DENTAL AMALGAM FILLINGS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-05-08 for DENTAL AMALGAM FILLINGS manufactured by Unk.

Event Text Entries

[1552002] Became disabled over time, diagnosed with ms and mercury toxicity by my doctor's major balance problems, peripheral neuropathy, paresthesia - numbness in extremities -, chronic fatigue, mental confusion, told going blind by 2 ophthalmologists, etc. After diagnosis of mercury toxicity, per tests, it was found that my major mercury source was dental amalgam fillings. - dr. (b) (6) - fp, dr. (b) (6) - neurologist, etc. - after replacement of amalgam fillings and detoxification, i over time fully recovered or significantly improved from all of these problems and now am again fully functional. Similar is true of thousands of others who had ms related to mercury. (b) (6). Dose or amount: 10 fillings plus 7 metal crown, route: dental. Diagnosis or reason for use: mercury toxicity re: tests; cavities. Event abated after use: yes.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5015880
MDR Report Key1685971
Date Received2010-05-08
Date of Report2010-05-08
Date of Event1992-01-01
Date Added to Maude2010-05-17
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
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

Generic NameDENTAL AMALGAM FILLINGS
Product CodeEJJ
Date Received2010-05-08
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Sequence No1
Device Event Key0
ManufacturerUNK
Manufacturer AddressUNK UNK


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2010-05-08

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