The Food and Drug Administration yesterday authorized for emergency use the first COVID-19 breathalyzer test for adults, which can detect the virus in breath samples in under three minutes under the supervision of a health care provider licensed or authorized to prescribe tests. Positive results should be treated as presumptive and confirmed with a molecular test. For more information, see the fact sheet for health care providers.

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The Department of Health and Human Services June 30 announced it will terminate emergency use authorization declarations for certain drugs and medical devices…
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Centers for Medicare & Medicaid Services Administrator Mehmet Oz, M.D., and CMS Deputy Administrator and Director of Medicaid and CHIP Dan Brillman sat…
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Flu and COVID-19 vaccination rates among all health care workers for the 2024-25 respiratory virus season was 76.3% and 40.2%, respectively, according to a…
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A study published March 18 by Science Advances estimated that more than 155,000 U.S. COVID-19 deaths were uncounted during the COVID-19 pandemic. Researchers…
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The Centers for Disease Control and Prevention Feb. 19 released a report on the low use of COVID-19 antiviral drugs among individuals age 65 and older, a…
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The Food and Drug Administration today released two guidance documents; one related to low-risk wellness products (including certain wearable devices) and the…