All information in the following is based on the German SPC. Information and availability may differ from country to country.
Sinupret® extract, Sinupret® forte, Sinupret®, Sinupret® Saft, Sinupret® Tropfen
Composition:
1 coated tablet of Sinupret extract contains as medicinally active ingredients: 160.00 mg dry extract (3-6:1) from gentian root; primrose blossoms; dock herb; elderflowers; Verbena (1:3:3:3:3). 1. Extracting agent: ethanol 51% (m/m).
Excipients: Glucose syrup 3.141 mg; Sucrose 133,736 mg; Maltodextrin 34,000 mg; Spray-dried Arabian gum; calcium carbonate; carnauba wax; Cellulose powder; microcrystalline cellulose; Chlorophyll powder 25% (E 140); dextrin (from corn starch); Hypromellose; indigo carmine; aluminium salt (E 132); Magnesium Stearate (Ph.Eur.) [vegetable]; riboflavin (E 101); highly dispersed silicon dioxide; highly dispersed hydrophobic silica; Stearic acid; Talc; Titanium dioxide (E 171).
1 coated tablet of Sinupret forte contains as medicinally active ingredients: verbena, powdered 36 mg; Gentian root, powdered 12 mg; garden sorrel, powdered 36 mg; Elderflower, powdered 36 mg; Primrose flowers with calyx, powdered 36 mg.
Excipients: Glucose syrup 2,750 mg; Lactose monohydrate 48,490 mg; sucrose (sucrose) 123,816 mg; Sorbitol 0.444 mg; calcium carbonate (E 170); Chlorophyll powder 25% (E 141); dextrin; Eudragite E 12.5; Gelatin; Indigo carmine, E 132, aluminium hydroxide; potato starch; corn starch; light magnesium oxide; Montan glycol wax; riboflavin (E 101); refined castor oil; shellac; highly dispersed silicon dioxide; Stearic acid; Talc; Titanium dioxide (E 171).
1 coated tablet of Sinupret contains as medicinally active ingredients: verbena, powdered 18 mg; Gentian root, powdered 6 mg; garden sorrel, powdered 18 mg; Elderflower, powdered 18 mg; Cowslip flowers with calyx, powdered 18 mg.
Other ingredients: glucose syrup 1.375 mg; Lactose monohydrate 24.245 mg; Sucrose (sucrose) 61,908 mg; Sorbitol 0.222 mg; calcium carbonate (E 170); Chlorophyll powder 25% (E 141); dextrin; Eudragite E 12.5; Gelatin; Indigo carmine, E 132, aluminium hydroxide; potato starch; corn starch; light magnesium oxide; Montan glycol wax; riboflavin (E 101); refined castor oil; shellac; highly dispersed silicon dioxide; Stearic acid; Talc; Titanium dioxide (E 171).
100 ml (120.8 g) Sinupret juice contains 41.7 g of an extract (1:38.5) of 1.1 g of a mixture of gentian root, verbena, sorrel, elderflower, primrose flowers with calyx (1:3:3:3); 1. Extracting agent: ethanol 59% (V/V), 2.–4. Extracting agent: purified water.
Excipients with known effect: Maltitol solution 78.8 g
This medicine contains 450 mg of alcohol (ethanol) per 7 ml, corresponding to 64 mg/ml.
100 g Sinupret drops contain 29 g extract (drug/extract ratio 1:11) from gentian root, cut; Verbena, sliced; garden sorrel, sliced; elderflowers, rubbed; primrose flowers with calyx, cut; (1:3:3:3:3); Extracting agent: ethanol 59% (V/V). Excipient with known effect: This medicine contains 456 mg of alcohol (ethanol) per 50 drops, corresponding to 152 mg/ml.
Indications:
Sinupret extract: For acute, uncomplicated inflammation of the paranasal sinuses (acute, uncomplicated rhinosinusitis). Sinupret extract is used in adults and adolescents from 12 years of age.
