Ok, Pfizer…
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Pfizer CEO Brags About Getting Briefed By the CIA, FBI On ‘The Spread Of Misinformation’
Speaking to the globalist Atlantic Council in a virtual meeting, Pfizer CEO Albert Bourla admitted that his corporation is “getting briefings from the CIA and FBI” on the “spread of misinformation” relating to COVID-19 vaccines.
Pfizer CEO Albert Bourla strangely admitted that the major pharmaceutical corporation is getting briefed on “the spread of misinformation” of COVID-19 vaccines from “the CIA and FBI” while speaking to the globalist Atlantic Council.
After explaining to the council that Pfizer was being “targeted” by “dark organizations,” Bourla said that they “were getting briefings from the CIA and FBI” about cyber attacks. “But also about the spread of misinformation,” he added.
People Who Spread “Misinformation” About COVID-19 Vaccines Are “Criminals,” Says Pfizer CEO
People who spread “misinformation” about COVID-19 vaccines are “criminals,” according to the CEO of Pfizer.
During an appearance at the globalist Washington D.C.-based think tank Atlantic Council, Pfizer CEO Albert Bourla blamed a “very small” group of people for circulating information that leads to people being vaccine hesitant.
“Those people are criminals,” he told Atlantic Council CEO Frederick Kempe. “They’re not bad people. They’re criminals because they have literally cost millions of lives.”
Bourla went on to suggest that life would only ever get “back to normal” once the unvaccinated have been vaccinated.
“The only thing that stands between the new way of life and the current way of life is, frankly, hesitancy to vaccinations,” he said.
The increasing shift towards demonizing people who question the safety and efficacy of vaccines as not just “conspiracy theorists,” but actual criminals who deserve prison time is accelerating.
FDA Knew About Numerous Adverse Events For Children ‘Related’ To Pfizer Vaccine, Approved It Anyway
The Food And Drug Administration (FDA) approved an emergency use authorization for the Pfizer-BioNTech vaccine for children as young as 5 years old despite the fact that its Pfizer-connected advisory committee knew about numerous adverse events that were reported in Pfizer’s clinical trials for children, including adverse events that were determined to be “related” to the clinical vaccine trial. The Briefing Packet for the FDA advisory committee meeting shows that the FDA advisers used clinical studies sponsored by BioNTech and conducted by or supported by Pfizer to approve the vaccine for young children. Talk about a conflict of interest! NATIONAL FILE reported on the FDA advisory committee’s massive Pfizer connections and how committee members have worked for Pfizer and are making money from the Pfizer vaccine. So what kind of adverse events were discovered in the clinical trials for children? The advisory committee meeting briefing packet, published by the FDA, shows that clinical trials found “related” illnesses including Lymphadenopathy, arthralgia, paresthesia, nervous tic, hematochezia (characterized by bloody stool, which sent the participant to the “emergency department”) pyrexia (fever), neutropenia (low white blood cell count), hypersensitivity reaction, angioedema, and rashes. Meanwhile, a case of the blood vessel disorder Henoch-Schoenlein purpura was reported but was conveniently classified as “non related” to the vaccine experiment.
Here is the “Vaccines and Related Biological Products Advisory Committee Meeting October 26, 2021 Briefing Document” published by the FDA. Page 15 lists an “OVERVIEW OF CLINICAL STUDIES.” Two clinical studies are listed. The first clinical study listed is “Phase 1/2/3 Registrational Study C4591001,” which was sponsored by BioNTech and conducted by Pfizer. The other clinical study listed is “Phase 1/2/3 Pediatric Study C4591007,” which is listed as being sponsored by BioNTech and supported by Pfizer. “Pediatric Study c4591007” is an ongoing study and it was used by the FDA for approval of the vaccine for ages 5 to 12. That’s right. The FDA meeting’s data was taken from an ongoing study conducted by the very makers of the vaccine. The information below comes from the FDA Briefing Packet’s review of Pfizer Pediatric Study C4591007.
British Medical Journal Publishes Damning Report Claiming Pfizer Faked Vaccine Data in Trials
Leading medical journal The BMJ has published an incendiary report exposing faked data, blind trial failures, poorly trained vaccinators, and a slow follow-up on adverse reactions in the phase-three trial of Pfizer’s Covid jab.
Central to the exposé is Brook Jackson, who, for two weeks, served as regional director at Ventavia Research Group, the company contracted to assist with the pivotal trial. She provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails supporting her concerns.
Jackson reveals that Ventavia staff who conducted quality-control checks were overwhelmed by the volume of problems they were identifying. She repeatedly informed her superiors of poor laboratory management, and patient safety and data integrity issues.
