BEUDAMED
    FDA Adverse Event Death Summary report: N

    EUFLEXXA

    MDR report key: 7772102 · Received August 9, 2018

    Report

    Report Number
    MW5079022
    Event Type
    Death
    Date Received
    August 9, 2018
    Date of Event
    June 15, 2018
    Report Date
    August 8, 2018
    Manufacturer
    FERRING PHARMACEUTICALS, INC.
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT'S DAUGHTER REPORTED THAT THE PT HAS PASSED AWAY. BILATERAL PRIMARY OSTEOARTHRITIS OF KNEE. THERAPY START DATE: (B)(6) 2017; THERAPY END DATE: (B)(6) 2018.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    607448 EUFLEXXA ACID, HYALURONIC INTRAARTICULAR MOZ FERRING PHARMACEUTICALS, INC. N10841A

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Death