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The CDC unanimously recommended the COVID-19 vaccine for 5 to 11 year olds, which has raised concerns about hidden incentives and liability immunity for manufacturers. The speaker questions the medical justification for vaccinating healthy children who have minimal risk from COVID-19 and already possess lifetime immunity. They argue that the potential harm from the vaccine outweighs the benefits, especially considering the limited testing done on children. The speaker compares the situation to the Tuskegee experiment, highlighting the lack of informed consent for children. They express shock and concern over the decision to vaccinate young children and believe it is an atrocity in the making. The speaker questions the justification of putting children at risk to protect others and emphasizes the importance of individual well-being.

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I am puzzled by Trump's support for mRNA vaccines and Peter Marks at the FDA. Marks, a key figure in Operation Warp Speed, now wants to use the same approach for cancer treatment. He advocates for speeding up drug approvals by easing FDA regulations. Marks controls information flow and defends the vaccine program, despite concerns like myocarditis. He is seen as the gatekeeper for vaccine information.

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Biden wants as many people as possible to get an annual COVID vaccine. The speaker claims that drug, food, and vaccine companies pay reviewers to approve their products. They believe that if everyone is required to get an annual vaccine, it will bring recurring money to these companies. Christopher Cole, an executive officer at the FDA, says the approval process for the vaccines will be gradual and eventually become an annual requirement like the flu shot. The speaker admits they don't completely agree with the process, especially for toddlers, as there may not be enough testing. However, all age groups are approved under emergency authorization, with the focus on the benefits outweighing the harm. The approval process for toddlers is related to COVID.

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

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Biden aims for annual COVID shots for everyone, benefiting drug companies financially. FDA executive Christopher Cole suggests gradual mandates, including for toddlers. Concerns raised about lack of complete testing for approval, especially for young children under emergency use authorization. Efficacy data standards lower for emergency use. COVID-related cases in toddlers justify approval process.

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Doctor Gruber discussed the need for further studies on myocarditis risk in pediatric populations before licensing the Pfizer vaccine. The FDA was aware of the risk before a meeting in July 2021. Vaccine mandates were not part of the FDA's considerations for licensure. Doctor Marks took over Gruber's responsibilities, appointed by Doctor Woodcock. The decision to approve the vaccine for children without proper testing is concerning, especially with reports of vaccine injuries. Congressional oversight is necessary for accountability and potential legislative reform. Marks pushed for a quicker timeline despite safety concerns, leading to the removal of top officials. The rush to mandate vaccines raises questions about prioritizing safety.

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The Food and Drug Administration granted final approval to the Pfizer COVID vaccine. Those hesitant due to its Emergency Use Authorization may now be more inclined to take it. The vaccine has been proven safe and effective and now has final approval. The speaker urges listeners to take the vaccine to save their life, and potentially the life of another.

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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.

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"The FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously green lighting four new COVID nineteen vaccines with twenty twenty five and twenty twenty six formulas." "The the reason for the revocation of that emergency youth authorization is because obviously the COVID pandemic and the public health emergency is over." "But just to correct the record because there's been a lot of misinformation on this, the FDA's decision does not affect the availability of COVID vaccines for Americans who want them." "We believe in individual choice. That's a promise both the president and the secretary have made, and it's a promise they have now delivered on."

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COVID-19 vaccines are described as safe and effective for various age groups, including children as young as five. Pfizer, Moderna, AstraZeneca, and Johnson & Johnson vaccines are highlighted. Studies and trials have confirmed the vaccines' safety and efficacy, with some showing high effectiveness in preventing symptomatic infections and severe disease. The FDA and European Medicines Agency have assessed and approved these vaccines. A booster shot different from the original vaccination is likely safe and effective. The vaccines are considered a key tool, along with mask-wearing and social distancing, to combat the spread of COVID-19 and return to normalcy.

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Joe Biden announced funding for a new vaccine, urging everyone to get it. Concerns have been raised about vaccine injuries, with reports of myocarditis, blood clots, and heart attacks. The pharmaceutical companies have not released their data on side effects. The speaker asks if the vaccine companies will be required to make this data public. The response is that they should, as transparency is important. The speaker emphasizes the need for facts to be made public immediately. They mention the unexpected nature of the pandemic and the devastating impact it has had globally. The conversation then shifts to President Biden's announcement of a new vaccine. The speaker questions whether the previous vaccine was ineffective and discusses the liability protection for pharmaceutical companies, which expires in December. They stress the importance of honesty and transparency from the companies regarding vaccine injuries. The speaker concludes by expressing the desperation of some people for the president's support in this matter.

