BEUDAMED
    FDA Adverse Event Summary report: N

    PERSANTINE

    MDR report key: 490440 · Received September 24, 2003

    Report

    Report Number
    MW4003579
    Date Received
    September 24, 2003
    Date of Event
    October 10, 2002
    Report Date
    September 5, 2003
    Manufacturer
    *
    Product Code
    JWM
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    COMPLAINANT WENT TO HOSPITAL TO UNDERGO A PERSANTINE THALLIUM STRESS TEST. THEY STATED THAT THEY ARE ALLERGIC TO HEPARIN, CODEINE, AND PENICILLIN. THE COMPLAINANT WAS ASKED THE NAME OF THE PERFORMING PHYSICIAN BUT THEY DID NOT KNOW IT. THEY DID STATED THAT IT WAS PERFORMED BY THE NUCLEAR MEDICINE DEPT. WHEN THE TEST WAS PERFORMED, PT NOTIFIED THEM THAT THEY HAD AN ITCHING AND BURNING SENSATION IN THEIR CHEST. THEY TOLD PT THE SENSATION WAS NORMAL AND WOULD GO AWAY BY ITSELF. PT WAS PRESCRIBED CORTISONE TO ALLEVIATE THE SYMPTOMS. THE SENSATIONS STILL PERSIST TO THIS DAY IN FLUCTUATING SEVERITIES. PT STATED THAT THEY ALSO NOTICED HAIR LOSS. PT STATED THAT THEY HAVE BEEN PRESCRIBED ROGAINE BY A DERMATOLOGIST AND THE HAIR RECOVERY HAS BEEN SLOW BUT IT IS GROWING BACK. THE COMPLAINANT STATED THAT THEY BELEIVE THAT THEIR ALLERGIES WERE IGNORED BY THE PHYSICIANS DESPITE THE FACT THAT THEY WERE LISTED ON THEIR ID BRACELET.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PERSANTINE THALLIUM STRESS TEST JWM * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *