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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.

According to VAERS, there have been 38,000 deaths from COVID shots. The speaker claims that under normal circumstances, the FDA would have pulled the shots, but instead, they've been put on the childhood vaccine schedule, with babies expected to get three shots by nine months old. The speaker states the shots are still under EUA status for those 12 and under, and are not fully FDA approved, yet are on the vaccine schedule. According to the CDC, nine million American children have received the latest version of these COVID shots. The speaker expresses concern about myocarditis in children. The speaker believes the shots should have been shut down a long time ago.

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.

Speaker 0 frames the issue as 'the corruption of science' and the 'capture of the agencies' by pharmaceutical industries, stating the goal is to restore integrity and credibility to science. Speaker 1 cites a CDC internal study: 'black boys who got the vaccine on time had a two hundred and sixty percent greater chance of getting an autism diagnosis than children who waited.' He adds that 'The chief chief scientist on that, Doctor. William Thompson, the senior said vaccine safety science at CDC, was ordered to destroy that data. And then they published it without that fact.' Finally, he asserts, 'So, you know that story. And you know of hundreds of stories like that. It happens all the time. We are being lied to by these agencies, and we're gonna change that right now.'

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.

I found blank inserts in vaccine information and a redacted 148-page study on myocarditis after COVID vaccination. There's a cover-up involving CDC, FDA, and other agencies worldwide. Pfizer withheld safety data for 55 years, revealing 1,223 deaths and 1,200 new adverse events post-vaccination. The FDA failed to regulate and disclose information on genetic transfer technology vaccines.

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.

There have been unprecedented injuries, disabilities, and deaths from COVID-19 vaccines. By January 22, 2021, 182 deaths were reported to the US vaccine adverse event reporting system. The FDA and CDC, who co-administer the program, lack experience in vaccine campaigns. Pfizer knew about 1,223 deaths within 90 days of their vaccine but kept it confidential. Moderna has not released their data. There are over 34,100 peer-reviewed papers on vaccine injuries, disabilities, and deaths.

The speaker found that the COVID vaccine has triggered 770 safety signals in the Veris system, a record number. The CDC failed to disclose this information, showing corruption. They refuse to provide access to data for analysis, preventing transparency. The speaker believes the vaccines are causing harm and increasing the risk of death. Access to data is restricted under the Freedom of Information Act, hindering efforts to uncover the truth. Cooperation and transparency are needed for scientific inquiry. Translation: The speaker discusses the alarming number of safety signals triggered by the COVID vaccine and criticizes the CDC for withholding this information. They highlight the lack of transparency in accessing data for analysis and express concerns about the vaccines' impact on public health. Collaboration and openness are essential for scientific investigation.

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 claims the medical landscape is dominated by COVID vaccine injuries, disabilities, and deaths, and that they submit multiple entries daily to VAERS, facing scrutiny and potential penalties for falsification. They state they diagnosed an executive in her late thirties with Guillain Barre syndrome from COVID-19 vaccination. The speaker estimates that only 1% of manuscripts on COVID vaccine injuries are being published, suggesting a tremendous bias, and that there are about 4,000 papers on the vaccine debacle, which is about 1% of reality. They claim to have never seen myocarditis, heart failure, or blood clots from eating frosted flakes, but are seeing people devastated by the shots. The speaker advocates for removing COVID-19 vaccines from the market, a critical reevaluation of the vaccine schedule, dropping all vaccine mandates, and rescinding the 1986 Vaccine Injury Compensation Act.

The speaker describes a committee conflict investigated by the office of inspector general and Congress, who urged change, but nothing happened. They claim medical malpractice by this group is evident in the approval of vaccines. The speaker states that in 1986 there were 11 vaccines, which increased to 69, then 92. They assert that, except for the COVID vaccine, none had a pre-licensing safety trial involving a true placebo. According to the speaker, these vaccines were introduced without safety studies, resulting in a lack of understanding regarding the risk profiles of these products. The speaker attributes this to corruption and agency capture.

