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    FDA MedWatch Report for Product Case ID 24390130 (Lupkynis)

    FDA MedWatch Report for Product Case ID 24390130 (Lupkynis)

    $69.00 USD
    $69.00 USD
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    Original Request: • Request for MedWatch Report for Product Case ID 24390130 • Suspect Product: Lupkynis • Reaction: Therapy Non-Responder; Polyarthritis; Autoimmune Haemolytic Anaemia; Dermatitis Bullous; Off Label Use; Lupus Nephritis • 23-year-old Female • Country of occurrence: DE • Manufacturer Control Number: DE-ALKEM LABORATORIES LIMITED-DE-ALKEM-2024-22062
    Tags: Pharma, Adverse Event, 2024
    • 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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