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Politics

Eighty Years Later, Biden and Johnson Revise the Atlantic Constitution for a New Period

CARBIS BAY, UK – UK President Biden and Prime Minister Boris Johnson signed a new version of the 80-year-old Atlantic Charter on Thursday, using their first meeting to redefine the Western alliance and what they see as the growing divide between troubled democracies and their autocratic rivals, led by Russia and China.

The two leaders unveiled the new charter as they tried to draw the world’s attention to emerging cyberattack threats, the Covid-19 pandemic that has turned the global economy on its head, and climate change it would hoped make clear that America First’s Trump era was over.

But the two men continued to grapple with old world challenges, including Mr Biden’s private admonition to the Prime Minister to take action that could spark sectarian violence in Northern Ireland.

The new charter, a 604-word declaration, was an attempt to outline a grand vision for global relations in the 21st century, just like the original, first drafted by Winston Churchill and Franklin D. Roosevelt, a declaration for a western one Commitment was to democracy and territorial integrity just months before the United States entered World War II.

“It was a policy statement, a promise that the UK and United States will meet the challenges of their time and that we will meet them together,” said Biden after his private meeting with Mr Johnson. “Today we are building on that commitment with a revitalized Atlantic Charter that has been updated to reaffirm that promise while addressing directly the key challenges of this century.”

The two men met at a seaside resort on the Cornish coast in England while Royal Navy ships were patrolling to protect the in-person meeting of the Group of 7 Industrialized Leaders, clearly trying to put themselves in the shape of Churchill and FDR . Looking at a small display of the original Atlantic Charter agreed on aboard a ship off Newfoundland in August 1941, less than four months before the attack on Pearl Harbor, Mr. Johnson noted that “this was the beginning of the alliance and “NATO.”

But Mr Biden’s advisors said they thought the charter had grown musty and did not reflect a world of diverse challenges – from cyberspace to China – in which Britain is a greatly reduced power.

Where the original charter provided for the “ultimate destruction of Nazi tyranny” and demanded freedom “to cross the high seas and oceans unhindered”, the new version focused on the “climate crisis” and the need to “protect biodiversity” . It is peppered with references to “emerging technologies”, “cyberspace” and “sustainable global development”.

As a direct reprimand for Russia and China, the new agreement calls on the Western allies to “resist interference through disinformation or other malicious influences, including in elections”. She assesses the threats to democratic nations in a technological age: “We reaffirm our shared responsibility for maintaining our collective security and international stability and resilience against the full spectrum of modern threats, including cyber threats.”

And it promises that “NATO will remain a nuclear alliance as long as there are nuclear weapons. Our NATO allies and partners will always be able to count on us, even if they continue to strengthen their own national armed forces. “

It would be hard to imagine that Mr Johnson, who nurtured his relationship with President Donald Trump, would sign such a document in the Trump era. Nonetheless, he is clearly addressing Mr Biden, who was born barely two years after the first charter was signed and who throughout his political life embraced the alliance it created.

The new charter specifically urges both countries to abide by “the rules-based international order,” a phrase that Trump and his staff tried unsuccessfully to banish from previous statements by Western leaders, believing it was a globalist threat represented Mr. Trump’s America First Agenda at home.

Updated

June 11, 2021 at 12:31 p.m. ET

Mr Biden also used his first full day abroad to officially announce that the United States will donate 500 million doses of the Pfizer BioNTech Covid vaccine to 100 poorer countries, a program that, according to official figures, will donate US $ 3.5 billion. Would cost $ 2 billion, including $ 2 billion in donations to the previously announced Covax consortium.

“Right now, our values ​​are asking us to do everything in our power to vaccinate the world against Covid-19,” said Biden. He brushed aside concerns that his government would use vaccine distribution as a diplomatic weapon in the world market.

“The United States is making these half a billion doses available without any conditions,” he said. “Our vaccine donations do not involve pressure for favors or possible concessions. We do this to save lives. To end this pandemic. That’s it. Period.”

But the donation, which is presented as a humanitarian action that was also in the US’s own interest, also carries a political message. Mr Biden’s advisors say this is a strong demonstration that democracies – and not China or Russia – are able to respond to the world’s crises, faster and more effectively.

By taking the lead in efforts to vaccinate the world and make resources available to meet its greatest public health challenges, officials said the United States is regaining a role it has been playing since the end of World War II tried to play.

