BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ASAP MODULE OF EMR

    MDR report key: 5018380 · Received August 17, 2015

    Report

    Report Number
    MW5055554
    Event Type
    Injury
    Date Received
    August 17, 2015
    Date of Event
    January 21, 2015
    Report Date
    August 17, 2015
    Manufacturer
    EPIC
    Product Code
    MMH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    1

    Narratives

    Description of Event or Problem · 1

    PATIENT WITH MULTIPLE MYELOMA ON CHEMOTHERAPY. AT ROUTINE CLINIC VISIT NOTED TO BE WEAK AND SWEATY, SO TRANSFERRED TO ER FOR EVAL AND TREATMENT. IN ER FOUND TO BE HYPOTENSIVE, TACHYCARDIC, CONFUSED, FEBRILE, PRESUMABLY DUE TO SEPSIS / SEPTIC SHOCK. DURING RESUSCITATION, UNABLE TO ENTER ORDERS FOR FLUIDS, MEDICATIONS, LAB WORK, X-RAYS IN THE TACHYCARDIC BECAUSE "CHART IS OPEN BY (B)(6) IN (B)(6) CLINIC WORKSTATION (B)(6)". CALLED CLINIC BUT CALL WENT TO VOICE MAIL. CALLED IT HELP DESK WHO SAID CALL CLINIC, THEN SAID THERE WAS NOTHING THEY COULD DO. WOULD NOT EVEN GO TO CLINIC TO SHUT DOWN WORKSTATION BECAUSE NUMBER PROVIDED DID NOT CORRESPOND TO THEIR WS IDS. ASKED OUR DEPT ADMINISTRATOR TO TAKE ON PROBLEM AS WE WERE BUSY W/ DIRECT CARE. AFTER ABOUT AN HOUR, PROBLEM EVENTUALLY WENT AWAY, ALTHOUGH DON'T KNOW WHY. PT GOT FLUIDS AND SOME (BUT NOT ALL) DRUGS, BUT COULD NOT GET LABORATORY OR RADIOLOGY RESULTS W/O A VALID ORDER IN SYSTEM. IT ALLEGEDLY REPORTED TO VENDOR, NO CORRECTIVE ACTION FORTHCOMING. CONCOMITANT MEDICAL PRODUCTS AND THERAPY DATES: NA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    542195 ASAP MODULE OF EMR EMR ORDER ENTRY MMH EPIC

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Life Threatening| R