April 23, 2021, Covid-19 vaccine and world news | CNN

April 23 coronavirus news

NEW YORK, NEW YORK - APRIL 07: Zenobia Brown, MD, of the Northwell Health house calls program prepares a dose of the Johnson & Johnson coronavirus (COVID-19) vaccine in the Astoria neighborhood of Queens borough on April 07, 2021 in New York City. NYC continues to have a 6.55 percent coronavirus (COVID-19) cases on a seven-day rolling average as the city continues to ramp up vaccinations. The city last week set a record of 524,520 coronavirus (COVID-19) vaccinations.  (Photo by Michael M. Santiago/Getty Images)
Dr. Gupta reacts to CDC's recommendation to resume J&J doses
04:26 - Source: CNN

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.

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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.

“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.

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.

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.

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

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. 

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. 

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.”

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.”

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.

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. 

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.

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.

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.

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.

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.

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.

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. 

CDC advisers begin J&J vaccine vote discussion

Members of the Advisory Committee on Immunization Practices have started discussions about what updated recommendation they may have for the Johnson & Johnson vaccine.

A vote is expected following the deliberations.

J&J says link to blood clots with its Covid-19 vaccine is "plausible" and suggests possible label change

A syringe is filled with a dose of the Johnson & Johnson Janssen Covid-19 vaccine at a vaccination site inside Reuther Hall at Forty Acres on March 13 in Delano, California.

Johnson & Johnson has agreed to revised language on the label of its Janssen coronavirus vaccine that warns of the danger of blood clots, a company official told US Centers for Disease Control and Prevention vaccine advisers on Friday.

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.

Johnson & Johnson Chief Medical Officer Dr. Joanne Waldstreicher said the company had worked out revised label language with the FDA.

“To that end, here is the language from our label that we have agreed upon with the FDA regarding thrombosis with thrombocytopenia.”

The revised language refers to blood clots in the brain combined with a blood clotting abnormality called thrombocytopenia. “Reports of adverse events following use of the Janssen Covid-19 vaccine … suggest an increased risk of thrombosis,” it reads, and says the relationship between the vaccine and the clots is “plausible.”

“In addition to the description of the event, health care professionals are alerted in the fact sheet to the signs and symptoms of thrombosis with thrombocytopenia in individuals who receive the COVID vaccine from Janssen,” Waldstreicher said.

“It also states that symptoms began approximately one to two weeks following vaccination, and that most people were females, aged 18 through 49, and that some cases have been fatal. Health care professionals are also directed to the published American Society of Hematology considerations, relevant to the diagnosis and treatment. In addition, the patient’s fact sheet contains a clear warning and instruction. J&J strongly supports this enhanced labeling.”

ACIP will vote later Friday on whether to change recommendations.

Johnson & Johnson says its coronavirus vaccine is valuable and protects against variants

Doses of the Johnson & Johnson COVID-19 vaccine are prepared at a clinic on March 25 in Los Angeles.

A Johnson & Johnson official argued Friday the company’s coronavirus vaccine is valuable to both the US and the world, saying it protects against variants and is easy to distribute.

The benefit of a one-shot vaccine is “critical,” Dr. Mathai Mammen, global head of Janssen Research and Development, told a meeting of US Centers for Disease Control and Prevention vaccine advisers. 

Plus, it’s easily stored at regular refrigerator temperatures for three months – as opposed to the Moderna and Pfizer vaccines, which must be stored frozen.

Some context: ACIP is meeting to discuss whether to change guidance for J&J’s Janssen vaccine.

The CDC and the US Food and Drug Administration recommended pausing its use after six reported cases of women who developed a rare blood clotting syndrome called thrombosis with thrombocytopenia syndrome, or TTS, after receiving Johnson & Johnson’s Janssen vaccine in the United States. Now the CDC says it has learned of 15 cases, including three deaths.

That total does not include one man who experienced clots after taking the vaccine as part of the clinical trial in the fall. That case was not included in the CDC’s analysis of cases seen after the vaccine was authorized and distributed to the public. 

Mammen said clinical trials have shown the Janssen vaccine offers protection quickly – within a week of the single dose. Plus, he said, it protects against concerning variants, including the B.1.351 variant that is now dominant in South Africa. The company’s data showed the vaccine had 82% efficacy in South Africa. 

Brazil's Sao Paulo state reports more than 20% decrease in weekly Covid-19 deaths 

Workers bury a coffin at the Vila Formosa cemetery in Sao Paulo, Brazil, on April 17.

The Brazilian state of Sao Paulo on Friday reported a 23.6% decrease in weekly deaths from Covid-19, after eight weeks of rising death numbers. 

The weekly average of Covid-19 deaths in Sao Paulo state is 621, compared to 813 deaths during the previous period. The average number of cases dropped 14.3%, from 14,921 to 12,784 infected.

