cancer complicates everything, too. i have neither.
COVID-19 Boots on the ground reports, what is happening in your town?
- Thread starter shaggyballs
- Start date
So does disinformation.
Good luck with your illogical sampling of dabbling.
Doctor.
Good luck with your illogical sampling of dabbling.
Doctor.
disinformation from the FDA
Editor’s note: And there it is, Fauci admits that lockdowns are a great tool to forcibly “vaccinate” people. This is equivalent to NAZI level tyranny and now that he is affiliated with Georgetown University, what does it say about that University?
If you click to watch the video on Youtube, it has a message below the video, “From an accredited US medical school. Learn how experts define health sources in a journal of the National Academy of Medicine”. This message is to let you know that Fauci is a credible source. They also want you to know that anyone not agreeing with the Government or the World Health Organization is not credible.
For those who can still critically think, there is no proof anywhere throughout human history that those teaching students (who know very little) versus those practicing for years in the field have more credentials or are anymore of an “expert”. Many would argue the opposite is true.
In the case of Fauci, he is a doctor who has never practiced medicine. He has been a government bureaucrat his entire life. His track record of being wrong, not to mention decisions in favor of big Pharma at the expense of living human beings throughout his career coupled with his serious lack of medical experience should disqualify him as an “expert” under any reasonable definition.
Google/Youtube’s inability to see this flaw should also disqualify Google/Youtube from being a qualified arbiter of trustworthy information.
Those who can still critically think should see this clearly.
In New Interview, Fauci Defends Lockdowns and Forced Shots
By Jordan SchachtelRecently retired government bureaucrat Anthony Fauci just appeared at a university virtual event titled, “Pandemic Lessons and Role of Faculty in Pandemic Preparedness with Dr. Anthony Fauci.” During the conversation, Fauci, who is now affiliated with Georgetown University, made it clear that he still supports locking down society in the name of a virus, adding that lockdowns are a great tool to forcibly “vaccinate” people.
I’ll save you 40 minutes of your life and quote some of the “highlights” from the interview, in which a Wayne State University professor asks Fauci about what he’s learned from his time overseeing a “pandemic response.” The video of the chat is available via YouTube below:
Fauci falsely claimed that New York City was overrun and had “cooler trucks outside because they had no places to put the bodies.”
“You had to have something to immediately shut down the tsunami of infection,” he states, adding, “that lockdown was absolutely justified.”
“Lockdown has a purpose,” the pseudoscientist continued. “One of the purposes, if you don’t have a vaccine, it’s to get more ventilators, get the hospitals better prepared … until you decompress the pressure on the hospitals.
Fauci wasn’t done yet. Here comes the truly evil insanity…
“If you have a vaccine available, you might want to lock down temporarily so you can get everybody vaccinated,” he suggests.
Rejecting the idea that lockdowns are a moral question, he added that “lockdowns have a place, but they are not a permanent solution.”
The conversation continued, with the longtime NIAID chief declaring that “climate change” is “playing a role” in causing outbreaks.
He then calls for an “international commitment to decrease the carbon imprint in society so you don’t have the kinds of crazy weather we’re having in this country.”
Yes, that’s a real quote.
He went on to blame the tragedy in Maui on climate change. “It’s completely, really amazing what’s happened with climate change,” he concludes.
now, in your own words... "i swerve to smell the tooth, the toll booth, and nuts sing on the roof..." a "loose" interpretation of reality that you give there..."truly evil insanity" LOL! obvious why you are not on a news group anywhere in the world. maybe you should apply to work for The Chump? he loves babbling rhetoric like that...
Bullshit.
Doctors have always been able to prescribe it.
The amount of fear he is propagating is completely unfounded.
You guys just really enjoy being terrified of whatever you are handed to fear.
If someone needs quotation marks around vaccination and pandemic response then they probably have an agenda...
But no worries there... let's just focus on the propaganda instead.
COVID-19 mRNA Vaccines Reduce A Major Beneficial Bacteria, Gut Biodiversity: Research
Saturday, Oct 28, 2023 - 07:10 PM
Authored by Marina Zhang via The Epoch Times (emphasis ours),
Research has shown that COVID-19 mRNA vaccines reduce bacteria belonging to the Bifidobacteria genus, a common and beneficial gut bacteria. COVID vaccination is also linked to reduced gut biodiversity.
(Stjrw/Shutterstock)Works by gastroenterologist Dr. Sabine Hazan, the CEO of ProgenaBiome, a microbiome genomic research laboratory, found that after COVID-19 vaccination, people's Bifidobacteria levels can fall by as much as 90 percent. Some of her unpublished data found that Bifidobacteria levels are negligible in vaccinated people.
Bifidobacteria are among the first microbes to colonize a baby's gastrointestinal tract as he or she passes through the mother's birth canal. They are believed to exert positive health effects on their host.
Bifidobacteria interact with the immune system, and their presence is linked with improved immunity against pathogens and cancer.
Dr. Hazan's prior works on hospitalized COVID-19 patients showed that patients who had severe COVID-19 tended to have no or low Bifidobacteria levels, whereas those with higher stores of Bifidobacteria tended to develop asymptomatic infection.
In her research, she came across a pair of siblings enrolled in the COVID-19 vaccine clinical trials.
