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Speaker 0 asked about a report and how concerning it is, questioning whether “10” is the real number. Speaker 1 said the main concern is that the report “dramatically understates the problem.” They argued that analyses rely on doctors and that it was difficult to obtain autopsies during the pandemic. Speaker 1 stated that medical professors did not want to know, resulting in very few autopsies. They said NIH, CDC, and FDA reviewed 96 autopsies of children and identified about 10 cases they considered possible or probable. Speaker 1 then pointed to VAERS, stating there are almost 1.7 million total adverse events and 39,000 deaths worldwide. They said that of the 39,000 deaths, 24% occurred on the day of vaccination or within one or two days. They acknowledged FDA officials say VAERS does not prove causation, but said that if someone was perfectly healthy and died on that day or within one or two days, they would assign blame. Speaker 1 also said there may be cases where people were already in bad health and vaccination “tipped them over,” with death ultimately caused by something else. Speaker 1’s “bigger revelation” was described as information they said was not covered by mainstream media. They stated that on 03/01/2021, Peter Marks, head of CBR within FDA, was briefed that their algorithm analyzing VAERS safety would hide and mask safety signals. Speaker 1 said that 26 days later, Marks ran a new algorithm that unmasked 49 cases of extreme masking and 25 safety signals, including sudden cardiac death, pulmonary infarction, Bell’s palsy, and different types of strokes. Speaker 1 said that in the next three months, similar data runs with the new algorithm showed more safety signals and more types of sudden death. They said the report described not “pin[ning] a badge” on doctor Anna Scharzman (identified as the dad of Speaker 1’s expert), ordering her to cease and desist, and continuing to use the algorithm the briefing warned would hide safety signals “to this day.” Speaker 1 said Peter Marks later went to work for Eli Lilly and claimed that the world is in denial. They stated they could not get the story broadcast or interviews on CBS, ABC, NBC, PBS, MS Now, or CNN, and said they challenged Jake Tapper, sending the report and requesting an additional appearance.

These ten deaths are the tip of the iceberg. There is a vast number of deaths in the peer reviewed literature. These have cases have already been vetted. We don't need FDA officials to comment to them on them. They're deeply concerning. And then our US CDC vaccine administration adverse event system, VAERS, has in total now, this is shocking for United States residents, nineteen thousand four hundred and eighty deaths. About two thousand of these have occurred right within forty eight hours of the shot, and then nineteen thousand two hundred seventy nine Americans reported to be permanently disabled. These are reported to VAERS by doctors like myself who have already determined the vaccine is the cause of the injury, disability, or death. Because if the vaccine was not the cause, then we wouldn't do the report to VAERS. So this is the VAERS does indicate causation by proxy of reporting. This is very important. The VAERS system, I'll say it again, indicates the vaccine is the cause of the problem because the doctor or the health care provider in the field at the scene who's examined the patient, examined the autopsy and the medical record information, examined the clinical record, the vaccine administration has determined the vaccine is the cause. Otherwise, a VAERS report would not be made. So this is very important. I would say at this point in time, both Macron and Prasad should immediately call for the COVID nineteen vaccines to be removed from the market. Every day they continue to delay on this, the more Americans will be hurt by boosters. We've already had several hundred deaths this year that have occurred on their watch. B, they should initiate a safety review of the 19480 deaths with an independent panel to review all the information. The CDC has the patients and their families' phone numbers, emails, addresses. There ought to be interviews of family members for the deceased, interviews of the patient themselves for injuries and disabilities to to get their side of the story. The CDC has all that information. The review should be done independently by people who are not CDC or FDA employees, And there should be multiple reviewers and should be an adjudication process and finally, a determination of causality for the vaccine. And then I would say, finally, the FDA officials, including Macari and Prasad, needs to start showing up to important proceedings in Washington. There have been multiple hearings on vaccine safety. One that I was the lead witness on, 05/21/2025. Yeah. We published a report indicating that there was a government cover up of COVID nineteen vaccine induced mild pericarditis, including fatal cases.

