Stay up to date with notifications from The Independent

Notifications can be managed in browser preferences.

US to restart use of Johnson & Johnson vaccine

Federal health officials end pause of single-dose shot after 15 patients among more than 8 million were diagnosed with rare blood clots

Alex Woodward
New York
Friday 23 April 2021 19:28 EDT
Comments
Biden announces Covid vaccines available for all adults

Your support helps us to tell the story

From reproductive rights to climate change to Big Tech, The Independent is on the ground when the story is developing. Whether it's investigating the financials of Elon Musk's pro-Trump PAC or producing our latest documentary, 'The A Word', which shines a light on the American women fighting for reproductive rights, we know how important it is to parse out the facts from the messaging.

At such a critical moment in US history, we need reporters on the ground. Your donation allows us to keep sending journalists to speak to both sides of the story.

The Independent is trusted by Americans across the entire political spectrum. And unlike many other quality news outlets, we choose not to lock Americans out of our reporting and analysis with paywalls. We believe quality journalism should be available to everyone, paid for by those who can afford it.

Your support makes all the difference.

Federal health agencies are lifting a pause on Johnson & Johnson’s Covid-19 vaccine, after the US Centers for Disease Control and Prevention uncovered 15 cases of a rare blood clot, three of which were fatal.

More than 8 million people in the US have received the Johnson & Johnson vaccine.

In its second meeting within 10 days, the CDC’s Advisory Committee on Immunization Practices argued that the benefits to the single-dose vaccine outweigh potential risks, and suggested that the vaccine come with a warning to those potentially receiving it.

The FDA and CDC allowed for the immediate administration of the vaccine following the panel’s guidance.

“In the end, this vaccine was shown to be safe and effective for the vast majority of people,” CDC Director Rochelle Walensky said on Friday.

FDA Commissioner Dr Janet Woodcock said the agency concluded that “the known and potential benefits of the ... vaccine outweigh its known and potential risks in individuals 18 years of age and older.”

“We are confident that this vaccine continues to meet our standards for safety, effectiveness and quality,” she said. “We recommend people with questions about which vaccine is right for them have those discussions with their health care provider.”

Roughly 10 million Johnson & Johnson vaccines are awaiting distribution in the US, as state and local governments had looked to the single-dose vaccine to ramp up innoculation efforts.

The pause “was essential to our ability to inform the public” of the rare condition linked to the vaccine, said Dr Jose R Romero, advisory panel chair.

Last week, officials recommended against the administration of the vaccine “out of an abundance of caution” after six women who received the shot – among more than 8 million people who the CDC has recorded receiving that vaccine – were diagnosed with a rare blood clot condition.

Nine additional women were reported with the condition on Friday. Three women died, seven were hospitalised and five are recovering, according to the board.

The CDC panel also issued additional guidance to doctors and health officials for patients who are diagnosed with clots within three weeks of receiving the vaccine.

Roughly 52 per cent of adults across the US have had at least one shot of the three available US vaccines, including Johnson & Johnson’s and the two-dose Pfizer and Moderna vaccines, according to the CDC.

The seven-day average for the number of daily shots is roughly 2.9 million per day.

Join our commenting forum

Join thought-provoking conversations, follow other Independent readers and see their replies

Comments

Thank you for registering

Please refresh the page or navigate to another page on the site to be automatically logged inPlease refresh your browser to be logged in