MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-10-05 for DENTAL AMALGAM manufactured by Unknown.
[27448627]
(b)(4). I had symptoms which fall within the spectrum of morgellons disease ("delusional parasitosis" which i now view as parenthesia due to mercury poisoning). My recovery was documented and published (see (b)(6)) as well as featured on the (b)(6) channel show "diagnose me" (can be seen at: (b)(6)).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5056790 |
| MDR Report Key | 5127036 |
| Date Received | 2015-10-05 |
| Date of Report | 2015-10-02 |
| Date of Event | 2007-02-07 |
| Date Added to Maude | 2015-10-05 |
| 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 | 3 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DENTAL AMALGAM |
| Product Code | EJJ |
| Date Received | 2015-10-05 |
| Device Availability | * |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNKNOWN |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other; 2. Required No Informationntervention | 2015-10-05 |