WHAT IS PFIZER AND THE FDA HIDING FROM THE AMERICAN PEOPLE REGARDING THE CLINICAL TRIALS OF THE FAKE “VACCINE”? WHY ARE THEY TRYING TO HIDE THE EMERGENCY USE TRIAL DATA FROM THE AMERICAN PEOPLE FOR 55 YEARS?

Here is one reason… THEY HAVE BEEN LYING TO THE WORLD ABOUT THE CHINA VIRUS AND THE FAKE VACCINE!

Pfizer lied about the number of individuals who died during thir COVID vaccine trials. The actual number of deaths during the clinical trials was 21 not 16 as was originally reported. This was four more deaths than the clinical trials control group (who didn’t get the fake vaccine).

So, if we understand correctly, the actual number of deaths in the Pfizer clinical trials was 21, which was 6 more than was reported, and 4 more than the unvaccinated control group, which tells us that the fake vaccine was even worse than a complete failure – it was / is deadly.

Does that hit home or what? The report says that the FDA LIED about how many people died in their emergency use trials, and the truth is that more people died after taking the fake vaccine than who didn’t take the vaccine. WOW! THAT IS NOT “FULL TRANSPARENCY” AT ALL!

According to the VAERS website there were 12,412 deaths linked to the Pfizer vaccine this year alone, but that number is probably way off (low) as well, as all of the other numbers are royally fucked-up.

SO WHAT THE FUCK IS PFIZER AND THE FDA HIDING? THE AMERICAN PEOPLE WANT TO KNOW!

The FDA is holding back information.

In response to a Freedom of Information Act request (FOIA) filed months ago the FDA has asked a federal judge to give them 55 years to release data related to the Pfizer COVID vaccines.

Americans are currently being forced by the regime to take this vaccine to hold a job but have no rights to see how this “vaccine” was approved.

But their grand-children may get to see the data in 55 years.

In response to a Freedom of Information Act request (FOIA) filed over three months ago, in August of 2021, the U.S. Food and Drug Administration (FDA) has asked a federal judge for 55 years to review its data before releasing it to the public in its entirety.

The data refers to the FDA’s decision to license what is now known as the Comirnaty vaccine against Covid-19, produced by Pfizer in collaboration with BioNTech. Back in November of 2020, when considering Pfizer-BioNTech’s request for emergency use authorization (EUA) of its product, the FDA promised that:

“In keeping with the FDA’s commitment to ensuring full transparency, dialogue and efficiency, the Vaccines and Related Biological Products Advisory Committee … will meet to discuss the totality and safety and effectiveness data provided … The FDA understands there is tremendous public interest regarding vaccines for COVID-19. We remain committed to keeping the public informed about the evaluation of the data … so that once available, the public and the medical community can have trust and confidence in receiving the vaccine for our families and ourselves.”

In September of 2021, when amending its EUA to include booster doses, the FDA reiterated its commitment to transparency, writing:

“As we learn more about the safety and effectiveness of COVID-19 vaccines … we will continue to evaluate the rapidly changing science and keep the public informed…”

The FDA noted at the time that it was studying data provided not only by Pfizer-BioNTech, but also from the “Israeli Ministry of Health, the University of Bristol, U.K. and the Centers for Disease Control and Prevention [CDC].”

Stand Up To Government Corruption and Hypocrisy – usbacklash.org