New Delhi [India], November 6 (ANI): Bharat Biotech's US partner Ocugen has announced that it had asked the US Food and Drug Administration (FDA) for Emergency Use Authorisation (EUA) of Covaxin for children below 18.
Washington [US], November 4 (ANI): Following formal recommendation of the Pfizer COVID-19 vaccine for children 5-11 by the US Food and Drug Administration (FDA), and the Centers for Disease Control (CDC), US President Joe Biden on Thursday (local time) urged parents and guardians to get thei
Washington [US], November 3 (ANI): Following rigorous review and authorization process by the US Food and Drug Administration (FDA), the Centers for Disease Control (CDC) on Tuesday (local time) has formally recommended the Pfizer COVID-19 vaccine for children 5-11.
Washington [US], October 26 (ANI/Xinhua): Advisors to the U.S. Food and Drug Administration (FDA) are set for a key meeting Tuesday on whether to recommend the Pfizer-BioNTech COVID-19 vaccine for children ages 5 to 11, as experts predicted younger kids will be eligible for the vaccine in e
Moscow [Russia], October 21 (ANI): Following the decision by the US Food and Drug Administration allowing individuals to receive booster shots that are different from their first COVID-19 vaccine doses, the Russian Direct Investment Fund (RDIF, Russia's sovereign wealth fund) reiterated that
Washington [US], October 21 (ANI): The US Food and Drug Administration (FDA) approved the use of third doses of the Moderna and Johnson and Johnson (Janssen) vaccines against the novel COVID-19 for eligible individuals.
Washington [US], October 16 (ANI): The United States will allow entry only to those foreign nationals who have been fully immunised with a coronavirus vaccine that has been approved either by the Food and Drug Administration (FDA) or the World Health Organization (WHO), the State Department
Hyderabad (Telangana) [India], October 9 (ANI/PNN): Optimus Pharma Private Limited today announced that it has received tentative approval from the United States Food and Drug Administration (FDA) for the generic equivalent of Rexulti® Tablets, 0.25 mg, 0.5 mg, 1 mg, 2 mg, 3 mg, and 4 m
Washington [US], October 1 (ANI): An antiviral pill has been found to reduce the risk of hospitalisation and deaths by 50 per cent in patients diagnosed with COVID-19 during clinical trials.
Washington [US], September 23 (ANI): US Food and Drug Administration (FDA) on Wednesday (local time) authorized booster shots of the Pfizer COVID-19 vaccine for those aged 65 and older and adults at high risk.
Mumbai (Maharashtra) [India], September 21 (ANI/PR Newswire): Glenmark Pharmaceuticals Ltd. (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Clindamycin Phosphate Foam, 1%, the generic version of Evoclin®1 Foam, 1%, of Mylan Pharm
Washington [US], September 18 (ANI): The US Food and Drug Administration advisory (FDA) committee on Friday (local time) voted unanimously to authorize Pfizer booster shots for use in people aged 65-plus and high-risk patients following a prior failed vote to approve third shots for all p