Stay Updated on Developing Stories

April 23 coronavirus news

What you need to know

  • Vaccine advisers to the US Centers for Disease Control and Prevention voted Friday to recommend resuming use of the Johnson & Johnson coronavirus vaccine.
  • India recorded the highest ever daily rise in cases worldwide for the second day in a row, as hospitals in the capital New Delhi run out of oxygen.
  • As US health officials race to get more Covid-19 shots into arms to control the virus, experts now warn vaccine supply will likely outstrip demand in the next few weeks.
Our live coverage has ended for the day.
7:36 p.m. ET, April 23, 2021

Vaccinations with J&J coronavirus vaccine can resume immediately, CDC director says

Vaccinations with Johnson & Johnson’s coronavirus vaccine may resume immediately, Centers for Disease Control and Prevention Director Dr. Rochelle Walensky said Friday.

The CDC and the US Food and Drug Administration lifted their recommendation for pausing use of the company’s Janssen vaccine after CDC advisers recommended it.

“We are no longer recommending a pause to the Johnson and Johnson vaccine,” Walensky said at a news conference. “I support the ACIP’s recommendation that the Johnson and Johnson Covid-19 vaccine be used for persons 18 years of age or older in the United States population under the FDA emergency use authorization, and I have signed this recommendation."

“With these actions, the administration of Johnson and Johnson's Covid-19 vaccine can resume immediately," Walensky added.

Certain women under the age of 50 may have a small risk of developing a rare blood clotting syndrome, Walensky said.

“There is likely an association but the risk is very low,” Walensky said.

 

7:22 p.m. ET, April 23, 2021

CDC and FDA lift pause on Johnson & Johnson coronavirus vaccine

A nurse prepares Johnson & Johnson Covid-19 vaccine doses on March 25, in Los Angeles, California. Frederic J. Brown/AFP/Getty Images

The US Centers for Disease Control and Prevention and the US Food and Drug Administration said they had lifted their recommend pause on use of Johnson & Johnson’s coronavirus vaccine Friday.

The agencies recommended the pause April 13 after learning of six cases of a rare blood clotting syndrome among women who had recently received the vaccine. Earlier Friday, the CDC’s Advisory Committee on Immunization Practices recommended lifting the pause.

“During the pause, medical and scientific teams at the FDA and CDC examined available data to assess the risk of thrombosis involving the cerebral venous sinuses, or CVST (large blood vessels in the brain), and other sites in the body (including but not limited to the large blood vessels of the abdomen and the veins of the legs) along with thrombocytopenia, or low blood platelet counts,” the agencies said in a joint statement. "The teams at FDA and CDC also conducted extensive outreach to providers and clinicians to ensure they were made aware of the potential for these adverse events and could properly manage and recognize these events due to the unique treatment required for these blood clots and low platelets, also known as thrombosis-thrombocytopenia syndrome (TTS).”

The CDC said it now has collected reports of 15 such cases, all in women and 13 of them in women under 50.

7:08 p.m. ET, April 23, 2021

More surveillance of asymptomatic Covid-19 in children could lower new infections, modeling study claims

New research suggests that quicker and more comprehensive monitoring for asymptomatic Covid-19 infection in children – such as testing in school – paired with vaccination of adults, may lower new infections in children to levels similar to vaccination.

In the study published in the medical journal JAMA Network Open on Friday, researchers modeled testing scenarios using Census data. People age 16 and older are now eligible to receive Covid-19 vaccines in the United States; so far, no vaccines are authorized for people younger than 16.

Study authors found that quickly identifying and contact tracing children to identify “silent infections” of Covid-19, where the disease is either presymptomatic or asymptomatic, combined with vaccination of 40-60% adults could significantly reduce the amount of disease.

In a different scenario, where silent infections remained undetected, researchers estimated that children would need an 81% vaccination rate, in addition to 40% of adults being vaccinated, in order to achieve a similar infection rate.

Researchers found that under conditions where vaccinations are only available for adults, even by identifying as few as 1 in 10 infections in children and isolating them within two days of infection, or 1 in 7 infections and isolating within 3 days after, the overall attack rate could be reduced to less than 5%.

According to study authors, these results can provide a map for continuing to reduce Covid-19 spread while waiting on Covid-19 vaccines to be authorized for use in children. 

 

5:52 p.m. ET, April 23, 2021

CDC advisers recommend resuming use of Johnson & Johnson coronavirus vaccine

A healthcare worker loads a syringe with the Johnson & Johnson Covid-19 vaccine on March 26, in Buffalo, West Virginia.  Stephen Zenner/Getty Images

Vaccine advisers to the US Centers for Disease Control and Prevention voted Friday to recommend resuming use of the Johnson & Johnson coronavirus vaccine.

