FDA Adverse Event Data FOIA

  • Oversight Actions
1 min. read

In this FOIA, we sought additional information regarding mifepristone safety data, including documents and reports from FDA’s newly identified safety signal (NISS) records, periodic safety reports (PSRs), and active risk identification and analysis (ARIA) system.

Submitted: 3/20/2026
30-day response due: 5/1/2026