Desperate to use the summit as a showcase for a post-Brexit identity with the Global Britain brand, Mr Johnson has also outlined ambitious plans to end the pandemic. Ahead of the summit, Mr Johnson urged leaders to commit to vaccinating everyone in the world against the coronavirus by the end of 2022.

Public health experts applauded Mr Biden’s announcement. If previous donations had been little more than a patch on a huge global vaccine deficit, the 500 million doses were more in line with the scale of the challenge, they said.

The announcement came when Covax, the vaccine-sharing partnership, struggled to deliver enough doses, especially as India blocked supplies from a large factory there to speed up its domestic vaccination campaign. Covax has shipped 82 million cans, less than a fifth of the shipment it expected by June.

But it continues to be difficult to get doses into people’s arms. Public health officials around the world have urged wealthy nations to start distributing their donations soon, rather than releasing additional doses at once later this year so that countries can administer the doses when they arrive.

In his meeting with Mr Johnson, Mr Biden also dealt with an old subject that he knows well: the British Territory of Northern Ireland. It first erupted as a source of tension between Mr Biden and Mr Johnson during the 2020 presidential campaign when Mr Biden warned on Twitter that “we cannot allow the Good Friday Agreement that brought peace to Northern Ireland to be sacrificed”. of Brexit. “He added that any trade deal between the United States and Britain would depend on preventing the return of a hard border between Northern Ireland and Ireland that lies within the European Union.

As a proud Irish American who loves to quote poetry by Yeats, Mr. Biden’s loyalty on this matter has never been in question. They are in stark contrast to Trump, who campaigned for Brexit and once urged Johnson’s predecessor Theresa May to sue the European Union. Mr Biden, on the other hand, described Brexit as a mistake.

The problem is that post-Brexit trade tensions in Northern Ireland have only increased since the election of Mr Biden. The UK has blamed the European Union for trade disruptions that resulted in some supermarket shelves in Northern Ireland being empty after the UK officially exited the bloc in January.

Negotiations over the arrangements, known as the Northern Ireland Protocol, are increasingly controversial, with Britain threatening to pull the plug if Brussels does not make concessions. Last week, the most senior American diplomat in London, Yael Lempert, bluntly expressed government concerns over mounting tensions against British Brexit chief negotiator David Frost.

News of the meeting surfaced in the Times of London on Wednesday evening when Mr Biden arrived in the country. While some analysts predicted it would overshadow Mr. Biden’s meeting with Mr. Johnson, others indicated that it served a purpose – publicly registering American concerns in a way that saved Mr. Biden the need to highlight the point in person.

White House officials have gone out of their way to say they do not want to be drawn into a dispute between London and Brussels. At the same time, they leave no doubt as to the depth of Mr. Biden’s feeling for the Good Friday Agreement conveyed through one of his Democratic predecessors, Bill Clinton.

“He’s not making threats or ultimatums,” National Security Advisor Jake Sullivan told Air Force One reporters. “He will simply convey his ingrained belief that we stand behind this protocol and must protect it.”

Mark Landler contributed the coverage from Falmouth, England, and Benjamin Mueller from London.

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Health

U.Ok. Approves Johnson & Johnson Vaccine

Britain’s drug regulator on Friday approved the use of the single-dose shots manufactured by Johnson & Johnson, the fourth coronavirus vaccine to be authorized in the country.

The authorization comes amid growing concerns about the spread in Britain of a coronavirus variant first detected in India. The number of cases of the variant, known as B.1.617.2, has doubled in a week, according to public data, and as of Thursday, nearly 7,000 cases had been detected.

“This fourth approved vaccine adds to our armory,” the British health secretary, Matt Hancock, said on Twitter. “When you’re eligible, get your jab.” Britain has also authorized the use of the vaccines manufactured by Moderna, Oxford-AstraZeneca and Pfizer-BioNTech.

More than 58 percent of Britain’s population has received at least one dose of a coronavirus vaccine, and 36 percent has been fully vaccinated. Britain opened vaccination to adults 30 and older this week, but most of the vaccination campaign’s efforts have in recent weeks focused on second injections.

Johnson & Johnson’s vaccine is 85 percent effective against severe illness from Covid-19, according to the British regulator.

The approval in Britain comes a day after Mexico gave emergency authorization to the same vaccine.

The Mexican government has previously authorized the vaccines from AstraZeneca and Pfizer, as well as Russia’s Sputnik V and China’s Sinovac and CanSino.

