BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA 10 MG/ ML

    MDR report key: 6954421 · Received October 17, 2017

    Report

    Report Number
    MW5072776
    Event Type
    Injury
    Date Received
    October 17, 2017
    Report Date
    October 13, 2017
    Manufacturer
    FERRING
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PATIENT'S WIFE REPORTED PATIENT HAD A BRAIN ABSCESS. NO ONSET DATE WAS PROVIDED. DOSE OR AMOUNT: 20 MG, FREQUENCY: WEEKLY FOR 3 WEEKS, ROUTE: INTRA-ARTICULAR. DIAGNOSIS OR REASON FOR USE: UNILATERAL PRIMARY OSTEOARTHRITIS, RIGHT KNEE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    734007 EUFLEXXA 10 MG/ ML ACID, HYALURONIC MOZ FERRING L15376A

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Other