Sinupret forte, Sinupret, Sinupret drops: For acute and chronic inflammation of the paranasal sinuses. Sinupret drops are used in children from 2 years of age, adolescents and adults.
Sinupret Juice: To improve the symptoms of acute inflammation of the paranasal sinuses. Sinupret juice is used in children from 2 years of age, adolescents and adults.
Contraindications:
Sinupret extract: Hypersensitivity to the active ingredient or any of the above-mentioned excipients. Gastric and/or duodenal ulcer. Not for use in children under 12 years of age. No use during pregnancy and breastfeeding. Patients with the rare hereditary fructose intolerance, glucose-galactose malabsorption, or sucrase-isomaltase deficiency should not take Sinupret extract.
Sinupret forte, Sinupret, Sinupret drops, Sinupret juice: Do not take if you have known hypersensitivity to any of the active ingredients or other ingredients.
Sinupret forte, Sinupret: Patients with the rare hereditary fructose intolerance, galactose intolerance, lactase deficiency, glucose-galactose malabsorption, or sucrase-isomaltase deficiency should not take Sinupret forte and Sinupret.
Sinupret forte: Not for use in children under 12 years of age.
Sinupret: Do not use in children under 6 years of age.
Sinupret Drops: Do not use in children under 2 years of age.
Sinupret Juice: Not for use in children under 2 years of age. Patients with the rare hereditary fructose intolerance should not take Sinupret juice.
Sinupret extract, Sinupret drops, Sinupret juice: Patients with a sensitive stomach or known stomach inflammation require special care when taking Sinupret juice. Sinupret juice is best taken after meals and with a glass of water.
Sinupret forte, Sinupret, Sinupret drops, Sinupret juice: Use during pregnancy and breastfeeding only after strict indications.
Side effects:
Sinupret extract: Common gastrointestinal complaints (e.g. nausea, flatulence, diarrhea, dry mouth, stomach pain). Occasionally, local hypersensitivity reactions of the skin (rash, redness, itching), systemic allergic reactions (angioedema, shortness of breath, facial swelling) and dizziness.
Sinupret forte, Sinupret: Occasionally gastrointestinal complaints (including stomach pain, nausea). Rarely, hypersensitivity reactions of the skin (rash, redness of the skin, itching) as well as severe allergic reactions (angioedema, shortness of breath, facial swelling).
Sinupret Drops, Sinupret Juice: Occasionally gastrointestinal complaints such as stomach pain, nausea, as well as hypersensitivity reactions of the skin such as rash, redness, itching. Severe allergic reactions such as angioedema, facial swelling, shortness of breath. Frequency not known.
Warnings:
Sinupret forte, Sinupret, Sinupret juice, Sinupret drops: Like all medicines, use during pregnancy and breastfeeding only after strict indications.
Sinupret drops: This medicine contains 456 mg of alcohol (ethanol) per 50 drops, corresponding to 152 mg/ml.
Sinupret Juice: This medicine contains maltitol solution and 450 mg of alcohol (ethanol) per 7 ml, equivalent to 64 mg/ml.
BIONORICA SE | 92308 Neumarkt
Co-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt Stand 03|24
Bronchipret® Juice TE, Bronchipret® Drops, Bronchipret® TP Film-coated Tablet, Bronchipret® Thyme Pastilles
Composition:
100 ml (equivalent to 112 g) Bronchipret juice TE contains: 16.8 g fluid extract of thyme herb (1 : 2 – 2.5); Extracting agent: ammonia solution 10 % (m/m): glycerol 85 % (m/m): ethanol 90 % (V/V): water (1 : 20 : 70 : 109); 1.68 g Ivy leaf fluid extract (1:1); Extracting agent: ethanol 70% (V/V). Excipients with known effect: This medicinal product contains 300 mg of alcohol (ethanol) per 5.4 ml corresponding to 56 mg/ml and 2.3 g of maltitol solution per 5.4 ml. Other ingredients: citric acid monohydrate, purified water, hydroxypropylbetadex, potassium sorbate (Ph. Eur.).
