GNH USA

Europe — EMA

Ledraxen

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

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 thrombo‑embolism in at‑risk patients. 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 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.

What are the side effects of Enoxaparin Sodium?

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.

What precautions apply to Enoxaparin Sodium?

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.

What does Enoxaparin Sodium interact with?

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

What is Ledraxen used for?+
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.
How does enoxaparin sodium work?+
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.
What is the usual dose of Ledraxen?+
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.
Is Ledraxen safe during pregnancy or breastfeeding?+
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.
How do I order Ledraxen from GNH USA?+
To order 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 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.
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. If temporary storage at controlled room temperature is necessary, keep the product below 30 °C and use within the manufacturer’s specified time frame.
How is Ledraxen administered?+
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.
What are the most serious risks associated with Ledraxen?+
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.
Who should not use Ledraxen?+
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.
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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