The United States Food and Drug Administration is a Federal agency of the Department of Health and Human Services. The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices, cosmetics, animal foods & feed and veterinary products. Read More
Scientists at the US Food and Drug Administration (FDA) are strongly against administering only single doses of the Moderna and Pfizer vaccines, as their efficacy has only been proven if people get two shots, The Wall Street Journal reports. ...
US President Joe Biden on Saturday said the approval of Johnson & Johnson's single-shot coronavirus vaccine by the US Food and Drug Administration (FDA) is "exciting news" but warned Americans against letting their guard down as the situation could d ...
A US Food and Drug Administration (FDA) advisory panel on Friday endorsed Johnson & Johnson's coronavirus vaccine and recommended the agency grant emergency authorisation. ...
The US Food and Drug Administration said on Wednesday that Johnson and Johnson's single-dose COVID-19 vaccine has met the requirements for emergency use authorisation. ...
A treatment, known as KEDRAB (Rabies Immune Globulin [Human]), currently used in the prevention of rabies has been demonstrated to be safe and effective for patients age 17 and under. ...