Search For "drug administration"
US lifts pause on use of Johnson & Johnson COVID-19 vaccine
Updated : 4 years, 10 months ago IST
Washington [US], April 24 (ANI): The US Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) have determined that the recommended pause regarding the use of Johnson & Johnson COVID-19 Vaccine in the US should be lifted and use of the vaccine should
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11 killed in oxygen tanker leak incident in Maharashtra's Nashik
Updated : 4 years, 10 months ago IST
Nashik (Maharashtra) [India], April 21 (ANI): Eleven people were killed in an oxygen tanker leak incident at Dr Zakir Hussain Hospital in Maharashtra's Nashik district, said Food and Drug Administration (FDA) Minister Rajendra Shingane on Wednesday.
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US revokes authorisation of one of Eli Lilly's COVID-19 monoclonal antibod
Updated : 4 years, 11 months ago IST
Washington [US], April 17 (ANI): The US Food and Drug Administration (FDA) said on Friday that it has revoked it emergency authorisation of Eli Lilly's COVID-19 monoclonal antibody treatment bamlanivimab when used on its own.
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South Africa suspends use of Johnson & Johnson COVID-19 vaccine
Updated : 4 years, 11 months ago IST
Johannesburg [South Africa], April 14 (ANI): South African Health Minister Zweli Mkhize on Tuesday said that the country will be suspending the use of the Johnson & Johnson COVID-19 vaccine after health concerns raised by the US Food and Drug Administration (FDA).
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FDA recommends pause in use of Johnson & Johnson COVID-19 vaccine
Updated : 4 years, 11 months ago IST
Washington [US], April 13 (ANI): The US Centers of Disease Control and Prevention (CDC) and the US Food and Drug Administration (FDA) have recommended "pause" in the use of Johnson and Johnson COVID-19 vaccine "out of an abundance of caution" over six reported cases in the US of a "rare and
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West expands partnership with Venus Remedies to launch safe syringes in In
Updated : 4 years, 11 months ago IST
Hyderabad (Telangana) [India], April 13 (ANI/NewsVoir): West Pharmaceutical Services, Inc. (West), a global leader in innovative solutions for injectable drug administration, recently announced its partnership with domestic Indian pharma company Venus Remedies Ltd. whose brand Cloti-Xa™
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Pfizer asks for expansion of emergency use authorization to vaccinate 12 t
Updated : 4 years, 11 months ago IST
New York [US], April 10 (ANI): Pfizer and BioNTech requested the US Food and Drug Administration (FDA) on Friday for an amendment to its emergency use authorization of its Covid-19 vaccine, to expand its use for children ages 12 to 15 in the United States.
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Amazon gets FDA green flag for its COVID-19 test kit
Updated : 4 years, 11 months ago IST
Washington [US], March 27 (ANI): The American multinational technology company, Amazon has received Food and Drug Administration authorization (FDA) for its COVID-19 test developed by its subsidiary STS Lab Holdco and the company is now intending to utilize it for its employee testing progra
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Glenmark Pharmaceuticals receives ANDA approval for Chlorpromazine Hydroch
Updated : 4 years, 11 months ago IST
Mumbai (Maharashtra) [India], March 24 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval from the United States Food & Drug Administration (US FDA) for Chlorpromazine Hydrochloride Tablets USP, 10 mg, 25 mg, 50 mg, 100 mg, and 200 mg, the generic v
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Glenmark Pharmaceuticals receives ANDA approval for Diltiazem Hydrochlorid
Updated : 4 years, 11 months ago IST
Mumbai (Maharashtra) [India], March 23 (ANI/PRNewswire): Glenmark Pharmaceuticals Limited (Glenmark) has received final approval by the United States Food & Drug Administration (U.S. FDA) for Diltiazem Hydrochloride Extended-Release Capsules USP, 60 mg, 90 mg, and 120 mg, the generic ver
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AstraZeneca plans to apply for US emergency nod for Covid-19 jab in April
Updated : 4 years, 11 months ago IST
Cambridge [UK], March 22 (ANI): AstraZeneca said on Monday that the company plans to apply for emergency use authorization from the US Food and Drug Administration for its Covid-19 vaccine in the first half of April.
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US promotes 'serial testing' for COVID-19 with streamlined approval
Updated : 4 years, 12 months ago IST
Washington [US], March 17 (ANI/Sputnik): The US government issued simplified rules for developers of coronavirus tests to promote serial screening, a process in which the same individual is tested multiple times within a few days, the Food and Drug Administration (FDA) said.
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