What is the recommended protocol for converting a patient from Lyrica (pregabalin) to gabapentin?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: October 14, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Protocol for Converting from Pregabalin (Lyrica) to Gabapentin

When converting from pregabalin to gabapentin, a gradual cross-titration approach is recommended with a dose ratio of approximately 1:6 (pregabalin:gabapentin), starting with gabapentin at 300 mg three times daily while tapering pregabalin over 1-2 weeks.

Conversion Ratio and Dosing Principles

  • The approximate dose conversion ratio is 1:6 for pregabalin to gabapentin (e.g., 300 mg of pregabalin is roughly equivalent to 1800 mg of gabapentin) 1
  • Gabapentin should be initiated at 300 mg three times daily (900 mg/day) and can be titrated up to 1800-3600 mg/day in divided doses 2
  • For most patients, efficacy is demonstrated at doses of 1800 mg/day, with limited additional benefit at higher doses 2

Cross-Titration Method

  • Begin with 50% of the original pregabalin dose plus 50% of the target gabapentin dose for 4 days 1
  • Gradually increase gabapentin while decreasing pregabalin over 1-2 weeks to minimize withdrawal symptoms 1, 3
  • For example, when converting from pregabalin 300 mg/day to gabapentin:
    • Days 1-4: Pregabalin 150 mg/day + Gabapentin 900 mg/day (300 mg TID)
    • Days 5-8: Pregabalin 75 mg/day + Gabapentin 1200-1500 mg/day
    • Days 9-14: Discontinue pregabalin + Gabapentin 1800 mg/day (600 mg TID) 1, 2

Dosage Adjustments for Special Populations

  • Both medications require dose adjustment in patients with renal impairment 1, 2
  • For patients with creatinine clearance 30-59 mL/min, reduce gabapentin to 400-1400 mg/day in divided doses 2
  • For patients with creatinine clearance 15-29 mL/min, reduce gabapentin to 200-700 mg/day 2
  • Elderly patients may require lower doses due to decreased renal function 2

Monitoring and Management

  • Monitor for breakthrough pain during the transition period 1
  • Watch for withdrawal symptoms (restlessness, agitation, anxiety, insomnia) if pregabalin is discontinued too rapidly 3, 4
  • Assess for common adverse effects including dizziness, somnolence, peripheral edema, and weight gain 5
  • Allow adequate trial time - gabapentin may require 2 months or more to achieve full efficacy compared to 4 weeks for pregabalin 1

Important Considerations

  • Avoid abrupt discontinuation of pregabalin to prevent withdrawal syndrome, which can include akathisia, anxiety, and flu-like symptoms 3, 4
  • Gabapentin has nonlinear pharmacokinetics at higher doses, which may require more frequent dosing compared to pregabalin's linear pharmacokinetics 1
  • Gabapentin may be less likely to reach therapeutic levels in clinical practice compared to pregabalin (only 46.2% of gabapentin patients vs. 89.3% of pregabalin patients reached therapeutic doses after 3 prescriptions) 6
  • Maximum time between gabapentin doses should not exceed 12 hours to maintain therapeutic effect 2

Common Pitfalls to Avoid

  • Attempting too rapid conversion, which may lead to withdrawal symptoms or inadequate pain control 3, 4
  • Failing to adjust doses based on renal function 1, 2
  • Not providing adequate overlap between medications during transition 1
  • Underestimating the total daily dose needed when converting (remember the 1:6 ratio) 1

References

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.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.