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The question asked whether the president believes the COVID vaccine should be available to and covered by insurance for all Americans regardless of age and preexisting conditions. The response notes that the FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously approving four new COVID-19 vaccines with 2025 and 2026 formulas. The revocation is described as a consequence of the COVID-19 pandemic and the public health emergency being over. To correct the record, it is stated that the FDA’s decision does not affect the availability of COVID vaccines for Americans who want them. The administration says, “We believe in individual choice,” a promise the president and the secretary have made and delivered on.

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The speaker believes that gradually we will move towards mandatory vaccination, which will likely be implemented after the presidential election next year. However, before that, there will be an intermediate step of vaccinating children. The Pfizer laboratory has completed its study and found that the vaccine is effective and well-tolerated in children aged five to eleven. They have submitted their request for commercialization to the FBI in the United States. Cuba has already started vaccinating children from the age of two. Therefore, the question of vaccinating children aged two and above will arise.

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The FDA recently revoked the emergency youth authorizations for three COVID vaccinations while simultaneously green lighting four new COVID nineteen vaccines with twenty twenty five and twenty twenty six formulas. The the reason for the revocation of that emergency youth authorization is because, obviously, the COVID pandemic the public health emergency is over. But just to correct the record because there's been a lot of misinformation on this, the FDA's decision does not affect the availability of COVID vaccines for Americans who want them. We believe in individual choice. That's a promise both the president and the secretary have made, and it's a promise they have now delivered.

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Children aged 5 to 11 can now get the COVID vaccine to protect older and vulnerable individuals. The vaccine has low side effects, with only a few cases of heart inflammation out of millions vaccinated in the US. Getting COVID poses a higher risk of heart inflammation than the vaccine. Vaccinating kids can reduce school disruptions and help safeguard older people.

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We're seeing the tip of the iceberg. So right now, I think probably the most prominent, demonstration of that, is, what secretary Kennedy did with changing the childhood schedule for COVID nineteen. In that, we were directed that only children with underlying conditions would be the ones that should qualify for vaccination. That's not what the data shows. Six month old to two year old, their underlying condition is youth. Fifty three percent of those children hospitalized last season had no underlying conditions. The data say that in that age range, you should be vaccinating your child. I understand that not everybody does it, but they have limited access by narrowing that recommendation. Insurance may not cover it.

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Biden's successful vaccination efforts have expanded the list of who can administer shots, including veterinarians. However, one person believes that getting the vaccine actually lowered their immune system and caused them to contract COVID-19. In Florida, a statewide grand jury is being called to investigate any wrongdoing related to COVID-19 vaccines. The speaker expects the Oxford AstraZeneca vaccine to be authorized in the UK soon, which they believe will have a significant impact on the pandemic. Despite concerns, another person eagerly awaits their Pfizer vaccine appointment. Vaccine hesitancy is attributed to false information circulating on social media, despite vaccines being proven safer than other drugs.

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The government urges people to get vaccinated to protect themselves and others. Businesses are encouraged to require vaccinations for employees. Approval for vaccines for children aged 5 to 11 is sought to ensure school safety. The recent FDA approval may help increase vaccination rates.

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The Trump administration's Operation Warp Speed developed a COVID vaccine quickly, but critics argue that the program protected drug companies from liability for vaccine injuries. The government's compensation program for harm caused by vaccines has been criticized for being bureaucratic, with only 8 payouts out of 12,000 claims filed. The issue of liability for vaccine manufacturers has been a topic of debate since Reagan's presidency. Some argue that those harmed by vaccines deserve accountability and that free speech is crucial in discussing the merits of vaccines. There is a call to end crony capitalism and lobbying in government, with a focus on preventing government officials from joining companies they previously dealt with. The government's actions during the COVID-19 pandemic, including vaccine mandates and the approval of mRNA shots for young babies, are seen as problematic. There is a desire for accountability and a promise to clean house in agencies like the CDC, NIH, and FDA to prevent similar situations in the future.

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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.

