BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MYCHCART

    MDR report key: 4834779 · Received June 3, 2015

    Report

    Report Number
    MW5043001
    Event Type
    Injury
    Date Received
    June 3, 2015
    Date of Event
    June 1, 2015
    Report Date
    June 3, 2015
    Manufacturer
    EPIC
    Product Code
    LNX
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    THE DROP DOWN MENU TO SPECIFY ROUTE OF ADMINISTRATION OF MEDICATIONS IS A SOURCE OF INNUMERABLE ERRORS. THE FIRST OPTION IS IM AND IS FREQUENTLY SELECTED BECAUSE OF ITS LOCATION AND CLOSE RESEMBLANCE TO IV. IT IS A FLAW THAT HAS BEEN CARRIED ON BY THE VENDOR FOR YEARS, ENDANGERING HUNDREDS OF PATIENTS, IF NOT THOUSANDS OVER TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    360750 MYCHCART CPOE/EHR LNX EPIC

    Patients

    Seq Age Sex Outcome Treatment
    1 81 YR Life Threatening