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    FDA FAERS Reports – Daybue (Troinetide) Adverse Events (From 1/1/2023; Case IDs: 239240521, 238170541, 237420811, 232756201, 232574331)

    FDA FAERS Reports – Daybue (Troinetide) Adverse Events (From 1/1/2023; Case IDs: 239240521, 238170541, 237420811, 232756201, 232574331)

    $69.00 USD
    $69.00 USD
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    Original Request Contents: Request FDA FAERS reports for adverse events for Daybue (troinetide) from 1/1/2023 to the latest available date, covering both brand and generic names; results to be emailed as PDF or Excel, accepting shorter form reports without narratives.
    • 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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