Medulla ossium Gl Medulla spinalis (tota) Gl Membrana sinus frontalis Gl Membrana sinus maxillaris Gl Membrana sinuum paranasalium Gl Membrana synovialis Gl Meniscus Gl Mesencephalon Gl Mesenchym Gl

x x x x x

652

x x x x x x x x

x x x x x x x x x

Preparation

Liqu. dil. for injection

Musculi glutaei Gl Musculus deltoideusKomplex Gl Musculus rectus abdominis Gl Musculus soleusKomplex Gl

x x

Nervi intercostales Gl Nervus abducens Gl Nervus accessorius Gl Nervus facialis Gl Nervus femoralis Gl Nervus glossopharyngeus Gl Nervus hypoglossus Gl Nervus ischiadicus Gl Nervus laryngeus recurrens Gl Nervus medianus Gl Nervus oculomotorius Gl Nervus opticus Gl Nervus peronaeus Gl Nervus phrenicus Gl Nervus pudendus Gl Nervus radialis Gl Nervus statoacusticus Gl Nervus tibialis Gl Nervus trigeminus Gl Nervus trochlearis Gl Nervus ulnaris Gl Nervus vagus Gl Nodi lymphatici Gl Nucleus ruber Gl

x x x x x x

Oesophagus Gl Ossicula auditus Gl Ovaria Gl

x x x

Pancreas Gl Papillae duodeni Gl Parametrium (dextrum) Gl

x x x

x x

x x x x x x x x x x x x x x x x x x

Preparation

Liqu. dil. for injection

Pars pallida Gl Patella Gl Penis Gl Pericardium Gl Periodontium Gl Periosteum Gl Peritonaeum Gl Pharynx Gl Pia mater encephali Gl Placenta (bovis) Gl Pleura Gl Plexus brachialis Gl Plexus cardiacus Gl Plexus coeliacus Gl Plexus gastricus Gl Plexus haemorrhoidalis Gl Plexus lumbalis Gl Plexus pelvinus Gl Plexus pulmonalis (Nervus vagus) Gl Plexus sacralis Gl Pons Gl Prostata Gl Pulmo Gl Pulpa dentis Gl Pylorus Gl

x x x x x x x x x x x x x x x x x x x

Rectum Gl Regio substantiae nigrae Gl Renes Gl Renes regio pyelorenalis Gl Reticuloendotheliales System Gl Retina et Chorioidea Gl

x x x x x

Sclera Gl

x

Sinus cavernosusKomplex Gl Sympathicus Gl

x

Tendo Gl

x

x x x x x x

x

x

Preparation

Liqu. dil. for injection

Testes Gl Thalamus Gl Thrombocyten Gl Thymus (Glandula) Gl Tonsilla pharyngea Gl Tonsillae palatinae Gl Trachea Gl Trigonum vesicae et Musculus sphincter Gl Truncus coeliacus Gl Tuba auditiva Gl Tuba uterina Gl Tunica mucosa intestini tenuis Gl Tunica mucosa nasi Gl Tunica mucosa recti Gl Tunica mucosa ventriculi Gl

x x x x x x x x

Ureter Gl Urethra feminina Gl Urethra masculina Gl Uterus Gl

x x x x

Vagina Gl Vaginae synoviales tendinum Gl Valva trunci pulmonalis Gl Valvula aortae Gl Valvula mitralis Gl Valvula tricuspidalis Gl Vena cava Gl Vena femoralis Gl Vena portae Gl Vena saphena magna Gl Ventriculus Gl Vertebra cervicalis Gl Vertebra coccygea Gl Vertebra lumbalis Gl Vesica fellea Gl Vesica urinaria Gl

x x

x x x x x x x

x x x x x x x x x x x x x x 653

Further Preparations for Internal Use Bitter Elixier Enzian Magentonikum Nierentonikum Passiflora Nerventonikum Plantago Hustensaft Akne-Kapseln Bolus alba comp. Pulver Chelidonium Kapseln Juniperus/Berberis comp., Kapseln Nervennahrung