"One sibling got placebo, and one got the vaccine. The one sibling that got the vaccine got harmed ... and she has no Bifidobacteria bacteria. Her brother, who got the placebo and was not harmed, has this Bifidobacteria," she told The Epoch Times.
The Importance of Bifidobacteria
The loss of Bifidobacteria was discovered by comparing microbiome diversity both before and after vaccination. Generally, the loss is transient, while it can persist for over nine months in more extreme cases.There are also rare cases where patients' Bifidobacteria population increases. Dr. Hazan spoke about a patient's Bifidobacteria population more than doubling a month after vaccination. However, at six to nine months postvaccination, the patient's number of Bifidobacteria had fallen to zero.
Dr. Hazan said it is unknown why some people's Bifidobacteria levels rise after vaccination.
Bifidobacteria are a common probiotic, and it is well-established that humans can consume them to improve gut health. In fact, products containing Bifidobacteria make up trillions of dollars in the market share of the probiotic market.
The absence of Bifidobacteria microbes is linked to chronic diseases, including diabetes, cancer, and autoimmune diseases. Some studies have shown that the administration of probiotic Bifidobacteria can help improve diabetic conditions and help fight cancer.
Loss of Other Microbes After Vaccination
Some patients may have other microbiomes missing after vaccination, and trying to track down what microbes the patient might have had before vaccination involves difficult forensics work, according to Dr. Hazan.One study by researchers from Hong Kong found that mRNA COVID-19 vaccine administration was directly linked to reduced gut biodiversity, resulting in a loss of at least 10 different microbes.
While some vaccinated people saw an increase in certain bacteria, vaccination reduced overall microbiome diversity.
The authors also noted that the risks of common adverse reactions like fever, headaches, pain at injection sites, and so on may also be linked to the bacteria in the gut. For example, patients with high Bifidobacteria tended to be less inclined to develop vaccine adverse reactions.
A gut microbiome with low biodiversity is associated with poor health and aging. After birth, babies develop a highly diverse gut microbiome. As they age, they lose this diversity as they develop diseases, take antibiotics and drugs, eat unhealthily, sleep less, etc.
Bifidobacteria can comprise up to 95 percent of the baby's gut microbiome during infancy. This then declines and stabilizes at under 10 percent in adulthood.
Yet Dr. Hazan has seen cases of babies breastfed by vaccinated mothers possessing no Bifidobacteria. The long-term consequences of this are unknown, especially since Bifidobacteria are involved in building a person's immune system.
The increasing awareness of the importance of the gut microbiome in health has led some parents to freeze their baby's first stool for fecal transplant in the future, internal physician Dr. Yusuf Saleeby told The Epoch Times. As the baby grows and his or her microbiome depletes, the fecal sample may be transplanted to correct the gut microbiome composition.
"If the child gets sick and there's dysbiosis, the parents can go back to the company ... and reinoculate those microbes back into the baby, to try to bring back what the baby should have had," he explained.
So do plenty of food and beverages.
Antibiotics are also quite effective at wiping out bifidobacteria.
Fear factory check there cowboy.
Antibiotics are also quite effective at wiping out bifidobacteria.
Fear factory check there cowboy.
if i eat tidepods would it remove the stain of the yellow condiment?
I wouldn't try it.
But considering that you swallow the bullshit that you do, you might well do just that.
But considering that you swallow the bullshit that you do, you might well do just that.
i imagine you swallowing something else
0 209 7 minutes read
Of course! This is what we have been saying all along and now there is even more documentation out showing that the fascists in our government were well aware of the dangers of the COVID shot, mainly in the form of damaging the hearts of the People.
Children’s Health Defense reports:
The White House and the Centers for Disease Control and Prevention (CDC) knew in April 2021 that the Pfizer COVID-19 mRNA vaccine was linked to heart damage on an unprecedented scale for a vaccine — but they hid that knowledge from the public while pushing vaccine mandates, according to emails obtained by DailyClout through a Freedom of Information Act (FOIA) request.
The emails show the White House communications team struggling to craft a cover-up message on email chains that included Dr. Anthony Fauci, then-director of the National Institute of Allergy and Infectious Diseases (NIAID) and chief medical advisor to President Biden; CDC Director Rochelle Walensky; Dr. Janet Woodcock, then-acting commissioner of the U.S. Food and Drug Administration (FDA), U.S. Surgeon General Vivek Murthy and Dr. Francis Collins, then-director the National Institutes of Health (NIH).
A number of high-level public health officials worked with upper-echelon leadership to craft a “Myocarditis Email” that minimized the relationship between COVID-19 mRNA vaccines and myocarditis,” said Amy Kelly, program director for the War Room/DailyClout Pfizer Documents Analysis Project.
According to Kelly, the officials included: Ian Sams, COVID-19 response and special assistant to the president and senior advisor and spokesman for the White House; Abbigail Tumpey, then-associate director for communication science for the CDC’s Public Health Infrastructure; and Dr. Dana Meaney-Delman, CDC lead on maternal immunization and CDC chief of Infant Outcomes Monitoring Research and Prevention Branch.
The FOIA emails were obtained by Edward Berkovich, one of 250 volunteer attorneys Kelly oversees on the DailyClout and War Room Project to analyze the court-ordered, FDA-released 450,000 pages of Pfizer’s records on its mRNA COVID-19 vaccine — records the drug maker tried unsuccessfully to keep private for 75 years.
The War Room-DailyClout Project was founded by bestselling author and journalist Naomi Wolf, a former advisor to the Clinton campaign, in collaboration with Steve Bannon, former advisor to President Trump and podcaster on “The War Room.”
In addition to volunteer attorneys, Kelly oversees approximately 3250 volunteer doctors, nurses, scientists and others who are reviewing the documents. They’ve issued 89 investigative reports, including the Oct. 18 report on the myocarditis cover-up evident in FOIA emails.
“Astonishingly, the emails reveal that the most senior of leaders, all the way up to the White House, knew about heart damage linked to mRNA vaccines,” Kelly said. “Yet they “colluded behind the scenes to conceal this side effect from the American people.”
Anyone can study the three FOIA releases of emails at dailyclout.io, Kelly said.
“What I think most important is to see who all is involved,” she said. “I believe 105 different people are on the emails, a whole slew of people at the White House, CDC, U.S. Department of Health and Human Services, NIAID, Pfizer, some children’s hospitals and organizations and some other external people,” Kelly said.
“My takeaway from seeing this is that everyone, all over the public health agencies, knew there was an issue” with myocarditis dangers linked to the COVID-19 vaccines, Kelly said. Yet “when you read through the emails, you see they are crafting messages to downplay the significance of myocarditis and the vaccines, all the the way up to the White House.”
Emails show the Israeli Ministry of Health tried to alert the CDC in late February 2021 to the problem, Kelly said.
“They said, ‘We’re seeing a myocarditis signal and we’re happy to share information with you,’” she said. “The CDC actually didn’t even respond to the first email as far as I can tell. So the Israeli Ministry of Health emailed again March 2, ‘Hey we’re seeing this myocarditis signal, we’re concerned, let’s discuss it if you want.’”
White House created 17-page script to ‘keep everyone on message’
The FOIA email trove was a frequent topic of discussion Saturday at the “Summit for Truth,” which brought together leaders of the health freedom movement at the Bethel Christian Fellowship church and community center in downtown Rochester, New York.
Wolf was the keynote speaker in a lineup that included Dr. Robert Malone, Dr. Ryan Cole, attorney Bobbie Ann Cox, and Brownstone Institute publisher and writer Jeffrey Tucker.
Wolf spoke about her journey from feminist icon to outcast from the liberal media establishment when she questioned the safety of the COVID-19 shots.
She has written two books on her experience investigating and reporting on the pandemic. They include, “The Bodies of Others: The New Authoritarians, COVID-19 and the War Against the Human,” and the forthcoming “Facing the Beast: Courage, Faith, and Resistance in a New Dark Age.”
During a panel discussion Saturday, Wolf called the White House involvement in a cover-up of vaccine dangers “absolutely shocking.”
Berkovich’s FOIA request was aided by “a whistleblower at the CDC,” Wolf said, who was “throwing the White House under the bus.”
"In addition to the pages he had asked for, he got 46 pages he didn’t request that showed the White House communications team was “freaking out at the highest levels in April of 2021, because news of blood clots and heart damage had reached them,” Wolf said.
“Instead of coming clean with the American people and pulling this injection off the market, they looped in Dr. Fauci, Dr. Collins, Dr. Walensky and created a script,” she said.
It was “a 17-page script, their word, which is wholly redacted, to keep everyone on message and downplay the dangers. And in fact if you recall from 2021, rather than pulling this injection off the market, they mandated it. They doubled down and mandated it.”
Wolf said the emails reveal “a massive crime.”
They show a template was prepared to email to “POTUS, which stands for president of the United States,” to keep the president up to date on the email discussions among the top U.S. public-health officials on myocarditis and vaccines, Wolf said.
“Dr. Wallensky was on the emails, Dr. Fauci, Dr. Collins,” she said. “The entire White House communications team was driving the discussion.”
“They were reacting to the fact that blood clots and heart damage had been presented to them at scale and that the American Association of Pediatrics was warning them about myocarditis in teens, a serious, sometimes fatal disease that needs constant management. Instead of coming clean with the American people…they doubled down and made a strategy to cover it up.”
Public-health officials went ahead with mandates for the Pizer COVID-19 vaccine, “knowing it was killing people,” Wolf said.
Dr. Peter McCullough, one of the most highly published cardiologists in the world, said the Pfizer COVID-19 vaccines should have been pulled from the market in January 2021, after “no more than 50 deaths” — the previous government standard to guarantee the safety of a biologic product.
McCullough said FDA records show the agency expected a myocarditis risk from the mRNA COVID-19 vaccines as early as Oct. 22, 2020.
Nearly two months later, Pfizer “covered up 38 additional deaths” linked to their vaccine before the Dec. 10, 2020 meeting of the FDA Vaccines and Related Biological Products Advisory Committee.
“If they had reported these deaths, there would have been a three- to four-fold excess cardiovascular risk with Pfizer in the core slides at the Dec. 10, 2020 meeting and Pfizer would never have been approved,” he said.
McCullough said the myocarditis cover-up has killed untold thousands of Americans.
He pointed to his research paper with other scientists including Dr. William Makis. They performed a systematic review of “all published autopsy reports involving COVID-19 vaccination-related myocarditis” through July 3, 2023.
The paper concluded “there is a high likelihood of a causal link between COVID-19 vaccines and death from suspected myocarditis in cases where sudden, unexpected death has occurred in a vaccinated person.”
McCullough and colleagues concluded that “urgent investigation is required for the purpose of risk stratification and mitigation in order to reduce the population occurrence of fatal COVID-19 vaccine-induced myocarditis.”
Dr. Bruce Boros, a Key West, Florida cardiologist who was one of the first American physicians to use ivermectin for early COVID-19 treatment based on his research of the emerging literature, said recent studies show that the RNA from the COVID-19 vaccines “goes right to the heart.”
A study that applied the Moderna and Pfizer vaccine to heart muscle cells in culture “showed direct evidence that within 48 hours there was heart dysfunction, mechanical and electrical chaos,” Boros said.
Young athletes dropping dead from heart failure at unprecedented rates are “almost assuredly suffering” myocarditis symptoms brought on by the shots, he said.
“Everybody who received the shot had some damage to the heart muscle,” Boros said. “They knew it in the preclinical studies and they covered it up. All the signals were there, the FDA went ahead and approved it anyway.
“It’s all a money game, a eugenics game, and they’re continuing to say you need to get a booster,” Boros said. “Now every child in the world should get this shot for a virus that has been falsely normalized as dangerous when the risk, especially for children, is essentially zero when it comes to death,” he said.
“It saddens me,” Boros concluded. “We need to remember this was created as a bioweapon, and hold our government accountable.”
Cross-posted with Sons of Liberty Media
Related:
FOIA Emails Reveal White House Covered Up COVID-19 Vaccine Heart Damage
Tim Brown October 28, 20230 209 7 minutes read
Of course! This is what we have been saying all along and now there is even more documentation out showing that the fascists in our government were well aware of the dangers of the COVID shot, mainly in the form of damaging the hearts of the People.
Children’s Health Defense reports:
The White House and the Centers for Disease Control and Prevention (CDC) knew in April 2021 that the Pfizer COVID-19 mRNA vaccine was linked to heart damage on an unprecedented scale for a vaccine — but they hid that knowledge from the public while pushing vaccine mandates, according to emails obtained by DailyClout through a Freedom of Information Act (FOIA) request.
The emails show the White House communications team struggling to craft a cover-up message on email chains that included Dr. Anthony Fauci, then-director of the National Institute of Allergy and Infectious Diseases (NIAID) and chief medical advisor to President Biden; CDC Director Rochelle Walensky; Dr. Janet Woodcock, then-acting commissioner of the U.S. Food and Drug Administration (FDA), U.S. Surgeon General Vivek Murthy and Dr. Francis Collins, then-director the National Institutes of Health (NIH).
A number of high-level public health officials worked with upper-echelon leadership to craft a “Myocarditis Email” that minimized the relationship between COVID-19 mRNA vaccines and myocarditis,” said Amy Kelly, program director for the War Room/DailyClout Pfizer Documents Analysis Project.
According to Kelly, the officials included: Ian Sams, COVID-19 response and special assistant to the president and senior advisor and spokesman for the White House; Abbigail Tumpey, then-associate director for communication science for the CDC’s Public Health Infrastructure; and Dr. Dana Meaney-Delman, CDC lead on maternal immunization and CDC chief of Infant Outcomes Monitoring Research and Prevention Branch.
The FOIA emails were obtained by Edward Berkovich, one of 250 volunteer attorneys Kelly oversees on the DailyClout and War Room Project to analyze the court-ordered, FDA-released 450,000 pages of Pfizer’s records on its mRNA COVID-19 vaccine — records the drug maker tried unsuccessfully to keep private for 75 years.
The War Room-DailyClout Project was founded by bestselling author and journalist Naomi Wolf, a former advisor to the Clinton campaign, in collaboration with Steve Bannon, former advisor to President Trump and podcaster on “The War Room.”
In addition to volunteer attorneys, Kelly oversees approximately 3250 volunteer doctors, nurses, scientists and others who are reviewing the documents. They’ve issued 89 investigative reports, including the Oct. 18 report on the myocarditis cover-up evident in FOIA emails.
“Astonishingly, the emails reveal that the most senior of leaders, all the way up to the White House, knew about heart damage linked to mRNA vaccines,” Kelly said. “Yet they “colluded behind the scenes to conceal this side effect from the American people.”
Anyone can study the three FOIA releases of emails at dailyclout.io, Kelly said.
“What I think most important is to see who all is involved,” she said. “I believe 105 different people are on the emails, a whole slew of people at the White House, CDC, U.S. Department of Health and Human Services, NIAID, Pfizer, some children’s hospitals and organizations and some other external people,” Kelly said.
“My takeaway from seeing this is that everyone, all over the public health agencies, knew there was an issue” with myocarditis dangers linked to the COVID-19 vaccines, Kelly said. Yet “when you read through the emails, you see they are crafting messages to downplay the significance of myocarditis and the vaccines, all the the way up to the White House.”
Emails show the Israeli Ministry of Health tried to alert the CDC in late February 2021 to the problem, Kelly said.