The speakers discuss a study of 325 autopsies of individuals who died shortly after receiving a COVID-19 vaccine. According to the speakers, this is the largest autopsy series of its kind. A rigorous review of the autopsies allegedly found that the vaccine caused or contributed to approximately 74% of the sudden deaths. This study is claimed to be a peer-reviewed paper that is going to be published. One speaker states that they are the senior author of this study. The speakers anticipate a "tsunami of evidence" regarding the harm caused by COVID-19 vaccines in children, pregnant women, and adults. They urge politicians to acknowledge and address this issue.

The speaker claims adverse events from the vaccine rollout were covered up and dismissed as rare and coincidental. They state that regulators approved the vaccines based on relative risk data (95%), which they describe as misleading, while the absolute risk reduction was only 0.84%, meaning 120 people had to be vaccinated to prevent one infection. The speaker alleges that Pfizer has 31 convictions, including withholding data, presenting false data, and bribing clinicians and regulators. They claim over 100 doctors have written to various health organizations, including the NHS and MHRA, about the vaccine program, but received only one response. The speaker concludes that science is dead because discussion, analysis, and debate are no longer allowed, and decisions are being made without scientific basis.

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus a month after rollout in November 2020. They allege Pfizer knew the third most common side effect was COVID. Within months, Pfizer supposedly needed to hire 2,400 staffers to process adverse event reports. The speaker asserts Pfizer and the FDA knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The speaker states the CDC initially claimed the injection materials stayed at the injection site, but Pfizer knew they biodistributed throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus one month after rollout in November 2020, and that "vaccine failure" was identified internally. They allege Pfizer knew they needed to hire 2,400 staffers to process adverse event reports shortly after rollout. The speaker further claims Pfizer knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but the government didn't inform parents of the elevated risk until August 2021. They state that contrary to CDC claims, the vaccine materials (lipid nanoparticles, mRNA, polyethylene glycol-coated industrial fat, and spike protein) do not stay in the injection site, but biodistribute throughout the body within 48 hours, accumulating in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries.

Insufficient measures were taken to ensure the safety of the vaccine, as important information regarding heart problems was withheld for a couple of years. The speaker mentions that they have previously discussed myocarditis for over two and a half years. A paper by Michels and colleagues revealed 38 deaths, which Pfizer did not disclose during the FDA meeting in December 2020. The deaths were not questioned by the committee or FDA, and had they been fully reported, there would have been a three to four times higher risk of cardiovascular death. With this data, it is unlikely that any FDA panel would have approved the vaccine.

The speaker discusses the underreporting of adverse events related to COVID-19 vaccines in the VAERS database, highlighting safety signals like myocarditis and death. They compare the number of deaths reported to VAERS to past incidents that prompted product removal, questioning why COVID-19 vaccines have not been halted. The speaker presents data showing a significant increase in adverse events with COVID-19 vaccines compared to other vaccines, particularly in younger age groups. They emphasize the need to follow standard procedures for analyzing safety signals and suggest that the CDC, HHS, and FDA are not properly addressing the issue.

Speaker 0 presented a chart and asserted that due to “radical transparency” they have access to close to 11,000,000 pages showing signals that were hidden in VAERS analyses. The speaker stated they uncovered that a signal on myocarditis was hidden, and they also recently uncovered a signal on ischemic stroke for people aged 65 and older in 2022–2023. They claimed both signals were downplayed, but that a hearing would be held next week and a draft report would be issued in conjunction with that hearing. The speaker alleged that Peter Marks was made aware on 03/26/2021 that the inventors of the algorithm analyzing VAERS data were going to mask adverse events, and that by using a different system they uncovered 49 examples of extreme masking, including 25 significant adverse events such as sudden cardiac death, Bell’s palsy, and pulmonary infarction. The speaker emphasized that this is not a matter requiring a sophisticated mathematical model to identify safety signals, stating that the chart shows deaths associated with vaccines dating back to 1990, with several hundred per year initially, and that in 2021 there were over twenty thousand deaths in a five-year span, contrasting with the FDA’s assertions that no signal exists. They characterized these as signals screaming that there has been a covering up to the present day. The speaker claimed that a number of individuals involved in the cover-up continue to work within HHS, the CDC, and the FDA. They requested a commitment that those people will be made available for interviews, and stated that they would subpoena others as needed to dig into the matter, announcing an intention to scrutinize the massive government apparatus and its handling of vaccine safety signals. The speaker concluded by reiterating their commitment to pursue interviews and investigations.

