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FDA Panel Votes 17-0 to Allow Experimental Pfizer Injections for Children 5-11 yrs

Today the United States Food and Drug Administration (FDA) vaccines advisory committee voted 17-0, with one abstention, to allow pharmaceutical giant Pfizer access to America’s child population aged 5 to 11 years, paving the way for a new round of mass injections of the highly controversial experimental mRNA gene therapy jab.

This sign-off was the result of intense industry lobby pressure on US elected representatives and federal officials in Washington DC, which sets stage for yet another fast-tracked, rubber-stamped ‘authorization’ in just days.

Big Pharma’s own private promotional mainstream media outlet, Bloomberg News, celebrated the announcement today as giddy investors prepare to reap even bigger financial gains from the US government’s newly established laissez faire regulatory process. This latest move will all but guarantee an unlimited pipeline for repeated “Covid booster shots” targeting the country’s school-aged children population. Moreover, the federal ‘seal of approval’ will also give school administrators increased license to demand total vaccine compliance as a requirement for a child to attend in-person teaching and other school activities.

In an incredible feat of propaganda gymnastics, pharmaceutical industry copywriters at Bloomberg exclaimed how the benefits of the experimental gene therapy injection exceed any risks:

“The benefits of a Covid-19 vaccine for young children made by Pfizer Inc. and BioNTech SE exceed its risks, according to a panel of U.S. experts, putting a shot for the youngest school-age children on track for a likely clearance.

The incredible claim that children are somehow at any noticeable risk of Covid-19 and that there are no serious risks of injecting the experimental mRNA gene-based compound into the bloodstreams of the country’s youth – goes against a growing body of data and peer reviewed science which clearly shows how children are statistically at near zero risk of ever getting seriously ill from Covid-19, let alone dying from it.

However, US regulators seem to have deliberately chosen to ignore mounting evidence of the increased risk of potential crippling and fatal heart inflammation directly resulting from injecting the genetically-modified compound. Incredibly, the FDA even admitted to these risks in their own recent reports, yet chose to minimize the obvious dangers in their final conclusion where they recommended fast-tracking the problematic mRNA ‘vaccine’ product.

Bloomberg goes on to advance another lie in its sub-headline, saying that, “Shots for kids, boosters could recharge U.S. immunization push,” implying that the experimental genetic injections provide immunity to COVID-19, which in fact they do not – something which the manufacturers have admitted from the very beginning of the unprecedented emergency roll-out.

Readers should note that the Pfizer-BioNTech Covid vaccine is still in clinical trials until what the company claims is the “estimated study completion date” of Jan. 31, 2023 (see here), so these are in effect, still experimental products – only the bigger uncontrolled trial has now been extended to the general population of the planet, something which is unprecedented in history, and which carries an infinite amount of unknown health and medical risks which no one, not least of all the pharmaceutical manufacturers pushing the product, could rightly claim to know.

Listen to the analysis by US media host Tucker Carlson:


READ MORE VACCINE NEWS AT: 21st Century Wire Vaccine Files




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