An Emergency Use Authorization (EUA) in the United States is an authorization granted to the Food and Drug Administration (FDA) under sections of the Federal...

PMC 7309195. PMID 32576276. Commissioner, Office of the (2024-03-04). "Emergency Use Authorization". FDA. "How Drugs are Reviewed in Canada". Government of Canada...

and Drug Administration (FDA) granted nirmatrelvir/ritonavir emergency use authorization (EUA) to treat COVID‑19. It was approved in the United Kingdom...

been granted an emergency use authorization (EUA) by the US Food and Drug Administration (FDA) and a conditional marketing authorization by the European...

medical use in the United Kingdom in November 2021. In December 2021, the US Food and Drug Administration (FDA) granted an emergency use authorization (EUA)...

have granted full or emergency use authorizations for 40 COVID-19 vaccines. Ten vaccines have been approved for emergency or full use by at least one stringent...

distribution," noting that this depended on the government granting emergency use authorization or product approval. California based laboratory, FOMAT, is part...

States. The Food and Drug Administration (FDA) first granted emergency use authorization to the Pfizer–BioNTech vaccine on December 10, 2020, and mass...

collaboration with Eli Lilly and Company. The drug was granted an Emergency Use Authorization by the U.S. Food and Drug Administration in November 2020, and...

(CDSCO) in India, on 5 May 2021, granted an Emergency Use Authorization to Roche (Genentech) and Regeneron for use of the casirivimab/imdevimab cocktail in...

From April to June 2020, there was an emergency use authorization for their use in the United States, and was used off label for potential treatment of...

Invivyd. The US Food and Drug Administration (FDA) issued an emergency use authorization for pemivibart in March 2024. In the US, pemivibart is authorized...

Lilly as a treatment for COVID-19. The medication was granted an emergency use authorization (EUA) by the US Food and Drug Administration (FDA) in November...

issued to Quidel the first emergency use authorization (EUA) for a COVID-19 rapid antigen test, a new category of tests for use in the ongoing pandemic....

help preventing and treating COVID-19. The data supporting the emergency use authorization (EUA) for bamlanivimab and etesevimab are based on a randomized...

Although Sotrovimab was used world-wide against SARS-CoV-2, including in the United States under an FDA emergency use authorization (EUA), the FDA canceled...

hospitalization or death. In November 2020, the FDA issued an emergency use authorization (EUA) for the combination of baricitinib with remdesivir, for...

(1). hdl:10665/340684. "Fact Sheet For Health Care Providers Emergency Use Authorization (EUA) Of Bamlanivimab and Etesevimab". U.S. Food and Drug Administration...

relaxed when the US Food and Drug Administration (FDA) updated the emergency use authorization (EUA) to permit undiluted frozen vials of the vaccine to be transported...

granted an emergency use authorization (EUA) by the US Food and Drug Administration (FDA) in April 2023. Vilobelimab was authorized for medical use in the...

emergency authorization for Pfizer–BioNTech's BNT162b2 COVID-19 vaccine for widespread use. On 11 December, the FDA gave emergency use authorization for...

granted emergency use authorization on December 17, 2020, and the Janssen (Johnson & Johnson) vaccine was granted emergency use authorization on February...

reaching clinical trials. It is currently in phase III. It received emergency use authorization in Iran on 9 September 2021. The vaccine is named after the Iranian...

(November 2020). "Expanded Access Programs, compassionate drug use, and Emergency Use Authorizations during the COVID-19 pandemic". Drug Discovery Today. 26...

the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for the use of peramivir based on safety data from phase I, phase...

authorized for emergency use in the US. In March 2024, pemivibart (Pemgarda), a monoclonal antibody drug, received an emergency use authorization from the US...

2021, the U.S. Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for Propofol‐Lipuro 1% to maintain sedation via continuous...

From April to June 2020, there was an emergency use authorization for their use in the United States, and was used off label for potential treatment of...

approval. In the United States, baricitinib is authorized under an emergency use authorization (EUA) for the treatment of COVID-19 in hospitalized people aged...

2021, the combination of nirmatrelvir and ritonavir was granted emergency use authorization by the US Food and Drug Administration (FDA) for the treatment...