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The discussion centers on concerns and policy questions regarding pediatric vaccines, their safety, and how authorities respond to families who choose not to vaccinate. Key points raised by Speaker 0: - Pediatric vaccination schedules are increasing, with currently up to about 30 doses from birth to 2 years. Some vaccines, such as the hepatitis B vaccine, the acellular pertussis (3-in-1) vaccine, and the influenza vaccine given after 6 months, contain additives such as thiomersal (mercury-containing compound) and aluminum adjuvants. There is worry among some about potential long-term effects on brain development from thiomersal and other additives. - Thiomersal in vaccines is described as an organomercury compound that decomposes to ethyl mercury; historical notes are given about its association, in some sources, with developmental disorders in the 1990s, and there is reference to materials from the Ministry of Health, Labour and Welfare explaining its presence in certain vaccines and associated documentation. - The vaccine components discussed include thiomersal in current hepatitis B vaccines (e.g., Belcevir or Veemegen trade names), and aluminum-containing compounds in combination vaccines and the cervical cancer vaccine (HPV). There are concerns about neurotoxicity and memory impairment reported in some sources, and questions are raised about how these substances are evaluated in light of pediatric metabolism and excretion. - The text also points to broader concerns about modern additives in foods (artificial sweeteners, neonicotinoids, tar dyes) as part of a context for questioning vaccine safety, though the central focus remains vaccines and their additives. Speaker 0 also emphasizes a paradox: despite declining birth rates, the number of children with developmental disorders such as ADHD, autism spectrum disorders, and learning disabilities has risen, leading to heightened parental anxiety about early vaccination (birth to 2 months). The speaker highlights that even if experts claim the amounts are tiny, parents’ concerns persist. A call is made to present attached documentation and graphs to explain these points, as well as the overall safety profile. Questions and responses about policy and practice: - Speaker 1 explains preventive vaccination law (Article 8 and 9) authorizing municipalities to issue guidance and reminder notices for vaccinations, including vaccines against measles, rubella (MR), HPV, and Japanese encephalitis (the latter appears in the discussion as often related to catch-up schedules). The notices are for encouragement, not coercive mandates. - On the issue of refusals and potential neglect: it is stated that vaccinating of unvaccinated children is not, by itself, considered neglect; the decision to not vaccinate does not automatically constitute abuse or neglect. The speaker emphasizes that the question is about ensuring access to vaccination information and avoiding punitive labeling. - The role of childcare facilities and schools: there is discussion about whether vaccination status affects eligibility or admission. It is clarified that vaccination history is part of health records but does not automatically disadvantage a child in admission processes. Authorities acknowledge that some educators may view non-vaccination as neglect, and there is a preference to improve information sharing and awareness so that staff understand vaccination matters without stigmatizing families. - The need for uniform understanding among healthcare workers and educators is stressed. It is suggested that vaccination-related information be shared between childcare, school administration, and health departments to minimize misunderstandings and to ensure equitable treatment. - There is acknowledgement of concerns about social attitudes toward families who opt out of vaccination, and a call to respect differing judgments while improving communication and education among professionals. Speaker 3 and 4 contribute: - They reiterate that in childcare settings, health screening and eligibility processes may consider vaccination history, but not in a way that inherently disfavors unvaccinated children. They also address the possibility of attitudes among staff about neglect, noting a need for consistent information, training, and collaboration to reduce stigma. - A broader aim is expressed: foster a society where mutual respect for different vaccination decisions is possible, supported by clear communication and shared information among healthcare providers and educators. Overall, the discussion distinguishes between official guidance and punitive actions, reinforces that unvaccinated status alone is not treated as neglect, and calls for better information-sharing and supportive responses to families navigating vaccination decisions.

Let's examine the contents of vaccines, particularly thimerosal, which is highly toxic and can cause serious health issues, including damage to the kidneys, respiratory system, and nervous system. It is also linked to reproductive and developmental toxicity, raising concerns about autism and other neurodevelopmental disorders. Thimerosal is a common preservative in vaccines, notably in the influenza vaccine, which is recommended annually for pregnant women, infants, and children. It's important to note that thimerosal is not added at the end of the manufacturing process; vaccines must be specifically produced to be thimerosal-free.

