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?
Excuse me if I don’t get excited about reports from the Gateway Pundit.
How do we know these docs from phmpt.org are legit?
https://phmpt.org/pfizers-documents/
We’ve been burned way too many times for me to jump on this bandwagon.
Those who know you’re lying know the truth, and liars and shills won’t be helped.
A restaurant salad bar has lettuce with E. Coli and no deaths and it prompts a nationwide investigation of the source and nationwide recalls.
1200 people die from the clot shots and the news is covered up and the government (which profits from the patents or holds lots of stock in the clotshot providers) tries to force everyone to take it, extending the jab to 5-to-12 year olds who statistically have <<<<0.01% deaths from the coof.
What’s that old saying again?
Oh yeah. “Sod Off, Swampy.”
Stuff it, troll.
Those opposed to the jabs are quoting for peer reviewed journals like the Lancet, the New England Journal of Medicine, the British Medical Journal, Science, Nature, and Circulation.
Nobody believes your lying propaganda anymore.
Only violence can save the republic.
Actually restore of the republic would be a better way to look at it.
Currently the republic is dead.
36mg? Per week??
That sounds like a treatment dose.
And, the American Heart Association.
Everything including the words “the” and “and” as the old saying goes.
There was a publication by a Harvard immunology professor a month or two back which showed no correlation between jab rates and infection rates across many countries and across over 2900 US counties.
Post your links that the jab rates are low in the U.K., for example.
Then note that those infected with Omicron are the jabbed; by definition this is true in Australia since they don’t allow the unjabbed to travel to their country.
Troll.
Hardly. 18mg twice per week is the recommended prophylaxis dosage for my weight range. I take it Mondays and Thursdays. An early treatment protocol would be 36mg-48mg daily for 5-7 days for my weight.
Have you reviewed the FLCCC I-Mask+ protocol? I suggest you do:
The problem with the use of Ivermectin is that it is being under prescribed and prescribed too late.
Ahhhh.....18 mg 2 x week. Got it.
I misread.....I thought you were taking 36 mg 2 x week. My apologies.
Yes....that sounds much better :-)
My prescribed dose is lower, but, I think hubby’s is close to what yours is.
First off, UK (which is both England and Scotland) vaccination rates are not that high.
Only, wrong....
“Furthermore, the UK’s vaccination program led most countries.
As of November 6, 2021, the official UK government website for COVID-19 vaccination data shows about 80% of its eligible population has received two doses, and 17% a third ‘booster’ dose”. ...
Add to those 90 deaths the people who barely survived and now have life threatening health problems.
Kaiser in Northern California started its big vaccination programs on 1/31/21 with the first shot in/at their big clinics or hospitals. Herds of us went in for the shot clinics across N.California.
Then, they had a big program on 2/21/21 for the second shot program.
Here, they used Pfizer’s vaccination. I think that you had to be 65 or 70 to get the first vaccination and then the second shot.
We have a lot friends and people, we know in our age group, 80+-10 years, who got the shots. Most of the women had minor problems if any.
Some of the guys had some weird and minor reactions. I had a temporary shingles reaction around the injection site and so did a few others.
Then, our shingles vaccinations apparently kicked in and the rashes disappeared with basically no problem about the 3rd day post Pfizer shot. One friend had the classic shingles breakout around his waist line, and he made and appointment with his PC doc. By the time his appt. came around, in a few days, the rash had disappeared. They had sent pictures to his PC showing the rash and then some after the disappearing act before the cancelled appt.. The Doc actually made a house call to see how the rash had disappeared.
None of our wives had anything besides an aching arm from the shots.
This was replicated with our family members across the nation. Basically, the wives had minimal reactions and the guys our ages had some aches and pains which went away.
Some of our younger relatives got hammered with the Moderna first 2 shots and really hammered with their recent booster shot this year. One previously very healthy early 50’s guy has missed over 2 weeks of work since his first Moderna booster. GI problems, dizziness and feeling like he got ran over by an all pro football team with off and on fever. He may have gotten the real crud a year ago between Thanksgiving and Christmas. Then a he got a second and third hammering with his second Moderna and recently his booster shot.
In summary, my age group 70-80+ with manageable diseases might be the only logical and ethical group which can have the vaccination. Only, if we want it.
It is basically and probably criminal to give any of these shots to anyone under 60-65.
If they get the crud or one of the variants, treat them as out patients. One of our DNA sons in his 50’s and 2 non DNA sons, who adopted us, had the Delta this past summer. They were treated as outpatients and have had good recoveries, and they are back to work and doing things with their families.
The money that can be made by the vaccine makers and their investors is enormous. Blanket immunity from any consequences for harm or deaths, total government funding of the jabs (companies can jack up the price as it’s 100% subsidized), multiple and probably endless ‘boosters’ to keep the money train rolling, etc.
Moderna stock is up almost 200% this year, and 1,600% the past five years. I coulda been rich!
“...for sharing public records with the public?”
I know, right?
Who would stoop so low as to do such a dastardly thing!
From my conversations with the injected (it ain’t vaccine, so don’t use the term), psychosis is already here - often was already latent psychosis, just waiting for a “trigger” for the rare psychosis.
How is this not breaking news on every single network?
“It is difficult to get a man to understand something, when his salary depends on his not understanding it.” - Upton Sinclair
Come Quickly Lord, Come Quickly Lord Jesus !
Amen ❤
There will never be a report on long term side effects.
Hand waiving and “confounding factors” will mean that there is no way to know what cancer is caused by the vaccine and what cancer you were going to get anyway.
Iatrogenics is real. What is happening now is madness, literal public madness.
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