Showing posts with label Pfizer. Show all posts
Showing posts with label Pfizer. Show all posts
Sign Petition FDA To Investigate Pfizer's Clinical Trial Fraud
Should the FDA investigate Pfizer's clinical trial fraud allegations? Or look the other way?
Pfizer's Data Dump Shows Only 12% Efficacy Rate for Vaccine
Pfizer released 80,000 pages of data pretty much showing that the vaccine efficacy at 12% is only a fraction of the 95% we were told. Here is a data source.
#PfizerDump #Pfizer #BREAKING #BreakingNews
— CramerSez (@CramerSez) May 3, 2022
PFIZER DATA DUMP PROVES THEY KNEW DRUG WAS ONLY 12% EFFECTIVE, AT BEST.
They also knew it could cause harm to the unborn. pic.twitter.com/qPdUwdFbpO
This thread shows how the manipulated the numbers.https://t.co/OUiv1TQ2tR https://t.co/OUiv1TQ2tR
— Brady Moon (@RockyMoonShine2) May 5, 2022
Wall Street Is Finally Paying Attention to the ‘Trust the Science’ Fraud
Blackrock’s Edward Dowd reveals how Big Pharma is going to become the next potential financial crisis.
As Pfizer try to ‘pump their stock’ Hedge Fund guru Dowd, takes us inside what he calls the third great fraud in his lifetime, in this new bombshell interview with Dr Naomi Wolf.
Will CDC's Rochelle Walensky be found guilty of fraud? She is testifying before a grand jury.
If you found this video informative I would suggested watching this video of Edward Dowd. Pfizer, FDA Hid Failed Clinical Trials Data, Says BlackRock Advisor
ICYMI: Oregon Sen. Kim Thatcher, Dennis Linthicum and Dr Ealy have filed Grand Jury Petition in 9th Circuit Court against CDC, Rochelle Walensky et al.
— rosecity_outrage (@rosecityoutrage) March 27, 2022
Suit alleges Covid data fraud, conspiracy, malfeasance, misappropriation of taxpayer $ and more. 👇🏻https://t.co/ChWNYC1fyt
Pfizer, FDA Hid Failed Clinical Trials Data, Says BlackRock Advisor
Article copied from Childrenshealthdefense.com.
In an interview with Naomi Wolf, former BlackRock investment advisor Edward Dowd explained why Wall Street lost faith in Pfizer and Moderna stocks when Pfizer and the U.S. Food and Drug Administration tried to hide clinical trial data.
In an interview with Naomi Wolf, of the Daily Clout, investment advisor Edward Dowd discussed why investors are dumping COVID-19 vaccine makers’ stocks.
Dowd, a former managing director with BlackRock from 2002 to 2012, grew BlackRock’s growth strategy from $2 billion-$14 billion over 10 years.
Wolf introduced Dowd:
“He’s the extraordinarily kind of courageous, well-informed whistleblower who has come forward to explain to audiences why in his view, Pfizer has committed a fraud.”
Dowd described how his initial caution about taking the experimental COVID vaccine led him to research data related to Pfizer’s clinical trials.
Dowd told Wolf:
“I learned from a friend in the biotech industry that Pfizer had failed its all-cause mortality endpoint in the initial trial … All-cause mortality is the gold standard in any drug trial at the FDA. When you fail that endpoint, the drug is not approved.”
When Big Pharma and the U.S. Food and Drug Administration (FDA) were unwilling to release vaccine safety data, Dowd grew even more skeptical about the vaccines, he said, and was compelled to speak out privately and publicly about what he believed was a major deception:
“I got more loud about fraud when the FDA decided to hide the clinical data for 75 years. I’m an investor, so let me just say how I think about the world. I don’t wait for people to tell me what just happened. My job was to come up with an analysis, mosaic and investment thesis, and then over time I’d be proven right.
“So I don’t wait for The New York Times, The Wall Street Journal or The Washington Post to tell me anything. Because by the time that happens, the opportunity to make money is lost. So I started screaming fraud as soon as I saw that — because it’s unprecedented to hide data from the public.”
It was a report from the CEO of a major life insurance company that confirmed Dowd’s doubts:
“If this vaccine was as deadly and injurious as we thought, we’d see the insurance companies and the funeral home results. These are databases that aren’t being hidden from us by the government. So, unfortunately, in early January, a signal was launched by One America.
“The CEO didn’t really know what he was saying or the implications of it — because he didn’t think it was the vaccine, but he got on a Chamber of Commerce call in Indiana, and he said that in the second half of 2021, he was seeing a 40% increase in all-cause mortality — non-COVID. And to put some meat on those bones, a 10% increase he said would be a three-standard deviation [increase], which in math in my world is a big deal.”
Dowd described the impact on the financial world and on his current work:
“Wall Street is listening to me now because they’re nervous and a lot of them are jabbed as well. And if you look at the stocks of Moderna and Pfizer, Moderna is down 70% and Pfizer is down 20 plus percent.
