FDA Full FAERS Reports – IZERVAY/Avacincaptad Pegol Intravitreal Solution (11/16/2024–11/22/2024, Electronic)

FDA Full FAERS Reports – IZERVAY/Avacincaptad Pegol Intravitreal Solution (11/16/2024–11/22/2024, Electronic)

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Original Request Contents: Request full FAERS reports for adverse events for IZERVAY (branded, marketed by Astellas Pharma Inc.) or avacincaptad pegol intravitreal solution (generic) between 11/16/2024 and 11/22/2024, provided electronically.
  • 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. Learn more about Fast-Track Requests here.

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