Pfizer Releases First 91+ Pages of COVID 19 Vaccine Documents, Reviewed by FDA For Comirnaty Approval

Pfizer releases first 91+ pages of its COVID vaccine trial data showing alarming numbers of vaccine adverse events.
December 2, 2021

Pfizer COVID 19 vaccine documents released! Finally Pfizer released Round 1 – the first 91+ Pages of it’s COVID 19 vaccine trial data, as part of a 500 pages per month judge ordered schedule; Delaying the full release of Pfizer’s COVID-vaccine trial until 2076. The First documents released by Pfizer show a “large increase of adverse event reports”, significant enough that Pfizer took action in “increasing the number of data entry and case processing colleagues” to handle the volume of adverse events; a stark contrast to the “safety and efficacy” touted by Pfizer and the media of their COVID-19 vaccine. The revelations in these documents have some wondering…if the volume of vaccine injuries were so high, why was Comirnaty ever approved?

FDA promises ‘full transparency’ asks judge to make public wait until the year 2076 (20,000 days)

Dozens of academics, professors and scientists from some of the most prestigious universities in the US, requested the data and information submitted to the FDA by Pfizer to license its COVID-19 vaccine. the FDA repeatedly promised “full transparency” with regard to Covid-19 vaccines, including reaffirming “the FDA’s commitment to transparency” when licensing Pfizer’s COVID-19 vaccine. 

Contrary to their promise of “full transparency”, the FDA ignored the data request. Experts then banded together and filed a lawsuit against the FDA, but the FDA still didn’t send any of the requested data. In fact Instead of complying with the request the FDA asked a federal judge to make the public wait until the year 2076 to disclose all of the data, and information it relied upon to license Pfizer’s COVID-19 vaccine.

The FDA asked the judge to let it produce the 329,000+ pages of documents Pfizer provided to the FDA to license its COVID vaccine at the rate of 500 pages per month, which means its production would not be completed earlier than 2076

It took the FDA precisely 108 days from when Pfizer started producing the records for emergency use licensure (on May 7, 2021) to when the FDA licensed the Pfizer vaccine (on August 23, 2021). According to the FDA, it conducted an intense, robust, thorough, and complete review and analysis of those documents in order to assure that the Pfizer vaccine was safe and effective for licensure. While it can conduct that intense review of Pfizer’s documents in 108 days, it now asks for over 20,000 days to make these documents available to the public

“So, let’s get this straight. The federal government shields Pfizer from liability.  Gives it billions of dollars.  Makes Americans take its product.  But won’t let you see the data supporting its product’s safety and efficacy.  Who does the government work for? “

FDA Asks Federal Judge to Grant it Until the Year 2076 to Fully Release Pfizer’s COVID-19 Vaccine Data

In other words it took roughly three and a half months for the FDA to conduct it’s own investigation and deem the Pfizer vaccine safe, while Pfizer now asks for 185x that amount of time to make documents available to the public. Something dishonest is going on here…

The fact that the Govt wants to allow a Pharmaceutical company to hide information until 2076, is evidence enough that nobody should be coerced by the government, and have their rights and freedoms; ability to have a job go outside, or travel, be contingent upon an medical procedure, especially an experimental treatment from a dishonest company trying to hide as much as it can from the public.

Public Health Experts File Lawsuit Against the FDA to obtain EUA documentation

Pfizer requests judge make public wait 20,000 days to fully release data to the public

FDA Releases first 91+ pages of documents regarding Approval of Pfizer’s COVID-19 vaccine

Approximately two months following the day the FDA was sued, and 3 months from when it first licensed Pfizer’s COVID-19 vaccine, the FDA released the first monthly round of the documents reviewed before licensing Pfizers COVID-19 vaccine.

The first found of documentation released, consisted of 91 PDF pages including 1 XPT file and 1 TXT file.

Cumulative Analysis of Post-Authorization Adverse Event Reports of [the Vaccine] Received Through 28-Feb-2021

One of the documents produced is a Cumulative Analysis of Post-Authorization Adverse Event Reports of [the Vaccine] Received Through 28-Feb-2021, which is a mere 2 ½ months after the vaccine received emergency use authorization (EUA).  This document reflects adverse events following vaccination that have completed Pfizer’s “workflow cycle,” both in and outside the U.S., up to February 28, 2021.

