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Structured benefit-risk evaluation for medicinal products: review of quantitative benefit-risk assessment findings in the literature.

Marie-Laure KürzingerLudivine DouarinIevgeniia UzunChantal El-HaddadWilliam HurstJuhaeri JuhaeriStéphanie Tcherny-Lessenot
Published in: Therapeutic advances in drug safety (2020)
Quantitative evaluation of the benefit-risk balance for medicinal products The review of the benefits and the risks associated with a medicinal product is called benefit-risk assessment. One of the conditions for a medicinal product to receive marketing authorization is to demonstrate a positive benefit-risk balance in which the benefits outweigh the risks. In order to enhance the transparency and consistency in the assessment of benefit-risk balance, frameworks and quantitative methods have been developed for decision making purposes and regulatory approvals of medicinal products. This article considers published quantitative benefit-risk evaluations which may have informed health care professionals and/or payor as well as contributed to decision making purposes in the regulatory setting for drug, vaccine and/or device approval.
Keyphrases
  • risk assessment
  • decision making
  • high resolution
  • human health
  • randomized controlled trial
  • transcription factor
  • emergency department
  • mass spectrometry
  • climate change
  • adverse drug
  • drug discovery