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Tag: Us Fda

US FDA Authorizes Pfizer-BioNTech Boosters For Kids Aged 12-15
US FDA Authorizes Pfizer-BioNTech Boosters For Kids Aged 12-15

The decision came as the Omicron variant is spreading rapidly across the US and has led to record high hospitalisations among younger people.

Pfizer's Covid Pill Will Take About 6-8 Months To Come To US Markets
Pfizer's Covid Pill Will Take About 6-8 Months To Come To US Markets

Pfizer has said that Paxlovid reduces the risk of hospitalisation or death in Covid-19 patients by 89 per cent.

US FDA approves 1st Oral Pill By Pfizer To Treat Covid
US FDA approves 1st Oral Pill By Pfizer To Treat Covid

The pill has also been approved for those at high risk for progression to severe Covid-19, including hospitalisation or death.

US FDA authorizes Pfizer-BioNTech vax for kids aged 5-11
US FDA authorizes Pfizer-BioNTech vax for kids aged 5-11

In that study, the vaccine was 90.7 per cent effective in preventing Covid, according to the FDA.

US FDA Panel Okays Pfizer Covid Vax For Kids Aged 5-11
US FDA Panel Okays Pfizer Covid Vax For Kids Aged 5-11

"Covid-19 is "the eighth-highest killer of kids in this age group over the past year,"

Allergic Reactions
Possible Allergic Reactions To Moderna Covid Vaccine Under Probe

New York: US-based drugmaker Moderna has confirmed that it has received a report from California’s health department that several individuals at one vaccination centre in San Diego were treated for possible allergic reactions after vaccination from one lot of the company’s Covid-19 vaccine. The company is “fully cooperating” with the California Department of Public Health […]

Regeneron
US FDA Authorizes Regeneron's COVID Treatment For Emergency Use

New York: The US Food and Drug Administration (FDA) has granted emergency use approval to the Regeneron Pharmaceuticals antibody treatment which was given to President Donald Trump after he was diagnosed with Covid-19. The emergency use authorisation is for the antibody cocktail casirivimab and imdevimab to be administered together — also known as REGN-COV2 or […]

FDA
US FDA Halts Approval For Plasma Therapy To Treat Covid: Report

New York: Blood plasma therapy that is being touted as the final resort to treat Covid-19 has not convinced the US Food and Drug Administration (FDA) as it has put the emergency use authorisation for blood plasma to treat the deadly respiratory disease on hold, the media reported. According to a report in The New […]

COVID-19 testing
Drug Controller General permits clinical trial of convalescent plasma in COVID-19 patients

New Delhi: The central drug regulator has given its go-ahead to a proposal by the Indian Council of Medical Research for the clinical trial of convalescent plasma in COVID-19 patients, as per the protocol developed by ICMR. The Drug Controller General of India said ICMR has submitted a list of institutes, which have shown an […]

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