BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LATEX GLOVE

    MDR report key: 53938 · Received December 6, 1996

    Report

    Report Number
    MW1010389
    Event Type
    Injury
    Date Received
    December 6, 1996
    Date of Event
    November 20, 1996
    Report Date
    November 21, 1996
    Manufacturer
    UNK
    Product Code
    LYY
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    PT ATE LUNCH IN A DELI KNOWN TO BE LATEX SAFE, STAYED APPROX 2HRS. PRIOR TO LEAVING, PT BEGAN TO NOTICE A SLIGHT ITCH. AS AFTERNOON AND EVENING PROGRESSED RPTR REQUIRED BENADRYL/50 PO Q 4, ATARAX 25 Q 6, PIRBUTEROL INHALER. PREDNISONE 50 MG. HOSP STAFF ATE AT DELI WHILE WEARING SCRUBS AND/OR WHITE COATS. COMPANION ALSO REACTED WHILE AT DELI. ON 11/21/96, SYMPTOMS OF ITCHING, CHEST TIGHTNESS AND COUGHING CONTINUED, REQUIRED USE OF PERBUTEROL INHALER. BENADRYL ATARAX AND PREDNISONE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LATEX GLOVE LATEX GLOVE LYY UNK * *

    Patients

    Seq Age Sex Outcome Treatment
    1 45 YR Required Intervention