Search For "us food and drug administration fda"
US FDA probing 'about five' allergic reactions to Pfizer COVID-19 vaccine
Updated : 5 years, 5 months ago IST
Washington [US], December 19 (ANI/Sputnik): The US Food and Drug Administration (FDA) is probing roughly five instances of individuals having allergic reactions to Pfizer and BioNTech's vaccine against COVID-19, Peter Marks, the director of the FDA's Center for Biologics Evaluation and Resea
Read More
US FDA plans to give Moderna authorisation for emergency use
Updated : 5 years, 5 months ago IST
Washington [US], December 18 (ANI): Advisors to the US Food and Drug Administration (FDA) voted in favour to recommend that the agency must give Emergency Use Authorisation (EUA) to Moderna's COVID-19 vaccine.
Read More
UPS, FedEx collaborate to ship Pfizer-BioNTech Covid-19 vaccines in US
Updated : 5 years, 5 months ago IST
Washington [US], December 13 (ANI): Rival US companies UPS and FedEx are working side-by-side to ship the Pfizer-BioNTech Covid-19 vaccine, after it was approved for emergency use by the US Food and Drug Administration (FDA) on Friday.
Read More
FDA panel nod to emergency use approval for Pfizer vaccine
Updated : 5 years, 5 months ago IST
Washington [US], December 11 (ANI): A panel of experts advising the US Food and Drug Administration (FDA) on Thursday recommended emergency approval for the Pfizer-BioNTech Covid-19 vaccine.
Read More
Moderna to request Emergency use authorisation, its vaccine 100% effective
Updated : 5 years, 5 months ago IST
Washington [US], November 30 (ANI): US biotech company Moderna on Monday announced that it plans to request an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) and conditional approval from the European Medicines Agency (EMA) after the final results from a lat
Read More
US allows emergency use of Eli Lilly's COVID-19 antibody treatment
Updated : 5 years, 6 months ago IST
Washington DC [US], November 10 (ANI): The US Food and Drug Administration (FDA) has approved an emergency use authorisation (EUA) for American pharmaceutical company Eli Lilly's experimental COVID-19 antibody treatment called 'bamlanivimab' for non-hospitalised patients with mild-to-moderat
Read More
Trump announces emergency authorization of convalescent plasma to treat C
Updated : 5 years, 9 months ago IST
Washington D.C. [US], August 24 (ANI): The US Food and Drug Administration (FDA) has authorised the use of convalescent plasma for the treatment of COVID-19 patients.
Read More
FDA issues first emergency use authorisation for COVID-19 pool testing
Updated : 5 years, 10 months ago IST
Washington D.C. [USA], July 19 (ANI): The US Food and Drug Administration (FDA) on Saturday (local time) issued an emergency use authorisation (EUA) to Quest Diagnostics that allows pool samples from up to four individuals to test for COVID-19.
Read More
Mylan gets DCGI nod for remdesivir in India, to launch at Rs 4,800 per via
Updated : 5 years, 10 months ago IST
Bengaluru (Karnataka) [India], July 7 (ANI): Global pharmaceutical major Mylan has got approval for its remdesivir from the Drug Controller General of India (DCGI) and will launch a generic version of Gilead Sciences' COVID-19 anti-viral in the country at Rs 4,800 for 100 mg/vial.
Read More
US FDA revokes emergency authorisation for HCQ championed by President Tru
Updated : 5 years, 11 months ago IST
Washington D.C. [US], June 15 (ANI): The US Food and Drug Administration (FDA) on Monday revoked the emergency use authorization for malaria drug hydroxychloroquine (HCQ) as a treatment for COVID-19, the use of which has been championed by President Donald Trump.
Read More
Zydus signs licensing agreement with Gilead to manufacture and market Remd
Updated : 5 years, 11 months ago IST
Ahmedabad (Gujarat) [India], June 13 (ANI): Healthcare major Zydus Cadila has signed a non-exclusive licensing agreement with Gilead Sciences Inc for the manufacturing and distribution of Remdesivir, the investigational drug which has been issued an emergency use authorisation by the US Food
Read More
COVID-19: Cipla enters into licensing pact with Gilead to manufacture and
Updated : 6 years ago IST
Mumbai (Maharashtra) [India], May 13 (ANI): Pharmaceutical major Cipla said on Wednesday it has signed a non-exclusive licensing agreement with Gilead Sciences Inc for manufacturing and distributing investigational medicine Remdesivir which has been issued an emergency use authorisation by t
Read More