What is the recommended dosing strategy to convert a patient from gabapentin (Neurontin) 1200mg per day to Lyrica (Pregabalin)?

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Gabapentin to Pregabalin Conversion

For a patient taking gabapentin 1200 mg/day (600 mg, 300 mg, 300 mg), convert to pregabalin 150 mg/day divided into 75 mg twice daily or 50 mg three times daily, using an approximate 6:1 conversion ratio. 1

Conversion Rationale

  • Pregabalin has linear pharmacokinetics compared to gabapentin's nonlinear, saturable absorption, making pregabalin dosing more straightforward and predictable 1
  • The typical conversion ratio is approximately 6:1 (gabapentin:pregabalin), meaning 1200 mg/day of gabapentin converts to approximately 150-200 mg/day of pregabalin 1
  • Pregabalin 150 mg/day has demonstrated efficacy in clinical trials for neuropathic pain conditions, making this an appropriate starting dose after conversion 1, 2

Specific Conversion Protocol

  • Day 1: Begin pregabalin 75 mg twice daily (total 150 mg/day) while discontinuing gabapentin 1
  • Alternative dosing: Pregabalin 50 mg three times daily (total 150 mg/day) can be used if the patient prefers more frequent dosing 1
  • Titration if needed: After 1 week, the dose can be increased to 300 mg/day (150 mg twice daily) if pain control is inadequate, as higher doses (>300 mg/day) are not consistently more effective and cause more adverse effects 1

Critical Considerations Before Conversion

  • Renal function assessment is mandatory before initiating pregabalin, as both gabapentin and pregabalin are eliminated unchanged by the kidneys and require dose reduction in renal impairment 1
  • For creatinine clearance <60 mL/min, dose adjustments are required for both medications 3, 1
  • In elderly patients, start at the lower end of the dosing range and monitor closely for dizziness and sedation 1

Expected Adverse Effects

  • Both medications produce similar dose-dependent side effects including dizziness, somnolence, peripheral edema, and dry mouth 1, 2
  • With pregabalin 150 mg/day, expect dizziness (23%), drowsiness (15%), and peripheral edema (10%) 2
  • These effects are typically mild to moderate and often subside within approximately 10 days 3, 4
  • Adverse effects can be managed by dose reduction rather than discontinuation 2

Efficacy Timeline

  • Allow 3-4 weeks at the target dose to properly evaluate efficacy, as neuropathic pain relief develops gradually 3
  • Pregabalin may provide faster onset of action compared to gabapentin due to its linear pharmacokinetics 1
  • In clinical trials, 33-50% of patients achieved at least 50% pain reduction with pregabalin 150-600 mg/day for neuropathic pain 5, 2

Common Pitfalls to Avoid

  • Do not abruptly discontinue gabapentin—however, at the relatively low dose of 1200 mg/day, direct switch to pregabalin is generally safe without a taper 1
  • Do not exceed 300 mg/day pregabalin initially, as higher doses are not consistently more effective and increase adverse effects 1
  • Do not fail to assess renal function before conversion, as this is non-negotiable for safe dosing 3, 1
  • Do not rush to declare treatment failure—allow the full 3-4 week trial period at the target dose 3

References

Guideline

Gabapentin vs. Pregabalin for Neuropathic Pain

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Pregabalin--profile of efficacy and tolerability in neuropathic pain].

Drugs of today (Barcelona, Spain : 1998), 2009

Guideline

Gabapentin Dosing Guidelines for Neuropathic Pain

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Pregabalin: new drug. Very similar to gabapentin.

Prescrire international, 2005

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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