FDA

The study found evidence of damage in 2.8% of participants, which is approximately 800 times greater than the anticipated rate of 0.0035%.

The U.S. Food and Drug Administration (FDA) changed the end date of a study it is requiring Pfizer to conduct because Pfizer requested a delay, the agency says.

In case you missed it, the CDC’s Immunization Safety Office Director, Dr. Tom Shimabukuro, recently admitted at an FDA Vaccines and Related Biological Products Advisory Committee (VRBAC) meeting that – yes – people have in fact, suffered “debilitating illness” and “lasting health problems” following COVID-19 “vaccination.”

Over 56,000 Covid-19 antigen rapid tests have been recalled in the US due to likely false results, and consumers are being advised to immediately stop using the product and return it to the distributor.

Molnupiravir, the oral pill for COVID-19, may actually be driving the emergence of new, potentially harmful, variants of the virus, according to a Wellcome Trust-funded study at the pre-print stage.

As a medical student and researcher, I staunchly supported the efforts of the public health authorities when it came to COVID-19.

MD/PhD student Kevin Bass said the scientific community should admit they made mistakes when dealing with COVID.

The health agency is "aware of these reports of people experiencing long-lasting health problems following COVID vaccination."

The Satanic Temple isn’t just promoting the killing of unborn babies in abortions anymore.

Of the 30,635 new HIV diagnoses in the U.S. in 2020, 68% (20,758) were among gay and bisexual men.