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

The FDA allegedly wanted to keep Pfizer's dossier hidden for 55 years, despite knowing about the high number of deaths associated with the vaccine. No safety review board has been called, and there has been no voluntary recall. The large number of deaths is a significant signal, with most occurring within a week of vaccination. There have been reports of blood clots, heart attacks, and fatal cases of myocarditis. The consistency of these adverse events in various systems and literature supports the association. Randomized trials have shown more deaths with Pfizer than with the placebo. The vaccines are believed to be causing deaths in unfortunate individuals due to a combination of factors, including the production of lethal spike proteins.

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.

The Dutch paper reveals a 36% higher risk of serious adverse events in the Pfizer vaccine group compared to the placebo. Despite this, the public was misled about the safety and effectiveness of the vaccines. Adverse reactions like stroke and heart attack were downplayed, making it difficult to link them to the vaccines. The truth is slowly coming to light, exposing the deception by big pharma, governments, and the media. Those responsible may face consequences in the future.

The speaker claims that Pfizer documents reveal evidence of a crime against humanity. They state that Pfizer knew the vaccines didn't work to stop COVID just one month after rollout and that the vaccines had vaccine failure and failure of efficacy. The speaker also highlights that Pfizer was receiving numerous reports of adverse events and had to hire staff to process the paperwork. They argue that the vaccines caused heart damage and other severe side effects, and that the materials in the vaccines biodistribute throughout the body, including the brain and ovaries. The speaker suggests that this is a deliberate bioweapon attack by the Chinese Communist Party and calls for justice.

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 claims the Pfizer documents reveal "the greatest crime against humanity in recorded history," with a specific focus on destroying reproduction, indicating a depopulation agenda. They allege Pfizer knew lipid nanoparticles were blocking women's ovaries and traversing the placenta, and that fetal deaths were due to maternal vaccine exposure. Charts purportedly show vaccinated nursing mothers were making babies sick, with one baby dying of multi-organ system failure. The speaker asserts Pfizer knew of an over 80% spontaneous abortion/miscarriage rate and warned vaccinated men about potential dangers to women/fetuses via semen. The injection travels throughout the body, accumulating in various organs including the ovaries and crossing the blood-brain barrier. The speaker claims Pfizer knew it was damaging minors' hearts and that White House documents reveal a cover-up attempt in April 2021.

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.

Multiple individuals share their experiences of adverse reactions and health issues following COVID-19 vaccination. Some report paralysis, loss of feeling, chronic pain, blood clots, heart problems, and other severe symptoms. Concerns are raised about the safety of vaccines, while others emphasize the overall effectiveness and rarity of serious adverse reactions. The CDC investigates deaths potentially linked to the Johnson & Johnson vaccine. A mother shares her daughter's debilitating condition after participating in the Pfizer vaccine trial. These personal accounts highlight the need for further examination and open discussion regarding vaccine-related injuries.

At the outset, a process was approved by the FDA for emergency use authorization. However, it was later discovered that the approved process was swapped out for one containing contaminants like DNA and a cancer-causing substance. Pfizer redacted 800 pages of the manufacturing process, hiding the fact that a carcinogen was included. This lack of transparency led to no informed consent and potential harm to individuals. The vaccine rollout included a trial with a 2.4 times higher adverse event rate, including the presence of a carcinogen.

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.

