What is the maximum recommended dose of gabapentin (Neurontin) per day?

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Last updated: December 22, 2025View editorial policy

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Maximum Recommended Dose of Gabapentin

The maximum recommended dose of gabapentin is 3600 mg per day, divided into three doses (1200 mg three times daily), as established by the FDA and supported by major guideline societies. 1, 2

Standard Maximum Dosing

  • The FDA-approved maximum dose is 3600 mg/day for adults, administered in three divided doses with no more than 12 hours between doses 1
  • The American Academy of Neurology and National Comprehensive Cancer Network confirm the target therapeutic dose range of 1800-3600 mg/day in three divided doses for neuropathic pain conditions 2
  • For postherpetic neuralgia specifically, the FDA notes that efficacy was demonstrated across the 1800-3600 mg/day range, though additional benefit above 1800 mg/day was not consistently demonstrated in clinical trials 1

Critical Dosing Considerations

Three-times-daily dosing is mandatory due to gabapentin's nonlinear, saturable absorption pharmacokinetics—once or twice daily dosing is ineffective 2, 3

  • Maximum single dose should not exceed 1200 mg as part of the 3600 mg daily total 4
  • Doses above 3600 mg/day have been administered to small numbers of patients for short durations and were well-tolerated, but this is not standard practice 1, 5
  • The maximum time interval between doses must not exceed 12 hours 1

Special Population Adjustments

Renal Impairment

Mandatory dose reduction is required based on creatinine clearance, as gabapentin is eliminated unchanged by the kidneys 1, 2:

  • CrCl ≥60 mL/min: 900-3600 mg/day (standard dosing) 1
  • CrCl 30-59 mL/min: 400-1400 mg/day in two divided doses 1
  • CrCl 15-29 mL/min: 200-700 mg/day as single daily dose 1
  • CrCl <15 mL/min: 100-300 mg/day as single daily dose 1
  • Hemodialysis patients: Maintenance dose based on CrCl plus supplemental 125-350 mg post-dialysis dose 1

Elderly Patients

  • Lower starting doses and slower titration are essential due to age-related decline in renal function 1, 2
  • Dose selection must be based on creatinine clearance values, not just age 1
  • Elderly patients face increased risk of falls, dizziness, and confusion at higher doses 6

Dose-Response and Safety Profile

Higher doses increase adverse events without proportional pain relief benefits:

  • A clear dose-response relationship exists for falls/fractures, with highest risk at doses ≥2400 mg/day (RR 1.90) 6
  • Common adverse events include dizziness (19%), somnolence (14%), peripheral edema (7%), and gait disturbance (14%) at therapeutic doses 7
  • Adverse event withdrawals occur in 11% of patients on gabapentin versus 8.2% on placebo 7

Condition-Specific Maximum Doses

  • Postherpetic neuralgia and diabetic neuropathy: 1800-3600 mg/day 2, 1, 7
  • Epilepsy (adults): Up to 2400 mg/day well-tolerated in long-term studies; 3600 mg/day administered to small numbers short-term 1
  • HIV-associated neuropathic pain: Maximum 2400 mg/day 2
  • Chronic unexplained cough: Maximum 1800 mg/day in two divided doses 2, 4

Critical Pitfalls to Avoid

  • Never exceed 3600 mg/day in routine clinical practice without compelling justification, as evidence for benefit above this dose is lacking 1, 2
  • Never use once or twice daily dosing for standard gabapentin—this is pharmacologically ineffective due to saturable absorption 2
  • Never discontinue abruptly—taper gradually over minimum 1 week to avoid withdrawal symptoms 1, 2
  • Never ignore renal function—failure to adjust for impaired creatinine clearance leads to drug accumulation and toxicity 1, 3

References

Guideline

Gabapentin Dosing Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Gabapentin Dosing and Administration

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Gabapentin dosing in the treatment of epilepsy.

Clinical therapeutics, 2003

Research

Gabapentin for chronic neuropathic pain in adults.

The Cochrane database of systematic reviews, 2017

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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