1 ml (equivalent to 1 g) Bronchipret drops oral liquid contains: 0.5 ml fluid extract of thyme herb (1 : 2 – 2.5), extracting agent: ammonia solution 10 % (m/m) : glycerol 85 % (m/m) : ethanol 90 % (V/V) : water (1 : 20 : 70:109). 0.03 ml of ivy leaf extract (1:1), extracting agent: ethanol 70% (V/V). Excipients with known effect: This medicine contains 500 mg of alcohol (ethanol) per 2.6 ml, corresponding to 192 mg/ml. Other ingredients: citric acid monohydrate, ethanol 96% (V/V), purified water, hydroxypropyl betadex (MS: 0.65), saccharin sodium dihydrate.
1 Bronchipret TP film-coated tablet contains: 60 mg dry extract of primrose roots (6-7:1), extracting agent: ethanol 47.4% (V/V); 160 mg dry extract of thyme herb (6-10:1), extracting agent: ethanol 70% (V/V). Other ingredients: glucose syrup 34 mg, lactose monohydrate 50 mg,
chlorophyllin a – copper complex trisodium salt (E 141), crospovidone, dimethicone, highly dispersed silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, peppermint flavor, polyacrylate dispersion 30%, povidone K25, propylene glycol, riboflavin (E 101), saccharin sodium, talc, titanium dioxide (E 171).
1 Bronchipret Thyme Pastille contains: 42.0 mg Thyme Herb Dry Extract (6-10:1); Extracting agent: ethanol 70% (V/V). Other ingredients: Arabian gum, Betadex, glucose syrup 8.9 mg, blackcurrant flavour (contains propylene glycol E 1520), maltitol solution 376.2 mg, sodium cyclamate, low-viscosity paraffin, saccharin sodium, silicon dioxide, highly dispersed, wild berry flavour (contains propylene glycol E 1520).
Indications:
Bronchipret Juice TE: To improve the symptoms of acute bronchitis with cough and colds with viscous mucus. The medicine is used in children from one year of age, adolescents and adults.
Bronchipret TP film-coated tablet: To improve the symptoms of acute bronchitis with cough and colds with viscous mucus.
Bronchipret drops: To improve the symptoms of acute inflammatory bronchial diseases and acute inflammation of the respiratory tract with the accompanying symptom "cough with viscous mucus". The medicine is used in children from 6 years of age, adolescents and adults.
Bronchipret Thyme Pastilles: To improve the symptoms of colds of the respiratory tract with viscous mucus and bronchitis.
Contraindications:
Bronchipret Juice TE: Do not use in case of known hypersensitivity to ivy, plants of the Aralia family, thyme or other lamiaceae (mint family), birch, mugwort, celery or any of the other ingredients. Do not use during pregnancy and breastfeeding due to insufficient examinations and in children under one year of age. Patients with the rare hereditary fructose intolerance should not take Bronchipret Juice TE.
Bronchipret Drops: Do not use in case of known hypersensitivity to ivy, plants of the Aralia family, thyme or other lamiaceae (mint family), birch, mugwort, celery or any of the other ingredients of the medicine. Do not use during pregnancy and breastfeeding and in children under 6 years of age due to insufficient examinations.
Bronchipret TP film-coated tablet: Do not use in case of known hypersensitivity to the active ingredients or other mints (Lamiaceae), birch, mugwort, celery or any of the other ingredients. Do not use during pregnancy and breastfeeding and in children under 12 years of age due to insufficient examinations. Patients with the rare hereditary galactose intolerance, lactase deficiency or glucose-galactose malabsorption should not take Bronchipret TP.
Bronchipret Thyme Pastilles: Do not use in case of known hypersensitivity to thyme or other mints (Lamiaceae), birch, mugwort, celery or any of the other ingredients. Do not use in children under 6 years of age, during pregnancy and breastfeeding due to insufficient examinations. Patients with the rare hereditary fructose intolerance or glucose-galactose malabsorption should not take Bronchipret Thyme Pastilles.
