BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AMALGAM FILLING

    MDR report key: 1685983 · Received May 7, 2010

    Report

    Report Number
    MW5015888
    Event Type
    Injury
    Date Received
    May 7, 2010
    Date of Event
    January 1, 1965
    Report Date
    May 7, 2010
    Manufacturer
    UNK
    Product Code
    EJJ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I WAS DIAGNOSED WITH MULTIPLE SCLEROSIS IN 1982. I NOW HAVE GONE TO A DOCTOR, WHO SAYS I HAVE MERCURY POISONING. I WENT AND HAD ALL MY MERCURY FILLINGS TAKEN OUT AND REPLACED WITH WHITE FILLINGS. MERCURY FILLINGS NEED TO BE STOPPED HERE IN THE USA. DIAGNOSIS OR REASON FOR USE: CAVITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 AMALGAM FILLING AMALGAM FILLING EJJ UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 7 YR Required Intervention