Members of the CDC’s Advisory Committee for Immunization Practices agreed the benefits of the vaccine outweigh the risks from rare blood clots linked with the vaccine.

The language of the vote said: “The Janssen Covid-19 vaccine is recommended for persons 18 years of age and older in the U.S. population under the FDA’s emergency use authorization.”

“The vote is 10 in favor, four opposed and one abstention. The motion carries,” Dr. Jose Romero, Arkansas secretary of health and chair of ACIP, said.
More context: The US Food and Drug Administration will update the label for the vaccine, indicating that women under the age of 50 should be aware of the risk of blood clots from the vaccine.

Earlier, Johnson & Johnson officials said they had agreed to updated language for the label.

CDC Director Dr. Rochelle Walensky will sign off and then the US Food and Drug Administration will prepare an amended emergency use authorization for the vaccine, Dr. Amanda Cohn, ACIP’s executive secretary, said at the meeting earlier.

“We are awaiting and anticipate that the FDA will be putting out a new, a newly approved EUA language,” Cohn said. “And additionally, we will be taking the input from today, along with this language that FDA will publish and both FDA and CDC will have communication materials and education materials including infographics, patient fact sheets."

 

5:43 p.m. ET, April 23, 2021

Canada's prime minister receives AstraZeneca vaccine as the country's Covid-19 case count rises

Canadian Prime Minister Justin Trudeau receives a dose of the AstraZeneca Covid-19 vaccine in Ottawa, Canada, on Friday, April 23. Adrian Wyld/CP/Bloomberg/ Getty Images

Canada’s Prime Minister Justin Trudeau received his first shot of the AstraZeneca vaccine Friday as the country’s Covid-19 case count rises to record levels.

Trudeau went to a local pharmacy with his wife, Sophie Gregoire Trudeau, where they both received the vaccine, Trudeau saying he was "very excited" and gave a thumbs up when it was done. 

Trudeau was also told after the vaccination that his second dose was not yet scheduled, and he would receive an email notice to schedule a follow-up shot. Canada’s vaccine rollout has suffered from supply issues and most second doses are being delayed by up to four months. 

Some context: About an hour after Trudeau received his vaccine, Canada’s expert advisory panel updated its guidance on AstraZeneca, saying it should be offered to all Canadians 30 or older. It had previously recommended it be administered only to those 55 or older although some provinces have already administered doses to those 40 and older. 

The panel also indicated that mRNA vaccines, either Pfizer or Moderna, should be "preferentially offered" and that a complete series of the AstraZeneca vaccine should be used if an individual does not wish to wait for an mRNA vaccine. 

Currently in most Canadian provinces, people aged 55 and younger have not yet been prioritized for an mRNA vaccine unless they are essential workers or they qualify in other categories like caregivers. 

The news on vaccines came as Canada released new modeling on the impact of new infections in the weeks to come. 

Daily case counts, hospitalizations and ICU admissions continue to increase as well as evidence that there is a troubling increase in mortality, now up more than 17% in the last week alone, according to Canada’s public health agency. 

Officials also said Friday that extensive restrictions and lockdowns across the country seem that have stalled the growth of the pandemic, although new daily case counts have perhaps plateaued at very high levels. 

4:34 p.m. ET, April 23, 2021

NFL modifies Covid-19 protocols for vaccinated team personnel 

National Football League commissioner Roger Goodell has modified the league's Covid-19 protocols due to the reduced risk of infection for vaccinated players.

Goodell outlined the amended protocols in a memo sent to all NFL teams on Friday. A source provided a copy of the memo to CNN. 

The NFL said that fully vaccinated team personnel will only be tested for Covid-19 once a week instead of daily tests. Last season, every personnel member was tested for the virus daily.

The memo also says that all fully vaccinated players and staff members will not need to quarantine if they come in close contact with an infected person.

Earlier this month: League spokesperson Brian McCarthy told CNN that the NFL will strongly encourage players to take the vaccine, but it will not be required.

The NFL Draft is scheduled to start on April 29 and conclude on May 1, in Cleveland, Ohio.

3:45 p.m. ET, April 23, 2021

CDC advisers are considering 4 choices on J&J vaccine, including a complete end to its use

Vaccine advisers to the US Centers for Disease Control and Prevention are considering four choices for changing the agency’s recommendation on Johnson & Johnson’s coronavirus vaccine, including label changes or a complete end to its use.

The CDC’s Advisory Committee on Immunization Practices is holding an emergency meeting and is expected to vote later Friday on recommendations.

At issue: The vaccine has been linked to 15 cases of a rare blood clotting condition called thrombosis with thrombocytopenia syndrome, or TTS, all among women. Three have died.

