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To study gastrointestinal adverse events associated umbralisib, idelalisib, duvelisib and alpelisib using the FDA adverse event reporting system (FAERS)

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Trial Profile

To study gastrointestinal adverse events associated umbralisib, idelalisib, duvelisib and alpelisib using the FDA adverse event reporting system (FAERS)

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 29 Sep 2022

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At a glance

  • Drugs Alpelisib (Primary) ; Duvelisib (Primary) ; Idelalisib (Primary) ; Umbralisib (Primary)
  • Indications Cancer
  • Focus Therapeutic Use

    • Most Recent Events

    • 29 Sep 2022 New trial record
    • 28 Aug 2022 Results presented at the 38th International Conference on Pharmacoepidemiology and Therapeutic Risk Management

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