“They said, ‘We’re seeing a myocarditis signal and we’re happy to share information with you,’” she said. “The CDC actually didn’t even respond to the first email as far as I can tell. So the Israeli Ministry of Health emailed again March 2, ‘Hey we’re seeing this myocarditis signal, we’re concerned, let’s discuss it if you want.’”
White House created 17-page script to ‘keep everyone on message’
The FOIA email trove was a frequent topic of discussion Saturday at the “Summit for Truth,” which brought together leaders of the health freedom movement at the Bethel Christian Fellowship church and community center in downtown Rochester, New York.
Wolf was the keynote speaker in a lineup that included Dr. Robert Malone, Dr. Ryan Cole, attorney Bobbie Ann Cox, and Brownstone Institute publisher and writer Jeffrey Tucker.
Wolf spoke about her journey from feminist icon to outcast from the liberal media establishment when she questioned the safety of the COVID-19 shots.
She has written two books on her experience investigating and reporting on the pandemic. They include, “The Bodies of Others: The New Authoritarians, COVID-19 and the War Against the Human,” and the forthcoming “Facing the Beast: Courage, Faith, and Resistance in a New Dark Age.”
During a panel discussion Saturday, Wolf called the White House involvement in a cover-up of vaccine dangers “absolutely shocking.”
Berkovich’s FOIA request was aided by “a whistleblower at the CDC,” Wolf said, who was “throwing the White House under the bus.”
"In addition to the pages he had asked for, he got 46 pages he didn’t request that showed the White House communications team was “freaking out at the highest levels in April of 2021, because news of blood clots and heart damage had reached them,” Wolf said.
“Instead of coming clean with the American people and pulling this injection off the market, they looped in Dr. Fauci, Dr. Collins, Dr. Walensky and created a script,” she said.
It was “a 17-page script, their word, which is wholly redacted, to keep everyone on message and downplay the dangers. And in fact if you recall from 2021, rather than pulling this injection off the market, they mandated it. They doubled down and mandated it.”
Wolf said the emails reveal “a massive crime.”
They show a template was prepared to email to “POTUS, which stands for president of the United States,” to keep the president up to date on the email discussions among the top U.S. public-health officials on myocarditis and vaccines, Wolf said.
“Dr. Wallensky was on the emails, Dr. Fauci, Dr. Collins,” she said. “The entire White House communications team was driving the discussion.”
“They were reacting to the fact that blood clots and heart damage had been presented to them at scale and that the American Association of Pediatrics was warning them about myocarditis in teens, a serious, sometimes fatal disease that needs constant management. Instead of coming clean with the American people…they doubled down and made a strategy to cover it up.”
Public-health officials went ahead with mandates for the Pizer COVID-19 vaccine, “knowing it was killing people,” Wolf said.
Dr. Peter McCullough, one of the most highly published cardiologists in the world, said the Pfizer COVID-19 vaccines should have been pulled from the market in January 2021, after “no more than 50 deaths” — the previous government standard to guarantee the safety of a biologic product.
McCullough said FDA records show the agency expected a myocarditis risk from the mRNA COVID-19 vaccines as early as Oct. 22, 2020.
Nearly two months later, Pfizer “covered up 38 additional deaths” linked to their vaccine before the Dec. 10, 2020 meeting of the FDA Vaccines and Related Biological Products Advisory Committee.
“If they had reported these deaths, there would have been a three- to four-fold excess cardiovascular risk with Pfizer in the core slides at the Dec. 10, 2020 meeting and Pfizer would never have been approved,” he said.
McCullough said the myocarditis cover-up has killed untold thousands of Americans.
He pointed to his research paper with other scientists including Dr. William Makis. They performed a systematic review of “all published autopsy reports involving COVID-19 vaccination-related myocarditis” through July 3, 2023.
The paper concluded “there is a high likelihood of a causal link between COVID-19 vaccines and death from suspected myocarditis in cases where sudden, unexpected death has occurred in a vaccinated person.”
McCullough and colleagues concluded that “urgent investigation is required for the purpose of risk stratification and mitigation in order to reduce the population occurrence of fatal COVID-19 vaccine-induced myocarditis.”
Dr. Bruce Boros, a Key West, Florida cardiologist who was one of the first American physicians to use ivermectin for early COVID-19 treatment based on his research of the emerging literature, said recent studies show that the RNA from the COVID-19 vaccines “goes right to the heart.”
A study that applied the Moderna and Pfizer vaccine to heart muscle cells in culture “showed direct evidence that within 48 hours there was heart dysfunction, mechanical and electrical chaos,” Boros said.
Young athletes dropping dead from heart failure at unprecedented rates are “almost assuredly suffering” myocarditis symptoms brought on by the shots, he said.
“Everybody who received the shot had some damage to the heart muscle,” Boros said. “They knew it in the preclinical studies and they covered it up. All the signals were there, the FDA went ahead and approved it anyway.
“It’s all a money game, a eugenics game, and they’re continuing to say you need to get a booster,” Boros said. “Now every child in the world should get this shot for a virus that has been falsely normalized as dangerous when the risk, especially for children, is essentially zero when it comes to death,” he said.
“It saddens me,” Boros concluded. “We need to remember this was created as a bioweapon, and hold our government accountable.”
