Emergency Use Authorization

The revision is a step toward finalizing the transition from Paxlovid's emergency use authorization to its new drug application label, initiated in late 2023.

An accurate reporting by Pfizer would have shown equal numbers of clinical trial deaths in the vaccine and ...

Commentary Recently, revelations by outstanding artist and writer/researcher/investigator Sasha Latypova about COVID genetic vaccines have shed light on the shady, ...

The Food and Drug Administration (FDA) has approved an unprecedented number of emergency use authorizations (EUAs) for drugs, ...

The National COVID-19 Emergency, first declared by President Trump in March 2020 in response to the COVID-19 pandemic, ...

Drug regulators over at the FDA granted a new Emergency Use Authorization to both Moderna and Pfizer for ...

A medical Army officer who discovered a sudden increase in disease coinciding with reports of side effects alongside ...

The latest trove of Pfizer documents was released by the FDA. These documents reveal information about the clinical ...

Are hospitals in USA full of COVID-19 Cases? No. Let's look at the data. Senator Rand Paul has ...

The U.S. Food and Drug Administration (FDA) announced Friday that it will have its advisory panel meet to ...

With illegal immigration surging at the southern border, President Joe Biden and Mexico's president spoke on Friday. What's their ...

President Joe Biden said on July 27 that his administration is considering mandating that all federal workers get ...

America’s Frontline Doctors, a nonprofit, filed a motion on July 19 seeking immediate injunctive relief to stop the ...

A number of doctors and parents have sued the U.S. Department of Health and Human Services (HHS) and ...

Pfizer and partner BioNTech on Friday submitted an application to the Food and Drug Administration (FDA) for emergency ...

The Food and Drug Administration (FDA) has granted an emergency use authorization (EUA) for a promising new drug ...

The U.S. Food and Drug Administration (FDA) has authorized the emergency use of the first antigen test for ...

The Food and Drug Administration (FDA) issued an emergency use authorization (EUA) of a diagnostic test for the ...

The Food and Drug Administration (FDA) warned on Monday that co-administering antiviral drug remdesivir with chloroquine phosphate or ...