“So my goal has been to raise consciousness across the country and the globe, by pointing out that even though the mainstream media is not going to save us — and it doesn’t seem like the politicians or the regulators are, because they’re in on it — we have to spread the word.”
Wolf asked Dowd about the repercussions of his public position:
“One of the things you’ve said, unequivocally, not mincing words — this is fraud. So if you are not right, that’s actionable, I believe, and Pfizer and Moderna could come at you with a libel suit or a slander suit. But I believe that has not happened yet. Will you speak to that?”
Dowd replied:
“I don’t have a medical license to take away. I don’t have a bar license to take away. I’m an investor. And throughout the history of Wall Street, investors have what we call a thesis. So I present this as a thesis — I’m a hundred percent convinced it’s fraud. I’ve laid out my case and it’s starting to appear, it’s coming to light that it is, but I can say this is freedom of speech. They can sue me if they want. I don’t suspect they will.”
Dowd said he’s been waiting for a “hit piece on me,” but there haven’t been any yet. He said because what he’s presenting is an investment thesis, he’s protected under free speech laws.
“Here’s the problem, Dowd said. “The proof of the fraud is showing up in real-life results. And that is becoming undeniable and impossible to hide.”
Read these related articles:
FDA Advisory Panel Votes 16-2 For No Booster Shots.
Dr. Steve Kirsch Bombshell Testimony at FDA Vaccine Hearing
(via Emerald Robinson) >> It’s official: the new vaccines are killing people. That’s what the data shows. 👇👇https://t.co/EzEiIf8KUi
— Giomerica (on GETTR @Giomerica) ✝️🇺🇸🍊🚛 (@ScottGiorgini) March 18, 2022
It’s always comforting when governments hide death data from the public. That is what I call a tell & prima facie evidence of fraud.
— Ed ☯️Free Thinker & Oracle (@DowdEdward) March 18, 2022
For those still in the matrix be sure to double up your mask, get your 4th booster & go march this weekend to virtue signal your support for 🇺🇦!
List of COVID Disinformation Spreaders That Need To Be Investigated
Steve Kirsch believe that all of these people are involved in “The proliferation of false or misleading narratives, which sow discord or undermine public trust in U.S. government institutions” and have collectively led to the tragic death of over 1M Americans.
Was Mass Vaccinating in the Public’s Interest or Pfizer’s?
Pfizer CEO Albert Bourla Reports $37B COVID Vaccine Sales in 2021
Pfizer reported global sales and alliance revenue from its abortion-tainted COVID vaccine brought in $36.78 billion in 2021, helping to more than double profits across its business operations compared with 2020.
In an earnings report issued Tuesday, the pharmaceutical giant also estimated that sales of its vaccine and anti-viral pill will top $54 billion in 2022, buoying shareholders’ hopes that profits at the company might soar for the second year in a row.
Pfizer CEO Albert Bourla said the company plans to aggressively expand the use of messenger RNA beyond just COVID vaccines, pointing to potential treatments of muscle, the liver and nervous system, despite warnings from many researchers that the use of mRNA technology carries significant risks.
Despite record earnings, Pfizer shares fell 3% yesterday on Wall Street due to lower than expected 2022 sales forecasts for its anti-viral pill, Paxlovid, which it sells at $530 a course in the United States.
Anti-viral pills like ivermectin, which health chiefs have sought to ban or restrict, typically sell for a few dollars when available, with several scientists suggesting the much-maligned pills are more effective than those produced by Pfizer.
Pfizer said its overall sales in 2022 across the company’s product range could reach $102 billion.
“In the early days of the COVID-19 pandemic, we committed to use all of the resources and expertise we had at our disposal to help protect populations globally against this deadly virus, as well as to offer treatments to help avoid the worst outcomes when infections do occur,” Bourla said yesterday. “We put billions of dollars of capital on the line in pursuit of those goals, not knowing whether those investments would ever pay off.”
Reacting to the earnings on Twitter, some commentators remarked on how beneficial mass-vaccination programs had been to the company’s balance sheet.
Bourla also said yesterday that Pfizer’s vaccine for the Omicron variant would not be ready for distribution until March, casting further doubt on calls from health officials and mainstream media outlets to vaccinate people now with shots made for previous variants.
The CEO acknowledged that the eradication of COVID is unlikely to be achieved because of mutations and the virus’ global spread, with some scientists previously warning that new vaccines were contributing to the growth of variants.Was mass vaccinating in the public’s interest or Pfizer’s? https://t.co/ojPAhfiCNE
— Lisa Boothe (@LisaMarieBoothe) February 8, 2022
Dr. Michael Yeadon, former Pfizer vice president and chief scientist for respiratory research, last week called on the media to apologize for their “lies” about vaccine safety as leaked data from the U.S. military indicated a 300% increase in miscarriages in 2021.
Yeadon, who spent 32 years in the industry leading new medicines research and retired from the pharmaceutical giant with the most senior research position in his field, was an author of a submitted petition to the European Medicines Agency (EMA) in December 2020 that raised substantial concerns regarding a lack of sufficient testing of the experimental COVID-19 gene-based vaccines before their emergency use authorizations.
