MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2008-07-14 for "MERCURY" AMALGAM FILLINGS manufactured by .
[19959393]
After 6 yrs of debilitating illness, i was diagnosed with heavy metal poisoning. My research resulted in the conclusion that the mercury poisoning was from the fillings in my mouth. Medical tests show an exorbitant amount of mercury being removed from my body. I am currently disabled with kidney, liver and digestive system problems. The american dental association and the fda's approval of the use of mercury fillings has caused me considerable health problems. Significant research has linked gynecological, endocrine, digestive, cognitive & psychological issues that i have endured over my lifetime. I am currently on disability. (see scanned pages)
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5007612 |
| MDR Report Key | 1075380 |
| Date Received | 2008-07-14 |
| Date of Report | 2008-06-12 |
| Date Added to Maude | 2008-07-18 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | "MERCURY" AMALGAM FILLINGS |
| Generic Name | NONE |
| Product Code | OIV |
| Date Received | 2008-07-14 |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 1043793 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Deathisabilit | 2008-07-14 |