"SILVER FILLINGS"

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-10-05 for "SILVER FILLINGS" manufactured by Still Everywhere U.s.a..

Event Text Entries

[1469838] Currently, i have 12 mercury amalgam fillings. I was "given" these all before i was age 12. I am also a recovering alcoholic, recovering drug addict, recovering sex addict; recovering "victim" of mercury poisoning. I work the 12 steps everyday. Taking full responsibility for my "diseases". If i had the money, i'd get these cursed things out today, however, i suffer from suicidal depression, and consequently dont' have much money, especially after paying the police and the state various fees for various misbehaviors, which i am now figuring out, predictably co-occur with mercury poisonings. May be this is all my fault. May be it is all your fault. Point is, i have been poisoned against my will as a child with a then-known neurotoxin, and now exhibit very clearly scientifically established well laid out obvious irrefutable incontestably undeniable symptoms of neurotoxic poisoning. If only there were a government agency that protected the citizenry, by regulating snake oil hucksters. Like i said, i am still suffering from neurotoxic poisoning. I hope someday to be able to afford getting this out of my body, and so may be to begin to live before i die. Event abated after use: no.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5017732
MDR Report Key1876066
Date Received2010-10-05
Date of Report2010-10-05
Date of Event1976-06-06
Date Added to Maude2010-11-09
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand Name"SILVER FILLINGS"
Generic NameMERCURY IMPLANTS
Product CodeEJJ
Date Received2010-10-05
Lot NumberWTF
Device AvailabilityY
Device Sequence No1
Device Event Key0
ManufacturerSTILL EVERYWHERE U.S.A.
Manufacturer AddressUS


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Life Threatening; 3. Other; 4. Required No Informationntervention 2010-10-05

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.