BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MORPHINE SULFATE ER

    MDR report key: 1680329 · Received May 6, 2010

    Report

    Report Number
    MW5015861
    Event Type
    Malfunction
    Date Received
    May 6, 2010
    Date of Event
    May 6, 2010
    Report Date
    May 6, 2010
    Product Code
    KYW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    MORPHINE SULFATE 60MG ER. MALLINCKRODT. LOT: 8380N72843. EXP: 08/11. FULL SEALED BOTTLE OF 100 TABS, ONLY CONTAINED 99 TABS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MORPHINE SULFATE ER NONE KYW 8380N72843

    Patients

    Seq Age Sex Outcome Treatment
    1