Search For "us food and drug administration fda"
Trump links acetaminophen use in pregnancy to autism; experts cite lack of
Updated : 7 months, 3 weeks ago IST
Speaking from the Oval Office, Trump stated that the US Food and Drug Administration (FDA) would soon notify physicians to limit the recommendation of Tylenol during pregnancy unless "medically necessary," such as for the treatment of fever, adding, "if you can't tough it out."
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Zumutor Biologics Inc announces FDA clearance of IND application of ZM008,
Updated : 2 years, 9 months ago IST
Boston [US]/Bangalore (Karnataka) [India], August 11: Zumutor Biologics Inc "Zumutor", a Boston based biopharmaceutical company focused on developing unique novel therapeutics in immuno-oncology (I-O) today announces that the US Food and Drug Administration (FDA) has granted the company's In
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US FDA Grants Breakthrough Designation for Blood Test to Help Diagnose Ina
Updated : 3 years, 4 months ago IST
Mumbai (Maharashtra) [India], January 3 (ANI/PRNewswire): Datar Cancer Genetics announced today that the US Food and Drug Administration (FDA) has granted 'Breakthrough Device Designation' for its 'TriNetra™-Glio', a blood test to help in the diagnosis of brain tumors. This is the thir
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Magnum receives USFDA 510k clearance for its surgical masks
Updated : 3 years, 9 months ago IST
New Delhi [India], August 26 (ANI/SRV): Magnum, one of the largest mask manufacturers from Mumbai, which has been in this industry for the last 29 years has recently received the US Food and Drug Administration (FDA) 510 (k) clearance, which is an approval by the United States government tha
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FDA denies authorization to market JUUL e-cigarettes over safety concerns
Updated : 3 years, 11 months ago IST
Maryland [US], June 24 (ANI): Citing safety concerns, the US Food and Drug Administration (FDA) issued marketing denial orders (MDOs) to JUUL Labs Inc. for their e-cigarettes among others which are currently marketed in the United States.
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US approves Pfizer, Moderna Covid-19 vaccines for youngest children
Updated : 3 years, 11 months ago IST
Washington [US], June 17 (ANI): The US Food and Drug Administration (FDA) authorized emergency use of the Moderna COVID-19 Vaccine and the Pfizer-BioNTech COVID-19 Vaccine for the prevention of COVID-19 to include use in children down to 6 months of age.
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FDA removes hold on clinical trial for phase 2,3 for COVAXIN-BBV152 says
Updated : 4 years ago IST
Malvern (Pennsylvania) [US], May 23 (ANI): Biotechnology company Ocugen on Monday announced that the US Food and Drug Administration (FDA) lifted the clinical hold on the Company's Phase 2, 3 clinical trials for COVAXIN™ (BBV152).
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US FDA limits use of Johnson & Johnson COVID-19 vaccine over blood clo
Updated : 4 years ago IST
Washington [US], May 6 (ANI): The US Food and Drug Administration (FDA) on Thursday said that the Johnson & Johnson vaccine that has been administered to more than 18 million Americans can potentially cause "life-threatening blood clots", and thereby warranted "limiting the authorized us
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COVID-19: FDA gives clearance to Covaxin for clinical trials in adults in
Updated : 4 years, 2 months ago IST
New Delhi [India], March 7 (ANI): Bharat Biotech's COVID-19 vaccine Covaxin has been given clearance for clinical trials in adults by the US Food and Drug Administration (FDA).
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US FDA grants the coveted Breakthrough Designation for early-stage prostat
Updated : 4 years, 3 months ago IST
Mumbai (Maharashtra) [India], February 15 (ANI/PR Newswire): Datar Cancer Genetics today announced that the US Food and Drug Administration (FDA) has granted 'Breakthrough Designation' for its blood test to detect early-stage prostate cancer. This is the second test from the Company that has
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US grants emergency use authorization for Merck's COVID-19 pill
Updated : 4 years, 5 months ago IST
Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Thursday said that it has granted an emergency use authorization for Merck's antiviral pill Molnupiravir that is used to treat COVID-19 patients.
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US FDA authorizes Pfizer's COVID antiviral pill for people aged 12
Updated : 4 years, 5 months ago IST
.Washington [US], December 23 (ANI): The US Food and Drug Administration (FDA) on Wednesday (local time) authorized Pfizer's Paxlovid COVID-19 pill for high-risk people aged 12 and over to treat coronavirus disease (COVID-19).
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