American Journal of Emergency Medicine
Volume 27, Issue 8 , Pages 911-915, October 2009

Incidence and onset of delayed seizures after overdoses of extended-release bupropion

  • Paul Starr, PharmD

      Affiliations

    • Maryland Poison Center/Department of Pharmacy Practice and Science, University of Maryland Baltimore, Baltimore, MD 21201
    • Corresponding Author InformationCorresponding author. Maryland Poison Center, University of Maryland School of Pharmacy, Level 01, Baltimore, Maryland 21201.
  • ,
  • Wendy Klein-Schwartz, PharmD

      Affiliations

    • Maryland Poison Center/Department of Pharmacy Practice and Science, University of Maryland Baltimore, Baltimore, MD 21201
  • ,
  • Henry Spiller, MS, RN

      Affiliations

    • Kentucky Regional Poison Center, Kosair Children's Hospital, Louisville, KY 40202
  • ,
  • Perri Kern, BSN, RN

      Affiliations

    • Regional Poison Control Center, Children's Hospital of Michigan, Detroit, MI 48201
  • ,
  • Susan E. Ekleberry, BS Pharmacy, RPh

      Affiliations

    • Central Ohio Poison Center, Nationwide Children's Hospital, Columbus, OH 43205
  • ,
  • Susan Kunkel, PharmD

      Affiliations

    • New Mexico Poison and Drug Information Center, University of New Mexico Health Sciences Center, Albuquerque, NM 87131

Received 7 April 2008; received in revised form 29 June 2008; accepted 2 July 2008.

Abstract 

Background

Delayed seizures have been reported with overdoses of bupropion extended-release (XL). This study systematically evaluates the frequency and timing of seizures and an association between other toxic effects (ie, agitation, tremors, and hallucinations) and seizures.

Methods

A 3-year multi–poison center observational study of hospitalized patients with ingestion of bupropion XL ≥600 mg in adults and ≥4 mg/kg in children was performed. Patients with coingestants or a medical history that could affect seizure occurrence were excluded. Data collection forms captured onset time of seizure(s), other symptoms, and treatment.

Results

One hundred seventeen patients met inclusion criteria: median age of 22 years (range, 1.3-65 years) with 16 children ≤ 3 years. Seizures occurred in 37 (31.6%) patients, with initial seizure at 0.5 to 24 hours after ingestion; 12 (32%) patients had initial seizure at > 8 hours. Subsequent seizures occurred in 49%. Children ages 1.3, 3, and 7 years, developed seizures. In patients ≥ 13 years of age, median dose with seizures was 4350 mg (range, 600-54 000) compared to 2400 mg (range, 600-9000) in patients without seizures. Agitation, tremors, and hallucinations occurred in 29.7%, 40.5%, and 18.9% of patients with seizures, respectively, compared with 12.5 %, 17.5%, and 10% in patients without seizures. The neurologic effects agitation (P = .045) and tremors (P = .005) occurred more frequently.

Conclusion

Delayed seizure onset suggests a minimum observation period of 24 hours after bupropion XL overdose. Although patients experiencing agitation or tremors may be at greater risk, seizures can occur without preceding central nervous system toxicity.

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PII: S0735-6757(08)00525-1

doi:10.1016/j.ajem.2008.07.004

American Journal of Emergency Medicine
Volume 27, Issue 8 , Pages 911-915, October 2009