BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENU CONTACT LENSE SOLUTION

    MDR report key: 702256 · Received April 14, 2006

    Report

    Report Number
    MW1038672
    Event Type
    Injury
    Date Received
    April 14, 2006
    Report Date
    April 14, 2006
    Manufacturer
    BAUSCH & LOMB
    Product Code
    LPN
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I USED RENU CONTACT LENS PRODUCTS FOR THE PAST FEW YEARS. IN THE LATE FALL/EARLY WINTER OF 2004, I DEVELOPED A SERIOUS EYE INFECTION. MY DR TOLD ME I HAD BOTH A VIRAL INFECTION AND A BACTERIAL INFECTION. I WENT WITHOUT CONTACTS FOR THREE MONTHS. LATER, I WAS ALLOWED TO WEAR THEM AGAIN, BUT THE SAME SYMPTOMS PRESENTED. THIS TIME, A DIFFERENT DR TOLD ME I HAD PINK EYE. ANOTHER TOLD MY I HAD CHRONIC DRY EYE. A THIRD PUT ME IN A MORE SENSITIVE CONTACT LENS WITH DIFFERENT SOLUTION. I HAVEN'T HAD PROBLEMS SINCE THEN. I SUSPECT, HOWEVER, THAT MY ISSUES MIGHT BE RELATED TO THE RENU SOLUTION SINCE MY SYMPTOMS WERE VERY SIMILAR: VERY RED. EVENT ABATED AFTER USE STOPPED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENU CONTACT LENSE SOLUTION * LPN BAUSCH & LOMB * *

    Patients

    Seq Age Sex Outcome Treatment
    1 32 YR Other