Search For "drug administration"
Philippines authorises emergency use of AstraZeneca COVID vaccine
Updated : 5 years, 1 month ago IST
Manila [The Philippines], January 28 (ANI/Sputnik): The Philippine Food and Drug Administration (FDA) has authorised the emergency use of the vaccine against the coronavirus developed by the AstraZeneca company, media reported on Thursday.
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Study: Colleges can prevent 96 pc of COVID-19 infections with common measu
Updated : 5 years, 2 months ago IST
Washington [US], January 13 (ANI): The combined effectiveness of three COVID-prevention strategies on college campuses--mask-wearing, social distancing, and routine testing--are as effective in preventing coronavirus infections as the Pfizer and Moderna vaccines approved by the U.S. Food and
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LASA receives WHO Nod for its Khed Unit in Ratnagiri
Updated : 5 years, 2 months ago IST
Mumbai (Maharashtra) [India], January 12 (ANI/NewsVoir): API major, Lasa Supergenerics Ltd. Received WHO Certificate of Good Manufacturing Practices from the Food and Drug Administration authorities for its manufacturing facility situated at Khed (Ratnagiri).
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Glenmark receives one ANDA approval and two tentative ANDA approvals - Tad
Updated : 5 years, 2 months ago IST
Mumbai (Maharashtra)[India], December 31 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark), a research-led global pharmaceutical company has received final approval by the United States Food & Drug Administration (U.S. FDA) for Tadalafil Tablets USP, 2.5 mg, 5 mg, 10 mg and 2
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Glenmark Pharmaceuticals receives ANDA tentative approval for Dabigatran E
Updated : 5 years, 2 months ago IST
Mumbai (Maharashtra) [India], December 21 (ANI/PRNewswire): Glenmark Pharmaceuticals Ltd (Glenmark) has received tentative approval by the United States Food & Drug Administration (U.S. FDA) for Dabigatran Etexilate Capsules, 75 mg, 110 mg, and 150 mg, the generic version of Pradaxa®
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US FDA probing 'about five' allergic reactions to Pfizer COVID-19 vaccine
Updated : 5 years, 2 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
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US FDA authorises Moderna Covid-19 vaccine for emergency use
Updated : 5 years, 2 months ago IST
Washington [US], December 19 (ANI): The United States Food and Drug Administration's (FDA) on Friday (local time) has authorised Moderna coronavirus vaccine for emergency use for people aged 18 years and above.
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US FDA plans to give Moderna authorisation for emergency use
Updated : 5 years, 2 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.
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Trump, White House staffers not among first to get COVID vaccine
Updated : 5 years, 3 months ago IST
Washington [US], December 14 (ANI): Days after the US Food and Drug Administration approved the Pfizer COVID-19 vaccine for emergency use, President Donald Trump on Sunday (local time) said that he along with the White House (WH) staffers would not be among the first in the country to get th
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UPS, FedEx collaborate to ship Pfizer-BioNTech Covid-19 vaccines in US
Updated : 5 years, 3 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.
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Pfizer Covid Vaccine will be administered in less than 24 hours, says Trum
Updated : 5 years, 3 months ago IST
Washington [US], December 12 (ANI): Soon after the US Food and Drug Administration on Friday approved Pfizer's COVID-19 vaccine for emergency use across the country, President Donald Trump said that the vaccine will be administered "in less than 24 hours."
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US FDA authorizes Pfizer's COVID-19 vaccine for emergency use
Updated : 5 years, 3 months ago IST
New York [US], December 12 (ANI): The US Food and Drug Administration authorized Pfizer's Covid-19 vaccine for emergency use on Friday for the prevention of coronavirus disease in individuals 16 years of age and older.
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