BEUDAMED
    FDA Adverse Event Other Summary report: N

    EUFLEXXA

    MDR report key: 20568738 · Received October 29, 2024

    Report

    Report Number
    MW5161886
    Event Type
    Other
    Date Received
    October 29, 2024
    Date of Event
    March 1, 2024
    Report Date
    October 23, 2024
    Manufacturer
    FERRING PHARMACEUTICALS INC.
    Product Code
    MOZ
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I RECEIVED EUFLEXXA INJECTIONS "(B)(6) 2024" STARTING WITH MY RIGHT KNEE. BOTH KNEES BECAME VERY PAINFUL AND STIFF. I HAD SWELLING IN BOTH OF MY LOWER LEGS AND FEET AND ENDED UP WITH A STRESS FRACTURE IN MY RINGTONE FOOT AS A RESULT OF WALKING ODD TO HELP ALLEVIATE THE KNEE PAIN. I ALSO LOST A LOT OF HAIR ON MY HEAD. REF REPORTS: MW5161887, MW5161888, MW5161889.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1897268 EUFLEXXA ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 74 YR Female AMLODIPINE.| ESTRADIOL.| IBUPROFEN.| ICOSAPENT.| METOPROLOL.| SERTRALINE.| ZEGERID.