BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DIPRIVAN

    MDR report key: 2750900 · Received October 6, 2008

    Report

    Report Number
    2750900
    Event Type
    Injury
    Date Received
    October 6, 2008
    Date of Event
    September 30, 2008
    Report Date
    October 6, 2008
    Manufacturer
    APP PHARMACEUTICALS, LLC
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    "BAD" DIPRIVAN MAY HAVE CAUSED PT TO BE MENTALLY CONFUSED AND UNABLE TO WALK AFTER CATARACT SURGERY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DIPRIVAN NONE FMF APP PHARMACEUTICALS, LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 73 YR Required Intervention