BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA INJ

    MDR report key: 6996245 · Received November 2, 2017

    Report

    Report Number
    MW5073104
    Event Type
    Injury
    Date Received
    November 2, 2017
    Date of Event
    October 30, 2017
    Report Date
    October 30, 2017
    Manufacturer
    UNK
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    SEVERE PAIN (PAIN SCALE 0-10, RATES AT 9) AND STATES IT GETS WORSE WHEN SHE LAYS DOWN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    776438 EUFLEXXA INJ EUFLEXXA INJ MOZ UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR