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In the Pfizer trial, more people died who received the vaccine than the placebo. The vaccine was meant to save lives, but more deaths occurred in the drug group. Saving one life required vaccinating 22,000 people, potentially saving 10,000 lives annually. However, data suggests at least 150,000 vaccine-related deaths. The focus on COVID lives saved overshadows vaccine deaths, with 117 kids possibly dying to save one life. Doctors fear discussing vaccine risks due to professional consequences.

In the Pfizer trial, more people died who received the vaccine than the placebo, contradicting the purpose of vaccines. Saving one life for every 22,000 vaccinated, the vaccine caused more deaths due to other reasons. Despite potentially saving 10,000 lives annually, around 150,000 deaths are linked to the vaccine. The focus on COVID lives saved overshadows vaccine-related deaths, especially concerning children. Doctors are silenced on the matter to avoid repercussions.

In this video, a diagnostic pathologist discusses the evidence presented by Pfizer to the FDA regarding COVID-19 vaccine trials in children aged 6 months to 4 years. The trial initially recruited 4,526 children, but 2,000 dropped out, raising concerns. The trial defined severe COVID as a slightly raised heart rate or increased breaths per minute. Six children in the vaccine group had severe COVID compared to one in the placebo group, suggesting a higher likelihood of the vaccine causing severe COVID. Additionally, 34 vaccinated children contracted COVID during the three-week period between doses, compared to 13 in the placebo group, indicating a 30% increased chance of catching COVID if vaccinated. The trial ignored significant data, ultimately comparing only three vaccinated children with COVID to seven in the placebo group to claim vaccine effectiveness.

According to the speaker, the COVID vaccine has caused more deaths in the last 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 different studies that estimate the likelihood of children getting myocarditis from the vaccine, ranging from 1 in 300 to 1 in 2,700. They argue that the risk of COVID-19 for healthy children is zero, based on studies that found no healthy American child who died from the virus. The speaker also discusses data from Pfizer's trial, highlighting neurological injuries and the case of a girl who is now wheelchair-bound after participating in the trial. They express concern about mandating the vaccine for children based on limited testing.

Behind the scenes communications from the BC Centre for Disease Control revealed that COVID-19 vaccines were 16 times more dangerous than flu shots for children. The data was manipulated before being released to the public, omitting comparisons to flu vaccines and downplaying serious adverse events. This lack of transparency raises concerns about health regulators withholding vital information from the public.

In this video, a diagnostic pathologist discusses the evidence presented by Pfizer to the FDA regarding COVID-19 vaccine trials in children aged 6 months to 4 years. The trial initially recruited 4,526 children, but 2,000 dropped out without explanation. The trial defined severe COVID as a slightly raised heart rate or increased breaths per minute. Six children in the vaccine group had severe COVID compared to one in the placebo group, suggesting a higher likelihood of the vaccine causing severe COVID. Additionally, 34 vaccinated children contracted COVID during the three-week period between doses, compared to 13 in the placebo group, indicating a 30% increased chance of catching COVID if vaccinated. The trial ignored significant data and only compared small numbers, concluding that the vaccine was effective based on three cases in the vaccine group and seven in the placebo group.

