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FDA Adverse Event Reports – Serious Cases for Spravato (2024; ~5,382 Cases)
FDA Adverse Event Reports – Serious Cases for Spravato (2024; ~5,382 Cases)
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Original Request Contents: Underlying adverse event reports for all serious cases related to Spravato (2024; approximately 5,382 cases)
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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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