Moderna

A new document from the Food and Drug Administration (FDA) stated the FDA does not "require demonstration of the prevention of infection or transmission" in order to authorize a vaccine.

"The monovalent Moderna and Pfizer-BioNTech COVID-19 vaccines are no longer authorized for use in the United States," the FDA says.

President Joe Biden signed a bill ending the COVID-19 national emergency in the US, but his administration launched a $5 billion program named Project Next Gen that aims to expedite the development of new COVID-19 vaccines and treatments, sparking concerns over government overreach and individual liberties, despite recent research indicating natural immunity may provide superior protection.

Since 2018, pork producers have been utilizing a livestock mRNA vaccine.

"On Monday, April 10, 2023, the President signed into law: H.J.Res. 7, which terminates the national emergency related to the COVID-19 pandemic," the White House announcement reads.

"Largest crime scene in history."

The World Health Organization acknowledged there are "comparatively low public health returns" for some groups receiving the COVID-19 booster.

Former chief judge of the U.S. Court of Federal Claims Susan Braden said the federal government's "statement of interest" in a Moderna lawsuit may present a "misuse of the law."

Republican Kentucky Sen. Rand Paul grilled Moderna CEO Stéphane Bancel on Wednesday over whether the shot is safe for teen boys, citing an increased risk of myocarditis.

Confidential documents from Pfizer reveal that the company was aware of potential risks of myocarditis following COVID-19 vaccinations in early 2022.