In a cited internal document from August 2020, shortly after the Pfizer trial began, a Ventavia executive identified three site staff members with whom to “go over e-diary issue/falsifying data, etc.” One employee was said to have been subsequently “verbally counseled for changing data” and “not noting late entry.”
Jackson reported her concerns to the US Food and Drug Administration (FDA), but was fired later the same day on the basis that she was “not a good fit.”
Disturbing Pfizer Ad Tells Kids They’ll Get Superpowers from COVID Jab
Pfizer was given the go-ahead this week from the CDC to give the experimental COVID vaccine to children.
Children have a greater chance of drowning, dying in a car wreck or dying from the flu than from the coronavirus.
Children are not forced to take the flu vaccine.
More children in Chicago have been shot this year than died from the coronavirus across the country.
But Pfizer sees a new market potential of one billion humans for their experimental product. And they’re going for it.
FDA Admits MORE Serious Adverse Effects From Pfizer Vaccine ‘May Become Apparent’ With Widespread Use
A Fact Sheet for Vaccine Providers published on the Food and Drug Administration (FDA) website admits that “Additional adverse reactions, some of which may be serious, may become apparent with more widespread use of the Pfizer-BioNTech COVID-19 Vaccine.” The Fact Sheet was issued in response to the FDA granting an emergency use authorization for the Pfizer vaccine for people aged 12 and older. The Fact Sheet also notes that the Pfizer vaccine carries risk of the heart conditions myocarditis and pericarditis in addition to numerous other ailments that have been reported in clinical trials, and that “immunocompromised persons…may have a diminished immune response to the Pfizer-BioNTech COVID-19 Vaccine.” Recent former FDA commissioner Scott Gottlieb (pictured above) is now on the board of directors of Pfizer. A contingent of recent Pfizer workers who serve on an FDA advisory committee are trying to get the FDA to authorize a Pfizer vaccine for children aged 5 to 11.
FDA Committee Members Reviewing Pfizer Vaccine For Children Have Worked For Pfizer, Have Big Pfizer Connections
The FDA’s Vaccines and Related Biological Products Advisory Committee is holding a virtual meeting Tuesday October 26 to discuss authorizing a Pfizer-BioNTech Coronavirus vaccine for children between the ages of 5 to 11 years old.
This committee has a lot of sway with the FDA and their findings will be relevant, considering the Biden administration is getting ready to ship vaccines to elementary schools and California has already mandated the vaccine for schoolchildren pending federal authorization.
But the meeting roster shows that numerous members of the committee and temporary voting members have worked for Pfizer or have major connections to Pfizer.
Members include a former vice president of Pfizer Vaccines, a recent Pfizer consultant, a recent Pfizer research grant recipient, a man who mentored a current top Pfizer vaccine executive, a man who runs a center that gives out Pfizer vaccines, the chair of a Pfizer data group, a guy who was proudly photographed taking a Pfizer vaccine, and numerous people who are already on the record supporting Coronavirus vaccines for children. Meanwhile, recent FDA Commissioner Scott Gottlieb is on Pfizer’s board of directors.
HERE’S THE MEETING ROSTER: Vaccines and Related Biological Products Advisory Committee October 26, 2021 Meeting Draft Roster.
Nothin’ to see here, folks…
Pfizer Scientist Flees After Being Caught On Tape Admitting COVID Antibodies Are Better Than Vaccines
Pfizer scientist Nick Karl, who privately admitted COVID antibodies are better than his company’s vaccine, was questioned by Project Veritas founder James O’Keefe while in public.
Nick Karl, who was not wearing a mask despite appearing to sit in a restaurant, was visibly surprised and upset when confronted by Project Veritas. He acknowledged his name, then became startled and refused to speak to O’Keefe as he abruptly rose and left the building.
Karl questioned, “I’m not doing this. Do not, absolutely not, what are you doing right now?” He then demanded to see video proving O’Keefe’s claims. When O’Keefe presented a tablet to view them, Karl fled the restaurant to his vehicle and drove away.
Karl, described by Project Veritas as an “experienced biochemist at Pfizer” with a history in pharmaceuticals, was caught in undercover video claiming that natural immunity provides a more robust antibody response to COVID-19 than the Pfizer vaccine.
“It’s just one antibody against one specific part of the virus,” said Karl while being recorded by a Project Veritas journalist. “When you actually get the virus, you’re going to start producing antibodies against like multiple pieces of virus.” Project Veritas also recorded two other Pfizer scientists who agree with this assessment.
Hellbound and Down 
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