According to the speaker, Pfizer documents reveal that one month after the vaccine rollout in November 2020, Pfizer knew the vaccines didn't stop COVID and identified vaccine failure. Within months, the company allegedly needed to hire 2,400 staffers to process adverse event reports. The speaker claims Pfizer knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this information wasn't shared with parents until August 2021. The speaker alleges that the CDC initially stated the injection materials stayed in the injection site, but Pfizer knew these materials biodistribute throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. The speaker asserts that there is no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

In the Pfizer trial, more people died who received the vaccine than the placebo. The clinical trial showed one life could be saved from COVID for every 22,000 people vaccinated. However, more people died in the trial from the vaccine itself. While vaccines may have saved 10,000 lives in a year, at least 150,000 people have been killed by the vaccine, according to VAERS data. The speaker claims that 150,000 deaths is the cost of saving 10,000 lives, and that the risk benefit is even worse for kids, where 117 kids are killed to save one life. Doctors are allegedly not allowed to talk about deaths caused by the vaccine.

In the message described, Speaker 0 highlights a key claim: the CDC and FDA were fully aware of the masking phenomenon within their empirical Bayesian analysis. The speaker emphasizes that this awareness was part of the information being conveyed in a letter to Bobby Kennedy. The central issue raised is not about general safety signals, but about the timing of deaths relative to vaccination. The speaker notes a concern that began earlier, stating that back in October there were discussions with Mike Eden about these injections. The concern is tied to what was observed in the data, specifically that “early on in March and April” the data appeared to be "screaming at us" when looking at thousands of deaths. The speaker provides a concrete statistic: “forty six percent of those deaths were occurring on the day of vaccination than one or two days.” The speaker then updates the figure, saying that they are “up to almost thirty nine thousand deaths” in total, and adds that “Twenty four percent of those deaths occurred on the day of vaccination or within one or two days.” The speaker asserts that this information “has been available month by month by month since about March, April 2021,” yet alleges that “the federal officials are still not acknowledging it.” Instead of acknowledging these signals, the speaker claims officials point to other metrics, stating they “go to these, you know, PRR, the proportional reporting ratios, or a more sophisticated” approach. The claim continues that when PRRs were showing safety signals, officials reacted as if, “oh, we're not using those. We're using empirical Bayesian analysis. They set the trigger.” In summary, the transcript presents a narrative in which the CDC and FDA are described as being aware of a masking phenomenon identified through empirical Bayesian analysis, with specific, alarming timing data linking a significant proportion of deaths to the day of vaccination or the following couple of days. The speaker contends this information has been publicly accessible on a monthly basis since early 2021, but accuses federal officials of not acknowledging it and of favoring a different analytic framework (PRR) or of claiming to use empirical Bayesian analysis after the fact, implying that the trigger for safety signals was set within that framework. The overall emphasis is on the alleged discrepancy between available data and official acknowledgment, as well as the choice of analytic methods used to interpret safety signals.

The speaker discusses the vaccine's link to death and disability, citing over 37,000 deaths globally reported on VAERS. They criticize regulators for not addressing this issue earlier and mention a conversation with Francis Collins about vaccine-related deaths. The speaker also mentions a conversation with Dr. Redfield, who admitted downplaying vaccine injuries to avoid creating hesitancy. Dr. Redfield acknowledged that there are more injuries than reported.

A recent study suggests that Pfizer may have excluded known deaths in the vaccine arm of its clinical trial from its data filing with the FDA in 2020. The study also found that trial subjects vaccinated with Pfizer's COVID-19 vaccine experienced a significant increase in cardiovascular deaths compared to placebo controls. This information was not disclosed by Pfizer when the FDA was evaluating the vaccine for emergency use. Additionally, researchers identified instances where Pfizer attributed potential vaccine-associated deaths to other causes, undermining vaccine safety data. The data presented to the FDA prior to the authorization of Pfizer's vaccine did not include all the deaths that occurred during the trial. The speaker raises concerns about the prioritization of profit over lives and warns against trusting Big Pharma.

