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

Inhixa

Active Ingredient:
Enoxaparin Sodium
Origin:
EU

Inhixa (Enoxaparin Sodium)

Enoxaparin Sodium, the active ingredient in Inhixa, is a low molecular weight heparin presented as an injectable solution for subcutaneous, intravenous, or hemodialysis use. It is employed to prevent and treat thromboembolic conditions in adult patients at risk of clot formation.
GNH India supplies Inhixa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Techdow Pharma Netherlands B.V.

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Indications & Clinical Uses

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

  • Deep vein thrombosis (DVT) prevention: reduces the risk of clot formation in surgical or immobilised patients.
  • Pulmonary embolism (PE) treatment: facilitates clot resolution and prevents recurrence.
  • Anticoagulation during hemodialysis: maintains circuit patency by inhibiting clotting during the procedure.

How It Works

  • Enoxaparin Sodium binds to antithrombin III, accelerating its inhibition of activated factor Xa and, to a lesser extent, thrombin (factor IIa). This selective blockade reduces thrombin generation and fibrin clot formation, providing anticoagulant activity without markedly affecting platelet function.

Side Effects

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

Common Side Effects

  • Injection site pain or bruising: local irritation at the administration site.
  • Minor bleeding: epistaxis, gum bleeding, or easy bruising.
  • Nausea or vomiting: gastrointestinal discomfort.
  • Headache: mild to moderate intensity.
  • Dizziness: transient light‑headedness.
  • Elevated liver enzymes: mild, transient changes in hepatic labs.

Serious or Rare Side Effects

  • Major hemorrhage: life‑threatening internal bleeding.
  • Heparin‑induced thrombocytopenia (HIT): immune‑mediated platelet drop.
  • Spinal or epidural hematoma: bleeding in the central nervous system after neuraxial procedures.
  • Severe allergic reaction: anaphylaxis or angioedema.
  • Disseminated intravascular coagulation (DIC): uncontrolled clotting and bleeding.
  • Acute renal failure: rare kidney impairment associated with high doses.

Precautions & Warnings

When using Enoxaparin Sodium, clinicians should observe several safety measures.

  • Renal impairment: assess kidney function and adjust dose as needed.
  • Surgery or invasive procedures: discontinue before to minimise bleeding risk.
  • Concomitant anticoagulants or antiplatelet agents: monitor closely for additive bleeding.
  • Pregnancy and lactation: use only if the benefit outweighs potential risk.
  • Platelet monitoring: check for thrombocytopenia indicative of HIT.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Enoxaparin Sodium can interact with several drug classes, affecting bleeding risk or anticoagulant effect.

Major Interactions (Avoid)

  • Other anticoagulants (e.g., warfarin, direct thrombin inhibitors): markedly increase bleeding.
  • Antiplatelet agents (aspirin, clopidogrel, ticagrelor): additive hemorrhagic risk.
  • Fibrinolytic therapy (tPA, streptokinase): potentiate bleeding complications.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): enhance mucosal bleeding.
  • Neuraxial anesthesia or spinal puncture: risk of spinal/epidural hematoma.

Moderate Interactions (Monitor Closely)

  • Glycoprotein IIb/IIIa inhibitors (abciximab, eptifibatide): may increase anticoagulant effect.
  • Certain antibiotics (e.g., penicillins, cephalosporins): can alter anti‑Xa activity.
  • Hormonal therapies (estrogen, oral contraceptives): modestly raise thrombosis risk.

Frequently Asked Questions

Inhixa contains Enoxaparin Sodium, a low molecular weight heparin indicated for preventing deep vein thrombosis, treating pulmonary embolism, and providing anticoagulation during hemodialysis procedures. It works by inhibiting clot‑forming factors to reduce the risk of thrombotic events.

Enoxaparin Sodium binds to antithrombin III, enhancing its ability to inactivate factor Xa and, to a lesser extent, thrombin (factor IIa). This selective inhibition reduces the generation of fibrin clots while preserving normal platelet function, delivering anticoagulant activity.

The dose of Inhixa is determined by the prescribing clinician based on the specific indication, patient weight, renal function, and treatment setting. Healthcare professionals calculate the appropriate regimen and adjust it as needed during therapy.

Enoxaparin Sodium is classified as a pregnancy category that should be used only when the potential benefit justifies the potential risk to the fetus. Limited data are available for breastfeeding; the decision should be made by a qualified healthcare provider.

To request Inhixa, 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 necessary import documentation.

Compared with unfractionated heparin, Enoxaparin Sodium offers more predictable pharmacokinetics, a longer half‑life, and does not usually require routine laboratory monitoring. It provides a lower risk of heparin‑induced thrombocytopenia and can be administered subcutaneously, offering greater convenience than many intravenous agents.

Inhixa should be stored at 2‑8 °C in a refrigerator, protected from light. Do not freeze or shake the vial. Keep the product in its original packaging until use to maintain stability and sterility.

Inhixa is given by subcutaneous injection, intravenous infusion, or added to the dialysis circuit, depending on the clinical indication. Administration technique follows standard aseptic practices, and the injection site should be rotated to minimise local irritation.

The most serious risks include major bleeding, heparin‑induced thrombocytopenia (HIT), spinal or epidural hematoma after neuraxial procedures, and rare allergic reactions such as anaphylaxis. Patients should be monitored closely for signs of bleeding or platelet count changes.

Inhixa is contraindicated in patients with active major bleeding, known hypersensitivity to Enoxaparin or other heparins, and those with severe uncontrolled hypertension. Caution is advised for individuals with a history of HIT, severe renal impairment, or recent spinal/epidural anesthesia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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