Succimer: the first approved oral lead chelator

Am Fam Physician. 1993 Dec;48(8):1496-502.

Abstract

The Centers for Disease Control and Prevention has redefined the threshold of concern for low-level lead toxicity, reducing it from a blood lead level of 25 micrograms per dL (1.21 mumol per L) to a blood lead level of 10 micrograms per dL (0.48 mumol per L), and has recommended universal screening of young children. Succimer (2,3-dimercaptosuccinic acid) is an effective oral lead chelating agent that has been approved for outpatient treatment of children with blood lead levels higher than 45 micrograms per dL (2.17 mumol per L). In the United States, clinical experience with succimer is limited; however, observed side effects, including gastrointestinal symptoms, rash and transient elevations of serum aminotransferase levels, are uncommon and mild. Isolated cases of neutropenia have been reported. Weekly monitoring of complete blood counts and serum aminotransferase levels is recommended during the 19-day treatment. Blood lead levels should be checked weekly to identify rebound from bone and soft tissue mobilization.

Publication types

  • Review

MeSH terms

  • Administration, Oral
  • Ambulatory Care
  • Clinical Trials as Topic
  • Drug Costs
  • Drug Eruptions / etiology
  • Drug Monitoring
  • Edetic Acid / therapeutic use
  • Female
  • Gastrointestinal Diseases / chemically induced
  • Humans
  • Lead Poisoning / blood
  • Lead Poisoning / drug therapy*
  • Lead Poisoning / epidemiology
  • Lead Poisoning / prevention & control
  • Lead Poisoning / urine
  • Mass Screening
  • Metabolic Clearance Rate
  • Neutropenia / chemically induced
  • Pregnancy
  • Succimer / pharmacology
  • Succimer / therapeutic use*
  • Transaminases / blood
  • United States
  • United States Food and Drug Administration

Substances

  • Edetic Acid
  • Succimer
  • Transaminases