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    FDA MedWatch Report for Myfortic Adverse Reactions – Case ID 24237687: Gastrointestinal Disorder, Proteinuria, Renal Failure, Streptococcal Bacteraemia.

    FDA MedWatch Report for Myfortic Adverse Reactions – Case ID 24237687: Gastrointestinal Disorder, Proteinuria, Renal Failure, Streptococcal Bacteraemia.

    $89.00 USD
    $89.00 USD
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    Original Request: • Request for MedWatch Report for Product Case ID 24237687 • Suspect Product: Myfortic • Reaction: Gastrointestinal Disorder; Proteinuria; Renal Failure; Streptococcal Bacteraemia; Urine Protein/Creatinine Ratio Increased; Cellulitis; Oedema • 68-Year-old male • Country of occurrence: US • Manufacturer Control Number: NVSC2024US165672
    • 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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