Product image of Hepsal (Heparin Sodium) supplied by GNH India

Hepsal

Active Ingredient:
Heparin Sodium
Origin:
EU

Hepsal (Heparin Sodium)

Hepsal is a prescription‑only medication that contains heparin sodium as its active ingredient. It is supplied as an injectable solution intended for intravenous administration. The product is marketed in the European Union and belongs to the anticoagulant drug class, used to reduce the risk of abnormal blood clot formation. Hepsal is typically stored under controlled temperature conditions and requires careful handling by healthcare professionals to maintain sterility and efficacy.

Manufacturer / TM Owner

Wockhardt Uk Ltd

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Indications & Clinical Uses

Hepsal is indicated for several clinical situations where prevention or treatment of thrombotic events is required.

  • Prevention and treatment of venous thromboembolism (VTE) in medical and surgical patients.
  • Prophylaxis of deep‑vein thrombosis (DVT) in patients undergoing orthopedic or general surgery.
  • Management of acute coronary syndromes, including unstable angina and myocardial infarction.
  • Treatment of confirmed pulmonary embolism (PE) to restore pulmonary perfusion.
  • Adjunct therapy during extracorporeal circulation procedures such as cardiopulmonary bypass.

Side Effects

Hepsal may cause a range of adverse reactions, which are generally classified by frequency and severity.

Common

  • Minor bleeding at the injection site or from mucous membranes (e.g., nosebleeds, gum bleeding).
  • Small bruising (ecchymosis) around the infusion site.
  • Transient elevation of liver enzymes.
  • Mild thrombocytopenia (low platelet count) detected on laboratory testing.
  • Local irritation or pain at the catheter insertion point.

Serious

  • Major hemorrhage, including intracranial or gastrointestinal bleeding.
  • Heparin‑induced thrombocytopenia (HIT) with a paradoxical risk of clotting.
  • Severe allergic reactions such as anaphylaxis or urticaria.
  • Spontaneous spinal or epidural hematoma causing neurologic deficits.
  • Disseminated intravascular coagulation (DIC) in rare cases.

Precautions & Warnings

Before using Hepsal, healthcare providers should evaluate patient‑specific factors and monitor for potential complications.

  • Assess bleeding risk, including recent surgery, trauma, or active gastrointestinal ulceration.
  • Obtain baseline complete blood count, especially platelet count, and repeat monitoring during therapy.
  • Review renal and hepatic function, as impairment may affect drug clearance.
  • Avoid use in patients with known hypersensitivity to heparin or pork‑derived products.
  • Consider alternative anticoagulation in pregnancy unless benefits outweigh risks.
  • Use caution in elderly patients due to increased bleeding susceptibility.

Avoid Interactions

Hepsal can interact with other medications, altering anticoagulant effects or increasing bleeding risk.

Avoid

  • Concurrent use with other anticoagulants (e.g., warfarin, direct oral anticoagulants) without close monitoring.
  • Combination with antiplatelet agents such as aspirin, clopidogrel, or NSAIDs that amplify bleeding.
  • Concomitant administration of fibrinolytic agents (e.g., alteplase, streptokinase).
  • Use with high‑dose corticosteroids that may affect platelet function.

Use with caution

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) at low doses, requiring periodic coagulation assessment.
  • Certain antibiotics (e.g., vancomycin, ceftriaxone) that may potentiate anticoagulant effect.
  • Herbal supplements such as ginkgo biloba, garlic, or fish oil that have mild antiplatelet activity.
  • Proton pump inhibitors that may interfere with platelet aggregation.

Frequently Asked Questions

Hepsal contains heparin sodium as its sole active pharmaceutical ingredient.

Hepsal is supplied as an injectable solution that is given by intravenous infusion under medical supervision.

Hepsal is used to prevent and treat venous thromboembolism, to provide deep‑vein thrombosis prophylaxis after surgery, to manage acute coronary syndromes, and to treat pulmonary embolism.

Hepsal should not be used in patients who have experienced heparin‑induced thrombocytopenia; alternative anticoagulants are recommended.

Routine monitoring includes activated partial thromboplastin time (aPTT), platelet counts, and occasionally anti‑Xa levels.

Yes, concurrent use of Hepsal and aspirin can increase bleeding risk and requires careful clinical monitoring.

Hepsal is classified as a prescription medication and should only be used in pregnancy when the potential benefit justifies the potential risk to the fetus.

Common adverse effects include minor bleeding, bruising at the infusion site, mild thrombocytopenia, and transient elevation of liver enzymes.

Serious reactions can include major hemorrhage, heparin‑induced thrombocytopenia, anaphylaxis, spinal or epidural hematoma, and disseminated intravascular coagulation.

Hepsal should be stored according to the manufacturer’s instructions, typically refrigerated and protected from light, and used before the expiration date.

Hepsal is usually given via a central or peripheral intravenous line, but the infusion rate and line size should follow institutional protocols.

The Anatomical Therapeutic Chemical (ATC) classification for Hepsal is B01AB01, indicating it is a heparin anticoagulant.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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