BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ACUVUE OASYS

    MDR report key: 1141983 · Received August 27, 2008

    Report

    Report Number
    MW5008134
    Event Type
    Injury
    Date Received
    August 27, 2008
    Date of Event
    August 22, 2008
    Report Date
    August 27, 2008
    Manufacturer
    JOHNSON & JOHNSON
    Product Code
    LPL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    I WENT TO THE EYE DOCTOR TO GET A REFILL ON MY CONTACT PRESCRIPTION AND WAS TOLD THAT I HAD AN EYE INFECTION. I STARTED USING EYE DROPS AND NOT WEARING MY CONTACTS. AFTER TWO WEEKS AND TWO APPOINTMENTS, I WAS REFERRED TO AN OPHTHALMOLOGIST. THE OPHTHALMOLOGIST PUT ME ON A DIFFERENT EYE DROP AND TOLD ME NOT TO WEAR CONTACTS FOR ANOTHER 2 WEEKS. IN 2008, I WENT BACK TO THE EYE DOCTOR AND WAS TOLD THAT I COULDN'T WEAR MY CONTACTS FOR ANOTHER MONTH AFTER ALREADY BEING OUT OF THEM FOR A MONTH. I WAS A LITTLE SUSPICIOUS OF MY DIAGNOSIS AND WHY THE INFECTION WASN'T GOING AWAY, SO I SEARCHED ON THE INTERNET. I DISCOVERED THAT MANY PEOPLE WHO WEAR THE CONTACTS THAT I WEAR, ACUVUE OASYS, HAD DEVELOPED SERIOUS VISION PROBLEMS AS A RESULT OF WEARING THEM. SO MY COMPLAINT IS AGAINST ACUVUE OASYS FOR CAUSING ME LOSS OF VISION AND KERATITIS ON MY CORNEA. DATES OF USE: A LITTLE MORE THAN A YEAR, 2007 - 2008. DIAGNOSIS OR REASON FOR USE: TO CORRECT VISION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACUVUE OASYS CONTACT LENSES LPL JOHNSON & JOHNSON

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR Other| S