With regard to the possibility of the shots endangering the fertility of women, Yeadon and his colleague, Dr. Wolfgang Wodarg, wrote, “There is no indication whether antibodies against spike proteins of SARS viruses would also act like anti-Syncytin-1 antibodies. However, if this were to be the case, this would then also prevent the formation of a placenta which would result in vaccinated women essentially becoming infertile.”
Such a possibility would need to be ruled out through standard experimentation before imposing such substances onto the entire population, according to the doctors.
“It’s important to note that none of these gene-based agents had completed what’s called ‘reproductive toxicology,’” Yeadon wrote in his recent statement. “Over a year later, this battery of tests in animals still has not been done. So there was and still is no data package supporting safety in pregnancy or prior to conception.”
The Centers for Disease Control and Prevention (CDC) released data in December showing a total of 965,843 reports of adverse events after COVID vaccines were submitted between Dec. 14, 2020, and Dec. 10, 2021, to the Vaccine Adverse Event Reporting System (VAERS).
The data included a total of 20,244 reports of deaths and 155,506 reports of serious injuries, including deaths, during the same period.
Judge Orders FDA To Show Pfizer Data Hidden From Public
I am pleased to report a federal judge rejected the FDA's request to produce the Pfizer Covid vaccine data at 500 pages per month and instead ordered a rate of 55,000 pages per month! Everyone should read the Judge's excellent 3-page decision available at https://t.co/ziqCs9fA9J
— Aaron Siri (@AaronSiriSG) January 6, 2022
On behalf of a client, my firm requested that the FDA produce all the data submitted by Pfizer to license its Covid-19 vaccine. The FDA asked the Court for permission to only be required to produce at a rate of 500 pages per month, which would have taken over 75 years to produce all the documents.
I am pleased to report that a federal judge soundly rejected the FDA’s request and ordered the FDA to produce all the data at a clip of 55,000 pages per month!
This is a great win for transparency and removes one of the strangleholds federal “health” authorities have had on the data needed for independent scientists to offer solutions and address serious issues with the current vaccine program – issues which include waning immunity, variants evading vaccine immunity, and, as the CDC has confirmed, that the vaccines do not prevent transmission.
1. The FDA shall produce the “more than 12,000 pages” articulated in its own proposal, see ECF No. 29 at 24, on or before January 31, 2022.
2. The FDA shall produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete.
3. To the extent the FDA asserts any privilege, exemption, or exclusion as to any responsive record or portion thereof, FDA shall, concurrent with each production required by this Order, produce a redacted version of the record, redacting only those portions as to which privilege, exemption, or exclusion is asserted.
4. The Parties shall submit a Joint Status Report detailing the progress of the rolling production by April 1, 2022, and every 90 days thereafter.[6]
SO ORDERED on this 6th day of January, 2022.
Evidence Mounting on Negative Efficacy of the Jabs
Do you know anyone who got the vaccine that has Covid?
— brandon 🇺🇸 (@gboslovesjesus) January 6, 2022
"The Danish government reported on Jan. 3 that only 24 percent of the people hospitalized with Omicron during late November and December were unvaccinated - while 76 percent were vaccinated, including 18 percent who were boosted."https://t.co/a0HKfxwahG
— Edmund Kudzayi (@EdmundKudzayi) January 7, 2022
Read the COVID-19 Positive Reddit Messageboard. It's hilarious.
Data from highly vaccinated countries suggests strongly that the answer is yes; vaccinated people are at higher risk of infection from Omicron.
Denmark has fewer than 6 million people - 1/60th as many as the United States.
Nearly all adults are vaccinated, mostly with the Pfizer mRNA vaccine that is the world’s supposed gold standard. Half have received the third “booster” doses. On Wednesday Denmark reported 28,000 Covid infections - equal to about 1.7 million in the United States.
The figures are similar in the United Kingdom, and all over Western Europe. Many countries are at 90 percent adult Covid vaccination levels, with boosters soaring. And they are all now in the midst of an epidemic of Covid contagion that dwarfs any that has come before.
The vaccines sure seem to have failed. That’s wrong, though.The reality is worse.The data from several countries now show clearly that infection rates are higher in vaccinated people.
We already know vaccine protection against earlier variants of Sars-Cov-2 falls sharply within months of the second dose, as the vaccine-generated antibodies fade.
But the new data go a step further, showing that previously vaccinated people are actually more likely to contract Omicron.
The government of Ontario has reported exactly the same pattern. So have Danish researchers, in a paper two weeks ago, when they found protection against Omicron turned negative three months after the second dose.
The vaccine fanatics have said that boosters are the answer against Omicron, that people who receive a third dose will regain protection.
This is - at best - a highly optimistic view. Remember the happy vaccine valley?
During the 2021 mass vaccination campaigns, Covid infections (whether Delta or the original strain) fell close to zero in the four months after the second dose, as antibodies peaked.
