BEUDAMED
    FDA Adverse Event Death Summary report: N

    SYNVISC PFS 8MG/ML (3X2ML)

    MDR report key: 21976056 · Received May 7, 2025

    Report

    Report Number
    MW5170006
    Event Type
    Death
    Date Received
    May 7, 2025
    Date of Event
    April 13, 2025
    Report Date
    April 30, 2025
    Manufacturer
    SANOFI GENZYME CORP/GENZYME CORPORATION
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PT DECEASED. CALLER'S NAME: (B)(6). CALLER'S RELATIONSHIP TO THE CUSTOMER: DAUGHTER. CUSTOMER'S DECEASED DATE: (B)(6) 2025. REASON OF DEATH UNK.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1820526 SYNVISC PFS 8MG/ML (3X2ML) ACID, HYALURONIC, INTRAARTICULAR MOZ SANOFI GENZYME CORP/GENZYME CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Female Death