FDA Adverse Event Injury Summary report: N

TWO TIER LYME DISEASE TESTING DEARBORN

MDR report key: 4231612 · Received October 31, 2014

Report

Report Number
MW5038950
Event Type
Injury
Date Received
October 31, 2014
Date of Event
June 15, 1985
Report Date
October 31, 2014
Product Code
LSR
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
WA, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I HAVE SUFFERED GREATLY DUE TO THE FRAUDULENT TESTING SCHEME KNOWN AS THE TWO TIER LYME DISEASE TESTING, AKA "DEARBORN". I WAS TESTED NUMEROUS TIMES FOR LYME DISEASE AFTER MY HEALTH STARTED DECLINING YEARS AGO USING THE TWO TIER LYME TESTS CURRENTLY IN PLACE. TESTS CAME BACK NEGATIVE EVEN THOUGH I WAS BITTEN BY A CLUSTER OF TINY TICKS NEARLY 25 YEARS AGO. I WAS ONCE AGAIN TESTED (B)(6) 2013. TESTS CAME BACK POSITIVE. I'M CURRENTLY SO SICK I AM NOT RESPONDING TO TREATMENT. IF I HAD BEEN PROPERLY DIAGNOSED EARLIER ON WITH MORE RIGOROUS TESTING I WOULD NOT BE ON DISABILITY, NOR WOULD I HAVE LOST THE HEALTHY, VIBRANT LIFE THAT I ONCE HAD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
698082 TWO TIER LYME DISEASE TESTING DEARBORN TWO TIER LYME DISEASE TESTING LSR

Patients

Seq Age Sex Outcome Treatment
1 51 YR Hospitalization| S