It’s a tricky question because all but two cases have been in women under the age of 50, and no cases have been reported among men since the vaccine has been in general use, although the CDC says it’s unlikely the risk is zero among men. 

CDC staff laid out several possible scenarios, all of which show that while resuming vaccination would result in more cases of blood clots, adding the J&J shot to the mix of available vaccines would save lives and keep people out of the hospital.

The committee’s four possible choices are:
  • Recommend against use for all persons
  • Reaffirm recommendation for all age and sex – US Food and Drug Administration to include warning statement with emergency use authorization
  • Recommend vaccination only for adults aged 50 or older
  • Reaffirm recommendations for use; women aged under 50 should be aware of the increased risk of TTS, and may choose another Covid-19 vaccine (ie mRNA vaccines)

Earlier, Johnson & Johnson officials said they had agreed with the FDA on new wording to add to the label saying the risk of blood clots is plausible and warning of the risks.

 

3:35 p.m. ET, April 23, 2021

CDC: Resuming use of J&J vaccine would save lives and result in at most a few dozen cases of rare blood clots

A dose of the Johnson & Johnson COVID-19 vaccine is prepared at an event put on by the Thornton Fire Department on March 6 in Thornton, Colorado. Michael Ciaglo/Getty Images

Resuming use of Johnson & Johnson’s coronavirus vaccine would save hundreds of lives and result in at most a few dozen cases of rare blood clots, a US Centers for Disease Control and Prevention analysis shows.

CDC’s Advisory Committee on Immunization Practices is holding an emergency meeting to discuss potential changes to guidance for who should get the vaccine.

CDC and the US Food and Drug Administration have paused use of the vaccine while they investigate the risk of a rare blood clotting syndrome called thrombosis with thrombocytopenia syndrome, or TTS. The CDC has reports of 15 cases, all in women, and 13 of them in women under the age of 50. Three have died.

The CDC’s Dr. Sara Oliver presented the results of several models laying out what might happen if the vaccine is used again, including with restrictions on use in certain groups. The CDC took into consideration deaths from coronavirus and the likelihood that people would get vaccinated more quickly if the Johnson & Johnson vaccine was in the mix.

“When resuming vaccination among all persons at least 18 years, we expect 26 to 45 TTS cases depending on vaccine uptake,” she said. But 600 to 1,400 deaths from Covid-19 would be prevented, and as many as 3,500 intensive care unit admissions would be prevented. 

If the vaccine were restricted to people over the age of 50, three TTS cases could be expected, but between 40 and 250 Covid-19 deaths would be prevented, and as many as 1,000 people would not need treatment in the ICU. 

For every million doses of vaccine given to women ages 18 to 49, 13 TTS cases can be expected, Oliver said. But 12 deaths from Covid-19 would be prevented and 127 ICU admissions would be prevented among those women if they had access to the Johnson & Johnson vaccine.

 The CDC did not consider a gender-based restriction, Oliver said, because it would be too hard to explain – even though the risk of blood clots appears to be very low among men.

“There are also benefits beyond efficacy. This vaccine is able to be shipped and stored at refrigerator temperatures, and as a single dose series, which may make it easier to reach some disproportionately affected groups,” Oliver said.

“We note that the benefits of vaccination apply to the whole population over a six month period and result from both direct and indirect effects,” she added.

 

3:36 p.m. ET, April 23, 2021

US adds more than 3 million Covid-19 vaccine shots

Otto Delcid is inoculated with the Pfizer-BioNTech Covid-19 vaccine by nurse Nicole Colon at the UMass Memorial Health Care COVID-19 Vaccination Center in the Mercantile Center in Worcester, Massachusetts, on April 22. Joseph Prezioso/AFP/Getty Images

The United States added more than 3.3 million Covid-19 vaccine shots to its cumulative tally Friday, according to data from the US Centers for Disease Control and Prevention. 

This is the largest single-day increase reported this week, but still leaves the United States short of the daily average peak reached in early April. 

The seven-day average of new Covid-19 shots reported administered continued to fall, and now sits at 2,862,758. This is the second consecutive day this average has been under 3 million. The United States has not seen a seven-day average for vaccination below 3 million for two days in a row since April 2.

The average pace of new shots reported administered has been greater than 3 million shots per day for most of April, reaching a peak of nearly 3.4 million shots per day on April 13.  

By the numbers: More than 200 million Covid-19 vaccine shots have been reported administered since President Biden took office, reaching a threshold the administration had set for Biden’s 100th day in office about a week early.

About 41% of the US population – over 137 million people – have received at least one dose of Covid-19 vaccine, and about 28% of the population – more than 90 million people – are fully vaccinated, CDC data shows. 

Note: Data published by the CDC may be delayed, and doses may not have been given on the day reported. 
Outbrain