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Synthetic factor Xa inhibitor

Fondaparinux sodium

Brand names: Arixtra

Fondaparinux sodium is a synthetic selective factor Xa inhibitor given by subcutaneous injection for the prevention and treatment of venous thromboembolism and in certain acute coronary syndromes.

Dosing — being independently re-sourced

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 and accelerates antithrombin-mediated inhibition of factor Xa, interrupting the coagulation cascade without directly inhibiting thrombin.

Prescribing in practice

  • It is largely renally cleared and accumulates in renal impairment, substantially increasing bleeding risk, so it is contraindicated or requires dose reduction depending on renal function and indication.
  • Bleeding is the principal hazard and there is no specific reversal agent, so it should be used cautiously around surgery and neuraxial procedures because of spinal or epidural haematoma risk.
  • Unlike heparin it does not usually cross-react in heparin-induced thrombocytopenia, but routine anti-Xa monitoring is not required.

Monitoring

Assess renal function and platelet count and watch for signs of bleeding rather than relying on routine coagulation monitoring.

Counselling the patient

  • This is a blood-thinning injection given under the skin.
  • Report unusual bruising, bleeding, black stools or blood in urine.
  • Tell any clinician planning surgery or a spinal procedure that you are using it.

Evidence & guidelines

Fondaparinux is supported by landmark venous thromboembolism prophylaxis and treatment trials and is recommended in NICE acute coronary syndrome and VTE guidance.

Reference: NICE NG89/NG185; ESC ACS guidelines; 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).

Related

Curated clinical cross-links plus same-class fallbacks.