18 ml, 180 ml 18 ml, 100 ml 180 ml , 450 ml 90 ml, 180 ml 90 ml (N1) 100 capsules (N1) 50 g (N1) 30 capsules (N1) 90 capsules (N1) 30 capsules (N1) 90 capsules (N1) 240 g

Eye Drops

Suppositories

Ointments

Package sizes: 5 single-dose containers (N1) x 0.5 ml 30 single-dose containers (N2) x 0.5 ml

Package size: 10 suppositories x 2 g (N1)

Package sizes: 10 g (N1), 30 g (N1), 100 g (N2)

Aconitum/China comp., Suppositorien Ammi visnaga comp., Suppositorien Belladonna comp., Suppositorien Cartilago comp., Suppositorien Carum carvi Zäpfchen Disci/Pulsatilla comp. cum Stanno, Suppositorien Disci/Viscum comp. cum Argento, Suppositorien Echinacea/Mercurius comp., Suppositorien Mercurialis comp., Suppositorien Passiflora Zäpfchen Quercus Hämorrhoidalzäpfchen Senecio comp., Suppositorien Silicea comp., Suppositorien

Arnika Salbe 30 g, 100 g Aurum comp., Unguentum 30 g Calcea Wund- und Heilcreme 10 g, 30 g, 100 g Camphora/Hypericum, Unguentum 30 g Cartilago comp., Unguentum 30 g, 100 g Cartilago/Mandragora comp., 30 g, 100 g Unguentum Cera/Aesculus comp., Unguentum 30 g, 100 g Colchicum comp., Unguentum 30 g Cuprum/Nicotiana, Unguentum 30 g Cuprum/Quarz comp., Unguentum 30 g, 100 g Disci comp. cum Pulsatilla, 30 g Unguentum Disci/Viscum comp. cum Stanno, 30 g, 100 g Unguentum Kupfer Salbe rot 30 g, 100 g Mercurialis Salbe 30 g, 100 g Nasenbalsam 10 g Nasenbalsam für Kinder 10 g Plantago Bronchialbalsam 30 g, 100 g Quercus Salbe 30 g, 100 g Rhus toxicodendron Salbe 30 g Rosatum Heilsalbe 30 g, 100 g Solum Salbe 30 g Viscum Mali e planta tota 3%, 30 g Unguentum

Belladonna e fructibus Augentropfen Belladonna ex herba Augentropfen Chelidonium comp. Augentropfen Cornea Levisticum comp. Augentropfen Echinacea Augentropfen Echinacea Quarz comp. Augentropfen Euphrasia Augentropfen Hornerz Corpus vitreum comp. Augentropfen Iris Lens comp. Augentropfen Lens Viscum comp. Augentropfen Mercurialis Augentropfen Nervus opticus comp. Augentropfen

Paediatric Suppositories

Ear Drops

Package size: 10 suppositories x 1 g (N1) Package size: 10 ml (N1) Aconit Ohrentropfen Levisticum Ohrentropfen

654

in arachis oil in olive oil

Aconitum/China comp., Suppositorien für Kinder Ammi visnaga comp., Suppositorien für Kinder Belladonna comp., Suppositorien für Kinder Carum carvi Kinderzäpfchen Echinacea/Mercurius comp., Suppositorien für Kinder Passiflora Kinderzäpfchen Silicea comp., Suppositorien für Kinder

655

Gels Package sizes:

30 g (N1), 100 g (N2)

Disci comp. cum Aesculo, Gelatum Echinacea/Viscum comp., Gelatum Majorana Vaginalgel Mundbalsam Narben Gel Rosmarinus/Prunus comp., Gelatum Silicea colloidalis comp., Gelatum Wund- und Brandgel

