BEUDAMED
    FDA Adverse Event Death Summary report: N

    EUFLEXXA

    MDR report key: 10918556 · Received November 25, 2020

    Report

    Report Number
    MW5098107
    Event Type
    Death
    Date Received
    November 25, 2020
    Date of Event
    September 25, 2020
    Report Date
    November 24, 2020
    Manufacturer
    FERRING PHARMACEUTICALS INC.
    Product Code
    MOZ
    UDI-DI
    55566410001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    PER EMAIL SENT, PATIENT PASSED AWAY (B)(6) 2020; ARWXP INFORMED TODAY, (B)(6). MEDICATION EXPIRATION DATE NOT REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1364278 EUFLEXXA ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS INC. 55566410001

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Death