Side effects:
Bronchipret juice TE: Occasionally gastrointestinal complaints such as cramps, nausea, vomiting. Rarely, hypersensitivity reactions with rashes. Hypersensitivity reactions with e.g. shortness of breath, hives and swelling of the face, mouth and/or throat are possible.
Bronchipret drops: Occasionally gastrointestinal complaints such as cramps, nausea, vomiting, diarrhea. Very rarely, hypersensitivity reactions, such as shortness of breath, rashes, hives and swelling of the face, mouth and/or throat.
Bronchipret TP film-coated tablet: Occasionally gastrointestinal complaints such as cramps, nausea, vomiting and diarrhea. Very rarely, hypersensitivity reactions, such as shortness of breath, rashes, hives, and swelling of the face, mouth, and/or throat.
Bronchipret Thyme Pastilles: Hypersensitivity reactions or allergic reactions of the skin and respiratory tract, such as shortness of breath, skin rashes, hives, as well as swelling of the face, mouth and/or throat (Quincke's edema) may occur. There may also be stomach and intestinal complaints such as cramps, nausea, vomiting. The frequency of these side effects is not known.
Warnings:
Bronchipret Juice TE contains maltitol solution as well as 300 mg alcohol (ethanol) per 5.4 ml corresponding to 56 mg/ml.
Bronchipret drops contain 500 mg of alcohol (ethanol) per 2.6 ml, corresponding to 192 mg/ml.
Bronchipret Thyme Pastilles contain propylene glycol, maltitol and glucose.
Bronchipret TP tablet contains glucose and lactose.
BIONORICA SE | 92308 NeumarktCo-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt
Booth: 09|25
Imupret® N Dragees, Imupret® N Drops
Composition:
1 coated tablet contains powdered drugs: marshmallow root 8 mg, oak bark 4 mg, chamomile flowers 6 mg, dandelion herb 4 mg, horsetail herb 10 mg, yarrow herb 4 mg, walnut leaves 12 mg. Other ingredients: glucose monohydrate, glucose syrup, lactose monohydrate, corn starch, potato starch, silicon dioxide (highly dispersed), stearic acid (vegetable), calcium carbonate, virgin castor oil, dextrin, montan glycol wax povidone (K25, K30), sucrose, shellac (wax-free), silicon dioxide (highly dispersed), talc. 100 ml of liquid contains: 100 ml extract (1:38) of 2.6 g of a mixture of marshmallow root, oak bark, chamomile flowers, dandelion herb, horsetail herb, yarrow herb and walnut leaves (4:2:3:4:5:4:4); Ethanol 59% (V/V). Excipient with known effect This medicinal product contains 210 mg of alcohol (ethanol) per 25 drops, equivalent to 152 mg/ml.
Indications:
Traditionally used at the first signs and during a cold, e.g. scratchy throat, sore throat, difficulty swallowing, coughing. Note: Imupret® N is a traditional herbal medicine that is registered for the indication only on the basis of many years of use. Imupret® N Dragees is used in children from 6 years of age, adolescents and adults. Imupret® N drops are used in children from 2 years of age, adolescents and adults.
Contraindications:
Do not use in case of known hypersensitivity to the active ingredients, to composite plants (e.g. mugwort, yarrow, chrysanthemum, margarite due to cross-allergies to active ingredients) due to so-called cross-reactions to chamomile flowers or any of the other ingredients. Pregnant and breastfeeding women are not recommended to take it because there are no data on its use. Coated tablets: Do not use in children under 6 years of age. Patients with the rare hereditary galactose intolerance, fructose intolerance, lactase deficiency, glucose-galactose malabsorption, or sucrase-isomaltase deficiency should not take Imupret® N coated tablets. Drops: Not for use in children under 2 years of age.
Side effects:
Rarely, allergic reactions (e.g., rash, urticaria) and gastrointestinal disorders may occur (≥ 1/10,000 to < 1/1,000).