The happy vaccine valley no longer exists. Boosters begin to fail essentially immediately against Omicron, despite the massive (and potentially dangerous) increase in anti-spike-protein antibodies they produce.
Here’s the most recent report on vaccine protection from the United Kingdom, from last week.
The black boxes represent protection against the Delta variant (which is overstated because of the healthy vaccine user bias, but put that fact aside). As you can see, peak protection against Delta starts around 90 percent two weeks after the second dose. It remains at 60 percent six months out. A third dose pushes it back to 90 percent, and it barely budges for the first 10 weeks.
But what’s true for Delta is NOT true for Omicron.
Even at their absolute peak, two doses of mRNA vaccines offer only 60 percent protection against Omicron. Within four months protection has fallen almost to zero. A booster returns protection to 70 percent, but two months later it has fallen to about 50 percent.
That’s a decline to 50 percent protection from Omicron (at most, because the unseen confounders will tend to overstate vaccine efficacy) within 10 weeks of a third dose. We have every reason to expect it too will plunge to zero within a few more weeks.
What then? A fourth dose? A fifth a few weeks after that? How much mRNA do the public health authorities intend to cram in us?
And what about the real terror, antibody-dependent enhancement?
Are the vaccines only driving infection with Omicron, or are they increasing the risk of serious illness too?
We don’t really know yet, in part because Omicron is milder across the board. In addition, the wave of cases has hit so fast that it will take time for serious illness to catch up. Finally, the problem of incidental hospitalizations (with, not from Covid) is worse and will further muddy the data.
That said, hospitalizations of vaccinated people with Omicron are rising very fast, and the gap between vaccinated and unvaccinated people is shrinking. The Danish government reported on Jan. 3 that only 24 percent of the people hospitalized with Omicron during late November and December were unvaccinated - while 76 percent were vaccinated, including 18 percent who were boosted. During the same period, unvaccinated people made up 45 percent of those hospitalized with earlier variants - yet more proof the vaccines simply do not work as well against Omicron as earlier variants.
Why are we encouraging people to get “vaccinated” or “boosted” with a “vaccine” that within a few weeks probably increases their risk of becoming infected with the newly dominant variant of Sars-Cov-2?
We were lucky with Omicron; it is apparently quite mild.
But we are now in a world where Sars-Cov-2 cannot be contained and where it will continue to mutate in both humans and animals in ways we cannot predict (some scientists believe that Omicron underwent most of its mutations in mice before before jumping back to humans).
Nor do we yet know whether and how vaccines will interfere with the development of immunity after Sars-Cov-2 infection and recovery; will they prevent our immune systems from developing antibodies to other parts of the coronavirus, or interfere with B- and T-cell maturation?
All we really know is that the vaccines don’t prevent infection for very long and for many healthy people have side effects that are significantly worse than coronavirus infection. Both those facts were true before Omicron. Both are doubly true now.
Yet the drive to vaccinate - and boost - continues.
Why?
Pfizer Clinical Trail Data Won't Be Released Until 2096. What Are They Hiding?
As attorney Siri writes “this is “Not a typo.” They are demanding 75 years of data secrecy. Yes, the FDA is agreeing to share about 12,000 pages in the first couple of months but thereafter they would release, at a snail’s...
Outrageous Lack of Transparency—Pfizer Now Asks Court for 75 Years to Hide Details of COVID-19 Vaccine Trial Results.
TrialSite has tracked attorney Aaron Siri and his client’s Freedom of Information Act (FOIA) case against Pfizer for full disclosure of clinical trials documentation. Siri shared in a previous post that the Food and Drug Administration (FDA) asked a federal judge to delay the full disclosure of all relevant documentation till 2076—55 years from now!
Siri, who is a partner with the law firm Siri Glimstad representing the Public Health and Medical Professionals for Transparency (PHMPT) countered to the court that Pfizer should disclose the entire batch of documentation within 108 days which just happens to be the amount of time it took for the Gold Standard regulatory agency to review and approve Pfizer’s vaccine. After the court-ordered both parties to submit updated briefs, now in what can only be considered an insult to injury, Pfizer “doubles down.” Meaning the pharmaceutical company now wants to hide the extent of all of the material information till 2096.
Here are some Tweets showing what they are hiding . . .
Tens of thousands of Serious Adverse Reactions, over 1200 dead in the first 90 days of this trial and Pfizer did everything they could to try to conceal & bury this data for 55 years. Our corrupt & negligent governments betrayed us must be held to account !https://t.co/lFFXGXrwtm
— Francis Boulle (@FrancisBoulle) December 6, 2021
Another account suspended. His crime? He dared post recently released OFFICIAL data that revealed 1,223 people died during Pfizer's trials out of ~43,000.
— Nick the Greek (@nick_the_geek78) December 2, 2021
We're not talking misinformation here but official data. This is utterly outrageous. pic.twitter.com/PBHj2MXxrV
Another account suspended. His crime? He dared post recently released OFFICIAL data that revealed 1,223 people died during Pfizer's trials out of ~43,000.
