Hepatophyte collection package 100 g

Instructions Hepatophyte collection package 100 g

Composition

active ingredients: 1 package (100 g) contains a mixture of medicinal plant raw materials: bean fruit flaps (Phaseoli fructus (sine semine)) 12 g, dandelion root (Taraxaci officinalis radix) 12 g, sand thistle flower (Helichrysi arenarii flos) 12 g, rosehip fruit (Rosae pseudo-fructus) 12 g, corn stigmas with stigmas (Zeae maydis styli cum stigmatis) 11 g, marigold flower (Calendulae flos) 11 g, galega herb (Galegae herba) 10 g, nettle leaf (Urticae folium) 10 g, milk thistle fruit (Silybi mariani fructus) 10 g.

Dosage form

Gathering.

Main physical and chemical properties: a mixture of pieces of various shapes of grayish-green color with brownish-red, yellow and white inclusions. Pleasant smell.

Pharmacotherapeutic group

Drugs used for liver and biliary tract diseases.

ATX code A05.

Pharmacological properties

Pharmacodynamics.

HEPATOPHYT promotes the restoration of liver cells (hepatocytes), improves the antitoxic function of the liver, enhances bile secretion, reduces the tone of the gallbladder and biliary tract, increases the concentration of bile acids and reduces the concentration of cholesterol. Moderately contributes to the reduction of blood sugar levels.

Indication

As part of complex therapy for liver and biliary tract diseases (chronic hepatitis, chronic cholecystitis, cholangitis, hypotonic type biliary dyskinesia); as part of complex therapy for diabetes mellitus.

Contraindication

Arterial hypertension of the 3rd degree, obstructive jaundice, cholelithiasis with stones more than 10 mm in diameter, low blood sugar, acute viral hepatitis, thrombophlebitis, increased blood clotting, acute poisoning of various etiologies; hypersensitivity to any components of the drug or other plants of the aster family (Compositae/Asteraceae).

Special safety measures.

It should be used with caution in patients with gastric and duodenal ulcers in the acute stage, cirrhosis of the liver, acute hepatitis, acute cholecystitis and acute pancreatitis; chronic pancreatitis or enterocolitis in the acute phase.

Interaction with other medicinal products and other types of interactions

Not installed.

Use during pregnancy or breastfeeding

There is no data on the safety and efficacy of the drug during pregnancy or breastfeeding, so it should not be prescribed during this period.

Ability to influence reaction speed when driving vehicles or other mechanisms

The drug does not affect the ability to drive or operate other mechanisms, but patients with existing vestibular disorders should exercise caution until their individual reaction is determined.

Method of administration and doses

Brew 2 tablespoons of the collection in 500 ml of boiling water, let it brew in a closed container for 1 hour, strain.

Adults and children over 7 years old should take ⅔ cup (150 ml) warm for
20-30 minutes before meals 3 times a day.

The duration of use is determined by the doctor. Usually the course of treatment does not exceed 4 weeks. If necessary, the course of treatment can be repeated as prescribed by the doctor.

Children

The drug is contraindicated in children under 7 years of age.

Overdose

Possible increased manifestations of adverse reactions.

Adverse reactions

The drug is usually well tolerated by patients. However, given the multicomponent composition of the drug, in some cases, as a rule, with individual hypersensitivity to any component of the drug or in violation of the recommended dosage regimen, the following adverse reactions may develop:

from the digestive system: nausea, vomiting, dyspepsia, heartburn, mild diarrhea;

Respiratory system: shortness of breath;

From the urinary system: increased diuresis;

Skin: allergic reactions, including itching, hyperemia, skin edema;

others: exacerbation of existing vestibular disorders.

In case of any negative reactions, you should consult a doctor.

Expiration date

2 years. Do not use after the expiry date stated on the packaging.

Storage conditions

In the original packaging at a temperature not exceeding 25 °C and out of the reach of children.

Packaging

100 g in a bag, enclosed in a pack.

Vacation category

Without a prescription.

Producer

LLC "Scientific and Production Pharmaceutical Company "AIM".

Location of the manufacturer and its business address

Ukraine, 61091, Kharkiv region, Kharkiv city, Kharkiv Divisions Street, 20, building "A-5".