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(Runtime 3:58)At a barbecue on campus last week, flames licked a set of sausage links as scientist Blake Foraker worked on achieving perfect grill…
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According to Novavax, the vaccine's manufacturer, it had a 100% efficacy against the original strain of the coronavirus and 93% efficacy against more worrisome variants that have subsequently appeared.
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The Food and Drug Administration says it's now OK to store the Pfizer COVID-19 vaccine at normal refrigerator temperatures for up to a month. This is much longer than was previously allowed under the FDA's emergency authorization and will make storage and distribution of the vaccine easier.
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The Food and Drug Administration said Monday that children 12 to 15 years old are now eligible to receive a key COVID-19 vaccine as the agency expanded its emergency use authorization for the Pfizer/BioNTech vaccine.
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The U.S. Food and Drug Administration says it is moving to ban menthol cigarettes and flavored cigars, based on the evidence of the addictiveness and harm of the products.
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The Food and Drug Administration and the Centers for Disease Control and Prevention announced Friday after the panel voted that the vaccine is safe and effective at preventing COVID-19, and its benefits outweigh the known risks.
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Peeling paint. Cracked buckets. Employees dragging unsealed bags of medical waste. Procedures ignored. Inadequately trained staff. All of these were problems noted by U.S. Food and Drug Administration inspectors at the Emergent BioSolutions factory in Baltimore – a facility that is intended to produce materials for the Johnson & Johnson COVID-19 vaccine.
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The Centers for Disease Control and Prevention says the blood clots are extremely rare but that it is reviewing the cases. The agency says it expects this pause to last for "a matter of days."
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Experts believe that the availability of at-home coronavirus tests could help slow the continued spread of the virus, which is contagious even when people are asymptomatic. Abbott's test will be available on grocery and drugstore shelves in the "coming weeks," according to a press release from the company. Quidel did not include a timeline in its release.
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A third COVID-19 vaccine is on the way, and this one requires only one shot for immunization. The Food and Drug Administration authorized Johnson & Johnson's vaccine for emergency use Saturday, a day after a panel of advisers to the agency voted unanimously (22-0) in its favor.