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The CDC has recommended COVID vaccines for everyone over the age of 6 months, which contradicts the UK's recommendation for those over 65. The CDC's communication does not mention the vaccines being safe and effective. They provide some data on the estimated risk of hospitalizations prevented per 1,000,000 doses, but there is limited information on adverse reactions. The speaker questions the CDC's thinking and highlights the high number of adverse reactions compared to the number of hospitalizations prevented. They also mention the increase in the price of COVID vaccines and raise concerns about the independence and trustworthiness of drug regulators. The symptoms of COVID are similar to those of a common cold for most people.

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Speaker 0 questions whether it is a conflict of interest for government employees who profit from the vaccine to dictate vaccine policies. Speaker 1 responds that the government should decide. Speaker 0 asks about the higher incidence of myocarditis among adolescent males after vaccination. Speaker 1 claims that the data shows less risk with the vaccine compared to getting COVID. Speaker 0 disagrees and presents peer-reviewed papers contradicting Speaker 1's claim. Speaker 0 questions the scientific soundness of mandating three vaccines for adolescent boys and suggests having a rational discussion about one vaccine. Speaker 1 defers to public health leaders. Speaker 0 criticizes the CDC's recommendation to vaccinate children multiple times and compares it to other countries' approaches. Speaker 1 admits to vaccinating their own children multiple times. Speaker 0 argues that the risk of myocarditis after vaccination should be weighed against the risk of the disease. Speaker 0 also expresses concern about conflicts of interest in government decision-making.

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In this video, an executive officer at the FDA named Christopher Cole discusses the government's desire to mandate annual COVID vaccines for everyone, including young children. He mentions the financial relationship between the FDA and big pharma, with drug companies paying the FDA millions of dollars to approve their products. Cole expresses concerns about the approval process for vaccines in young children, stating that there haven't been enough tests done. He also mentions the lack of protection for whistleblowers and the pressure to stay silent within the government. Overall, the video raises concerns about the safety and efficacy of mandating annual vaccines for all age groups.

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No children died from COVID in 2020, so there is no need for them to be vaccinated. The government's role in this situation cannot be denied, and many Americans are outraged and angered by the lack of accountability. The worst thing to happen to our country and the world, in my opinion, is the ongoing vaccine mandates.

The Peter Attia Drive Podcast

#137 - Paul Offit, M.D.: An expert perspective on COVID-19 vaccines
Guests: Paul Offit
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In this episode of The Drive podcast, host Peter Attia interviews Dr. Paul Offit, a pediatrician and vaccine expert. Offit discusses his extensive background in infectious diseases and vaccines, including his role in the development of the rotavirus vaccine. The conversation focuses on the COVID-19 vaccine landscape, detailing the four main strategies for vaccine development: mRNA vaccines, viral vector vaccines, protein subunit vaccines, and inactivated or live attenuated vaccines. Offit explains the unprecedented speed of COVID-19 vaccine development, attributing it to initiatives like Operation Warp Speed, which mitigated financial risks for pharmaceutical companies. He emphasizes the importance of understanding the safety and efficacy of vaccines, particularly in light of past vaccine failures, such as the RotaShield vaccine, which was withdrawn due to safety concerns. The discussion also covers the historical context of vaccine hesitancy, particularly stemming from the fraudulent Wakefield study linking vaccines to autism. Offit expresses frustration over the persistence of anti-vaccine sentiments but acknowledges that public perception has shifted positively in recent years. Attia and Offit delve into the specifics of vaccine trials, explaining the phases of clinical trials and the significance of statistical analysis in determining vaccine efficacy. They discuss the importance of monitoring long-term effects and the challenges of distributing vaccines, especially given the logistical requirements for mRNA vaccines that need ultra-cold storage. Offit shares insights on the immune response generated by vaccines, highlighting the role of neutralizing antibodies and memory cells. He expresses cautious optimism regarding the potential for COVID-19 vaccines to provide lasting immunity, drawing parallels with other vaccines that have proven effective over time. The conversation concludes with Offit addressing the potential for future vaccines for children and the ethical considerations surrounding vaccine distribution. He emphasizes the need for continued research and monitoring to ensure the safety and effectiveness of vaccines as they roll out to the public. Overall, the episode provides a comprehensive overview of the current state of COVID-19 vaccine development and the complexities involved in ensuring public health.
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