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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.

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 claims Pfizer knew a month into November 2020 rollout that the vaccine did not stop COVID, and that mandates, job losses, school closures, and two-tier society followed a lie. They allege the injection did not stay in the deltoid; the materials biodistribute within forty eight hours, cross the blood-brain barrier, and accumulate in organs including the liver, adrenals, spleen, lymphatic system, and ovaries, with the second dose increasing ovarian accumulation. Pfizer allegedly hired 2,400 staff to process adverse events, totaling over forty two thousand between 2020 and 2021; top side effects were myalgia and joint pain, followed by COVID. Catastrophic events included heart damage, myocarditis, pericarditis, thrombotic events, neurological and autoimmune disorders, and eye damage, plus twelve hundred deaths in three months. By April 2021 minors showed myocarditis; FDA/CDC/Israeli MOH were aware; FOIA revealed a 17-page script urging parents to vaccinate minors; Ron Johnson uses work to push unredaction.

Maddy DeGary, a participant in Pfizer's COVID-19 vaccine trial for 12 to 15-year-olds, suffered serious injuries post-vaccination. Pfizer initially downplayed her condition as abdominal pain, misleading the FDA. Despite being wealthy, only after an email to FDA officials did Pfizer admit to DeGary's injuries. FDA's response was lackluster, showing no concern for Pfizer's misconduct. The failure to report all adverse events corrupts the trial process, with no repercussions for Pfizer's actions.

Speaker 0 questions understanding of vaccine causing myocarditis, mentioning Pfizer's awareness. Speaker 1 doubts if vaccine was tested for stopping transmission before market release. Speaker 0 believes vaccination was optional, not forced.

Florida's surgeon general raised concerns about the safety of COVID vaccines, while the federal government continues to promote them. This video tells the story of Maddie, a child who participated in Pfizer's vaccine study. After receiving the second dose, Maddie experienced severe symptoms including chest pain, abdominal pain, and loss of feeling in her legs. Despite seeking medical help, her symptoms were dismissed as anxiety. Maddie's case was not properly reported, and the FDA granted emergency use of the vaccine for children based on this study. Other children also experienced serious adverse effects, including heart problems and death. Maddie was eventually diagnosed with chronic inflammatory demyelinating polyneuropathy. The government and those involved in the study declined to comment. Maddie's parents are hopeful for her recovery but have lost trust in the medical system.

Pfizer submitted their full approval application on May 18, 2021. The original required action due date was January 18, 2022. Doctor Marks worked with doctors Kraus and Gruber on the approval process. They proposed October 2021 for approval, but Doctor Marks requested September 15, 2021. Doctor Marks wanted it approved even faster, but they declined. Doctor Marks and former FDA Commissioner Woodcock relieved doctors Kraus and Gruber from their roles due to pressure to approve the vaccine faster. Doctor Marks made the decision to speed up the approval process due to increasing COVID-19 deaths and the belief that an approved vaccine would encourage more people to get vaccinated. There were discussions about vaccine mandates, and a licensed vaccine would allow for mandates. Concerns were raised about the workload and safety signals regarding myocarditis in young men. There were no direct conversations with the Department of Defense regarding the vaccine approval. Doctor Marks desired approval by August 20th, and it was ultimately approved on August 23rd. The military mandate was issued on August 24th.

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.

Vaccine recommendations typically come from the Advisory Committee of Immunization Practices (an outside consulting committee at CDC) and VRBPAC (within FDA), which recommends vaccine licensure. These committees only adopted evidence-based medicine about twelve years ago. The speaker states that during their administration, they want safety studies prior to vaccine licensure and recommendation. They claim vaccines are exempt from pre-licensing safety testing, and the COVID vaccine was the only one tested in a full placebo trial. They assert that the other 76 shots children receive between birth and 18 have not been safety tested against a placebo, meaning the risk profile is not understood. The speaker intends to remedy this.

The speaker discusses concerns about the origins of COVID-19 and the risks of childhood vaccination. Dr. McCullough warns about the dangers of vaccinating children and presents findings on heart inflammation post-vaccination. A study from Tokyo, New York, and Houston reveals that vaccinated individuals experience a 46% increase in heart workload. The speaker urges for a reevaluation of vaccine safety and calls for an end to vaccine mandates.

