BEUDAMED
    FDA Adverse Event Other Summary report: N

    RENU WITH MOISTURE LOC

    MDR report key: 758456 · Received June 20, 2006

    Report

    Report Number
    MW1040334
    Event Type
    Other
    Date Received
    June 20, 2006
    Date of Event
    May 2, 2006
    Report Date
    May 31, 2006
    Manufacturer
    BAUSCH & LOMB
    Product Code
    LPN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I USED RENU WITH MOISTURELOC FROM MID MARCH TO THE BEGINNING OF MAY 2006. ON MAY 2, I STARTED HAVING EXTREME PAIN IN MY LEFT EYE, ON MAY 3, MY RIGHT EYE. I FIRST SAW AN OPTOMETRIST. I THEN SAW AN OPHTHALMOLOGIST WHO STARTED AGGRESSIVE TREATMENT IMMEDIATELY WITH DROPS (2).

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 41 YR Other