Tinzaparin
Brand names: Innohep
Tinzaparin is a low molecular weight heparin given by subcutaneous injection for the prophylaxis and treatment of venous thromboembolism, including in pregnancy and in cancer-associated thrombosis.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It binds antithrombin to accelerate inhibition of activated factor Xa more than thrombin, producing a predictable anticoagulant effect with a longer half-life than unfractionated heparin.
Prescribing in practice
- Bleeding is the main risk, and the drug accumulates in significant renal impairment so use with caution and consider anti-Xa monitoring or an alternative as renal function declines, particularly in the elderly.
- It is contraindicated with active major bleeding and a history of heparin-induced thrombocytopenia, and neuraxial anaesthesia requires careful timing relative to dosing to avoid spinal haematoma.
- Treatment doses are calculated by body weight and given once daily, and some multidose presentations contain benzyl alcohol making them unsuitable in pregnancy and neonates.
Monitoring
Monitor full blood count for thrombocytopenia, renal function, and signs of bleeding, using anti-Xa activity rather than activated partial thromboplastin time where monitoring is needed.
Counselling the patient
- You or a carer can be taught to give the injection under the skin, rotating sites.
- Report unusual bruising, bleeding that will not stop, or black stools.
- Do not stop suddenly without advice if treating a clot.
Evidence & guidelines
Its efficacy in venous thromboembolism prophylaxis and treatment is supported by randomised trials and reflected in NICE guidance and the SPC.
Reference: MHRA SPC Innohep; IRIS Study (Renal Impairment); NICE NG89; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
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