FDA

Originally published May 11, 2023 2:00 pm PDT The World Health Organization (WHO) has announced that monkeypox is no longer considered a global public health...

The FDA analysts also raised concerns about whether women with medical conditions that should preclude them from taking the pill, primarily breast cancer and undiagnosed vaginal bleeding, would avoid the product.

The FDA issued a warning last week to stop using a particular COVID at-home test due to the potential for bacterial contamination in the product’s solution.

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.

Far-left Oregon Governor Tina Kotek announced Thursday that the state has partnered with Oregon Health Science University (OHSU) to stash a three-year supply of mifepristone, the first drug used in a two-drug medication abortion procedure. 

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

"As Attorney General, I will always fight to protect children because gender transition interventions are experimental," says AG Bailey.

2021 filings reveal Pfizer had reason to believe its COVID-19 vaccine's effectiveness waned, although the company did not choose to release the information until months after the revelation.

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

Three people have died and four people have had eyeballs removed after using eyedrops linked to a drug-resistant bacterial disease.