Dr. Menares and an interlocutor debate the science behind pediatric COVID vaccination and routine immunizations, focusing on transmission, hospitalization, and risk. - The interlocutor asks whether the COVID vaccine prevents transmission. Speaker 1 answer: the vaccine can reduce viral load in individuals who are infected, and with reduced viral load, there is reduced transmission. The interlocutor reframes, insisting that the vaccine does not prevent transmission and notes decreasing effectiveness over time, citing Omicron data showing around 16% reduction when there is a reduction. - On hospitalization for children 18 and under: Speaker 0 asserts the vaccine does not reduce hospitalization for 18-year-olds; statistics are inconclusive due to small numbers of hospitalizations in that age group (approximately 76 million people aged 18 in the country, with 183 deaths and a few thousand hospitalizations in 2020–2021; numbers have since dropped). The argument emphasizes a need to discuss the issue. - On death for children 18 and under: Speaker 0 says the vaccine does not reduce the death rate; claims there is no statistical evidence that it reduces deaths. Speaker 1 responds with a more cautious stance: “It can,” but Speaker 0 counters, calling that an insufficient answer. - The discussion references the vaccine approval process and ongoing debates in vaccine committees. The interlocutor states that when the vaccine was approved for six months and older, the discussion acknowledged no proof of reduction in hospitalization or death. The argument asserts that the justification for vaccination is based on antibody generation rather than clear hospitalization/death data. The interlocutor contends that immunology measurements (antibody production) do not necessarily justify vaccination frequency. - The core debate centers on what the science supports for vaccinating six-month-olds and the benefits versus risks. The interlocutor argues there is no hospitalization or death benefit for vaccination in this age group, and notes a known risk of myocarditis in younger populations, estimated somewhere between six and ten per ten thousand, which the interlocutor claims is greater than the risk of hospitalization or death being measurable. - The exchange then shifts to changing the childhood vaccine schedule, particularly the hepatitis B vaccine given to newborns when the mother is not hepatitis B positive. The interlocutor asks for the medical or scientific reason to give a hepatitis B vaccine to a newborn with an uninfected mother, arguing that the discussion should focus on whether to change the schedule rather than declaring all vaccines as good or bad. - Speaker 1 says they agreed with considering the science and would not pre-commit to approving all ACIP recommendations without the science. Speaker 0 disagrees, asserting their position that the debate should center on the medical rationale for these specific vaccines and schedules, not on a blanket endorsement of vaccines. - Throughout, the dialogue emphasizes examining the medical reasons and evidence for specific vaccines and schedules, rather than broad generalizations about vaccines.

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.

COVID-19 vaccinations protect children from severe illness and reduce community spread, which goes against the science. Only 15 children between 0-19 years old died during the pandemic. Increased death tolls and adverse events arose after the COVID shots were rolled out. Before that, there was no pandemic, and children who died had serious comorbidities. Positive PCR tests were fraudulent due to high cycle thresholds between 40-45, leading to many false positives, making the test useless. The test's creator stated before his 2019 death that it was not designed to diagnose viral illnesses.

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.

In the Pfizer trial, more people died who received the vaccine than the placebo, raising concerns about vaccine safety. While the vaccine may save lives from COVID, data suggests at least 150,000 deaths may be linked to the vaccine. The focus on COVID prevention overlooks the potential harm caused by the vaccine, with a risk-benefit ratio of 117 children potentially dying to save one life. Doctors are silenced on this issue, leading to a lack of transparency in vaccine-related deaths.

A child named Maddie DeGary experienced severe side effects after receiving the COVID vaccine during clinical trials. She felt pain at the injection site and developed intense abdominal and chest pain. Concerns have been raised about the vaccine's safety, with claims of thousands of deaths in the United States. The vaccine's effectiveness has also been questioned, as a reanalysis of the trials suggested a higher likelihood of serious adverse events from the vaccine compared to hospitalization from COVID. Despite heavy promotion and potential coercion, vaccination rates for the booster shot remain low, with only 7% of adults and 2% of children receiving it. Many adults express reluctance to get vaccinated or vaccinate their children.

Pfizer presented evidence to the FDA on their trial for 6-month to 4-year-old children. Out of 4,526 children, 3,000 dropped out of the trial, which is concerning. The trial defined severe COVID as a slightly raised heart rate or increased breaths per minute. In the vaccine group, 6 children aged 2 to 4 had severe COVID compared to 1 in the placebo group. One child in the trial was hospitalized after vaccination. The trial twisted the data by ignoring cases of COVID during the 3-week gap between doses and the 8-week gap after the second dose. Ultimately, they only compared a small number of cases, claiming the vaccine was effective.

