What dystopian world are we living in? You just can’t make this stuff up! The mRNA gene-altering medical device, that has never been used on humans before, was only was under stage 3 trials for 3 months in humans with placebo then that continued in the global population since. Over 20,000 have died from the Pfizer shots in the US, Europe and UK as recorded by their government reporting systems, which are known to be under reported by at least 10 times. Now the death shot has been given full FDA “approval” for humans 16 years and older. See below for explanation.
Welcome to the future. Gene altered transhumans with graphene-oxide based biocircuitry is the plan for those few who survive the death shots.
The totally corrupt and captured US FDA has explained in their own document this way.
Today, the U.S. Food and Drug Administration approved the first COVID-19 vaccine. The vaccine has been known as the Pfizer-BioNTech COVID-19 Vaccine, and will now be marketed as Comirnaty (koe-mir’-na-tee), for the prevention of COVID-19 disease in individuals 16 years of age and older. The vaccine also continues to be available under emergency use authorization (EUA), including for individuals 12 through 15 years of age and for the administration of a third dose in certain immunocompromised individuals.
“The FDA’s approval of this vaccine is a milestone as we continue to battle the COVID-19 pandemic. While this and other vaccines have met the FDA’s rigorous, scientific standards for emergency use authorization, as the first FDA-approved COVID-19 vaccine, the public can be very confident that this vaccine meets the high standards for safety, effectiveness, and manufacturing quality the FDA requires of an approved product,” said Acting FDA Commissioner Janet Woodcock, M.D. “While millions of people have already safely received COVID-19 vaccines, we recognize that for some, the FDA approval of a vaccine may now instill additional confidence to get vaccinated. Today’s milestone puts us one step closer to altering the course of this pandemic in the U.S.”
Since Dec. 11, 2020, the Pfizer-BioNTech COVID-19 Vaccine has been available under EUA in individuals 16 years of age and older, and the authorization was expanded to include those 12 through 15 years of age on May 10, 2021. EUAs can be used by the FDA during public health emergencies to provide access to medical products that may be effective in preventing, diagnosing, or treating a disease, provided that the FDA determines that the known and potential benefits of a product, when used to prevent, diagnose, or treat the disease, outweigh the known and potential risks of the product.FDA.gov
Here’s a disease with a 99.9% plus recovery rate for most humans under 70 years old that has been given an approved drug they call a vaccine which it isn’t because it does not prevent disease nor transmission. In fact, in many countries now most hospitalised individuals with the so-called COVID-19 disease are fully vaxxed.
This is what is next. Because it is now approved, even though the human stage 3 trials were to go to 2022 more and more borders, businesses, agencies, services will require the death shot and COVID passport to enter or participate.
NEWSFLASH: It turns out that Pfizer vaxxine has not been approved. It is all a con job.
Watch this! Media TRICK/CON about FDA ‘Approval’
In a chilling shell game, the following has been done:
- Pfizer has had its EUA extended.
- A product that cannot yet be purchased (maybe never?) has been provisionally approved subject to 9 additional studies which will be completed in 2024. I’m referring here to the hypothetical BioNTech-branded version of the Pfizer-branded vaccine.
The two vaccines here, Pfizer and BioNTech, are identical, or essentially so.
They are however legally distinct. Pfizer has complete protection from legal liability. BioNTech would not (if it ever comes to market, unlikely). Only approved vaccines on the children’s schedule have immunity from liability for the manufacturers, since 1986; the vaccines for adults only do not get this protection.
The rational for this shell game is to be able to report in the press that Pfizer has been approved. But it hasn’t. It’s doppelgänger has been (provisionally) approved.
And now that Pfizer has been “approved”, the mandates can move forward at full speed.
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