Apixaban (Eliquis) Dosing and Usage for Anticoagulation
The standard dosing of apixaban for patients requiring anticoagulation varies by indication, with 5 mg twice daily for atrial fibrillation, 10 mg twice daily for the first 7 days followed by 5 mg twice daily for DVT/PE treatment, and 2.5 mg twice daily for extended prevention of recurrent DVT/PE after at least 6 months of treatment. 1
Dosing by Indication
Atrial Fibrillation
- Standard dose: 5 mg orally twice daily 2, 1
- Reduced dose (2.5 mg twice daily) if patient has at least two of the following:
Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) Treatment
- Initial treatment: 10 mg orally twice daily for the first 7 days 2, 1
- Maintenance treatment: 5 mg orally twice daily after the first 7 days 2, 1
- Duration: Typically 3-6 months, depending on clinical scenario and risk factors 4
Prevention of Recurrent DVT/PE
- 2.5 mg orally twice daily after at least 6 months of treatment for DVT or PE 2, 1
- This reduced dose has been shown to be effective for secondary prevention while potentially reducing bleeding risk 2, 4
Prophylaxis Following Hip or Knee Replacement Surgery
Special Populations and Considerations
Renal Function
- No dose adjustment needed for mild to moderate renal impairment 1, 5
- Use with caution in severe renal impairment (CrCl <15 mL/min) 2, 5
- Apixaban is approximately 27% renally cleared, making it less dependent on renal function than some other anticoagulants 5
Hepatic Impairment
- Avoid in severe hepatic impairment 2
- Use with caution in patients with elevated liver enzymes (>2x upper limit of normal) or total bilirubin >1.5x upper limit of normal 2
Elderly Patients
- Age alone does not require dose reduction unless other criteria are met 3
- Patients with isolated advanced age showed consistent benefits with the 5 mg twice daily dose compared to warfarin 3
Patients Undergoing Procedures
- Discontinue apixaban at least 48 hours prior to elective surgery or invasive procedures with moderate/high bleeding risk 1
- Discontinue at least 24 hours prior to procedures with low bleeding risk 1
- Restart after adequate hemostasis has been established 1
Patients with Atrial Fibrillation Undergoing PCI
- Apixaban has been studied in combination with P2Y12 inhibitors in patients with AF undergoing PCI 6
- Clopidogrel is the preferred P2Y12 inhibitor when combined with apixaban due to lower bleeding risk 2
- Appropriately dosed apixaban (both standard and reduced doses) showed favorable outcomes compared to vitamin K antagonists in this population 6
Practical Administration Considerations
- Apixaban can be taken with or without food 5
- If a dose is missed, take as soon as possible on the same day and resume twice-daily dosing; do not double the dose 1
- Half-life is approximately 12 hours 5
- No routine anticoagulation monitoring is required 4
Switching Between Anticoagulants
- From warfarin to apixaban: Discontinue warfarin and start apixaban when INR is below 2.0 1
- From apixaban to warfarin: Discontinue apixaban and begin both parenteral anticoagulant and warfarin at the time the next dose of apixaban would have been taken 1
- From apixaban to other anticoagulants: Discontinue apixaban and begin the new anticoagulant at the usual time of the next apixaban dose 1
Common Pitfalls and Caveats
- Inappropriate dose reduction: In clinical practice, reduced doses are sometimes prescribed to patients who don't meet criteria, potentially compromising efficacy 6
- Failure to adjust dose based on multiple criteria: Patients with at least two dose-reduction criteria should receive the reduced dose of 2.5 mg twice daily 1, 3
- Drug interactions: While apixaban has limited clinically relevant interactions with most medications, strong dual inhibitors of CYP3A4 and P-gp may increase apixaban exposure 5
- Missed doses: Patients should be educated about the importance of adherence and proper management of missed doses 1
- Perioperative management: Failure to appropriately time the discontinuation and resumption of apixaban around procedures can increase bleeding or thrombotic risk 1