Food and Drug Administration

In an exclusive interview with The Defender, Dr. Paul Marik said patients are dying “unnecessarily and unlawfully” because the hospital where he is director of the ICU prioritizes expensive drugs like Remdesivir while banning more effective and less costly treatments.

"The entire purpose of the FOIA is to assure government transparency"

In an analysis presented during a meeting of the American Heart Association, Dr. Steven Gundry, a pioneer in infant heart transplant surgery, said mRNA COVID vaccines put many patients at higher risk of a new acute coronary syndrome, such as a heart attack.

In a November 12, 2021, blog post, Maryanne Demasi, Ph.D., reviews how the benets of the COVID-19 shots have been exaggerated by the drug companies and misrepresented to the public by an uncritical media. She has previously given many lectures on how the drug companies conated absolute and relative risks for statin drugs.

Abhorrence of NIH experiments shows institutional cruelty as a neglected but potent political issue.

The FDA released documents it reviewed before licensing the Pfizer jab showing a "large increase of adverse event reports."

Covid-19 boosters from Pfizer-BioNTech, Moderna now cleared for all U.S. adults remain authorized under emergency use, but not approved by the FDA. QUICK FACTS: The Food...

The US Food and Drug Administration (FDA) may take 55 years to release all the documents it used to declare Pfizer’s Covid-19 vaccine safe, a group of doctors and professors claim.

Pfizer somehow miscounted — or publicly misreported, or both — the number of deaths in one of the most important clinical trials in the history of medicine.

VAERS data released today by the CDC included a total of 875,653 reports of adverse events from all age groups following COVID vaccines, including 18,461 deaths and 135,400 serious injuries between Dec. 14, 2020, and Nov. 5, 2021.