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 thrombo‑embolism in at‑risk patients.
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 is a low molecular weight heparin used in the prevention and treatment of venous thrombo‑embolic disorders.

  • Prevention of deep vein thrombosis (DVT) in surgical patients: reduces the incidence of postoperative clot formation.
  • Treatment of acute deep vein thrombosis: facilitates clot resolution and prevents propagation.
  • Prevention and treatment of pulmonary embolism: provides anticoagulation to lower the risk of embolic events.
  • Anticoagulation during haemodialysis: maintains circuit patency by inhibiting clot formation.

How It Works

  • Enoxaparin sodium potentiates antithrombin III, enhancing its inhibition of factor Xa and, to a lesser extent, factor IIa (thrombin). This selective blockade reduces thrombin generation and fibrin clot formation, thereby providing anticoagulant protection without markedly affecting platelet function.

Side Effects

Adverse reactions may occur with any anticoagulant therapy.

Common Side Effects

  • Injection‑site bruising or pain: mild local irritation at the administration site.
  • Minor bleeding: such as epistaxis, gum bleeding or easy bruising.
  • Nausea or gastrointestinal discomfort: occasional transient upset.
  • Headache: mild to moderate intensity.

Serious or Rare Side Effects

  • Major bleeding: internal hemorrhage including gastrointestinal or intracranial bleeding.
  • Heparin‑induced thrombocytopenia (HIT): immune‑mediated platelet decline with paradoxical thrombosis.
  • Spinal or epidural hematoma: risk when combined with neuraxial anesthesia.
  • Severe allergic reaction: anaphylaxis, urticaria or angioedema.
  • Paradoxical thrombosis: clot formation despite therapy.

Precautions & Warnings

Careful assessment and monitoring are required when using enoxaparin.

  • Renal function: adjust dose or avoid use in severe renal impairment.
  • Platelet count: monitor regularly for thrombocytopenia, especially after 5‑10 days.
  • Concomitant anticoagulants: avoid or use with caution to reduce bleeding risk.
  • Active bleeding: contraindicated in patients with ongoing hemorrhage.
  • Surgical procedures: discontinue appropriately before neuraxial or invasive surgery.
  • Storage: Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Enoxaparin may interact with several drug classes, requiring clinical vigilance.

Major Interactions (Avoid)

  • Other anticoagulants (e.g., warfarin, direct oral anticoagulants): markedly increase bleeding risk.
  • Antiplatelet agents (e.g., aspirin, clopidogrel): additive antithrombotic effect.
  • Thrombolytic therapy (e.g., alteplase): synergistic hemorrhagic potential.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): heightened gastrointestinal bleeding.
  • Neuraxial anesthesia or spinal puncture: risk of spinal hematoma.

Moderate Interactions (Monitor Closely)

  • Certain antibiotics (e.g., vancomycin, quinolones): may alter anticoagulant activity.
  • ACE inhibitors or ARBs: potential for enhanced anticoagulant effect.
  • Diuretics: may affect plasma volume and drug concentration.
  • Hormonal contraceptives or hormone replacement therapy: modest increase in thrombotic risk.
  • Lipid‑lowering agents (e.g., statins): occasional impact on platelet function.

Frequently Asked Questions

Ledraxen, containing enoxaparin sodium, is used to prevent and treat venous thrombo‑embolism such as deep vein thrombosis and pulmonary embolism, and to provide anticoagulation during haemodialysis procedures.

Enoxaparin sodium enhances the activity of antithrombin III, which selectively inhibits factor Xa and, to a lesser extent, factor IIa (thrombin). This reduces thrombin generation and fibrin clot formation, delivering anticoagulant protection.

The prescribed dose of Ledraxen is determined by the treating clinician based on the specific indication, patient weight, renal function and other clinical factors. Dosing regimens are individualized and should follow the prescriber’s instructions.

The safety of enoxaparin sodium in pregnancy or lactation has not been definitively established. Use is generally reserved for situations where the benefit outweighs potential risk, and decisions should be made by a qualified healthcare professional.

To order Ledraxen, 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 import documentation.

Compared with unfractionated heparin, enoxaparin offers more predictable pharmacokinetics, once‑ or twice‑daily dosing, and a lower risk of heparin‑induced thrombocytopenia. Direct oral anticoagulants provide oral administration but differ in reversal options and renal clearance considerations.

Ledraxen should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen or shaken. If temporary storage at controlled room temperature is necessary, keep the product below 30 °C and use within the manufacturer’s specified time frame.

Ledraxen is administered by subcutaneous injection, intravenous infusion, or added to the haemodialysis circuit as directed by a healthcare professional. The injection site should be rotated, and aseptic technique must be observed.

The most serious risks include major bleeding events, heparin‑induced thrombocytopenia (HIT), and spinal or epidural hematoma when used with neuraxial anesthesia. Prompt medical attention is required if signs of severe bleeding or thrombocytopenia appear.

Ledraxen is contraindicated in patients with active major bleeding, known hypersensitivity to enoxaparin or heparin products, and those who have a history of heparin‑induced thrombocytopenia. Caution is also advised for individuals with severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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