FLAMIN-HEALTH
UkraineThe drug is used for chronic cholecystitis, chronic hepatitis, and biliary dyskinesia.
Frequently asked questions
How should Flamin-health be taken correctly?
Tablets should be taken orally 30 minutes before meals, swallowing with a small amount of water. Adults and children aged 14 and older are usually prescribed 1 tablet 3 times a day (the dose may be increased to 2 tablets 2-3 times a day). Children aged 10 to 14 years — 1 tablet 2 times a day; children aged 5 to 10 years — 1 tablet 1 time a day. The course of treatment lasts from 10 to 40 days.
What side effects can Flamin-health cause?
Rarely, allergic reactions (rash, itching, urticaria, skin redness) or increased blood pressure may occur. With prolonged use, cholestasis may develop.
Who should not take this drug?
Contraindications include hypersensitivity to the components, jaundice (obstructive), the presence of gallstones larger than 10 mm, exacerbation of peptic ulcer disease, as well as acute inflammation of the liver, gallbladder, bile ducts, or pancreas.
Can the drug be combined with other medicines?
The drug can be used together with other agents for the treatment of the liver and biliary tract. It also enhances the effect of metronidazole and aminoquinoline when treating giardiasis. However, if you are taking any other medicines simultaneously, you should inform your doctor.
Are there any special precautions regarding administration?
Caution should be exercised in individuals with increased gastric acidity. Since the drug contains lactose, people with sugar intolerance must consult a doctor. During pregnancy and breastfeeding, use is only possible upon a doctor's decision, if the benefit outweighs the risk.
Instructions for use
INSTRUCTIONS FOR MEDICAL USE OF THE MEDICINAL PRODUCT FLAMIN-ZDOROVYE (FLAMIN-ZDOROVYE)
Composition:
Active substance: 1 tablet contains flamin, calculated as the content of total flavonoids 70% – 50 mg;
Excipients: lactose monohydrate; potato starch; corn starch; magnesium carbonate light; calcium stearate.
Pharmaceutical form. Tablets.
Main physicochemical properties: yellow or yellowish-brown tablets with speckles, with a faint specific odor, flat cylindrical shape, beveled edges.
Pharmacotherapeutic group. Agents used in liver and biliary tract disorders. ATC code A05AA.
Pharmacological Properties
Pharmacodynamics
A flavonoid-containing polyphenolic medicinal agent derived from the flower heads of Helichrysum arenarium (immortelle). Contains flavonoid glycosides (salipurposide, isosalipurposide, kaempferol, apigenin), bitter substances, tannins, sterins, essential oils, and other biologically active compounds (organic acids, carotenoids, polysaccharides).
Increases bile secretion, alters the "cholesterol/bile acids" ratio, increases bile cholate content, and prevents the formation of gallstones. Exhibits a spasmolytic effect on the smooth muscle of the sphincters of the gallbladder and biliary ducts. By stimulating gastric juice secretion, it promotes better digestion of food. Demonstrates hypocholesterolemic and hepatoprotective effects. The drug reduces inflammatory processes in the liver parenchyma and biliary tract, improves hepatic circulation. The most important aspect of its pharmacodynamics is the ability to stabilize liver cell and subcellular membranes, which is based on its antioxidant effect.
Pharmacokinetics
Not studied.
Clinical characteristics.
Indications.
Chronic cholecystitis, chronic hepatitis, biliary tract dyskinesia.
Contraindications.
Hypersensitivity to the components of the drug; obstructive jaundice, cholelithiasis with stones larger than 10 mm in diameter, peptic ulcer exacerbation, acute inflammatory diseases of the liver, gallbladder and biliary tract, and pancreas.
Interaction with other medicinal products and other forms of interaction.
The drug can be used in combination with other medicinal products prescribed for liver and biliary tract disorders.
The drug enhances the activity of metronidazole and aminoquinolines in the treatment of giardiasis.
If simultaneous use of any other medicinal products is required, a physician should be informed.
Special precautions for use.
Use with caution in patients with increased gastric acid secretion.
The medicinal product contains lactose. If the patient has known intolerance to certain sugars, consult a physician before taking this medicinal product.
Use during pregnancy or breastfeeding.
Special considerations for use of the medicinal product during pregnancy or breastfeeding have not been studied. The medicinal product may be used only if, in the opinion of the physician, the expected benefit to the mother outweighs the potential risk to the fetus or infant.
Ability to influence reaction rate while driving or operating machinery.
Does not influence.
Dosage and Administration.
For oral administration to adults and children aged 5 years and older, taken 30 minutes before meals, swallowed with a small amount of water.
Adults and adolescents aged 14 years and older: 50 mg (1 tablet) three times daily. If necessary, the dose may be increased to 100 mg (2 tablets) two to three times daily.
Children aged 10 to 14 years: 50 mg (1 tablet) twice daily.
Children aged 5 to 10 years: 50 mg (1 tablet) once daily.
The duration of treatment is 10 to 40 days (depending on the nature, severity, and course of the disease). If necessary, the treatment course may be repeated upon physician's recommendation.
Children. The medication is indicated for treatment of children aged 5 years and older.
Overdose.
Cases of overdose have not been reported.
Adverse reactions.
The drug is usually well tolerated. Rarely, allergic reactions (including skin rashes, urticaria, itching, hyperemia) are possible; increased arterial pressure (in patients with arterial hypertension). With prolonged use, cholestatic manifestations are possible.
Shelf life. 5 years.
Storage conditions. Store in the original packaging at a temperature not exceeding 25 °C.
Keep out of reach of children.
Packaging. Tablets № 10×3 in blisters in a box; № 30 in a container in a box.
Availability. Over-the-counter.
Manufacturer. LIMITED LIABILITY COMPANY "CORPORATION "ZDOROVYA".
Manufacturer's location and address of business activity.
Ukraine, 61013, Kharkiv region, city of Kharkiv, Shevchenka street, 22.
The original data is available in the language of the country of manufacture.
Data source: State Register of Medicinal Products of Ukraine
Data last verified: August 13, 2026