Product image of Heparin Sodium Panpharma (Heparin Sodium) supplied by GNH India

Heparin Sodium Panpharma

Active Ingredient:
Heparin Sodium
Origin:
EU

Heparin Sodium Panpharma (Heparin Sodium)

Heparin Sodium Panpharma is a pharmaceutical product containing the active ingredient heparin sodium. It is supplied in an injectable form for intravenous or subcutaneous administration, though specific strength and dosage form are not disclosed. Classified as an anticoagulant and antithrombotic, it works by enhancing antithrombin III activity to inhibit clotting factors. The product is marketed in the European Union and requires a prescription for clinical use.

Manufacturer / TM Owner

Panpharma

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Indications & Clinical Uses

Heparin Sodium Panpharma is indicated for several antithrombotic applications where rapid anticoagulation is required. It is commonly employed in hospital settings to prevent and treat clot‑related conditions.

  • Prevention and treatment of venous thromboembolism, including deep‑vein thrombosis and pulmonary embolism.
  • Prophylaxis of deep vein thrombosis in surgical patients or those with limited mobility.
  • Anticoagulation during cardiac surgery, cardiopulmonary bypass, and extracorporeal dialysis procedures.
  • Management of clot formation in indwelling catheters and vascular access devices.
  • Adjunct therapy in acute coronary syndromes when rapid anticoagulation is needed.

Side Effects

Adverse reactions to Heparin Sodium Panpharma vary in frequency and severity, ranging from mild laboratory changes to rare but serious complications.

Common

  • Minor bleeding at injection sites or from mucous membranes.
  • Small decreases in platelet count without clinical symptoms.
  • Transient elevation of liver enzymes detected on routine labs.
  • Localized bruising or hematoma formation around the injection area.

Serious

  • Heparin‑induced thrombocytopenia (HIT) with paradoxical clot formation.
  • Major hemorrhage affecting internal organs or central nervous system.
  • Spontaneous spinal or epidural hematoma leading to neurologic deficits.
  • Severe allergic reactions such as anaphylaxis or angioedema.

Precautions & Warnings

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

  • History of heparin‑induced thrombocytopenia or known hypersensitivity to heparin.
  • Active bleeding, recent intracranial surgery, or uncontrolled hypertension.
  • Severe liver disease or marked thrombocytopenia (platelet count <50 × 10⁹/L).
  • Concomitant use of other anticoagulants, antiplatelet agents, or thrombolytics.
  • Pregnancy (category B) – benefits must outweigh potential fetal risk.
  • Renal impairment requiring dose adjustment and close laboratory monitoring.

Avoid Interactions

Heparin Sodium Panpharma may interact with other medicines, altering anticoagulant effect or increasing bleeding risk; careful assessment is essential.

Avoid

  • Concurrent use with direct thrombin inhibitors (e.g., dabigatran) or factor Xa inhibitors (e.g., rivaroxaban, apixaban).
  • High‑dose aspirin or other non‑steroidal anti‑inflammatory drugs (NSAIDs) that impair platelet function.
  • Systemic fibrinolytic agents such as alteplase or streptokinase.

Use with caution

  • Warfarin or other vitamin K antagonists, especially during initiation of heparin therapy.
  • Glycoprotein IIb/IIIa inhibitors used in interventional cardiology.
  • Certain antibiotics (e.g., vancomycin, cefoperazone) that may potentiate anticoagulant activity.

Frequently Asked Questions

Heparin Sodium Panpharma potentiates antithrombin III, which then inhibits thrombin (factor IIa) and factor Xa, reducing the conversion of fibrinogen to fibrin and preventing clot formation.

It is supplied as an injectable solution for intravenous bolus or infusion and for subcutaneous injection, depending on the therapeutic goal and patient condition.

Patients at risk of or diagnosed with venous thromboembolism, those undergoing cardiac surgery, dialysis, or requiring prophylaxis for deep‑vein thrombosis are typical candidates.

Activated partial thromboplastin time (aPTT) or anti‑Xa levels are commonly measured to ensure therapeutic anticoagulation while minimizing bleeding risk.

It is classified as pregnancy category B in the EU, indicating that animal studies have not shown risk, but it should be used only if the potential benefit justifies any potential fetal exposure.

A sudden drop in platelet count (often >50% from baseline) accompanied by new thrombosis, skin necrosis, or systemic clots suggests HIT and requires immediate evaluation.

Heparin Sodium Panpharma is an unfractionated heparin with a broader range of molecular weights, requiring laboratory monitoring, whereas low‑molecular‑weight heparins have more predictable pharmacokinetics and often do not need routine monitoring.

In addition to aPTT, platelet counts, liver enzymes, and sometimes serum potassium may be monitored because heparin can cause mild hepatic enzyme elevations and affect electrolyte balance.

No specific dietary restrictions are required, but patients should avoid foods or supplements that significantly increase bleeding risk, such as high‑dose vitamin K or herbal products with anticoagulant properties.

Store the vial or ampoule at controlled room temperature, protected from light, and keep it out of reach of children. Do not freeze.

Seek immediate medical attention; protamine sulfate can be administered as an antidote to neutralize excess heparin activity, guided by clinical assessment and laboratory values.

Yes, protamine sulfate is the specific reversal agent for unfractionated heparin, administered intravenously in a dose calculated based on the amount of heparin given.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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