WASHINGTON -- The head of the Food and Drug Administration said Friday his agency has provided new guidance to the White House after data suggested that a rapid COVID-19 test used by President Donald ...
New York Post may be compensated and/or receive an affiliate commission if you buy through our links. Featured pricing is subject to change. COVID-19 — it’s still a thing, which means it’s always a ...
The public will no longer need a prescription or a visit to a health provider to take take a combined COVID and flu test at home. The U.S. Food and Drug Administration on Thursday announced it has ...
HHS will begin distributing Abbott’s 15-minute COVID-19 test to states in mid-September and will let states decide how to use them, The Hill reported. The tests received emergency authorization from ...
Taking a COVID-19 test at home seems simple enough: If you get a line, you're positive for the coronavirus. But what if your ...
The FDA has extended the shelf life for some COVID-19 tests. Now that allergy season is here, many are finding themselves with symptoms asking: Is it allergies or a cold? COVID? Something else? Since ...
Molecular tests are far superior to rapid antigen tests—and now you can get them for home use. Last week, I was about to go on a date, and because I'm severely immunocompromised, we agreed he would ...
The Food and Drug Administration on Wednesday authorized the first rapid coronavirus test that doesn’t need any special computer equipment to get results. The 15-minute test from Abbott Laboratories ...
The maker of a rapid coronavirus test widely used across the United States and distributed by the federal government has warned that its device can produce false negatives if a special solution is ...
Lab officials say Abbott’s rapid COVID-19 test poses a greater risk of infection to those administering it than other types of diagnostic tests, Kaiser Health News reported. HHS has said the test ...
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