In other news around the world:

  • The regional government of Madrid announced on Friday that it would use AstraZeneca’s vaccine for second doses for people under 60, going against a recommendation by Spain’s central government to switch to Pfizer-BioNTech’s vaccine for the second shot. While European Union regulators have said AstraZeneca’s vaccine is safe, it has continued to create tension in Spain, one of the countries that suspended its use briefly in March after reports of blood clots.

  • The Indian government is in talks with Pfizer to obtain 50 million doses of the company’s coronavirus vaccine starting this summer, but is still considering the drug manufacturer’s demand for indemnity from costs related to severe side effects, officials have said.

  • Hong Kong on Thursday recorded no new coronavirus cases for the first time in seven months, a promising sign in the Chinese territory’s efforts to quash a wave of infections that began in November. The city has gone more than a month without recording more than 15 daily cases, increasing calls for the authorities to relax social-distancing measures.

  • Vietnam ordered religious establishments to suspend large gatherings after a cluster of infections was linked to a Protestant congregation in Ho Chi Minh City, part of a nationwide surge in cases. Of more than 6,300 total cases recorded in the Southeast Asian nation since the start of the pandemic, half have come in the past month, the state-run Vietnam News Agency reported.

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Politics

Over 100 Million Johnson & Johnson Covid Vaccine Doses on Maintain

The House Democrats launched a full investigation into Emergent after the New York Times documented months of problems at the plant, including a failure to properly disinfect equipment and protect it from viral and bacterial contamination. The committee released a series of confidential audits previously reported by The Times that identified a number of violations of manufacturing standards, as well as a June 2020 report from a leading federal manufacturing expert stating that Emergent did not have had trained staff and adequate quality control systems.

Lawmakers are looking to see if corporate officials used ties with the Trump administration to win a $ 628 million federal contract and whether Emergent executives accepted the award despite known shortcomings. You’ll also see Mr. Kramer’s sale of $ 10 million worth of Emergent stock this year and hundreds of thousands of dollars in cash awards made by Emergent’s board of directors to its top executives.

New York Democrat Representative Carolyn Maloney complained that aspiring officials “appeared to have wasted tax dollars while filling their own pockets”. Mr Krishnamoorthi sharply asked Mr Kramer if he would consider handing over his $ 1.2 million bonus to American taxpayers from 2020 onwards.

“Congressman, I will not make that commitment,” replied Mr. Kramer evenly.

“I didn’t think so,” replied Krishnamoorthi-san.

Regarding his stock deals, Mr. Kramer said they were “done according to a plan approved by the company” and in “a quiet time that was also approved by the company”. He added, “My participation has been completely removed from these stores.”

At the beginning of the hearing, Mr. Kramer testified that possible contamination of the Johnson & Johnson cans “has been identified by our quality control procedures, as well as by controls and deliberations. However, when questioned, he later admitted that it was picked up from a Johnson & Johnson laboratory in the Netherlands.

While the Democrats were pushing Mr Kramer for information about how vaccines are made, the Republicans tried to defend the company and tried to change the subject by talking about the unproven theory that the coronavirus emerged from a laboratory in China, the “Lies of the Communist Party of China” and masked mandates as well as the demand of the Biden government for a renunciation of an international agreement on intellectual property, which is strongly rejected by the pharmaceutical industry.

“You are a reputable company that did Yeoman’s job protecting this land on biological defense!” Tennessee Republican Representative Mark Green once exclaimed, adding, “So you gave your people a bonus for their incredible work.”

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Health

Boris Johnson says variant from India extra transmissible

British Prime Minister Boris Johnson speaks during a televised press conference at 10 Downing Street on February 22, 2021 in London, England.

Leon Neal | Getty Images News | Getty Images

LONDON – British Prime Minister Boris Johnson warned on Friday that the variant of the coronavirus, first discovered in India, has the potential to prevent the easing easing currently underway in the country.

The UK is now set to accelerate the second dose of vaccine for those over 50 and clinically at risk due to concerns about the Indian variant.

At a news conference on Friday, Johnson said the variant was more transmissible than other strains but warned it was not clear by how much. The English chief physician Chris Whitty speaks alongside Johnson, added that there is “confidence” that it is “more transferable” than the variants already circulating in the country.

Whitty said, “Earlier this week we said we thought it was as transferable as B.1.1.7 and possibly even more. There is now confidence … that this variation is more transferable than B.1.1.7 . “

The B.1.1.7 variant, known as the UK or Kent strain, has an unusually high number of mutations and is associated with more efficient and faster transmission of the coronavirus. British scientists first discovered this mutation in September last year, and it was the dominant strain in the United States by April

Johnson added that there is currently no evidence that the variant would dodge the vaccines that are being used across the country.

“But I have to measure myself with you, this new variant could seriously disrupt our progress,” said Johnson.

“And I have to emphasize that we will do everything we can to protect the public.”

Data on the new variant, released Thursday by Public Health England, showed the number of cases across the UK had increased from 520 last week to 1,313 this week, with most cases in North West England and some clusters concentrated in London.

The introduction of vaccines in the UK was one of the fastest in the world. Almost 70% of the adult population received at least one shot. Vaccines are available to anyone over the age of 38, but the government has said they could be made available to younger people in multi-generational households.

The next phase of England’s exit from the lockdown is slated for Monday, when the conviviality, hospitality and indoor entertainment will resume.

– CNBC’s Elliot Smith contributed to this article.

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Health

Hug with ‘care and customary sense,’ Boris Johnson says

British Prime Minister Boris Johnson briefs on the coronavirus disease (COVID-19) pandemic during a virtual press conference at 10 Downing Street in central London on March 18, 2021.

Tolga Akmen

LONDON – British Prime Minister Boris Johnson confirmed on Monday that England will move into the next phase of its program to ease the coronavirus lockdown on May 17th.

Indoor facilities such as cinemas and hotels are reopening, but with some capacity constraints. Pubs and restaurants are allowed to welcome customers back indoors, and indoor mixing is allowed to resume for groups of up to six people.

People can also meet outdoors in groups of up to 30 people.

Johnson said the social distancing rules for public spaces remain in place, but people can make their own judgment in private.

When asked about the hug, Johnson said at a news conference Monday, “People should do it when they see fit, when they think the risks are very, very small.”

“But you should use care and common sense. And people who are not vaccinated must have a clearly higher risk of transmission than those who have been vaccinated,” he added.

Johnson has been heavily criticized for the initial response to the coronavirus pandemic. With more than 127,000 reported deaths, the UK has one of the worst death rates in Europe and the world.

But Johnson has also been at the forefront of a successful vaccination campaign that saw more than 50% of the country’s population receive at least one dose of vaccine.

International travel can be resumed next Monday in most cases, although quarantines and testing would for the most part be required upon return to the UK. The government hopes to lift all restrictions on social contact by June 21st.

Around noon on Monday, UK chief medical officers agreed to lower the country’s Covid-19 alert level from 4 – meaning transmission is high or increasing exponentially – to level 3, meaning the epidemic is in general circulation.

– CNBC’s Holly Ellyatt contributed to this article.

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Health

Johnson & Johnson JNJ earnings Q1 2021 beat estimates

Johnson & Johnson’s coronavirus disease (COVID-19) vaccines will be seen at Northwell Health’s South Shore University Hospital in Bay Shore, New York on March 3, 2021.

Shannon Stapleton | Reuters

Johnson & Johnson on Tuesday reported $ 100 million in first-quarter sales of its Covid-19 vaccine, which is on hold in the US while federal health officials investigate a rare blood clotting problem.

When it released its first quarter financial results, the company also reported earnings and sales that exceeded Wall Street’s expectations.

According to Refinitiv’s average estimates, J&J has fared compared to Wall Street expectations as follows:

  • Adjusted earnings per share: $ 2.59 per share versus $ 2.34 expected.
  • Revenue: $ 22.32 billion versus $ 21.98 billion expected.

The New Jersey-based company’s share price fell slightly in premarket trading after the report.

J & J’s pharmaceuticals business, which developed the single-shot vaccine Covid, had sales of $ 12.19 billion, up 9.6% year over year. Results were driven by sales of the company’s multiple myeloma drugs Darzalex and Stelara, a treatment for Crohn’s disease.

The company’s consumer unit, which makes products like Neutrogena Face Wash and Listerine, had sales of $ 3.5 billion, down 2.3% year over year. J&J executives told investors the decline was due to an “unfavorable comparison” with the previous year when people were stocking over-the-counter products due to the virus.

