BEUDAMED
    FDA Adverse Event Death Summary report: N

    EUFLEXXA 20 MG/2ML

    MDR report key: 17595255 · Received August 21, 2023

    Report

    Report Number
    MW5144817
    Event Type
    Death
    Date Received
    August 21, 2023
    Report Date
    August 17, 2023
    Manufacturer
    UNKNOWN
    Product Code
    MOZ
    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

    (B)(6) CAREGIVER OF PATIENT REPORTED THAT PATIENT PASSED AWAY (B)(6) 2023. INJECT ONE PRE-FILLED SYRINGE INTRA-ARTICULARLY INTO BOTH KNEES EVERY WEEK FOR 3 WEEKS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    50458 EUFLEXXA 20 MG/2ML ACID, HYALURONIC, INTRAARTICULAR MOZ UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Male Death