Apixaban Dosing for Nonvalvular Atrial Fibrillation and Venous Thromboembolism
For nonvalvular atrial fibrillation, prescribe apixaban 5 mg orally twice daily as the standard dose, reducing to 2.5 mg twice daily ONLY when patients meet at least TWO of three criteria: age ≥80 years, body weight ≤60 kg, or serum creatinine ≥1.5 mg/dL. 1
Atrial Fibrillation Dosing Algorithm
Standard Dosing
- The FDA-approved standard dose is 5 mg orally twice daily for most patients with nonvalvular atrial fibrillation 1
- This dosing demonstrated a 21% reduction in stroke or systemic embolism compared to warfarin (HR 0.79,95% CI 0.66-0.95) and a 31% reduction in major bleeding in the ARISTOTLE trial 2, 3
Dose Reduction Criteria (Must Meet ≥2 of 3)
Critical pitfall: Reducing the dose based on only ONE criterion is off-label and may lead to inadequate anticoagulation with increased stroke risk 4, 5. Studies show that 60.8% of patients receiving reduced-dose apixaban did not meet proper criteria for dose reduction 6, and inappropriately underdosed patients may face increased thromboembolic risk 4.
Renal Function Considerations
- For CrCl >30 mL/min: Apply standard dosing algorithm (5 mg twice daily unless ≥2 dose-reduction criteria met) 3
- For CrCl 15-30 mL/min: Use 5 mg twice daily unless ≥2 dose-reduction criteria are met 2, 3
- For end-stage renal disease on hemodialysis: Start 5 mg twice daily, reduce to 2.5 mg twice daily only if age ≥80 years OR body weight ≤60 kg 2, 3
- For CrCl <15 mL/min NOT on dialysis: Apixaban is contraindicated 2, 1
Venous Thromboembolism Dosing
Acute DVT/PE Treatment
- Initial 7 days: 10 mg orally twice daily 1
- After 7 days: 5 mg orally twice daily for completion of treatment course 1
Extended Treatment (Recurrence Prevention)
- After completing at least 6 months of anticoagulation for DVT or PE, use 2.5 mg orally twice daily for extended prophylaxis 1
Post-Surgical VTE Prophylaxis
- Following hip or knee replacement: 2.5 mg orally twice daily starting 12-24 hours after surgery 1
- Duration: 35 days for hip replacement, 12 days for knee replacement 1
Important caveat: The evidence for apixaban in cancer-associated VTE is limited, with only 2.7% of patients in the AMPLIFY trial having active cancer 7. Consider alternative agents with stronger evidence in this population 7.
Monitoring Requirements
- Assess renal function before initiation and at least annually thereafter 3
- Monitor renal function more frequently if CrCl 30-50 mL/min or other risk factors for deterioration exist 2, 3
- Evaluate body weight periodically, particularly in patients near the 60 kg threshold 3
- No routine coagulation monitoring is required 2
- Assess clinically for signs of bleeding or thromboembolism 2
Switching Between Anticoagulants
From Warfarin to Apixaban
From Apixaban to Warfarin
- Discontinue apixaban and begin both parenteral anticoagulant AND warfarin at the time of the next scheduled apixaban dose 1
- Continue parenteral anticoagulant until INR reaches therapeutic range 1
From Other DOACs to Apixaban
- Simply discontinue the other DOAC and start apixaban at the time the next dose of the previous DOAC would have been due 2, 1
Special Populations
Patients with Prior Stroke/TIA
Patients Requiring Antiplatelet Therapy
- After coronary intervention, use apixaban with clopidogrel (NOT aspirin) after a brief periprocedural period to reduce bleeding risk while maintaining efficacy 2, 3
- For stable coronary disease without recent PCI, apixaban monotherapy is appropriate—adding antiplatelet therapy increases bleeding without clear benefit 2