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  2. Wearable cardioverter defibrillator - Wikipedia

    en.wikipedia.org/wiki/Wearable_cardioverter...

    A wearable cardioverter defibrillator (WCD) is a non-invasive, external device for patients at risk of sudden cardiac arrest (SCA). [1] It allows physicians time to assess their patient's arrhythmic risk and see if their ejection fraction improves before determining the next steps in patient care. It is a leased device.

  3. List of COVID-19 pandemic legislation - Wikipedia

    en.wikipedia.org/wiki/List_of_COVID-19_pandemic...

    Second COVID-19 tier regulations in England; United States. Coronavirus Preparedness and Response Supplemental Appropriations Act, 2020 – March 2020;

  4. Treatment and management of COVID-19 - Wikipedia

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

    As of February 2021, in the United States, only remdesivir had FDA approval for certain COVID-19 patients, [67] and while early research had suggested a benefit in preventing death and shortening illness duration, this was not borne out by subsequent trials. [68] [needs update]

  5. FDA reportedly plans to authorize emergency use of largely ...

    www.aol.com/news/fda-reportedly-plans-authorize...

    The Food and Drug Administration will authorize the emergency use of the antiviral remdesivir on COVID-19 patients as soon as Wednesday, a senior administration official told The New York Times.

  6. Rethinking coronavirus, growing questions about the use of ...

    www.aol.com/article/news/2020/04/08/doctors...

    Early reporting on coronavirus deaths from China, Italy and the U.S. show that more than half — and as many as two-thirds — of COVID-19 patients who are placed on ventilators don’t survive.

  7. Food and Drug Administration Safety and Innovation Act

    en.wikipedia.org/wiki/Food_and_Drug...

    The Food and Drug Administration Safety and Innovation Act of 2012 (FDASIA) is a piece of American regulatory legislation signed into law on July 9, 2012.It gives the United States Food and Drug Administration (FDA) the authority to collect user fees from the medical industry to fund reviews of innovator drugs, medical devices, generic drugs and biosimilar biologics.

  8. FDA authorizes emergency use of coronavirus drug remdesivir - AOL

    www.aol.com/fda-authorizes-emergency-coronavirus...

    The Food and Drug Administration on Friday issued an emergency-use authorization for remdesivir in a bid to help patients get quicker access to the first antiviral to show promise against Covid-19 ...

  9. 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 ...