Starting on Saturday, restaurants, beauty salons, cinemas, gyms, and other recreational establishments will be able to reopen with attendance restrictions in Sao Paulo state.

Last week, shopping malls were able to open at 25% capacity, as well as religious events. The curfew from 8 p.m. to 5 a.m. local time has yet to be lifted.

Since the beginning of the pandemic, Sao Paulo state has registered at least 2,793,750 cases and 90,810 deaths from the novel coronavirus, according to the state’s health ministry.

Rare blood clots cause symptoms 1 to 2 weeks after Covid-19 vaccination, CDC expert says

So far, patients with a rare and dangerous blood clotting syndrome linked with Johnson & Johnson’s coronavirus vaccine have started showing symptoms one to two weeks after getting the vaccine, a US Centers for Disease Control and Prevention expert said Friday.

And symptoms are similar to those seen among people who experienced blood clots after getting AstraZeneca’s vaccine in Europe and the UK, the CDC’s Dr. Tom Shimabukuro told a meeting of the CDC’s Advisory Committee on Immunization Practices.

The CDC and the US Food and Drug Administration recommended pausing the use of the Johnson & Johnson vaccine after six reported cases of women who developed a rare blood clotting syndrome called thrombosis with thrombocytopenia syndrome, or TTS, after receiving the Johnson & Johnson vaccine in the United States. Now 15 cases have been reported, Shimabukuro said – all of them among women.

During the clinical trial of the vaccine last fall, one man experienced clots 21 days after taking the vaccine, according to J&J. That was case was previously presented to CDC, but was not included in the agency’s analysis of cases seen after the vaccine was authorized and distributed to the public. 

“So to sum up, TTS is rare but clinically serious and potentially life threatening adverse event that has been observed in association with the Janssen Covid-19 vaccine,” Shimabukuro said.

“Symptom onset appears to occur at least several days after vaccination, typically around one to two weeks after vaccination,” he added.

“The clinical features of TTS following the Janssen Covid-19 vaccine appear similar to what is being observed following the AstraZeneca Covid-19 vaccine in Europe. It is important to recognize TTS early and initiate appropriate treatment.”

The main danger is using a common blood thinner called heparin. Other blood thinners are safe to use, and experts are also recommending use of an immune product called IVIG to restore the balance of blood-clotting cells.

“We will certainly continue our enhanced surveillance for this,” Shimabukuro said.

ACIP is expected to vote on any changes to its guidance for J&J’s vaccine later Friday. If ACIP recommends changes to the vaccine label – such as a warning, or changes to who it recommends should get the vaccine – CDC Director Dr. Rochelle Walensky will sign off and then the FDA will have to make any label changes. 

US has more than 9 million Johnson & Johnson doses ready to go if pause lifts

The US has more than nine million doses of Johnson & Johnson’s vaccine ready to be administered if federal health officials lift their recommended pause of the one-shot vaccine, CNN has learned. 

President Biden’s coronavirus adviser Jeff Zients told CNN there are more than nine million doses that have already been distributed to states, tribes, territories and federal channels that are ready to go depending on the conclusion reached by the independent vaccine advisory panel Friday.

If the pause lifts, it’s still unclear how soon those shots will start going into arms, including whether it could take hours or days. Dr. Rochelle Walensky, director of the US Centers for Disease Control and Prevention, will have to approve the recommendation reached by the independent panel. 

UK is looking at ways to help India with Covid-19 pandemic, prime minister says

Britain's Prime Minister Boris Johnson leaves 10 Downing Street in London on April 21.

The United Kingdom is looking at what can be done to help India with the Covid-19 pandemic, UK Prime Minister Boris Johnson told reporters on Friday. 

On Friday, India reported the world’s highest daily rate of Covid-19 for the second day in a row, according to a CNN tally of figures from the Indian Ministry of Health, as Delhi hospitals call for emergency oxygen supplies amid shortages.

No blood clot cases linked with Moderna and Pfizer coronavirus vaccines, CDC expert says

Pharmacist Fedelis Onyimba prepares to administer a Moderna COVID-19 vaccine dose at First Baptist Church of Highland Park on March 18 in Landover, Maryland.

No blood clots have been associated with coronavirus vaccines made by Moderna or Pfizer, a US Centers for Disease Control and Prevention expert said Friday.

The CDC’s Advisory Committee on Immunization Practices is meeting to discuss whether to change guidance for J&J’s Janssen vaccine. The CDC and the US Food and Drug Administration recommended pausing its use after six reported cases of women who developed a rare blood clotting syndrome called thrombosis with thrombocytopenia syndrome, or TTS, after receiving Johnson & Johnson’s Janssen vaccine in the United States. But no cases have been firmly linked with other vaccines used in the US. 

