What is the recommended dose of Eliquis (apixaban)?

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Last updated: October 7, 2025View editorial policy

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Recommended Dosing of Apixaban (Eliquis)

The standard dose of apixaban for most patients with nonvalvular atrial fibrillation is 5 mg taken orally twice daily. 1

Standard Dosing by Indication

  • Nonvalvular Atrial Fibrillation (NVAF): 5 mg orally twice daily 2, 1
  • Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE) Treatment: 10 mg orally twice daily for the first 7 days, followed by 5 mg orally twice daily 2, 1
  • DVT/PE Prevention after Hip or Knee Replacement Surgery: 2.5 mg orally twice daily, starting 12-24 hours after surgery 1
    • For hip replacement: continue for 35 days 1
    • For knee replacement: continue for 12 days 1
  • Reduction in Risk of Recurrent DVT/PE: 2.5 mg orally twice daily after at least 6 months of treatment for DVT or PE 1

Dose Reduction Criteria

For Nonvalvular Atrial Fibrillation

The dose should be reduced to 2.5 mg twice daily if the patient has at least two of the following characteristics 2, 1:

  • Age ≥80 years
  • Body weight ≤60 kg
  • Serum creatinine ≥1.5 mg/dL (133 μmol/L)

Special Considerations for Renal Function

  • Normal to Moderate Renal Impairment: No dose adjustment needed for patients with creatinine clearance >30 mL/min 2
  • Severe Renal Impairment: For patients with end-stage renal disease on hemodialysis, 5 mg twice daily with reduction to 2.5 mg twice daily if age ≥80 years or body weight ≤60 kg 2

Clinical Evidence Supporting Dosing Recommendations

  • The ARISTOTLE trial demonstrated that apixaban 5 mg twice daily reduced stroke or systemic embolism by 21% compared with warfarin, with a 31% reduction in major bleeding and 11% reduction in all-cause mortality 2
  • Patients with only one dose-reduction criterion still benefit from the standard 5 mg twice daily dose, showing similar efficacy and safety profiles compared to those with no dose-reduction criteria 3
  • Inappropriate dose reduction (using 2.5 mg twice daily when not indicated) may compromise efficacy without providing additional safety benefits 4, 5

Temporary Interruption for Procedures

  • For elective surgery or invasive procedures with moderate/high bleeding risk: discontinue apixaban at least 48 hours prior 1
  • For procedures with low bleeding risk: discontinue at least 24 hours prior 1
  • For high hemorrhagic risk procedures (e.g., neurosurgery): consider longer interruption periods of up to 3-5 days 2
  • Resume apixaban as soon as adequate hemostasis has been established 1

Important Warnings

  • Premature Discontinuation: Stopping apixaban increases thrombotic risk; if discontinuation is necessary for reasons other than bleeding, consider alternative anticoagulation 1
  • Missed Dose: If a dose is missed, take it as soon as possible on the same day and resume twice-daily administration; do not double the dose 1
  • Spinal/Epidural Hematoma Risk: Patients receiving neuraxial anesthesia or undergoing spinal puncture are at risk; monitor frequently for neurological impairment 1

Switching Between Anticoagulants

  • From warfarin to apixaban: Discontinue warfarin and start apixaban when INR is below 2.0 1
  • From apixaban to warfarin: Consider bridging with parenteral anticoagulant until INR reaches acceptable range 1
  • Between apixaban and other anticoagulants: Begin the new anticoagulant at the time the next dose of the previous anticoagulant would have been taken 1

Apixaban offers predictable anticoagulation without the need for routine monitoring, making it an attractive alternative to traditional vitamin K antagonists like warfarin for many patients requiring anticoagulation 6.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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