Search For "fda"
FDA Pune issues circular to chemists to maintain record of buyers purchasi
Updated : 4 years, 2 months ago IST
Pune (Maharashtra) [India], January 13 (ANI): Food and Drug Administration (FDA) of Pune has issued a circular to all the chemists and other medical retailers instructing them to maintain a record of all the customers buying self-testing COVID RAT kits.
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Researchers find prominent drug to treat Alzheimer's disease
Updated : 4 years, 2 months ago IST
Washington [US], January 8 (ANI): A recent clinical study has identified sildenafil, FDA-approved therapy for erectile dysfunction and pulmonary hypertension, as a promising drug candidate to treat Alzheimer's disease.
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Study finds sildenafil as candidate drug for Alzheimer's disease
Updated : 4 years, 2 months ago IST
Washington [US], January 3 (ANI): A new study by the Cleveland Clinic has found that sildenafil, an FDA-approved therapy for erectile dysfunction and pulmonary hypertension, is a promising drug candidate to help prevent and treat Alzheimer's disease.
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Employees of Pakistan's Federal Directorate of Education to go on strike a
Updated : 4 years, 2 months ago IST
Islamabad [Pakistan], December 31(ANI): The teaching and non-teaching staff of Pakistan's Federal Directorate of Education has called out to go on strike from January 10, 2022 against the Imran Khan government over the controversial clauses of the Islamabad Capital Territory (ICT) Local Gove
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Rapid antigen tests less sensitive for detecting Omicron variant infection
Updated : 4 years, 2 months ago IST
Washington [US], December 29 (ANI): The Food and Drug Administration in the US has said that rapid antigen tests are less sensitive for detecting Omicron variant infections.
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US grants emergency use authorization for Merck's COVID-19 pill
Updated : 4 years, 3 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, 3 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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Pfizer's COVID-19 antiviral pill marks significant step forward in path ou
Updated : 4 years, 3 months ago IST
Washington [US], December 15 (ANI): US President Joe Biden on Tuesday (local time) said that Pfizer's COVID-19 antiviral pill mark a significant step forward in the path out of the pandemic.
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US FDA grants breakthrough designation for early-stage breast cancer detec
Updated : 4 years, 4 months ago IST
Mumbai (Maharashtra) [India], November 20 (ANI/PRNewswire): Datar Cancer Genetics, a leading cancer research company today announced that the US Food and Drug Administration (FDA) has granted 'Breakthrough Designation' for its blood test to detect early-stage Breast Cancer.
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COVID-19: US FDA expands emergency use authorizations for Pfizer, Moderna
Updated : 4 years, 4 months ago IST
Washington [US], November 19 (ANI): The US Food and Drug Administration on Friday (local time) expanded the emergency use authorization (EUA) for the Pfizer and Moderna COVID-19 vaccine boosters signaling that the shots can be given to anyone aged 18+ at least six months after completion of
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Biden administration buys 10 million Pfizer's antiviral COVID-19 pills
Updated : 4 years, 4 months ago IST
Washington [US], November 18 (ANI): Biden administration on Thursday (local time) announced that they have purchased 10 million treatment courses of Pfizer's antiviral COVID-19 pill.
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Philippines approves China's Sinovac COVID-19 vaccine as booster shots
Updated : 4 years, 4 months ago IST
Manila [Philippines], November 16 (ANI/Xinhua): The Philippines' Food and Drug Administration (FDA) has approved the use of China's Sinovac CoronaVac vaccine and three other brands as booster shots against the COVID-19, FDA Director General Enrique Domingo said Tuesday.
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