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FDA Licensed Hep-B V^ccine based on: -Data from just 147 kids -No Placebo Control -Monitored safety for FIVE DAYS. This v^ccine is given to newborn babies on their first day of life in the US. Is this enough safety data for you?

The HighWire

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301,223 views • 2 years ago •via X (Twitter)

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Gen Belisarius2 years ago

Here's the dirty secret: None of the vaccines on the Child and Adolescent Immunization Schedule have double blind long term RCT utilizing an inert placebo. The Clinical trials use older vaccines (often being replaced because they are unsafe), combinations of vaccines, test vaccine sans antigen, experimental vaccines as the placebo. So if the tested vaccine is as safe as unsafe it's safe! (got that). Oh, btw might as well tell you, you know at those wellness visits when the pediatrician says time for 5 vaccine injections (or 6,7,8+), yeah, no RCT trials on number of combination of vaccines given being safe or not. It's all a lie. You are led to believe they are safe, truth is they have never been properly tested & data released. Your Doctor was told in medical school they are safe, gold standard, so they never looked or really thought about it, which makes sense since they get paid huge % of their annual income based on % of their patients (your children) who receive all the injections plus often money for each one! They have a mortgage and bills, how they look at it, and also they must be safe. Factor all this in.

A&Z MD2 years ago

@uTobian All pharmacological recommendations need to be thoroughly investigated.

ConservativeDeadHead2 years ago

@QuillWalter So how many newborns are having unprotected sex or sharing needles? The concept of giving this poison at birth is ridiculous.

J’s Cat2 years ago

@DeaceOnline No, and that’s why my son didn’t get it. The pushback we received over rejecting that one vaccine opened my mind over childhood vaccines…then COVID made me research every other vaccine on the market I had not worked on in my career. I will never give him another vaccine.

Buckman5422 years ago

I thought the Plandemic was bad, then went down the Childhood Vax rabbit hole & couldn't believe WTF I was hearing. Started w/Aaron Siri's interview w/Del on Plotkin, then watched "Vaxxed" & the rest is history. Thank U HW for opening my eyes....we R dealing w/Eugenicists!

Blade2 years ago

I was dumb enough to take it many years ago and it injured me. I'll never take another vaccine. Lesson learned.

Anthony Holland2 years ago

Why the fook do babies need an hepatitis vaccine for. Am i missing something here .Can some one explain to me simply please

Molly Rutherford, MD2 years ago

A few friends/patients have recently given birth & I told them “don’t give that hep B shot to your newborn…the nurses & doctors will likely judge you & roll their eyes at you…ignore them”

Loh2 years ago

Most of us didn’t think to question their science . Thanks to convid I am finding fraud left , right and centre. Vaxx scam is one of many.

YouShowMe2 years ago

For those who care to see

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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

24,561 views • 5 months ago

Just watched this new breakdown by Aaron Siri on the original clinical trial that put the hepatitis B vaccine on the day-1 newborn schedule. The numbers he reads straight from the 1986 study and today’s FDA insert: - 147 infants - Safety monitoring: 5 days after each dose - No saline placebo Source docs in the first reply so everyone can check for themselves. What caught your attention?

Just watched this new breakdown by Aaron Siri on the original clinical trial that put the hepatitis B vaccine on the day-1 newborn schedule. The numbers he reads straight from the 1986 study and today’s FDA insert: - 147 infants - Safety monitoring: 5 days after each dose - No saline placebo Source docs in the first reply so everyone can check for themselves. What caught your attention?

Camus

119,851 views • 10 months ago

"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

26,877 views • 3 months ago

"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 views • 1 year ago

Dr. Joseph Ladapo, Joseph A. Ladapo, MD, PhD, gives Del Bigtree his TOP 3 COVID B**STER CONCERNS. 1 - No Safety Data 2- Multiple Studies Show V*ccine Increases Risk of Infection 3- Persistent and Growing Myocarditis Concerns Watch the full segment from The HighWire here:

Dr. Joseph Ladapo, Joseph A. Ladapo, MD, PhD, gives Del Bigtree his TOP 3 COVID B**STER CONCERNS. 1 - No Safety Data 2- Multiple Studies Show V*ccine Increases Risk of Infection 3- Persistent and Growing Myocarditis Concerns Watch the full segment from The HighWire here:

The HighWire

114,362 views • 3 years ago

The hepatitis B vaccine given to your child on their first day of life was approved based on a trial of 147 children, followed for five days after each dose, with no placebo group. I have not found another drug tested that poorly, on that small a group, for that short a period, anywhere in my investigation. Here's how you find that out for yourself. Search "FDA licensed vaccines," and every vaccine your doctor recommends will come up. Pull up the CDC's childhood vaccine schedule and look at what you're actually being asked to give, sometimes five vaccines on a single day. Click on one and find the package insert, the same kind of warning label wrapped around every drug you've ever taken, the one almost no doctor has actually read when it comes to vaccines. Go to section 6.1. That's the section the FDA used to decide the product was safe enough for the public. It's one paragraph. Read it for Recombivax HB and you'll see the numbers for yourself. I'm not inventing the idea that vaccines carry risk. It's documented. This is just the beginning of the journey. The FDA is handing you their best evidence for safety. This is what it looks like. And it is not good enough.

The hepatitis B vaccine given to your child on their first day of life was approved based on a trial of 147 children, followed for five days after each dose, with no placebo group. I have not found another drug tested that poorly, on that small a group, for that short a period, anywhere in my investigation. Here's how you find that out for yourself. Search "FDA licensed vaccines," and every vaccine your doctor recommends will come up. Pull up the CDC's childhood vaccine schedule and look at what you're actually being asked to give, sometimes five vaccines on a single day. Click on one and find the package insert, the same kind of warning label wrapped around every drug you've ever taken, the one almost no doctor has actually read when it comes to vaccines. Go to section 6.1. That's the section the FDA used to decide the product was safe enough for the public. It's one paragraph. Read it for Recombivax HB and you'll see the numbers for yourself. I'm not inventing the idea that vaccines carry risk. It's documented. This is just the beginning of the journey. The FDA is handing you their best evidence for safety. This is what it looks like. And it is not good enough.

Del Bigtree

57,378 views • 22 days ago

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 views • 9 months ago

👀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 views • 9 months ago

"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

263,254 views • 1 year ago

🔥 Aaron Siri EXPOSES the safety review process for Hep B shots as a sham. “How many Hepatitis B vaccines are there that they give to babies in the first day of life?” “Two.” “How many days are safety monitored after injection in the clinical trials … to become a vaccine?” “Five.” “How many kids were in the trial?” “147.” “What was the control?” "None." “Does that sound like a safety review? Why would they do that?” “Because that’s just how the economics work.” “The original sin is the passage of the National Childhood Vaccine and Injury Act.” “That set into motion… the economic framework and then the regulatory framework that allowed for clinical trials that are completely defective.” “They do not assess safety beforehand.” “That is a very, very serious problem.” Aaron Siri

🔥 Aaron Siri EXPOSES the safety review process for Hep B shots as a sham. “How many Hepatitis B vaccines are there that they give to babies in the first day of life?” “Two.” “How many days are safety monitored after injection in the clinical trials … to become a vaccine?” “Five.” “How many kids were in the trial?” “147.” “What was the control?” "None." “Does that sound like a safety review? Why would they do that?” “Because that’s just how the economics work.” “The original sin is the passage of the National Childhood Vaccine and Injury Act.” “That set into motion… the economic framework and then the regulatory framework that allowed for clinical trials that are completely defective.” “They do not assess safety beforehand.” “That is a very, very serious problem.” Aaron Siri

Children’s Health Defense

15,482 views • 7 months ago

🤯 SHOCKING: Aaron Siri Exposes the Lack of Safety Data Behind the Hepatitis B Vaccine for Newborns "COVID vaccines have over 6 months of safety review...Hepatitis B given to newborns had 5 days of safety monitoring after injection. 30,000 people in the COVID-19 vaccine clinical trial...[Hepatitis B had 147 kids]." Aaron Siri Jan Jekielek ICAN - Informed Consent Action Network The HighWire

🤯 SHOCKING: Aaron Siri Exposes the Lack of Safety Data Behind the Hepatitis B Vaccine for Newborns "COVID vaccines have over 6 months of safety review...Hepatitis B given to newborns had 5 days of safety monitoring after injection. 30,000 people in the COVID-19 vaccine clinical trial...[Hepatitis B had 147 kids]." Aaron Siri Jan Jekielek ICAN - Informed Consent Action Network The HighWire

Chief Nerd

1,221,220 views • 3 years ago

You would assume vaccines for newborns are tested more carefully than anything else we give a child. They’re not. The hepatitis B vaccine, injected on day one of life, was tested on just 147 babies. No saline placebo group. No comparison group. And the safety follow-up lasted only five days. FIVE DAYS. That is not science. It’s also not informed consent. That is blind faith. For some, it’s religion. These are exactly the issues we expose in my film, An Inconvenient Study. Check out the full conversation with Alec Lace and watch the film for free at

You would assume vaccines for newborns are tested more carefully than anything else we give a child. They’re not. The hepatitis B vaccine, injected on day one of life, was tested on just 147 babies. No saline placebo group. No comparison group. And the safety follow-up lasted only five days. FIVE DAYS. That is not science. It’s also not informed consent. That is blind faith. For some, it’s religion. These are exactly the issues we expose in my film, An Inconvenient Study. Check out the full conversation with Alec Lace and watch the film for free at

Del Bigtree

46,422 views • 8 months ago

The The New York Times and its kin don’t care that after pharma got financial immunity for vaccine injuries in 1986, chronic disease in children, especially immune related diseases, exploded as the number of first year vaccine injections rose from 3 in 1986 to 29 today. They don't care that vaccine products licensed in that period, including novel polio and infant hep B vaccines, were licensed based on clinical trials monitoring safety for only days after injection. Their reporting to the public is: shut up and inject your children without question. No questions allowed. Especially not legitimate ones. Asking questions means you want everyone to have polio. Just read the three petitions my firm filed on behalf of ICAN - Informed Consent Action Network and determine for yourself whether they raise legitimate concerns. SOURCES: ICAN's FDA petitions: Polio Hep b Aluminum adjuvants First year injections from 3 in 1986 to 29 today: Childhood chronic disease from under 13% in 1980s to over 50% today: Chart with links to FDA sources for safety duration and control for each childhood vaccine:

The The New York Times and its kin don’t care that after pharma got financial immunity for vaccine injuries in 1986, chronic disease in children, especially immune related diseases, exploded as the number of first year vaccine injections rose from 3 in 1986 to 29 today. They don't care that vaccine products licensed in that period, including novel polio and infant hep B vaccines, were licensed based on clinical trials monitoring safety for only days after injection. Their reporting to the public is: shut up and inject your children without question. No questions allowed. Especially not legitimate ones. Asking questions means you want everyone to have polio. Just read the three petitions my firm filed on behalf of ICAN - Informed Consent Action Network and determine for yourself whether they raise legitimate concerns. SOURCES: ICAN's FDA petitions: Polio Hep b Aluminum adjuvants First year injections from 3 in 1986 to 29 today: Childhood chronic disease from under 13% in 1980s to over 50% today: Chart with links to FDA sources for safety duration and control for each childhood vaccine:

Aaron Siri

169,655 views • 1 year ago

Frightening… “NONE of the vaccines on the CDC’s routine Childhood Schedule were licensed by the FDA based on long-term, placebo-controlled trials…and their follow-up lasted just 3 days to a few months…and most trials had NO placebo group at all…”

Frightening… “NONE of the vaccines on the CDC’s routine Childhood Schedule were licensed by the FDA based on long-term, placebo-controlled trials…and their follow-up lasted just 3 days to a few months…and most trials had NO placebo group at all…”

Liz Churchill

74,432 views • 11 months ago

The Hepatitis B vaccine is given on Day 1 of life. The most fragile moment your child will ever be. Fresh out of the womb. You'd assume - you'd demand - that a product injected into a hours-old newborn was tested with the highest possible scientific rigor. Here's what the package insert actually says: 147 children. 5-day observation window. No placebo group. That's it. That's the study. If your baby died on day six, the trial missed it. If something went wrong on day ten, the trial missed it. The manufacturers can say "no babies died in our trial" because the trial ended before they'd ever know. Meanwhile, Grandpa's Viagra got a 10-year safety study. And here's what makes me absolutely furious: The FDA will let a Stage 4 cancer patient, someone who is dying, wait years for a drug showing real promise in trials because "safety protocol must be followed." We'll let terminal patients die in the name of scientific rigor. But a perfectly healthy baby, born to a perfectly healthy mother who just tested negative for Hepatitis B (a sexually transmitted disease) gets injected on Day 1 of life based on a 5-day study of 147 kids. No placebo. No long-term follow-up. No justification. Someone explain that to me. Because I'm still waiting for an answer.

The Hepatitis B vaccine is given on Day 1 of life. The most fragile moment your child will ever be. Fresh out of the womb. You'd assume - you'd demand - that a product injected into a hours-old newborn was tested with the highest possible scientific rigor. Here's what the package insert actually says: 147 children. 5-day observation window. No placebo group. That's it. That's the study. If your baby died on day six, the trial missed it. If something went wrong on day ten, the trial missed it. The manufacturers can say "no babies died in our trial" because the trial ended before they'd ever know. Meanwhile, Grandpa's Viagra got a 10-year safety study. And here's what makes me absolutely furious: The FDA will let a Stage 4 cancer patient, someone who is dying, wait years for a drug showing real promise in trials because "safety protocol must be followed." We'll let terminal patients die in the name of scientific rigor. But a perfectly healthy baby, born to a perfectly healthy mother who just tested negative for Hepatitis B (a sexually transmitted disease) gets injected on Day 1 of life based on a 5-day study of 147 kids. No placebo. No long-term follow-up. No justification. Someone explain that to me. Because I'm still waiting for an answer.

Del Bigtree

112,929 views • 7 months ago