BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UTERINE ARTERY EMBOLIZATION

    MDR report key: 388863 · Received April 16, 2002

    Report

    Report Number
    MW1024753
    Event Type
    Injury
    Date Received
    April 16, 2002
    Date of Event
    April 1, 1997
    Report Date
    April 11, 2002
    Manufacturer
    *
    Product Code
    KRD
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    AFTER UNDERGOING UTERINE ARTERY EMBOLIZATION PT EXPERIENCED FOUL VAGINAL ODOR, VAGINAL DISCHARGE WITH PUS AND BLOOD, PAIN IN LLQ, DEPRESSION, LOSS OF EMPLOYMENT, AND UTERINE INFECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UTERINE ARTERY EMBOLIZATION * KRD * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other| R