The speakers discuss a broad denial about vaccine injuries and the idea that, despite evidence, the medical establishment and political figures push the narrative that vaccines are safe and effective. They claim that many people who are vaccinated want to move on and avoid acknowledging serious side effects, including turbo cancers, undetected myocarditis, and neurological issues, and that autoimmune disease is being attributed to other causes. They argue that the medical establishment, federal health agencies, and some members of Congress who produce supportive content, such as segments like Steve Colbert’s, advocate for taking the shot. They question how many people were killed or died from the shot, asserting that Bayer’s data shows “close[ly]” to thirty-nine thousand worldwide, and that if only ten percent are reported, the true number would be in the hundreds of thousands. They claim there are millions of adverse events, but that this is denied and covered up. The speakers contend that the shot was not a real vaccine. They describe it as gene therapy rather than a traditional vaccine. They explain a sequence in which a vaccine is typically an attenuated or killed virus that requires adjuvants like aluminum or mercury to stimulate the immune system, because the attenuated or killed virus may not work well on its own. In contrast, they say this shot is mRNA, which is modified so it does not degrade. They describe how it is put into a lipid nanoparticle designed to permeate barriers like the blood-brain barrier, and they assert it would never stay in the arm, distributing all over the body. They claim the lipid nanoparticle allows the mRNA to enter cells, hijack cellular structures, and cause the cells to express spike protein, which the body then attacks as foreign. When asked who is responsible, they reference a “doctor Frankenstein” figure and name Francis Collins, head of the NIH, and Anthony Fauci as possible figures in question. The response indicates that while they consider all of them criminally liable, they would say it is primarily Fauci, with acknowledgment that people like Collins are implicated as well.

A study of 325 autopsies found that in 73.9% of cases, the vaccine was either the direct cause of death or significantly contributed to it. The deaths occurred within one to two weeks after the last shot. Over 50% of these deaths had a cardiovascular cause. According to the speaker, these findings contradict the official narrative from the CDC and FDA, which maintains that there is no evidence linking deaths to the vaccine, except for a few acknowledged cases after the Janssen vaccine. The speaker claims this research represents the largest series of autopsies indicating patients died from the vaccine, challenging the government's position.

The speaker claims that aligning deaths in the vaccine trial to intervention arms shows the vaccine was never life-saving. They allege that at the time of vaccine approval, there were more deaths in the vaccinated arm, but four deaths in the vaccinated arm within the data reporting period were not publicly announced. The speaker states that loved ones of two patients called the clinical site on the day of their death. They felt it was their ethical duty to inform the TGA and Ken Paxton about these hidden deaths. Publicly available data stated four deaths in the placebo arm and two in the vaccine arm. The speaker questions delays in reporting deaths, noting discrepancies in reporting rates between the vaccinated and placebo arms. The speaker wrote to Professor Tony Lawler of the TGA, who allegedly stated there were no hidden deaths and that no deaths in the vaccine arm were due to the vaccine. The speaker highlights that out of 38 total deaths in the six-month period (21 vaccinated, 17 placebo), only seven autopsies were done. Ten of the 21 deaths in the vaccinated arm were categorized as sudden adult death, with some individuals found dead shortly after vaccination.

Speaker 0 describes finding vaccine insert materials with no printed content and says this is disheartening and “disgusting,” then adds that it “gets better” and that “more” continues to happen. Speaker 0 claims the CDC redacted every word of a 148-page study on myocarditis after COVID vaccination, and that when they asked to have the study printed, the entire document was redacted. They question what the study could have contained that required redaction and say this is “even scarier.” Speaker 1 says they are witnessing “an active cover up” of a “colossal consumer product safety debacle” affecting the entire world. They claim that in the United States the CDC, National Institutes of Health, and FDA are actively involved, and that similar actions occur in the UK with the MHRA, in Europe with European medicine agencies, and in Australia with the Therapeutic Goods Administration. Speaker 1 states that each of these regulators requires product companies to produce ninety days of safety monitoring after a product comes out, describing this as a regulatory dossier. They say that if problems arise and are reported to a company (such as Pfizer), the company must report, compile, and produce a report that is made publicly available. Speaker 1 claims that for Pfizer, whose first vaccine was approved 12/10/2020, Pfizer did not produce a report after the ninety days. They add that when people asked what was happening, Pfizer allegedly did not disclose what occurred, leading to court proceedings. Speaker 1 states that the FDA’s lawyer allegedly said the dossier should not be released for fifty-five years, and that after pressure, the Pfizer dossier was eventually released. They then claim Pfizer recorded 1,223 deaths with their product within ninety days of release and recorded over 1,200 new adverse events. Speaker 1 also says the FDA worked to cover this up, and that FDA should have regulated Pfizer with at least monthly meetings and full disclosure about “novel vaccines,” which they describe as a “genetic transfer technology platform,” the first time human beings had been injected with foreign genetic material in world history. Speaker 1 ends by stating that two thirds of the world’s population took these.

