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FDA MedWatch Report for Farxiga, Jardiance, Lupkynis Adverse Reactions – Case ID 24271750: Rash Pruritic, Back Pain, Pruritus, Rash.
FDA MedWatch Report for Farxiga, Jardiance, Lupkynis Adverse Reactions – Case ID 24271750: Rash Pruritic, Back Pain, Pruritus, Rash.
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Original Request: • Request for MedWatch Report for Product Case ID 24271750 • Suspect Product: Farxiga; Jardiance; Lupkynis • Reaction: Rash Pruritic; Back Pain; Pruritus; Rash • 63-year-old Male • Country of occurrence: Not Specified • Manufacturer Control Number: US-AstraZeneca-2024A192219
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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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