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FDA Adverse Event Reports – Librela (Bedinvetmab) in Dogs
FDA Adverse Event Reports – Librela (Bedinvetmab) in Dogs
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Original Request: I would liked to request records regarding reported adverse events received on librela
(bedinvetmab) under the Freedom of Information Act. All adverse events reported in all dogs.
If possible please include adverse events reported from US release date up until today’s date
8/13/2024 or as late as can be included.
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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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