BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ESSURE

    MDR report key: 3781403 · Received April 30, 2014

    Report

    Report Number
    MW5035822
    Event Type
    Injury
    Date Received
    April 30, 2014
    Date of Event
    August 10, 2010
    Report Date
    April 17, 2014
    Manufacturer
    BAYER
    Product Code
    HHS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    HEAVY CONTINUOUS BLEEDING THAT LEAD TO ANEMIA AND IRON DEFICIENCY. FATIGUE, JOINT PAIN, VISION PROBLEMS, ANXIETY ATTACKS, DEPRESSION, LOWER BACK PAIN, ABDOMEN PAIN, HIGH BLOOD PRESSURE. #MEDWATCHER #MW156149.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    260828 ESSURE HHS BAYER

    Patients

    Seq Age Sex Outcome Treatment
    1 45.000 YR Other CYTOMEL,SYNTHROID,LEXAPRO,CLARITIN.SINGULAIR,LISIN