BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UTERINE ARTERY EMBOLIZATION

    MDR report key: 935986 · Received October 23, 2007

    Report

    Report Number
    MW5004239
    Event Type
    Injury
    Date Received
    October 23, 2007
    Date of Event
    March 1, 2007
    Report Date
    October 23, 2007
    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

    SEVERE LLQ PAIN FOR THREE AND A HALF WEEKS EVERY MONTH. PAIN WORSENING OVER THE SIX MONTHS SINCE UAE. IN THE SIXTH MONTH POST UAE, EXPERIENCING TEMPERATURE ELEVATION, VOMITING, SIGNIFICANT DIARRHEA. IR AND GYNECOLOGIST REFUSED TO SPEAK WITH PT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 YR Other