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  2. The best FDA-approved at-home COVID tests - AOL

    www.aol.com/lifestyle/at-home-covid-tests...

    The Flowflex COVID-19 Antigen Home Test is currently the only at-home COVID test cleared by the FDA’s premarket review pathway. That means this test is approved beyond just emergency use, but ...

  3. FDA authorizes over-the-counter combined COVID-19 and flu test

    www.aol.com/fda-authorizes-over-counter-combined...

    Similar to other virus test kits on the market, the Healgen product entails using a nasal swab sample to detect if it shows the presence of proteins from SARS-CoV-2 (the virus that causes COVID-19 ...

  4. COVID-19 testing in the United States - Wikipedia

    en.wikipedia.org/wiki/COVID-19_testing_in_the...

    In December, the FDA authorized the use of a rapid testing kit developed by Brisbane, Australia-based Ellume Health. The test is available for purchase without a prescription for about $30 and can give results in about 20 minutes. [62] [63] The FDA approved the test for people with and without COVID symptoms. [63]

  5. Is it COVID-19, a cold or the flu? Your guide to seasonal ...

    www.aol.com/lifestyle/covid-19-flu-colds-back...

    COVID-19 often shares a lot of the same symptoms as influenza, including stuffy or runny nose, sore throat, cough, muscle aches, fatigue and fever or chills. But unlike the flu, COVID symptoms can ...

  6. Emergency Use Authorization - Wikipedia

    en.wikipedia.org/wiki/Emergency_Use_Authorization

    An Emergency Use Authorization (EUA) in the United States is an authorization granted to the Food and Drug Administration (FDA) under sections of the Federal Food, Drug, and Cosmetic Act as added to and amended by various Acts of Congress, including by the Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (PAHPRA), as codified by 21 U.S.C. § 360bbb-3, to allow the use of a ...

  7. Food and Drug Administration - Wikipedia

    en.wikipedia.org/wiki/Food_and_Drug_Administration

    The United States Food and Drug Administration (FDA or US FDA) is a federal agency of the Department of Health and Human Services.The FDA is responsible for protecting and promoting public health through the control and supervision of food safety, tobacco products, caffeine products, dietary supplements, prescription and over-the-counter pharmaceutical drugs (medications), vaccines ...

  8. FDA approves testing pooled samples to speed up coronavirus ...

    www.aol.com/fda-approves-testing-pooled-samples...

    The first COVID-19 diagnostic test to be authorized for pooled samples, it can allow for testing on up to four individual swab specimens at a time, the FDA said. FDA approves testing pooled ...

  9. Treatment and management of COVID-19 - Wikipedia

    en.wikipedia.org/wiki/Treatment_and_management...

    The principal for obstetric management of COVID-19 include rapid detection, isolation, and testing, profound preventive measures, regular monitoring of fetus as well as of uterine contractions, peculiar case-to-case delivery planning based on severity of symptoms, and appropriate post-natal measures for preventing infection.