BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA

    MDR report key: 7142229 · Received December 21, 2017

    Report

    Report Number
    MW5074192
    Event Type
    Injury
    Date Received
    December 21, 2017
    Date of Event
    December 20, 2017
    Manufacturer
    FERRING PHARMACEUTICALS INC.
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD THE 3RD EUFLEXXA INJECTION. IMMEDIATELY AFTERWARD I HAD SEVERE KNEE PAIN, TO WHERE I COULD NOT PUT WEIGHT ON IT. I HAD NOT HAD ANY PROBLEM WITH THE FIRST 2 INJECTIONS. ARTHRITIS, TORN MINISCUS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    920463 EUFLEXXA EUFLEXXA MOZ FERRING PHARMACEUTICALS INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR