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This is Aaron Siri deposing Dr. Stanley Plotkin, often called the godfather of vaccines, under oath. The Hepatitis B vaccine was licensed after safety was monitored for just 5 days following each dose. Five. When asked plainly whether 5 days is enough time to detect adverse reactions that occur... after 5 days, the answer was simple: No. The manufacturer’s own insert lists reported post-vaccination events including: 🛑Guillain-Barré syndrome. 🛑Multiple sclerosis and exacerbation of MS. 🛑Myelitis. 🛑Seizures. 🛑Peripheral neuropathy. 🛑Encephalitis. And yet, before licensure, there was no randomized, placebo-controlled trial - the study you would need to prove causation. We often hear how "hard" it is to prove causation. That wasn’t disputed. It was admitted. This isn’t rhetoric or speculation here; it’s sworn testimony. If “safe and effective” is the standard, then evidence matters. Watch the deposition:show more

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👀The Plotkin Deposition - Part III In Part III, Stanley Plotkin confirms a series of facts that are rarely acknowledged publicly, but matter deeply for informed consent: • Hepatitis B vaccines (Recombivax HB & Engerix-B) were licensed after safety monitoring of 4–5 days, with no placebo control groups • Serious neurological and autoimmune conditions are listed in manufacturer inserts — yet causation was never tested pre-licensure • Once a vaccine is placed on the CDC schedule, Plotkin admits it becomes “ethically difficult” to ever perform a proper placebo-controlled safety study • IPV (polio) safety was monitored for just 48 hours, and it was administered alongside DTP, making attribution of injury impossible • MMR: Plotkin cannot cite a single randomized, placebo-controlled pre-licensure safety trial despite decades of use • Gardasil (HPV) trials combined aluminum-adjuvant controls with saline placebo — masking the fact that the saline-only group showed 0% autoimmune events • Drugs given to sick adults undergo safety follow-up for years, while vaccines given to healthy babies are monitored for days ...AND MORE Watch The Plotkin Deposition – Part III and share your thoughts below.

👀The Plotkin Deposition - Part III In Part III, Stanley Plotkin confirms a series of facts that are rarely acknowledged publicly, but matter deeply for informed consent: • Hepatitis B vaccines (Recombivax HB & Engerix-B) were licensed after safety monitoring of 4–5 days, with no placebo control groups • Serious neurological and autoimmune conditions are listed in manufacturer inserts — yet causation was never tested pre-licensure • Once a vaccine is placed on the CDC schedule, Plotkin admits it becomes “ethically difficult” to ever perform a proper placebo-controlled safety study • IPV (polio) safety was monitored for just 48 hours, and it was administered alongside DTP, making attribution of injury impossible • MMR: Plotkin cannot cite a single randomized, placebo-controlled pre-licensure safety trial despite decades of use • Gardasil (HPV) trials combined aluminum-adjuvant controls with saline placebo — masking the fact that the saline-only group showed 0% autoimmune events • Drugs given to sick adults undergo safety follow-up for years, while vaccines given to healthy babies are monitored for days ...AND MORE Watch The Plotkin Deposition – Part III and share your thoughts below.

The HighWire

15,354 görüntüleme • 7 ay önce

Lawyer Aaron Siri says he was shocked when he saw how limited the safety monitoring was for licensed Hep B vaccines. “Here’s the Hep B vaccine. This is the package insert for Recombivax HB.” “434 doses of Recombivax HB 5 micrograms were administered to 147 healthy infants and children up to 10 years of age who were monitored for 5 days after each dose.” “First time I read this, I thought, there’s no way this can be it. There’s no way they licensed this product to be given to millions of babies based on that.” “No control group, not monitoring safety long enough, and not enough kids in it. It’s useless.” “That is what the FDA relied upon.” Aaron Siri

Lawyer Aaron Siri says he was shocked when he saw how limited the safety monitoring was for licensed Hep B vaccines. “Here’s the Hep B vaccine. This is the package insert for Recombivax HB.” “434 doses of Recombivax HB 5 micrograms were administered to 147 healthy infants and children up to 10 years of age who were monitored for 5 days after each dose.” “First time I read this, I thought, there’s no way this can be it. There’s no way they licensed this product to be given to millions of babies based on that.” “No control group, not monitoring safety long enough, and not enough kids in it. It’s useless.” “That is what the FDA relied upon.” Aaron Siri

Children’s Health Defense

24,545 görüntüleme • 3 ay önce

"No Vaccine On The Childhood Schedule Has Ever Been Tested Against A True Placebo." Del Bigtree "No Vaccine Has Ever Been Thoroughly Safety Tested." The Hep-B Vaccine Used Injected Aluminum As The 'Placebo...' 'Safety Tested' On 147 Children For Only 5 Days Before Approval. Every Single⏬Vaccine Safety Trial Period Is Listed In The Package Insert Under Section 6.1, Which States How Long The Trial Participants Were Observed To 'Prove Safety Of The Vaccine' Before Given CDC & FDA Approval. Think the vaccines have gone thru a long robust safety trial to prove they are 'safe & effective'? All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, not vaccines... Hep-B Vaccine: Administered to 147 infants & children who were monitored for 5 days, then granted approval. Gardasil HPV Vaccine: Safety was evaluated using vaccination report card (VRC)- aided surveillance for 14 days. Hep-A Vaccine: Test subjects were followed for safety for 14 days. Influenza A Vaccine: Participants were monitored for adverse events for 28 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored daily for 7 days. DTaP & TDaP Vaccines: Participants were monitored for 14 days. Chicken Pox Vaccine: Subjects were observed for adverse reactions for 42 days. Shingles Vaccine: Test subjects were followed for 7 days. Prevnar Pneumonia Vaccine: Participants were monitored for 7 days. RSV Vaccine: Safety monitored for 30 days. MMR Vaccine: Participants were followed for 42 days. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. No true placebo in a vaccine clinical trial skews all results & makes all vaccines appear "safe & effective" because the adverse events, side effects & Injuries in both groups are the same. List⏬Of 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo Was Injected Aluminum Adjuvant. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine. Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. COVID-19 Vaccine Clinical Trial...Placebo Was Meningitis Vaccine. 👇Hep-B Vaccine Package Insert👇 👇Gardasil HPV Vaccine Package Insert👇 👇Hep-A Vaccine Package Insert👇 Speaker: Alex Clark & Del Bigtree Podcast: Alex Clark

"No Vaccine On The Childhood Schedule Has Ever Been Tested Against A True Placebo." Del Bigtree "No Vaccine Has Ever Been Thoroughly Safety Tested." The Hep-B Vaccine Used Injected Aluminum As The 'Placebo...' 'Safety Tested' On 147 Children For Only 5 Days Before Approval. Every Single⏬Vaccine Safety Trial Period Is Listed In The Package Insert Under Section 6.1, Which States How Long The Trial Participants Were Observed To 'Prove Safety Of The Vaccine' Before Given CDC & FDA Approval. Think the vaccines have gone thru a long robust safety trial to prove they are 'safe & effective'? All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, not vaccines... Hep-B Vaccine: Administered to 147 infants & children who were monitored for 5 days, then granted approval. Gardasil HPV Vaccine: Safety was evaluated using vaccination report card (VRC)- aided surveillance for 14 days. Hep-A Vaccine: Test subjects were followed for safety for 14 days. Influenza A Vaccine: Participants were monitored for adverse events for 28 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored daily for 7 days. DTaP & TDaP Vaccines: Participants were monitored for 14 days. Chicken Pox Vaccine: Subjects were observed for adverse reactions for 42 days. Shingles Vaccine: Test subjects were followed for 7 days. Prevnar Pneumonia Vaccine: Participants were monitored for 7 days. RSV Vaccine: Safety monitored for 30 days. MMR Vaccine: Participants were followed for 42 days. 'True Placebo' Is Saline As The Comparative In A Vaccine Control Trial. That's Not What The Gov't Uses. No true placebo in a vaccine clinical trial skews all results & makes all vaccines appear "safe & effective" because the adverse events, side effects & Injuries in both groups are the same. List⏬Of 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo Was Injected Aluminum Adjuvant. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo Was Aluminum Adjuvant & Hep-A Vaccine. Hepatitis A Clinical Trial...Placebo Was Hep-B Vaccine. Influenza A Clinical Trial...Placebo Was Influenza B Vaccine. Meningitis Vaccine Clinical Trial...Placebo Was DTaP Vaccine. Pertussis Vaccine Clinical Trial...Placebo Was Diphtheria & Tetanus Vaccine. Prevnar-13 Pneumonia Clinical Trial...Placebo Was Prevnar-7 Vaccine. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine. Chicken Pox Vaccine Clinical Trial...Placebo Was Diluted Chicken Pox Vaccine. Shingles Vaccine Clinical Trial...Placebo Was Diluted Shingles Vaccine. COVID-19 Vaccine Clinical Trial...Placebo Was Meningitis Vaccine. 👇Hep-B Vaccine Package Insert👇 👇Gardasil HPV Vaccine Package Insert👇 👇Hep-A Vaccine Package Insert👇 Speaker: Alex Clark & Del Bigtree Podcast: Alex Clark

Valerie Anne Smith

46,282 görüntüleme • 1 yıl önce

"It Is A Myth That Vaccines Are Safe & Necessary...If I Had My Young Children Today, They Would Not Get A Single Vaccine." Dr Pierre Kory, MD "SIDS Occurs At 2, 4 & 6 Months Of Age...Right After Vaccination." "The Gov't Refuses To Do A True Placebo Safety Trial On Any Vaccine." Vaccines have not gone thru a long robust safety trial to prove they are 'safe & effective.' All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, but vaccines are not safety monitored this way. Hep-B Vaccine: Tested on only 147 infants & children, then monitored for 5 days & granted CDC approval. Hep-A Vaccine: Subjects were monitored for safety, 14 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored for 7 days. Prevnar Pneumonia Vaccine: Study volunteers were monitored for 7 days. MMR Vaccine: Subjects were followed for 42 days. RSV Vaccine: Participants were monitored for 30 days. DTaP & TDaP Vaccines: Subjects were monitored for 14 days. Gardasil HPV Vaccine: Trial participants were surveilled for 14 days. Vaccines have not been safety trialed against a saline placebo. They have all used Aluminum adjuvant or another vaccine as the placebo in clinical trials. Gardasil HPV Clinical Trial: placebo was the Hep-A Vaccine & Aluminum Adjuvant. Hepatitis A Clinical Trial: placebo was the Hep-B Vaccine. Influenza A Clinical Trial: placebo was the Influenza B Vaccine. Meningitis Vaccine Clinical Trial: placebo was the DTaP Vaccine. Pertussis Vaccine Clinical Trial: placebo was the Tetanus & Diphtheria Vaccine. Polio Vaccine Clinical Trial: placebo was Diluted Polio Vaccine. Vaxelis 6 in 1 Vaccine Trial: placebo was the DTaP, Polio, HIB & Hep-B Vaccines. Hepatitis B Clinical Trial: placebo was Aluminum Adjuvant. The countries that have the most infant vaccines on their childhood schedules, have the highest infant mortality. The United States is #1 in infant vaccines & #1 in infant mortality, of all industrialized nations. 97% of infants who die of SIDS, do so within 7 days being vaccinated. 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 👇Health Outcomes: Vaxxed Versus UnVaxxed👇 Speaker: Dr Pierre Kory, MD Video: @that_barefootgirlv

"It Is A Myth That Vaccines Are Safe & Necessary...If I Had My Young Children Today, They Would Not Get A Single Vaccine." Dr Pierre Kory, MD "SIDS Occurs At 2, 4 & 6 Months Of Age...Right After Vaccination." "The Gov't Refuses To Do A True Placebo Safety Trial On Any Vaccine." Vaccines have not gone thru a long robust safety trial to prove they are 'safe & effective.' All other pharmaceuticals are safety trialed for 2-6yrs before approval by the CDC & FDA, but vaccines are not safety monitored this way. Hep-B Vaccine: Tested on only 147 infants & children, then monitored for 5 days & granted CDC approval. Hep-A Vaccine: Subjects were monitored for safety, 14 days. Meningitis Vaccine: Local & systemic adverse reactions were monitored for 7 days. Prevnar Pneumonia Vaccine: Study volunteers were monitored for 7 days. MMR Vaccine: Subjects were followed for 42 days. RSV Vaccine: Participants were monitored for 30 days. DTaP & TDaP Vaccines: Subjects were monitored for 14 days. Gardasil HPV Vaccine: Trial participants were surveilled for 14 days. Vaccines have not been safety trialed against a saline placebo. They have all used Aluminum adjuvant or another vaccine as the placebo in clinical trials. Gardasil HPV Clinical Trial: placebo was the Hep-A Vaccine & Aluminum Adjuvant. Hepatitis A Clinical Trial: placebo was the Hep-B Vaccine. Influenza A Clinical Trial: placebo was the Influenza B Vaccine. Meningitis Vaccine Clinical Trial: placebo was the DTaP Vaccine. Pertussis Vaccine Clinical Trial: placebo was the Tetanus & Diphtheria Vaccine. Polio Vaccine Clinical Trial: placebo was Diluted Polio Vaccine. Vaxelis 6 in 1 Vaccine Trial: placebo was the DTaP, Polio, HIB & Hep-B Vaccines. Hepatitis B Clinical Trial: placebo was Aluminum Adjuvant. The countries that have the most infant vaccines on their childhood schedules, have the highest infant mortality. The United States is #1 in infant vaccines & #1 in infant mortality, of all industrialized nations. 97% of infants who die of SIDS, do so within 7 days being vaccinated. 👇Vaccinated Versus Unvaccinated Study👇 👇Vaccine Induced Neurodevelopment Disorders👇 👇Health Outcomes: Vaxxed Versus UnVaxxed👇 Speaker: Dr Pierre Kory, MD Video: @that_barefootgirlv

Valerie Anne Smith

260,637 görüntüleme • 11 ay önce

The results of the study at the heart of our award-winning film “An Inconvenient Study” are shocking. A complaint I hear often is that the study is too small - that there aren’t enough children in the unvaccinated group. For contrast, the Hepatitis-B vaccine that we give newborns only had 147 children in it, with no control and no placebo. They were monitored for 5 days. So, a 5-day safety study with 147 children was good enough for the Hep-B approval, but a study with twenty thousand kids, two thousand of which were unvaccinated, followed for multiple years, is not? Think about that. Weston A. Price Foundation

The results of the study at the heart of our award-winning film “An Inconvenient Study” are shocking. A complaint I hear often is that the study is too small - that there aren’t enough children in the unvaccinated group. For contrast, the Hepatitis-B vaccine that we give newborns only had 147 children in it, with no control and no placebo. They were monitored for 5 days. So, a 5-day safety study with 147 children was good enough for the Hep-B approval, but a study with twenty thousand kids, two thousand of which were unvaccinated, followed for multiple years, is not? Think about that. Weston A. Price Foundation

Del Bigtree

115,850 görüntüleme • 8 ay önce

“Unless you're comparing a vaccine against saline, how can you say it’s safe?” Dr. Sherri Tenpenny just exposed Pharma’s “safe and effective” narrative as a complete sham. “There has never been—on any one of the vaccines that are currently given—a truly placebo-controlled trial where in one set of children they were given the new vaccine, and then the other set of children it was a true saline placebo.” “All of the vaccine trials are a vaccine compared to another vaccine,” Alex Clark: “How long were the majority of the safety trials done on the vaccines on the childhood schedule?” Dr. Tenpenny: “The average length of time is probably somewhere between 15 and 30 days.” “It’s been as short as 4 days.” “When they brought the first hepatitis B vaccine to market, they followed to see if there were any side effects for 5 days.” “The second hepatitis B vaccine that came to market, they followed side effects for 4 days.” “That is not a safety trial.” “It can take months to years to develop autoimmune diseases, neurological complications, other types of things like [gastrointestinal] disorders.” “Encephalitis can start right away, but it can be slow brewing for a long period of time.” Dr Sherri Tenpenny

“Unless you're comparing a vaccine against saline, how can you say it’s safe?” Dr. Sherri Tenpenny just exposed Pharma’s “safe and effective” narrative as a complete sham. “There has never been—on any one of the vaccines that are currently given—a truly placebo-controlled trial where in one set of children they were given the new vaccine, and then the other set of children it was a true saline placebo.” “All of the vaccine trials are a vaccine compared to another vaccine,” Alex Clark: “How long were the majority of the safety trials done on the vaccines on the childhood schedule?” Dr. Tenpenny: “The average length of time is probably somewhere between 15 and 30 days.” “It’s been as short as 4 days.” “When they brought the first hepatitis B vaccine to market, they followed to see if there were any side effects for 5 days.” “The second hepatitis B vaccine that came to market, they followed side effects for 4 days.” “That is not a safety trial.” “It can take months to years to develop autoimmune diseases, neurological complications, other types of things like [gastrointestinal] disorders.” “Encephalitis can start right away, but it can be slow brewing for a long period of time.” Dr Sherri Tenpenny

Children’s Health Defense

49,833 görüntüleme • 8 ay önce

"Never a Placebo-Controlled Group": How Our Children's Vaccines Were Licensed on a Foundation of Flimsy Science. We are told the vaccine schedule is the most tested and safest in medical history. But what if that claim collapses under the weight of the actual data? Attorney Aaron Siri delivers a stunning fact that should halt every parent and citizen in their tracks: "Almost all childhood vaccines were licensed based on trials in which safety was reviewed for days or weeks after injection, underpowered, not enough kids, and there was never a placebo-controlled group for a single of the routine childhood vaccines injected into children, not one of them." Let that sink in. Not one. The gold standard of scientific research—the placebo-controlled trial—was abandoned for the entire routine childhood vaccine schedule. Why the Double Standard? For prescription drugs, companies run years-long, placebo-controlled trials. Why? Not ethics—economics. They are liable for damages. A harmful drug means financial ruin. For vaccines, the incentive is perversely flipped. With liability removed, the corporate boardroom's bottom-line calculus is simple: do the absolute minimum required for licensure. The Hep B Example is Jaw-Dropping Proof. The Combovax HB vaccine, given to babies on their first day of life, was licensed based on a "trial" that: - Monitored safety for just FIVE DAYS. - Included only 147 children. - Had NO control group whatsoever. This isn't just inadequate; it's scientifically indefensible. The recent COVID vaccine trials, often criticized as rushed, were vastly more comprehensive than this. The Root Cause? The Liability Shield. There is no doubt: if vaccine manufacturers were financially liable for injuries, the safety science would be exhaustive. They would never risk their profits on such flimsy data. The absence of liability created an absence of scientific rigor. This isn't conspiracy. It's cold, hard corporate calculus, and our children are the ones living in the experiment. It's long past time to demand the same gold-standard safety proof for vaccines that we demand for every pill we swallow.

"Never a Placebo-Controlled Group": How Our Children's Vaccines Were Licensed on a Foundation of Flimsy Science. We are told the vaccine schedule is the most tested and safest in medical history. But what if that claim collapses under the weight of the actual data? Attorney Aaron Siri delivers a stunning fact that should halt every parent and citizen in their tracks: "Almost all childhood vaccines were licensed based on trials in which safety was reviewed for days or weeks after injection, underpowered, not enough kids, and there was never a placebo-controlled group for a single of the routine childhood vaccines injected into children, not one of them." Let that sink in. Not one. The gold standard of scientific research—the placebo-controlled trial—was abandoned for the entire routine childhood vaccine schedule. Why the Double Standard? For prescription drugs, companies run years-long, placebo-controlled trials. Why? Not ethics—economics. They are liable for damages. A harmful drug means financial ruin. For vaccines, the incentive is perversely flipped. With liability removed, the corporate boardroom's bottom-line calculus is simple: do the absolute minimum required for licensure. The Hep B Example is Jaw-Dropping Proof. The Combovax HB vaccine, given to babies on their first day of life, was licensed based on a "trial" that: - Monitored safety for just FIVE DAYS. - Included only 147 children. - Had NO control group whatsoever. This isn't just inadequate; it's scientifically indefensible. The recent COVID vaccine trials, often criticized as rushed, were vastly more comprehensive than this. The Root Cause? The Liability Shield. There is no doubt: if vaccine manufacturers were financially liable for injuries, the safety science would be exhaustive. They would never risk their profits on such flimsy data. The absence of liability created an absence of scientific rigor. This isn't conspiracy. It's cold, hard corporate calculus, and our children are the ones living in the experiment. It's long past time to demand the same gold-standard safety proof for vaccines that we demand for every pill we swallow.

Camus

38,809 görüntüleme • 10 ay önce

Bird Flu vaccine trial truth straight from product inserts On behalf of ICAN, we have submitted FOIA requests with regard to the bird flu H5N1 vaccines. The bird flu H5N1 is back in the news. Let's look at the three licensed H5N1 vaccines. The first one was licensed by GSK. In a clinical trial where, after the first year, those that got the vaccine had four times the rate of new immune mediated diseases, four times the rate. And then there is the product by Seqirus. In that clinical trial, there were 11 deaths in the vaccinated group and one in the placebo group. That trial was for adults. There was also a trial for children that only had 329 children in it, and 26% of them reported an adverse event within 21 days. And then finally, there is an H5N1 vaccine licensed by Sanofi. And in that one, it only had 151 adults in the clinical trial. That's it. Within the first 56 days after vaccination, there were four serious adverse events, including one death in a population of only 151 adults. Before you take one of these three products, if that is something anybody out there is considering, it might be a good idea to go to the FDA website, pull up the package insert, go to section 6.1, and you can read exactly the information I just went through. Aaron Siri - 03/05/2025 TheHighWire Episode 414 Fowl Play: Support ICAN: PS: It only took a few minutes to find the following 2 product insert examples, as Aaron explained. - Sanofi Pasteur H5N1 vaccine: Product insert: - Biomedical Corporation of Quebec H5N1 vaccine: Product insert:

Bird Flu vaccine trial truth straight from product inserts On behalf of ICAN, we have submitted FOIA requests with regard to the bird flu H5N1 vaccines. The bird flu H5N1 is back in the news. Let's look at the three licensed H5N1 vaccines. The first one was licensed by GSK. In a clinical trial where, after the first year, those that got the vaccine had four times the rate of new immune mediated diseases, four times the rate. And then there is the product by Seqirus. In that clinical trial, there were 11 deaths in the vaccinated group and one in the placebo group. That trial was for adults. There was also a trial for children that only had 329 children in it, and 26% of them reported an adverse event within 21 days. And then finally, there is an H5N1 vaccine licensed by Sanofi. And in that one, it only had 151 adults in the clinical trial. That's it. Within the first 56 days after vaccination, there were four serious adverse events, including one death in a population of only 151 adults. Before you take one of these three products, if that is something anybody out there is considering, it might be a good idea to go to the FDA website, pull up the package insert, go to section 6.1, and you can read exactly the information I just went through. Aaron Siri - 03/05/2025 TheHighWire Episode 414 Fowl Play: Support ICAN: PS: It only took a few minutes to find the following 2 product insert examples, as Aaron explained. - Sanofi Pasteur H5N1 vaccine: Product insert: - Biomedical Corporation of Quebec H5N1 vaccine: Product insert:

Judy A. Mikovits PhD

17,837 görüntüleme • 1 yıl önce

Prevnar 7 was licensed for infants at two, four, and six months of age with no placebo-controlled trial. There was no ethical reason to skip one. Instead, the control used in the clinical trial was another experimental vaccine, an investigational meningococcal conjugate vaccine that had never been licensed either. A JAMA article authored by FDA scientists acknowledged this approach can mask serious adverse events. Prevnar 7 then became the control used to license Prevnar 13. In that trial, serious adverse events including death, hospitalization, and permanent disability were reported in 8.2% of Prevnar 13 recipients and 7.2% of Prevnar 7 recipients. Prevnar 13 then became the control used to license Prevnar 15. Serious adverse events were reported in 9.6% of Prevnar 15 recipients and 8.9% of Prevnar 13 recipients. The FDA called it safe. Each generation of this vaccine was tested against the last one, and the last one was never tested against a true placebo. Aaron Siri calls it a pyramid scheme of safety, with a baseline that has never been shown to be safe at all.

Prevnar 7 was licensed for infants at two, four, and six months of age with no placebo-controlled trial. There was no ethical reason to skip one. Instead, the control used in the clinical trial was another experimental vaccine, an investigational meningococcal conjugate vaccine that had never been licensed either. A JAMA article authored by FDA scientists acknowledged this approach can mask serious adverse events. Prevnar 7 then became the control used to license Prevnar 13. In that trial, serious adverse events including death, hospitalization, and permanent disability were reported in 8.2% of Prevnar 13 recipients and 7.2% of Prevnar 7 recipients. Prevnar 13 then became the control used to license Prevnar 15. Serious adverse events were reported in 9.6% of Prevnar 15 recipients and 8.9% of Prevnar 13 recipients. The FDA called it safe. Each generation of this vaccine was tested against the last one, and the last one was never tested against a true placebo. Aaron Siri calls it a pyramid scheme of safety, with a baseline that has never been shown to be safe at all.

The HighWire

32,370 görüntüleme • 1 ay önce

"The Big Problem With 'Trusting The science' Is Who's Behind The science." Dr Eric Berg "When You Test A Drug, It's Against A Placebo." "Vaccines Are Not Tested Against Placebos...They Are Tested Against Another Active Vaccine." "That's Like Testing Whiskey Against Bourbon." 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo used was Aluminum Adjuvant & only safety tested for 5 days. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo used was Aluminum Adjuvant & Hep-A Vaccine. Only safety tested for 14 days. Hepatitis A Clinical Trial...Placebo used was Hepatitis-B Vaccine & participants were monitored for 14 days. Influenza A Clinical Trial...Placebo used was Influenza B Vaccine & clinical trial volunteers were followed for 28 days. Meningitis Vaccine Clinical Trial...Placebo used was the DTaP Vaccine & adverse reactions were monitored for 7 days. Pertussis Vaccine Clinical Trial...Placebo used was the Diphtheria & Tetanus Vaccine. Participants were followed for 14 days. Prevnar-13 Pneumonia Clinical Trial...Placebo used was the Prevnar-7 Vaccine & volunteers were monitored for 7 days. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine & patients were monitored for 2 days. Chicken Pox Vaccine Clinical Trial...Placebo used was diluted Chicken Pox Vaccine & trial volunteers were monitored for 42 days. Shingles Vaccine Clinical Trial...Placebo used was diluted Shingles Vaccine & participants were followed for 7 days. mNEXSPIKE Covid Vaccine Clinical Trial...Placebo used was SPIKEVAX Covid Vaccine & only safety tested 7 days. Without informed consent & without the use of a saline placebo skews all results & makes all vaccines appear "safe & effective" because the adverse events & side effects in both groups are the same. The US CDC Government's belief on placebos as stated on the CDC website... 1⃣ "Testing a new vaccine against a saline injection is considered unethical." 2⃣ "Depriving half of the trial participants of an older vaccine(which is approved to use as placebo) & giving them a true saline placebo instead would not be fair: it would actually be unethical." 3⃣ "Saline injections don’t cause a sore arm, which might unwittingly reveal to the 'double blind volunteers' that they are in the placebo group. Those who get the experimental vaccine & those who get placebo must be kept secret." 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 👇Vaccine Excipients Used In Vaccines👇 Speaker: Dr. Eric Berg DC Video: @toxins_in_children

"The Big Problem With 'Trusting The science' Is Who's Behind The science." Dr Eric Berg "When You Test A Drug, It's Against A Placebo." "Vaccines Are Not Tested Against Placebos...They Are Tested Against Another Active Vaccine." "That's Like Testing Whiskey Against Bourbon." 'Placebos' Used In Vaccine Clinical Trials As Listed From The Package Inserts For Common Vaccines: Hepatitis B Clinical Trial...Placebo used was Aluminum Adjuvant & only safety tested for 5 days. Vaxelis 6 in 1 Vaccine Trial...Placebo Was DTaP, Polio, HIB & Hep-B Vaccines. HPV Gardasil Clinical Trial...Placebo used was Aluminum Adjuvant & Hep-A Vaccine. Only safety tested for 14 days. Hepatitis A Clinical Trial...Placebo used was Hepatitis-B Vaccine & participants were monitored for 14 days. Influenza A Clinical Trial...Placebo used was Influenza B Vaccine & clinical trial volunteers were followed for 28 days. Meningitis Vaccine Clinical Trial...Placebo used was the DTaP Vaccine & adverse reactions were monitored for 7 days. Pertussis Vaccine Clinical Trial...Placebo used was the Diphtheria & Tetanus Vaccine. Participants were followed for 14 days. Prevnar-13 Pneumonia Clinical Trial...Placebo used was the Prevnar-7 Vaccine & volunteers were monitored for 7 days. Polio Vaccine Clinical Trial...Placebo Was Diluted Polio Vaccine & patients were monitored for 2 days. Chicken Pox Vaccine Clinical Trial...Placebo used was diluted Chicken Pox Vaccine & trial volunteers were monitored for 42 days. Shingles Vaccine Clinical Trial...Placebo used was diluted Shingles Vaccine & participants were followed for 7 days. mNEXSPIKE Covid Vaccine Clinical Trial...Placebo used was SPIKEVAX Covid Vaccine & only safety tested 7 days. Without informed consent & without the use of a saline placebo skews all results & makes all vaccines appear "safe & effective" because the adverse events & side effects in both groups are the same. The US CDC Government's belief on placebos as stated on the CDC website... 1⃣ "Testing a new vaccine against a saline injection is considered unethical." 2⃣ "Depriving half of the trial participants of an older vaccine(which is approved to use as placebo) & giving them a true saline placebo instead would not be fair: it would actually be unethical." 3⃣ "Saline injections don’t cause a sore arm, which might unwittingly reveal to the 'double blind volunteers' that they are in the placebo group. Those who get the experimental vaccine & those who get placebo must be kept secret." 👇Pediatric Vaccine Clinical Trial Placebos👇 👇Vaccine Trial Placebo Development👇 👇Vaccine Excipients Used In Vaccines👇 Speaker: Dr. Eric Berg DC Video: @toxins_in_children

Valerie Anne Smith

113,112 görüntüleme • 10 ay önce

👀The Plotkin Deposition - Part V - Under oath, Dr. Stanley Plotkin confirmed the following: • Vaccines on the childhood schedule are manufactured using aborted fetal cell strains (MRC-5, WI-38), derived from electively aborted fetuses • Those cell strains originated from fetuses aborted for social and psychiatric reasons • Human DNA and protein fragments remain in final vaccine products • Millions to trillions of fragments of human DNA may be present per dose • No study exists proving the safety of injecting those DNA fragments into infants • Polio vaccines were grown on monkey kidney cells, later found contaminated with SV40 • Porcine circovirus was unintentionally found in rotavirus vaccines after release • Vaccine ingredients have repeatedly entered the market before contaminants were discovered • Aluminum adjuvants can bind not only to antigens, but also to manufacturing byproducts and impurities • Serious adverse events listed across product inserts are real, even if causation is later disputed • He receives compensation from all four major vaccine manufacturers When asked directly whether safety data exists for many of these exposures, the answer was repeated again and again: “I don’t know.” “There is no study.” “That data doesn’t exist.” This is the scientific record finally spoken aloud. Watch the final part of The Plotkin Deposition – Part V.

👀The Plotkin Deposition - Part V - Under oath, Dr. Stanley Plotkin confirmed the following: • Vaccines on the childhood schedule are manufactured using aborted fetal cell strains (MRC-5, WI-38), derived from electively aborted fetuses • Those cell strains originated from fetuses aborted for social and psychiatric reasons • Human DNA and protein fragments remain in final vaccine products • Millions to trillions of fragments of human DNA may be present per dose • No study exists proving the safety of injecting those DNA fragments into infants • Polio vaccines were grown on monkey kidney cells, later found contaminated with SV40 • Porcine circovirus was unintentionally found in rotavirus vaccines after release • Vaccine ingredients have repeatedly entered the market before contaminants were discovered • Aluminum adjuvants can bind not only to antigens, but also to manufacturing byproducts and impurities • Serious adverse events listed across product inserts are real, even if causation is later disputed • He receives compensation from all four major vaccine manufacturers When asked directly whether safety data exists for many of these exposures, the answer was repeated again and again: “I don’t know.” “There is no study.” “That data doesn’t exist.” This is the scientific record finally spoken aloud. Watch the final part of The Plotkin Deposition – Part V.

The HighWire

16,124 görüntüleme • 7 ay önce

"There's no way this can be it" Federal regulations require vaccine package inserts to summarize the clinical trial relied upon to license the product for safety. Here is what the Recombivax HB package insert says in that section. "In three clinical studies, 434 doses of Recombivax HB were administered to 147 healthy infants and children up to 10 years of age who were monitored for five days after each dose." There was no control group, five days of safety monitoring, and 147 infants in the trial. That's the data the FDA accepted to license this product for administration to millions of babies. Aaron Siri couldn't believe it, and neither could we.

"There's no way this can be it" Federal regulations require vaccine package inserts to summarize the clinical trial relied upon to license the product for safety. Here is what the Recombivax HB package insert says in that section. "In three clinical studies, 434 doses of Recombivax HB were administered to 147 healthy infants and children up to 10 years of age who were monitored for five days after each dose." There was no control group, five days of safety monitoring, and 147 infants in the trial. That's the data the FDA accepted to license this product for administration to millions of babies. Aaron Siri couldn't believe it, and neither could we.

The HighWire

26,693 görüntüleme • 1 ay önce

👀The Plotkin Deposition - Part IV This is not opinion. This is sworn testimony. In Part IV of the Stanley Plotkin deposition, the record gets uncomfortable. Fast. Under oath, the world’s most celebrated vaccine authority admits: • There has never been a study comparing the total health outcomes of fully vaccinated children vs. completely unvaccinated children • The Institute of Medicine reviewed 158 serious vaccine injury claims, and for 135 of them, concluded the evidence was insufficient to determine causation • He helped review those reports while consulting for multiple vaccine manufacturers, a conflict not disclosed in the reports • Vaccines are recommended even when science cannot determine whether they cause certain injuries • Aluminum adjuvants can persist in the body, be taken up by immune cells, and travel to the brain - something he acknowledged is possible • Studies showing concerning outcomes are dismissed as “predatory,” yet he agrees they warrant larger, better studies • Despite billions in revenue and taxpayer-funded vaccine purchases, no comprehensive safety comparison has ever been done Perhaps most telling: When asked whether doctors should wait for science before declaring vaccines do not cause autism, his answer was clear: “Do I wait? No.” Watch Part IV of The Plotkin Deposition and decide for yourself whether “safe and effective” is science or policy.

👀The Plotkin Deposition - Part IV This is not opinion. This is sworn testimony. In Part IV of the Stanley Plotkin deposition, the record gets uncomfortable. Fast. Under oath, the world’s most celebrated vaccine authority admits: • There has never been a study comparing the total health outcomes of fully vaccinated children vs. completely unvaccinated children • The Institute of Medicine reviewed 158 serious vaccine injury claims, and for 135 of them, concluded the evidence was insufficient to determine causation • He helped review those reports while consulting for multiple vaccine manufacturers, a conflict not disclosed in the reports • Vaccines are recommended even when science cannot determine whether they cause certain injuries • Aluminum adjuvants can persist in the body, be taken up by immune cells, and travel to the brain - something he acknowledged is possible • Studies showing concerning outcomes are dismissed as “predatory,” yet he agrees they warrant larger, better studies • Despite billions in revenue and taxpayer-funded vaccine purchases, no comprehensive safety comparison has ever been done Perhaps most telling: When asked whether doctors should wait for science before declaring vaccines do not cause autism, his answer was clear: “Do I wait? No.” Watch Part IV of The Plotkin Deposition and decide for yourself whether “safe and effective” is science or policy.

The HighWire

23,365 görüntüleme • 7 ay önce

Sen. Blumenthal: "You're not a Medical Doctor [or] Immunologist or biologist?" Aaron Siri: "Or Vaccinologist, NO, but I depose them regularly, including the World's leading ones". Dem Senator Richard Blumenthal wasn't prepared for Aaron Siri, who deposed the godfather of vaccinology, Dr. Stanley Plotkin. Dr. Plotkin admitted in that deposition the Hep B vaccine only had 5 days of safety review. In the new movie "An Inconvenient Truth", the head of infectious disease at Henry Ford Health System, Dr. Marcus Zervos, also admitted that "The proper safety studies haven't been done" on vaccines recommended within the CDC schedule. As Del Bigtree points out, after depositions and multiple lawsuits won, they found out "the entire science behind vaccine safety, was nothing but a complete fraud".

Sen. Blumenthal: "You're not a Medical Doctor [or] Immunologist or biologist?" Aaron Siri: "Or Vaccinologist, NO, but I depose them regularly, including the World's leading ones". Dem Senator Richard Blumenthal wasn't prepared for Aaron Siri, who deposed the godfather of vaccinology, Dr. Stanley Plotkin. Dr. Plotkin admitted in that deposition the Hep B vaccine only had 5 days of safety review. In the new movie "An Inconvenient Truth", the head of infectious disease at Henry Ford Health System, Dr. Marcus Zervos, also admitted that "The proper safety studies haven't been done" on vaccines recommended within the CDC schedule. As Del Bigtree points out, after depositions and multiple lawsuits won, they found out "the entire science behind vaccine safety, was nothing but a complete fraud".

Humanspective

516,822 görüntüleme • 10 ay önce

💉Not a single routine injected childhood vaccine on the CDC schedule has ever been licensed based on a placebo-controlled trial. When another vaccine was used as the control, that vaccine was also never licensed based on a placebo-controlled trial. Every product on the schedule traces back through a chain of vaccines-used-as-controls, and at the bottom of that chain, there is no placebo. Aaron Siri spent ten years fighting the FDA for the clinical trial documents that prove it, and every one of them is cited in chapter 10 of "Vaccines, Amen." "That is a categorical fact. And for any reporters out there, instead of calling Paul Offit when you run out of here, why don't you actually go to chapter 10 and look at the underlying FDA licensure documents that we spent 10 years clawing out of FDA's hands for yourselves."

💉Not a single routine injected childhood vaccine on the CDC schedule has ever been licensed based on a placebo-controlled trial. When another vaccine was used as the control, that vaccine was also never licensed based on a placebo-controlled trial. Every product on the schedule traces back through a chain of vaccines-used-as-controls, and at the bottom of that chain, there is no placebo. Aaron Siri spent ten years fighting the FDA for the clinical trial documents that prove it, and every one of them is cited in chapter 10 of "Vaccines, Amen." "That is a categorical fact. And for any reporters out there, instead of calling Paul Offit when you run out of here, why don't you actually go to chapter 10 and look at the underlying FDA licensure documents that we spent 10 years clawing out of FDA's hands for yourselves."

The HighWire

39,641 görüntüleme • 1 ay önce

🚨Debunking Grok: Polio Vaccine Trials You’ve Never Been Shown Aaron Siri breaks down the licensing data for today’s polio vaccine, IPOL. It was licensed in 1990, and in its clinical trial, safety was only reviewed for three days after injection. THREE. DAYS. There was no control group. This is not the Salk or Sabin vaccine most people think of. This version uses Vero cells, monkey kidney cells modified to replicate indefinitely. Del notes that although some claim the original IPV was tested against a saline placebo, the modern IPOL vaccine was never tested against that earlier product. When pressed on whether the Salk vaccine truly had a saline placebo, Siri is clear. It did not. The control injection contained formalin, antibiotics, dye, and other ingredients. By any definition, that is not an inert placebo.

🚨Debunking Grok: Polio Vaccine Trials You’ve Never Been Shown Aaron Siri breaks down the licensing data for today’s polio vaccine, IPOL. It was licensed in 1990, and in its clinical trial, safety was only reviewed for three days after injection. THREE. DAYS. There was no control group. This is not the Salk or Sabin vaccine most people think of. This version uses Vero cells, monkey kidney cells modified to replicate indefinitely. Del notes that although some claim the original IPV was tested against a saline placebo, the modern IPOL vaccine was never tested against that earlier product. When pressed on whether the Salk vaccine truly had a saline placebo, Siri is clear. It did not. The control injection contained formalin, antibiotics, dye, and other ingredients. By any definition, that is not an inert placebo.

The HighWire

39,252 görüntüleme • 8 ay önce

Did you know that there was no pre-license clinical trial on the MMR vaccine before it was mass administered? This is one of my favorite parts from the Siri and Plotkin deposition, and demonstrates how horrible vaccine science really is. Share this with anyone who is adamant about vaccines being properly safety tested, especially the MMR vaccine, which has been at the root of the autism discussion for decades. Make sure they know exactly who Plotkin is, and his importance and prestige in vaccinology. You can see Plotkin panicking internally as he begins to figure out that Siri isn't going to let him weasel out of the fact that there are no proper studies discerning the safety of the MMR vaccine, and Plotkin eventually says he won't provide any studies, and he just has to "read his book". That book being the Vaccination Bible. Siri eventually forces it out of Plotkin that the MMR vaccine studies never had a saline placebo group. This is a perfect example of what a great lawyer pursuing truth looks like. Siri says: "So you're claiming something happened, but you're not willing to provide any proof that it happened?" Plotkin: "....the proof is in the publications (his book), which you can read if you like". Plotkin gives the same line about how "these vaccines have been studied for 50 years", and Siri responds with basically "I know you just want us to take your word for it, but I prefer to rely on science, peer reviewed publications, and clinical trials. I know you're getting upset about me trying to ask for the data" and then explains what is required for a vaccine to be approved per the FDA with placebo controls. After some more deliberation, Siri asks Plotkin to provide him anything in regards to a study that had a placebo group, and Plotkin eventually has to say HE DOESN'T KNOW IF IT HAD A PLACEBO GROUP, and he would have to go back and look at the individual study. Think about this for a second... Godfather of vaccines. One of the most controversial vaccines in history in regards to autism and various injuries, and he doesn't know if there was a placebo control used in a study for it? Come on... This continues for a couple more minutes before Plotkin has to give up and say "I will look for the studies and provide them to you after the deposition". Guess what? He never provided those studies, as expected. Same thing Fauci did to RFK when asked. They know these studies don't exist, but they put on a show to save face. This is being knowingly dishonest. This is lying under oath. This is so wrong because the result of this lie and lack of proper safety studies is people being harmed or killed, or kids being brain damaged for life and suffering immensely. It's unforgiveable. There isn't a jail cell small enough for these criminals. One of the most damning clips from the deposition. Aaron Siri is a beast and deserves immense respect, on par with RFK.

Did you know that there was no pre-license clinical trial on the MMR vaccine before it was mass administered? This is one of my favorite parts from the Siri and Plotkin deposition, and demonstrates how horrible vaccine science really is. Share this with anyone who is adamant about vaccines being properly safety tested, especially the MMR vaccine, which has been at the root of the autism discussion for decades. Make sure they know exactly who Plotkin is, and his importance and prestige in vaccinology. You can see Plotkin panicking internally as he begins to figure out that Siri isn't going to let him weasel out of the fact that there are no proper studies discerning the safety of the MMR vaccine, and Plotkin eventually says he won't provide any studies, and he just has to "read his book". That book being the Vaccination Bible. Siri eventually forces it out of Plotkin that the MMR vaccine studies never had a saline placebo group. This is a perfect example of what a great lawyer pursuing truth looks like. Siri says: "So you're claiming something happened, but you're not willing to provide any proof that it happened?" Plotkin: "....the proof is in the publications (his book), which you can read if you like". Plotkin gives the same line about how "these vaccines have been studied for 50 years", and Siri responds with basically "I know you just want us to take your word for it, but I prefer to rely on science, peer reviewed publications, and clinical trials. I know you're getting upset about me trying to ask for the data" and then explains what is required for a vaccine to be approved per the FDA with placebo controls. After some more deliberation, Siri asks Plotkin to provide him anything in regards to a study that had a placebo group, and Plotkin eventually has to say HE DOESN'T KNOW IF IT HAD A PLACEBO GROUP, and he would have to go back and look at the individual study. Think about this for a second... Godfather of vaccines. One of the most controversial vaccines in history in regards to autism and various injuries, and he doesn't know if there was a placebo control used in a study for it? Come on... This continues for a couple more minutes before Plotkin has to give up and say "I will look for the studies and provide them to you after the deposition". Guess what? He never provided those studies, as expected. Same thing Fauci did to RFK when asked. They know these studies don't exist, but they put on a show to save face. This is being knowingly dishonest. This is lying under oath. This is so wrong because the result of this lie and lack of proper safety studies is people being harmed or killed, or kids being brain damaged for life and suffering immensely. It's unforgiveable. There isn't a jail cell small enough for these criminals. One of the most damning clips from the deposition. Aaron Siri is a beast and deserves immense respect, on par with RFK.

Inversionism

759,976 görüntüleme • 3 yıl önce