Section 13 · Monograph

Apixaban

Reviewed Nov 2026FDA label
EliquisFactor Xa inhibitor (DOAC)
Forms
Tab: 2.5, 5mg
Dose
AF stroke prevention: 5mg BID (2.5mg BID if 2 of: age 80+, weight 60kg or less, creatinine 1.5+)
MOA
Direct factor Xa inhibition

Black Box Warning

  • Premature discontinuation increases the risk of thrombotic events including stroke — if stopped for a reason other than bleeding, cover with another anticoagulant
  • Spinal/epidural hematoma risk with neuraxial anesthesia or puncture, potentially causing long-term or permanent paralysis

Indications

  • Reduce risk of stroke and systemic embolism in nonvalvular atrial fibrillationFDA-labeled
  • Treatment and secondary prevention of DVT/PE; postoperative VTE prophylaxisFDA-labeled

Mechanism of Action

  • Direct, selective, reversible factor Xa inhibitor

Full Dosing

Adult / usual

  • AF: 5mg twice daily; 2.5mg twice daily if at least 2 of: age 80 or older, weight 60kg or less, serum creatinine 1.5mg/dL or more
  • Strong dual CYP3A4/P-gp inhibitors: reduce dose by 50% (avoid if already 2.5mg twice daily)
  • Hold before procedures according to bleeding risk

Contraindications

  • Active pathological bleeding
  • Severe hypersensitivity to apixaban

Drug Interactions

  • Strong dual CYP3A4/P-gp inhibitors (ketoconazole, ritonavir) increase levels
  • Strong inducers (rifampin, carbamazepine, phenytoin) lower levels — avoid
  • NSAIDs, antiplatelets and SSRIs increase bleeding risk

Adverse Effects

  • Bleeding (GI, intracranial)
  • Anemia
  • Nausea

Monitoring Parameters

  • Renal function and CBC at least yearly (more often in CKD)
  • Age, weight and creatinine criteria for dose
  • Bleeding signs

Pregnancy & Lactation

  • Limited data; avoid in pregnancy (LMWH preferred)
  • Avoid during breastfeeding

References

  1. ELIQUIS (apixaban) Prescribing Information — DailyMed (NIH) search

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