Can gabapentin (anticonvulsant) be used to treat anxiety?

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Gabapentin for Anxiety Treatment

Gabapentin is not recommended as a first-line treatment for anxiety disorders, but may be considered as a second-line option when first-line treatments have failed or are contraindicated. 1

Evidence-Based Treatment Hierarchy for Anxiety

  • SSRIs and SNRIs are the recommended first-line pharmacological treatments for anxiety disorders with substantial evidence supporting their efficacy 1
  • Cognitive behavioral therapy (CBT) is recommended as a first-line non-pharmacological treatment for anxiety disorders 1
  • Benzodiazepines may be used for short-term management of severe anxiety but carry risks of dependence and are not recommended for long-term use 1
  • Gabapentin may be considered when first-line treatments have failed or are contraindicated 1, 2

Clinical Evidence for Gabapentin in Anxiety

  • Limited high-quality evidence exists for gabapentin's efficacy in generalized anxiety disorder, with most support coming from case reports rather than randomized controlled trials 3, 2
  • A systematic review found that gabapentin may have benefit for some anxiety disorders, although there are no robust studies specifically for generalized anxiety disorder 2
  • In a controlled trial with breast cancer survivors, gabapentin (300mg and 900mg) showed significant anxiolytic effects compared to placebo at both 4 and 8 weeks 4
  • An experimental study demonstrated that gabapentin (800mg) attenuated anxiety in healthy volunteers during simulated public speaking 5

Specific Clinical Considerations

  • The Canadian Clinical Practice Guideline lists gabapentin as a second-line drug for social anxiety disorder 6
  • Lower doses (300mg) may be effective for most patients with mild to moderate anxiety, while higher doses may be needed for those with severe baseline anxiety 4
  • Gabapentin may be particularly useful in patients with comorbid conditions that might benefit from its use, such as neuropathic pain, seizures, or insomnia 1
  • For patients reluctant to take benzodiazepines or those with a history of substance use, gabapentin may offer an alternative therapy with lower abuse potential 4

Safety Concerns and Monitoring

  • Gabapentinoids (including gabapentin) have been associated with tolerance, dependence, addiction, and withdrawal symptoms, similar to benzodiazepines 7
  • In 2019, gabapentinoids were classified as controlled substances (Class C) in some countries due to these risks 7
  • Deaths involving pregabalin (a related gabapentinoid) have been rising, particularly when used concomitantly with opioids or other drugs 7
  • Regular evaluation of treatment response using standardized anxiety measures is recommended 1

Practical Prescribing Approach

  • Start with lower doses (300mg daily) and titrate based on response and tolerability 4
  • Monitor for side effects including somnolence, dizziness, and peripheral edema 2
  • Evaluate efficacy after 4-8 weeks of treatment 4
  • Consider discontinuation if no meaningful improvement is observed 7
  • When discontinuing, taper gradually to minimize withdrawal symptoms 3

Limitations of Current Evidence

  • Most studies on gabapentin for anxiety are short-term and don't account for long-term effects of tolerance and dependence 7
  • Variation in dosing between studies makes it difficult to establish optimal dosing guidelines 2
  • Studies vary in whether gabapentin is used as monotherapy or adjunctive treatment 2
  • Different primary outcomes between trials complicate direct comparisons 2

References

Guideline

Gabapentin for Anxiety Treatment

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Gabapentin Therapy in Psychiatric Disorders: A Systematic Review.

The primary care companion for CNS disorders, 2015

Research

Treatment of Generalized Anxiety Disorder with Gabapentin.

Case reports in psychiatry, 2017

Research

Effects of gabapentin on anxiety induced by simulated public speaking.

Journal of psychopharmacology (Oxford, England), 2003

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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