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COVID-19 Federal Responses: Monday, February 14, 2022

COVID-19 Federal Responses: Monday, February 14, 2022
  • A study found that the effectiveness of booster shots wanes over time. Effectiveness against hospitalization fell from 91% two months post-booster to 78% at four months.
  • The Occupational Safety and Health Administration (OSHA) continues to develop permanent COVID-19 safety standards.
  • Pfizer postponed its request to receive emergency use authorization for the first two shots—of an expected three-dose series—for its COVID-19 vaccine for children under five. The FDA delayed its meeting of advisers planned for February 15 to wait for more information on the three-dose trial.
  • The FDA granted emergency use authorization to Eli Lilly’s monoclonal antibody treatment, bebtelovimab, for patients 12 and older who are at high risk of developing a severe case of COVID-19. The Federal government already purchased enough courses to treat 600,000 patients, and will begin shipping them to states now that it has received authorization.

White House and Federal Agencies

  • The Centers for Disease Control and Prevention (CDC) published new guidance for health plans about how they should cover over-the-counter at-home COVID-19 tests.
  • The Occupational Safety and Health Administration (OSHA) continues to develop permanent COVID-19 safety standards.
  • Surgeon General Dr. Vivek Murthy participated in a Q&A on COVID-19.

Economy, Vaccines, Testing and Treatment

  • Pfizer postponed its request to receive emergency use authorization for the first two shots—of an expected three-dose series—for its COVID-19 vaccine for children under five.
    • The company had asked the Food and Drug Administration (FDA) to approve a two-dose series of shots while gathering data on the effect of a third dose after two doses failed to produce an effective immune response.
    • The FDA delayed its meeting of advisers planned for February 15 to wait for more information on the trial of three doses.
  • The FDA granted emergency use authorization to Eli Lilly’s monoclonal antibody treatment bebtelovimab for patients 12 and older who are at high risk of developing a severe case of COVID-19.
    • The Federal government already purchased enough courses to treat 600,000 patients, and will begin shipping them to states now that it has received authorization.
  • A study found that the effectiveness of booster shots wanes over time. Effectiveness against hospitalization fell from 91% two months post-booster to 78% at four months.
  • The American Medical Association (AMA) published guidelines for minimizing the risk of transmitting SARS-CoV-2 during mouth to mouth resuscitation, such as using bag valve masks and certain protective equipment.

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