The speaker believes all vaccines are suspect. As an emergency medicine physician, the speaker thought vaccines only contained a dead or attenuated virus and saline. In September 2000, after reading a package insert and researching vaccines, the speaker was mortified to learn that a child receiving all scheduled vaccines gets almost 13,000 micrograms of aluminum, almost 600 micrograms of mercury, and over 200 chemicals. The speaker states that this is why vaccines have never been proven safe, and vaccination is like injecting foreign matter into a baby.

Flu vaccines are administered annually starting at six months old, with nine branded options available in the U.S. A CDC document lists all vaccine ingredients, revealing that three flu vaccines contain hydrocortisone, a corticosteroid known to suppress the immune system. This raises questions about the effectiveness of flu vaccines, which are marketed to boost immunity. Additionally, one vaccine contains Madine Darby canine kidney cells, which are highly susceptible to the flu virus. Other concerning ingredients include formaldehyde and polysorbate 80, which can affect the blood-brain barrier. The hepatitis B vaccine also contains MRC-5 cells derived from a fetus, prompting further scrutiny about the ingredients in vaccines and their implications for health.

We documented six sixty 1 trials using inert placebo controls. We confirmed that all 16 antigens routinely recommended for children have been studied in placebo controlled trials. The claim that childhood vaccines haven't been tested against placebos is demonstrably false. Of the 661 trials, 567 were not a routine injected vaccine for disease on the CDC's childhood schedule; the remaining 94 studies, 70 did not involve healthy children; of the remaining 24, 21 did not involve a US licensed vaccine. That leaves us with three studies, three, that were claimed to have an inert control that were relied upon to license a routine injected childhood vaccine. One varicella trial was only a few 100 people and underpowered; it was an inert control but actually neomycin. Gardasil 4: control group mostly aluminum adjuvant; few 100 labeled inert control but not inert. Gardasil 9: saline after three Gardasil 4 doses. So, zero trials.

Speaker 0 describes a highly significant and controversial issue surrounding human papillomavirus (HPV) vaccines, including Gardasil and Cervarix, and reports that lawsuits are occurring worldwide. In Japan, there have been major lawsuits with hundreds of plaintiffs, including young women and girls, though the fundamental problem, according to the speaker, centers on contamination with DNA impurities. The speaker states that from the early days of the Ministry of Health, Labour and Welfare in Japan, the core issue has been the contamination with DNA impurities in vaccines, and that this problem had already become clear by 2012 in a widely cited paper. The speaker explains that by 2012, a paper described the DNA contamination in Gardasil-related vaccines, specifically noting residual DNA fragments from HPV types 16 and 18 associated with the vaccine’s aluminum adjuvant particles. The claim is that vaccine samples contained residual HPV DNA fragments that were directly bound to aluminum adjuvant particles, and that PCR tests confirmed these DNA fragments were identical to the HPV sequences described in the paper. The speaker emphasizes that researchers around the world—doctors and researchers listening to women and girls’ voices—noticed unusual, severe post-vaccination symptoms in children and young women, and saw potential links between these symptoms and the residual HPV DNA attached to adjuvants. The testimony references samples gathered from multiple countries (Australia, Bulgaria, France, India, New Zealand, Poland, Russia, Spain, and the United States) and asserts that nearly all of the Gardasil/HPV vaccine lots examined contained residual HPV DNA attached to aluminum adjuvant particles. The speaker mentions that in the specific investigation, sixteen samples of Gardasil-4 contained residual HPV DNA fragments bound to aluminum adjuvant particles, and that all samples tested via PCR showed the same DNA sequence as described in the 2012 paper. The speaker claims that in 2014, the vaccine program for cervical cancer halted in Japan, and that the subsequent attention brought this issue to light publicly. The discussion attributes the major role to a Japanese expert, Ishii Ken (Ishii-sensei), described as a leading figure in Japan’s vaccine adverse-event research. The speaker recounts that, in the years around 2012–2014, efforts involved international collaboration with HR/HSA, FDA, and others, although logistical obstacles caused delays. The speaker notes that in 2012, 16 vaccine packages were distributed in nine countries for examination and that contamination persisted in all samples. They credit Japan with acting as a global relay for disseminating information about DNA contamination and its potential health implications. Further, the speaker references a broader context: the later emergence of literature discussing how DNA contamination might relate to adverse neurological or systemic symptoms, and the evolution of guidelines on acceptable residual DNA in vaccines. The discussion mentions that WHO and FDA guidelines permit changing permissible DNA limits over time, with higher thresholds introduced for manufacturing and regulatory purposes, raising questions about what constitutes safety and what is permissible in drug development. The dialogue closes with Speaker 1 alluding to the seriousness of the issue, noting deaths in the context of messenger-type vaccines and subsequent debates about vaccine safety, while acknowledging that those opposed to this view are also active.