We're not talking misinformation here but official data. This is utterly outrageous. pic.twitter.com/PBHj2MXxrVThis is why @pfizer trial data was asked to be kept a secret for 55 years.
— From the Desk of NikP@EL (@npuk1) December 5, 2021
Over a 90-day trial, resulted in
42,086 people having adverse effects
1,223 people died pic.twitter.com/Y27s5FH9ph
Pfizer trial data which 30 pages got released after the court rejected the request for data to stay hidden for 55 years shows that 1223 out 42 086 people died within 90 days after taking the jab.
— king Keith (@KaConfessor) December 6, 2021
Link: https://t.co/IOzvP6Jv4w pic.twitter.com/vGzvsSitHl
Yes! The Pfizer Booster Trial data submitted to the 9/17/21 VRBPAC meeting indicated that 34/268 ppl tested positive w/in 28 days of the boost.
— Jean Rees (@JeanRees10) December 6, 2021
What would that look like in the real world?
Now, we know. Negative VE the first month after the booster. https://t.co/78MZ1xS362 pic.twitter.com/kWhTKs7jYN
NO WONDER PFIZER AND THE FDA WANTED TO HIDE THE DATA FOR 55 YEARS….CRIMINAL.
— Jimmy 🩸54 (@cawthorme) December 7, 2021
Out of 42 reported pregnancy outcomes in the Pfizer trial, 25 spontaneous abortions occurred.
Description of missing information 👇👇👇 pic.twitter.com/w5YB1jI5Nq
MUST SEE YOUTUBE: FDA Says It Now Needs 75 Years to Fully Release Pfizer Trial Data| Facts Data https://t.co/V140DIwO1N via @YouTube pic.twitter.com/QKZTGzqWWQ
— Climate Realists (@ClimateRealists) December 9, 2021
Pfizer Knew from their own trials the shots were maiming/killing lots of people, But they pushed for FDA approval anyway, and tried to delay releasing data till 2075, first documents released confirm this, over 1200 deaths in the trials. #Pfizer #Scandal #VaccineSideEffects pic.twitter.com/Ebv9YDikBI
— BB8TEE (@BB8TEE) December 4, 2021
Court Orders FDA To Comply With FOIA Docs Request
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.
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.
This is criminal! Am I reading this correctly? 2.9% of adverse effects are recorded as deaths. Why hasn’t this been removed from the market? Other vaccines in development have been discontinued for even a single death in testing.
— Ags Win (@aggiesportsfan) December 2, 2021
“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.”
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.
Smoking gun confidential Pfizer document exposes FDA criminal cover-up of VACCINE DEATHS… they knew the jab was killing people in early 2021… three times more WOMEN than MEN
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?
Pfizer CEO Albert Bourla Lied & Pushed Misinformation Months Ago
Pfizer CEO is publically commenting about stopping the spread of vaccine misinformation.
The irony: months back Pfizer CEO touted their product had 84% efficacy at 6 months from the 2nd shot. This info was then echoed by the government to push mandates with the vaccine being so effective.
Israel and other countries do large-scale independent testing and find Pfizer to have 16%-20% efficacy at 6 months from the 2nd dose. It's the exact reason that Israel pushed for boosters asap.
Now the US government is pushing boosters and admitting the vaccine wains way quicker than initially thought.
Where did Pfizer get this info? It was clear misinformation was being pushed by the manufacturers to sell their product and they aren't being held accountable.
How many Americans got the Pfizer jab after reading these stats? Thinking it would be 2 jabs and they're good for well over 6 months. Now they are being told they will need boosters every 4-6 months.
Soon we will follow Israel's move and double jabbed Americans past 6 months won't even be counted as vaccinated.
Pfizer loves this. Every jab is money in their pockets.
CEO of Pfizer arrested by the FBI, charged with fraud
— Chief Erican, MBA (@EricanSA) November 8, 2021
Pfizer lied about the effectiveness of the vaccines & misled customers about the serious side effects the vaccines can produce. Pfizer is accused of paying off governments & the mainstream media to stay silent. #pfitzergate https://t.co/eS40uF2rkY pic.twitter.com/2YXobQ1EJB
Former Pfizer VP Sounds The Alarm on Athlete Deaths
You might be wondering why there have been so many news stories, even coming from mainstream media sites, which report young people including athletes suddenly dying or having injuries? The former VP at Pfizer, Dr. Michael Yeadon connects this sudden increase in youth deaths and injuries directly to the COVID jabs.
Individual reports of the deaths and permanent disabilities of young football, cricket, rugby, and hockey players, dancers, and more are everywhere all of a sudden. But how is no mainstream media outlet putting these all together and calling it out as a huge problem?
Dr. Michael Yeadon has had enough and is making a connection. He’s called out this spate of deaths and injuries for what it is: the effects of the COVID jabs. We’ll take a look at what Dr. Yeadon has said and link all the reports of these athletes and young people, their deaths injuries and testimonies, and let you decide for yourself.
