Thursday, June 30, 2022

FDA Panel Advisor Admits Agency "LOST" Clinical Trial Data for Placebo Group Before Approving Experimental Vaccine for Babies and Toddlers

The Food and Drug Administration (FDA) authorized the mRNA vaccine for emergency use in young children

  • In addition to ignoring the mountain of evidence showing the vaccines are regularly causing life-threatening injuries, the FDA 'experts' routinely skipped crucial steps in the testing process, allowing them to manipulate the data in order to suit their desired outcomes.

No efficacy data

  • "There is no efficacy data," Zhang explained. "We have lost the placebo groups, so we cannot really say anything about the duration of vaccine efficacy after that time point."
  • Unfortunately, we are limited to the results that we have shown you in the slide with the data cut off.

Despite all of this, the FDA dutifully approved the vaccine for babies and toddlers despite no efficacy data

  • Recent data has shown that they are actually more susceptible to long-term vaccine injury after taking the experimental mRNA jab, especially among young boys
  • Cases of myocarditis have exploded among young Americans, hitting unprecedented levels ever since the vaccine was made available to those aged 12-17

 

https://www.thegatewaypundit.com/2022/06/fda-panel-advisor-admits-agency-lost-clinical-trial-data-placebo-group-approving-experimental-vaccine-babies-toddlers-video/ 

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