Hepatitis B is contracted through sexual activity and IV drug use. The speaker believes babies do not need the hepatitis B vaccine. The hepatitis B vaccine contains 250 micrograms of aluminum. The speaker states that after Thimerosal was removed from vaccines, the hepatitis B vaccine was moved from being given to teenagers to newborns. The speaker claims the amount of aluminum in the vaccine is five times the adult daily maximum.

The speaker argues that modern childhood vaccines contain a variety of unusual and controversial ingredients. They list specific components as included in vaccines: gelatin from boiled pigskin, chicken embryo protein, blood from the hearts of cow fetuses, DNA fragments from human fetuses, oil extracted from shark livers, proteins from worm ovaries, and DNA fragments from monkey kidneys. The speaker compares this mix to a Shakespearean recipe, saying, “eye of Newt, toe of frog, lizard's leg, tongue of dog,” and evokes a mental image of Gates, Offit, and Hotez in a witch’s brew assembling these substances. They then enumerate additional ingredients in modern childhood vaccines: formaldehyde (described as bad), polysorbate 80 (linked to infertility), and potassium chloride (noting it is the chemical used in third injections in lethal injections by executioners, though acknowledging infants receive far less). The list continues with sodium borate and Triton X, described as being in spermicides, and until very recently, ethyl mercury. The speaker questions why there are so many different ingredients and references a source from a book (and a hint that ChatGPT can provide it) that purportedly explains “a kind of insane reason for each of these.” The speaker emphasizes the insistence that each ingredient has a very important purpose, countering the idea that one does not need to understand the science. They state they do not want mercury injected into their kids, using that as a personal stance against the presence of mercury in vaccines. The overall message is a strong distrust of vaccine ingredients, highlighted by vivid comparisons, lists of chemical and biological components, and a personal declaration against mercury.

For the past 23 years, I've focused on raising awareness about vaccine-related issues, asserting that vaccines are unsafe, ineffective, unnecessary, and harmful. Initially, I believed vaccines contained only dead or weakened viruses and saline. However, after reading a package insert in September 2000, I discovered that children receiving the full vaccination schedule are exposed to nearly 13,000 micrograms of aluminum, 600 micrograms of mercury, and over 200 different chemicals. This revelation shocked me, highlighting that vaccines have never been proven safe. Vaccinating a child means injecting foreign substances into a precious life.

"72 mandated vaccines by the age of 18." They start injecting pregnant women second trimester. "In 1986, congress gave big pharma carte blanche, put in whatever you want. You have absolutely no liability." "And in that year, the vaccine schedule tripled." "Babies are getting seven shots at the same time." "This shot is experimental and on and you it did not get FDA approval. That was a complete fraud." "under an EUA, emergency use authorization." The synthetic mRNA is a program that they put into your body. It instructs your cells to produce the spike protein. The spike protein in itself creates the disease. It also contains fetal cell lines, kidney cells, retinal cells, lung cells. These are immortal meaning that they are cancerous. The COVID contained polyethylene glycol. Seventy percent of people are allergic to this. Luciferase. The shot contains a bioluminescent dye.

In 1989, 10 shots were given as part of the vaccine schedule. Compared to other Western countries, we give twice as many shots. The question is, do we really need all these vaccines? We should educate ourselves and make informed decisions as parents. We can't assume that those in charge of public health always have our best interests at heart. Some doctors seem hesitant to learn more about vaccines, which can save lives and prevent diseases. It's important to note that the pharmaceutical industry heavily influences medical schools and the American Academy of Pediatrics. Vaccines are a booming business, worth billions of dollars. We need doctors to prioritize prevention and overall health, even if it means taking a financial hit.

