Advancing drug safety science by integrating molecular knowledge with post‐marketing adverse event reports

Abstract Promising drug development efforts may frequently fail due to unintended adverse reactions. Several methods have been developed to analyze such data, aiming to improve pharmacovigilance and drug safety. In this work, we provide a brief review of key directions to quantitatively analyzing ad...

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Библиографические подробности
Главные авторы: Theodoros G. Soldatos (Автор), Sarah Kim (Автор), Stephan Schmidt (Автор), Lawrence J. Lesko (Автор), David B. Jackson (Автор)
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Опубликовано: Wiley, 2022-05-01T00:00:00Z.
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