This story was up to date at 8:35 p.m.
April 23, 2021 — Use of the Johnson & Johnson COVID-19 vaccine ought to resume in the USA for all adults, the FDA and CDC stated Friday, though well being care suppliers ought to warn sufferers of the danger of creating the uncommon and severe blood clots that brought about the businesses to pause the vaccine’s distribution earlier this month.
“What we’re seeing is the general fee of occasions was 1.9 instances per million folks. In ladies 18 to 29 years there was an approximate 7 instances per million. The danger is even decrease in ladies over the age of fifty at .9 instances per million,” CDC Director Rochelle Walensky, MD, stated in a information briefing Friday night..
In the long run, the potential advantages of the vaccine far outweighed its dangers.
“When it comes to advantages, we discovered that for each 1 million doses of this vaccine, the J&J vaccine may stop over 650 hospitalizations and 12 deaths amongst ladies ages 18-49,” Walensky stated. The potential advantages to ladies over 50 have been even higher: It may stop 4700 hospitalizations and 650 deaths.
“In the long run, this vaccine was proven to be secure and efficient for the overwhelming majority of individuals,” Walensky stated at a press briefing on Friday night time.
The advice to proceed the vaccine’s rollout got here barely 2 hours after a CDC Advisory Committee on Immunization Practices voted to advocate the pause be lifted. The vote was 10-4 with one abstention.
The choice additionally consists of directions for the warning directed at ladies beneath 50 who’ve an elevated danger of a uncommon however severe blood clot dysfunction known as thrombosis with thrombocytopenia syndrome (TTS).
As of April 21, 15 instances of TTS, all in ladies and 13 of them in ladies beneath 50, have been confirmed amongst 7.98 million doses of the J&J vaccine administered within the U.S. Three ladies have died.
The FDA and CDC advisable the pause on April 13 after reviews that 6 ladies developed a blood clotting dysfunction 6 to 13 days after they obtained the J&J vaccine.
William Schaffner, MD, an infectious illness professional at Vanderbilt College in Nashville, and a non-voting ACIP member, stated in an interview the panel made the fitting suggestion.
He applauded each the choice to restart the vaccine and the up to date warning info that “will clarify [TTS] extra totally to folks, notably ladies, who’re coming to be vaccinated.”
As to ladies within the danger group needing to have a alternative of vaccines, Schaffner stated that can be addressed otherwise throughout the nation.
“Each supplier is not going to have different vaccines of their location so there can be many alternative methods to do that. You’ll have to get this info and choose which web site you’re going to relying on which vaccine is out there if this matter is essential to you,” he famous.
ACIP made at this time’s choice after a 6-hour emergency assembly to listen to proof on advantage of Johnson & Johnson’s protecting advantages in opposition to COVID-19 vs. danger of TTS.
Within the CDC-FDA press briefing, Walensky identified that over the previous few days, as regulators have reviewed the uncommon occasions, newly recognized sufferers had been handled appropriately, with out the usage of heparin, which isn’t suggested for treating TTS.
Because of this, regulators felt like their messages had gotten out to medical doctors who now knew how you can take particular precautions when treating sufferers with the dysfunction.
She stated the Johnson & Johnson shot remained an essential possibility as a result of it was handy to present and simpler to retailer than the opposite vaccines at present licensed within the U.S.
Peter Marks, MD, the director of FDA’s Heart for Biologics Analysis and Analysis, stated the company had already added info describing the danger of the uncommon clotting dysfunction to its reality sheets for sufferers and medical doctors.
Janet Woodcock, appearing commissioner of the FDA, stated vaccination facilities may resume giving the “one and completed” photographs as early as tomorrow morning.