Can levetiracetam (Keppra) cause somnolence?

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Last updated: February 14, 2026View editorial policy

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Can Keppra Make You Sleepy?

Yes, levetiracetam (Keppra) commonly causes somnolence (sleepiness), which is one of its most frequently reported side effects.

Incidence of Somnolence

In Adults with Partial Onset Seizures

  • 14.8% of levetiracetam-treated adults reported somnolence compared to 8.4% of placebo patients in controlled trials 1
  • At higher doses (4000 mg/day without titration), approximately 45% of patients experienced somnolence 1
  • Somnolence was considered serious in 0.3% of treated patients 1
  • About 3% of patients discontinued treatment specifically due to somnolence, compared to 0.7% of placebo patients 1

In Pediatric Patients

  • 22.8% of levetiracetam-treated children experienced somnolence, compared to 11% of placebo patients in controlled trials 1

Timing and Pattern

  • Somnolence occurs most frequently within the first 4 weeks of treatment 1
  • This side effect is part of a broader pattern of CNS adverse events that also includes fatigue (asthenia) and coordination difficulties 1

Comparative Safety Profile

Levetiracetam is generally better tolerated than older antiepileptic drugs like phenytoin or valproic acid, according to the American Academy of Neurology 2, 3

  • The American Heart Association recommends levetiracetam over phenytoin or valproic acid due to its better overall tolerability profile 2
  • When oral loading was used in patients with epilepsy, 89% reported no adverse effects, while only 11% experienced transient tiredness or lightheadedness 2

Clinical Significance

Severity and Management

  • In most cases, somnolence is mild to moderate and transient 4, 2
  • The dose was reduced in 1.4% of treated patients due to somnolence 1
  • Only 0.3% of patients required hospitalization due to somnolence 1

Common Pitfalls to Avoid

  • Do not assume somnolence will resolve immediately—it typically improves after the first month but may persist in some patients 1
  • Higher doses carry substantially higher risk—the jump from standard dosing to 4000 mg/day increases somnolence rates from ~15% to ~45% 1
  • Renal dysfunction requires dose adjustment as levetiracetam is predominantly renally eliminated, which could exacerbate CNS side effects if not properly adjusted 2

Additional Context from Research

Systematic reviews confirm that somnolence is the most statistically significant adverse effect associated with levetiracetam compared to placebo 5. A comprehensive safety review of 3,347 patients found that somnolence, along with asthenia and dizziness, occurred most frequently during the first month of treatment 6.

References

Guideline

Adverse Effects of Levetiracetam

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Levetiracetam Safety Profile in Pediatric Patients

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

The adverse effects profile of levetiracetam in epilepsy: a more detailed look.

The International journal of neuroscience, 2014

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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