FDA Adverse Event
Other
Summary report: N
ALCON LASER
MDR report key: 86345
·
Received June 21, 1996
Report
- Report Number
- 86345
- Event Type
- Other
- Date Received
- June 21, 1996
- Date of Event
- February 6, 1996
- Report Date
- April 2, 1996
- Manufacturer
- ALCON LABORATORIES
- Product Code
- HQF
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- IL, US
- Reporter Occupation
- PHYSICIAN
Narratives
Description of Event or Problem · 1
PT HAD 3 FOCAL LASER TREATMENTS. 2/7/95 R #60 0.1 100 MICRONS 150-200 MV, 2/21/95 (L) #42 0.1 100 200 MV, 7/25/95 (L) #28 0.1 100 250 MV ON 6/13/95 C/O SOME DECREASE IN V/A L EYE. ON 9/19/95 C/O DECREASE IN V/ACUITY: ON 2/6/96 C/O MUCH WORSE VISION DIM AND BLURRING TOWARDS CENTER. ON 2/6/96 DIAGNOSED AS SUBRETINAL NEOVASCULARIZATION. STILL ATTEMPTING TO FOLLOW-UP 3 PTS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ALCON LASER | LASER | HQF | ALCON LABORATORIES | 532 LASER | -- |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 61 YR | Other |