BEUDAMED
    FDA Adverse Event Injury Summary report: N

    APPLE WATCH

    MDR report key: 18780502 · Received February 23, 2024

    Report

    Report Number
    MW5151944
    Event Type
    Injury
    Date Received
    February 23, 2024
    Date of Event
    February 9, 2024
    Report Date
    February 9, 2024
    Manufacturer
    APPLE INC.
    Product Code
    QDA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IN
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I CHECKED MY BLOOD PRESSURE BEFORE AND AFTER TAKING THIS MEDICATION, BUT STILL IT IS SAME. BLOOD PRESSURE CHECKED USING APPLE WATCH. I DONT KNOW WHY THERE IS NO PROPER MECHANISM FOR REPORTING A SIDE EFFECT IN INDIA. NEED PROPER REPORTING CHANNEL IN INDIA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    102502 APPLE WATCH ELECTROCARDIOGRAPH SOFTWARE FOR OVER-THE-COUNTER USE QDA APPLE INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 53 YR Male NUROKIND GOLD