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For years, I claimed that none of the 72 vaccines mandated for children underwent proper safety testing in placebo-controlled trials. When I confronted Fauci about this, he couldn't provide the study he claimed existed. After suing him, we received confirmation that no such study was ever conducted. The lack of liability and safety testing saves pharmaceutical companies significant costs, leading to a rush to add unnecessary vaccines to the schedule. This has resulted in a dramatic increase in chronic diseases among American children since 1989, including a rise in neurological disorders and autism, which has skyrocketed from 1 in 10,000 to 1 in 34 today.

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The Institute of Medicine reported in 2011 that over 150 vaccine-related injuries have not been studied, and the CDC has repeatedly been ordered to conduct these studies but has refused. The pharmaceutical companies producing vaccines, such as Merck, Sanofi, Glaxo, and Pfizer, have faced over $35 billion in penalties for misconduct. Trust in these companies is misplaced without solid scientific evidence. While vaccines should remain available for those who choose them, there is a need for rigorous scientific scrutiny. The FDA has misled the public in the past, as seen with Vioxx and opioids, raising concerns about their credibility regarding vaccine safety. The focus should be on ensuring public health, not pharmaceutical profits.

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According to the speaker, most vaccines have never been tested in a randomized, placebo-controlled trial to evaluate their safety. The speaker claims that vaccines contain aluminum compounds because many dead vaccines don't mount an immune response without them. The speaker alleges that in a Gardasil vaccine study, the placebo group received an aluminum adjuvant instead of a true placebo, resulting in similar side effect profiles between the active vaccine and placebo groups. The speaker asserts that Merck used a novel aluminum compound and that data suggests aluminum in vaccines is profoundly toxic. The speaker states that the only true randomized controlled trial involving a vaccine was conducted on sheep with blue tongue disease. The results allegedly showed that the aluminum in the vaccine was toxic, causing the sheep to become sick, unsociable, and, in some cases, die. The speaker concludes that the assumption that aluminum adjuvants in vaccines are safe is unfounded and has never been tested.

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Bill Gates and WHO promoted the DTP vaccine, which was withdrawn in the US due to safety concerns. Despite this, it was given to African and Asian children. Danish scientists found that girls who received the vaccine were 10 times more likely to die from various illnesses. The vaccine's dangers were not noticed for 30 years due to lack of placebo-controlled trials, highlighting a widespread issue in vaccinology.

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Congress investigated ACIP over two decades ago, finding conflicts of interest. In 2002/2003, four of five people who added the rotavirus vaccine had direct financial interest; one voted the rotavirus vaccine onto the schedule and sold his rotavirus vaccine for $186 million. Congress found that 97% of ACIP members had undisclosed conflicts. According to the speaker, a critical issue is adding new vaccines without pre-licensing safety studies. In 1986, there were 11 vaccines on the schedule; now, children must take 69 to 92 vaccines to stay in school in some states, none of which have been safety tested in pre-licensing placebo-controlled trials. The speaker states that the people in charge are now gone, and new, credentialed scientists and physicians will be brought onto the ACIP panel to do evidence-based medicine and make objective public health determinations based on science.

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Changes to ACIP are occurring after over two decades of congressional investigation. In 2002/2003, a government oversight committee found conflicts of interest, citing that four out of five people who added the rotavirus vaccine to the schedule had direct financial interest in it. One individual voted the rotavirus vaccine onto the schedule and then sold his rotavirus vaccine in development for $186 million. That year, Congress stated that 97% of ACIP members had undisclosed conflicts. The speaker claims that adding new products to the schedule without pre-licensing safety studies is malpractice. In 1986, there were 11 vaccines on the schedule, but now children must take between 69 and 92 vaccines to stay in school in some states, and none have been safety tested in prelicensing placebo-controlled trials. The speaker states that the people in charge are now gone, and new credentialed scientists and physicians will be brought onto the ACIP panel to do evidence-based medicine and follow the science.

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A lawsuit against Merck alleges mishandling of Gardasil safety tests. Internal emails reveal Merck knew the vaccine was contaminated with HPV DNA fragments, which can trigger harmful immune responses when bound to the vaccine's aluminum adjuvant. Pathologist Dr. Soo Han Lee discovered high levels of HPV DNA in vaccines in 2011. These DNA fragments can activate the immune system, potentially leading to autoimmune disorders like POTS, and in rare cases, death. Internal emails allegedly show Merck downplayed the risks and tried to convince regulators not to test for HPV DNA. Merck's chief medical officer admitted they never looked for HPV DNA in their vaccine, instead using flawed testing methods. The lawsuit raises questions about regulatory oversight and Dr. Lee is set to testify in February. The speaker advocates for transparency, thorough safety studies, and informed consent regarding vaccines.

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None of the 72 vaccines for children have been tested against a placebo. The speaker sued HHS in 2016 to find placebo studies for vaccines, but none were found. The safety testing for the polio vaccine was only 48 hours, while the hepatitis b vaccines were tested for 4-5 days. This means that any adverse events occurring after that time period were not considered. Without placebo testing, the risk profile of current vaccines is unknown, and it cannot be determined if vaccines cause more harm than good. The speaker questions the ethics of mandating medical products with unknown risks for children.