Cross-posted with Sons of Liberty Media
Related:
- Cardiologist: Over 7M Americans May Have Some Form Of HEART INJURY Due To COVID-19 Vaccines (Video)
- COVID Jabs Did NOT Save Millions Of Lives: “Highly Improbable,” Says New Study
- Died suddenly: 8-year-old boy used in Covid vax promotional ad
- COVID Shots Tied To 17 MILLION ‘Vaccine Deaths’
- Immunology Expert Warns mRNA Shots For COVID Must Be ‘Banned’
Oh look, we get more of the same.
Keep banging the drum.
No one is listening anymore.
Keep banging the drum.
No one is listening anymore.
then quit replying to something you don't read or listen to. wanker.
10/27/23
According to an analysis, published this month in the International Journal of Vaccine Theory, Practice, and Research, of Pfizer-BioNTech COVID-19 vaccine clinical trial data, the vaccine makers hid fatality data from regulators in order to qualify for Emergency Use Authorization.
By
Angelo DePalma, Ph.D.
Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product.
The vaccine makers also failed to account for a large number of subjects who dropped out of the trial.
Together, these strategies kept regulators and the public ignorant of a 3.7-fold increase in cardiac deaths among subjects who received the vaccine, according to analysis in the International Journal of Vaccine Theory, Practice, and Research.
The authors of the paper described it as a “forensic analysis,” defined by the U.S. National Institute for Standards and Technology as “the use of scientific methods or expertise to investigate crimes or examine evidence that might be presented in a court of law.”
What the analysis shows
Corinne Michels, Ph.D., retired distinguished professor of biology at Queens College, New York, led the DailyClout Pfizer/BioNTech Documents Investigations Team on what the authors claim was the first independent examination of original data from the Pfizer-BioNTech COVID-19 mRNA vaccine (BNT162b2) clinical trial.
Investigators looked at each of the 38 deaths occurring between July 27, 2020, the start of phase 2/3 of the Pfizer-BioNTech vaccine trial, and March 13, 2020, the end date culminating in Pfizer-BioNTech’s 6-month interim report.
This trial phase involved 44,060 subjects. Half received a dose of BNT162b2, half got a placebo consisting of an inactive sterile salt solution.
The trial was unusual because at week 20 after the FDA issued the EUA for the vaccine, trial subjects in the placebo group were allowed to switch to the vaccinated group and receive their first BNT162b2 shot.
https://www.amazon.com/Vax-Unvax-Childrens-Health-Defense-Kennedy/dp/1510766960/
Switching from the placebo to the vaccinated group — or “unblinding” — normally occurs when the benefit of the drug is so great that not treating subjects becomes unethical. For example, investigators might consider unblinding a cancer trial if at some point all untreated patients deteriorated or died but all treated patients improved.
Unblinding conditions may be specified in the study design, but they usually involve input or review from medical ethicists.
Of 20,794 unblinded placebo subjects in the Pfizer trial, 19,685 received at least one dose of BNT162b2.
Normally the decision to unblind a vaccine trial would be based on the product’s safety and effectiveness in reaching certain endpoints or objectives. Endpoints for a drug to prevent viral infections might be a positive test or self-reported COVID-19 illness (the “case” numbers that drove much of COVID-19 policy), illness requiring hospitalization or death.
But, perhaps unexpectedly, after 33 weeks the data revealed no significant difference between deaths in the vaccinated and placebo groups for the initial 20-week placebo-controlled portion of the trial.
After week 20, after most former placebo subjects had received the vaccine, deaths among those in the vaccine group continued unabated.
The authors revealed “inconsistencies” between data presented in Pfizer-BioNTech’s 6-month interim report and subsequent publications by Pfizer-BioNTech trial site administrators:
“Most importantly, we found evidence of an over 3.7-fold increase in the number of deaths due to cardiac events in the BNT162b2 vaccinated individuals compared to those who received only the placebo.”
This means that 79% of relevant deaths were not recorded in time to be included in Pfizer’s regulatory paperwork.
By not including relevant subject deaths in the case report, Pfizer obscured cardiac adverse event signals, allowing the EUA to proceed unchallenged.
How did Pfizer get around legal, ethical obligations?
The Pfizer-BioNTech data, obtained through a Freedom of Information Act lawsuit, uncovered four additional deaths in the vaccine group and one more in the placebo group — but Pfizer failed to include these data in their FDA submission despite an explicit study design requirement to do so.
These data, and how they differ from what Pfizer-BioNTech reported in their applications, are summarized in Table 3 of Michels’ study.
One case involved a 63-year-old woman who died 41 days after receiving the shot, but whose death only entered the data pool 37 days later. Another was a 58-year-old woman whose death 72 days after vaccination went unreported for 26 days.
Had Pfizer-BioNTech met their legal and ethical obligation to report all serious adverse events their data would have shown equal deaths in placebo and vaccine groups — which would have shown no clear benefit for the vaccine.
How were they able to skirt those obligations?
For one, they were able to hide behind the the 2005 Public Readiness and Emergency Preparedness (PREP) Act, which provided an almost impenetrable liability shield for vaccine manufacturers for “medical countermeasures” in response to any “public health emergency.”
Second, because COVID-19 was viewed as a national health emergency, regulators abandoned the established, patient-centered, safety-based approval process requiring years of preclinical animal testing — and Pfizer-BioNTech unsurprisingly went along.
