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When the Covid-19 pandemic hit, the then-Stanford professor was one of the loudest critics of lockdowns, school closures and ...
Novavax on Thursday tried to calm investors spooked by the delay of full approval of its COVID vaccine shot by U.S.
The U.S. Food and Drug Administration said on Wednesday it will hold a meeting of experts on May 22 to discuss COVID-19 ...
Vinay Prasad, named to lead the FDA agency tasked with regulating vaccines and gene therapy, has made controversial comments ...
For years, U.S. vaccine experts have issued a universal recommendation for Covid vaccines. That could change soon.
19h
Green Matters on MSNCOVID-19 Vaccine Deemed Safe Long Term in New Study, Most Common Side Effects RevealedA half-decade since the pandemic, countless individuals and families have been left wondering: what is the long-term safety ...
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In most people with mild to moderate COVID, it can last 7–10 days. Symptomatic people can spread the infection to others from ...
Placebo testing has been part of the process since the 1940s. It’s unclear what additional measures would achieve — but it may slow development.
Senior leaders at the FDA began pushing Moderna and Pfizer to file for full, formal approval of their COVID vaccines for ...
The EU Court found the head of the European Commission, Ursula von der Leyen, responsible for concealing information about ...
In recent interviews, Health and Human Services Secretary Robert F. Kennedy Jr. has minimized the risk COVID-19 poses to kids ...
13h
AFP on MSNJudgment day in EU chief's Covid vaccine texts caseA top court is to rule Wednesday on whether the EU failed the transparency test by declining to release text messages sent by ...
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