The former VP of Pfizer, Dr. Yeadon, recently called out the COVID jabs for their danger early on and warned of their deadly potential. And now his dire predictions are coming true. But the mainstream media with the collusion of governments and health authorities are trying to cover up the evidence.
Dr. Yeadon has pulled together a couple dozen recent examples of athletes dying and becoming permanently injured, and notes how rare such occurrences used to be, whereas in the past few weeks it seems to be a daily occurrence.
He also explained the deaths and injuries, saying, “These vaccines induce the body to manufacture unregulated amounts of virus spike protein. Not only are the amounts uncontrolled in any way, we also have no idea, in any individual, WHERE in the body this dangerous protein is made.”
This scientific expert concluded, “I surmise that all these sports people are being injured & killed by the COVID-19 vaccines. Young people are NOT at risk from this virus & also are poor at passing it on. There is therefore NO REASON why these people have been vaccinated, and it’s pressure from their clubs & leagues that’s made them comply.”
So let’s take a look at these cases. Each of these stories have been compiled and shared recently on Dr. Michael Yeadon’s Telegram channel, but as you can see most have been reported by mainstream media sites.
Slovak Player Boris Sádecký Passes Away
Young Saurashtra cricketer Avi Barot dies after suffering cardiac arrest
Fabrice N’Sakala of Besiktas recovering in hospital after on-field collapse
Jens (27) collapses on the football field and dies: “This is not… (Maldegem)
Jente van Genechten, 25, footballer collapses on field due to heart attack
Benjamin Taft, 31, German footballer collapses after game, passes away due to heart attack
Rune Coghe, 18, Belgian footballer suffers cardiac arrest on pitch
Helen Edwards, referee taken off court during World Cup qualifier due to heart issues
Dimitri Lienard, 33, FC Strasbourg midfielder collapses during game
Barcelona star Sergio Aguero admitted to hospital for ‘cardiac exam’ after chest pain during match
Emil Palsson: Footballer collapses from cardiac arrest during game in Norway
Antoine Méchin, 31, French triathlete suffers pulmonary embolism following Modern
Luis Ojeda, 20, Argentine football player unexpectedly passes away
Greg Luyssen, 22, Belgian pro cyclist ends career due to heart issues
Teen equestrian star Cienna Knowles hospitalised with blood clots after Pfizer vaccine
World Class Athletes Suffer Vaccine Injuries
WORLDWIDE SURGE OF SPORTS PEOPLE SUFFERING SUDDEN HEALTH ISSUES AND DEATH
Anna Terentyeva, the leading soloist of the Perm Ballet, has passed away
Miss World contestant, 24, dies suddenly at home after failing to show up for work
This list could go on and on, so we must heed the advice of so many doctors who are calling out these COVID jabs. These include Dr. Michael Yeadon, Dr. Elizabeth Lee Vliet of Truth for Health Foundation, Dr. Peter McCullough, Dr. Robert Malone, and so many more. They have come out risking their own careers to spread the truth about what’s happening.
We really have to say right now, as do the many conferences of Dr. Vliet we have the privilege to air … stop the shot!
Who Are The 'Disinformation' Enemies of Truth?
The only way to know who your enemy is in the age of disinformation is to follow the money.
China's Wuhan laboratory is owned by GlaxoSmithKline which owns Pfizer the company that makes the vaccines. Dr. Fauci funded the research at the Wuhan lab through NIH. GlaxoSmithKline is managed by the Private Equity finance division of Black Rock which manages the finances of Open Foundation Group for George Soros which manages the French Accent Group. Soros owns the German company that built the Wuhan laboratory which was bought by the German Alliance which has Vanguard as a shareholder. Black Rock, Vanguard and Alliance control the central banks and also have a large stake in Microsoft where Bill Gates is the Chairman. Bill Gates is a shareholder of Pfizer and BioNTech and a sponsor of the World Health Organization.
Over the past two decades, the Bill and Melinda Gates Foundation has donated “a bit more than $10 billion” into mainly three groups: the Global Alliance for Vaccines and Immunization, the Global Fund to Fight AIDS, Tuberculosis and Malaria, and the Global Polio Eradication Initiative.
What's is REALLY in the Coivd 19 Vaccines
Israeli Physicians, Scientists Advise FDA of ‘Severe Concerns’ Regarding Reliability and Legality of Official Israeli COVID Vaccine Data
An independent Israeli group of physicians, lawyers, scientists, and researchers called the Professional Ethics Front today advised the U.S. Food and Drug Administration (FDA) regarding the upcoming FDA discussion on administering COVID-19 vaccines to children aged 5-11, expressing “severe concerns” regarding the reliability and legality of official Israeli COVID vaccine data.
