BEUDAMED
    FDA Adverse Event Other Summary report: N

    EPIC

    MDR report key: 16953426 · Received May 17, 2023

    Report

    Report Number
    MW5117633
    Event Type
    Other
    Date Received
    May 17, 2023
    Report Date
    May 17, 2023
    Manufacturer
    EPIC SYSTEMS CORPORATION
    Product Code
    OUG
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENT ADMITTED TO HOSPITAL LATE EVENING ON "X/XX". JUST AFTER MIDNIGHT, PATIENTS HOME MEDICATIONS (KEPPRA, ONFI AND ZYRTEC) WERE ENTERED BY PROVIDER, BUT TIMED FOR TOMORROW. ORDERS WERE VERIFIED TO START ON "X/XX" (2 DAYS AFTER). WE CONTINUE TO SEE ISSUES WITH EPIC'S "TOMORROW" BUTTON LEADING TO UNINTENTIONAL TIMING OF MEDICATIONS. FORTUNATELY THIS WAS CAUGHT THE NEXT MORNING ON ROUNDS BY A CLINICAL SPECIALIST, BUT COULD HAVE HAD A NEGATIVE IMPACT ON PATIENT'S CARE IF MISSED.(B)(6). SUBMISSION ID: (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    650566 EPIC MEDICAL DEVICE DATA SYSTEM OUG EPIC SYSTEMS CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown KEPPRA| ONFI| ZYRTEC