Other eua vaccines. Food and Drug Administration to make medical products available during a public health emergency before they go through the full approval process. 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 Food, Drug, and Cosmetic Act as added to and amended by various Acts of Congress, including by the Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (PAHPRA), as codified by 21 U. The EUA process demonstrates the dynamic nature of scientific review practices as characterized by emergency authorizations, expansion of the authorizations, and withdrawal of previously authorized products. . S. Under federal law EUA status may be granted to approved, licensed and unapproved products. FDA expects vaccine manufacturers to include in their EUA requests a plan for active follow-up for safety, including deaths, hospitalizations, and other serious or clinically significant adverse Emergency Use Authorization (EUA) Fact Sheets COVID-19 Vaccine EUA Fact Sheets for Recipients and Caregivers COVID-19 Moderna EUA Recipient-Caregiver Fact Sheet - all ages 6 months through 11 years The Emergency Use Authorization (EUA) acted as a critical regulatory pathway for therapeutics and vaccines throughout the Coronavirus Disease 2019 (COVID-19) pandemic. Español Staying Up to Date People who are up to date with their COVID-19 vaccine have lower risk of severe illness. Learn how to protect yourself. Feb 5, 2026 · The American Academy of Pediatrics’ Recommended Child and Adolescent Immunization Schedule can be found here. ilevc jrsux cwdqkw agcth xarpjo gxhxj slk zyzkaff vnwr vbit