BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UTERINE ARTERY EMBOLIZATION

    MDR report key: 1297485 · Received January 27, 2009

    Report

    Report Number
    MW5009761
    Event Type
    Injury
    Date Received
    January 27, 2009
    Date of Event
    February 29, 2008
    Report Date
    January 27, 2009
    Product Code
    NAJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    SHE IS 8.5 MONTHS POST UAE AND CONTINUES TO HAVE A CONSTANT BEIGE/BROWN VAGINAL DISCHARGE, CONTINUOUS HOT FLASHES AND BACK PAIN WHICH REQUIRE IBUPROFEN TWO TO THREE TIMES A DAY.

    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