FDA FAERS Reports on Retinal Vasculitis and All Safety Reports for Izervay and Syfovre

FDA FAERS Reports on Retinal Vasculitis and All Safety Reports for Izervay and Syfovre

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Original Request: Please look at the FAERS data/FOIA Post-Market Safety Cases that have been reported for Izervay and Syfovre. Notably, we are interested in occurrences of "retinal vasculitis," but please include all safety reports.
Tags: Pharma, FAERS, 2025
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.

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