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RT: The US Food and Drug Administration (FDA) has revoked its emergency use authorizations for two kinds of monoclonal antibodies treatments produced by Regeneron and Eli Lilly. The regulator said the two therapeutics were “highly unlikely to be active against the omicron variant.”
Opioid-related overdose deaths are one of the leading causes of death in the United States.
A SARS-like cluster of circulating bat coronaviruses shows potential for human emergence
Consumers, restaurants, and retailers should not drink, cook with, sell, or serve “Real Water” alkaline water, until more information is known about the cause of the illnesses.
The rollout of Covid-19 vaccine could then begin in the United States in a matter of days
FDA has scheduled a meeting of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) on Dec. 10
The development of safe and effective vaccines to prevent SARS-CoV-2 infection and/or COVID-19 is essential to help bring the pandemic under control.
The administration proposed labeling a Covid-19 vaccine authorization a ‘pre-licensure,’ which FDA says would undermine its procedures.
Beginning October 1, Gilead will be responsible for distributing Veklury in the United States upon conclusion of the previous distribution agreement with the U.S. Federal government.
Defendants Allegedly Attempted to Avoid Government Regulation by Selling Products Through a Company They Deceptively Named Genesis II Church
More than 100 vaccines are being tested worldwide
Siemens Healthineers Receives FDA Emergency Use Authorization for its SARS-CoV-2 Total Antibody Test that Delivers Superior Clinical Performance Siemens Tarrytown, NY | Jun 01, 2020 • Total antibody test...
Health Editor's Note: Read this FDA communication listing restrictions for the use of hyroxychloroquine, chloroquine, and azithromycin. The use of these medications may cause...
The FDA has not approved Genesis’s product for any use