Pfizer knew within three months of rollout that 1,225 people had died. By April 2021, Pfizer was aware that minors' hearts were being damaged by the injection, with warnings coming from the Israeli health ministry and a pediatric group. Email chains, obtained through FOIA requests, show this information was sent to Dr. Fauci, Dr. Walensky, the President, and White House staffers. A "freak out conference" ensued, allegedly to plan how to lie to the American people, resulting in a 17-page redacted script. The claim is that in April and May 2021, authorities stated that pericarditis and myocarditis in young men and teenagers were transient, mild, and rare, despite allegedly knowing otherwise. This was followed by a summer-long propaganda campaign using influencers and TikTok personalities to encourage young people to get injected.

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.

I recently heard stories of people losing their children to Pfizer injections, some experiencing immediate or gruesome deaths. The FDA knew about potential risks like cancer from as far back as 2013, but suddenly in 2020, these concerns were ignored. This seems like a premeditated crime, with regulators aware of the dangers. Military involvement in pushing these products is suspicious.

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.

I recently met someone whose 18-year-old daughter developed cancer after receiving the Pfizer vaccine. I've heard from many parents who lost children to these injections, some experiencing immediate and horrific deaths. They repeatedly share their stories with lawmakers, highlighting a significant crime that must end. The FDA was aware of the potential cancer risks associated with these vaccines, as outlined in guidance documents from 2013 and 2015. These documents instructed manufacturers to study risks like cancer, fertility issues, and cardiovascular problems, and deemed it unethical to test on healthy volunteers. Yet, by 2020, these concerns were seemingly overlooked. This raises serious suspicions about the intentions behind the vaccine rollout, suggesting a premeditated crime where regulators and the military may have colluded with pharmaceutical companies.

This is the story of Maddie, a 12-year-old girl who participated in Pfizer's COVID vaccine study for children. After receiving the second dose, Maddie experienced severe symptoms including chest pain, abdominal pain, and loss of feeling in her legs. Despite her deteriorating condition, doctors dismissed her symptoms as anxiety. Maddie was hospitalized multiple times and diagnosed with chronic inflammatory demyelinating polyneuropathy. The family believes that Pfizer, the FDA, and the study leaders tried to cover up Maddie's case. The FDA granted emergency use of Pfizer's vaccine for children based on this study, but there were no official hearings on vaccine side effects. The family's trust in the government and medical professionals has been shattered.

A study of 1,700,000 children found heart damage only in COVID-vaccinated children, with zero heart-related problems in unvaccinated children. The study also found that no children, vaccinated or unvaccinated, died from COVID-19. The COVID shots offered little protection, with many children becoming infected after 14-15 weeks. The study, led by Oxford University's Professor Kome d Andrews, investigated Pfizer's vaccine safety and effectiveness in 5-15 year olds registered with the UK's national healthcare system. Myocarditis and pericarditis cases only emerged in the vaccinated group. The speaker asserts emergency use authorization was given despite evidence the injections were not safe, which Pfizer and the FDA allegedly knew. The speaker claims future injection rollouts need more scrutiny and alleges globalists plan to force regular injections via digital ID systems to prevent future pandemics. The speaker urges scrutiny of everything from big pharma.

According to the speaker, the COVID vaccine has resulted in more deaths in the past 8 months than 72 other vaccines combined over the past 30 years. They claim that children are most at risk of suffering from heart attacks due to myocarditis, with a 50% chance of death or requiring a heart transplant within 5 years. The speaker mentions studies showing that healthy children have zero risk of dying from COVID, while the risk of myocarditis from the vaccine is much higher. They also discuss data from Pfizer's trial, highlighting the case of a girl who experienced severe side effects and is now wheelchair-bound. The speaker questions the decision to mandate the vaccine for children based on limited testing.

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.

A physician who experienced an adverse reaction to the Moderna COVID shot states that the COVID shots should never have been authorized for children and pregnant women. After receiving the Moderna shot, the speaker developed transverse myelitis, autonomic dysfunction, and an unspecified immune disorder, leading to medical retirement. The speaker is now co-chair of React19, representing Americans injured by the COVID shots. The speaker claims that the clinical trials were rushed, safety data was withheld or altered, and reporting systems like VAERS and V-Safe have failed. The speaker questions whether regulatory agencies have a conflict of interest. The speaker alleges that instead of proving safety and efficacy, the COVID-19 shots were assumed to be safe and effective, with short follow-up data, and were given to pregnant/lactating women and children without long-term safety data. The speaker is appreciative that the COVID-19 shots have been removed from the childhood vaccination schedule for healthy children, but much damage has already been done. The speaker advocates for recognition, research, medical care, and compensation for those injured by the COVID-19 shots.