Warnings:
The user should consult a doctor or other qualified person working in a health care profession if symptoms persist or if side effects other than those mentioned in the package leaflet occur. Dragees: Contains glucose, lactose, sucrose. Drops: This medicine contains 210 mg of alcohol (ethanol) per 25 drops, corresponding to 152 mg/ml.
BIONORICA SE | 92308 Neumarkt Stand: 08|24Co-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt
Tonsipret® Tableten, Tonsipret® Tropfen
Composition:
1 tablet contains: Capsicum annuum Dil. D3 75.0 mg; Guaiacum Dil. D3 75.0 mg; Phytolacca americana Æ 50.0 mg. Other ingredients: lactose monohydrate 250.0 mg, potato starch, magnesium stearate (Ph. Eur.) [vegetable].
10 g (= 10.9 ml) drops contain: Capsicum annuum Dil. D4 4.0 g; Guaiacum Dil. D4 4.0 g; Phytolacca americana Dil. D1 2.0 g. Excipient with known effect: This medicinal product contains 114 mg of alcohol (ethanol) per 5 drops, corresponding to 440 mg/ml.
Areas of application:
Homeopathic medicine for inflammatory diseases of the throat. The areas of application are derived from the homeopathic remedy pictures. These include: Acute throat and tonsillitis (tonsillitis).
Contraindications:
Do not use during pregnancy and breastfeeding. The drugs should not be used in children under one year of age because there is no sufficiently documented experience. In case of hypersensitivity to the active ingredients or any of the excipients. Tablets: Patients with the rare hereditary galactose intolerance, lactase deficiency or glucose-galactose malabsorption should not take Tonsipret tablets.
Side effects:
In rare cases, nausea and stomach discomfort, very rarely allergic skin reactions. When taking a homeopathic medicine, the existing symptoms may temporarily worsen (initial aggravation).
Warnings:
Drops: Tonsipret® drops contain 114 mg of alcohol (ethanol) per 5 drops, corresponding to 440 mg/ml.
BIONORICA SE | 92308 NeumarktCo-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt
Booth: 02|24
Canephron® Uno, Canephron® N Dragees, Canephron® N Drops
Composition:
Canephron® Uno Active ingredients: 1 coated tablet contains: Tagaury powder (Centaurium erythraea Rafin s.l., herba) 36 mg, lovage root powder (Levisticum officinale Koch, radix) 36 mg, rosemary leaf powder (Rosmarinus officinalis L., folium) 36 mg.
Canephron® N Dragees Active ingredients: 1 coated tablet contains: Centaury powder 18 mg, lovage root powder 18 mg, rosemary leaf powder 18 mg. Other ingredients Canephron® Uno / Canephron® N Dragees: lactose monohydrate, magnesium stearate (Ph. Eur.) [vegetable], corn starch, povidone K 25, silicon dioxide (highly dispersed), calcium carbonate, virgin castor oil, iron(III) oxide (E172), dextrin (from corn starch), glucose syrup, montan glycol wax, povidone K 30, sucrose (sucrose), shellac (wax-free), riboflavin (E101), talc, titanium dioxide (E171).
Canephron® N drops Active ingredients: 100 ml (=98 g) oral liquid contains an extract (1:56) of 1.8 g of a mixture of rosemary leaves, lovage root and centaury (1:1:1); 1. AZM: ethanol 59% (V/V), 2.–4. AZM: purified water. Excipients with known effect: This medicine contains 760 mg of alcohol (ethanol) per 5.0 ml, corresponding to 152 mg/ml (19% V/V).
Indications:
Canephron® Uno: Traditional herbal medicine for the supportive treatment and supplementation of specific measures for minor complaints (such as frequent urination, burning during urination and increased urination) in the context of inflammatory diseases of the urinary tract.
Canephrone® N: Traditionally used as a supportive treatment and to supplement specific measures for mild symptoms associated with inflammatory diseases of the urinary tract.
Canephron® Uno, Canephron® N: For flushing the urinary tract to reduce the deposition of kidney semolina. Canephron® N drops is used in adolescents from 12 years of age and adults.
