FDA Adverse Event Injury Summary report: N

BAUSCH AND LOMB RENU MOISTURE LOC

MDR report key: 702458 · Received April 11, 2006

Report

Report Number
MW1038560
Event Type
Injury
Date Received
April 11, 2006
Date of Event
October 1, 2005
Report Date
April 11, 2006
Manufacturer
BAUSCH & LOMB
Product Code
LPN
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

WENT TO FAMILY DOCTOR WITH C/O RIGHT EYE PAINFUL AND RED, LEFT CONTACT OUT FOR 10 DAYS THEN FLARED UP WITH WORSE WITH NEW CONTACT LENS; WENT TO CONTACT LENS DOCTOR TREATED FOR 1 WEEK, NOT GETTING BETTER; WENT TO OPHTHALMOLOGIST ON 10/17/2005; TRIED MANY DIAGNOSES WITHOUT SUCCESS; WENT TO CORNEAL SPECIALIST ON DECEMBER 12 THOUGHT IT WAS HERPES, NO BETTER; ON JANUARY 25TH WENT TO ANOTHER EYE DOCTOR AND CULTURED FUNGAL INFECTION AND TREATED; TOOK PILLS FIRST FOR 60 DAYS AND NOW CONTINUED VORICONAZOLE DROPS; USING CONTACT LENS FOR 35 DAYS; RIGHT EYE FOR DISTANCE VISION; CQ5 SOFT CONTACT DAILY LENS FOR PAST 10 YEARS; REPORTED TO DEPT OF PUBLIC HEALTH.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 BAUSCH AND LOMB RENU MOISTURE LOC * LPN BAUSCH & LOMB * 6842600

Patients

Seq Age Sex Outcome Treatment
1 65 YR Other| R