Product image of Heparin Sodium Wockhardt Uk (Heparin Sodium) supplied by GNH India

Heparin Sodium Wockhardt Uk

Active Ingredient:
Heparin Sodium
Origin:
EU

Heparin Sodium Wockhardt Uk (Heparin Sodium)

Heparin Sodium Wockhardt Uk is an injectable anticoagulant that contains the active ingredient heparin sodium. It is supplied as a sterile intravenous solution intended for use under medical supervision. The product conforms to European Union standards and is classified as a prescription‑only medication. By potentiating antithrombin III, it helps inhibit thrombin and factor Xa, reducing the risk of pathological clot formation in patients at risk of thrombosis.

Manufacturer / TM Owner

Wockhardt Uk Ltd

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Indications & Clinical Uses

Heparin Sodium Wockhardt Uk is used in clinical settings to prevent and treat thromboembolic conditions where rapid anticoagulation is required.

  • Prevention and treatment of deep vein thrombosis (DVT) in hospitalized or immobile patients.
  • Prevention and treatment of pulmonary embolism (PE) following surgery or trauma.
  • Anticoagulation during cardiac, vascular, or cardiopulmonary bypass procedures.
  • Maintenance of circuit patency in extracorporeal dialysis or hemofiltration systems.
  • Prophylaxis of clot formation in patients with atrial fibrillation undergoing invasive procedures.
  • Adjunctive anticoagulation in patients receiving thrombolytic therapy for acute myocardial infarction.

Side Effects

Heparin Sodium Wockhardt Uk may be associated with a range of adverse effects, which are generally categorized by frequency and clinical significance.

Common

  • Minor bleeding at the injection site or from mucous membranes.
  • Small bruising (ecchymosis) in areas of venipuncture.
  • Transient elevation of liver enzymes.
  • Nausea or mild gastrointestinal discomfort.
  • Transient low platelet count without clinical significance.
  • Mild headache or dizziness.

Serious

  • Major hemorrhage, including intracranial or gastrointestinal bleeding.
  • Heparin‑induced thrombocytopenia (HIT) with a rapid drop in platelet count.
  • Allergic reactions such as rash, itching, or anaphylaxis.
  • Spinal or epidural hematoma when used in neuraxial procedures.
  • Acute adrenal insufficiency due to bilateral adrenal hemorrhage.

Precautions & Warnings

When prescribing Heparin Sodium Wockhardt Uk, clinicians should evaluate patient‑specific factors and monitor for conditions that increase bleeding risk.

  • Assess baseline coagulation parameters (aPTT, PT/INR) before initiation.
  • Review history of heparin‑induced thrombocytopenia or other heparin allergies.
  • Use caution in patients with active gastrointestinal ulcers, recent surgery, or intracranial lesions.
  • Adjust dose or avoid use in severe renal or hepatic impairment.
  • Monitor platelet counts regularly to detect HIT early.
  • Avoid concurrent use with other anticoagulants or antiplatelet agents unless medically justified.
  • Consider pregnancy status, as safety data are limited.

Avoid Interactions

Heparin Sodium Wockhardt Uk can interact with several medications, influencing anticoagulant effect or bleeding risk.

Avoid

  • Concurrent use with other parenteral anticoagulants such as low‑molecular‑weight heparin or direct thrombin inhibitors.
  • Combination with potent antiplatelet agents (e.g., clopidogrel, ticagrelor) without close monitoring.
  • Co‑administration with fibrinolytic drugs (e.g., alteplase, streptokinase) due to heightened hemorrhagic potential.

Use with caution

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs) and aspirin may increase minor bleeding; monitor gastrointestinal tolerance.
  • Certain antibiotics (e.g., vancomycin, cefazolin) can alter platelet function; observe for signs of HIT.
  • Herbal supplements such as ginkgo biloba, garlic, or high‑dose vitamin E may potentiate anticoagulation; assess patient use.

Frequently Asked Questions

Heparin Sodium Wockhardt Uk potentiates antithrombin III, which in turn inhibits thrombin (factor IIa) and factor Xa, reducing the conversion of fibrinogen to fibrin and thereby preventing clot formation.

The product is supplied as a sterile solution for intravenous injection and is administered under the supervision of a qualified healthcare professional.

It is indicated for the prevention and treatment of deep vein thrombosis, pulmonary embolism, anticoagulation during cardiac and vascular surgery, and for maintaining patency of extracorporeal circuits such as dialysis or hemofiltration.

Common adverse effects include minor injection‑site bleeding, bruising, transient elevation of liver enzymes, mild nausea or gastrointestinal discomfort, low platelet counts without clinical impact, and occasional headache or dizziness.

Serious reactions to watch for are major hemorrhage (including intracranial or gastrointestinal bleeding), heparin‑induced thrombocytopenia (HIT), severe allergic responses such as anaphylaxis, spinal or epidural hematoma, and acute adrenal insufficiency due to bilateral adrenal hemorrhage.

Platelet counts should be measured at baseline and then regularly (e.g., every 2–3 days) during treatment to detect a rapid decline that may indicate HIT.

Patients with a documented history of HIT should not receive heparin products, including Heparin Sodium Wockhardt Uk, because of the risk of recurrence.

Baseline coagulation studies such as activated partial thromboplastin time (aPTT) and prothrombin time/international normalized ratio (PT/INR) are recommended, along with a complete blood count to assess platelet levels.

Concurrent use of other parenteral anticoagulants, potent antiplatelet agents, and fibrinolytic drugs should be avoided unless closely monitored because of the increased risk of bleeding.

Severe renal or hepatic dysfunction may alter the pharmacodynamics of heparin; dose adjustments or alternative anticoagulation strategies should be considered in these patients.

Safety data for heparin use in pregnancy are limited for this specific product; clinicians should weigh potential benefits against unknown risks and follow local guidelines.

The product should be stored at controlled room temperature, protected from light, and kept in its original packaging until use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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