FDA Adverse Event Injury Summary report: N

CT SCAN

MDR report key: 15499295 · Received September 27, 2022

Report

Report Number
MW5112318
Event Type
Injury
Date Received
September 27, 2022
Date of Event
June 18, 2022
Report Date
September 25, 2022
Manufacturer
UNK
Product Code
JAK
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

CT SCAN OF BRAIN, I WAS SCANNED MULTIPLE TIMES AT ONCE, EACH TIME AT A OVERDOSE OF 15 MSV. I WAS SCARED AT LEAST SIX TIMES IN ONE SITTING AT THAT DOSE EQUALING AT LEAST 90 MSV. I AM SUFFERING GREAT SIDE EFFECTS AND HARM. EXCRUCIATING PAIN IN MY BRAIN CONSTANTLY, ALONG WITH OTHER SYMPTOMS AND GETTING WORSE. FDA SAFETY REPORT ID# (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2863883 CT SCAN SYSTEM, X-RAY, TOMOGRAPHY, COMPUTED JAK UNK

Patients

Seq Age Sex Outcome Treatment
1 41 YR Female Life Threatening| S