Is parkinsonism a side effect of lamotrigine?

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Parkinsonism as a Side Effect of Lamotrigine

Parkinsonism is a documented but uncommon side effect of lamotrigine. While lamotrigine is generally well-tolerated and preferred for its favorable side effect profile compared to older antiseizure medications, it has been associated with various movement disorders including parkinsonism in some patients.

Evidence for Lamotrigine-Associated Parkinsonism

  • A literature review identified 13 cases of parkinsonism associated with lamotrigine use among 108 cases of lamotrigine-related movement disorders from 19 countries 1
  • Movement disorders associated with lamotrigine typically develop within 6 months of starting the medication in 81% of cases 1
  • In most cases (83%), these movement disorders resolve within 1 month after lamotrigine withdrawal 1

Spectrum of Movement Disorders Associated with Lamotrigine

Lamotrigine can cause various movement disorders beyond parkinsonism:

  • Tics (29 cases), dyskinesias (21 cases), myoclonus (14 cases), dystonia (10 cases), and akathisia (10 cases) have been reported 1
  • Unusual side effects including tremor, unsteadiness, chorea, and eye movement abnormalities have been documented in pediatric patients 2
  • These movement disorders typically resolve upon discontinuation of lamotrigine 2, 1

Risk Factors and Clinical Considerations

  • The mean lamotrigine dose at movement disorder onset was reported to be 228 mg 1
  • Males appear to be more commonly affected than females 1
  • Epilepsy was the most common indication for lamotrigine use in patients who developed movement disorders 1

Management of Lamotrigine-Associated Parkinsonism

  • The most common and effective management strategy is lamotrigine withdrawal 1
  • Careful dose adjustment may be considered before complete withdrawal, evaluating the risk-benefit ratio on a case-by-case basis 1
  • When monitoring patients on lamotrigine, clinicians should regularly assess for the emergence of movement disorders 3

Lamotrigine in Clinical Practice

  • Despite these potential side effects, lamotrigine is considered a preferred option for seizure control due to its overall good tolerability 3
  • Lamotrigine is often preferred over enzyme-inducing antiepileptic drugs because it has fewer drug interactions with steroids, chemotherapy, and targeted therapies 3
  • In studies of driving performance, chronic lamotrigine use did not result in clinically meaningful driving impairment, suggesting that cognitive and motor functions are generally preserved with long-term use 3

Contrasting Evidence

  • Some research suggests lamotrigine may actually have beneficial effects on parkinsonian symptoms in certain patients with bipolar disorder 4
  • However, experimental studies in rat models of Parkinson's disease found that lamotrigine failed to demonstrate antiparkinsonian activity 5

Clinical Monitoring Recommendations

  • Patients starting lamotrigine should be monitored for the emergence of movement disorders, particularly within the first 6 months of treatment 1
  • If parkinsonism or other movement disorders develop, consider dose reduction or discontinuation of lamotrigine 1
  • Regular follow-up visits should include assessment for potential drug-related side effects, including movement disorders 3

References

Research

Unusual side effects of lamotrigine therapy.

Journal of child neurology, 2003

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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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