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An Evaluation of Postmarketing Reports with an Outcome of Death in the US FDA Adverse Event Reporting System.

Kathryn MarwitzS Christopher JonesCindy M KortepeterGerald J Dal PanMonica A Muñoz
Published in: Drug safety (2021)
Understanding the origins and characteristics of ICSRs with an outcome of death supports meaningful evaluations and interpretations of FAERS data. A wide variability in ICSR quality exists, even in those reports with the most serious outcome.
Keyphrases
  • adverse drug
  • electronic health record
  • big data
  • quality improvement
  • drug induced