by Brian Shilhavy
Editor, Health Impact News
Almost 2 years ago, on May 5, 2020, we published an article reporting that not a single test being used to allegedly detect the COVID-19 virus was approved by the FDA, and that the ones that were granted emergency use authorizations (EUAs) were admitted to be unreliable by the FDA and the pharmaceutical manufacturers.
I included testimony from a reader of Health Impact News who had 43 years of experience in Clinical Diagnostics and was appalled that our nation was being locked down over an alleged virus for which there was no accurate test. See:
Fast forward now 2 years to today, and the only thing that has changed over these faulty tests is that now there are a lot more of them that have been given EUAs, and still none of them have been granted FDA approval.
This was published on the FDA Roundup News Release on April 1, 2022:
- COVID-19 testing updates:
- As of today, 425 tests and sample collection devices are authorized by the FDA under emergency use authorizations (EUAs). These include 293 molecular tests and sample collection devices, 84 antibody and other immune response tests and 48 antigen tests. There are 74 molecular authorizations and 1 antibody authorization that can be used with home-collected samples. There is one EUA for a molecular prescription at-home test, two EUAs for antigen prescription at-home tests, 15 EUAs for antigen over-the-counter (OTC) at-home tests, and three for molecular OTC at-home tests.
- The FDA has authorized 28 antigen tests and nine molecular tests for serial screening programs. The FDA has also authorized 910 revisions to EUA authorizations.
I read this on the blog of Dr. Meryl Nass over the weekend who wrote:
Just in case you thought that FDA would help to standardize the tests that are used in the US to diagnose COVID-19, you were sorely mistaken. Yesterday, FDA announced the current number of tests it has “authorized” for this purpose: 425 different tests.
Just in case you thought FDA might inform the public as to the most accurate tests, or provide information so that we can compare the different tests to aid in choosing or interpreting them, you would again be mistaken.
Finally, if you thought after two years it was time for FDA to actually start “approving” some tests, so that we might feel secure that they met established standards, you would again be wrong.
It has become only too obvious that the EUA is a trick being used by our federal health agencies to ensure the persistence of COVID confusion, while eliminating all responsibility and liability from the agencies themselves, the manufacturers and all those who administer the products or tests. (Source.)
Notice in the FDA update from April 1st that they have “also authorized 910 revisions to EUA authorizations.”
We have previously reported on how the CDC withdrew their EUA request on certain PCR tests at the end of 2021 because they claimed that some of these COVID tests could not distinguish between an influenza virus, or a COVID-19 virus. See:
CDC to Withdraw Emergency Use Authorization for RT PCR Test Because It Cannot Distinguish Between SARS-CoV-2 and the Flu
Jon Rappoport also wrote about this recently:
We have also previously reported how the CDC changed how they reported deaths at the end of 2020, because the statistics at the end of the year were not showing excess deaths in the year the COVID “pandemic” started, and they added about 400,000 deaths to make COVID appear to be a serious killer virus, which then hid the real increase in deaths that occurred in 2021 after the COVID-19 vaccines were rolled out. See:
This is the biggest scam in the history of the world, as the flu disappeared in 2020 and still remains absent here in 2021, because there just are not enough sick people dying to inflate both flu and COVID numbers.
The Disappearance of the Annual Flu Which was Replaced with COVID-19 Shows Corruption at its Highest Level at the CDC
And the real tragedy that this corruption has caused, besides the fact that the COVID-19 vaccines are destroying people’s lives, is that this group of upper respiratory symptoms that used to be called “influenza” but is now called “COVID-19” is very easily treatable, by either using older drugs that are generally safe such as Ivermectin, or even natural products such as high-dose Vitamin C IV treatment.
But to make sure these existing treatments do not interfere with the new vaccines and drugs that have been given EUAs by the FDA, the FDA has issued 215 warning letters for “Fraudulent Coronavirus Disease 2019 (COVID-19) Products” to protect the pharmaceutical industry and their EUA products “by pursuing warning letters, seizures, injunctions or criminal prosecutions against products and firms or individuals” that dare to defy the FDA by using unauthorized products to actually heal people. (Source.)
So those profiting from a new drug given an EUA like Remdesivir, which we now see kills 25% of the patients who take it, or the experimental COVID-19 vaccines that now have over 1.2 million reports of deaths and injuries in VAERS, face no consequences for the dangers of their products.
But if a doctor heals someone using Vitamin C which has no serious side effects, it is the doctor using Vitamin C who can be arrested as a criminal and lose their career while the criminals at the FDA, CDC, and pharmaceutical companies go free and are sanctioned in their criminal acts.
Welcome to the new world of “medicine” where EUAs for a fake pandemic are perpetuated indefinitely for the profit of Big Pharma, but at the expense of American lives lost from withholding real cures.
Comment on this article at HealthImpactNews.com.
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