Timing of death reports raises questions
Michels also raised issues regarding total death reports and their timing.
Since the death total from both study groups, 38, appeared “surprisingly low” to study authors — particularly during a pandemic — they undertook their own analysis based on population mortality expectations at the time.
Assuming that age-adjusted death rates for the study subjects were similar to those of the general population, they estimated that 222 subjects should have died from July 27, 2020, to March 13, 2021. The reported number, 38, is just 18% of the expected number.
Michels explained this by the large number, 4.2% of “discontinued subjects.” The most concerning of these were subjects “lost to follow-up,” which means missing scheduled visits or other required activities.
Pfizer-BioNTech tried to reach these subjects via phone, certified mail or through their emergency contact but despite their efforts could not account for 395 subjects who had dropped out.
The authors wrote:
“These are not insignificant numbers and could easily account for the low number of deaths reported in this safety period of the trial. Given the importance of knowing the status of each trial subject, there should have been greater effort to locate these individuals.
“Additionally, Pfizer/BioNTech was responsible for oversight of the trial sites. Sites with excessive numbers of lost to follow-up should have been evaluated for performance.”
Michels was also concerned over how certain trial centers had many dropped-out subjects while others had none or just a few.
Ninety-six of 153 trial sites (63%) reported 0 or 1 subjects lost to follow-up and 34 (22%) reported 2-5 dropouts. But four sites reported more than 20 subjects lost to follow-up, amounting to about 5% of all trial subjects.
Since the vaccine makers were responsible for trial site oversight, the authors wrote, “Sites with excessive numbers of lost to follow-up should have been evaluated for performance.”
Finally, based on the data, it appears Pfizer-BioNTech was in no hurry to enter death reports before the EUA submission deadline, particularly for the BNT162b2 group.
Of the 38 reported deaths only one case was added on the day the subject died. Delays of 20+ and 30+ days were common.
One death took 72 days to find its way into the database, and all were entered as occurring on the reporting day, not on the actual date of death.
Of the eight subjects in the vaccine group that should have been reported by Dec. 10, 2020, the EUA application cutoff, the average reporting delay was 17.5 days for subjects in the vaccine group, but just 5.9 days for deaths among subjects in the placebo group.
childrenshealthdefense.org
10/27/23
How Pfizer Hid Nearly 80% of COVID Vaccine Trial Deaths From Regulators
According to an analysis, published this month in the International Journal of Vaccine Theory, Practice, and Research, of Pfizer-BioNTech COVID-19 vaccine clinical trial data, the vaccine makers hid fatality data from regulators in order to qualify for Emergency Use Authorization.
By
Angelo DePalma, Ph.D.
Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product.
The vaccine makers also failed to account for a large number of subjects who dropped out of the trial.
Together, these strategies kept regulators and the public ignorant of a 3.7-fold increase in cardiac deaths among subjects who received the vaccine, according to analysis in the International Journal of Vaccine Theory, Practice, and Research.
The authors of the paper described it as a “forensic analysis,” defined by the U.S. National Institute for Standards and Technology as “the use of scientific methods or expertise to investigate crimes or examine evidence that might be presented in a court of law.”
What the analysis shows
Corinne Michels, Ph.D., retired distinguished professor of biology at Queens College, New York, led the DailyClout Pfizer/BioNTech Documents Investigations Team on what the authors claim was the first independent examination of original data from the Pfizer-BioNTech COVID-19 mRNA vaccine (BNT162b2) clinical trial.
Investigators looked at each of the 38 deaths occurring between July 27, 2020, the start of phase 2/3 of the Pfizer-BioNTech vaccine trial, and March 13, 2020, the end date culminating in Pfizer-BioNTech’s 6-month interim report.
This trial phase involved 44,060 subjects. Half received a dose of BNT162b2, half got a placebo consisting of an inactive sterile salt solution.
The trial was unusual because at week 20 after the FDA issued the EUA for the vaccine, trial subjects in the placebo group were allowed to switch to the vaccinated group and receive their first BNT162b2 shot.
https://www.amazon.com/Vax-Unvax-Childrens-Health-Defense-Kennedy/dp/1510766960/
Switching from the placebo to the vaccinated group — or “unblinding” — normally occurs when the benefit of the drug is so great that not treating subjects becomes unethical. For example, investigators might consider unblinding a cancer trial if at some point all untreated patients deteriorated or died but all treated patients improved.
Unblinding conditions may be specified in the study design, but they usually involve input or review from medical ethicists.
Of 20,794 unblinded placebo subjects in the Pfizer trial, 19,685 received at least one dose of BNT162b2.
Normally the decision to unblind a vaccine trial would be based on the product’s safety and effectiveness in reaching certain endpoints or objectives. Endpoints for a drug to prevent viral infections might be a positive test or self-reported COVID-19 illness (the “case” numbers that drove much of COVID-19 policy), illness requiring hospitalization or death.
But, perhaps unexpectedly, after 33 weeks the data revealed no significant difference between deaths in the vaccinated and placebo groups for the initial 20-week placebo-controlled portion of the trial.
After week 20, after most former placebo subjects had received the vaccine, deaths among those in the vaccine group continued unabated.
