US lifts pause, allowing J&J COVID-19 vaccinations to resume

Lauran Neergaard and Mike Stobbe
Associated Press
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U.S. health officials lifted an 11-day pause on COVID-19 vaccinations using Johnson & Johnson’s single-dose shot on Friday, after scientific advisers decided its benefits outweigh a rare risk of blood clot.

The government uncovered 15 vaccine recipients who developed a highly unusual kind of blood clot, out of nearly 8 million people given the J&J shot. All were women, most under age 50. Three died, and seven remain hospitalized.

FILE - This Saturday, March 6, 2021, file photo, shows vials of Johnson & Johnson COVID-19 vaccine at a hospital pharmacy.

But ultimately Friday, the Food and Drug Administration and Centers for Disease Control and Prevention decided that J&J’s one-and-done vaccine is critical to fight the pandemic – and that the small clot risk could be handled with warnings to help younger women decide if they should use that shot or an alternative.

“Above all else, health and safety are at the forefront of our decisions,” CDC Director Dr. Rochelle Walensky said in a statement. “Our vaccine safety systems are working. We identified exceptionally rare events – out of millions of doses” of the J&J shot and will continue to monitor them.

The U.S. decision – similar to how European regulators are rolling out J&J’s shot – comes after CDC advisers earlier Friday voted 10-4 to resume vaccinations but panelists made clear that they must come with warnings about the risk. The group debated but ultimately steered clear of outright age restrictions.

“This is an age group that is most at risk (of the clotting) that is getting vaccine predominately to save other peoples’ lives and morbidity, not their own. And I think we have a responsibility to be certain that they know this,” said Dr. Sarah Long of Drexel University College of Medicine, who voted against the proposal because she felt it did not go far enough in warning women.

The committee members all agreed the J&J vaccine “should be put back into circulation,” panel chairman Dr. Jose Romero, Arkansas’ health secretary, said in an interview after the vote. “The difference was how you convey the risk … It does not absolve us from making sure that people who receive this vaccine, if they are in the risk group, that we inform them of that.”

European regulators earlier this week made a similar decision, deciding the clot risk was small enough to allow the rollout of J&J’s shot. But how Americans ultimately handle J&J’s vaccine will influence other countries that don’t have as much access to other vaccination options.

Dr. Paul Stoffels, J&J’s chief scientific officer, pledged that the company would work with U.S. and global authorities “to ensure this very rare event can be identified early and treated effectively.” J&J already was working with the FDA on a warning label for the shot.

At issue is a weird kind of blood clot that forms in unusual places, such as veins that drain blood from the brain, and in patients with abnormally low levels of the platelets that form clots. Symptoms of the unusual clots, dubbed “thrombosis with thrombocytopenia syndrome,” include severe headaches a week or two after the J&J vaccination – not right away – as well as abdominal pain, nausea.

The government initially spotted six cases of the rare clots, with nine more cases coming to light in the last week or so. But even the first needle-in-a-haystack reports raised alarm because European regulators already had uncovered similar rare clots among recipients of another COVID-19 vaccine, from AstraZeneca. The AstraZeneca and J&J shots, while not identical, are made with the same technology.

European scientists found clues that an abnormal platelet-harming immune response to AstraZeneca’s vaccine might be to blame – and if so, then doctors should avoid the most common clot treatment, a blood thinner called heparin.

That added to U.S. authorities’ urgency in pausing J&J vaccinations so they could tell doctors how to diagnose and treat these rare clots. Six patients were treated with heparin before anyone realized that might harm instead of help.

Dr. Jesse Goodman of Georgetown University closely watched Friday’s deliberations and said people should be made aware of the clotting risk but that it shouldn’t overshadow the benefits of COVID-19 protection.

“We need to treat people as adults, tell them what the information is and give them these choices,” said Goodman, a former vaccine specialist at the FDA.

Two-dose vaccines from Pfizer and Moderna, which are made differently and haven’t been linked to clot risks, are the mainstay of the U.S. vaccination effort. But many states had been counting on the easier-to-store, one-and-done option to also help protect hard-to-reach populations including people who are homeless or disabled.

The CDC’s advisers struggled to put the rare clot cases into perspective. COVID-19 itself can cause a different type of blood clots. So can everyday medications, such as birth control pills.

The side effect debate isn’t the only hurdle facing J&J. The FDA separately uncovered manufacturing violations at a Baltimore factory the company had hired to help brew the vaccine. No shots made by Emergent BioSciences have been used – J&J’s production so far has come from Europe. But it’s unclear how the idled factory will impact J&J’s pledge to provide 100 million U.S. vaccine doses by the end of May and 1 billion doses globally this year.

Detroit will evaluate the decision and "find an appropriate way to offer a Johnson and Johnson vaccine option," John Roach, spokesman for Mayor Mike Duggan, said late Friday.

The Michigan Department of Health and Human Services didn't indicate when Johnson & Johnson shots would start being used again in the state. 

Instead the department emphasized that Michigan recently reached a milestone of 6 million doses of the vaccine administered in just over four months. Nearly 34% of the state's 8.1 million adults 16 years and older had been fully vaccinated through Friday, according to the state health department's website. The most recent one million vaccines were administered in a record 11 days, department spokeswoman Lynn Sutfin said Friday.

The pause in the Johnson & Johnson vaccine had been blamed for a recent decline in COVID-19 vaccinations in Michigan.

The state administered 567,115 doses of the vaccine during the week of April 17, a 16% decrease from the nearly 658,700 doses administered during the week of April 10, according to data on the state health department’s website. It was the first time the number had dipped since the beginning of March.

At the same time, doses shipped to Michigan by the federal government declined about 8% from 914,760 doses during the week of April 10 to 840,710 doses last week, according to state data.

Ford Field’s Federal Emergency Management Agency mass vaccination site also experienced a drop in doses administered in the past week. A Ford Field researcher blamed the Johnson & Johnson pause for the drop.

The J&J pause “may have slowed down administration,” Michigan Department of Health and Human Services spokeswoman Lynn Sutfin said.

Ford Field is more than five weeks into its eight-week operation. It was scheduled on Thursday to use Johnson & Johnson vaccine for the seventh and eighth weeks of operation, but had contingency plans if the pause hadn’t been lifted.

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AP health writer Matthew Perrone and Detroit News staff contributed.

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