Pfizer/BioNTech’s COVID-19 “vaccine”, which is actually a gene therapy, has been given emergency use authorization for children ages 5-11. Exactly no one should be shocked by this.

“The authorization was based on the FDA’s thorough and transparent evaluation of the data that included input from independent advisory committee experts who overwhelmingly voted in favor of making the vaccine available to children in this age group,” the agency said on Friday.

Today, we authorized the emergency use of the Pfizer-BioNTech COVID-19 Vaccine for the prevention of #COVID19 to include children 5 through 11 years of age. https://t.co/Tz0S9s4eyz pic.twitter.com/dc18AWIHKQ

— U.S. FDA (@US_FDA) October 29, 2021

Earlier this week, the FDA’s vaccines advisory committee voted 17-0, with one abstention, to approve the emergency use of the vaccine for children. The jabs would be administered three weeks apart, in two 10-microgram doses – a third of the dose currently recommended for everyone 12 and older.

The panel’s decision was based on data presented by Pfizer, which tracked 2,268 children in the 5-11 age group who received either the recommended regimen or a placebo. Only three of the vaccinated developed symptomatic Covid-19 compared to 16 in the placebo group, according to the study conducted in August and September. -RT

“Vaccinating younger children against [Covid]-19 will bring us closer to returning to a sense of normalcy,” said acting FDA Commissioner Janet Woodcock in a statement on Friday. “Our comprehensive and rigorous evaluation of the data pertaining to the vaccine’s safety and effectiveness should help assure parents and guardians that this vaccine meets our high standards.”

That’s laughable. Does anyone actually believe that the FDA did a “rigorous” evaluation of any data? Anyone with common sense should have known that this was going to be the outcome. These psychopaths were going to approve this shot no matter what, regardless of how many adverse side effects there are and no matter what the “data” says.

Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, said the agency was “committed to making decisions that are guided by science that the public and healthcare community can trust. We are confident in the safety, effectiveness, and manufacturing data behind this authorization,” he said.

Oh and those pesky side effects like myocarditis? It doesn’t matter because apparently, the “benefits” outweigh the risks. Even though children have a statically irrelevant risk of dying from COVID (which isn’t anything new, just the common cold and the flu renamed) they want parents to give them a shot that could enlarge their hearts. We live in crazy times, folks.