reSee.it - Related Video Feed

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.

The speaker expresses disappointment that the existence of myocarditis was known very early on. They claim to have written to Fauci in 2020 and 2021 about lymphopenia and the failure to clear the virus, asserting that this failure was also known early on. The speaker states the perception of 95% efficacy was inaccurate and suggests there were perverse incentives at play, and now the consequences must be recognized. Another speaker then states that this is why Fauci needed a pardon.

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 speakers discuss the lack of accurate data on vaccine-related deaths and adverse effects. They mention various investigations and studies conducted internationally, highlighting statistical signals of increased deaths during vaccination campaigns across Europe. They also mention issues with data in England, where a delay between vaccination and death results in vaccinated individuals being classified as unvaccinated. This artificially inflates the number of unvaccinated deaths. An English study shows that vaccinated individuals make up a higher percentage of deaths compared to their population percentage. These findings raise concerns about the effectiveness of vaccines and the accuracy of government data.

According to the speaker, vaccination eligibility should only have been granted after a doctor determined it was advisable for an individual case, because—except for a single exception—virtually no one under 60 would have faced a chance of serious complications from coronavirus. The speaker claims that therefore, people under 60 should not have been vaccinated, and that filling sports halls with vaccination sites was completely contrary to the purposes for which the vaccines were authorized by the EMA. The speaker further argues that evaluating vaccine safety required that side effects be properly recorded. They quote the EMA as saying it expects many reports of side effects occurring during or shortly after vaccination, meaning that complaints must be reported in the first period of vaccination. The speaker then says that the government supported a policy in which these complaints were not reported in the first 14 days after vaccination because the vaccine would need 10 to 14 days to become effective. The speaker claims that all complaints in that time were instead attributed to coronavirus, calling this both fraudulent and deliberately endangering human lives. The speaker also refers to an ongoing “gigantic so-called unexplained excess mortality.” In summary, they state that the EMA information is devastating for the vaccination policy of Rutte and De Jonge, claiming the government knew the vaccines would not protect against virus transmission but did not share that information with the public. The speaker says the government pushed the vaccines on citizens with “lies,” concealed side effects, and endangered the health of everyone who took the vaccine. They conclude that the vaccination campaigns should be stopped as soon as possible because they are not safe and do not meet EMA requirements. The speaker ends by saying the government and all political parties that supported this should be held accountable for their “lies and deception,” and then hands the word to Jojim Koers.

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.

The speaker claims that the COVID vaccine is toxic and could have caused the deaths of 17 million people worldwide. They suggest that there is a temporary increase in all-cause mortality following vaccine rollouts, which is consistent across different countries. Another speaker points out that normally, deaths decrease in the summer, but during the vaccine campaign, there are spikes in mortality, even in the Southern Hemisphere where it should be low. They mention that this pattern is seen during booster rollouts as well. This phenomenon is described as unprecedented.

The speaker claims that the vaccine is toxic and could have caused the deaths of 17 million people worldwide. They argue that after each vaccine rollout, there is a temporary increase in overall mortality. This pattern is observed consistently across countries with sufficient data. Another speaker points out that typically, deaths decrease in the summer and increase in the winter, but during the COVID vaccine campaign, there are spikes in mortality right after the campaigns, even in the summer. They mention that this pattern is seen in both the northern and southern hemispheres. The speakers emphasize that this is a new phenomenon.

The speaker claims that the vaccine is toxic and could have killed 17 million people worldwide. They argue that after each booster rollout, there is a peak in all cause mortality, which is consistently observed across different countries. Another speaker points out that normally, deaths decrease in the summer, but during the COVID vaccine campaign, there are spikes in mortality right after vaccine campaigns, even in the Southern Hemisphere where it should be a low death period. They mention that this pattern is seen in all 17 countries they studied. Overall, they emphasize that these observations are unprecedented.

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.

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.

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.

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.

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."

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.

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.