The medical device unit grossed $ 6.57 billion, up 7.9% as the pandemic recovery improves. The unit was badly hit last year when the pandemic forced hospitals to postpone elective surgeries and Americans stayed at home.

J & J’s chief financial officer Joseph Wolk told CNBC Tuesday that the three businesses are “healthier” than they were last year when they entered the pandemic.

The company increased its profit and sales forecast for the year. J&J now expects full year earnings of $ 9.42 to $ 9.57 per share, compared to its previous guidance of $ 9.40 to $ 9.60 per share. Revenue is expected to range between $ 90.6 billion and $ 91.6 billion, compared to its previous forecast of $ 90.5 billion to $ 91.7 billion.

J & J’s Covid vaccine was suspended in the US after six women developed a rare but potentially life-threatening bleeding disorder. One woman died and another was in critical condition.

The six women developed a condition known as cerebral sinus thrombosis within about two weeks of receiving the shot, US health officials said. CVST is a rare form of stroke that occurs when a blood clot forms in the venous sinuses of the brain. It can eventually leak blood into the brain tissue and cause bleeding.

The Chief Medical Officer of the White House, Dr. Anthony Fauci said last week the hiatus would give US health officials the time they need to thoroughly investigate the cases and “find some common ground among the women involved”.

Vamil Divan, an analyst at Mizuho Securities, said in a notice to investors Tuesday that he expects security concerns about the J&J shot to fuel further demand for Pfizer’s mRNA-based vaccine.

During an earnings meeting with investors, J&J executives said the company was working to “restore confidence in the vaccine” after reports of rare blood clots shocked some patients.

“We hope by making people aware of it [of the risk,] Not only do we use clear diagnostic and therapeutic guidelines to restore confidence in our vaccine, ”said Dr. Paul Stoffels, Scientific Director of J & J.

Wolk told CNBC that the company is working with US regulators to ensure they have all the information they need to make a decision about using the J&J vaccine. He expects the US to make a decision by the end of this week. A key body of the Centers for Disease Control and Prevention is due to meet on Friday to make a recommendation on the vaccine.

“We remain very confident and hope the benefit-risk profile will work,” he told CNBC’s Squawk Box, adding that the company continues to expect 100 million doses to be released in the first half of this year will, if the US investigation is conducted on the clot cases, “go well.”

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World News

Fauci Expects Choice on Utilizing Johnson & Johnson Vaccine Friday

A decision to resume administration of Johnson & Johnson’s coronavirus vaccine should be made this Friday when a panel of experts advising the Centers for Disease Control and Prevention says Dr. Anthony S. Fauci, the country’s leading infectious disease expert, is to meet.

“I think we will make a decision by then,” said Dr. Fauci on Sunday on CNN’s State of the Union program.

“I don’t want to be one step ahead of the CDC, the FDA and the Advisory Committee,” he added, but said he expected experts to recommend “some kind of warning or restriction” on using the vaccine.

Federal health officials recommended suspending vaccine injections Tuesday while investigating whether this was related to a rare bleeding disorder. All 50 states except Washington, DC and Puerto Rico have stopped giving the vaccine.

The unusual disorder includes blood clots in the brain combined with low levels of platelets, blood cells that typically promote clotting. The combination, which can lead to coagulation and bleeding at the same time, was initially documented in six women between the ages of 18 and 48 who had received the vaccine one to three weeks earlier. One of the women died and another was hospitalized in critical condition.

This pattern has raised questions about whether vaccinations could be resumed in men or in the elderly. However, with women filling more healthcare positions for which vaccination has been prioritized, it is not clear how the problem could affect men as well. Two more cases of the coagulation disorder were identified on Wednesday, including one in a man who received the vaccine in a clinical trial.

Of the 129.5 million people in the United States who received at least one dose of a Covid-19 vaccine, more than seven million have received Johnson & Johnson’s. If there is a link between the vaccine and the coagulation disorder, the risk remains extremely low, according to experts.

“It is an extremely rare occurrence,” said Dr. Fauci on the ABC program “This Week”. The break should give experts time to gather more information and warn doctors about the clotting disorder so they can make more informed treatment decisions, said Dr. Fauci, who appeared on four television news programs on Sunday morning.

European regulators have investigated similar cases of the unusual coagulation disorder in people who received the AstraZeneca vaccine. Some European countries have now stopped giving this vaccine completely, while others have restricted its use in younger people.