The volume of Adverse Events was so significant that pfizer made a statement to address the vaccine injuries on Pg. 6:

“Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases…” and that Pfizer “has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports” including “increasing the number of data entry and case processing colleagues” and “has onboarded approximately [REDACTED] additional fulltime employees (FTEs).”

First 91+ pages of documents regarding Emergency Use Approval of Pfizer’s COVID-19 vaccine

In other words Pfizer felt it necessary to share that they had to physically hire multiple additional full time employees (FTEs), simply to handle the sheer volume of adverse events being reported…does that sound like a treatment that should be slated for FDA approval?

Volume of Adverse Events Reports | Pfizer COVID 19 Vaccine Documents Released

According to the documentation released by Pfizer 2.5 months following EUA Pfizer received a total of 42,086 reports containing 158,893 “events.” Most of the adverse event reports:

  • Were located in the USA (possibly a limitation in interfacing or collecting Adverse events from other countries; due to a lack of technology or effort)
  • Disproportionately occurred in women (29,914 vs. 9,182 provided by men)
  • Occurred in individuals between ages 31 and 50 years old (13,886 vs 21,325 for all other age groups combined, with another 6,876 whose ages were unknown).
  • Were classified as “Nervous system disorders” (25,957 reports)

Were no stranger to adverse events…In fact we created a vaccine adverse reactions page on WokeGuru, with a mere fraction of the vaccine injuries we could find, including injuries from covid-19 vaccine manufacturers: Pfizer / BioNTech, Moderna, Johnson&Johnson, and AstraZeneca.

Nothing to see here says the FDA

“The findings of these signal detection analyses are consistent with the known safety profile of the vaccine.”

Pfizer in First 91+ pages of documents regarding Emergency Use Approval of Pfizer’s COVID-19 vaccine

So if they knew these vaccine adverse events were going to occur in the large volume they did, why did they have to hire more people to handle the volume of vaccine injuries?

“The data do not reveal any novel safety concerns or risks requiring label changes and support a favorable benefit risk profile of to the BNT162b2 vaccine.”

Pfizer in First 91+ pages of documents regarding Emergency Use Approval of Pfizer’s COVID-19 vaccine

It would seem to, that if Pfizer had to hire more full time employees simply to handle the high volume of adverse events, the data did in fact reveal “novel safety concerns” and “risks”…

In what reality does tens of thousands of vaccine injuries warrant a “favorable risk profile? Pfizer talks as though the tens of thousands of debilitating vaccine injuries; which may forever impact the lives of those people, were just numbers in some equation that Pfizer determined was ok. Quite frankly I don’t see how anyone could interpret this as anything less than putting profit before human lives.

Pfizer & BioNTech Development Timeline

It’s important to point out that when the FDA fully approved the Comirnaty COVID-19 vaccine on Aug 23 2021, this was for a separate product, different from the Pfizer Vaccine being administered; Comirnaty was not yet manufactured or distributed. There is conflicting information from Pfizer and the media, which implied that Comirnaty was the same as the COVID-19 vaccines being administered by Pfizer under EUA; this is not the case. In fact in a recent court case Federal Judge Allen Winsor Rejected the Department of Defense (DOD) claim, that the EUA and Comirnaty vaccines are interchangeable.

This is important, because Emergency Use Approval protects pharmaceutical companies from injuries or compensation caused by the vaccine. In other words Pfizer is not liable for injuries from an EUA vaccine. However when a vaccine is fully FDA approved, the company is now liable for injuries and damages and they are no longer protected from liability. If you are injured as a result of taking Pfizer’s “Comirnaty” COVID-19 vaccine, you can sue Pfizer for damages and they are liable to compensate you.

If you are unsure who to believe there is one way to confirm, if the vaccine you may want to receive is the EUA product, or the fully FDA approved “Comirnaty”, simply ask to see the vial from which your vaccine is being administered; if it doesn’t have “Comirnaty” clearly on the label, then it is not the FDA approved product, and under the provisions of EUA Pfizer is not liable if you are injured by the vaccine.

Dec 11 2020

FDA Issues Initial Pfizer COVID-19 vaccine

Pfizer received initial FDA Emergency Use Authorization for it’s COVID-19 vaccine.

