FDA Adverse Event
Injury
Summary report: N
*
MDR report key: 819312
·
Received February 13, 2007
Report
- Report Number
- MW1041919
- Event Type
- Injury
- Date Received
- February 13, 2007
- Date of Event
- January 1, 1989
- Report Date
- January 29, 2007
- Manufacturer
- *
- Product Code
- EJJ
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- CT, US
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
NINETEEN EIGHTY NINE - NINETY ONE - RECEIVED MANY MERCURY AMALGAM FILLINGS AT HEALTH CLINIC. HEALTH DECLINED - 1995 BRAIN SURGERY, 1996 - 2006 HAD 8 ABDOMINAL SURGERIES - 2 HEAD SURGERIES, PROBLEMS WITH BREATHING, SLEEPING, DIGESTION, CHRONIC FATIGUE, IBS, IC, IN 2006 HOSPITALIZED WITH SEVERE NEUROLOGIC PROBLEMS. FILLINGS (MERC) REMOVED IMPROPERLY 05/06 - GOT VERY, VERY, VERY SICK.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | AMALGAM FILLINGS | EJJ | * | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 36 YR | Hospitalization| O| S |