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.

"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."

The speaker asserts that the vaccines given this morning in hospitals across America to newborns and others contain a long list of ingredients, including gelatin from boiled pig skin, chicken embryo protein, blood from the hearts of cow fetuses, human fetus DNA, oil extracted from shark liver, proteins from worm ovaries, monkey kidney DNA fragments, and then proceeds to mention the chemical ingredients formaldehyde, polysorbate eighty, potassium chloride, phenyl, borax, aluminum salts, mercury, and Triton X-100 (which is used in spermicides). The speaker emphasizes that potassium chloride is the ingredient used as the third injection when we execute people by lethal injection, noting that it is a smaller dose for infants, and explicitly states that they are not claiming it’s the same dose. The speaker then lists: formaldehyde, polysorbate eighty, and potassium chloride among the chemicals, followed by assertions that this combination includes substances the speaker believes people would not want to inject into their children. The speaker highlights the idea that parents should not inject their babies with something they don’t understand, and asserts that millions of Americans do exactly that every time they go to CVS or Long’s Drugs. The speaker paints a scenario where a 23-year-old assistant pharmacist—described as someone who doesn’t know what he’s mixing and doesn’t know what questions he’s supposed to ask—figures it out and gives your baby an injection, and notes that people go along with it.

We couldn't find a prelicensing safety trial for any of the 72 vaccines doses 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.

Pentacel is five in one vaccination by Sanofi Pasteur. It covers diphtheria, tetanus, pertussis, polio, Hib, indicated for six weeks through four years, with four doses at two, four, six months, and between fifteen and eighteen months. Section five warns: Guillain Barre syndrome; a review by the Institutes of Medicine found evidence of a causal relationship between this vaccine and Guillain Barre syndrome. It contains one point five milligrams of aluminum phosphate as an adjuvant, polysorbate eighty, residual formaldehyde, bovine serum albumin, streptomycin, neomycin, polymyxin B. All this in a two month old. Pentacel has not been evaluated for carcinogenic or mutagenic potential or impairment of fertility. Translation. We don't know if this vaccine could lead to cancer or impair this child's ability with fertility later in life.

The speakers discuss the vaccination landscape around human papillomavirus (HPV) vaccines, focusing on a controversial issue they claim has been known and disseminated since early on: contamination with DNA (DNA residuals) from Deinococcus or related genetic material in vaccines and the implications of aluminum adjuvants used in Gardasil/Gardasil 9. - They begin by asserting that HPV vaccines, including Gardasil/Sil, have been the subject of remarkable legal actions worldwide, including four major lawsuits in Japan. They note that historically, in Japan, many young women and girls stood as plaintiffs, and that the core problem they highlight is the DNA contamination issue (referred to as “ディー エ ヌ エー 混 入 汚 染 問 題”). - The claim is that from early on, the Japanese Ministry of Health, Labour and Welfare and others acknowledged this contamination as central. They reference a 2012 paper that reportedly made the DNA contamination problem very clear, naming pathogens such as Human Papillomavirus, HPV, and DEIN? They describe that vaccine particles (HBV? HPBL DNA fragments) were found to be directly bound to aluminum adjuvant particles in Gardasil, implying a mechanism by which residual DNA could be involved in adverse effects. - The speakers say that the 2012 study, and subsequent work, led to attention from doctors worldwide who listened to the voices of women and girls and wondered what was happening with the vaccine recipients. They claim that samples showed that residual HPV DNA fragments were consistently present and directly linked to aluminum adjuvant particles, and that “PCR” detection indicated the same DNA sequences across samples. They mention that the 2012 paper’s findings were followed by reporting that, by 2014, vaccination had been suspended in Japan earlier than many would have expected. - They recount a process in which major scientists from various countries (France, the UK, and others) were involved in investigating adenoviral or genetic components (they reference Shihan? and others) and that the Japan-based researchers, including Ishii Ken, were central figures. They describe meetings, PowerPoint presentations at a hotel, and a sequence of visits to the UK and the US (including HR-related planning with U.S. FDA and the UK authorities) that were interrupted by closures in the Obama era, leading to documentation and discussions about the safety concerns. - The speakers claim that by the 2012 report and again by 2014, all vaccine samples from multiple countries contained residual DNA, and that Japan became a hub for disseminating awareness of these issues globally. They state that the issue was present not only in the early Gardasil (Gardasil-4) but also in later forms, with references to Gardasil-9 and the idea that the DNA contamination and adjuvant interactions could contribute to immune and neurological symptoms in recipients, particularly in women and girls. - They discuss changes to WHO and FDA guidelines on residual DNA limits, noting a progression from 10 picograms to higher thresholds over time, implying corporate interests in allowing higher residual DNA quantities in vaccines. They emphasize that the shift in limits is tied to pharmaceutical companies’ needs, not human biology changes, and argue that Japan highlighted the problem of Deinance-DNA contamination during the cervical cancer vaccine era, signaling that researchers, journalists, and victims were aware long before others. - Finally, Speaker 1 adds that two points became clear a year earlier: the disruption of messenger RNA–type vaccines as a response to safety concerns, and the subsequent rise in adverse outcomes after widespread vaccination, including deaths, which they claim intensified opposition to these vaccines. Note: The summary presents the speakers' claims and sequencing of events as described in the transcript without evaluation or endorsement.

