FDA Restricts the Use of Sotrovimab

Contact:
 Communications Office
 NewsMedia@flhealth.gov
 850-245-4111

Tallahassee, Fla. — On April 5, 2022, the U.S. Food and Drug Administration (FDA) revised the Emergency Use Authorization (EUA) for sotrovimab. The revised EUA does not allow providers to administer this treatment within the United States.

This decision leaves the State of Florida with only a single monoclonal antibody treatment, bebtelovimab.

The FDA based its decision on the Centers for Disease Control and Prevention’s (CDC’s) Nowcast estimates. Unlike previous revisions on EUAs that stopped treatments at an estimate of 80%, the authorization for sotrovimab removed its use at 50%. According to CDC’s current estimate, 40% of COVID-19 cases in Florida would still benefit from this life-saving treatment.

As is tradition at the FDA, this change comes after a single live virus pre-print study with no clinical data. Florida disagrees with decisions on preventions and treatments without being provided any supporting clinical data.

For more information, please contact the FDA at 1-(888)-463-6332.

To find locations with prevention and treatment options, visit the Florida Department of Health treatment locator.

 

About the Florida Department of Health

The department, nationally accredited by the Public Health Accreditation Board, works to protect, promote and improve the health of all people in Florida through integrated state, county and community efforts.

Follow us on Twitter at @HealthyFla and on Facebook. For more information about the Florida Department of Health please visit www.FloridaHealth.gov.

 

Corrections & Clarifications


Original Published 7:43 PM ET, Wed April 06, 2022 | C&C on 9:57 AM ET, Mon April 11, 2022
Original: This decision leaves the State of Florida with only a single post-exposure monoclonal antibody treatment, bebtelovimab.
C&C: This decision leaves the State of Florida with only a single monoclonal antibody treatment, bebtelovimab.
RFC: Re-word this content to be consistent with the EUA.



Originally published at https://www.floridahealth.gov/newsroom/2022/04/20220406-fda-restricts-use-sotrovimab.pr.html

business banners

Latest posts

Marine Upholstery Makes Miami Boats More Comfortable and Easy to Use

Marine upholstery is especially important for boats in Miami, where strong sun, high humidity, and constant saltwater exposure can quickly affect interior materials. In...

ROI Amplified Expands Services to Deliver Strategic Digital Marketing Solutions for Political Campaigns Nationwide

Full Service Digital Marketing Agency ROI Amplified Top Hubspot Partner Award- ROI Amplified TAMPA, FL, UNITED STATES, March 3, 2026 /EINPresswire.com/ --...

Diana Hamilton to Appear on Women In Power TV

FL, UNITED STATES, November 25, 2025 /EINPresswire.com/ -- Diana Hamilton, electrical industry leader and founder of NW Technical Training...

Discover “Recycle Right Miami-Dade: The Youth Collective”

The Miami-Dade Department of Solid Waste Management (DSWM) invites the community to experience “Recycle Right Miami-Dade: The Youth Collective,” an inspiring exhibition on display...

Boyne Capital Announces the Sale of McKee Utility to MasTec

Boyne Capital, announced today the sale of its portfolio company, McKee Utility Contractors, LLC to MasTec, Inc. at an enterprise...

MIAMI REALTORS® Launching Homestead Letters; 10th Set of Letters to Benefit South Florida

MIAMI — The MIAMI Association of REALTORS® (MIAMI), in collaboration with the National Association of REALTORS® (NAR) and the City of Homestead, proudly announces...
celebrity reality tv