BEUDAMED
    FDA Adverse Event Death Summary report: N

    SYNVISC

    MDR report key: 16397963 · Received February 16, 2023

    Report

    Report Number
    MW5114999
    Event Type
    Death
    Date Received
    February 16, 2023
    Date of Event
    December 21, 2022
    Report Date
    February 14, 2023
    Manufacturer
    GENZYME CORPORATION
    Product Code
    MOZ
    UDI-DI
    58468009001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE PATIENT'S SON REPORTED THAT THE PATIENT PASSED AWAY ON (B)(6) 2022. NO ADDITIONAL INFORMATION DOCUMENTED. THE FOLLOWING PRODUCT INFORMATION REFLECTS THE LAST DISPENSE BY (B)(6) PHARMACY (DELIVERED 30NOV2021) AND WAS NOT PROVIDED BY THE PRIMARY REPORTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1374506 SYNVISC ACID, HYALURONIC, INTRAARTICULAR MOZ GENZYME CORPORATION ARSP011E 58468009001

    Patients

    Seq Age Sex Outcome Treatment
    1 85 YR Male Death