Patients with COVID ... shots? U.S. regulators strictly limited who can receive Johnson & Johnson's COVID-19 vaccine due to the ongoing risk of rare but serious blood clots. The FDA said the ...

advised consumers Monday not to use over-the-counter COVID-19 tests by Cue Health and to throw them out. The FDA issued a warning ... risk of vaping, smoking Kids and young adults who use social ...

The FDA is recommending that anyone who still has any home COVID tests left from Cue Health should throw them away. According to the agency, its inspectors discovered that the diagnostics company ...

Cue Health, headquartered in San Diego, received emergency use FDA authorization for two COVID-19 tests early in the pandemic to help people detect if they were infected with the virus.

The Food and Drug Administration warned consumers Monday to not use Cue Health’s at-home Covid-19 tests. This follows an FDA warning letter to the company last week that said Cue was not ...

Health care company Cue Health received emergency use authorization for two COVID-19 tests from the FDA early on in the pandemic to help people detect whether they have been infected with the virus.

After that, the FDA approved the company’s updated COVID booster shot, making it available alongside shots from Moderna and Pfizer. The Sanofi deal was announced a few months after Novavax reported Q4 ...

Following a meeting of an advisory panel this week, the World Health Organization (WHO) recommended drugmakers to update their COVID-19 vaccine formulations to reflect the currently dominant SARS ...

SINGAPORE – As the Covid-19 virus continues to evolve, the Ministry of Health (MOH) and Singapore’s Expert Committee on Immunisation (ECI) continue to recommend an additional dose in 2024 for ...

An FDA rejection of MDMA, the abbreviation of the drug's chemical name, would deal a major setback to the effort. Clinical trials have inspired optimism in the drug for its potential to help the ...