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Pfizer seeks emergency use authorisation for its COVID-19 vaccine in India
"Pfizer India has submitted an application on December 4 to the DCGI seeking emergency use au…
PTI
India allows emergency use of Merck's new drug Molnupiravir for treatment of mild-to-moderate COVID-19 cases
An expert panel of the country's central drug authority has recommended granting emergency use auth…
PTI
Rivals Serum Institute and Bharat Biotech come together after fear of ban on vaccine exports
Bharat Biotech CEO Krishna Ella and Serum Institute of India (SII) CEO Adar Poonawalla issued a joi…
FDA allows emergency use of anti-viral vaccine Remdesivir to treat COVID-19 patients
According to Gilead, the EUA is based on available data from two global clinical trials – the Natio…
PTI
ICMR experts reject inclusion of Molnupiravir in COVID-19 treatment guidelines for fourth time citing safety concerns
Responding to a question over Molnupiravir's inclusion in the treatment guidelines amid doctors …
PTI
Remdesivir expected to be available for COVID-19 patients from next week: top company official
The Food and Drug Administration (FDA) gave emergency use authorisation (EUA) for the use of invest…
PTI
Cipla inks licensing pact with Gilead Sciences for potential COVID-19 treatment drug remdesivir
The EUA is based on available data from two global clinical trials – US National Institute for All…
PTI
Amazon is now selling an FDA-authorized at-home saliva COVID-19 test for $110. All you do is spit in a tube and send it to an LA lab via prepaid shipping.
Amazon is selling the first at-home saliva test to get emergency use authorization (EUA) from the F…
Kate Duffy
Pfizer says kids under 5 may not get shots until mid-2022 after trial found low-dose vaccine didn't work in kids aged 2-5
A low dose of Pfizer's vaccine worked well in babies, but not so well in 2- to 5-year-olds. It mean…
Hilary Brueck
Dr. Fauci says he expects babies and toddlers will have a COVID-19 vaccine by spring 2022
Dr. Anthony Fauci told Insider, if he had to guess, Pfizer will conclude its trial in the coming mo…
Hilary Brueck
Moderna's COVID-19 vaccine could get FDA authorization today, with distribution starting at the weekend, health secretary Alex Azar says
Health and Human Services Secretary Alex Azar called the vaccine "exceptionally safe" and said the …
Grace Dean
US FDA approves emergency use of Remdesivir for COVID-19 patients
The US Food and Drug Administration (FDA) has granted Emergency Use Authorization (EUA) for the e…
Cipla shares gain over 3 pc as co launches generic remdesivir for COVID-19 patients
Remdesivir is the only USFDA-approved EUA for treatment for adult and paediatric patients hospitali…
PTI
Things to keep in mind before taking your teen for Covid-19 vaccination
Sharma noted that the Zydus vaccine ZyCov-D has been approved for people between the age of 15…
Roche India rolls out first batch of its antibody drugs Casirivimab and Imdevimab against COVID-19
Roche India on Monday announced the rollout of its first batch of the antibody cocktail (Casirivima…
COVID-19: Jubilant Life inks licensing agreement with Gilead for remdesivir
The EUA is based on available data from two global clinical trials -- US National Institute for Al…
PTI
'Covaxin likely to be available for public use by Feb' (IANS Exclusive)
New Delhi, Dec 8 (IANS) Covaxin, the COVID vaccine candidate by Hyderabad-based vaccine manufacture…
Brazil's health minister shook hands with a maskless Boris Johnson at the UN. Then he tested positive for COVID-19.
Marcelo Queiroga tweeted on Tuesday that he tested positive for COVID-19, just one day after meetin…
Jake Epstein
Shortfall in Phase-III Covaxin trial target, can delay rollout: AIIMS doctor (IANS Special)
New Delhi, Dec 18 (IANS) The rollout of Covid-19 vaccine by Bharat Biotech for the general public m…
Health Ministry charts out preparatory activities for Covid-19 vaccine roll-out
New Delhi, Dec 8 (IANS) From line-listing of prioritised groups, strengthening cold chain infrastru…