Active substanceActivated charcoal + Bile + Stinging nettle leaves + Garlic seed bulbActivated charcoal + Bile + Stinging nettle leaves + Garlic seed bulb
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  • Dosage form: & nbspcoated tablets
    Composition:
    Active components:

    Bile condensed in terms of dry matter or bile dry - 0.080 g

    Dried garlic - 0.040 g

    Nettle leaves - 0.005 grams

    Activated carbon - 0.025 g

    Excipients: Magnesium oxide - 0.0042 g, starch potato - 0.04026 g, talc 0.004312 g, silicon dioxide colloid (aerosil) 0.012587 g, calcium stearate 0.0021 g, sucrose (sugar) 0.109895 g, magnesium hydroxycarbonate (magnesium carbonate basic ) - 0.062361 g, titanium dioxide - 0.001667 g, povidone (polyvinylpyrrolidone low molecular weight medical 12600 ± 2700) - 0.002382 g, tropeolin 0 - 0.00006 g, beeswax - 0.000176 g.

    Description:

    The tablets covered with a cover, round biconcave forms, yellow color, without a smell. Two layers are visible on the cross-section.

    Pharmacotherapeutic group:Cholagogue
    ATX: & nbsp

    A.05.A.X   Other drugs for the treatment of bile duct diseases

    Pharmacodynamics:

    The combined agent,enhancing the formation of bile and bile acids; reduces the processes of putrefaction and fermentation in the intestine.

    The action of bile is caused by the reflex influence on the secretory function of the liver parenchyma. Bile strengthens also the secretory and motor functions of the gastrointestinal tract.

    Substances contained in garlic, enhance the secretory and motor functions of the gastrointestinal tract, stimulate the secretion of bile.

    The leaves of the nettle have choleretic and anti-inflammatory properties.

    Activated carbon is an adsorbent that binds toxic substances in the gastrointestinal tract.

    Pharmacokinetics:The drug is well absorbed in the gastrointestinal tract. Cholic and chenodeoxycholic acids contained in the preparation are subjected to 7α-dehydroxylation in the intestine. Chenodeoxycholic acid, in addition, is metabolized in the liver: conjugated to amino acids, secreted in bile, whence it is again released into the intestine, then partially reabsorbed; the remainder is excreted through the intestine.
    Indications:

    As part of complex therapy for chronic reactive hepatitis, cholangitis, beskamennom (nekalkuleznom) cholecystitis,dyskinesia of bile ducts by hypokinetic type, atonic constipation, postcholecystectomy syndrome.

    Contraindications:Hypersensitivity to the components of the drug, calculous cholecystitis, obstructive jaundice, acute hepatitis, acute and subacute liver dystrophy, gastric ulcer and duodenal ulcer in the acute phase, acute pancreatitis, sugarase / isomaltase deficiency, glucose intolerance, glucose-galactose malabsorption, age up to 12 years.
    Carefully:Not described.
    Pregnancy and lactation:Perhaps if the potential benefit to the mother exceeds the potential risk to the fetus and the baby. Consultation of the doctor is necessary.
    Dosing and Administration:Inside after eating. Adults - 1-2 tablets 3-4 times a day. Children over 12 years - 1 tablet 3 times a day. The course of treatment is 3-4 weeks. With an exacerbation of the disease take 1 tablet 2-3 times a day for 1-2 months. Repeated courses of treatment are carried out with an interval of 3 months after a doctor's consultation. Before using the drug in children, you should consult your doctor.
    Side effects:

    Allergic reactions are possible; diarrhea; increased activity of "hepatic"transaminase in the serum. If side effects occur, stop taking the medication and consult a doctor.

    Overdose:Diarrhea, nausea, heartburn, itchy skin are possible. Treatment: symptomatic.
    Interaction:Preparations containing aluminum hydroxide, colestramine, colestipol reduce absorption and reduce the effect of the drug. Simultaneous reception is inexpedient.
    Special instructions:At a diabetes it is necessary to consider, that in structure of a preparation enters saccharose. One tablet contains about 0.1 g of sucrose (sugar), which corresponds to 0.01 XE; in the maximum daily dose of the drug contains about 0.8 g of sucrose (sugar), which corresponds to 0.08 XE.
    Effect on the ability to drive transp. cf. and fur:The use of the drug does not affect the management of vehicles and the employment of other potentially hazardous activities that require an increased concentration of attention and speed of psychomotor reactions.
    Form release / dosage:
    The tablets are coated.
    Packaging:

    For 10 or 24 tablets, coated in a contoured cell packaging of polyvinylchloride film and aluminum foil printed lacquered.

    5 contour mesh packages (10 coated tablets each) or 1 circuit pack (24 coated tablets each), along with instructions for use in a pack of cardboard or contour mesh packages together with an equal number of instructions for use in a group package.

    Storage conditions:

    Store in a dry, protected from light place at a temperature of 15 to 25 ° C.

    Keep out of the reach of children.

    Shelf life:4 years. Do not use after the expiration date.
    Terms of leave from pharmacies:Without recipe
    Registration number:P N001511 / 01
    Date of registration:24.04.2008 / 10.05.2017
    Expiration Date:Unlimited
    The owner of the registration certificate:DALHIMFARM, OJSC DALHIMFARM, OJSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp11.07.2017
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