Another COVID-19 antibody-drug has been given emergency use approval by the U.S. Food and Drug Administration. The said drug was developed by GlaxoSmithKline and Vir Biotechnology.
Based on the Food and Drug Administration, the studies suggest that the ban on menthol would help individuals to quit smoking. The FDA noted that menthol makes tobacco more palatable and the flavor facilitates progression to regular smoking, especially to youth and young adults.
An advisory panel to the U.S. Food and Drug Administration (FDA) voted unanimously on Friday to recommend that the agency approve the use of Johnson & Johnson's COVID-19 vaccine in adults.
The U.S. Food and Drug Administration (FDA) gave emergency use authorization to Pfizer's COVID-19 vaccine on Friday night, paving the way for the millions of vulnerable individuals to get inoculated within days.
White House Chief of Staff Mark Meadows said Food and Drug Administration (FDA) Commissioner Stephen Hahn's job could be on the line if his agency will not quickly approve Pfizer Inc.'s COVID-19 vaccine.
Pfizer's COVID-19 vaccine will be going through an FDA committee vote on Thursday, the last step to reach approval, as two allergic reactions reported in the UK raised concerns.
The Pfizer coronavirus vaccine is poised to get approval from the U.S. Food and Drug Administration (FDA) after a scientific evaluation released on Tuesday confirmed it offered strong protection.