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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.

Dr. McCulloch states that COVID vaccines, in some people, result in death, sometimes on the first day of the shot. He believes this should trigger a black box warning on the product immediately. He claims that the currently available COVID vaccine package inserts do not contain the word "death" as of today. Therefore, Americans are not fairly informed.

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.

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.

I testified in the US Senate on December 7, 2022, stating that the vaccine is causing a significant number of deaths. The vaccine fulfills the criteria for causality according to the Bradford Hill tenets. As of December 23, 2022, the CDC reported over 6,000 Americans who died shortly after receiving the vaccine, but this number is likely underestimated.

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.

We submitted a vaccine injury paper to The Lancet on COVID vaccine-related sudden deaths. The paper, co-authored by Dr. Peter McCullough, is the largest autopsy series in the world with 325 cases. 74% of sudden deaths were linked to the vaccine. Despite pressure, the paper passed peer review and will be published. More evidence is emerging on the harm of COVID vaccines, urging politicians to act preemptively.

Speaker 0 asks about a report and how concerning it is, suggesting that if the reported figure is 10, there is a “real number” that could be higher. Speaker 1 says the main concern is that the analysis “dramatically understates the problem.” They describe the difficulty of getting autopsies during the pandemic and say medical professors didn’t want to perform them, resulting in very few autopsies. They state that NIH/CDC/FDA reviewed 96 pediatric autopsies and concluded about 10 were possible or probable. Speaker 1 then argues that safety signals were “screaming,” and points to VAERS. They claim there are almost 1.7 million total adverse events and 39,000 deaths worldwide. They say 24% of the 39,000 deaths occurred on the day of vaccination or within one or two days. Speaker 1 also references the point that VAERS doesn’t prove causation, while stating that if a person who was “perfectly healthy” died that day or within one or two days, they would “be blaming” the jab. They add that in some cases people may have been in bad health already, with death tipped over by another cause. Speaker 1 says the “bigger revelation,” which they claim was unveiled three weeks ago and is “still not being covered by the mainstream media,” involves FDA’s VAERS algorithm. They state that on 03/01/2021, Peter Marks (head of CBER/FDA’s division approving vaccines and surveilling post-approval safety) was briefed that their algorithm analyzing VAERS would “hide and mask safety signals.” They say that 26 days later, a new algorithm unmasked safety signals, producing 49 cases of extreme masking revealed and 25 safety signals, including sudden cardiac death, pulmonary infarction, Bell’s palsy, and different types of strokes. They claim that similar data runs over the next three months showed more safety signals and more sudden death. Speaker 1 further claims that FDA did not “pin a badge” on Anna Scharzman, referred to as the father of their expert, and instead “shunned her off to the side,” ordered her to cease and desist, and decided to use the algorithm they had been warned would hide safety signals, which they say is still being used. Speaker 1 states that Peter Marks left for Eli Lilly and claims “the entire world” is in denial. They say they have been unable to broadcast the story or get interviews on CBS, ABC, NBC, PBS, MSNBC, or CNN, and that they challenged Jake Tapper, who they say agreed to read the report but has not invited them back yet.

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.

And do you have any signs to back up your your opinion? The best data are autopsies. So in the largest autopsy series published to date, I know because I'm the senior author. Of all the deaths examined and we re reviewed them. We had an adjudication committee. We had ways of arbitration deciding on did the vaccine cause death. The answer is of these cases that came in for autopsy after vaccination, seventy three point nine percent of individuals, it was determined that the vaccine was the cause of death. First off, there's Hocher and colleagues who's sitting right behind me.

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.

We submitted a vaccine injury paper to The Lancet about COVID-19 vaccine-related sudden deaths. The paper was taken down due to pressure from the pharmaceutical industry but has now passed peer review and will be published. It found that 74% of sudden deaths were caused by the vaccine. More evidence is emerging about the harm of COVID-19 vaccines, and politicians should act before it's too late.

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.

Professor Lawler stated there were no breaches of good clinical practice and no hidden deaths in the Pfizer trial, also claiming that none of the deaths were attributed to the vaccine and the initial conclusions remain valid. In response, the speaker says they reanalyzed the data and found more deaths in the vaccinated arm (21) compared to the placebo arm (17). In the vaccinated arm, 10 deaths were categorized as sudden adult death or found dead, but only two had autopsies. One autopsy result is available and showed sudden cardiac death. The other is still pending. The speaker questions how it can be stated that deaths are not due to the vaccine when autopsy results are pending or not performed, especially in cases of sudden death. The speaker has repeatedly asked the TGA for the evidentiary basis for the statement that none of the deaths were due to the vaccine, but has not received a reply.

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.

I recently testified in the US Senate on December 7th, 2022. I want to be very clear: the vaccine is killing people, and it's killing large numbers of people. It fulfills all the criteria for the Bradford Hill tenets of causality for a medicinal product causing death. As of December 23rd, 2022, the CDC has recorded over sixteen thousand Americans that have died within a few days of taking the vaccine, and that's probably a gross underreport. I was recently at a conference in Romania on the COVID crisis. There was a lot of work trying to unpack what we actually understand, and I saw a credible estimate of something like seventeen million deaths globally from this technology. When you scale up to billions, it's not hard to reach a number like that with a technology this dangerous.

In the largest autopsy series to date, the speaker states that they are the senior author. After examining deaths and reviewing them with an adjudication committee, it was determined whether the vaccine caused death. According to the speaker, in 73.9% of cases that came in for autopsy after vaccination, the vaccine was determined to be the cause of death. The first author is Holsher and colleagues.

The speaker discusses a review of 325 autopsies, which they claim is the largest autopsy series in the world, of COVID-19 vaccinated individuals who died shortly after vaccination. According to the speaker, this review found that the vaccine caused or contributed to approximately 74% of the sudden deaths. The speaker states that this information will be published in a peer-reviewed paper. The speaker anticipates a "tsunami of evidence" regarding the harm caused by COVID-19 vaccines to children, pregnant women, and adults. The speaker urges politicians to "get ahead of this" issue now.

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.

Speaker 0 asks Speaker 1 to explain the process of how the vaccine causes myocarditis and pericarditis. Speaker 1 mentions rare reports of myocarditis and pericarditis associated with vaccination. Speaker 0 insists on an explanation of the mechanism, but Speaker 1 does not provide a direct answer. Speaker 1 emphasizes that all medicines have benefits and side effects and refers to the benefit-risk ratio. Speaker 0 continues to press for an explanation of the biochemical pathway, but Speaker 1 agrees to provide a response later. The transcript ends with Speaker 2 confirming Speaker 1's agreement to give a further response.

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.