BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ESSURE

    MDR report key: 4771771 · Received May 14, 2015

    Report

    Report Number
    MW5042689
    Event Type
    Injury
    Date Received
    May 14, 2015
    Date of Event
    April 28, 2015
    Report Date
    May 2, 2015
    Manufacturer
    BAYER
    Product Code
    HHS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    (B)(4). PELVIC PAIN, HEAVY BLOOD, HEADACHES, DIZZIED, ALLERGIES, HAIR AND NAIL LOSS, NUMBED LEFT LEG AND ARM,. VITAMIN D DEFICIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    315142 ESSURE HHS BAYER

    Patients

    Seq Age Sex Outcome Treatment
    1 34.000 YR Other