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Most people are unaware that vaccines contain aluminum. Studies have shown that aluminum and mercury, both present in vaccines, are highly toxic when combined. The safety data sheet for thimerosal, a mercury-containing compound, clearly states that it should never be combined with aluminum. However, the FDA failed to consider this when assessing the safety of vaccines. The CDC conducted studies on the vaccine safety data link (VSD) to prove that thimerosal was safe, but the results showed elevated risks of autism. The CDC then manipulated the data to downplay the risks. The Institute of Medicine (IOM) conducted flawed studies that wrongly concluded that thimerosal is not linked to autism. The CDC and pharmaceutical companies have actively worked to suppress the truth about thimerosal's harmful effects.

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The speaker claims that when the rotavirus vaccine was approved, four out of five board members had direct financial interests in it, working for the companies that made the vaccine or receiving grants to do clinical trials on it. One board member, Paul Offit, allegedly voted to add the rotavirus vaccine to the schedule while he had a rotavirus vaccine in development. The speaker says that because it's now on the schedule, his developing vaccine is virtually guaranteed to get on the schedule. The rotavirus vaccine that Offit voted on was withdrawn within a year because it was causing intussusception in kids. Offit's vaccine then replaced it. The speaker states that Offit and his business partners sold that vaccine to Merck for $186,000,000. The speaker says that Offit told Newsweek that he won the lottery and that it's been said of him that he voted himself rich.

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We couldn't find any prelicensing safety trials for the 72 vaccines doses that are recommended for American children. Unlike other medications, vaccines were exempt from conducting safety trials that compare health outcomes between a placebo group and a vaccine group. This lack of safety trials is concerning considering the widespread use of these vaccines.

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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.

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"Roll back in the time machine to August 2014, that is when Bill Thompson made the admission that the CDC had lied and hid the fact that the MMR vaccine was associated with autism." "Doctor Thompson freely admitted that he had covered it up and his associates at the CDC also covered it up." "Thimerosal causes autism like features and that's the way I would say it." "I'm completely ashamed of what I did." "Colleen is the center director. Frank is the director of immunization safety, and Marshall is the branch chief." "Doctor Julie Gerberding was head of the CDC at the time. Coincidentally, she went on to a lucrative career at Merck, the manufacturer of the MMR vaccine." "I'm like, oh my god. I cannot believe we did what we did. But we did."

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"Birtucil is probably the single worst mass vaccine that we've ever seen." "This vaccine targets millions of preteens and teens for whom the risk of dying from cervical cancer is zero." "Death rates in the Gardasil trials were thirty seven times the death rates for cervical cancer." "Children who take that vaccine, the Gardasil vaccine, are thirty seven times more likely to die from the vaccine than they are to die from cervical cancer." "So the problem with Gardasil, like most vaccines, is it was never tested against a true placebo, an inert placebo." "And the CDC and HHS say, if you don't test it against a true placebo, it's not science." "The entity that is actually performing the study is and paying for this study is Merck." "Merck got to decide which injuries were being caused by Gardasil and which were just bad coincidences." "They were able to license something that is insanely dangerous."

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Big problem with trusting the science is not the science part, it's who's behind the science part, primarily in the area of vaccines for children. Normally, when you study a drug, you compare it with a placebo, so that way you can truly test the side effects on something, but that is not how they test children's vaccines. This so called placebo control is not really a true placebo control because it's not inert. It's an active vaccine with something called an adjuvant. The big one that they've been using for a long time is aluminum. My question is, how can you really truly test the safety and effectiveness of something if you're looking at the relative safety of an active vaccine to another active vaccine with adjuvants. That just muddies the water to this whole safe and effective claim that you keep hearing over and over and over.

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The speaker discusses the issue of unvaccinated individuals and the lack of studies conducted by the government. They argue that giving the vaccine to everyone absolves the government of understanding its effects. However, they found studies in plain sight that compared vaccinated and unvaccinated children. Over 100 such studies are featured in the book, with very few coming from the federal government. The FDA claims it is not their job to conduct these studies, but the problem lies in the funding of studies by those who stand to profit from the products. The Centers for Disease Control and Prevention (CDC) should be evaluating the risks associated with vaccines, especially when given together, but they have been negligent in doing so. The speaker suggests that vaccines should undergo placebo-controlled trials like other drugs.

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The speaker states they searched for years for a pre-licensing safety trial of the 72 vaccine doses effectively mandated for American children. They claim that every other medication requires a safety trial comparing health outcomes in a placebo group versus a vaccine group before FDA licensing. The speaker assumed this was also done for vaccines. They state they found out that vaccines were exempt from this requirement.

