MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-05-07 for AMALGAM FILLING manufactured by Unk.
[1552468]
I was diagnosed with multiple sclerosis in 1982. I now have gone to a doctor, who says i have mercury poisoning. I went and had all my mercury fillings taken out and replaced with white fillings. Mercury fillings need to be stopped here in the usa. Diagnosis or reason for use: cavity.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5015888 |
| MDR Report Key | 1685983 |
| Date Received | 2010-05-07 |
| Date of Report | 2010-05-07 |
| Date of Event | 1965-01-01 |
| Date Added to Maude | 2010-05-17 |
| 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 | AMALGAM FILLING |
| Generic Name | AMALGAM FILLING |
| Product Code | EJJ |
| Date Received | 2010-05-07 |
| Lot Number | UNK |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNK |
| Manufacturer Address | UNK UNK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2010-05-07 |