BEUDAMED
    FDA Adverse Event Injury Summary report: N

    AMALGAM MERCURY

    MDR report key: 12954611 · Received December 6, 2021

    Report

    Report Number
    MW5105878
    Event Type
    Injury
    Date Received
    December 6, 2021
    Date of Event
    October 1, 2008
    Report Date
    December 3, 2021
    Manufacturer
    UNK
    Product Code
    OIV
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    REPORTER CALLED TO REPORT THAT IN (B)(6) 2008 HIS SON HAD ONE TOOTH NUMBER THIRTEEN FILLED WITH AMALGAM MERCURY BY A DENTIST IN (B)(6) AND THAT HIS SON HAS BEEN ILL AND DISABLED EVER SINCE. HE REPORTS THAT HIS SON IS UNABLE TO ENJOY LIFE OR FAMILY; THAT HE USED TO A VARSITY TENNIS PLAYER AND HAD AN ACTIVE SOCIAL LIFE. REPORTER STATES THAT HE HAS SPENT OVER FOUR HUNDRED THOUSAND DOLLARS TO FIND OUT WHAT IS WRONG WITH HIS SON. REPORTER STATES THAT HE WAS ADVISED TO HAVE THE FILLING REMOVED AND SINCE REMOVAL HE HAS GOTTEN TWENTY TO THIRTY PERCENT BETTER. "NO ONE HAS BEEN ABLE TO HELP MY SON GET BETTER AFTER THIS AMALGAM FILLING HAS MADE HIM SICK AND DISABLED. NO ONE CARES ABOUT THIS IN THE USA. WE HAVE BEEN EVERYWHERE TRYING TO FIND OUT WHAT IS WRONG; EVEN THE (B)(6) COULD NOT TELL US."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1843338 AMALGAM MERCURY AMALGAM MERCURY OIV UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR Male Other| S