MERCURY DENTAL AMALGAM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-08-06 for MERCURY DENTAL AMALGAM manufactured by Henry Schein, Inc..

Event Text Entries

[1362069] I am reporting on the adverse reactions of the mercury amalgam fillings placed in my mouth when i was still an adolescent. I was what one would call an allergic and sensitive child. After having the amalgams placed, my health began to exhibit strange symptoms geographic tongue, tinea versicolor, autoimmune issues, etc. More importantly, my mother is a medical professional, and had she known that mercury was a 50 percent component of amalgam fillings, she never would have let a dentist near anyone in our family. Recently, in addition to my other diagnoses, i was diagnosed with adhd and heavy metal toxicity. I had my mercury amalgam fillings removed in (b)(6)2010. At this point, my symptoms ranged from general erethism, spontaneous lactation, agoraphobia, miscarriages, migraines, brain fog, fibromyalgia, cfs, inability to learn new things, difficulty reading, fits of rage, mood swings, multiple food allergies -including gluten and dairy- etc. And just to be clear, my agoraphobia was so debilitating, i had to withdraw from a major university under full academic scholarship in 2000. The two days post-removal, i had not felt better than i had felt in years. It was instantaneous, but not long lasting. I will not say how, for fear that the fda will ban any treatment not directly profiting the pharmaceutical industry, but i will say that people are getting better regardless of what the fda chooses to allow in these archaic dental devices. I will submit with request under supervision of my attorney.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5017039
MDR Report Key1798744
Date Received2010-08-06
Date of Report2010-08-06
Date Added to Maude2010-08-17
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

Brand NameMERCURY DENTAL AMALGAM
Generic Name"SILVER FILLINGS" 50 % MERCURY
Product CodeEJJ
Date Received2010-08-06
Device AvailabilityN
Device Sequence No1
Device Event Key0
ManufacturerHENRY SCHEIN, INC.


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2010-08-06

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