BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UTERINE ARTERY EMBOLIZATION

    MDR report key: 1811927 · Received August 18, 2010

    Report

    Report Number
    MW5017141
    Event Type
    Injury
    Date Received
    August 18, 2010
    Date of Event
    January 28, 2010
    Report Date
    August 18, 2010
    Product Code
    NAJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    FOR THE PAST 7 MONTHS SINCE UNDERGOING UAE, SHE HAS EXPERIENCED LOSS OF ORGASM, HAIR LOSS, INSOMNIA, AND BI-WEEKLY MENSTRUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UTERINE ARTERY EMBOLIZATION NONE NAJ

    Patients

    Seq Age Sex Outcome Treatment
    1 Other