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Adverse Drug Reaction Risk Measures: A Comparison of Estimates from Drug Surveillance and Randomised Trials.

Raphaelle Beau-LejdstromSarah CrookAlessandra SpanuTsung YuMilo A Puhan
Published in: Pharmaceutical medicine (2020)
Spontaneous reporting of suspected ADRs is an important tool for regulatory agencies and pharmaceutical companies in making decisions and detecting drug safety signals. Although there was moderate-to-strong agreement between ADR risk estimates from drug surveillance and RCTs for one drug, this study illustrates the current recommendations not to use disproportionality measures as valid proxies for risk estimates.
Keyphrases
  • adverse drug
  • electronic health record
  • drug induced
  • emergency department
  • public health
  • clinical trial
  • randomized controlled trial
  • open label
  • transcription factor