Note: Canephron® Uno and Canephron® N are traditional herbal medicines that are registered for the indication solely on the basis of many years of use.
Contraindications:
Canephron® Uno, Canephron® N: Do not use in case of hypersensitivity to the active ingredients, to other apiaceae (e.g. anise, fennel), to anethol (component of essential oils) or any of the excipients, in children under 12 years of age, during breastfeeding and in cases of rare hereditary fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase deficiency, galactose intolerance or lactase deficiency; none Irrigation therapy for oedema due to impaired heart or kidney function and/or when reduced fluid intake has been recommended.
Canephron® Uno: Not used for peptic ulcer;
Canephrone® N: No use for stomach ulcers.
Canephron® N drops: No use during pregnancy.
WARNINGS:
Canephron® N Dragees and Canephron® Uno contain glucose, sucrose (sugar), lactose. Canephron® N drops contain 760 mg of alcohol (ethanol) per 5.0 ml, corresponding to 152 mg/ml (19% V/V).
Side effects:
Canephron® Uno, Canephron® N: Common gastrointestinal complaints (e.g. nausea, vomiting, diarrhea).
Canephron® Uno: Hypersensitivity reactions (rash, itching, facial edema), frequency not known.
Canephrone® N: Allergic reactions, frequency not known.
BIONORICA SE | 92308 Neumarkt
Co-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt Stand: 02|24
Agnucaston® 20 mg film-coated tablets, Agnucaston® film-coated tablets
Active ingredient:
Dry extract of monk's pepper fruits
Composition:
Agnucaston® 20 mg film-coated tablets Active ingredient: 1 film-coated tablet contains: 20.0 mg dry extract of monk's pepper fruit (7–11:1), extracting agent: ethanol 70% (V/V). Other ingredients: povidone 30, highly dispersed silicon dioxide, potato starch, lactose monohydrate (50 mg), microcrystalline cellulose, croscarmellose sodium, magnesium stearate (Ph. Eur.) [vegetable], Opadry amb II (consisting of polyvinyl alcohol, talc, titanium dioxide (E 171), glycerol monocaprylocaprate and sodium dodecyl sulfate).
Agnucaston® film-coated tablets: 1 film-coated tablet contains: 4.0 mg chasteberry dry extract (7–11:1), extracting agent: ethanol 70% (V/V). Other ingredients: lactose monohydrate 25.0 mg, ammonium methacrylate copolymer (type A), iron(III) oxide (E 172), indigo carmine (E 132) aluminum salt, potato starch, magnesium stearate (Ph.Eur.)[vegetable], macrogol 6000, microcrystalline cellulose, povidone (30), highly dispersed silicon dioxide, talc, titanium dioxide (E 171).
Indications:
Agnucastone® 20 mg film-coated tablets: Herbal medicine for the treatment of premenstrual syndrome in women aged 18 years and older.
Agnucaston® film-coated tablets: menstrual tempo abnormalities, premenstrual syndrome, mastodynia.
Contraindications:
Agnucastone® 20 mg: film-coated tablets In case of hypersensitivity to the active ingredient or any of the excipients. Patients with rare hereditary galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine. Its use during pregnancy is not recommended because there are no data. Use during breastfeeding is not recommended, as study data indicate an influence on milk production. No use in children and adolescents under 18 years of age due to lack of sufficiently documented experience.
Agnucaston® film-coated tablets: In case of hypersensitivity to the active ingredient or any of the other ingredients. Patients with the rare hereditary galactose intolerance, lactase deficiency or glucose-galactose malabsorption should not take Agnucastone® film-coated tablets. Do not take during pregnancy as there is insufficient experience. Agnucastone® should not be used during breastfeeding, as the study data indicate an influence on milk production. No use in children and adolescents under 18 years of age due to lack of sufficiently documented experience.
Side effects:
Agnucastone® 20 mg film-coated tablets: Severe allergic reactions with facial swelling, dyspnea and difficulty swallowing, headache, dizziness, gastrointestinal disorders (such as nausea, abdominal pain), allergic skin reactions (such as rash and hives), acne and menstrual irregularities. There is no information on the frequency of occurrence of these possible side effects.
