Check it out


Quote:

FDA Panel Advisor Admits Agency “LOST” Clinical Trial Data for Placebo Group Before Approving Experimental Vaccine for Babies and Toddlers By Julian Conradson June 29, 2022 Earlier this month the Food and Drug Administration (FDA) authorized the mRNA vaccine for emergency use in young children, aged six months to five years old, after its advisory committee voted in favor of the experimental treatment, claiming that it has passed its clinical hurdles and is effective in preventing symptomatic infection without causing worrisome side effects. However, in addition to ignoring the mountain of evidence showing the vaccines are regularly causing life-threatening injuries – especially in healthy children and young people, the FDA ‘experts’ have routinely skipped crucial steps in the testing process, allowing them to manipulate the data in order to suit their desired outcomes. This inexcusable act of criminal malpractice was confirmed this month by the team leader of the FDA’s clinical review staff, Rachel Zhang, who explained during an advisory panel zoom call that the agency had lost the results from the placebo group during its clinical trials related to the decision to approve the experimental jab for America’s youngest children. Without this data from the placebo group, the effectiveness of the vaccine cannot be measured against those who did not receive the treatment. Therefore, the clinical trial is meaningless. But the gaping hole in the results apparently doesn’t matter to the ‘experts’ at the FDA, who went ahead with the EUA approval anyway. “There is no efficacy data,” Zhang explained. “I guess it will have to come from real-world effectiveness,” she added glibly. In other words, babies and toddlers are essentially vaccine guinea pigs that will provide the lost data. Remember, Zheng is the team leader of the FDA’s clinical review staff, which oversees the approval of new medical treatments. From Zheng: “…We have lost the placebo groups, so we cannot really say anything about the duration of vaccine efficacy after that. There’s no more efficacy data, basically, after that time point. So, unfortunately, we are limited to – in this study – would be the results that we have shown you in the slide with the data cut off. The latest one [placebo group data] would be the May 31st one, and that still is, unfortunately, very few cases… …I guess it will have to come from real-world effectiveness.”  How does something like this even happen? They don’t even have to come up with a viable excuse anymore. This is literally on par with the old ‘dog ate my homework’ line. What a joke.

https://archive.ph/hUpuL#selection-431.0-563.182

Julian Conradson writes for the Gateway Pundit.    Enough said LOL.

Check out its record of trash journalism HERE.

It's a farrago of misinformation, distortions of fact, and blatant lies, and
can safely be ignored as a vehicle of truth or accuracy.

Sorry Sir lastnail.      ;)

Julian Conradson    ;D

Shooting the messenger again :D LOL

lol... the Bobbsey twins logged out at almost exactly the same time a few minutes ago and now they've both just logged in again - at exactly the same time.

;D

Now they've both gone again.

Synchronised stupidity would be a good description.

;D

Sir lastnail wrote on Nov 9^th, 2022 at 9:47pm:

Check it out [quote]FDA Panel Advisor Admits Agency “LOST” Clinical Trial Data for Placebo Group Before Approving Experimental Vaccine for Babies and Toddlers By Julian Conradson June 29, 2022 Earlier this month the Food and Drug Administration (FDA) authorized the mRNA vaccine for emergency use in young children, aged six months to five years old, after its advisory committee voted in favor of the experimental treatment, claiming that it has passed its clinical hurdles and is effective in preventing symptomatic infection without causing worrisome side effects. However, in addition to ignoring the mountain of evidence showing the vaccines are regularly causing life-threatening injuries – especially in healthy children and young people, the FDA ‘experts’ have routinely skipped crucial steps in the testing process, allowing them to manipulate the data in order to suit their desired outcomes. This inexcusable act of criminal malpractice was confirmed this month by the team leader of the FDA’s clinical review staff, Rachel Zhang, who explained during an advisory panel zoom call that the agency had lost the results from the placebo group during its clinical trials related to the decision to approve the experimental jab for America’s youngest children. Without this data from the placebo group, the effectiveness of the vaccine cannot be measured against those who did not receive the treatment. Therefore, the clinical trial is meaningless. But the gaping hole in the results apparently doesn’t matter to the ‘experts’ at the FDA, who went ahead with the EUA approval anyway. “There is no efficacy data,” Zhang explained. “I guess it will have to come from real-world effectiveness,” she added glibly. In other words, babies and toddlers are essentially vaccine guinea pigs that will provide the lost data. Remember, Zheng is the team leader of the FDA’s clinical review staff, which oversees the approval of new medical treatments. From Zheng: “…We have lost the placebo groups, so we cannot really say anything about the duration of vaccine efficacy after that. There’s no more efficacy data, basically, after that time point. So, unfortunately, we are limited to – in this study – would be the results that we have shown you in the slide with the data cut off. The latest one [placebo group data] would be the May 31st one, and that still is, unfortunately, very few cases… …I guess it will have to come from real-world effectiveness.”  How does something like this even happen? They don’t even have to come up with a viable excuse anymore. This is literally on par with the old ‘dog ate my homework’ line. What a joke.

Me thinks that a lot of palms may have been greased, just to look the other way

big pharma farm old sick people the way i farm steers.
they like their old people fat, diabetic and hypertensive so they can get their billions of dollars providing drugs as the cure when good nutrition and exercise is actually the cure.

but young babies and toddlers dont have blood pressure and cholesterol and diabetes from years of eating corporate garbage (yet).

how to farm them , the way i farm young calves?

i know
jab them 20 times before they hit preschool ( the current number of jabs that a child gets in oz).

scare the public with horror stories through the controlled corporate media and offer yourself and your expensive "gear" as the salvation.

use the word "safety' a lot.

appeal to the fearful chode who has extreme death anxiety and thinks immortality is his birthright.

get government to mandate 20 vaccines or the kid cant get family tax benefit.

chuck in another 3 for covid.
this should be available without 7 years of testing ONLY for emergency use but hell, people wont notice,

keep those rivers of gold coming.

practice diverse farming techniques.

the people are just cattle to be farmed
maybe stick an ear tag on the babies so they are easier to control  ::) ::) ::)

government and big food and big pharma are the arsonist and the fire brigade  ;D ;D

https://media.gab.com/system/media_attachments/files/119/986/388/original/ca2ffa9c11d5abd0.png

Carl D wrote on Nov 9^th, 2022 at 10:44pm:

Now they've both gone again. Synchronised stupidity would be a good description. ;D

A lying sack of sh*t aptly describes you.

Covid is mild and no more dangerous than the flu and that the pandemic is now over.

Where's the link Dunce? There isn't one because you are a liar. I bet you have lied all through your life. Telling people you have this degree and that qualification when in fact you are just a lying sack of sh*t. You probably faked your school reports too.

What a dunce you are.

One link is I am asking and I will happily f*^k off from this forum. Here is your opportunity.

But there is no link is there because you are a liar.