GNH USA

Europe — EMA

Ledraxen

GNH USA supplies Ledraxen (Enoxaparin Sodium), a low molecular weight heparin for VTE prevention, DVT/PE treatment, and anticoagulation during haemodialysis.

Enoxaparin Sodium

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

What is Enoxaparin Sodium used for?

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.

What are the side effects of Enoxaparin Sodium?

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.

What precautions apply to Enoxaparin Sodium?

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.

What does Enoxaparin Sodium interact with?

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

What is Ledraxen used for?+
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.
How does enoxaparin sodium work?+
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.
What is the usual dose of Ledraxen?+
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.
Is Ledraxen safe during pregnancy or breastfeeding?+
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.
How do I order Ledraxen from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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.
How does Ledraxen compare with other anticoagulants?+
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.
What are the storage and handling requirements for Ledraxen?+
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.
How is Ledraxen administered?+
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.
What are the most serious risks associated with Ledraxen?+
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.
Who should not use Ledraxen?+
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.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Enoxaparin Sodium
Route
Haemodialysis , Intravenous Use , Subcutaneous Use
Manufacturer
Venipharm
Origin
EU

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