BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA INJ 10MG/ML

    MDR report key: 6199341 · Received December 19, 2016

    Report

    Report Number
    MW5066867
    Event Type
    Injury
    Date Received
    December 19, 2016
    Date of Event
    December 19, 2016
    Report Date
    December 19, 2016
    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

    ALLERGY WITH SYNVISC.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    838609 EUFLEXXA INJ 10MG/ML EUFLEXXA INJ 10MG/ML MOZ UNK 55566410001
    838610 EUFLEXXA INJ 10MG/ML EUFLEXXA INJ 10MG/ML MOZ UNK 55566410001

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR