FDA Adverse Event Injury Summary report: N

DENTAL AMALGAM

MDR report key: 4117327 · Received September 20, 2014

Report

Report Number
MW5038320
Event Type
Injury
Date Received
September 20, 2014
Report Date
September 20, 2014
Product Code
EKH
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I AM DISABLED WITH CHRONIC MERCURY POISONING (CONFIRMED BY A PORPHYRINS PANEL), WITH NO KNOWN EXPOSURE ASIDE FROM 12 DENTAL AMALGAMS FOR 40 YEARS. MY 23ANDME TEST SHOWS SOME POSSIBLE GENETIC SUSCEPTIBILITIES TO TOXIC METALS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
585879 DENTAL AMALGAM DENTAL AMALGAM EKH

Patients

Seq Age Sex Outcome Treatment
1 Disability