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FDA FAERS Adverse Event Reports – Leqembi/Lecanemab Case IDs
FDA FAERS Adverse Event Reports – Leqembi/Lecanemab Case IDs
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Original Request: I am writing to request, under the Freedom of Information Act, the following FDA Adverse Event Reporting System (FAERS) records, noted below by case number, pertaining to the drug leqembi (brand name) or lecanemab (generic): 23319617 21828248 22853291 23272251 22954105 21856064 21959204 22235964 22018092 22035372 22110894 22762686
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- 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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