BEUDAMED
    FDA Adverse Event Injury Summary report: N

    COMPRESSOR,NEBULIZER, CHARACTER, PUP

    MDR report key: 19822385 · Received July 24, 2024

    Report

    Report Number
    1417592-2024-00768
    Event Type
    Injury
    Date Received
    July 24, 2024
    Date of Event
    June 23, 2024
    Report Date
    July 24, 2024
    Manufacturer
    MEDLINE INDUSTRIES, LP
    Product Code
    BTI
    UDI-DI
    00888277678166
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE NEBULIZER "STOPPED MISTING" THE "ALBUTEROL" MEDICATION CAUSING HER DAUGHTER TO DEVELOP A "CONGESTIVE COUGH". THE CUSTOMER REPORTED HER DAUGHTER TAKES THE MEDICATION "AS NEEDED" TO TREAT HER "ASTHMA". THE CUSTOMER REPORTED AFTER THE COUGH DEVELOPED SHE CALLED HER PHYSICIAN WHO PRESCRIBED "PREDNISONE ORAL MEDICATION FOR 5 DAYS". THE CUSTOMER DID NOT REPORT ANY SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW-UP CARE RELATED TO THE REPORTED INCIDENT. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS MEDWATCH IS BEING FILED. IF ANY FURTHER RELEVANT INFORMATION IS IDENTIFIED OR OBTAINED, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED.

    Description of Event or Problem · 0

    ACCORDING TO THE CUSTOMER, ON (B)(6) 2024 THE NEBULIZER "STOPPED MISTING" THE "ALBUTEROL" MEDICATION CAUSING HER DAUGHTER TO DEVELOP A "CONGESTIVE COUGH".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2343609 COMPRESSOR,NEBULIZER, CHARACTER, PUP BTI MEDLINE INDUSTRIES, LP 6462212 00888277678166

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other