Active substanceSodium HeparinSodium Heparin
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  • Dosage form: & nbspgel for external use
    Composition:1 g of gel contains:
    active substance: heparin sodium - 1000 ME (0.00833 g with the activity of heparin sodium 120 IU / mg);
    Excipients: Ethanol (ethyl alcohol) 0.24 g, methyl parahydroxybenzoate (nipagine, methylparaben) 0.0012 g, propyl parahydroxybenzoate (nipazole, propylparaben) 0.0003 g, diethanolamine (2,2-iminodiethanol) up to 0.014 g to obtain a gel with a pH of 7.5 to 8.7, a carbomer (carbopol) - up to 0.015 g, water (purified water) - up to 1 g.
    Description:The gel is colorless or with a slight yellowish tint, transparent, with a specific odor.
    Pharmacotherapeutic group:Anticoagulant direct action for topical application
    ATX: & nbsp

    B.01.A.B.01   Heparin

    Pharmacodynamics:Direct anticoagulant, has anti-inflammatory, antiproliferative, anti-edematous and analgesic effect. Reduces platelet aggregation, binds to antithrombin III, preventing the passage of prothrombin in thrombin. Oppresses the activity of thrombin.Reduces the activity of hyaluronidase, increases the fibrinolytic properties of the blood. Trombles® improves microcirculation and activates tissue metabolism, thereby accelerating the processes of resorption of hematomas and thrombi, eventually restoring the permeability of veins, clinically it is accompanied by a pronounced analgesic and anti-inflammatory effect.
    Pharmacokinetics:An insignificant amount of heparin is absorbed from the surface of the skin into the systemic circulation. The maximum concentration of heparin in the blood is noted 8 hours after the application. The elimination of heparin, mainly occurs through the kidneys, half-life of 12 hours.
    Indications:Thrombophlebitis of superficial veins; localized infiltrates and swelling of soft tissues; subcutaneous hematomas (including hematomas after phlebectomy), injuries and bruises of joints, tendons, muscle tissue.
    Contraindications:Hypersensitivity to the components of the drug; ulcerative-necrotic, purulent processes on the skin; traumatic violation of the integrity of the skin; increased tendency to bleeding, thrombocytopenia.
    Pregnancy and lactation:It is possible to use the drug during pregnancy and lactation, if the potential benefit to the mother exceeds the risk to the fetus and the baby.
    Dosing and Administration:Outwardly. The gel column, 3-10 cm long, is lightly rubbed onto the skin over the affected area 1-3 times a day. The gel is used daily, on average from 3 to 7 days. The duration of treatment is determined by the doctor.
    Side effects:With prolonged use of the drug, local reactions are possible in the form of skin hyperemia, allergic reactions.
    Overdose:Due to low systemic absorption, an overdose is unlikely.
    Interaction:The combined use of the gel with indirect anticoagulants can cause lengthening of the isotrobin time.
    The gel is not prescribed topically at the same time as non-steroidal anti-inflammatory drugs, tetracyclines, antihyetamine drugs.
    Special instructions:The drug should not be used for bleeding, as well as for open wounds, mucous membranes and purulent processes.
    Form release / dosage:Gel for external use 1000 IU / g.
    Packaging:For 10, 20, 30, 40, 50 g in aluminum tubes or in polyethylene laminated tubes.Each tube together with instructions for medical use of the drug is placed in a pack of cardboard.
    Storage conditions:At a temperature of no higher than 25 ° C.
    Keep out of the reach of children.
    Shelf life:3 years. Do not use the drug after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LS-000112
    Date of registration:19.02.2010 / 29.12.2011
    The owner of the registration certificate:NIZHFARM, JSC NIZHFARM, JSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp2016-01-13
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