Product image of Ivor (Bemiparin Sodium) supplied by GNH India

Ivor

Active Ingredient:
Bemiparin Sodium
Origin:
EU

Ivor (Bemiparin Sodium)

Bemiparin Sodium, the active ingredient in Ivor, is a low molecular weight heparin presented as a subcutaneous injection for subcutaneous use. It is employed to prevent venous thromboembolism, treat deep vein thrombosis, and reduce thromboembolic complications in patients undergoing surgery. The drug activates antithrombin III, leading to inhibition of factor Xa and, to a lesser extent, factor IIa. Its predictable pharmacokinetic profile allows once‑daily administration in most clinical settings.

GNH India supplies Ivor as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Rovi Pharma Industrial Services S.A.U.

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Indications & Clinical Uses

  • Bemiparin Sodium is indicated for anticoagulation in several clinical scenarios related to venous clot formation.
  • Prevention of venous thromboembolism: reduces incidence of deep vein thrombosis and pulmonary embolism in at‑risk patients.
  • Treatment of deep vein thrombosis: facilitates clot resolution and prevents propagation of existing thrombi.
  • Surgical prophylaxis of thromboembolic complications: lowers risk of postoperative clot formation in patients undergoing major surgery.

How It Works

  • Bemiparin Sodium belongs to the low molecular weight heparin class and exerts its anticoagulant effect by binding to antithrombin III. This complex accelerates the inhibition of activated factor Xa, and to a lesser degree factor IIa (thrombin), thereby interrupting the coagulation cascade and preventing fibrin clot formation. Its selective inhibition provides a more predictable response compared with unfractionated heparin.

Side Effects

Bemiparin Sodium may be associated with a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Injection site pain or erythema
  • Bruising or hematoma at the injection site
  • Mild bleeding (e.g., epistaxis, gum bleeding)
  • Nausea
  • Headache
  • Dizziness

Serious or Rare Side Effects

  • Major hemorrhage (intracranial, gastrointestinal)
  • Thrombocytopenia, including heparin‑induced thrombocytopenia (HIT)
  • Severe allergic reactions (anaphylaxis, urticaria)
  • Spinal or epidural hematoma following neuraxial procedures
  • Skin necrosis at the injection site
  • Pulmonary embolism despite therapy

Precautions & Warnings

  • When prescribing Bemiparin Sodium, clinicians should consider several safety aspects.
  • Renal impairment: assess renal function and monitor anti‑Xa levels if needed.
  • History of bleeding disorders: evaluate risk before initiating therapy.
  • Concurrent use of other anticoagulants or antiplatelet agents: avoid unless medically justified.
  • Pregnancy and lactation: use only if potential benefit outweighs risk.
  • Surgical procedures: discontinue prior to major surgery according to clinical guidelines.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light.

Avoid Interactions

Bemiparin Sodium can interact with other medicines that affect hemostasis.

Major Interactions (Avoid)

  • Warfarin: additive anticoagulant effect increasing bleeding risk.
  • Direct oral anticoagulants (e.g., apixaban, rivaroxaban): combined therapy may cause severe hemorrhage.
  • Thrombolytic agents (e.g., alteplase): heightened risk of major bleeding.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may increase minor bleeding.
  • Antiplatelet drugs (e.g., clopidogrel, aspirin): additive effect on platelet inhibition.
  • Selective serotonin reuptake inhibitors (SSRIs): potential for impaired platelet aggregation.

Frequently Asked Questions

Ivor contains Bemiparin Sodium, a low molecular weight heparin used to prevent venous thromboembolism, treat established deep vein thrombosis, and provide prophylaxis against clot formation in patients undergoing major surgery.

Bemiparin Sodium binds to antithrombin III, accelerating the inhibition of factor Xa and, to a lesser extent, factor IIa (thrombin). This blocks key steps in the coagulation cascade, reducing the formation of fibrin clots.

The prescribed dose of Ivor is determined by the treating physician based on the patient’s clinical condition, weight, renal function, and indication. Dosing regimens are not standardized in this description.

Safety data for Bemiparin Sodium in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

To request Ivor, 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 and any necessary import documentation.

Compared with unfractionated heparin, Bemiparin Sodium (Ivor) offers more predictable pharmacokinetics, a lower risk of heparin‑induced thrombocytopenia, and once‑daily dosing. Relative to newer oral agents, it requires subcutaneous injection but provides rapid onset and is reversible with protamine sulfate if needed.

Ivor should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the product protected from moisture and direct light to maintain stability.

Ivor is given by subcutaneous injection, typically into the abdominal wall or thigh. Administration technique follows standard aseptic injection practices, and the injection site should be rotated to minimize local irritation.

The most serious risks include major bleeding events such as intracranial or gastrointestinal hemorrhage, heparin‑induced thrombocytopenia (HIT), and rare but severe allergic reactions. Prompt medical attention is required if any of these occur.

Ivor is contraindicated in patients with active major bleeding, known hypersensitivity to bemiparin or other heparins, and those with a history of heparin‑induced thrombocytopenia. Caution is also advised for individuals with severe renal impairment or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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