BEUDAMED
    FDA Adverse Event Other Summary report: N

    ALCOHOL PAD

    MDR report key: 19424856 · Received May 29, 2024

    Report

    Report Number
    MW5155520
    Event Type
    Other
    Date Received
    May 29, 2024
    Report Date
    May 29, 2024
    Manufacturer
    UNK
    Product Code
    LKB
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    FOR A PATIENT WITH PRIMARY LANGUAGE OF SPANISH. RX# (B)(6) RECEIVED ON (B)(6) 2023. FIRST INPUT ON (B)(6) 2023 BY TECHNICIAN. E-SCRIPT SIG READ: "TEST 2 BY MISC. (NONDRUG; COMBO ROUTE) ROUTE EVERY DAY" WITH MESSAGE TO PHARMACY "INCREASED FREQUENCY." PRESCRIPTION INPUTTED AS "USELO PARA ANALIZER SU AZUCAR EN LA SANGRE UNA VEZ AL DIA (USE TO TEST BLOOD SUGAR ONCE DAILY). QUANTITY DISPENSED 100, DAY SUPPLY INPUTTED AS 50. PRESCRIPTION DIRECTIONS, QUANTITY. AND DAY SUPPLY INPUTTED WERE NOT CONSISTENT, AND PHARMACIST FAILED TO CLARIFY DURING FINAL PRESCRIPTION REVIEW. BELIEVED THAT THE DIRECTIONS SHOULD HAVE READ TO TEST TWICE DAILY, BUT THIS WAS NOT CONSISTENT WITH OTHER PRESCRIPTIONS FOR TESTING SUPPLIES (LANCETS AND ALCOHOL PADS). ISMP, 5200 BUTLER PIKE, PLYMOUTH MEETING, PA 19462 I PHONE: 215-947-7797 I EMAIL: [email protected]. SUBMISSION ID: (B)(4). REF REPORT: MW5155519.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    298893 ALCOHOL PAD PAD, ALCOHOL, DEVICE DISINFECTANT LKB UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown