GNH USA

Europe — EMA

Ledraxen

GNH USA supplies Ledraxen (Enoxaparin Sodium), a low molecular weight heparin for prevention of deep vein thrombosis, treatment of pulmonary embolism

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 solution for subcutaneous, intravenous, and haemodialysis use. It prevents and treats blood clots in patients at risk of deep vein thrombosis, pulmonary embolism, or requiring anticoagulation during dialysis.

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

What is Enoxaparin Sodium used for?

Enoxaparin sodium is a low molecular weight heparin used to prevent and treat thromboembolic disorders.

- Prevention of deep vein thrombosis: reduces the incidence of DVT in surgical or immobilised patients. - Treatment of pulmonary embolism: facilitates clot resolution and prevents recurrence of emboli. - Anticoagulation during hemodialysis: maintains circuit patency and reduces clot formation during dialysis sessions.

What are the side effects of Enoxaparin Sodium?

Enoxaparin sodium may cause a range of adverse reactions, from mild to severe.

Common Side Effects: - Injection site bruising or pain - Minor bleeding (e.g., gum, nosebleeds) - Nausea or vomiting - Headache - Elevated liver enzymes - Mild anemia

Serious or Rare Side Effects: - Major hemorrhage (intracranial, gastrointestinal) - Heparin‑induced thrombocytopenia (HIT) - Allergic reactions (rash, urticaria, anaphylaxis) - Skin necrosis at injection sites - Spinal or epidural hematoma - Acute adrenal hemorrhage

What precautions apply to Enoxaparin Sodium?

Before using Ledraxen, consider the following safety measures.

- Assess bleeding risk: evaluate patient history for recent surgery or bleeding disorders. - Monitor platelet count: check regularly for signs of heparin‑induced thrombocytopenia. - Adjust dose in renal impairment: reduce dosage in patients with decreased kidney function. - Avoid concomitant anticoagulants: do not combine with other blood thinners unless clinically indicated. - Use caution in pregnancy: only if benefits outweigh potential risks. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Enoxaparin Sodium interact with?

Enoxaparin sodium can interact with several medications that affect haemostasis.

Major Interactions (Avoid): - Other anticoagulants (warfarin, direct thrombin inhibitors) - Antiplatelet agents (aspirin, clopidogrel) - Fibrinolytic therapy (tPA, streptokinase) - Non‑steroidal anti‑inflammatory drugs (NSAIDs) - Spinal or epidural anesthesia (risk of hematoma)

Moderate Interactions (Monitor Closely): - Factor Xa inhibitors (rivaroxaban, apixaban) – increased bleeding risk. - Certain antibiotics (e.g., vancomycin) – may potentiate anticoagulant effect. - Renal‑clearing drugs – monitor renal function and adjust dose as needed.

Frequently asked questions

What is Ledraxen used for?+
Ledraxen contains enoxaparin sodium, a low molecular weight heparin used to prevent deep vein thrombosis, treat pulmonary embolism, and provide anticoagulation during haemodialysis procedures. It works by inhibiting clot formation in patients at risk of thromboembolic events.
How does enoxaparin sodium work?+
Enoxaparin sodium enhances the activity of antithrombin III, which accelerates the inhibition of factor Xa and, to a lesser extent, thrombin (factor IIa). This reduces thrombin generation and fibrin formation, thereby limiting the development of blood clots while preserving normal haemostatic balance.
What is the usual dose of Ledraxen?+
The specific dose of Ledraxen is determined by the prescribing clinician based on the patient’s indication, weight, renal function, and overall risk profile. Healthcare professionals calculate the appropriate amount and administration schedule for each individual case.
Is Ledraxen safe to use during pregnancy or breastfeeding?+
Safety data for enoxaparin sodium in pregnancy and lactation are limited. It may be used during pregnancy only if the potential benefits justify the potential risks to the fetus. Breastfeeding mothers should consult their healthcare provider, as the drug can be excreted in breast milk.
How do I order Ledraxen from GNH USA?+
To request Ledraxen, 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 import documentation.
How does Ledraxen compare with other anticoagulants?+
Compared with unfractionated heparin, enoxaparin sodium (Ledraxen) offers more predictable pharmacokinetics, a longer half‑life, and does not require routine laboratory monitoring in most patients. It provides a lower risk of heparin‑induced thrombocytopenia but still carries bleeding risk similar to other anticoagulants.
What are the storage and handling requirements for Ledraxen?+
Ledraxen should be stored at 2‑8 °C (refrigerated), protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use to maintain stability and sterility.
How is Ledraxen administered?+
Ledraxen is administered by subcutaneous injection, intravenous injection, or via the haemodialysis circuit, depending on the clinical indication. The exact route, injection site and technique are determined by the prescribing clinician and nursing staff.
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), and rare allergic reactions that can lead to anaphylaxis. Patients should be monitored closely for signs of bleeding or platelet count changes.
Who should not use Ledraxen?+
Ledraxen is contraindicated in patients with active major bleeding, known hypersensitivity to enoxaparin or other LMWHs, and those with severe uncontrolled hypertension. Caution is also advised for individuals with a history of HIT, recent spinal or epidural procedures, or severe renal impairment without dose adjustment.
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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