30 g 30 g 30 g, 100 g 10 g, 30 g 30 g 30 g 30 g 30 g

Oils for Embrocations and Massages

Dispersion Bath Oils

Package sizes: 50 ml (N1), 100 ml (N2), 500 ml (N3)

in olive oil

in arachis oil Aconit Schmerzöl Birken Rheumaöl mit Arnika Birken Rheumaöl ohne Arnika Hypericum ex herba 5%, Oleum Kampfer Johanniskrautöl Malvenöl Melissenöl Primula Muskelnähröl in almond oil Oleum Petrae comp in olive oil Solum Öl

50, 100 ml 50, 100 ml 100 ml 50, 100 ml 100 ml 50, 100 ml 50, 100 ml 100 ml

100 ml

50, 100, 500 ml

Aconitum e tubere W 5%, Oleum Aesculus e semine W 5%, Oleum Arnica e floribus W 5%, Oleum Betula e foliis W 5%, Oleum Calendula e floribus W 10%, Oleum Camphora 5%, Oleum Chamomilla e floribus W 10%, Oleum Citrus, Oleum aethereum 10% Equisetum ex herba W 5%, Oleum Eucalyptus, Oleum aethereum 10% Lavandula, Oleum aethereum 10% Levisticum e radice W 5%, Oleum Melissa ex herba W 5%, Oleum Oxalis e planta tota W 10%, Oleum Pinus pumilio, Oleum aethereum 10% Prunus spinosa e floribus W 5%, Oleum Rheuma-Badeöl Rosa e floribus 10%, Oleum Rosmarinus, Oleum aethereum 10% Thymus, Oleum aethereum 5% Urtica dioica ex herba W 5%, Oleum Viscum Mali ex herba W 5%, Oleum

656

Preparations for Compresses, Lavages, Baths 50 ml (N1) 100 ml (N1) 100 ml 100 ml (N1) 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml 100 ml (N1) 100 ml 100 ml (N1) 100 ml 100 ml 100 ml

Aesculus-Essenz Aesculus/Prunus comp., Essenz Akne-Gesichtsdampfbad Akne-Gesichtsmaske Akne-Wasser Arnika Essenz Arnika Wundtuch Borago-Essenz Brandessenz Calendula-Essenz Echinacea-Essenz Echinacea Mund- und Rachenspray Equisetum-Essenz Hamamelis-Essenz Mundbalsam flüssig Oxalis-Essenz Prunus-Essenz Quercus-Essenz Resina laricis-Bademilch Solum Badezusatz Thuja-Essenz

100 ml (N1) 100 ml (N1) 100 ml (N1) 100 ml (N1) 100 ml (N1) 100 ml 5 pieces 100 ml (N1) 100 ml (N1) 100 ml (N1) 500 ml (N3) 100 ml (N1) 50 ml (N1) 100 ml (N1) 100 ml (N1) 50 ml (N2) 100 ml (N1) 100 ml (N1) 100 ml (N1) 100 ml (N1) 500 ml (N3) 100 ml (N1) 500 ml (N3) 100 ml (N1)

657

WALA Medicinal Products Available by Prescription Only under Art. 48 of the German Medicines Act (AMG)

WALA Medicinal Products for General Sale

Aconitum e tubere W 5% Ammi visnaga comp. Ammi visnaga comp

Arnica e floribus W 5%, Oleum Arnika Essenz Arnika Wundtuch Bitter Elixier Calendula e floribus W 10%, Oleum Chamomilla e floribus W 10%, Oleum Citrus, Oleum aetheroleum 10% Eucalyptus, Oleum aetheroleum 10% Lavandula, Oleum aetheroleum 10% Levisticum e radice W 5%, Oleum Melissa ex herba W 5%, Oleum Nervennahrung

Colchicum comp Colchicum comp. Unguentum Conchae comp. Gelsemium comp. Mandragora officinarum e radice D2 Mandragora officinarum e radice D3 Strophanthus kombe e semine D3 Veratrum comp.

658

Oil Suppositories Paediatric suppositories Liqu. dil. f. inj. Ointment Liqu. dil. f. inj. Liqu. dil. f. inj. Liqu. dil. f. inj. Liqu. dil. f. inj. Liqu. dil. f. inj. Liqu. dil. f. inj.

