CDC Withdraws request for FDA Emergency Use Authorization (EUA) of the PCR Diagnostic Panel!

https://www.cdc.gov/csels/dls/locs/2021/07-21-2021-lab-alert-Changes_CDC_RT-PCR_SARS-CoV-2_Testing_1.html

As has been reported since the very beginning, the RT-PCR_SARS-CoV-2_Test was never intended to be used to diagnose SARS-CoV2, which is why it was NEVER APPROVED by the FDA for this purpose.

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“In the United States, because of a shortage of tests and testing facilities during the early months of the pandemic tests were primarily used for diagnoses to identify a person with an active infection associated with signs or symptoms of COVID-19 or who had definite or suspected recent exposure to the virus,” the report found.

“Later, the Federal Drug Administration (FDA) approved testing to be extended to screen for infection in individuals WITHOUT known or suspected exposure to SARS-CoV-2 living in congregate settings, such as long-term care facilities or prisons. Side Note: The very same protocols introduced and implemented by Dr Anthony Fauci in the 1980's when he was hired by the Regan administration to cure HIV-AIDS.

Finally, periodic screening programs have been developed for educational institutions, sport teams, and the workplace to detect asymptomatic, pre-symptomatic, and symptomatic infected individuals early and isolate them to reduce them infecting others.”

Read The Report:

False Positive Results With SARS-CoV-2 RT-PCR Tests and How to Evaluate a RT-PCR-Positive Test for the Possibility of a False Positive Result

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WHAT IF!

You and a friend are in an automobile accident and are subsequently taken to a near by hospital.

The FIRST thing that takes place in that hospital is that both are given the SARS-CoV-2 RT-PCR Test.

The next thing that takes place, depending on the test results, is that patients who test posative are moved into the CoVID ward. Sounds reasonable doesn't it?

"The over-diagnosis of SARS-CoV-2 infection has multiple potential adverse effects the inconvenience, financial and psychological issues affecting those misdiagnosed; the possible exposure of uninfected individuals to infected people in hospital or congregate living areas; misdiagnosed persons foregoing social distancing and the masks use because they think that they are immune from COVID-19; and temporary closure of a business because of the need to quarantine coworkers.

In addition, the over-diagnosis can inflate the number of asymptomatic infections in public health statistics." READ ABOVE REPORT!

This information is not new. It has been well documented since 2019. The Inventor of the test stated that the test was not designed to diagnose CoVID -19

Yet the test was used as the gold standard of SARS-CoV-2 testing throughout the "pandemic".