Product image of Ledraxen (Enoxaparin Sodium) supplied by GNH India

Ledraxen

Active Ingredient:
Enoxaparin Sodium
Origin:
EU

Ledraxen (Enoxaparin Sodium)

Enoxaparin Sodium, the active ingredient in Ledraxen, is a low molecular weight heparin presented as a sterile injectable solution for subcutaneous, intravenous and haemodialysis use. It is employed to prevent and treat venous thromboembolic disorders and to provide anticoagulation during renal replacement therapy.

GNH India supplies Ledraxen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Venipharm

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Indications & Clinical Uses

Ledraxen, a low molecular weight heparin, acts on the coagulation cascade to reduce clot formation in several clinical settings.

  • Venous thromboembolism prophylaxis: Reduces the risk of deep‑vein thrombosis and pulmonary embolism in surgical and medically immobilised patients.
  • Deep‑vein thrombosis and pulmonary embolism treatment: Facilitates clot resolution and prevents extension of existing thrombi.
  • Anticoagulation during haemodialysis: Provides safe anticoagulation to maintain circuit patency without excessive bleeding.

How It Works

  • Enoxaparin Sodium binds to antithrombin III, accelerating its inhibition of activated factor Xa and, to a lesser extent, factor IIa (thrombin). This selective blockade reduces thrombin generation and fibrin formation, thereby limiting clot propagation while preserving some hemostatic function.

Side Effects

Adverse reactions may occur with any anticoagulant therapy.

Common Side Effects

  • Injection site pain or bruising: Local discomfort at the administration site.
  • Minor bleeding: Nosebleeds, gum bleeding, or easy bruising.
  • Nausea or mild gastrointestinal upset.

Serious or Rare Side Effects

  • Major bleeding: Intracranial, gastrointestinal or retroperitoneal hemorrhage.
  • Heparin‑induced thrombocytopenia (HIT): Immune‑mediated platelet decline with paradoxical thrombosis.
  • Spinal or epidural hematoma: Bleeding in the spinal canal after neuraxial procedures.
  • Severe allergic reaction: Anaphylaxis, urticaria or angioedema.

Precautions & Warnings

Careful assessment and monitoring are required when using Ledraxen.

  • Renal impairment: Adjust dose or monitor anti‑Xa activity in patients with reduced kidney function.
  • Surgery or invasive procedures: Discontinue before the procedure to minimise bleeding risk.
  • Concomitant anticoagulants: Avoid or closely monitor when used with other anticoagulant agents.
  • Antiplatelet therapy: Use with caution together with aspirin, clopidogrel or similar drugs.
  • Pregnancy and lactation: Reserve for situations where benefit outweighs potential fetal or neonatal risk.
  • Store at 2-8°C: Keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Enoxaparin may interact with several drug classes, altering its safety profile.

Major Interactions (Avoid)

  • Concurrent use with other anticoagulants (e.g., warfarin, direct thrombin inhibitors).
  • Combination with antiplatelet agents such as aspirin or clopidogrel.
  • Co‑administration with fibrinolytic therapy (e.g., alteplase).

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) that increase bleeding tendency.
  • Selective serotonin reuptake inhibitors (SSRIs) or other serotonergic agents.
  • Renally cleared drugs (e.g., aminoglycosides) that may affect enoxaparin clearance.

Frequently Asked Questions

Ledraxen contains enoxaparin sodium, a low molecular weight heparin used to prevent venous thromboembolism, to treat established deep‑vein thrombosis and pulmonary embolism, and to provide anticoagulation during haemodialysis procedures.

Enoxaparin sodium binds to antithrombin III, greatly enhancing its ability to inhibit factor Xa and, to a lesser extent, factor IIa (thrombin). This reduces thrombin generation and fibrin clot formation, thereby limiting clot propagation.

The dose of Ledraxen is individualized by the prescribing clinician based on the specific indication, patient weight, renal function and procedural requirements. Only a qualified health professional should determine the appropriate regimen.

Enoxaparin sodium is classified as a pregnancy category that should be used only when the potential benefit justifies any potential risk to the fetus. Limited data are available for breastfeeding; the decision should be made by the treating physician.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain where required) and necessary import documentation.

Compared with unfractionated heparin, enoxaparin offers more predictable pharmacokinetics, a longer half‑life and does not require routine laboratory monitoring. Compared with direct oral anticoagulants, it is administered parenterally and is preferred in settings such as haemodialysis or when rapid reversal is needed.

Ledraxen should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability.

Ledraxen is given by subcutaneous injection, intravenous infusion, or added to the haemodialysis circuit as directed by the clinician. The injection site should be rotated for subcutaneous use, and aseptic technique must be observed.

The most serious risks include major bleeding events such as intracranial or gastrointestinal hemorrhage, heparin‑induced thrombocytopenia (HIT) which can paradoxically cause clotting, and spinal or epidural hematoma following neuraxial procedures.

Ledraxen is contraindicated in patients with active major bleeding, known hypersensitivity to enoxaparin or other heparins, and those with severe thrombocytopenia. Caution is advised in individuals with uncontrolled hypertension, recent major surgery, or a history of HIT.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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