BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ESSURE

    MDR report key: 3983317 · Received August 6, 2014

    Report

    Report Number
    MW5037604
    Event Type
    Injury
    Date Received
    August 6, 2014
    Date of Event
    September 11, 2013
    Report Date
    August 4, 2014
    Manufacturer
    BAYER
    Product Code
    HHS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    (B)(4). SEVERE CRAMPING, SWELLING IN MY FEET, HOT FLASHES, HEAVY BLEEDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    459512 ESSURE HHS BAYER

    Patients

    Seq Age Sex Outcome Treatment
    1 36.000 YR Other