Europe — EMA
Hepathromb
Learn about Hepathromb, a European heparin sodium anticoagulant, its uses, side effects, precautions, and drug interactions.
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What is 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.
What is Heparin Sodium used for?
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.
What are the side effects of Heparin Sodium?
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.
What precautions apply to Heparin Sodium?
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.
What does Heparin Sodium interact with?
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
What is Hepathromb and what active ingredient does it contain?+
How does heparin sodium, the component of Hepathromb, work as an anticoagulant?+
In which clinical situations might Hepathromb be prescribed?+
What are the most common side effects reported with heparin sodium therapy?+
What serious adverse reactions should patients be monitored for while using Hepathromb?+
What laboratory tests are recommended before starting Hepathromb therapy?+
Can Hepathromb be used during pregnancy?+
Which medications should be avoided when a patient is receiving Hepathromb?+
Which drugs require caution when combined with Hepathromb?+
How should healthcare providers monitor patients on Hepathromb for safety?+
Is there a specific route of administration for Hepathromb?+
What therapeutic class does Hepathromb belong to?+
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