An internal NIH CDC FDA meeting in October 2020 anticipated side effects from a vaccine, including myocarditis, blood clots, and paralysis. Despite these warnings, the vaccine received emergency use authorization in December 2020. By June 2021, the CDC and FDA held emergency meetings regarding heart damage linked to the vaccine, particularly affecting young boys. A report in the New England Journal of Medicine documented a fatal case of myocarditis. In Connecticut, two healthy teenage boys died unexpectedly after vaccination, with autopsies confirming fatal myocarditis as the cause. Despite these serious risks, fatal myocarditis is still not mentioned on consent forms for the vaccine.

A Pfizer whistleblower has revealed documents indicating over 158,000 reports of adverse reactions from December 2020 to February 2021, including serious issues like spontaneous abortions. This raises concerns about the intentional release of the vaccine and the knowledge of its potential to cause severe health problems, including heart attacks and infertility. The FDA's efforts to keep these documents hidden for 75 years suggest awareness of these dangers. The continued availability of the vaccine is alarming, especially considering that other vaccines have been removed for far fewer adverse cases. Those involved in this situation must be held accountable.

Pfizer knew a month into the rollout, November 2020, that this vaccine did not work to stop COVID. Everything that followed—the mandates, the lost jobs, the closures, children not allowed back to school if they didn’t take the shot, the armed forces compelled to take it, pilots compelled—was built on a lie of vaccine efficacy. The most common side effect of getting vaccinated is COVID, and Pfizer understood that the vaccine’s efficacy and vaccine failure showed it did not stop COVID. They also knew the injection did not stay in the deltoid. Europeans through the EMA and public health entities described side effects as chills, fever, fatigue, needing to lie down, but Pfizer knew that was a lie. In Pfizer documents, charts show that the materials—the spike protein, the mRNA, the lipid nanoparticles, and polyethylene glycol—biodistribute within forty-eight hours and leave the injection site to biodistribute to major organs throughout the body, crossing the blood-brain barrier. This may have contributed to personality changes in some loved ones who took the injection. They also accumulate in the liver, the adrenals, the spleen, the lymphatic system, and in women, the ovaries. The first injection accumulates in ovaries; the second injection more so. Experts could not find any mechanism whereby this material left the body in either gender. By the first booster, surgeries on vaccinated women reported fully blocked ovaries, among other damage. Pfizer knew that. They also hired 2,400 full-time staff to process reports of serious adverse events, starting to receive them during the 2020-2021 period. In Pfizer documents, over forty-two thousand serious adverse events were tallied from November 2020 to February 2021, with many individuals experiencing multiple events. The top documented side effects included myalgia (muscle pain), followed by joint pain, then COVID itself, and then a catastrophic tally of serious side effects including heart damage (myocarditis, pericarditis), problems with the aorta, thrombotic events (blood clots in various locations), neurological events (tremors, Guillain-Barré, dementia, epilepsy-like seizures), autoimmune disorders, and eye damage including blindness. Reproductive damage was noted: miscarriages and other issues. Twelve hundred deaths in three months were recorded as not statistically random; they were old with prior conditions, yet doctors noted causality concerns and recorded them. Pfizer knew by April 2021 that minors were injured by the vaccine, specifically myocarditis and pericarditis. Minors sustained heart damage, with thirty-five minors affected. The Israeli Ministry of Health warned the CDC and the Biden administration about minor heart damage, but FOIA requests later showed active conversations up to the White House regarding myocarditis in minors. Instead of withdrawing or advising parents, a 17-page document was produced as a script to persuade parents to vaccinate their minors, supplemented by a TikTok influencer campaign encouraging young people to get injected. These communications indicated that kids would sustain deadly heart damage, and still proceeded. Senator Ron Johnson is using the work to unredact those documents and hold hearings about the cover-up. Pfizer knew all of these things.