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Hepathromb

Active Ingredient:
Heparin Sodium
Origin:
EU

Hepathromb (Heparin Sodium)

Hepathromb is a pharmaceutical product that contains the active ingredient heparin sodium. It is supplied in an unspecified dosage form and strength, and is marketed within the European Union. As an anticoagulant belonging to the antithrombotic therapeutic class, Hepathromb works by enhancing the activity of antithrombin III to inhibit clotting factors. The product is intended for use under medical supervision and appropriate clinical monitoring by qualified healthcare professionals.

Manufacturer / TM Owner

Esteve Pharmaceuticals Gmbh

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Indications & Clinical Uses

Hepathromb is used in clinical settings where anticoagulation is required to prevent or treat thrombotic events.

  • Prevention of venous thromboembolism in patients undergoing surgery or immobilization.
  • Management of acute coronary syndromes where clot formation is a risk.
  • Adjunct therapy during hemodialysis to maintain circuit patency.
  • Treatment of established deep vein thrombosis or pulmonary embolism under supervision.
  • Prophylaxis of clot formation in patients with atrial fibrillation undergoing certain procedures.
  • Support of anticoagulation during cardiopulmonary bypass when rapid reversal may be needed.

Side Effects

Side effects associated with heparin sodium, the active component of Hepathromb, vary in frequency and severity.

Common

  • Minor bruising or bleeding at injection sites.
  • Small hematomas.
  • Mild thrombocytopenia (platelet count reduction).
  • Nausea or mild headache.

Serious

  • Major hemorrhage (internal or external).
  • Heparin‑induced thrombocytopenia (HIT) with risk of thrombosis.
  • Allergic reactions such as urticaria or anaphylaxis.
  • Elevated liver enzymes indicating hepatic involvement.

Precautions & Warnings

When prescribing or administering Hepathromb, healthcare professionals should consider several precautionary measures to ensure patient safety.

  • Assess baseline coagulation parameters and platelet count before initiation.
  • Review patient history for bleeding disorders, recent surgery, or trauma.
  • Monitor for signs of bleeding during therapy, especially in the gastrointestinal and intracranial regions.
  • Adjust dose or discontinue if significant thrombocytopenia develops.
  • Use caution in patients with renal or hepatic impairment, as drug clearance may be altered.
  • Avoid use in pregnancy unless benefits outweigh risks, after specialist consultation.

Avoid Interactions

Heparin sodium can interact with other medications, affecting its anticoagulant effect or increasing bleeding risk.

Avoid

  • Concurrent use of other anticoagulants such as warfarin, direct oral anticoagulants, or low‑molecular‑weight heparins.
  • Antiplatelet agents like clopidogrel or aspirin when combined may amplify bleeding.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) that impair platelet function.

Use with caution

  • Certain antibiotics (e.g., vancomycin) that may potentiate anticoagulation.
  • Thrombolytic agents used in acute clot dissolution.
  • High‑dose corticosteroids that can affect platelet stability.

Frequently Asked Questions

Hepathromb is a pharmaceutical product marketed in the European Union that contains the active ingredient heparin sodium, an anticoagulant used to reduce blood clot formation.

Heparin sodium potentiates antithrombin III, which in turn inhibits thrombin (factor IIa) and factor Xa, leading to reduced conversion of fibrinogen to fibrin and decreased clot formation.

Hepathromb may be used for prevention of venous thromboembolism after surgery, management of acute coronary syndromes, during hemodialysis, treatment of deep vein thrombosis or pulmonary embolism, prophylaxis in atrial fibrillation procedures, and as part of anticoagulation during cardiopulmonary bypass.

Common side effects include minor bruising or bleeding at the injection site, small hematomas, mild reductions in platelet count, nausea, and mild headache.

Serious reactions can include major internal or external hemorrhage, heparin‑induced thrombocytopenia (HIT) that may paradoxically cause thrombosis, severe allergic responses such as anaphylaxis, and elevated liver enzymes indicating possible hepatic involvement.

Baseline coagulation tests such as activated partial thromboplastin time (aPTT), platelet count, and assessment of liver and kidney function are typically recommended before initiating therapy.

The safety of Hepathromb in pregnancy has not been established; it should only be used if the potential benefits outweigh the risks and after consultation with a specialist.

Concurrent use of other anticoagulants (e.g., warfarin, direct oral anticoagulants, low‑molecular‑weight heparins), antiplatelet agents like aspirin or clopidogrel, and NSAIDs should be avoided due to increased bleeding risk.

Caution is advised when Hepathromb is used with certain antibiotics such as vancomycin, thrombolytic agents, and high‑dose corticosteroids, as these can potentiate anticoagulant effects or affect platelet function.

Providers should regularly assess bleeding signs, monitor platelet counts for thrombocytopenia, check coagulation parameters, and evaluate liver and kidney function throughout treatment.

Hepathromb is administered via the cutaneous route, typically as a subcutaneous injection, in accordance with clinical guidelines.

Hepathromb belongs to the antithrombotic therapeutic class and is classified as an anticoagulant.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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