FDA Adverse Event Summary for Tums, Tums Ultra, Tislelizumab, Capivasertib, Foscarbidopa/Foslevodopa, and Infliximab-dyyb (Jan–Mar 2025)

FDA Adverse Event Summary for Tums, Tums Ultra, Tislelizumab, Capivasertib, Foscarbidopa/Foslevodopa, and Infliximab-dyyb (Jan–Mar 2025)

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Original Request: Please provide me with data summarizing reports of adverse events associated with the following drugs between Jan. 1, 2025 and March 18, 2025: Tums and Tums Ultra, tislelizumab, capivasertib, foscarbidopa/foslevodopa, and infliximab-dyyb.
Tags: Pharma, Adverse Event, 2025
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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