The speaker questions how many people injected with mRNA products knew they weren't receiving a traditional vaccine, suggesting many, including medical professionals, are unaware due to the perception of conspiracy. The speaker claims there was a sufficient safety signal in VAERS to halt the rollout in January, citing almost 90,000 VAERS entries and nearly 700 deaths within the first month. They state that historically, products causing over 50 deaths have been pulled from the market. The speaker questions why the CDC, HHS, and FDA aren't investigating this data.

Dr. McCulloch is asked to weigh in. Speaker 1 responds that he has presented at FDA advisory meetings and advised companies for decades on regulatory science. He states that when a product definitely results in death, and there are thousands of peer-reviewed papers on this, the COVID vaccines in some people sadly result in death—some on the very first day they take the shot. He argues that this must be a black box warning on the product immediately. He says he checked the package inserts for the currently available products, noting that the ones Senator Blumenthal wants to pursue, and what the Governor still wants to pursue, and what the FDA still wants administered, do not have the word “death” in the package insert. He asserts that Americans are not fairly informed. Speaker 0 asks whether Speaker 1 doubts that the COVID injection caused some deaths, and asks for his view on the numbers listed on VAERS (thirty-seven thousand, six hundred seven, per the prompt) and whether he has any science to back up his opinion. Speaker 1 replies that the best data are autopsies. He references the largest autopsy series published to date and notes that he is the senior author. He says they examined deaths after vaccination, had an adjudication committee and methods of arbitration to decide whether the vaccine caused death, and that in these autopsy cases, seventy-three point nine percent of individuals, it was determined that the vaccine was the cause of death. He mentions Holsher and colleagues, who are right behind him. Speaker 0 reiterates the FDA’s own laws, asking that this be included in the package insert, correct? Speaker 1 confirms, noting that in 2021 Dr. Carol Tocetta, working with the Daily Cloud, wrote about Peters’ marks in 2023 and asked, “where’s the black box warning? Where is it?”

Speaker 0 states that the committee now has over 8,000,000 pages of information. In the first tranche, they discovered that someone in the federal health agencies, through interagency communication, hid the signal and admitted there was a signal on myocarditis, but they hid it and didn’t warn the public or doctors. This is described as one instance of corruption and lies told by the CDC, with many more to be rolled out. He notes that they held their first hearing in permanent subcommittee investigation on that hiding of the signal myocarditis and that they have heard a lot of studies. He mentions that, as he has looked into science, it has been thoroughly corrupted, and he requests to enter a data sheet into the record, saying he has been publishing this chart since early 2021. He references being on talk radio shows where they get deplatformed due to censorship in the Biden administration. He then presents what he calls “the facts” about the VAERS system, which was touted in October 2020 as a great safety surveillance system on COVID. A few months later, they denigrated their own system. Despite this, VAERS shows that there have been 38,742 deaths reported on VAERS worldwide associated with the COVID vaccine. He specifies that 9,252 of those deaths occurred on the day of vaccination within one or two days.

A Pfizer whistleblower within the company released documents showing that there were over 158,000 reports of adverse reactions from 12/01/2020 through 02/28/2021. The reports include serious adverse reactions and spontaneous abortions. The whistleblower states that the FDA was well aware and wanted these documents hidden for seventy five years. According to the speaker, the documents prove that the adverse events were intentionally released and that officials knew all along that the vaccine was going to cause massive heart attacks and strokes and deaths and infertility and miscarriages. The speaker claims the list of adverse effects goes on, including neurological issues, and questions how this vaccine remains on the market, noting that vaccines have been removed where ten cases of a child getting sick occurred. The speaker describes the situation as evil, intentional, and asserts that those involved must be held accountable.

