BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EROXON

    MDR report key: 20673329 · Received November 8, 2024

    Report

    Report Number
    MW5162399
    Event Type
    Malfunction
    Date Received
    November 8, 2024
    Report Date
    November 6, 2024
    Manufacturer
    FUTURE MEDICAL IN BRITAIN UK/FUTURA MEDICAL DEVELOPMENTS LIMITED
    Product Code
    QWW
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I ONLY CONSIDERED USING THE PRODUCT CALLED EROXON. BUT 90-95% OF THE FEEDBACK FROM THOSE THAT USED IT SAID IT DID NOT WORK! HOW DOES THE FDA APPROVE A PRODUCT THAT 90% DOES NOT WORK. WHERE IS THE DATA AND PROOF IT WORKS. BECAUSE ACTUAL FEEDBACK SAYS OTHERWISE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1349728 EROXON NON-MEDICATED TOPICAL FORMULATION FOR TREATMENT OF ERECTILE DYSFUNCTION QWW FUTURE MEDICAL IN BRITAIN UK/FUTURA MEDICAL DEVELOPMENTS LIMITED

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Male