Speaker 0: I find information like this, you know, inserts for the vaccine. Paper's there, and there's nothing printed on it. I find that very interesting, disheartening, disgusting, and lots of other words, but then it gets better. It just keep wait. There's more. It just keeps happening. The CDC redacts every single word of a 148 page study on a myocarditis after COVID vaccination. So I asked research to print the study for me. 148 pages. The entire thing is redacted. What good does a study do if there's nothing there? Then I wanna know, wait, what might have been there that they needed to redact it? That's even scarier. Speaker 1: We're witnessing an active cover up of a colossal consumer product safety debacle that is is basically affecting the entire world. Mhmm. So in The United States, our CDC, National Institutes of Health, and the FDA are actively involved in a cover up. And the same is occurring in The UK with the MHRA, Europe with European medicine agencies, and Australia with the Therapeutic Goods Administration. Something is going on that's very big. Each one of these companies that puts out a product has an obligation to produce ninety days of safety monitoring after their product comes out. It's a regulatory dossier. If somebody has a problem with the new product and they call the company like Pfizer, Pfizer has to report, write down what happened, and they have to collate that in a report and produce it and make it publicly available. When it came to ninety days with Pfizer, the first vaccine that came out, remember Pfizer was approved 12/10/2020. Pfizer didn't produce the report. And then people started asking, well, what's happening with your vaccine? And Pfizer would not disclose what happened. And then it went to court. And the lawyer for the FDA stepped in and said they don't wanna release Pfizer's dossier for fifty five years. Mhmm. Oh. Fifty five years. And the the the plaintiff pushed. And finally, slowly, the Pfizer dossier came out. Pfizer recorded one thousand two hundred and twenty three deaths with their product within ninety days of release. People were calling Pfizer in desperation watching their family members die after taking the vaccine. Pfizer recorded over twelve hundred new adverse events, new problems that doctor Boden has talked to you about that we are grappling with the entire time. But the point is our FDA worked to cover this up. The FDA should be regulating this company. FDA should have been having at least monthly meetings and fully disclosing what was going on with these novel vaccines, which are a genetic transfer technology platform.

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.

Maddy DeGary, a participant in Pfizer's 12-15 year old COVID-19 vaccine trial, suffered serious injuries post-vaccination. Pfizer misrepresented her condition as "functional abdominal pain" to the FDA. Despite efforts to bring attention to her true injuries, the FDA showed little concern and failed to hold Pfizer accountable for withholding information. This lack of transparency undermines the integrity of the trial process.

Recent studies have raised serious concerns about the COVID-19 vaccines, particularly regarding potential shedding effects. A new study published in the International Journal of Vaccine Theory found that women indirectly exposed to vaccinated individuals reported significant menstrual irregularities, with over 70% experiencing symptoms shortly after exposure. Additionally, research confirmed the presence of residual DNA in vaccine vials, which could pose risks, including potential integration into human DNA, leading to health issues like cancer. Reports also indicate that heart conditions in vaccinated individuals are worsening over time. Accusations have emerged against Pfizer for allegedly concealing deaths during vaccine trials. These findings highlight the urgent need for further investigation into the safety and long-term effects of COVID-19 vaccines.

The speaker claims the Pfizer documents reveal the "greatest crime against humanity in recorded history," with a specific focus on destroying reproduction, indicating a depopulation agenda. They assert Pfizer knew lipid nanoparticles were blocking women's ovaries and traversing the placenta, determining fetal deaths were due to maternal vaccine exposure. The speaker alleges Pfizer knew vaccinated nursing mothers were making babies sick, citing charts showing thousands of babies experiencing vomiting, edema, and convulsions, with one death from multi-organ system failure. They claim no one is warning vaccinated mothers about the risks to their babies. According to the speaker, Pfizer documents show over an 80% spontaneous abortion/miscarriage rate and warn vaccinated men to avoid intercourse with women of childbearing age or use two forms of contraception. The speaker states Pfizer knew the injection travels throughout the body, accumulating in various organs including the ovaries, and damaging the hearts of minors. They claim lawyers have FOIA documents showing a White House scramble in April 2021 to cover this up.

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.

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.

Pfizer documents show an 80% miscarriage rate in pregnant women. 236 out of 270 records were lost. Babies in utero were exposed to the vaccine, leading to deaths. Breast milk was poisoned by vaccine components, causing convulsions and deaths. Newborns may have air sacs between lungs and chest walls, leading to respiratory distress. Pfizer knew about this issue 2 years prior.

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.

I spent 9 months researching the Pfizer vaccine with whistleblowers and scientists. Trials showed a 1 in 800 risk of serious harm from the vaccine, higher than COVID hospitalization rates. Other vaccines were pulled for less harm. Serious harm included hospitalization, disability, and life-changing events, with 40% related to clotting disorders.

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.

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”