FDA Adverse Event
Injury
Summary report: N
ELECTROSHOCK
MDR report key: 36137
·
Received August 27, 1996
Report
- Report Number
- MW1009818
- Event Type
- Injury
- Date Received
- August 27, 1996
- Date of Event
- January 1, 1963
- Report Date
- August 27, 1996
- Manufacturer
- UNK
- Product Code
- GXC
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- TX, US
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
PT RECEIVED THREE ELECTROSHOCK TREATMENTS AT THE STATE HOSP IN 1963. AFTERWARDS WAS COMPLETELY DISORIENTED FOR A PERIOD OF SEVERAL MONTHS. WAS FORCED TO EDUCATE SELF ALL OVER AGAIN. HAD TO LEARN TO MULTIPLY NUMBERS, TO ADD, TO USE AN ADULT VOCABULARY AGAIN. HAD TO LEARN AGAIN HOW TO DRIVE A CAR. SUFFERS TO THIS DAY FROM PERMANENT, IRREVOCABLE MEMORY LOSS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ELECTROSHOCK | ELECTRICAL CONVULSIVE THERAPY UNIT | GXC | UNK | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 34 YR | Disability |