Biden administration chief medical adviser Dr. Anthony Fauci is defending President Joe Biden’s decision to announce that vaccine booster shots would be available for most Americans by Sept. 20 despite no indication that key regulators would approve them in time.
Fauci, head of the National Institute of Allergy and Infectious Diseases since 1984, told “Meet the Press” that Biden’s plan was always contingent on authorization by the FDA.
“I think people are not understanding the difference of planning for something and actually what element of that, what proportion of it, you’re actually going to roll out,” he said. “And that’s exactly what happened.”
Americans who are vaccinated and are waiting for a third shot need to remain patient, Fauci said. Meanwhile, data from the Johnson & Johnson and Moderna vaccines are still needed.
“We’re working on that right now to get the data to the FDA, so they can examine it and make a determination about the boosters for those people,” he said. “They’re not being left behind, by any means.”
It isn’t clear when a final FDA decision could come on booster doses for those aged 65 and up, while the Centers for Disease Control and Prevention has scheduled a meeting next week to distribute boosters around the United States.
“We recommend that people wait until you fall into the category when it’s recommended,” he said, adding that there is “always a theoretical risk” because relevant studies haven’t been performed yet on Pfizer vaccines.
On Sept. 17, the advisory panel voted 16–3 against recommending the Pfizer booster for people under the age of 65. Some members of the board said they are concerned about potential links between the booster and myocarditis, a type of heart inflammation.
Dr. James Hildreth, a voting member on the FDA expert panel, said he has “a serious concern of myocarditis in young people,” while others expressed concern about the data Pfizer presented to the agency. Pfizer had argued that over several months, its vaccine efficacy had dropped and thereby warranted the need for additional doses.
The Epoch Times has contacted the FDA for comment.