Fda

Rapid Covid home tests are more likely to give a false negative with the heavily-mutated Omicron variant compared to earlier strains, the US Food and Drug Administration (FDA) said Tuesday.

The US Food and Drug Administration (FDA) on Thursday authorized Merck's Covid pill for high risk adults, a day after a similar pill by Pfizer was given the green light.

The US Food and Drug Administration (FDA) on Wednesday authorized Pfizer's Covid pill for high-risk people aged 12 and over, a major milestone in the pandemic that will allow millions to access the treatment.

The Maharashtra Food and Drug Administration (FDA) has seized stocks of a medicine that makes misleading claim to cure diabetes after raiding the premises of a pharma distributor here, FDA officials said on Wednesday.

The USFDA has determined that the inspection classification of the facility is VAI, the company said in a statement.

The US Food and Drug Administration (FDA) on Thursday expanded authorization of the Pfizer-BioNTech Covid booster to include 16- and 17-year-olds.

India-based pharma giant, Zydus Cadila received final approval from US Food and Drug Administration (FDA) for Glycopyrrolate injection that is used before surgery to decrease the volume of secretions from the mouth, lungs and stomach.

A study, published in the Journal of Exposure Science & Environmental Epidemiology, states that traces of some harmful chemicals were found in burritos, pizzas, burgers and several other fast foods.

Ocugen, Bharat Biotech's US partner for COVID-19 vaccine Covaxin, on Wednesday said it has submitted Investigational New Drug Application (IND) to the US Food and Drug Administration to conduct clinical trials.

The US Food and Drug Administration (FDA) on Wednesday authorized using a so-called "mix and match" strategy for eligible people who require a booster shot of a Covid vaccine after their primary series.

The US Food and Drug Administration (FDA) is preparing to allow "mix and match" coronavirus vaccine boosting, in which people get a different additional shot to the dose they initially received, US media reported.

Drug maker Johnson & Johnson asked the US Food and Drug Administration (FDA) on Tuesday to authorize booster shots of its Covid-19 vaccine for people over the age of 18.

The United States on Wednesday authorized the use of boosters of Pfizer's Covid-19 vaccine for people aged over 65, or adults at high-risk of severe disease as well as those in high-exposure jobs.

Lupin shares have so far this year fallen 2.73 per cent, sharply underperforming the benchmark Sensex which has advanced 23.6 per cent.

Molecular Biology Consortium based at Berkeley Lab's Advanced Light Source (ALS) claims to have discovered an antibody that can neutralise all known SARS-CoV-2 strains, including the new mutants.

Rapid Covid home tests are more likely to give a false negative with the heavily-mutated Omicron variant compared to earlier strains, the US Food and Drug Administration (FDA) said Tuesday.

The US Food and Drug Administration (FDA) on Thursday authorized Merck's Covid pill for high risk adults, a day after a similar pill by Pfizer was given the green light.

The US Food and Drug Administration (FDA) on Wednesday authorized Pfizer's Covid pill for high-risk people aged 12 and over, a major milestone in the pandemic that will allow millions to access the treatment.

The Maharashtra Food and Drug Administration (FDA) has seized stocks of a medicine that makes misleading claim to cure diabetes after raiding the premises of a pharma distributor here, FDA officials said on Wednesday.

The USFDA has determined that the inspection classification of the facility is VAI, the company said in a statement.

The US Food and Drug Administration (FDA) on Thursday expanded authorization of the Pfizer-BioNTech Covid booster to include 16- and 17-year-olds.

India-based pharma giant, Zydus Cadila received final approval from US Food and Drug Administration (FDA) for Glycopyrrolate injection that is used before surgery to decrease the volume of secretions from the mouth, lungs and stomach.

A study, published in the Journal of Exposure Science & Environmental Epidemiology, states that traces of some harmful chemicals were found in burritos, pizzas, burgers and several other fast foods.

Ocugen, Bharat Biotech's US partner for COVID-19 vaccine Covaxin, on Wednesday said it has submitted Investigational New Drug Application (IND) to the US Food and Drug Administration to conduct clinical trials.

The US Food and Drug Administration (FDA) on Wednesday authorized using a so-called "mix and match" strategy for eligible people who require a booster shot of a Covid vaccine after their primary series.

The US Food and Drug Administration (FDA) is preparing to allow "mix and match" coronavirus vaccine boosting, in which people get a different additional shot to the dose they initially received, US media reported.

Drug maker Johnson & Johnson asked the US Food and Drug Administration (FDA) on Tuesday to authorize booster shots of its Covid-19 vaccine for people over the age of 18.

The United States on Wednesday authorized the use of boosters of Pfizer's Covid-19 vaccine for people aged over 65, or adults at high-risk of severe disease as well as those in high-exposure jobs.

Lupin shares have so far this year fallen 2.73 per cent, sharply underperforming the benchmark Sensex which has advanced 23.6 per cent.

Molecular Biology Consortium based at Berkeley Lab's Advanced Light Source (ALS) claims to have discovered an antibody that can neutralise all known SARS-CoV-2 strains, including the new mutants.