Liquid bath additive Essence Wet wipe Syrup Liquid bath additive Liquid bath additive Liquid bath additive Liquid bath additive Liquid bath additive Liquid bath additive Liquid bath additive Medicinal honey Oxalis e planta tota W 10%, Liquid bath Oleum additive Pinus pumilio, Oleum Liquid bath aetheroleum 10% additive Prunus spinosa e floribus W 5%, Liquid bath Oleum additive Rheuma Badeöl Liquid bath additive Rosa e floribus 10%, Liquid bath Oleum additive Thymus, Liquid bath Oleum aetheroleum 5% additive Urtica dioica ex herba W 5%, Liquid bath Oleum additive Viscum Mali ex herba W 5%, Liquid bath Oleum additive

659

WALA Medicinal Products Contraindicated During Pregnancy and Breastfeeding

Medicinal product

Contraindicated during pregnancy

Contraindicated while breastfeeding

Toxicologically relevant

Medicinal product

Echinacea Mund- und Rachenspray

x

Enzian Magentonikum

x

x

Acorus calamus

Juniperus/Berberis comp., Kapseln

x

x

Acorus calamus, Juniperus communis

Kampfer Johanniskrautöl

x

x

Camphor

Myristica sebifera comp.

x

x

Kalium bichromicum (potassium dichromate)

Nierentonikum

x

Passiflora Zäpfchen

x

x

Valeriana officinalis

Salix/Rhus comp.

x

x

Dryopteris filix-mas, Pteridium aquilinum

Salix/Rhus comp.

x

x

Dryopteris filix-mas, Pteridium aquilinum

Solum Badezusatz

x

Symphytum e radice D2

x

Akne-Gesichtsdampfbad

x

x

Tropaeolum majus (benzyl isothiocyanate)

Akne-Kapseln

x

x

Juniperus communis, Rhamnus frangula

Aquilinum comp.

x

x

Dryopteris filix-mas, Pteridium aquilinum

Aquilinum comp.

x

x

See Injection

Arnica e floribus W 5%, Oleum

x

Arnika Essenz

x

Arnika Wundtuch

x

Bitter Elixier

x

Camphora/Hypericum, Unguentum

x

Tincture for external use Hard capsules

Liquid dilution for injection Globuli velati

Arnica flowers

x

Toxicologically relevant

Sage oil

Spray for application to the oral cavity Liquid for internal use

Soft capsules

Arnica flowers

Liquid dilution for injection

Arnica flowers

Syrup

x

Acorus calamus

Suppositories

x

Camphor

Liquid dilution for injection

Tincture for external use Wet wipes Syrup

Ointment

x

x

Citrullus colocynthis

Soft capsules

Chelidonium/Colocynthis

Contraindicated while breastfeeding

Oily embrocation

Liquid bath additive

Chelidonium Kapseln

Contraindicated during pregnancy

x

x

Citrullus colocynthis

Globuli velati

Juniperus communis

Globuli velati

Possible bacterial contamination of the peat extract

Liquid bath additive

x

Pyrrolizidine alkaloids

Colchicum comp.

x

x

Colchicine

Liquid dilution for injection

Colchicum comp.

x

x

Colchicine

Tincture for external use

Colchicum comp., Unguentum

x

x

Colchicine

Veratrum e radice D4

x

x

Alkaloids

Cuprum/Quarz comp., Unguentum

x

x

Rosemary oil (cineole, camphor)

Veratrum e radice D3 und D4

x

x

Alkaloids

Globuli velati

Globuli velati

Thuja-Essenz

Liquid dilution for injection Ointment

Contraindicated Contraindicated Thuja occidentalis (thujone) for use on mufor use on mucous membranes cous membranes

Liquid dilution for injection

Ointment

660

661

WALA Medicinal Products Contraindicated in Children

Medicinal product

Contraindicated Reason in children under

Medicinal product

Contraindicated Reason in children under

Aconit Schmerzöl

6 years

Eucalyptus, Oleum aethereum 10%

2 years

Essential oils: eucalyptus oil (cineole)

