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Tuesday 21 December 2021

The CDC Withdraw the Emergency Use of ​The PCR Test ​In 10 Days’ Time​, Why Is It Still Being Used In The UK?

[The Expose]: Back in July 2021, The Centers for Disease Control and Prevention (CDC) announced that its PCR test has failed its full review and will have its Emergency Use Authorization revoked.

The Innova SARS-CoV-2 Antigen Rapid Qualitative Test, the CDC’s benchmark COVID diagnostic testing system, will be withdrawn for Emergency Use by the end of 2021 due to an inordinate frequency of false-positive and negative results.

The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death,” the FDA stated on its website.

After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only(source).

“CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives” (source). 

The FDA goes on to explain the risks associated with false positives and negatives:

False-negative results may lead to delayed diagnosis or inappropriate treatment of SARS-CoV-2, which may cause patient harm including serious illness and death. False-negative results can also lead to further spread of the SARS-CoV-2 virus, including when presumed negative patients are grouped into cohorts in health care, long-term care, and other facilities based on false test results.

False-positive results could lead to a delay in the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness, which could be another life-threatening disease that is not SARS-CoV-2. False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results (source)

Although the CDC was also a distributor of the RT-PCR Diagnostic Panel they advised that from September 30, 2021, they would no longer happen and that laboratories should transition away from the Diagnostic Panel by the end of 2021 (source). Why would the CDC wait until the end of 2021 to cease the use of the RT-PCR Test?

We are now almost at the second anniversary of the commencement of the governments across the globe terrorising their own people by claiming that there was a deadly new virus due to an initial 44 “cases” of pneumonia with unknown aetiology being discovered.

However, this was a virus that was so deadly, but we had to be tested for it to see if we had it or not....<<<Read More>>>...