In 1989, the vaccine schedule increased from 10 to 24 vaccines, all containing thimerosal with mercury. Children are injected with 400 times the amount of mercury considered safe by the FDA or EPA. A newborn receives a hepatitis B shot, but under EPA guidelines, would have to be 275 pounds to safely absorb it. In 1988, autism affected 1 in 2,500 children; now it affects 1 in 166. Additionally, 1 in 6 children have learning, neurological, speech, or language disorders, ADD, or hyperactivity, all connected to autism. The federal government claims there's no good science linking vaccines to autism, but science is often diluted in politics. While it can't be proven now, intuitively, the speaker believes that thimerosal causes autism.

Vaccines contain various ingredients, including viruses, ethylmercury, aluminum, phenol formaldehyde, antifreeze, foreign RNA and DNA, animal DNA, and nanotechnology. These components can pass through the blood-brain barrier. The SV 40 virus, which could be deadly, was a result of undisclosed research. The scientist who discovered it, Dr. Mary Sherman, was killed, and her work was likely confiscated. The fear of germs persists, but having a strong immune system can protect against them.

- Approximately 3.6 million newborns are born in the United States each year. The American Academy of Pediatrics (AAP) recommends that every single one of them receive an intramuscular dose of vitamin K1. - The package insert for vitamin K for the newborn includes a black box warning—the highest level of warning required by the FDA. It states that severe reactions, including fatalities, have occurred during and immediately after intravenous and intramuscular injections of vitamin K. - The package insert notes that the product contains aluminum, which may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration, and premature neonates are particularly at risk. - In section 13.1 of the package insert, it states: “Studies of carcinogenicity, mutagenesis, or impairment of fertility have not been conducted.” Translation: there is no information on whether the product could lead to cancer or interfere with reproductive health later in life. - The package insert also notes that deaths have occurred after intramuscular administration and references the black box warning. It states that whenever possible, the FDA package insert says vitamin K should be given by the subcutaneous route, yet the AAP recommends an intramuscular dose of vitamin K1. - The contrast highlighted is that the AAP’s recommendation for universal IM administration appears in the package insert, despite the FDA’s stated possibility of subcutaneous administration as a preferred route when feasible, and despite historical reports of severe adverse events and fatalities linked to IM (and IV) injections of vitamin K.

The speaker traces the origins and contents of vaccines from their earliest forms to modern childhood vaccines, presenting a sequence of claimed ingredients and comparisons. - The concept of a vaccine is said to have started from the word cowpox, with the idea that “cow pus” was used. Pus from cows was rubbed into wounds on people, leading to early vaccines. - They claim that practitioners experimented for a long time with various substances, including horse pus and cow pus from an infected horse’s hoof, rubbed into people. - Early vaccines are described as being steeped for years in a mix of ox bile, glycerin, and potato slices, which the speaker notes sounds like a joke but asserts to be true. - The evolution then moves to more modern-but-old-time ingredients, listing dried rabbit spinal cords, duck embryos, chicken blood, human bile (because it shouldn’t be wasted), ground-up rat spleens, and boiled pigskin as examples of earlier vaccine components. Switching to modern day vaccines, the speaker enumerates what is said to be present in today’s childhood vaccines: - Gelatin from boiled pigskin, described as similar to the old ingredient. - Chicken embryo protein. - Blood from the hearts of cow fetuses. - DNA fragments from human fetuses. - Oil extracted from shark livers. - Proteins from worm ovaries. - DNA fragments from monkey kidneys. The speaker then invokes a Shakespearean reference to Macbeth—“eye of Newt, toe of frog, lizard’s leg, tongue of dog”—to emphasize the appearance of a witch’s brew-like mixture in the composition of vaccines, suggesting that Gates, Offit, and Hotez are “sitting around in their witch’s brew putting this stuff together.” Further modern ingredients in childhood vaccines are listed: - Formaldehyde, described as bad. - Polysorbate eighty, claimed to be linked to infertility. - Potassium chloride, called out as the chemical injected as the third injection in lethal injections by executioners, noting that infants receive far less of it than executed individuals. - Sodium borate. - Triton X. - Ethyl mercury, stated as having been used “until very recently.” The speaker concludes with a strong personal stance: “I don’t want mercury injected into my kids. Period.” They recount a memory of a broken light requiring hazmat handling for mercury, contrasting that with the alleged injection of mercury into babies, and labeling the overall situation as crazy.

As a child, there were only 3 shots in 1960, but today's kids face 108 shots. After 13 shots at one visit, there's a 40% chance of brain injury and autism if a child has a seizure.

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.

Speaker 0 discusses the idea that doctors will say a preservative-free form is not necessarily safe. The claim is that a preservative-free label does not guarantee safety. The discussion then focuses on Polysorbate eighty (Polysorbate 80). It is stated that there are ten milligrams of Polysorbate eighty in the preparation being discussed. Polysorbate eighty is described as being used in research studies, particularly in cancer research for brain cancer drugs, because it is used to compare the drug with Polysorbate eighty and because it “opens up the blood brain barrier” which helps the drug get into the brain. The speaker asserts that Polysorbate eighty does the same thing when administered to babies, enabling the blood-brain barrier to be opened, and then, immediately after that, the hepatitis B vaccine is given with two hundred fifty micrograms of aluminum. The aluminum is said to have access to the brain immediately because of the Polysorbate eighty that is in the vitamin K shot. The speaker references a 2016 statement of concern about Gardasil, noting that Gardasil injections at that time contained fifty micrograms of Polysorbate eighty, and there was concern about polysorbate eighty causing premature ovarian failure. The claim is that polygsorbate eighty is used in clinical studies to induce infertility. The discussion then contrasts the amounts: when the vitamin K shot is injected, Amphastar has ten milligrams of Polysorbate eighty. So the concern is that there is a comparison between fifty micrograms in Gardasil and ten milligrams (which is two hundred times that amount). This discrepancy raises the question posed by the speaker: is the vitamin K shot a factor in the infertility problems that are claimed to be occurring in young people today?

We documented six sixty 1 trials using inert placebo controls and confirmed that all 16 antigens routinely recommended for children have been studied in placebo controlled trials. The claim that childhood vaccines haven't been tested against placebos is demonstrably false. Drilling into the 661 trials, 567 were not a routine injected vaccine for disease on the CDC's childhood schedule; the remaining 94 studies, 70 did not involve healthy children; of the remaining 24, 21 did not involve a US licensed vaccine. That leaves three studies claimed to have an inert control used to license a routine injected childhood vaccine. One varicella trial had only a few hundred participants and, though called inert, used neomycin instead. The Gardasil 4 trial's control group largely received an aluminum adjuvant injection; a few hundred labeled inert were not inert. The Gardasil 9 trial used a saline injection only after three doses of Gardasil 4. The result: zero trials used a placebo as well as a true inert control to license a routine injected vaccine on the CDC schedule.