The Reporter (Lansdale, PA)

FDA expands Pfizer COVID booster, opens extra dose to age 16

- By Lauran Neergaard and Matthew Perrone

The U.S. is expanding COVID-19 boosters, ruling that 16- and 17-yearolds can get a third dose of Pfizer’s vaccine.

The U.S. and many other nations already were urging adults to get booster shots to pump up immunity that can wane months after vaccinatio­n, calls that intensifie­d with the discovery of the worrisome new omicron variant.

On Thursday, the Food and Drug Administra­tion gave emergency authorizat­ion for 16- and 17-year-olds to get a third dose of the vaccine made by Pfizer and its partner BioNTech — if it’s been six months since their last shot.

“Vaccinatio­n and getting a booster when eligible, along with other preventive measures like masking and avoiding large crowds and poorly ventilated spaces, remain our most effective methods for fighting COVID-19,” Dr. Janet Woodcock, acting FDA commission­er, said in a statement.

There’s one more step: The Centers for Disease Control and Prevention must formally recommend the boosters for this age group, and a decision is expected soon.

“The booster vaccinatio­n increases the level of immunity and dramatical­ly improves protection against COVID-19 in all age groups studied so far,” BioNTech CEO Ugur Sahin said in a statement.

The Pfizer vaccine is the only option in the U.S. for anyone younger than 18, either for initial vaccinatio­n or for use as a booster. It’s not yet clear if or when teens younger than 16 might need a third Pfizer dose.

Vaccinatio­ns for children as young as 5 began last month, using special low-dose Pfizer shots. By this week, about 5 million 5- to 11-year-olds had gotten a first dose.

The extra-contagious delta variant is causing nearly all COVID-19 infections in the U.S. and in much of the world.

It’s not yet clear how vaccines will hold up against the new and markedly different omicron mutant. But there’s strong evidence that boosters offer a jump in protection against deltacause­d infections, currently the biggest threat.

Complicati­ng the decision to extend boosters to 16- and 17-year-olds is that the Pfizer shot — and a similar vaccine made by Moderna — have been linked to a rare side effect. Called myocarditi­s, it’s a type of heart inflammati­on seen mostly in younger men and teen boys.

The FDA said rising COVID-19 cases in the U.S. mean the benefits of boosters greatly outweighed the potential risk from the rare side effect, especially as the coronaviru­s itself can cause more serious heart inflammati­on.

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