A child named Maddie DeGary experienced severe side effects after receiving the COVID vaccine during clinical trials. She felt pain at the injection site and developed intense abdominal and chest pain. Concerns have been raised about the number of deaths associated with the vaccine, with claims of 17,000 recorded deaths in the United States alone. A reanalysis of Pfizer and Moderna's trials suggested that the vaccines had a higher likelihood of causing serious adverse events compared to being hospitalized with COVID. Despite these concerns, the vaccines were heavily promoted and even mandated in some cases. Vaccination rates for the latest COVID booster remain low, with only 7% of adults and 2% of children receiving the shot.

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 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.

According to VAERS, there have been 38,000 deaths from COVID shots, but instead of being pulled, the FDA has doubled down and put the shots on the childhood vaccine schedule. Babies are expected to get three COVID shots by nine months old. The shots are still under EUA status for the under 12 age group and are not fully FDA approved, yet they are on the vaccine schedule. The CDC states that nine million American children have received the latest version of these COVID shots. There is concern about myocarditis. It is believed that the shots should have been shut down a long time ago.

Dr. Claire Craig, a diagnostic pathologist and co-chair at the Heart Group, discusses the evidence presented by Pfizer to the FDA regarding their trial on children aged 6 months to 4 years old. She highlights the concerning drop-off rate of 3,000 out of 4,526 children in the trial and questions the reasons behind it. Dr. Craig points out that the trial defined severe COVID based on minor symptoms such as a slightly raised heart rate or increased breaths per minute. She raises concerns about the higher number of severe COVID cases in the vaccine group compared to the placebo group. Additionally, she criticizes the manipulation of data by ignoring significant periods and focusing on small numbers to claim vaccine effectiveness.

Excitement surrounds the discussion of Pfizer's top-selling drugs as of 2019, which includes four medications and one vaccine. The clinical trials for these drugs involved long-term safety follow-ups, often lasting several years with placebo control groups to assess various health impacts. In contrast, the vaccine Prevnar had only a six-month safety review, using another vaccine as a control rather than a true placebo. This raises concerns about the thoroughness of safety evaluations for childhood vaccines, which are administered multiple times in the first six months of life. The disparity in study lengths suggests that economic interests may drive pharmaceutical companies to minimize safety testing to expedite market entry, raising questions about regulatory oversight.

According to Pfizer documents, one month after the vaccine rollout in November 2020, Pfizer knew the vaccines didn't stop COVID and identified vaccine failure. Internal documents showed COVID was the third most common side effect. Within months, Pfizer hired 2,400 staffers to process adverse event reports. By May 2021, Pfizer and the FDA knew the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The CDC initially claimed the injection materials stayed in the injection site, but Pfizer knew the materials biodistribute throughout the body within 48 hours, settling in the brain, liver, adrenals, and spleen. In women, they accumulate in the ovaries, and there's no known mechanism for the body to eliminate the lipid nanoparticles from the ovaries.

Pfizer's claim of 96% efficacy for their vaccine was questioned. The study and data were not independently verified, and Pfizer wanted to keep the data hidden for 75 years. The true effectiveness of the vaccine, based on absolute risk reduction, is less than 1%. More people died and were harmed in their trials compared to the placebo group. The vaccine's safety was questionable from the start, and it is not effective. Additionally, appropriate studies were not conducted for new variants.

The evidence shows that out of 344 babies in a Pfizer trial, only 3 completed it, with reasons like hospitalization and death leading to discontinuation. Less than 1% of babies finished the trial, yet it's claimed to be safe. The speaker questions the safety of these injections, citing reports of babies experiencing symptoms similar to sudden infant death syndrome.

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.

None of the vaccines, including the COVID vaccine, have undergone proper testing. No childhood vaccine has completed a placebo-controlled clinical trial with sufficient duration and power to confirm its safety before being administered to millions of children in America. This is not an opinion; it can be verified by anyone visiting the FDA website, where the package inserts and clinical trial documents are available for review.