Speaker 0 says they found “information like this,” such as vaccine insert paper, with “nothing printed on it,” which they call disheartening and disgusting. They add that it “just keeps happening” and claim the CDC redacts “every single word” of a 148-page study on a myocarditis after COVID vaccination. Speaker 0 says they asked someone to print the study, and that the entire 148 pages are redacted. They ask what a study does if “there’s nothing there,” and they ask what might have been there that required redaction. Speaker 1 says they are “witnessing an active cover up” involving “a colossal consumer product safety debacle” affecting the entire world. They claim that in the United States, the CDC, National Institutes of Health, and FDA are actively involved in a cover up, and that similar cover ups are occurring in the UK with the MHRA, in Europe with European medicine agencies, and in Australia with the Therapeutic Goods Administration. Speaker 1 states that each company that puts out a product has an obligation to produce “ninety days of safety monitoring” after the product comes out, describing it as a regulatory dossier. They claim that if someone has a problem and reports it to a company like Pfizer, Pfizer must report, write down what happened, collate it into a report, and make it publicly available. Speaker 1 says that when the ninety days elapsed for Pfizer’s first vaccine approved on 12/10/2020, Pfizer “didn’t produce a report.” They add that people asked what was happening with the vaccine, and Pfizer allegedly would not disclose what happened, leading to a court case. Speaker 1 says the lawyer for the FDA stepped in to say they did not want to release Pfizer’s dossier for fifty-five years. Speaker 1 then says that after the plaintiff pushed, the Pfizer dossier “slowly” came out. They claim Pfizer recorded one thousand two hundred and twenty-three deaths with their product within ninety days of release, and they say people called Pfizer in desperation watching family members die after taking the vaccine. Speaker 1 also claims Pfizer recorded “over twelve hundred” new adverse events and refers to “doctor Boden” discussing problems they say they have been grappling with. They conclude by claiming the FDA worked to cover this up and should have been regulating the company with at least monthly meetings and full disclosure about novel vaccines, described by Speaker 1 as a genetic transfer technology platform and as the first time human beings were injected with foreign genetic material in world history, after which “they were getting it full on.” Speaker 1 ends by saying “Two thirds of the world’s population took”

A study of 325 autopsies found that in 73.9% of cases, the COVID-19 vaccine was either the direct cause of death or significantly contributed to it. The deaths occurred within one to two weeks after the last shot, and in over 50% of cases, the single cause of death was cardiovascular. This contradicts the official narrative from the CDC and FDA, which maintains that there is no evidence linking deaths to the vaccine, except for a few acknowledged cases after the Janssen vaccine. According to the speaker, these autopsy results are incontrovertible evidence that patients died from the vaccine, challenging the government's stance. The findings have gained significant attention online and on social media.

Speaker 0 states that death rates from the vaccine are extraordinarily high, claiming there have been more deaths in eight months than in all the billions of vaccines combined over the last thirty years for this one vaccine, totaling seventeen thousand recorded deaths in the United States, and asserts the death rate is much higher, “probably 40 times.” The speaker says the risk from the vaccine is completely untenable and that if people knew the truth they would not be taking this vaccine, and that the benefits after six months are apparently zero or even subzero. Speaker 0 references British data, claiming that people who are vaccinated are actually more likely in many age categories to get COVID than people who are unvaccinated, and asserts this outcome was predicted. The speaker alleges that Pfizer knew this would happen, citing their clinical trial, which they say was only six months long; at the end of that period, they claim twenty people died in the vaccine group and fourteen in the placebo group of all-cause mortality. They further claim there were five heart attacks in the vaccine group and only one in the placebo group, concluding that the chance of dying of a heart attack when vaccinated is five hundred percent greater than if one is unvaccinated. Speaker 0 contends that Pfizer knew they were going to kill a lot of people and proceeded to do so anyway. They insist that people need access to those studies to understand what they describe as deceptive, criminal deception that has supposedly been imposed upon them.