Posted on 12/02/2021 9:12:19 AM PST by Red Badger
The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.
The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.
In a shameless effort to bury the information, the FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.
In other words, Elon will make it to Mars way before the documents would be fully released – in the year 2076.
A motion that was also filed by the same group of doctors and scientists is currently pending in federal court that would force the FDA to expedite processing and releasing these documents.
Meanwhile, the FDA still has to comply with the original order to begin turning over documents. Lo and behold, the first release is a bombshell.
According to an official Pfizer document that is titled Cumulative Analysis of Post-Authorization Adverse Event Records Reports, in just the first 90 days of the vaccine’s roll out under the FDA’s EUA – from December 1st. 2020 – February 28th, 2021 – there were TENS OF THOUSANDS of reported adverse reactions, including OVER 1200 DEATHS.
https://twitter.com/iGNORANTCHiMP/status/1465992238689923081
The report only included adverse events to the vaccine that researchers considered “serious cases,” there were thousands more submissions that were left out of this data.
Any cases deemed “non-serious” would be processed within 90 days, but this report was released before 90 days of Pfizer’s vaccine being available had even passed.
“Due to the large numbers of spontaneous adverse event reports received for the product, the MAH has prioritised the processing of serious cases, in order to meet expedited regulatory reporting timelines and ensure these reports are available for signal detection and evaluation activity.
Non-serious cases are processed as soon as possible and no later than 90 days from receipt. Pfizer has also taken a multiple actions to help alleviate the large increase of adverse event reports.”
In all, the report states that there were a total of 42,086 case reports of individuals who had an adverse reaction to Pfizer’s vaccine worldwide, with the largest number (13,739) coming from the United States and from the UK (13,404).
According to the documents women (29,914) were over 3x more likely to experience a reaction than men (9182). A total of 1223 individuals had a fatal reaction to the experimental Pfizer vaccine.
https://twitter.com/iGNORANTCHiMP/status/1465999494177345537
How did the FDA not immediately pull the experimental jab out of circulation? Let alone grant multiple extensions of the EUA to Pfizer while working with the fraudulent Biden regime to push a needle into the arm of every single American.
The document also makes it clear that the data only includes “recorded adverse events,” which even the author admits is likely just a portion of the true number of adverse reactions that took place.
Again, keep in mind, this is within the first 90 days of the Pfizer jab’s availability.
From the Pfizer document:
“Reports are submitted voluntarily, and the magnitude of underreporting is unknown.
Some of the factors that may influence whether an event is reported include: length of time since marketing, market share of the drug, publicity about a drug or an AE, seriousness of the reaction, regulatory actions, awareness by health professionals and consumers of adverse drug event reporting, and litigation.”
https://twitter.com/iGNORANTCHiMP/status/1466018418981752837
Pfizer’s “confidential” Covid-19 vaccine adverse reaction review ends with thousands of conditions that are of “special interest” and could possibly develop after taking their experimental jab. The single-space typed list continues for an astonishing 9 pages.
Yet somehow the paper concludes that the “review of available data” was good enough and demonstrated a “favorable benefit-risk balance” for the rushed vaccine.
What’s the benefit-risk balance on a virus that has a 99.9% recovery rate? The benefit – at least for Pfizer – is clear; It doesn’t matter how many otherwise healthy lives are lost – they are CASHING IN to the tune of $1,000 PER SECOND with a projected $36 BILLION in profit this year from the vaccine alone – it’s criminal.
The full document can be found here.
The FDA clearly agreed with Pfizer, extending the EUA despite the high number of deaths and serious reactions in the short amount of time Pfizer’s jab had been available.
What else are they hiding?
Meh. Drop in the bucket as far as they’re concerned.
Evil. money-grubbing b@stards.
Pro vaxxers lie all the time. I just read a couple in this thread.
Yep, The Usual Suspects are on this thread like stink on Mitt...
Even assuming your math is correct, I am not willing to risk the long term side effects for a minimal improvement in survivability risk. Now add into that equation the questionable efficacy of the shot and I think it makes the decision quite clear. I’ll take my 36mg of Ivermectin per week and a 100% guarantee that I won’t have to deal with side effects long term.
***
Well THIS is telling:
@Ignorantchimp Twitter account is now suspended; manifestly for sharing public records with the public.
for sharing public records with the public?........................
Choices after one knows all the relevant facts available is not the issue I take here. What I think should upset everybody is the lying and censorship of the relevant facts. The CDC maintained for months that it was not able to establish any deaths were caused by the jabs despite the gigantic spike in reported VAERs deaths compared to other vaccines. Is it even plausible that there was any honest effort and that them looking into it was not a total sham? Or was the CDC just not able to review these documents either? And if not why the hell not? Why did the FDA let the CDC spin nonsense when they knew for a fact that it did kill people? Saying it might be worth taking still because the number killed was low compared to those that took it avoids the fact that they intentionally gave the false impression it was perfectly safe. There should be an investigation and this incompetence or dishonesty needs to have consequences.
How will it ever be proven that those effects were a result of the shots, years later?——————————————————————————————————————— It will be proven by comparison to the un vaccinated control group. The control grou they are so desperately trying to eliminate via mandatory vaccination policy
The media is fully complicit.
They are the propaganda tentacle of this whole CCP CONTROLLED government we now have.
The usual suspects took awhile to arrive, but then did so at about the same time. I wonder if they are independent, coordinated or independent with some central resource?
Under socialism, everything is done for “the collective” ... including dying from a “vaccine” that still doesn’t work.
Maybe, but most of them will make sure to dump it saying “Well OSHA said so!”
We should have never given immunity to vax makers.
You might as well take up smoking too. Your chance of dying from lung cancer after your first month of smoking is less than your chance of dying from the vaccine in the first month.
(from the article): "The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA)
request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency. "
Diogenesis :" KNOWINGLY then they made money in the stock market
as more people and children and fetuses died
(and more to come), but they made profit
and so much royalties for the CDC. "
"MENGELE PRIZE coming around the mountain."
(My comment/tik) Now we know what the indemnification from lawsuits was all about, if true and that Pfizer knew at the time
when they and the Federal gov. declared :
" Safe and Effective".
The only way to enact this injection "Under Emergency Authorization" (UEA) is to eliminate any alternative medication procedure, which NIH/CDC has effectively done.
The term "vaccine" had to be changed by the CDC to accommodate the mRNA injection of a synthetic genetic biologic injection.
All done, but at what costs to humanity, Constitutional rights, vaccine passports, family divisiveness, mask mandates, travel and educational restrictions ?
And still we don't have a legal definition of the true original covid-19 source, even though it appears to have been genetically spliced in a laboratory.
An unexplained Plandemic. Go figure !
Release the litigation hounds.
” How could anyone, in good conscience, push this poison?”
You answered your own question.
Yeah, let’s get KRAKEN....................
Note that Andrew Cuomo's media advisor was pulling the puppet strings of PMSNBC's Katy Tur behind the scenes [all on group texts], and Chris Cuomo was coordinating hits on his brother's accusers behind the scenes, using XiNN network resources.
Food for thought.
“They will blame it on Trump in 3-2-1”
there’s no doubt whatsoever that the National Socialist Democrat Party, their media propagandist toadies, social media, and the deep state will indeed blame all of this on Trump, but only starting AFTER he announced his re-election bid ... until then, dementia joe can do no wrong, no matter how many thousands he kills with the vaccine and no matter how many hundreds of thousands he murders by withholding cheap, effective treatments such as HCQ and IVR ...
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