The authors revealed “inconsistencies” between data presented in Pfizer-BioNTech’s 6-month interim report and subsequent publications by Pfizer-BioNTech trial site administrators:
“Most importantly, we found evidence of an over 3.7-fold increase in the number of deaths due to cardiac events in the BNT162b2 vaccinated individuals compared to those who received only the placebo.”
This means that 79% of relevant deaths were not recorded in time to be included in Pfizer’s regulatory paperwork.
By not including relevant subject deaths in the case report, Pfizer obscured cardiac adverse event signals, allowing the EUA to proceed unchallenged.
How did Pfizer get around legal, ethical obligations?
The Pfizer-BioNTech data, obtained through a Freedom of Information Act lawsuit, uncovered four additional deaths in the vaccine group and one more in the placebo group — but Pfizer failed to include these data in their FDA submission despite an explicit study design requirement to do so.
These data, and how they differ from what Pfizer-BioNTech reported in their applications, are summarized in Table 3 of Michels’ study.
One case involved a 63-year-old woman who died 41 days after receiving the shot, but whose death only entered the data pool 37 days later. Another was a 58-year-old woman whose death 72 days after vaccination went unreported for 26 days.
Had Pfizer-BioNTech met their legal and ethical obligation to report all serious adverse events their data would have shown equal deaths in placebo and vaccine groups — which would have shown no clear benefit for the vaccine.
How were they able to skirt those obligations?
For one, they were able to hide behind the the 2005 Public Readiness and Emergency Preparedness (PREP) Act, which provided an almost impenetrable liability shield for vaccine manufacturers for “medical countermeasures” in response to any “public health emergency.”
Second, because COVID-19 was viewed as a national health emergency, regulators abandoned the established, patient-centered, safety-based approval process requiring years of preclinical animal testing — and Pfizer-BioNTech unsurprisingly went along.
Timing of death reports raises questions
Michels also raised issues regarding total death reports and their timing.
Since the death total from both study groups, 38, appeared “surprisingly low” to study authors — particularly during a pandemic — they undertook their own analysis based on population mortality expectations at the time.
Assuming that age-adjusted death rates for the study subjects were similar to those of the general population, they estimated that 222 subjects should have died from July 27, 2020, to March 13, 2021. The reported number, 38, is just 18% of the expected number.
Michels explained this by the large number, 4.2% of “discontinued subjects.” The most concerning of these were subjects “lost to follow-up,” which means missing scheduled visits or other required activities.
Pfizer-BioNTech tried to reach these subjects via phone, certified mail or through their emergency contact but despite their efforts could not account for 395 subjects who had dropped out.
The authors wrote:
“These are not insignificant numbers and could easily account for the low number of deaths reported in this safety period of the trial. Given the importance of knowing the status of each trial subject, there should have been greater effort to locate these individuals.
“Additionally, Pfizer/BioNTech was responsible for oversight of the trial sites. Sites with excessive numbers of lost to follow-up should have been evaluated for performance.”
Michels was also concerned over how certain trial centers had many dropped-out subjects while others had none or just a few.
Ninety-six of 153 trial sites (63%) reported 0 or 1 subjects lost to follow-up and 34 (22%) reported 2-5 dropouts. But four sites reported more than 20 subjects lost to follow-up, amounting to about 5% of all trial subjects.
Since the vaccine makers were responsible for trial site oversight, the authors wrote, “Sites with excessive numbers of lost to follow-up should have been evaluated for performance.”
Finally, based on the data, it appears Pfizer-BioNTech was in no hurry to enter death reports before the EUA submission deadline, particularly for the BNT162b2 group.
Of the 38 reported deaths only one case was added on the day the subject died. Delays of 20+ and 30+ days were common.
One death took 72 days to find its way into the database, and all were entered as occurring on the reporting day, not on the actual date of death.
Of the eight subjects in the vaccine group that should have been reported by Dec. 10, 2020, the EUA application cutoff, the average reporting delay was 17.5 days for subjects in the vaccine group, but just 5.9 days for deaths among subjects in the placebo group.
How Pfizer Hid Nearly 80% of COVID Vaccine Trial Deaths From Regulators
According to an analysis, published this month in the International Journal of Vaccine Theory, Practice, and Research, of Pfizer-BioNTech COVID-19 vaccine clinical trial data, the vaccine makers hid fatality data from regulators in order to qualify for Emergency Use Authorization.
childrenshealthdefense.org
I read most of the stuff that you post.
Without my posts this entire thread would just be your copypasta.
I'd hate to leave an idiotic echo chamber unmonitored.
Without my posts this entire thread would just be your copypasta.
I'd hate to leave an idiotic echo chamber unmonitored.
well then you must have a comprehension deficit.
i'd be perfectly happy to continue on my own with no need of your involvement.
i'd be perfectly happy to continue on my own with no need of your involvement.
It's not that difficult to understand.
You want to spam copypasta and scare people while you attempt to justify your fear.
I don't think that is what is best for the average reader.
I have taken upon myself to season your spam with counterpoints and raze barely concealed conjecture that many might have taken as truth.
You want to spam copypasta and scare people while you attempt to justify your fear.
I don't think that is what is best for the average reader.
I have taken upon myself to season your spam with counterpoints and raze barely concealed conjecture that many might have taken as truth.
the morass of your moral terpitude is staggering. so again i would recommend buggering off.
