Is U.S. Public Health’s big bet on mRNA paying off?
Are government regulators minimizing the availability of COVID vaccine options in the United States in order to protect our health, or are there many other factors in play — that are completely unrelated to our health — being considered behind the curtain?
The U.S. COVID-19 vaccine market has been shut out to outside competition for almost a year. Despite these shots being marketed and sold as akin to a cure to a coronavirus, they have catastrophically failed to achieve that result. Despite COVID-19 being declared the pandemic of the century, American regulatory agencies remain adamantly opposed to opening the market to more participants.
COVID shots were both marketed by Big Pharma and authorized by the government under the core claim that they prevent transmission
With the United States shattering records for recorded COVID-19 cases across the board, it’s time to dissect all of the revisionist history in the waters these days….
On December 11, 2020, the FDA issued emergency use authorization (EUA) to Pfizer and BioNTech for their COVID-19 vaccine. The U.S. government has since spent billions of taxpayer dollars on hundreds of millions of Pfizer shots.
On December 18, 2020 the FDA issued an EUA to Moderna for their COVID-19 vaccine. The U.S. government has since spent billions of taxpayer dollars on hundreds of millions of Moderna shots.