BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EHR

    MDR report key: 8487684 · Received April 4, 2019

    Report

    Report Number
    MW5085625
    Event Type
    Injury
    Date Received
    April 4, 2019
    Date of Event
    March 25, 2019
    Report Date
    March 29, 2019
    Manufacturer
    UNK
    Product Code
    OUG
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I DISCOVERED THAT IN MY EHR, MY ALPHA-GAL ALLERGY IS SPECIFICALLY LISTED AS A 'NON DRUG ALLERGY.' THIS IS WRONG. WHEN I TRIED TO CONTACT MY DR TO GET IT CHANGED, THEY SAID THEY 'DID NOT SEE THAT IN THEIR SYSTEM'. I OF COURSE, HAVE NO WAY TO KNOW IF THEY WERE LOOKING AT THE SAME THING I WAS. BOTTOM LINE THOUGH IS THAT INFO IS IN THE SYSTEM SOMEWHERE, AND IT NEEDS TO BE FIXED. THIS COULD BE A LIFE THREATENING ISSUE. HTTP://MYCW39.ECLINICALWEB.COM/REGION6/JSP/100MP/LOGIN_OTP.JSP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    274952 EHR MEDICAL DEVICE DATA SYSTEM OUG UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Required Intervention