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?
“Y’all think this is shocking, just wait a few years when they will have the data for the long term side effects.”
How will it ever be proven that those effects were a result of the shots, years later?
“ This would be useful information if we knew how many shots were given during the 90 day period”
I get it. It’s okay to kill people just as long as it is a low percentage!
It only makes sense that the unvaccinated should be sued.
From their overall numbers for that 2 and 1/2 months timeframe:
Recovered/Recovering 19582
Recovered with sequelae 520
Not recovered at the time of report 11361
Fatal 1223
Unknown 940
They need to separate "recovered" from "recovering."
"Recovering," by definition, means they haven't recovered yet.
Therefore, the number "Not recovered at the time of the report" really wasn't 11361, it was some larger number.
And, while Pfizer may have shipped out the first doses on Dec 1st (per their report here), the first dose given wasn't publicly acknowledged until December 14th, 2020: US administers 1st doses of Pfizer coronavirus vaccine.
So the timeframe for this Adverse Event report is really 10 weeks (not 3 months).
That Twitter account has already been suspended.
That’s strange....Gee, I wonder why? ..................................
Whichever it may be: Let the games begin!
Surprise... Surprise...
Now, who would have thought that these scumbags were screwing with the sheeple who meekly submitted to the jab... /s
The media is complicit in this cover up along with a ton of politicians in both parties.
I hope to heck not, but it might be very easy to prove. It would really suck if everyone around me started dropping like flies from a vaccine for an illness that was over 99% survivable. I hope to heck the vaccine doesn’t cause prion illnesses down the road.
Buzzards...................
Where are the Frerpers arguing that the gigantic spike in VAERs reported deaths were just due to negative publicity and not the jabs?
Why wouldn’t they find some nondescript info to realease?
Buzzards? That’s probably the media.
“A total of 1223 individuals had a fatal reaction to the experimental Pfizer vaccine.”
I have nothing but disdain for Pharma and would never put mRNA in my body.
But the above quote is fear mongering bullsh!t.
Nobody knows, yet, why these people died.
It will end up in the lap of corporations who pushed it on their employees.
Military and federal workers out of luck i suppose.
Against who? Pfizer is protected by law?
See my post at 38. Agreed - these deaths were people who got the shot and then died. Correlation does not necessarily equal causation.
Another GP lie.
Why post lies from known liars?
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