Agnucaston® film-coated tablets: Severe allergic reactions with facial swelling, shortness of breath and difficulty swallowing have been reported. (allergic) Skin reactions (e.g. rash, urticaria), headaches, dizziness, gastrointestinal complaints (e.g. nausea, abdominal pain), acne and cycle irregularities can occur. There is no information on the frequency of occurrence of these possible side effects. At the first sign of a hypersensitivity reaction, Agnucastone® should not be taken again.
Warnings: Contains lactose
BIONORICA SE | 92308 Neumarkt
Co-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt Stand: 03|25
Mastodynone® Homeopathic Blend, Tablets
Composition:
10 g (10.8 ml) Mixture contains: 2.0 g Agnus castus Ø; 1.0 g Caulophyllum thalictroides Dil. D4; 1.0 g Cyclamen Dil. D4; 1.0 g Ignatia Dil. D6; 2.0 g Iris Dil. D2; 1.0 g Lilium tigrinum Dil. D3. Excipient with known effect: This medicine contains 390 mg of alcohol (ethanol) per 30 drops, corresponding to 420 mg/ml.
1 tablet contains: 162.0 mg Agnus castus Ø; 81.0 mg Caulophyllum thalictroides dil. D4; 81.0 mg Cyclamen Dil. D4; 81.0 mg Ignatia Dil. D6; 162.0 mg Iris Dil. D2; 81.0 mg Lilium tigrinum Dil. D3. Other ingredients: lactose monohydrate, potato starch, magnesium stearate (Ph. Eur.).
Indications:
Homeopathic medicine for gynaecology. The areas of application are derived from the homeopathic remedy pictures. These include: pre-period bleeding symptoms such as a feeling of tightness and swelling in the breasts (mastodynia), discomfort during period bleeding and irregular period bleeding (menstrual cycle disorders). In the event of persistent, unclear or recurring symptoms, a doctor should be consulted, as it may be a disease that requires medical treatment.
Contraindications:
Hypersensitivity to the active ingredients or any of the excipients. Patients with the rare hereditary galactose intolerance, lactase deficiency or glucose-galactose malabsorption should not take mastodynon® tablets. Do not take under 18 years of age and during pregnancy. Intake during breastfeeding is not recommended, as the study data indicate an influence on milk production.
Side effects: Severe allergic reactions with facial swelling, shortness of breath and difficulty swallowing have been reported. (allergic) Skin reactions (e.g. rash, urticaria), headaches, dizziness, gastrointestinal complaints (e.g. nausea, abdominal pain), acne and cycle irregularities can occur. There is no information on the frequency of occurrence of these possible side effects. At the first signs of a hypersensitivity reaction, mastodynolone® should not be taken again.
Warnings:
Mixture: This medicine contains 390 mg of alcohol (ethanol) per 30 drops, corresponding to 420 mg/ml.
Tablets: Contain lactose.
BIONORICA SE | 92308 Neumarkt
Co-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt Stand: 08|24
Klimadynon® film-coated tablets
Active ingredient:
dry extract of Cimicifuga rootstock.
Composition:
1 film-coated tablet Klimadynon® contains: 2.8 mg dry extract of Cimicifuga rootstock
(Cimicifuga racemosa (L.) Nutt., rhizoma) (5–10:1), extraction agent: ethanol 58% (V/V).
Other ingredients: lactose monohydrate 17.2 mg, calcium hydrogen phosphate dihydrate, ammonium methacrylate copolymer (type A) (Ph. Eur.), iron(III) oxide (E 172), iron(III) hydroxide oxide × H2O (E 172), macrogol 6000, magnesium stearate (Ph. Eur.) [vegetable], potato starch, talc, sodium hydroxide, sorbic acid (Ph. Eur.), titanium dioxide (E 171).
Areas of application:
Herbal medicine used to relieve menopausal symptoms such as hot flashes and excessive sweating.
