Bamlanivimab and Etesevimab Injection

IMPORTANT WARNING:

Bamlanivimab and etesevimab injection is currently being studied for the treatment and prevention of coronavirus disease 2019 (COVID-19) caused by the SARS-CoV-2 virus.

Only limited clinical trial information is available at this time to support the use of bamlanivimab and etesevimab injection for the treatment of COVID-19. More information is needed to know how well the combination of bamlanivimab and etesevimab work for the treatment and prevention of COVID-19 and the possible adverse events from it.

Bamlanivimab and etesevimab injection has not undergone the standard review to be approved by the FDA for use. However, the FDA has approved an Emergency Use Authorization (EUA) to allow certain non-hospitalized adults and children and in hospitalized or non-hospitalized children and infants less than 2 years of age who have mild to moderate COVID-19 symptoms to receive bamlanivimab and etesevimab injection.

IMPORTANT NOTICE:

On January 24, 2022, FDA reissued the emergency use authorization (EUA) for bamlanivimab and etesevimab stating that the combination regimen is not authorized for treatment of mild to moderate COVID-19 in geographic regions where infection is likely to have been caused by a non-susceptible SARS-CoV-2 variant based on available information including variant susceptibility to these drugs and regional variant frequency. Given the prevalence of the Omicron variant in the United States, bamlanivimab and etesevimab is not recommended for use anywhere for mild to moderate disease at the present time.

Information about Bamlanivimab and Etesevimab Injection

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