BEUDAMED
    FDA Adverse Event Other Summary report: N

    EPIC SYSTEM

    MDR report key: 17586208 · Received August 18, 2023

    Report

    Report Number
    MW5144794
    Event Type
    Other
    Date Received
    August 18, 2023
    Report Date
    June 28, 2023
    Manufacturer
    EPIC SYSTEMS CORPORATION
    Product Code
    OUG
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENT WAS ADMITTED TO THE HOSPITAL X2 WITHIN A MONTH FOR VARIOUS HEALTH CONDITIONS INCLUDING HEPATIC FAILURE. UPON ADMISSION THE FIRST TIME, THE PATIENT WAS PLACED ON RISPERIDONE. PHARMACY HAD CONSULTED THE PATIENT'S LONG TERM CARE SERVICE AND THEY STATED HE IS NO LONGER TAKING THE RISPERIDONE. DESPITE THIS, THE MEDICATION WAS AGAIN STARTED INPATIENT A SECOND TIME WHEN THE PATIENT WAS ADMITTED LATER ON. CONFUSION OCCURRED AS THE MED APPEARED TO STILL BE AN ACTIVE FILL PER THE EPIC SYSTEM. PRESCRIPTION PROCESSING SOFTWARE COMMUNICATION, POOR/LACKING (NONSPECIFIC). ISMP, (B)(6). SUBMISSION ID: (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1035154 EPIC SYSTEM MEDICAL DEVICE DATA SYSTEM OUG EPIC SYSTEMS CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown RISPERIDONE.