FDA Authorizes more Boosters without any Clinical Trials

The newest COVID-19 “updated booster” doses, created for the Omicron variety, have been approved by the Food and Drug Administration (FDA) without being subjected to human testing, making people waiting in line for the shots the test subjects.

The vaccinations will be tested on mice rather than on humans, and they will be authorized for use by the general public months before the end of human trials. According to Fox, the FDA authorized the new Omicron injections on Wednesday.

The U.S. Food and Drug Administration announced in a statement that it had amended the emergency use authorizations (EUAs) for the Moderna COVID-19 vaccine and the Pfizer-BioNTech COVID-19 vaccine to allow for the use of bivalent formulations of the vaccines as a single booster dose at least two months after primary or booster vaccination.

“Two messenger RNA (mRNA) components of SARS-CoV-2 virus, one of the original strain of SARS-CoV-2 and one in common with the BA.4 and BA.5 lineages of the omicron variant of SARS-CoV-2,” are included in the new injections, which the FDA is calling to as “updated boosters.”

The government will force the immunization on all Americans despite it never having been tested on people. The FDA will also depend on data from current COVID-19 vaccinations and past generations of boosters in addition to tests on mice. The FDA was urged not to distribute the booster injections without adequate study in an opinion piece written by two health professionals in June.

Paul A. Offit, a pediatrician, professor of pediatrics, director of the Vaccine Education Center at the Children’s Hospital of Philadelphia, and a member of the Vaccines and Related Biological Products Advisory Committee, co-wrote the article with John P. Moore, a virologist and professor of microbiology and immunology at Weill Cornell Medicine.

“I’m uneasy that we would move forward, that we would administer millions or tens of millions of doses to people, based on mice evidence,” Offit told the Wall Street Journal.

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