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 4500 IU/mL injection for subcutaneous use. It is employed to prevent and treat thromboembolic conditions such as deep vein thrombosis and pulmonary embolism in surgical, post‑operative, medical and dialysis patients. The medication reduces the risk of clot formation during periods of prolonged immobilization and after major orthopedic procedures.

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 Pharma B.V.

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Indications & Clinical Uses

Tinzaparin sodium, a low molecular weight heparin, is used to prevent and treat thromboembolic disorders.

  • Prophylaxis of deep vein thrombosis in surgical patients: prevents clot formation after surgery.
  • Treatment of acute deep vein thrombosis: facilitates clot resolution and reduces recurrence.
  • Treatment and secondary prevention of pulmonary embolism: limits embolic events and supports recovery.
  • Prevention of clotting in hemodialysis circuits: maintains circuit patency during dialysis sessions.

How It Works

  • Tinzaparin sodium binds to antithrombin III, markedly enhancing its ability to inactivate factor Xa and, to a lesser extent, factor IIa (thrombin). By accelerating the inhibition of these key coagulation enzymes, the drug reduces thrombin generation and fibrin formation, thereby preventing the development and propagation of pathological blood clots. The selective inhibition of factor Xa provides a predictable anticoagulant response with a lower risk of platelet interaction compared with unfractionated heparin.

Side Effects

Tinzaparin sodium may cause a range of adverse reactions, most of which are related to its anticoagulant activity.

Common Side Effects

  • Injection site pain or erythema: mild discomfort at the injection site.
  • Bruising or hematoma: localized bleeding under the skin.
  • Minor bleeding: such as gum or nosebleeds.
  • Transient thrombocytopenia: mild decrease in platelet count.

Serious or Rare Side Effects

  • Major bleeding: gastrointestinal or intracranial hemorrhage.
  • Heparin‑induced thrombocytopenia (HIT): immune‑mediated platelet activation.
  • Spinal or epidural hematoma: bleeding in the spinal canal after neuraxial procedures.
  • Severe allergic reaction: anaphylaxis or urticaria.

Precautions & Warnings

When using Tinzaparin sodium, clinicians should consider several safety measures to minimize bleeding risk and other complications.

  • Renal impairment: adjust dose or monitor anti‑Xa levels in patients with reduced kidney function.
  • Pregnancy: category B, use only when benefit outweighs potential risk to the fetus.
  • Concomitant anticoagulants: avoid or closely monitor when combined with warfarin, DOACs or other heparins.
  • Surgical or invasive procedures: discontinue before major surgery to reduce bleeding risk.
  • Platelet monitoring: check platelet counts regularly to detect heparin‑induced thrombocytopenia.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Tinzaparin sodium can interact with other medicines that affect haemostasis, requiring careful management.

Major Interactions (Avoid)

  • Other anticoagulants (e.g., warfarin, direct oral anticoagulants): additive bleeding risk.
  • Thrombolytic agents (e.g., alteplase): increased risk of severe hemorrhage.
  • High‑dose antiplatelet drugs (e.g., clopidogrel): heightened bleeding potential.

Moderate Interactions (Monitor Closely)

  • Nonsteroidal anti‑inflammatory drugs (NSAIDs): may exacerbate minor bleeding.
  • Selective serotonin reuptake inhibitors (SSRIs): potential for increased mucosal bleeding.
  • ACE inhibitors: monitor for rare reports of enhanced anticoagulant effect.

Frequently Asked Questions

Innohep contains tinzaparin sodium, a low molecular weight heparin indicated for prevention of deep vein thrombosis in surgical patients, treatment of acute DVT, treatment and secondary prevention of pulmonary embolism, and to keep hemodialysis circuits free of clots.

Tinzaparin sodium binds antithrombin III, greatly increasing its inhibition of factor Xa and, to a lesser extent, thrombin (factor IIa). This blocks the conversion of prothrombin to thrombin, reducing fibrin formation and preventing clot propagation.

The dose of tinzaparin sodium is individualized by the prescribing clinician based on the specific indication, patient weight, renal function and risk factors. Dosing regimens are provided in the product label and should be followed as directed by a qualified health professional.

Tinzaparin sodium is classified as pregnancy category B, indicating that animal studies have not shown risk and there are no adequate human studies. It may be used during pregnancy only if the potential benefit justifies the potential risk to the fetus, and it is excreted in breast milk in small amounts; breastfeeding decisions should be made with a physician.

To request Innohep, 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 if needed) and the necessary import documentation.

Compared with unfractionated heparin, tinzaparin sodium offers more predictable pharmacokinetics, a longer half‑life and once‑daily dosing for many indications, with a lower risk of heparin‑induced thrombocytopenia. Direct oral anticoagulants provide oral administration but lack the ability to be reversed easily in emergencies, whereas Innohep can be partially reversed with protamine sulfate.

Innohep should be stored refrigerated at 2‑8 °C, protected from light, and must not be frozen or shaken. Before use, allow the vial to reach room temperature if required, and inspect for particulate matter or discoloration. Follow aseptic technique for subcutaneous injection.

Innohep is supplied as a sterile solution for subcutaneous injection. The appropriate dose is drawn into a sterile syringe and injected into the fatty tissue of the abdomen, thigh or upper arm, avoiding areas of bruising or irritation. Injection technique and site rotation should follow the prescribing information.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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