What are the guidelines for Eliquis (apixaban) dosages?

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Last updated: September 21, 2025View editorial policy

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Guidelines for Eliquis (Apixaban) Dosages

The standard dose of Eliquis (apixaban) is 5 mg twice daily for most patients, with specific dose reduction to 2.5 mg twice daily required for patients who meet at least two of the following criteria: age ≥80 years, body weight ≤60 kg, or serum creatinine ≥1.5 mg/dL. 1

Standard Dosing for Atrial Fibrillation

For patients with non-valvular atrial fibrillation:

  • Standard dose: 5 mg twice daily 2, 1
  • Reduced dose: 2.5 mg twice daily (only if patient meets ≥2 of the following criteria):
    • Age ≥80 years
    • Body weight ≤60 kg
    • Serum creatinine ≥1.5 mg/dL 2, 1

Dosing for Other Indications

Deep Vein Thrombosis (DVT) and Pulmonary Embolism (PE)

  • Initial treatment: 10 mg twice daily for the first 7 days
  • Maintenance treatment: 5 mg twice daily after the first 7 days
  • Extended prevention: 2.5 mg twice daily after at least 6 months of treatment 1

Prophylaxis Following Hip or Knee Replacement Surgery

  • 2.5 mg twice daily starting 12-24 hours after surgery
  • Duration: 35 days for hip replacement; 12 days for knee replacement 1

Renal Dosing Considerations

Apixaban has lower renal clearance (27%) compared to other direct oral anticoagulants, making it potentially preferable in patients with renal impairment 2, 3:

Creatinine Clearance (CrCl) Recommended Dosing
>30 mL/min Standard dosing (5 mg twice daily or 2.5 mg twice daily if meeting dose reduction criteria)
15-30 mL/min Standard dosing (5 mg twice daily or 2.5 mg twice daily if meeting dose reduction criteria)
<15 mL/min or on dialysis 2.5 mg twice daily (regardless of other criteria) [3]

The ARISTOTLE trial data showed that apixaban caused less bleeding than warfarin in patients with CrCl 25-30 mL/min, with even greater reductions in bleeding compared to patients with CrCl >30 mL/min 4.

Drug Interactions

Dose adjustments are necessary when apixaban is co-administered with certain medications:

  • P-glycoprotein and strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole, ritonavir, clarithromycin):

    • For patients already on 5 mg twice daily: Reduce to 2.5 mg twice daily
    • For patients already on 2.5 mg twice daily: Avoid apixaban use 2
  • P-glycoprotein and CYP3A4 inducers (e.g., rifampin, carbamazepine, phenytoin, St. John's wort):

    • Avoid concurrent use due to reduced apixaban effectiveness 2

Temporary Interruption for Procedures

When interrupting apixaban for surgical or invasive procedures 1:

  • Low bleeding risk procedures: Discontinue apixaban at least 24 hours before procedure
  • Moderate to high bleeding risk procedures: Discontinue apixaban at least 48 hours before procedure
Procedure Bleeding Risk Last Apixaban Dose Before Procedure
Low bleeding risk 1 day before (CrCl >25 mL/min)
High bleeding risk 2 days before (CrCl >25 mL/min)

For patients with lower CrCl, consider holding for an additional 1-3 days, especially for high bleeding risk procedures 2.

Important Clinical Considerations

  • Off-label underdosing is common but not recommended: Studies show that approximately 15-17% of patients receive lower-than-recommended doses of apixaban 5. This practice should be avoided as it may compromise stroke prevention without improving safety.

  • Single dose-reduction criterion: Patients with only one dose-reduction criterion (e.g., only age ≥80 years) should receive the standard 5 mg twice daily dose. Research shows these patients derive consistent benefits with the standard dose compared to warfarin 6.

  • Missed doses: If a dose is missed, take it as soon as possible on the same day and resume the normal twice-daily schedule. Do not double the dose to make up for a missed dose 1.

  • Switching between anticoagulants:

    • From warfarin to apixaban: Start apixaban when INR is below 2.0
    • From apixaban to warfarin: Consider overlapping with parenteral anticoagulant until INR reaches acceptable range 1

By following these evidence-based guidelines for Eliquis dosing, clinicians can optimize both efficacy in preventing thromboembolic events and safety regarding bleeding risk.

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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