The US drug regulatory authority has declined to grant emergency use authorisation (EUA) for Covaxin, India’s Covid-19 vaccine, for children aged between 2 and 18 years. The vaccine’s dev...

The US Food and Drug Administration (FDA) on Thursday authorized Merck's Covid pill for high risk adults amid a winter surge of cases driven by the highly infectious Omicron variant. The decision...

The Food and Drug Administration on Friday authorised booster shots of both the Pfizer-BioNTech and Moderna vaccines for everyone 18 and older, opening up eligibility to tens of millions more fully va...

More than 650 people in 37 states have been sickened in a salmonella outbreak linked to imported onions, federal health officials said on Wednesday. The Food and Drug Administration said that an inve...

If you love the Netflix show, Bridgerton, tickets just went live for a 90-minute ball in March called “The Queen’s Ball: A Bridgerton Experience”. It will take place in US citie...

US regulators on Thursday said transplant recipients and others with severely weakened immune systems can get an extra dose of the Pfizer or Moderna COVID-19 vaccines to better protect them as the del...

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The knights have nearly reached. The fortress is under siege and the archers are raining fire. The villagers are trying their best to farm inside the town to feed the soldiers. It hasn’t rained ...

The Food and Drug Administration on Tuesday gave an emergency green light to the first rapid coronavirus test that can be run from start to finish at home, paving a potential path for more widespread ...

Nine drug companies issued a joint pledge on Tuesday that they would “stand with science” and not put forward a vaccine until it had been thoroughly vetted for safety and efficacy. The co...