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

Klexane

Active Ingredient:
Enoxaparin Sodium
Origin:
EU

Klexane (Enoxaparin Sodium)

Enoxaparin sodium, the active ingredient in Klexane, is a low molecular weight heparin presented as a sterile solution for subcutaneous and intravenous use. It is employed to prevent and treat deep vein thrombosis, pulmonary embolism, and other thromboembolic disorders in at‑risk patients.

GNH India supplies Klexane as a licensed, GDP‑compliant international pharmaceutical supplier, delivering the product to hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, supporting patient care across multiple continents and regulatory environments, and ensuring consistent quality throughout.

Manufacturer / TM Owner

Sanofi A/S

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Indications & Clinical Uses

  • Enoxaparin sodium is a low molecular weight heparin used in the prevention and treatment of venous thromboembolism.
  • Deep vein thrombosis: prevention and treatment of DVT in surgical and medical patients.
  • Pulmonary embolism: treatment of acute PE and prevention of recurrence.
  • Venous thromboembolism prophylaxis: prophylaxis after orthopedic or abdominal surgery.
  • Anticoagulation during hemodialysis: provides anticoagulation for patients undergoing haemodialysis.
  • Acute coronary syndromes: adjunct anticoagulant therapy in ACS management.

How It Works

  • Enoxaparin binds to antithrombin III, markedly enhancing its inhibition of factor Xa and, to a lesser extent, factor IIa (thrombin). This reduces thrombin generation and fibrin formation, thereby interrupting the coagulation cascade and preventing clot propagation in the venous system.

Side Effects

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

Common Side Effects

  • Injection site bruising or pain.
  • Minor bleeding such as epistaxis or gum bleeding.
  • Nausea or mild gastrointestinal discomfort.
  • Headache.
  • Transient elevation of liver enzymes.
  • Local erythema at the injection site.

Serious or Rare Side Effects

  • Major hemorrhage, including intracranial or gastrointestinal bleeding.
  • Heparin‑induced thrombocytopenia (HIT).
  • Allergic reactions such as rash, urticaria, or anaphylaxis.
  • Spinal or epidural hematoma following neuraxial procedures.
  • Severe hypotension.
  • Skin necrosis at the injection site.

Precautions & Warnings

  • Before initiating enoxaparin therapy, several safety considerations are essential.
  • Renal impairment: adjust dose or monitor anti‑Xa activity in patients with reduced kidney function.
  • Bleeding risk: assess for active bleeding or high‑risk lesions prior to use.
  • Pregnancy: category B; use only when the clinical benefit outweighs potential risk.
  • Surgery or invasive procedures: discontinue appropriately before major operations to reduce bleeding.
  • Concomitant anticoagulants: avoid combined use with other anticoagulants unless clinically indicated.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

Avoid Interactions

Enoxaparin can interact with other medicines, affecting bleeding risk or anticoagulant effect.

Major Interactions (Avoid)

  • Concurrent unfractionated heparin: additive anticoagulation increases bleeding.
  • Combined warfarin therapy: potentiates anticoagulant effect and raises INR.
  • Use with potent antiplatelet agents (e.g., clopidogrel) in high‑bleeding‑risk patients.

Moderate Interactions (Monitor Closely)

  • NSAIDs (ibuprofen, naproxen): may increase minor bleeding.
  • Thrombolytic agents (alteplase, streptokinase): additive anticoagulant effect.
  • SSRIs or SNRIs (fluoxetine, venlafaxine): potential for increased bleeding tendency.

Frequently Asked Questions

Klexane contains enoxaparin sodium, a low molecular weight heparin indicated for the prevention and treatment of venous thromboembolic disorders such as deep vein thrombosis and pulmonary embolism, as well as for anticoagulation during hemodialysis and in acute coronary syndromes.

Enoxaparin binds to antithrombin III, accelerating its inhibition of factor Xa and, to a lesser extent, factor IIa (thrombin). This reduces thrombin generation and fibrin clot formation, thereby interrupting the coagulation cascade and preventing clot propagation.

The dose of Klexane is individualized and determined by the prescribing clinician based on the specific indication, patient weight, renal function, and risk factors. Dosing regimens are not standardized and should follow the prescriber’s order.

Enoxaparin sodium is classified as pregnancy category B. It may be used during pregnancy when the potential benefit justifies the potential risk to the fetus. Limited data are available for breastfeeding, and use should be discussed with a healthcare professional.

To order Klexane, submit an enquiry on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and necessary import documentation.

Compared with unfractionated heparin, enoxaparin (Klexane) has more predictable pharmacokinetics, a longer half‑life, and does not usually require routine laboratory monitoring. It provides a higher ratio of anti‑Xa to anti‑IIa activity, resulting in a lower risk of heparin‑induced thrombocytopenia.

Klexane should be stored at 2‑8 °C in a refrigerator, protected from light, and must not be frozen. If removed from refrigeration for administration, it may be kept at controlled room temperature for a limited period as specified in the product labeling.

Klexane is administered by subcutaneous injection, typically into the abdomen or thigh. In certain clinical settings, such as during hemodialysis, it may be given intravenously. Administration technique and site rotation are guided by the prescribing clinician.

The most serious risks include major bleeding (including intracranial or gastrointestinal hemorrhage), heparin‑induced thrombocytopenia (HIT), spinal or epidural hematoma after neuraxial procedures, and severe allergic reactions. Patients should be monitored closely for signs of these events.

Klexane is contraindicated in patients with active major bleeding, severe thrombocytopenia (platelet count < 50 × 10⁹/L), known hypersensitivity to enoxaparin or other heparins, and in those who have had a recent spinal or epidural anesthesia unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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