Regulators expected to OK Pfizer boosters for older Americans this week
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[September 20, 2021]
By Michael Erman
(Reuters) - U.S. regulators are expected to
authorize a third booster shot of the Pfizer Inc/BioNTech SE COVID-19
vaccine for older and some high-risk Americans early this week in time
for the government to roll them out by Friday as hoped.
The Food and Drug Administration is expected to give the nod to the
shots for at least this group in the days ahead of a meeting of advisers
to the U.S. Centers for Disease Control and Prevention scheduled for
Wednesday afternoon. The CDC panel will discuss more precise
recommendations for how the shots will be administered.
On Friday, an FDA advisory committee voted to recommend emergency
authorization of the additional Pfizer shots for Americans 65 and older
and those at high risk of severe illness.
The panel had earlier decided against recommending broader approval,
saying there was not enough evidence to support broad use, and that they
wanted to see more safety data, especially concerning the risk of heart
inflammation in younger people after vaccination.
The FDA is not bound to follow the panel's recommendation but usually
does.
The agency could revisit the booster shots for a broader authorization
in the future. Top FDA members have been split on the necessity of the
boosters, with interim head Janet Woodcock backing them and some of the
agency's top scientists arguing they are not needed yet.
Despite the narrowed scope of the proposed authorization, the panel's
recommendation would cover most Americans who got their shots in the
earliest stages of the U.S. vaccination campaign and whose immunity may
be waning.
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A vial labelled with the Pfizer-BioNTech coronavirus disease
(COVID-19) vaccine is seen in this illustration picture taken March
19, 2021. REUTERS/Dado Ruvic/Illustration
Norman Baylor, chief executive of Biologics
Consulting and former director of FDA’s Office of Vaccines Research
and Review, said the decision gives FDA additional time to
understand what data is required to approve booster shots broadly.
"It does give them some space," Baylor said.
Health officials signaled they expect boosters will ultimately be
recommended for a broad swath of the population, but advised
Americans not to seek booster doses until they have the nod from the
FDA.
President Joe Biden's chief medical adviser, Dr. Anthony Fauci, told
CNN on Sunday that the data needed to determine the advisability of
booster shots of the Moderna Inc and Johnson & Johnson COVID-19
vaccines is just weeks away.
Some countries, including Israel and Britain, have already begun
COVID-19 booster campaigns. The United States authorized extra shots
for people with compromised immune systems last month and some 2
million people had already received a third shot, according to the
CDC.
(Reporting by Michael Erman; Editing by Stephen Coates)
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