Dr. Fauci also expressed frustration that “a worryingly large segment of Republicans” who have criticized many of the coronavirus restrictions have expressed reluctance to vaccinate. “It’s almost paradoxical,” he said. “On the one hand, they want to be released from the restrictions, on the other hand, they don’t want to be vaccinated. It just makes almost no sense. “

Dr. Fauci said he expects all students to be eligible for a vaccination before school starts in the fall, with younger children being eligible by Q1 2022 at the latest.

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World News

Skilled Panel to C.D.C. to Vote on Johnson & Johnson Vaccine Pause

An advisory committee from the Centers for Disease Control and Prevention discussed the Johnson & Johnson Covid-19 vaccination break during a Wednesday afternoon meeting while investigating a possible association with a small number of rare blood clots.

The emergency meeting follows Tuesday’s announcement by the Food and Drug Administration to investigate six cases of rare and severe blood clots in women aged 18 to 48, one of whom died. All of the women had received the Johnson & Johnson vaccine before developing the clot, although it is unclear whether the vaccine was responsible. As of Tuesday, more than seven million people in the United States had received the shot, and another 10 million cans had been shipped to the states, according to CDC data.

Following the call from federal health officials, all 50 states, Washington, DC and Puerto Rico on Tuesday quickly paused or advised vendors to stop administering the vaccine. The U.S. military, government-run vaccination centers, and a variety of private companies, including CVS, Walgreens, Rite Aid, Walmart, and Publix, also paused the injections.

The Advisory Committee on Immunization Practices (ACIP) is a panel of independent experts who advise the CDC on its vaccine policy. During the meeting, the experts will review and debate data from the rare blood clots, including a seventh case, and will later hear comments from the public before a possible vote on how to proceed. You could vote to recommend, for example, that the break continue, or to indicate that it should only apply to a specific age or gender.

Federal officials said Tuesday the hiatus could only last a few days, though it depends on what officials learned from the investigation. They said the break will give officials more time to alert doctors that patients with these rare blood clots should not be given the drug heparin, the standard treatment doctors give for typical blood clots, and that they also have time to to see if there are more cases.

The worrying coagulation disorder among vaccine recipients is different – and much less common – than the typical blood clots that occur in hundreds of thousands of people each year. In addition to having clots in the brain, the seven women also had remarkably low levels of platelets, parts of the blood that help make normal clots. The panel experts discussed the known background rates of each disease in the general population, but noted that insufficient data was available to accurately estimate how often they occur simultaneously.

“At the moment we believe these events are extremely rare, but we are also not sure we have heard of all possible cases as this syndrome may not be easily identified as being associated with the vaccine,” said Dr. Rochelle P. Walensky, the CDC director said at a White House press conference about the pandemic on Wednesday.

The US surgeon general Dr. Vivek Murthy reiterated Wednesday that the break in Johnson & Johnson’s vaccinations gives public health officials a chance to investigate the cases and discuss them with health professionals. He added that breaks are common when new vaccines and drugs are introduced.

“We are only doing the necessary care to ensure that everything is safe so that we can continue our vaccination efforts,” said Dr. Murthy on “CBS This Morning”.

The committee’s assessment will be of vital importance at a time when the nation is trying to vaccinate as many people as possible to curb the steady buildup of cases, especially when worrying variants become more prominent. Some public health experts were disappointed with the FDA’s recommendation to suspend the Johnson & Johnson vaccine, arguing that preventing these extremely rare side effects was not worth the compromise of slowing the vaccination campaign and potentially increasing public confidence in vaccines Generally undermine.

What You Need To Know About The Johnson & Johnson Vaccine Break In The United States

    • On April 13, 2021, U.S. health officials called for an immediate halt to use of Johnson & Johnson’s single-dose Covid-19 vaccine after six recipients in the U.S. developed a rare blood clot disorder within one to three weeks of vaccination.
    • All 50 states, Washington, DC, and Puerto Rico have temporarily suspended use of the vaccine or suspended from recommended vendors. The U.S. military, government-run vaccination centers, and a variety of private companies, including CVS, Walgreens, Rite Aid, Walmart, and Publix, also paused the injections.
    • Fewer than one in a million Johnson & Johnson vaccinations are currently being studied. If there is indeed a risk of blood clots from the vaccine – which has yet to be determined – the risk is extremely small. The risk of contracting Covid-19 in the United States is much higher.
    • The hiatus could complicate the country’s vaccination efforts at a time when many states are facing spikes in new cases and are trying to address vaccine hesitation.
    • Johnson & Johnson has also decided to delay the launch of its vaccine in Europe amid concerns about rare blood clots, which is taking another blow to the vaccine surge in Europe. South Africa, devastated by a contagious variant of the virus found there, also stopped using the vaccine. Australia announced that it would not buy cans.

