Hepatrombin (Hepatrombin)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
Read on
Active substanceHeparin sodium + [Allantoin + Dexpanthenol]Heparin sodium + [Allantoin + Dexpanthenol]
Similar drugsTo uncover
  • Hepatrombin
    ointment externally 
    Hemofarm AD     Serbia
  • Hepatrombin
    gel externally 
    Hemofarm AD     Serbia
  • Hepatrombin
    gel externally 
    Hemofarm AD     Serbia
  • Hepatrombin
    ointment externally 
    Hemofarm AD     Serbia
    • Dosage form: & nbspgel for external use
    Composition:

    100 g of gel contain:

    active ingredients: heparin sodium 50 000 ME *, allantoin 0.250 g, dexpanthenol 0.250 g;

    Excipients: carbomer 1,100 g, levomentol 0.020 g, disodium edetate 0.100 g, trolamine 0.590 g, pine mountain oil 0.080 g, pine ordinary oil 0.080 g, lemon oil 0.020 g, sorbitol 2,000 g, isopropanol 25.370 g, macrogol glycerol prilocaprate 0,200 g, polysorbate-80 1,000 g, water 68.860 g.

    * 1 mg of sodium heparin contains not less than 180 IU in terms of dry matter

    Description:Colorless, clear gel with a characteristic odor.
    Pharmacotherapeutic group:Anticoagulant direct action for topical application
    ATX: & nbsp

    C.05.B.A.53   Heparin in combination with other drugs

    C.05.B.A   Heparin-containing preparations for topical application

    Pharmacodynamics:Combined preparation for topical application. Heparin prevents the formation of blood clots, has anti-edematous and anti-inflammatory effect, improves local blood flow. Allantoin has an anti-inflammatory effect, stimulates metabolic processes in tissues and promotes cell proliferation. Dexpanthenol improves the absorption of heparin, stimulates granulation and epithelialization of tissues.
    Indications:Thrombosis, thrombophlebitis, varicose veins; sports injuries, tendovaginitis; inflammatory infiltrates.
    Contraindications:Hypersensitivity to the components of the drug, violation of the integrity of the skin, infected skin lesions, children under 5 years.
    Pregnancy and lactation:Possible use of the drug in the III trimester of pregnancy. Caution should be given in the I and II trimester of pregnancy and during breastfeeding.
    Dosing and Administration:

    Outwardly.

    About 5 cm of the gel is applied in a thin layer, rubbing lightly massaging movements from the bottom upwards 2 times a day (morning and evening) for 10-14 days (with thrombosis and thrombophlebitis massaging is not recommended).

    The recommended course of treatment is 1 month.

    During pregnancy (III trimester) is applied externally.

    About 5 cm of the gel is applied in a thin layer, rubbing lightly massaging movements upward 2 times a day (morning and evening) on ​​the inner surface of the shin of each leg for 10-14 days (with thrombosis and thrombophlebitis massaging is not recommended).The recommended course of treatment is 1 month.

    Side effects:Allergic reactions (skin rash, skin hyperemia, urticaria, angioedema).
    Overdose:Overdose is unlikely in connection with low systemic absorption of active substances.
    Interaction:Clinically significant interactions with other drugs have not been identified. However, if the drug is used concomitantly with other drugs applied to the skin, special caution is recommended.
    Effect on the ability to drive transp. cf. and fur:The drug does not affect the ability to drive vehicles and mechanisms.
    Form release / dosage:Gel for external use (500 ME + 2.5 mg + 2.5 mg) / g.
    Packaging:For 40 g of the drug in an aluminum tube, ukuporennuyu screwed on the lid of plastic. The tube opening is protected by an aluminum membrane. The cap is a monolithic structure, including a device for piercing the membrane. Tuba, together with instructions for use, is placed in a cardboard box.
    Storage conditions:

    Store at a temperature of 15 to 25 ° C.

    Keep out of the reach of children!

    Shelf life:

    3 years.

    Do not use after the expiry date printed on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:П N011078 / 02
    Date of registration:18.08.2010 / 29.01.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:Hemofarm ADHemofarm AD Serbia
    Manufacturer: & nbsp
    Representation: & nbspHEMOFARM A.D. HEMOFARM A.D. Serbia
    Information update date: & nbsp27.03.2017
    Illustrated instructions
      Instructions
      Up