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 use. It is employed to prevent and treat venous thromboembolic disorders in adult patients at risk of clot formation.
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 is a low molecular weight heparin used in the management of venous thromboembolism and related surgical prophylaxis.

  • Deep vein thrombosis: prevention and treatment of clot formation in the deep veins of the lower extremities.
  • Pulmonary embolism: prevention and treatment of embolic obstruction in the pulmonary arteries.
  • Surgical thromboprophylaxis: reduction of postoperative thromboembolic events in patients undergoing major surgery.

How It Works

  • Tinzaparin sodium binds to antithrombin III, enhancing its inhibitory activity against factor Xa and, to a lesser extent, factor IIa (thrombin). This accelerates the inactivation of these clotting factors, leading to reduced thrombin generation and inhibition of fibrin clot formation, thereby providing anticoagulant protection.

Side Effects

Adverse reactions may occur with any anticoagulant therapy.

Common Side Effects

  • Injection site pain or erythema: mild discomfort at the subcutaneous injection site.
  • Bruising or hematoma: localized bleeding under the skin.
  • Minor bleeding: such as gum or nosebleeds.
  • Nausea: occasional gastrointestinal upset.

Serious or Rare Side Effects

  • Severe bleeding: life‑threatening hemorrhage in any organ system.
  • Heparin‑induced thrombocytopenia (HIT): immune‑mediated drop in platelet count with paradoxical clot risk.
  • Spinal or epidural hematoma: bleeding in the spinal canal after neuraxial procedures.
  • Allergic reaction: urticaria, angioedema, or anaphylaxis.
  • Elevated liver enzymes: abnormal hepatic function tests.

Precautions & Warnings

Use of Innohep requires careful assessment of patient‑specific risk factors.

  • Renal impairment: adjust dosing and monitor anti‑Xa levels in patients with reduced kidney function.
  • Hepatic disease: consider increased bleeding risk and monitor liver function.
  • Concomitant anticoagulants: avoid or closely monitor when used with other anticoagulant or antiplatelet agents.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Elderly patients: increased susceptibility to bleeding; monitor closely.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Tinzaparin sodium may interact with several drug classes, affecting bleeding risk or anticoagulant efficacy.

Major Interactions (Avoid)

  • Other anticoagulants (e.g., warfarin, direct oral anticoagulants): additive anticoagulant effect leading to severe bleeding.
  • Thrombolytic agents (e.g., alteplase): heightened risk of hemorrhage.
  • Neuraxial anesthesia or spinal puncture: increased chance of spinal/epidural hematoma.

Moderate Interactions (Monitor Closely)

  • Antiplatelet drugs (e.g., aspirin, clopidogrel): may modestly increase bleeding tendency.
  • Non‑steroidal anti‑inflammatory drugs (NSAIDs): can exacerbate gastrointestinal bleeding.
  • Selective serotonin reuptake inhibitors (SSRIs) or serotonin‑norepinephrine reuptake inhibitors (SNRIs): may enhance mucosal bleeding.

Frequently Asked Questions

Innohep, containing tinzaparin sodium, is indicated for the prevention and treatment of deep vein thrombosis, the management of pulmonary embolism, and the prophylaxis of thromboembolic events in patients undergoing major surgery.

Tinzaparin sodium binds to antithrombin III, markedly increasing its ability to inhibit factor Xa and, to a lesser extent, factor IIa (thrombin). This reduces thrombin generation and fibrin clot formation, providing anticoagulant protection.

The dose of Innohep is individualized by the prescribing clinician based on the patient’s indication, weight, renal function, and risk factors. Exact dosing regimens are determined by the treating physician.

Safety data for tinzaparin sodium in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare professional.

To place an order, 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.

Innohep (tinzaparin) has a longer half‑life and a higher anti‑Xa to anti‑IIa activity ratio compared with some other LMWHs, allowing once‑daily dosing in many cases. Its safety and efficacy profile is comparable, but specific clinical choices depend on patient characteristics and institutional protocols.

Innohep should be stored at 2‑8 °C (refrigerated), protected from light, and must not be frozen or shaken. Keep the product in its original packaging until use.

Innohep is given by subcutaneous injection, typically into the abdominal wall or thigh. The injection site should be rotated to reduce local irritation, and aseptic technique must be followed.

The most serious risks include severe or uncontrolled bleeding, heparin‑induced thrombocytopenia (HIT), and spinal or epidural hematoma following neuraxial procedures. Prompt medical attention is required if any of these events are suspected.

Innohep is contraindicated in patients with active major bleeding, known hypersensitivity to tinzaparin or any heparin product, and those with a history of heparin‑induced thrombocytopenia. Caution is also advised for individuals with severe renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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