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Dr. Plotkin testified that there are two hepatitis B vaccines on the market: Engerix B by Glaxo and Recombivax HB by Merck. The clinical trial experience for Recombivax HB states that safety was monitored for only 5 days after each dose, which may not be long enough to detect autoimmune or neurological issues. There is no mention of a control group in the clinical trials. The manufacturer insert also reports hypersensitivity reactions, arthritis, autoimmune diseases, and nervous system disorders like Guillain Barre syndrome and multiple sclerosis after vaccination. However, no randomized placebo-controlled study was conducted before licensure. It would be ethically difficult to conduct such a study today, even though the vaccine is recommended by the CDC.

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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.

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Most people are unaware that vaccines contain aluminum. Studies have shown that aluminum and mercury, when combined, are highly toxic. The safety data sheet for thimerosal, a mercury-containing compound, clearly states that it should not be combined with aluminum. However, the FDA failed to consider this when assessing the safety of vaccines. The CDC conducted a study on vaccine side effects, but manipulated the data to downplay the risks of thimerosal. The Institute of Medicine (IOM) was paid by the CDC to review the evidence, but their conclusions were flawed and biased. The CDC and pharmaceutical companies worked together to protect themselves from lawsuits, while disregarding the potential harm caused by thimerosal.

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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.

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According to the speaker, vaccines have never been tested in a randomized, placebo-controlled trial to evaluate their safety. The speaker claims that vaccines contain aluminum compounds because many dead vaccines don't mount an immune response without them. The speaker alleges that in a Gardasil vaccine study, the placebo group received an aluminum adjuvant instead of a true placebo, so the side effect profiles of the active vaccine and placebo groups were the same. The speaker asserts that Merck used a novel aluminum compound and that data shows aluminum in vaccines is toxic. The speaker states that the only completely randomized controlled trial was on sheep using a vaccine for blue tongue disease. The speaker claims the aluminum was toxic, the sheep became sick, their behavior changed, and many died compared to the placebo group. The speaker concludes that the presumption that aluminum as an adjuvant is safe is unfounded and has never been tested.

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Gardasil is claimed to be the worst mass vaccine ever, targeting preteens and teens at zero risk of dying from cervical cancer. It's alleged that death rates in Gardasil trials were thirty-seven times higher than cervical cancer death rates, implying children are thirty-seven times more likely to die from the vaccine than from cervical cancer. The claim is that Gardasil, like most vaccines, wasn't tested against a true inert placebo, which the CDC and HHS require for scientific validity. Merck, who funded and performed the study, allegedly decided which injuries were caused by Gardasil, writing off others as coincidences. This was possible because the control group received aluminum neurotoxins, causing injuries identical to those in the Gardasil group, allowing Merck to avoid reporting vaccine injuries and license a dangerous product.

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For years, I claimed that none of the 72 vaccines mandated for children underwent safety testing in placebo-controlled trials. Despite Tony Fauci's denials, I challenged him to provide evidence. He admitted he didn't have it on hand and promised to send it, but I never received it. After suing him, his lawyers confirmed there was no such study. The lack of liability and safety testing allows pharmaceutical companies to profit significantly, as the government mandates vaccines for millions of children. This has led to a surge in unnecessary vaccines, contributing to a dramatic rise in chronic diseases among American children since 1989, including conditions like autism, which has increased from 1 in 10,000 to 1 in 34.

Keeping It Real

VACCINES: HONEST ANSWERS with Dr. Joel Warsh

Guests: Dr. Joel Gator Warsh

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The episode presents a wide‑ranging, data‑driven discussion about vaccines with Dr. Joel Warsh, a pediatrician and epidemiology trained clinician who authored a book aimed at balancing vaccine questions with evidence. The conversation centers on how vaccine safety is communicated, the medical community’s approach to risk, and why concerns persist among parents who notice rising autoimmune and allergic conditions, chronic illnesses, and debates over autism. Warsh stresses that vaccines are not anti‑vaccine; rather, the aim is open dialogue, rigorous safety review, and better public understanding of benefits versus harms. He notes that many questions get short shrift in public discourse, and he advocates transparency, nuance, and ongoing research rather than absolutist declarations about safety being “debunked.” The dialogue dives into core concepts of safety testing and trial design, explaining the difference between inert placebo controls and comparisons against other vaccines or existing vaccines. The guests discuss how safety signals are collected, the role of VAERS, and whether long‑term, large‑scale data can convincingly rule out rare adverse events. They debate the interpretation of data around autism, noting the scarcity of comprehensive, prospective studies across all vaccines beyond MMR and thimerosal and arguing that unanswered questions should prompt more research rather than definitive dismissals. A substantial portion is devoted to the ethical and societal questions of mandates, coercion, and herd immunity. The hosts explore how individual risk assessments intersect with the social contract to protect vulnerable populations, acknowledging that definitions of “safe” and “enough” vary widely. They discuss vaccine technologies—old versus new—and adjuvants, including aluminum and trace metals, as well as the development of mRNA vaccines, their testing history, and what “emergency use” really means. Throughout, the conversation emphasizes the importance of listening to skeptical voices, testing assumptions, and pursuing healthier, safer vaccines while avoiding vilification of dissenting views. The episode concludes with calls for more balanced media coverage and collaborative dialogue among scientists, clinicians, policymakers, and parents to restore trust and improve vaccine safety in practice.