FDA Summary Narratives for Semaglutide FAERS Cases: 24431673, 24556422, 24556421, 24546950, 24566981, 24589385, 24578484, 24616184, 24622224, 24611285, 24644491, 24634599

FDA Summary Narratives for Semaglutide FAERS Cases: 24431673, 24556422, 24556421, 24546950, 24566981, 24589385, 24578484, 24616184, 24622224, 24611285, 24644491, 24634599

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Original Request: I would like to request copies of the summary narratives produced for the following adverse events related to semaglutide. Please send these in electronic format over email. (Case ID) 24431673, 24556422, 24556421, 24546950, 24566981, 24589385, 24578484, 24616184, 24622224, 24611285, 24644491, 24634599
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

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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