Akne-Kapseln

10 years

Juniperus communis, Rhamnus frangula

Juniperus/Berberis comp.,Kapseln

12 years

Acorus calamus (ß-asarone)

Echinacea pallida

Kampfer Johanniskrautöl

2 years

Camphor

Symphytum officinale (pyrrolizidine alkaloids)

Majorana Vaginalgel

6 years

Origanum majorana (arbutin, hydroquinone)

Contraindicated on account of the severity of the primary condition

Melissenöl

6 years

Origanum majorana (arbutin, hydroquinone)

Contraindicated on account of the severity of the primary condition

Mundbalsam

2 years

Essential oils: peppermint oil (menthol)

Contraindicated on account of the severity of the primary condition

Nasenbalsam

2 years

Essential oils: eucalyptus oil (cineole), cajeput oil

Camphor

Oleum camphoratum comp.

12 years

Camphor

Oleum Petrae comp.

12 years

Camphor

Plantago Bronchialbalsam

2 years

Camphor, essential oils: eucalyptus oil (cineole)

Resina laricis-Bademilch

6 years

Terebinthina laricina

Essential oils: rosemary oil (cineole, camphor)

Salix/Rhus comp.

4 years

Dryopteris filix-mas

Echinacea pallida

Salix/Rhus comp.

4 years

Dryopteris filix-mas

Thuja-Essenz

Tincture for external use

Essential oils: rosemary oil (cineole, camphor), thyme oil; terebinthina laricina

12 years for appli- Thuja occidentalis (thujone) cation to mucous membranes

Veratrum e radice D3

6 years

Alkaloids

Acorus calamus (ß-asarone)

Veratrum e radice D4

6 years

Alkaloids

Camphor

Oily embrocation

Bath additive, liquid

Hard capsules

Argentum nitricum comp.

2 years

Liquid dilution for injection

Arnika Salbe

Oily embrocation

1 year

Ointment

Birken Rheumaöl mit Arnika

2 years

Oily embrocation

Birken Rheumaöl ohne Arnika

2 years

Oily embrocation

Bryonia/Stannum

6 years

Liquid dilution for injection

Camphora 5%, Oleum

2 years

Bath additive, liquid

Camphora/Hypericum, Unguentum

7 years

Camphor

2 years

Chelidonium majus

12 years

Colchicine

2 years 1 year

Globuli velati

Echinacea Mund- und Rachenspray

4 years 2 years

Gel

Enzian Magentonikum

Liquid to be taken internally

662

Liquid dilution for injection Globuli velati

Echinacea pallida

Spray for application to the oral cavity

Echinacea/Viscum comp., Gelatum

Ointment

Liquid for external use

Ointment

Echinacea e planta tota D6

Gel

Ointment

Ointment

Cuprum/Quarz comp., Unguentum

Oily embrocation

Oily embrocation

Globuli velati

Colchicum comp., Unguentum

Gel

Oily solution for injection

Ointment

Chelidonium/Colocynthis

Soft capsules

12 years

Globuli velati

Liquid dilution for injection

663

Compendium of Medicines Cat. No.: 410 000 136 / 1H Translation of the 31st German edition from September 2009 © 2011 WALA Heilmittel GmbH PO Box 1121 73085 Bad Boll/Eckwälden Germany Phone: +49 (0)7164 930-0 Fax: +49 (0)7164 930-297 [email protected] www.wala.de www.walaarzneimittel.de www.dr.hauschka.de www.dr.hauschka-med.de Translated by Hilary Coleman Revised and proofread by Angela Stintzing, Agnes Mitzakoff Typeset by submedia, fresh media solutions; Stuttgart www.submedia.de Printed by RöslerDruck GmbH; Schorndorf www.roeslerdruck.de

WALA®, WALA® Logo, viaWALA®, Dr.Hauschka®, Dr.Hauschka Med ®, Dr.Hauschka CulturCosmetic®, CulturCosmetic® and Dr.Hauschka Design are registered trade marks of the company WALA Heilmittel GmbH.

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