BEUDAMED
    FDA Adverse Event Other Summary report: N

    PHARMACY SYSTEM

    MDR report key: 19042329 · Received April 3, 2024

    Report

    Report Number
    MW5153538
    Event Type
    Other
    Date Received
    April 3, 2024
    Report Date
    April 3, 2024
    Manufacturer
    UNKNOWN
    Product Code
    NEP
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    THE PHARMACIST TYPED "AS DIRECTED" IN THE SYSTEM, THE SIGS CODE CHANGED TO "LEFT EAR" DIRECTED. THE PHARMACY SYSTEM REQUIRED TO PUT A BRACKET ( [ ] ) IN BETWEEN ANY FREE TEXT. THE PHARMACIST FORGOT TO PUT IN THE BRACKET. TRANSCRIPTION ERROR/MISUNDERSTOOD ORDER INACCURATE INFORMATION (LABEL/LABELING). (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2374121 PHARMACY SYSTEM SYSTEM/DEVICE, PHARMACY COMPOUNDING NEP UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown