FDA Panel Advisor Says Agency 'Lost' Essential Covid Vax Trial Data for Kids, Babies

An FDA panel advisor admitted that the agency “lost” the placebo group data essential for knowing the effectiveness of the Covid-19 vaccine in kids. . .and then authorized the vax for little kids 6 months old and up anyway. Which makes the clinical trials for kids as meaningless as a Joe Biden mumblefest. This follows on a series of revelations indicating that the US government and vaccine companies know how dangerous the Covid vaccines are but simply don’t care.

As a study from Israel found that the Pfizer-BioNTech Covid-19 vaccine increases the risk for myocarditis threefold, the US FDA gave the Moderna and Pfizer Covid vaccines emergency use authorization (EUA) for children under 5 years—based on Pfizer study data on 10 children. Except that evidence has shown the dosages approved on June 17 for little children and teens from the Moderna shot were so toxic when previously used on adults that, when administered to kids, the dosages could well turn out to be deadly. Then the FDA proposed the “future framework” for Moderna and Pfizer Covid vaccines, allowing the companies to change their vaccine formulas without conducting clinical trials (with help from the Bill Gates-funded World Health Organization).

If you’re not already convinced this is all deliberate, murderous evil, then check out this story on Gateway Pundit:

“[I]n 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. . .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 [emphasis added].

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?”

How indeed? It happens when the government wants money and control (including population control) so much that it knowingly gives a deadly and unproven vaccine to babies. Welcome to the New World Order.