BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HNA MILLENNIUM PHARMNET

    MDR report key: 390085 · Received April 18, 2002

    Report

    Report Number
    1931259-2002-00004
    Event Type
    Malfunction
    Date Received
    April 18, 2002
    Date of Event
    April 3, 2002
    Report Date
    April 15, 2002
    Manufacturer
    CERNER CORP.
    Product Code
    MMH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE ISSUE INVOLVES THE PHABATCHREPORT.EXE APPLICATION USED WITHIN THE MILLENNIUM PHARMNET SYSTEM. THE ISSUE OCCURS WHEN THE USER DISCONTINUES A MEDICATION FROM THE MEDICATION ADMINISTRATION RECORD (MAR). THE DISCONTINUED MEDICATION CONTINUES TO APPEAR ON THE MAR. THE BEHAVIOR WAS OBSERVED TO OCCUR WHEN AN ORDER WITH A FUTURE DISCONTINUE ACTION IS UPDATED. AFTER BEING IDENTIFIED AS AN ORDER THAT REQUIRES A DISCONTINUE ACTION (MAKING THE FUTURE DISCONTINUE ACTION EFFECTIVE ONCE THE DISCONTINUE DATE AND TIME HAS PASSED), THE PHARMACY SHAREABLE (PHA_SHRORDER.EXE) FAILS TO UPDATE THE MAR. AFTER THE FUTURE DISCONTINUES ACTION IS UPDATED, THE ORDER CONTINUED TO DISPLAY ON THE REPORTS AS AN ACTIVE MEDICATION. CERNER HAS NOT BEEN MADE AWARE OF ANY ADVERSE PATIENT CARE EVENTS THAT RESULTED FROM THIS ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HNA MILLENNIUM PHARMNET SOFTWARE MMH CERNER CORP. RELEASE 500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA