"There's no way this can be it" Federal regulations require vaccine...

Uploaded: 2026-07-10T17:22:00.000Z
Duration: PT41.733S
Channel: The HighWire

2:03

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 views • 3 months ago

1:15

"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

5:53

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 • 8 months ago

1:23

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 views • 1 year ago

3:10

Parents this is beyond alarming. The Pentacel five in one vaccine is approved for infants as young as six weeks old. It’s given as a four dose series and contains aluminum, polysorbate 80, and formaldehyde. There were no safety studies done against an inert placebo group. During the clinical trials, five infants died. Listen to what I have to say about it.

Dr. Dawn Michael

15,868 views • 25 days ago

1:50

🔥 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 • 6 months ago

5:36

🤯 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

1,220,944 views • 3 years ago

2:03

"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 views • 11 months ago

1:58

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 views • 1 month ago

4:45

This is what the FDA relied upon to license the Hep B vaccine before unleashing this product for injection into newborn babies in America—and then administering it again, and a third time, before six months of age.

Aaron Siri

55,152 views • 1 month ago

0:31

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

301,223 views • 2 years ago

4:29

🚩 Aaron Siri Deposes Dr. Stanley Plotkin, 'The Godfather of Vaccines', on the Limited Safety Testing Done on the Hepatitis B Vaccine Siri: "Is five days long enough to detect an autoimmune issue that arises after five days?" Plotkin: "No" Siri: "Is five days long enough to detect any neurological disorder that arose from the vaccine after five days?" Plotkin: "No" Siri: "There is no control group, correct?" Plotkin: "Does not mention any control group, no." Siri: "In to establish whether it's causal between the vaccine and the condition, you need a randomized placebo-controlled study but that was not done for this Hepatitis B vaccine before licensure was it?" Plotkin: "No" Aaron Siri

Chief Nerd

109,626 views • 3 years ago

1:45:52

👀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 • 7 months ago

0:51

🚨"He can't support vaccine safety...No one can.." Who is Stanley Plotkin? Aaron Siri: "We subpoenaed him to provide all the data to support the safety of all the vaccines, the clinical trial data, post-licensure safety data, ingredient safety, all of it. And instead of responding with, 'Here's the mountain of science,' he responded by getting a lawyer and moving in a separate court to squash that subpoena. Has never produced a single document. And obviously, in the almost eight years since, as we've continued to press the FDA, 'Get those documents.' We know why. He can't support vaccine safety. Nobody can." Watch the full episode at

The HighWire

18,863 views • 9 months ago

2:12

Twelve Infants Perish in Clinical Trial for RSV Shot - FDA Recommends Anyway Four of the twelve infants’ deaths in the AstraZeneca trial were from cardiac arrest, and two died of SIDS (Sudden Infant Death Syndrome). The FDA claimed the deaths were “unrelated” to AstraZeneca’s monoclonal antibody injection, but how often do you hear about four babies naturally dying of cardiac arrest in a clinical trial setting? “This is hugely important,” stressed #CHDTV Polly Tommey. “The pediatricians are going to push this. The doctors, as soon as the babies are born, they’re going to give these babies this RSV jab.”

Children’s Health Defense

329,964 views • 3 years ago

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This is what the FDA relied upon to license the Hep B vaccine before unleashing this product for injection into newborn babies in America—and then administering it again, and a third time, before six months of age.

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?