FDA Authorizes Pfizer’s Coronavirus Vaccine for Emergency Use

Saturday, December 12, 2020

 

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The Food and Drug Administration (FDA) issued an emergency use authorization (EUA) for Pfizer-BioNTech's coronavirus vaccine, the agency announced on Friday night.

"This vaccine will be made free for all Americans," President Trump said in a video message following the announcement. "Through our partnership with FedEx and UPS, we have already begun shipping the vaccine to every state and zip code in the country. The first vaccine will be administered in less than 24 hours.

According to Axios:

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"Why it matters: It's a major milestone in the U.S. fight against COVID-19, clearing the way for the initial rollout of a vaccine that has been found to be 95% effective with no serious side effects.

What to watch: A Department of Health and Human Services official told Axios that Operation Warp Speed is working with governors to ensure that vaccine distribution begins 'within 24 hours' of the FDA's authorization.

636 locations equipped with ultra-cold storage capacity across all 50 states will receive about 2.9 million doses in the initial Pfizer shipment, according to Operation Warp Speed officials.

An equal number will be held for the second dose of the vaccine, which is meant to be administered 21 days later."

READ FDA AUTHORIZATION LETTER HERE

Health care workers and nursing home residents are expected to be the first to receive the vaccine, with Governors deciding where the vaccine will go in their state and who will get them first. 

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The U.K. became the first country to grant emergency approval to the Pfizer vaccine on December 2, followed by Bahrain and Canada.

The FDA will meet later this month to consider granting an EUA for Moderna's vaccine, which has been found to be 94.5% effective.

An EUA is not a full approval. Rolling out the vaccine is contingent upon companies generating more data needed to support full approval, including ongoing placebo-controlled trials to understand the long-term effects.

 
 

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