HONOLULU – The U.S. Food and Drug Administration (FDA) today granted Emergency Use Authorization for Johnson & Johnson’s COVID-19 vaccination. With the FDA authorization, the U.S. Centers for Disease Control & Prevention’s Advisory Committee on Immunization Practices will soon issue recommendations on who should receive the vaccine and how it should be distributed.
“Today’s announcement validates the FDA’s findings that this vaccine is safe and effective at preventing severe illness, hospitalization, and death,” Hawai‘i State Health Director Dr. Elizabeth Char said. “Johnson & Johnson’s one-dose regimen and less stringent handling requirements will bolster Hawaii’s vaccination efforts. We look forward to reviewing the CDC’s recommendations so we can make informed distribution decisions.”
The Johnson & Johnson vaccine is effective in preventing severe illness, hospitalization and death from COVID-19. Unlike previous vaccines approved by the FDA, this vaccine requires only one dose, and its less stringent storage requirements make it easier to transport and use.
Once the CDC makes recommendations on who should receive the vaccine, state leaders will be able to move forward in coordinating distribution.
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PDF: Following FDA approval Hawaii awaits national guidelines on use of Johnson & Johnson vaccine
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