“We are aware that the state of Israel is perceived as ‘the world laboratory’ regarding the safety and efficacy of the Pfizer-BioNTech COVID-19 vaccine, as reflected by statements made by Dr. Albert Bourla, Dr. Anthony Fauci, and other senior figures in leading health authorities throughout the world,” the letter reads. “It is therefore our understanding that the data and information coming from Israel play a crucial role in critical decision-making processes in regards to COVID-19 vaccination policies. We thus see it of utmost importance to convey a message of warning and raise our major concerns regarding potential flaws in the reliability of the Israeli data with respect to the Pfizer-BioNTech COVID-19 vaccine, as well as many significant legal and ethical violations that accompany the data collection processes.”
The letter elaborates: “We believe that the significant failures underlying the Israeli database, which have been brought to our attention by numerous testimonies, impair its reliability and legality to such an extent that it should not be used for making any critical decisions regarding the COVID-19 vaccines.”
America’s Frontline Doctors (AFLDS) spoke to Haifa and Reichman Universities Health and Risk Communication lecturer Dr. Yaffa Shir Raz, one of the letter’s authors, about their findings and conclusions:
This document briefly outlines the main failures that lead to this unfortunate, albeit inevitable, conclusion,” the notice reads. “We emphasize that we can expand and clarify further, as well as provide references, in relation to each of the failures described below:
“1. Lack of a Public and Transparent Adverse Events Reporting System: The first prerequisite for granting a permit for use of any new medicinal preparation is the setup of adverse events (AEs) collection systems that would allow appropriate management of risks and generation of alarm signals. All the more so when it concerns a mass vaccination campaign of a first-in-human use of an experimental preparation to the citizens of an entire country, which serves as a global model. Despite the advanced technological systems available to the Israeli HMOs, and contrary to common standards in Western countries, there exists no proper and transparent AEs reporting system in Israel, such as the US VAERS system, that is accessible to the public, and thus no appropriate tracking of AEs occurring after the administration of the COVID-19 vaccine.
“Healthcare professionals or citizens in Israel, who wish to submit reports of AEs following vaccination, are unable to do so. As such, there is no possibility for either of these populations to also search through the data, rendering impossible the examination of the reported AEs by other citizens, physicians and independent researchers. Instead, there is only an online AEs reporting form available on the MOH’s website. This form, however, was for many months not useful, since it did not allow the inclusion of personal contact information. The free text field intended to describe the AEs comprised a limited number of characters and the symptoms list available to choose from was limited as well and included only mild AEs terms.
“A petition to the Israeli Supreme Court of Justice has led the Ministry of Health (MOH) to implement the above-mentioned necessary improvements to the form. Unfortunately, the modification of the form was made very late, after the majority of the adult population had already been vaccinated. Furthermore, since the report is not publicized in a transparent manner, the MOH is the only recipient and thus the sole owner of the data and the decision-making authority on the utilization and distribution of it.
“Moreover, no tracking and monitoring of even the most sensitive populations, such as pregnant women and the elderly, is taking place. For example, as part of the ‘National Senior Population Protection from the COVID-19 Program’ in Israel, a reporting system was activated in April 2020, which presented detailed reports almost daily on COVID-19 eruptions, on hospitalizations and on mortality in nursing homes. However, on December 29th, 2020, the very day the vaccination campaign commenced in nursing homes, the publication of these reports was abruptly discontinued, and has never been resumed since.
“2. Severe Impairments in Healthcare Professionals’ Adverse Events Reporting System: We reveal that physicians and medical teams in Israel encounter great obstacles when attempting to report AEs following Pfizer-BioNTech COVID-19 vaccination to the MOH. We have testimonies of physicians, who attest to the complexity of filling the AEs reports to the MOH, claiming that reporting is almost impractical in the incredibly stressful working conditions of medical teams in Israel during this period. As a result of these tremendous difficulties, there is an immense underreporting of AEs by healthcare professionals in Israel, and AEs are only rarely reported in exceptional cases. The physicians’ testimonies that we have obtained also show that reported AEs are not openly publicized, or made available to the healthcare professionals themselves.
“Even more disturbing is the fact that the few reports, which the Israeli MOH does publicize about the AEs observed after receiving the Pfizer-BIONtech COVID-19 vaccine, are not consistent with the testimonies of physicians regarding severe adverse events (SAEs) that they themselves have reported to the MOH. Thus, for example, in a discussion before the Advisory Committee of the FDA on September 17th, 2021, the head of the Israeli Health Services, Dr. Alroy-Preis, claimed that only one case of myocarditis was observed after the 3rd vaccine dose out of three million people who received the 3rd vaccine dose in Israel. This claim does not reconcile with research findings from all over the world, including findings from Israel, that were published in the medical literature, according to which the rate of myocarditis observed after receiving the Pfizer-BioNtech COVID-19 vaccine stands at 1:3,000-6,000. The claim of Dr. Alroy-Preis also stands in contrast to reports given by a handful of brave Israeli doctors about cases of myocarditis and other SAEs observed in close proximity to the Pfizer-BioNtech COVID-19 vaccine.