Dec 11 2020

May 10 2021

Re-Issue / Extension of Pfizer EUA

FDA reissues Pfizer COVID vaccine EUA, for individuals 12-15 and 16yrs+.

May 10 2021

August 23 2021

Comirnaty FDA Full Approval

Pfizer & BioNTech partnership COVID-19 labeled “Comirnaty” receives FDA approval (If the vial does not have “Comirnaty” on the label it’s not the FDA approved product.)

August 23 2021

Oct 29 2021

FDA expands EUA for Pfizer COVID Vaccine to children 5-11

FDA expanded Pfizer’s Emergency use Authorization of the Pfizer-BioNTech COVID-19 Vaccine to include children 5-11 years of age.

Oct 29 2021

Nov 17 2021

Pfizer Releases first 91 pages of vaccine documents

Pfizer Releases the first 91 pages of COVID 19 Vaccine Documents reviewed by FDA prior to approval

Nov 17 2021

Dr. John Campbell Discusses Other data integrity issues in Pfizer’s vaccine trial

On a separate but related topic Dr. John Campbell discusses data integrity issues present in Pfizer’s initial COVID vaccine trial; released by Pfizer Employee whistleblower. It’s quite alarming that a trial was reviewed and approved with this level of incompetence and error in the trial.

COVID Vaccine Injuries

We have an expanded library of COVID vaccine injuries with hundreds of stories of vaccine injuries as well as videos of some of the more severe reactions. Here is a sample of some of the covid vaccine injuries:

Astrazeneca Covid Vaccine Trial Brianne Dressen Var Vae Covid 19 Vaccine Injury 1-1
Astrazeneca Covid Vaccine Trial Brianne Dressen Var Vae Covid 19 Vaccine Injury 2-1
Aaron Siri Esq Managing Partner Of Siri And Glimstad Var Vae Covid 19 Vaccine Injury-1
Covid Vaccine Trial Suzanna Newell Var Vae Covid 19 Vaccine Injury-1
Covid Vaccine Trial Kellai Rodriguez Var Vae Covid 19 Vaccine Injury-1


Pfizer and the FDA both promised a commitment to “full transparency”, but contrary to their words, have tried instead to keep critical vaccine documents that should be publicly available, away from the general public. The pharmaceutical company made bold claims regarding the safety and efficacy of their COVID-19 vaccine; If it’s as safe as they say, what is there to hide?…why have they tried so desperately to block and delay release of their COVID vaccine trial data? Only time will tell, as Pfizer’s COVID-19 vaccine trial documents, are slowly released to the public at 500 pages per month. The the release far off into the future at 2076, some of us may not live to see the truth of Pfizer’s COVID vaccine.


  1. AmarilloMama -

    I believe that they should have to release all of their documents now, not in 55 years… That is ridiculous. Most people who survive this genocide and tyrannical take over of the planet will be living in a horror show in less time than this 55 years. The FDA is another compromised agency that has already failed the American People and Minorities around the world. I believe that Bill Gates, Investors and Fauchi should be investigated. This vaccine was invented at least 6 years before the public even heard of the Covid 19 virus. My grandmother died from one of Fauchi’s shots…. Swine Flu. I was pregnant during the time when that vaccine and my OBGYN was trying to get me to take that vaccine. I had to keep refusing until I gave up and went to an East Indian female doctor. Not once did she ask me to take the vaccine. This intentional genocide must stop NOW. And all who have created this mess globally should be arrested, put on trial, and hung. That includes most of the governments who are or have become tyrannical demanding deprivation of human rights to work, to visit elders, family, friends, the right to travel, and go about a normal life. The families who have been broken up, divorced, lost a loved one, lost their business due to shut down and all other’s should be compensated for their loss their careers and jobs, their disabilities and their property lost due to the loss of income and employment. I think we can connect the dots to those behind all of this fraudulent scam upon all of humanity… so that they can depopulate the planet, and take complete control of all resources and humanity as their slaves.

  2. Tnt -

    Even if the fda releaes trial data documents, who the heck trusts that the FDA will not manipulate these documents and edit them and release false/fraudulent docs. They are asking for 75 yrs lol! Plenty of time to falsify docs.. duh!
    It’s poison, they are nazi sellouts with nazi plandemic fraudci-Berrick doctors along with poison genetic nazi shots.. simple as that

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