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Heparibene Na

Active Ingredient:
Heparin
Origin:
EU

Heparibene Na (Heparin)

Heparibene Na is a pharmaceutical product containing the active ingredient heparin, supplied in an injectable form for intravenous or subcutaneous administration. It is marketed in the European Union and is available only by prescription. Heparin is an anticoagulant that works by enhancing antithrombin III activity to inhibit clotting factors. Heparibene Na is used under medical supervision for preventing and treating thromboembolic conditions such as deep vein thrombosis and pulmonary embolism.

Manufacturer / TM Owner

Teva Gyógyszergyár Zrt

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Indications & Clinical Uses

Heparibene Na is indicated for several clinical situations where inhibition of clot formation is required.

  • Prevention and treatment of deep vein thrombosis (DVT) in at‑risk patients.
  • Prevention and treatment of pulmonary embolism (PE) following DVT or as primary therapy.
  • Prophylaxis of thromboembolic events in patients undergoing major surgery, such as orthopedic or abdominal procedures.
  • Management of acute coronary syndromes, including unstable angina and non‑ST‑segment elevation myocardial infarction, when anticoagulation is indicated.
  • Treatment of other thrombotic disorders as determined by a healthcare professional.

Side Effects

Adverse reactions to Heparibene Na vary in frequency and severity; they are classified as common or serious.

Common

  • Minor bleeding at the injection site.
  • Nosebleeds (epistaxis).
  • Hematuria (blood in urine).
  • Mild thrombocytopenia (reduced platelet count).

Serious

  • Major hemorrhage, including intracranial or gastrointestinal bleeding.
  • Heparin‑induced thrombocytopenia (HIT) with risk of thrombosis.
  • Allergic reactions such as rash, urticaria, or anaphylaxis.
  • Elevated liver enzymes indicating hepatic injury.

Precautions & Warnings

Before initiating Heparibene Na, clinicians should evaluate several precautionary factors to minimize risk.

  • Assess patient history for bleeding disorders, recent surgery, or trauma.
  • Review renal and hepatic function, as impairment may affect drug clearance.
  • Monitor platelet counts regularly to detect heparin‑induced thrombocytopenia.
  • Use caution in pregnant or lactating women; benefits must outweigh potential risks.
  • Avoid concurrent use of other anticoagulants or antiplatelet agents unless specifically indicated.
  • Adjust dose in patients with severe obesity or low body weight under medical guidance.
  • Ensure appropriate laboratory monitoring (e.g., activated partial thromboplastin time) during therapy.

Avoid Interactions

Heparibene Na may interact with other medications, altering its anticoagulant effect or increasing bleeding risk.

Avoid

  • Concurrent use of other anticoagulants (e.g., warfarin, direct oral anticoagulants) without careful monitoring.
  • Combination with antiplatelet drugs such as aspirin, clopidogrel, or non‑steroidal anti‑inflammatory drugs (NSAIDs).

Use with caution

  • Concurrent administration of fibrinolytic agents (e.g., alteplase) due to additive bleeding risk.
  • Use with certain antibiotics (e.g., vancomycin) that may potentiate anticoagulation.
  • Concomitant therapy with corticosteroids or hormonal contraceptives that can affect coagulation parameters.

Frequently Asked Questions

Heparibene Na contains heparin, which binds to antithrombin III and accelerates its inhibition of thrombin (factor IIa) and factor Xa, thereby reducing clot formation.

Heparibene Na is supplied as an injectable solution and can be given either intravenously or subcutaneously according to the prescribing clinician’s instructions.

It is commonly prescribed for prevention and treatment of deep vein thrombosis, pulmonary embolism, postoperative thromboembolic prophylaxis, and certain acute coronary syndromes.

Common adverse effects include minor injection‑site bleeding, nosebleeds, hematuria, and mild reductions in platelet count.

Regular platelet count monitoring is recommended, especially during the first two weeks of therapy, to detect any significant decline that could indicate HIT.

Activated partial thromboplastin time (aPTT) is often measured to assess anticoagulant effect, and platelet counts are checked to screen for thrombocytopenia.

Concurrent use of other anticoagulants (e.g., warfarin, direct oral anticoagulants) and antiplatelet agents such as aspirin or NSAIDs should generally be avoided unless closely monitored.

Heparin products may be used in pregnancy when the benefits outweigh potential risks, but the decision must be made by a qualified healthcare professional.

Dose adjustment and more frequent monitoring of coagulation parameters are advised for patients with significant hepatic or renal dysfunction.

Heparibene Na is administered by injection and has a rapid onset and short half‑life, whereas warfarin is oral, requires several days to achieve effect, and is monitored using INR.

The patient should seek immediate medical attention; healthcare providers may discontinue the drug and consider reversal agents such as protamine sulfate.

Yes, protamine sulfate can neutralize the anticoagulant effect of heparin when administered under medical supervision.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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