“One of these physicians, Dr. Yoav Yehezkelli, who was among the founders of the Israeli Outbreak Management Team, wrote on his Facebook page that he personally treated in his clinic a 17-year-old boy, who suffered from myocarditis several days after the 3rd vaccine dose, and he knows of two additional cases among the boy’s classmates. Dr. Yoav Yehezkelli added that he reported the myocarditis case that he treated (and additional SAEs cases) to the MOH through the online reporting system, as well as via personal reports to MOH officials, but his reports were quickly dismissed as having no link to the vaccine, without thorough examination of the cases. Dr. Yehezkelli also mentioned that he encountered other patients in his clinic, who were hospitalized after suffering from AEs in close proximity to receiving Pfizer-BioNTech COVID-19 vaccines, and the hospital supposedly failed to report said AEs to the MOH. We have affidavits from nine other physicians, who have also treated cases of myocarditis or know of such cases, but have abandoned their attempts at reporting to the MOH having tackled immense difficulty or, alternatively, reported to the MOH and did not get any response. It is statistically improbable that a small cohort of physicians should witness these many COVID-19 vaccine injuries if Dr. Alroy-Preis’s claim was accurate.
“3. Data Distortion: Recently, two serious incidents in which data presented by the MOH was distorted have been revealed.
“The first one was the deletion of thousands of citizens’ responses to a post by the MOH. In response to an MOH post that read ‘Let’s talk about the adverse events’, and claimed that the vaccine is completely safe and that SAEs are extremely rare, tens of thousands of responses from the public were posted, with many reporting AEs, including SAEs, which they suffered after the vaccine. But instead of examining the responses and addressing them, about half of them were deleted.
“The second event occurred about two weeks ago. Based on MOH dashboard data, an analysis conducted by members of the Israeli Public Emergency Council for the Corona Crisis (PECC) demonstrated that the Pfizer-BioNtech COVID-19 3rd vaccine dose effectiveness is much lower than that claimed in the New England journal of Medicine study presented by Dr. Sharon Alroy-Preis to the FDA panel on September 17th, 2021. Within 24 hours of the release of the PECC analysis, the relevant dashboard data history was completely re-written. The PECC released screenshots of both the original and “rectified” data.
“4. Legal and Ethical Violations in Data Collection Processes: Not only is the data coming from Israel regarding the safety and efficacy of the PfizerBioNtech COVID-19 vaccine apparently unreliable, but also the collection method is controversial, and claimed to be neither legal nor ethical. The Pfizer-BioNtech COVID-19 vaccines are administered to the Israeli population without their informed consent, which is required by the GCP chapter of IHC-6 and carried out in other countries. This is a clear violation of the Nuremberg Code Rules, the Patient’s Bill of Rights, and the Israeli MOH directives for clinical trials on humans. Moreover, the Israeli citizens are under tremendous pressure to get vaccinated, almost to the point of coercion.
“Should the ‘Outbreak Management Team’ decide on a 3rd dose of the vaccine to the immunocompromised patients, it is not clear how many we can vaccinate, and it requires approval of the Helsinki committee (medical trial approval committee) and Pfizer’s approval. We are committed to Pfizer, to vaccinate only by the vaccination regimen established by them”. This is a statement made by Prof. Hezi Levi, former CEO of the Israeli MOH on July 5th, 2021. The evident conclusion is that the 3rd vaccine dose operation is an experiment requiring approval of the Helsinki Committee in charge of approving human medical experiments in Israel. Such an approval has never been issued. Moreover, the 3rd vaccine dose operation refers only to the immunocompromised population, and thus is even more unethical in healthy individuals, especially in young healthy individuals, shown to be at a higher risk for myocarditis.
“We are deeply concerned with the failure of the Vaccine Safety Committee (VSC) to fulfill its designated role. The VSC is responsible in Israel for vaccine safety and the official arm designated to monitor and collect safety data. It has not issued a single position paper on its behalf or raised a single red flag to raise wareness/bring attention to SAE cases and has never gathered in full assembly. Additionally, one of the public representative, who is a pediatrician (allergist, immunologist), never knew that he was appointed and did not attend any of the meetings, even when they did take place.”
The Israeli Professional Ethics Front concludes its notice to the FDA: “In accordance with the accepted perception established after World War II, the findings of experiments obtained in illegal and immoral ways should not be relied upon. We believe that the same rules should apply to the findings of the current experiment in Israel, since these findings were obtained through significant legal and ethical infringements. Our conclusion is further reinforced by the significant doubts about the reliability of the data reported by Israel, as detailed above, and the consequent major concern that their use might be misleading and thus disrupt the decision-making processes pertaining to the Pfizer-BioNtech COVID-19 vaccines.
“In the Book of Leviticus, it is said ‘Do not stand idly by while your neighbor’s blood is shed.’ In the spirit of those words, we implore the committee to take into consideration our urgent warnings and adopt utmost precaution when referring to the Israeli data concerning the safety and efficacy of the Pfizer-BioNtech COVID-19 vaccines.”
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