Product image of Innohep (Tinzaparin Sodium) supplied by GNH India

Innohep

Active Ingredient:
Tinzaparin Sodium
Origin:
EU

Innohep (Tinzaparin Sodium)

Tinzaparin sodium, the active ingredient in Innohep, is a low molecular weight heparin presented as a sterile solution for subcutaneous, intravenous, and haemodialysis use. It is employed to prevent and treat venous thromboembolism in adult patients at risk.

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

Manufacturer / TM Owner

Leo Laboratories Limited

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Indications & Clinical Uses

Innohep (tinzaparin sodium) is used in the venous thromboembolism pathway to prevent and manage clot formation.

  • Deep vein thrombosis (prevention): reduces incidence of clot formation in at‑risk patients.
  • Deep vein thrombosis (treatment): facilitates resolution of existing thrombi and prevents extension.
  • Pulmonary embolism (prevention): lowers risk of embolic events in patients with DVT or other risk factors.
  • Haemodialysis (anticoagulation): provides anticoagulant support during extracorporeal dialysis circuits.

How It Works

  • Tinzaparin sodium binds to antithrombin III, markedly enhancing its inhibition of activated factor Xa and, to a lesser extent, thrombin (factor IIa). This accelerates the inactivation of clotting factors within the coagulation cascade, thereby reducing thrombin generation and preventing the formation and propagation of fibrin clots.

Side Effects

Tinzaparin sodium may be associated with bleeding‑related and immune‑mediated reactions.

Common Side Effects

  • Injection site pain or erythema.
  • Minor bruising or hematoma at the injection site.
  • Mild gastrointestinal bleeding.
  • Transient thrombocytopenia.
  • Elevated liver enzymes.

Serious or Rare Side Effects

  • Major hemorrhage (intracranial, gastrointestinal).
  • Heparin‑induced thrombocytopenia (HIT) with paradoxical thrombosis.
  • Spinal or epidural hematoma.
  • Severe allergic reaction (anaphylaxis).
  • Disseminated intravascular coagulation (rare).

Precautions & Warnings

When prescribing Innohep, clinicians should evaluate patient‑specific risk factors and monitor therapy closely.

  • Renal impairment: assess dosing and monitor anti‑Xa levels.
  • History of bleeding: weigh benefits against increased bleeding risk.
  • Concurrent anticoagulants or antiplatelet agents: avoid or adjust therapy to limit bleeding.
  • Pregnancy: use only if potential benefit justifies potential risk to fetus.
  • Upcoming surgery or invasive procedures: discontinue according to clinical guidelines.
  • Store at ambient temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Tinzaparin sodium can interact with several agents that affect hemostasis or drug metabolism.

Major Interactions (Avoid)

  • Other parenteral anticoagulants (e.g., unfractionated heparin, fondaparinux): additive anticoagulant effect.
  • Direct thrombin inhibitors (e.g., dabigatran): increased bleeding risk.
  • Thrombolytic agents (e.g., alteplase): synergistic hemorrhagic potential.

Moderate Interactions (Monitor Closely)

  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): may exacerbate gastrointestinal bleeding.
  • Selective serotonin reuptake inhibitors (SSRIs) or SNRIs: heightened bleeding tendency.
  • Corticosteroids: potential for mucosal bleeding.
  • ACE inhibitors: rare reports of enhanced anticoagulant effect.

Frequently Asked Questions

Innohep contains tinzaparin sodium, a low molecular weight heparin indicated for the prevention and treatment of deep vein thrombosis, the prevention of pulmonary embolism, and for anticoagulation during haemodialysis procedures.

Tinzaparin sodium binds to antithrombin III, greatly increasing its ability to inhibit factor Xa and, to a lesser extent, thrombin (factor IIa). This blocks key steps in the coagulation cascade, reducing clot formation and propagation.

The dose of Innohep is individualized by the prescribing clinician based on the patient’s indication, weight, renal function, and overall bleeding risk. Exact dosing regimens are established in the product’s prescribing information.

Safety data for tinzaparin in pregnancy and lactation are limited. Use is generally reserved for situations where the therapeutic benefit outweighs potential risks to the fetus or infant, and should be decided by a qualified healthcare professional.

Enquiries are submitted via the product page on gnhindia.com, where you specify the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and import documentation.

Innohep (tinzaparin) has a relatively higher anti‑Xa to anti‑IIa activity ratio compared with some other LMWHs, which may influence monitoring requirements. Clinical efficacy for VTE prevention and treatment is comparable, but individual patient factors and institutional protocols often guide the choice of LMWH.

Innohep should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight and extreme temperature fluctuations to maintain stability.

Innohep is supplied as a sterile solution for injection and is administered subcutaneously, intravenously, or via the haemodialysis circuit, depending on the clinical indication. Administration technique follows standard aseptic injection practices and institutional protocols.

The most serious risks include major bleeding events such as intracranial or gastrointestinal hemorrhage, heparin‑induced thrombocytopenia (HIT) which can paradoxically cause thrombosis, and rare spinal or epidural hematomas that may lead to neurological impairment.

Innohep is contraindicated in patients with known hypersensitivity to tinzaparin or any component of the formulation, active major bleeding, or a history of heparin‑induced thrombocytopenia. Caution is also advised in severe renal impairment and in patients undergoing high‑risk surgery.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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