Speaking at the press conference, Jeffrey D. Zients, the White House pandemic coordinator, said the hiatus would not disrupt the momentum of the country’s vaccination campaign in general.

“In the short term, we expect some impact on the daily average as Johnson & Johnson locations and dates move to Moderna and Pfizer vaccines,” he said. “We have more than enough Pfizer and Moderna vaccines to continue or even accelerate the current rate of vaccination.”

Noah Weiland, Denise Grady and Madeleine Ngo contributed to the coverage.

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Health

U.S. Requires Pause on Johnson & Johnson Vaccine After Blood Clotting Instances

Dr. Marks said the federal government hadn’t issued an order to suspend the vaccine, adding that health care providers could decide that for a given patient, the benefits of a shot outweigh the risks. “We’re not going to stop this provider from giving the vaccine because it might be right,” he said.

The decision is a new blow for Johnson & Johnson. Late last month, the company discovered that employees at a subcontracted facility in Baltimore had accidentally contaminated a batch of vaccine, forcing the company to throw away the equivalent of 13-15 million cans. That facility would handle the delivery of the vaccine to the US from Johnson & Johnson’s Dutch plants, which were federal certified earlier this year.

FDA certification of the Baltimore facility has now been delayed while inspectors investigate quality control issues and severely reduce the supply of Johnson & Johnson vaccines. The sudden drop in available doses sparked widespread complaints from governors and state health officials who had anticipated much larger deliveries of Johnson & Johnson’s vaccine this week than they did.

States have used the vaccine in a variety of settings, including at mass vaccination sites and on college campuses. The vaccine’s one-shot approach has proven popular, and officials have directed it to temporary, rural, and isolated communities where second-dose follow-up is more complicated.

It is common for regulators to investigate “safety signals” in new vaccines and other medical products. Very often the signals do not turn out to be critical. However, concerns about Johnson & Johnson’s vaccine echoes concerns about AstraZeneca’s vaccine, which European regulators investigated last month after some recipients developed blood clots.

Of 34 million people who received the vaccine in the UK, the European Union and three other countries, 222 had blood clots associated with low platelet levels. The majority of these cases occurred within the first 14 days after vaccination, mainly in women under 60 years of age.

On April 7, the European Medicines Agency, the main regulator, concluded that the disorder is a very rare side effect of the vaccine. Researchers in Germany and Norway published studies on April 9, suggesting that the AstraZeneca vaccine, on very rare occasions, caused people to make antibodies that activated their own platelets.

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World News

The Johnson & Johnson Vaccine: Dwell Updates on States, Blood Clotting and Europe

Here’s what you need to know:

Credit…Mary Altaffer/Associated Press

Injections of Johnson & Johnson’s single-dose coronavirus vaccine came to a sudden halt in much of the United States on Tuesday after federal health agencies called for a pause in the vaccine’s use following the emergence of a rare blood clotting in six recipients.

All six were women between the ages of 18 and 48 and all developed the illness within one to three weeks of vaccination. One woman died and a second woman in Nebraska has been hospitalized in critical condition.

Nearly seven million people in the United States have received Johnson & Johnson shots so far, and roughly nine million more doses have been shipped out to the states, according to data from the Centers for Disease Control and Prevention.

“We are recommending a pause in the use of this vaccine out of an abundance of caution,” Dr. Peter Marks, director of the Food and Drug Administration’s Center for Biologics Evaluation and Research, and Dr. Anne Schuchat, principal deputy director of the C.D.C., said in a joint statement. “Right now, these adverse events appear to be extremely rare.”

At a news conference later on Tuesday morning, Dr. Marks said that “on an individual basis, a provider and patient can make a determination whether or not to receive the vaccine” manufactured by Johnson & Johnson.

