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HomeNewsFDA Coronavirus (COVID-19) Update: September 3rd, 2020

FDA Coronavirus (COVID-19) Update: September 3rd, 2020

U.S. Food and Drug Administration (FDA)Silver Spring, MD – The U.S. Food and Drug Administration (FDA) continued to take action in the ongoing response to the COVID-19 Coronavirus pandemic:

On September 1st, 2020, the FDA approved an abbreviated new drug application for cisatracurium besylate USP 20 mg/10mL, which is indicated to facilitate tracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation.


Side effects of cisatracurium besylate injection include bradycardia, hypotension, flushing, bronchospasm, and rash. This drug is listed in the FDA Drug Shortage Database.

The FDA remains deeply committed to facilitating access to medical products that are experiencing increased demand.

As part of the FDA’s effort to protect consumers, the agency issued a warning letter jointly with the Federal Trade Commission to 1 Party At A Time for selling an unapproved product with fraudulent COVID-19 Coronavirus claims. The company sells BetterFly, a niacin containing product, with false or misleading claims that the product can mitigate, prevent, treat, diagnose, or cure COVID-19 Coronavirus in people.

There are currently no FDA-approved products to prevent or treat COVID-19 Coronavirus. FDA requested that 1 Party At A Time immediately stop selling this unapproved and unauthorized product. Consumers concerned about COVID-19 Coronavirus should consult with their health care provider.

Wednesday, the FDA updated its guidance, “Investigational COVID-19 Convalescent Plasma,” to provide additional information related to the recently issued Emergency Use Authorization (EUA) for the use of COVID-19 convalescent plasma to treat hospitalized patients with COVID-19 Coronavirus.

This update includes a discussion regarding FDA’s intent to exercise temporary enforcement discretion regarding the IND requirements for the use of this product when blood establishments, hospitals, and health care providers collect plasma that does not meet the Conditions of Authorization of the EUA. T

he revised guidance continues to provide recommendations for health care providers who wish to administer and study convalescent plasma under an Investigational New Drug Application. In addition, the agency updated the web page, “Recommendations for Investigational COVID-19 Convalescent Plasma,” which also provides this information.

Testing updates:

To date, the FDA has currently authorized 238 tests under EUAs; these include 192 molecular tests, 42 antibody tests, and 4 antigen tests.

About the U.S. Food and Drug Administration

The U.S. Food and Drug Administration (FDA), an agency within the U.S. Department of Health and Human Services, protects the public health by assuring the safety, effectiveness, and security of human and veterinary drugs, vaccines and other biological products for human use, and medical devices. The agency also is responsible for the safety and security of our nation’s food supply, cosmetics, dietary supplements, products that give off electronic radiation, and for regulating tobacco products.


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