Thread by @JoshWalkos

Did you know? Childhood vaccine trials are purposely designed to obscure the true incidence of adverse events of the vaccine being tested.

A new pediatric vaccine is never tested during its formal approval process against a neutral solution (saline)placebo. Think about that one.

Then, when the “next generation” vaccine comes along, its pre-licensing clinical trials will always compare the new vaccine to the current vaccine and never to a placebo. By doing this they can never ensure that the true rate of AE’s are never known. They think we’re idiots.

Imagine that, instead of triple blinding the trial & the control group receiving a saline placebo to test against the old generation and new generation, they simply use another vaccine in the control group. This will cause AE’s and muddy the data comparatively.

For example and you can look this up. The package insert for Glaxo-Smith-Kline’s (GSK) hepatitis A vaccine (Havrix) reads:

“Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a vaccine cannot be directly compared to rates in the clinical trials of another vaccine, and may not reflect the rates observed in practice.”

Well that’s reassuring, I definitely want to plunge a needle into my child’s arm now.

This is just the beginning. I’m going to provide more shocking facts that before would get me banned immediately. It’s sad you have to get informed consent from someone on twitter isn’t it?

This is RCT 101. You can’t have a bio active placebo in the control group if you are testing the safety of a product. The only explanation for this is to ensure AE’s occur in both groups so that the true amount of AE’s are “plausibly”concealed. This is good enough for the FDA.

Pfizer unblinded their trials.

“The Vaccine Transition Option offers all participants 12 years & older the choice to learn whether they received the study vaccine or placebo, & for those who received the placebo,to have the option to receive the study vaccine”

Because Science.

covidvaccinestudy.com/participants

How the Vaccine Transition Option works:
•If you choose the Vaccine Transition Option, your study site will schedule a time for you to be unblinded (that is, learn whether you were in the study vaccine or placebo group) in the coming weeks.

•If you find out that you were in the placebo group and would like to receive the study vaccine, you will have an in-person visit where you will be provided with a new informed consent document that the study doctor will review with you and your parent or guardian before signing

Then, you will receive your first dose of the study vaccine.
•You will receive a second dose of the study vaccine about 21 days later and follow an updated study schedule that includes follow-up and illness visits.

How can the data be reliable if they unblinded participants?

Looks like the clowns 🤡 in or associated with the 77th PsyOp brigade have been alerted to someone being truthful about vaccines. You’ll notice them by there lack of evidence and shit attitudes.