Following a subpoena to HHS, a timeline reveals that on 02/28/2021, Israeli health officials notified the CDC of myocarditis reports, especially in young people, after the Pfizer vaccine. On April 12, a DOD consultant raised concerns to the CDC and FDA about monitoring cardiac adverse events, stating, "If you do not ask, you will not see it." In mid-April 2021, CDC officials discussed myocarditis safety signals with mRNA vaccines based on DOD and Israeli data but didn't immediately warn the public. By April 2021, VAERS reported 2,926 worldwide deaths within 30 days of injection, with 46% occurring on days zero, one, or two. The speaker claims that when he raised this issue, he was censored. From May 17-21, 2021, CDC officials discussed a formal health warning on myocarditis, noting underreporting to VAERS. On May 24, officials asked if VAERS was signaling for myopericarditis and were told yes for ages 16-24. From May 25-27, the CDC updated Pfizer and Moderna but not the public. On May 26, the FDA didn't concur with the warning, and the CDC and FDA decided to nix it, publishing less formal clinical considerations instead. An FDA official raised concerns about even posting those. The CDC then edited clinical considerations, removing advice to restrict patients with myocarditis from rigorous activity.

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.

The speaker claims the Biden administration covered up science related to the COVID shot. Information related to vaccine complications was allegedly censored as COVID vaccine hesitant content. The speaker alleges the heart inflammation in young, healthy men and boys was not disclosed as soon as it should have been, resulting in thousands of kids developing myocarditis unnecessarily. The speaker suggests the administration knew the shot didn't stop transmission but kept it secret. The head of the FDA is cited as saying the Biden administration suppressed information about myocarditis damage to children. The speaker believes this sounds criminal, especially considering mandates for school, work, and travel.

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 CDC planned to analyze VAERS data for COVID-19 vaccine safety signals using Proportional Reporting Ratio (PRR), where a score above two would trigger further inquiry. ICANN requested the PRR results via FOIA and found "incredibly concerning results," with some harms having PRRs of 30, 50, or 100. The CDC then switched to Empirical Bayesian (EB) analysis by the FDA. ICANN requested this data via FOIA, leading to two federal lawsuits before the data was released. This data was also "very concerning." Both the PRR analysis and the EB data are available on the ICANN website. The speaker encourages independent scientists to analyze and publish on the data, which confirms "incredibly concerning reports of harm from the COVID-19 vaccine." The speaker claims federal health officials hid this data from the public.

Speaker says his committee now has over 8,000,000 pages of information and that federal health agencies hid the signal about myocarditis, claiming "CD somebody in the federal health agencies, interagency communication, hid the signal. Admitted there was a signal on my architis and they hid it. They didn't warn the public. They didn't warn doctors." He calls this "one instance of corruption and lies told by the CDC" and says more will be rolled out. He notes "our first hearing in permanent subcommittee investigation on that hiding of the signal myocarditis." He asserts science has been "thoroughly corrupted" and presents "data" to enter into the record. Citing censorship during the Biden administration, he cites VAERS: "thirty eight thousand seven hundred and forty two deaths reported on VAERS worldwide associated with COVID vaccine. Thirty eight thousand seven hundred forty two. Nine thousand two hundred fifty two of those deaths occurred on the day of vaccination within one or two days." He adds, "There's not any good study on that. This is hard evidence."

Documents show they had received over 158,000 reports of adverse reactions from 12/01/2020 through 02/28/2021, including serious adverse reactions and spontaneous abortions. It is claimed that the FDA was well aware and wanted these documents hidden for 75 years because it proves the information was intentionally released and would cause massive heart attacks and strokes, deaths, infertility, and miscarriages, with neurological issues also cited. The speaker asserts that this vaccine is still on the market and contrasts it with vaccines that were removed after ten cases of a child getting sick. The statements describe the situation as evil and intentional, and say whoever is involved must be held accountable.

The speaker claims a committee experienced typical conflict, but a specific conflict was particularly obvious. The Office of Inspector General and Congress investigated and urged change, but nothing happened. The speaker asserts this group committed medical malpractice by approving vaccines, increasing the number from 11 in 1986 to 69 and then 92. They state that, except for the COVID vaccine, none had pre-licensing safety trials with a true placebo. According to the speaker, these vaccines were introduced without safety studies, meaning the risk profiles are unknown. The speaker attributes this to corruption and agency capture.

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.

The speaker discusses redacted information on vaccine inserts and a cover-up involving the CDC, FDA, and other agencies regarding vaccine safety monitoring. Pfizer failed to produce safety monitoring reports, leading to court battles and eventual disclosure of 1,223 deaths and 1200 adverse events within 90 days of vaccine release. The FDA is accused of covering up this information, despite the unprecedented use of genetic transfer technology in vaccines.

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.

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.