FDA Authorizes COVID-19 Vaccine For Emergency Use In U.S.
Pfizer and BioNTech's vaccine is the first to receive an emergency authorization from the Food and Drug Administration. Officials say it may be ready for widespread inoculations within days.
Federal officials have authorized emergency use of the COVID-19 vaccine produced by Pfizer and BioNTech in a landmark decision that promises to alter the fight against the coronavirus radically in the United States.
The U.S. Food and Drug Administration released its letter to Pfizer granting the authorization Friday evening.
The FDA's authorization, which comes just one day after an advisory panel overwhelmingly offered its endorsement, makes the vaccine the first to obtain a green light for widespread distribution in the United States.
Health and Human Services Secretary Alex Azar, speaking with ABC's Good Morning America, said Friday he expects that "we could be seeing people [in the U.S.] getting vaccinated Monday or Tuesday of next week."
In the first push after authorization, the government expects 2.9 million doses of vaccine to go out. Shipments are expected to begin within 24 hours. Government officials have said they'll be able to supply enough doses of vaccine for 20 million people by the end of the year.
"We have clear evidence that the vaccine is highly effective at least three months after getting the first dose, and given the other data they presented, I think it's likely to be effective for much longer," Dr. Paul Offit told NPR's Morning Edition on Friday in advance of the FDA announcement.
Offit is the director of the Vaccine Education Center at Children's Hospital of Philadelphia and one of the 17 members of the advisory board to vote to recommend the vaccine Thursday. Four of the advisers voted against it, while one abstained.
"We know that the vaccine has been given to tens of thousands of people safely. So we can say, at least with comfort, that it doesn't cause an uncommon, serious side effect," he said, adding the caveat that this doesn't necessarily rule out the possibility that a rare side effect may crop up later.
"But I think we know enough. You know, when you agree to move forward with a product, it's not whether you know everything. It's whether you know enough to say that the benefits outweigh what at this point are theoretical risks," Offit added.
That's a key consideration with the authorization process, which has unfolded against the backdrop of a pandemic currently killing record numbers of people per day in the United States. Nearly 300,000 people in the U.S. have died of COVID-19 since the start of the year, according to data compiled by Johns Hopkins University — a staggering death toll that now exceeds the number of Americans killed in battle during all of World War II.
That means an urgent quandary for health regulators around the world, many of whom, including in the U.S., have departed from the usual approval process to ensure a speedier response to the pandemic. The FDA has relaxed its usual review mechanism to allow drugs, tests and vaccines to get out more quickly than the usual, more stringent requirements for full-blown approval would otherwise allow. This speedier path is called emergency use authorization.
The Pfizer vaccine, which is administered in a pair of doses three weeks apart, has been demonstrated to be 95% effective in clinical trials.
But it's not the only vaccine to show promising results.
Another vaccine, this one produced by Moderna, has been more than 94% effective in trials and is currently awaiting its own authorization by the FDA. At a public meeting on Dec. 17, a panel of expert advisers to the agency will meet to consider the evidence for the vaccine and make a recommendation about it.
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