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Hepaxane

Active Ingredient:
Enoxaparin Sodium
Origin:
EU

Hepaxane (Enoxaparin Sodium)

Hepaxane is a prescription medication that contains the active ingredient enoxaparin sodium, a low‑molecular‑weight heparin, provided as an injectable solution for subcutaneous, intravenous, or haemodialysis administration. It is marketed in the European Union and is classified as an anticoagulant used to reduce the risk of blood clot formation in clinical settings. It is supplied in sterile vials and must be administered by a healthcare professional.

Manufacturer / TM Owner

Chemi S.P.A.

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Indications & Clinical Uses

Hepaxane is used in clinical practice to prevent and treat thromboembolic conditions where anticoagulation is indicated.

  • Prophylaxis of deep vein thrombosis (DVT) in patients undergoing orthopedic surgery or prolonged immobilization.
  • Treatment of acute DVT and pulmonary embolism, including extension therapy.
  • Prevention of clot formation during haemodialysis procedures.
  • Anticoagulation in patients with unstable angina or non‑ST elevation myocardial infarction when combined with other antiplatelet agents.
  • Bridging anticoagulation for patients transitioning between oral anticoagulants and surgical procedures.

Side Effects

The safety profile of enoxaparin sodium reflects the pharmacologic activity of low molecular weight heparins and includes both frequent and rare adverse events.

Common

  • Minor bruising or bleeding at the injection site.
  • Small amounts of nosebleed or gum bleeding.
  • Mild skin irritation or erythema around the administration area.

Serious

  • Significant bleeding such as gastrointestinal hemorrhage or intracranial bleed.
  • Thrombocytopenia, including heparin‑induced thrombocytopenia (HIT).
  • Allergic reactions ranging from rash to anaphylaxis.

Precautions & Warnings

Before initiating Hepaxane therapy, clinicians should evaluate patient‑specific factors and monitor for conditions that may increase the risk of bleeding or other complications.

  • History of active bleeding, recent surgery, or trauma.
  • Severe renal impairment, as drug clearance is reduced.
  • Concomitant use of other anticoagulants, antiplatelet agents, or thrombolytics.
  • Known hypersensitivity to enoxaparin, heparin, or any excipients.
  • Pregnancy and lactation status should be assessed, as safety data are limited.
  • Baseline platelet count and periodic monitoring to detect thrombocytopenia.

Avoid Interactions

Enoxaparin sodium can interact with several medications, potentially altering anticoagulant effect or increasing bleeding risk.

Avoid

  • Other injectable or oral anticoagulants (e.g., warfarin, direct oral anticoagulants) without appropriate dose adjustment.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) and aspirin at high doses.
  • Systemic thrombolytic agents (e.g., alteplase, streptokinase).

Use with caution

  • Antiplatelet drugs such as clopidogrel or ticagrelor.
  • Selective serotonin reuptake inhibitors (SSRIs) and other serotonergic agents.
  • Concomitant corticosteroids or other agents that may impair platelet function.

Frequently Asked Questions

Enoxaparin sodium enhances antithrombin III activity, which inhibits clotting factor Xa and, to a lesser extent, factor IIa (thrombin), thereby reducing the formation of fibrin clots.

Yes, Hepaxane is indicated for prophylaxis of deep vein thrombosis and for therapeutic anticoagulation in conditions such as acute DVT and pulmonary embolism.

Hepaxane can be administered subcutaneously, intravenously, or via the haemodialysis circuit, depending on the clinical indication.

Renal function influences the clearance of enoxaparin; dose adjustment or careful monitoring is recommended in patients with severe renal impairment.

Typical local reactions include minor bruising, mild bleeding, and occasional skin irritation or erythema at the injection site.

Enoxaparin is a low molecular weight heparin with more predictable pharmacokinetics, a longer half‑life, and a greater inhibition of factor Xa relative to unfractionated heparin.

In most cases, Hepaxane is discontinued prior to surgery to reduce bleeding risk; the timing depends on the type of surgery and the patient’s renal function.

Routine monitoring is not required, but anti‑Xa activity assays can be used in special populations such as those with renal failure or extreme body weight.

Safety data for enoxaparin in pregnancy are limited; clinicians should weigh potential benefits against risks and consider alternative anticoagulation strategies when appropriate.

HIT is an immune‑mediated reaction that can occur with heparin products, including low molecular weight heparins like enoxaparin, leading to a drop in platelet count and paradoxical clot formation.

There are no specific dietary restrictions, but patients should avoid excessive intake of vitamin K–rich foods if they are also on vitamin K antagonists.

The product should be kept in its original packaging, protected from light, and stored at controlled room temperature, typically between 15 °C and 30 °C.

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GNH India Pharmaceuticals Limited

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Last updated:

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