Contraindications:
Hypersensitivity to the active ingredient or any of the excipients. Patients with the rare hereditary galactose intolerance, absolute lactase deficiency or glucose-galactose malabsorption should not take Klimadynon®. Its use in pregnancy is not recommended due to insufficient examinations. Do not use during breastfeeding.
Side effects:
In connection with the use of Cimicifuga rhizoma-containing medicines, cases of liver injury (including hepatitis, jaundice,
Changes in liver values) have occurred. Allergic skin reactions (hives, skin itching, rash), facial edema, peripheral oedema and gastrointestinal complaints (e.g. dyspeptic complaints, diarrhoea) have been reported. The frequency of these adverse reactions cannot be estimated on the basis of the available data.
Warnings:
Contains lactose.
BIONORICA SE | 92308 Neumarkt
Co-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt Stand: 06|24
Digestopret®
Active ingredient:
Peppermint oil (Mentha x piperita L., aetheroleum).
Composition:
1 enteric-coated softgel contains: 0.2 ml (= 182 mg) peppermint oil (Mentha x piperita L., aetheroleum). Other ingredients: gelatin, glycerol, purified water, ethylcellulose, sodium alginate, medium-chain triglycerides, stearic acid, oleic acid.
Areas of application:
To treat the symptoms of irritable bowel syndrome (irritable colon), which manifest themselves in abdominal pain, flatulence, bloating, constipation or diarrhoea.
Contraindications:
Do not use in case of hypersensitivity to the active ingredient, menthol or any of the above-mentioned excipients, in children under 12 years of age, in pregnant women, during breastfeeding and in patients with liver disease, cholangitis, achlorhydria, gallstones or other biliary diseases; Do not take it at the same time as histamine H2 receptor antagonists, proton pump inhibitors or other medicines with peppermint oil.
Side effects:
Often heartburn, perianal burning, blurred vision, dry mouth, nausea and vomiting; Frequency not known: Stomach discomfort (in sensitive individuals), urine and bowel movements with menthol odor, dysuria, inflammation of the glans, allergic reactions to menthol with headache, bradycardia, muscle tremor, ataxia, anaphylactic shock and erythematous rash.
BIONORICA SE | 92308 NeumarktCo-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt
Stand: 04|23
Silimarit® 86.5 mg hard capsules
Active ingredient:
dry extract of milk thistle fruits
Composition:
1 hard capsule contains 136.0-160.0 mg dry extract of milk thistle fear (50-70:1) corresponding to 86.5 mg silymarin (calculated as silibinin, HPLC); Extracting agent: acetone.
Other ingredients: highly dispersed silicon dioxide, dextrin, lactose monohydrate, magnesium stearate (Ph. Eur.), gelatine, sodium dodecyl sulfate.
Areas of application:
For supportive treatment of chronic inflammatory liver disease, cirrhosis and toxic liver damage in adolescents aged 12 years and older and adults. Note: Drug therapy does not replace the avoidance of liver-damaging causes (e.g. alcohol). In case of jaundice, a doctor should be consulted. This medicine is not suitable for the treatment of acute poisoning.
Contraindications:
Hypersensitivity to milk thistle fruit and/or other composite plants or any of the other ingredients of the medicine.
Use during pregnancy and breastfeeding is not recommended.
Patients with the rare hereditary galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take Silimarit 86.5 mg hard capsules.
Side effects:
Diseases of the gastrointestinal tract: Mild gastrointestinal symptoms such as dry mouth, nausea, stomach upset, stomach irritation and diarrhoea. Diseases of the nervous system: headaches. Immune system disorders: Hypersensitivity reactions (allergic reactions) such as dermatitis, urticaria, rash, pruritus, anaphylaxis, and asthma.
The frequency of occurrence of the mentioned side effects is not known.
BIONORICA SE | 92308 Neumarkt
Co-sales: PLANTAMED Arzneimittel GmbH | 92308 Neumarkt
Booth: 05|25