Shimabukuro told ACIP that 2.7 million doses of Pfizer/BioNTech coronavirus vaccine and 2.5 million doses of Moderna’s vaccine had been included in CDC’s Vaccine Safety Database as of April 17. He said 10 cases of a rare type of brain blood clot called CVST were reported afterward but five were ruled out because of the medical histories of the patients, and five more were ruled out because patients did not develop a low level of platelets. It’s the combination of blood clots and low platelet counts that is linked with the vaccines.

ACIP is expected to vote on any changes to its guidance for J&J’s vaccine later Friday. If ACIP recommends changes to the vaccine label — such as a warning, or changes to who it recommends should get the vaccine — CDC Director Dr. Rochelle Walensky will sign off and then the FDA will have to make any label changes.

CDC director: Swift action needed on paused J&J shot as there's demand for convenient single-dose shot

A Premise Health healthcare worker loads a syringe with the Covid-19 Johnson & Johnson Janssen vaccine on March 26 in Buffalo, West Virginia.

Dr. Rochelle Walensky, director of the US Centers for Disease Control and Prevention, said Friday the risk-benefit analysis of the Johnson & Johnson Covid-19 vaccine considers who would prefer the single-dose vaccine or wouldn’t otherwise have access to one of the two-dose vaccines currently authorized in the United States. 

The CDC has been working hard over the last week to determine if there have been any additional cases of blood clots among those people who have received the Johnson & Johnson Covid-19 vaccine, Walensky said. 

The J&J vaccine rollout has been on pause since April 13, after a small number of people experienced blood clots after taking the shot. 

Walensky said the agency’s analysis will be presented during the Advisory Committee on Immunization Practices meeting currently underway.

AstraZeneca vaccine benefits outweigh risks, European Medicines Agency officials say

A vial of the AstraZeneca COVID-19 vaccine is seen at a medical center on March 20 in Bridport, England.

European Medicines Agency officials said at a news conference on Friday that the benefits of the AstraZeneca vaccine outweigh the risks, and that they will continue to review “very rare cases” of blood clots.

“Importantly, the data show that the benefits of vaccination increased with age and increasing levels of infection in the community,” said Dr. Peter Arlett, head of Pharmacovigilance and Epidemiology Department at the European Medicines Agency.

Arlett also said the European Medicines Agency is stepping back from reporting the numbers on blood clots, as the agency wants to contextualize the numbers and the risk.

Earlier this month, the EMA said a particular combination of unusual blood clots with low blood platelet counts should be listed as a side effect of the AstraZeneca vaccine, but stopped short of recommending its use be limited. The agency previously said the positive benefits of AstraZeneca’s vaccine outweigh the risks. 

CDC recommends that pregnant people get the Covid-19 vaccine, director says

Dr. Rochelle Walensky, director of the US Centers for Disease Control Prevention, speaks during a White House Covid-19 briefing on April 23.

Dr. Rochelle Walensky, director of the US Centers for Disease Control Prevention, said Friday that the CDC recommends that pregnant people get the Covid-19 vaccine.

Her comment follows a new study that found no safety concerns among a large group of pregnant people who received the vaccine in their third trimester, and no safety concerns for their babies.

The CDC vaccine guidelines online have not been updated. They currently say that pregnant women may receive a Covid-19 vaccine when one is available, and getting vaccinated is a personal choice, but do not say the vaccine is recommended. CNN reached out to the CDC for further clarification. 

On Wednesday, the New England Journal of Medicine published preliminary findings from CDC scientists that determined that the mRNA Covid-19 vaccines made by Pfizer and Moderna do not appear to pose any serious risk during pregnancy. Last month, another study published in the American Journal of Obstetrics and Gynecology found mRNA Covid-19 vaccines are effective in pregnant and lactating women, and they can pass protective antibodies to newborns. 

Clinical trials of the vaccines did not include pregnant people so there was limited data on the safety of vaccination in pregnant people and babies. Scientists intend to follow up with the pregnant people in the study to assess the long-term safety of the vaccine during pregnancy.

READ MORE

Some promising news for pregnant people
US has the opportunity to overcome the Covid-19 pandemic but a major challenge lies ahead, expert says
US may soon reach a tipping point on Covid-19 vaccine demand. Here’s why that’s concerning
FDA report details flaws at Emergent facility making Johnson & Johnson Covid-19 vaccine
India’s health care system close to collapse

READ MORE

Some promising news for pregnant people
US has the opportunity to overcome the Covid-19 pandemic but a major challenge lies ahead, expert says
US may soon reach a tipping point on Covid-19 vaccine demand. Here’s why that’s concerning
FDA report details flaws at Emergent facility making Johnson & Johnson Covid-19 vaccine
India’s health care system close to collapse