United States health officials lifted their recommended pause on the Johnson and Johnson (J&J) vaccine April 23, after 11 days of the hold. After conducting a review of available data and reaching out to healthcare providers across the U.S., the U.S. Food and Drug Administration (FDA) and Centers for Disease…
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Third coronavirus vaccine approved by FDA
On Feb. 27, the United States Food and Drug Administration (FDA) issued another emergency use authorization for a coronavirus vaccine developed by Johnson & Johnson. This is the third COVID-19 vaccine that has been approved by the FDA for emergency use. With the approval, hopes rise for expanded vaccine outreach.…
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