While the move was framed as a recommendation to health practitioners in the states, the federal government is expected to pause administration of the vaccine at all federally run vaccination sites. Federal officials expect that state health officials will take that as a strong signal to do the same. Within two hours of the announcement, Gov. Mike DeWine of Ohio, a Republican, advised all health providers in his state to temporarily stop giving Johnson & Johnson shots. In New York, the health commissioner, Dr. Howard Zucker, said the state would halt the use of the vaccine statewide while federal officials evaluate the safety risks. Appointments for Johnson & Johnson’s shot on Tuesday at state mass sites would be honored with Pfizer doses, Dr. Zucker said.

Several other states quickly followed the call from federal health agencies on Tuesday to pause the administration of Johnson & Johnson’s vaccine after six women in the United States developed a rare disorder involving blood clots within about two weeks of vaccination.

The other states include: Connecticut, Georgia, Illinois, Indiana, Maine, Maryland, Massachusetts, Minnesota, Missouri, New Jersey, Nebraska, Oregon, Texas, Utah, Vermont and Virginia.

CVS and Walgreens, the nation’s largest retail pharmacy chains, also said that they would immediately stop Johnson & Johnson vaccinations. Both companies said they were emailing customers whose appointments would be canceled and would reschedule appointments when able.

Dr. Janet Woodcock, the acting commissioner of the F.D.A., said at the news conference Tuesday that the pause was only expected to last “a matter of days,” although she said the time frame depends on “what we learn in the next few days.” Dr. Schuchat said at the same briefing that the pause was enacted in part to “prepare the health care system to recognize and treat patients appropriately.”

Scientists with the F.D.A. and C.D.C. will jointly examine possible links between the vaccine and the disorder and determine whether the F.D.A. should continue to authorize use of the vaccine for all adults or limit the authorization.

“For people who recently got the vaccine within the last couple of weeks, they should be aware, to look for any symptoms. If you receive the vaccine and develop severe headaches, abdominal pain, leg pain or shortness of breath, you should contact your health care provider and seek medical treatment,”Dr. Schuchatsaid. She emphasized that an emergency meeting of the C.D.C.’s outside advisory committee, which has been scheduled for Wednesday, to discuss how to handle the vaccine in the future is made up of independent experts. Officials also stressed that no serious safety problems have emerged with either of the other two federally authorized vaccines, developed by Pfizer-BioNTech and Moderna.

The move could substantially complicate the nation’s vaccination efforts at a time when many states are confronting a surge in new cases and seeking to address vaccine hesitancy. Regulators in Europe and elsewhere are concerned about a similar issue with another coronavirus vaccine, developed by AstraZeneca and Oxford University researchers. That concern has driven up some resistance to all vaccines, even though the AstraZeneca version has not been authorized for emergency use in the United States.

The vast majority of the nation’s vaccine supply comes from Pfizer-BioNTech and Moderna, which together deliver more than 23 million doses a week of their two-shot vaccines.

But while shipments of the Johnson & Johnson vaccine have been much more limited, the Biden administration had still been counting on using hundreds of thousands of doses every week. In addition to requiring only a single dose, the vaccine is easier to ship and store than the other two, which must be stored at extremely low temperatures.

Jeffrey D. Zients, the White House Covid-19 response coordinator, said Tuesday the pause “will not have a significant impact” the Biden administration’s plans to deliver enough vaccine to be able to inoculate all 260 million adults in the United States by the end of May. With the Johnson & Johnson setback, federal officials expect there will only be enough to cover fewer than 230 million adults. But a certain percentage of the population is expected to refuse shots, so the supply may cover all the demand.

Mr. Zients said the administration will still “reach every adult who wants to be vaccinated” by the May 31 target.

Federal officials are concerned that doctors may not be trained to look for the rare disorder if recipients of the vaccine develop symptoms of it. The federal health agencies said Tuesday morning that “treatment of this specific type of blood clot is different from the treatment that might typically be administered” for blood clots.

“Usually, an anticoagulant drug called heparin is used to treat blood clots. In this setting, administration of heparin may be dangerous, and alternative treatments need to be given,” the statement said.

In a news release, Johnson & Johnson said: “We are aware that thromboembolic events including those with thrombocytopenia have been reported with Covid-19 vaccines. At present, no clear causal relationship has been established between these rare events and the Janssen Covid-19 vaccine.” Janssen is the name of Johnson & Johnson’s division that developed the vaccine.

In the United States alone, 300,000 to 600,000 people a year develop blood clots, according to C.D.C. data. But the particular blood clotting disorder that the vaccine recipients developed, known as cerebral venous sinus thrombosis, is extremely rare.

All of the women developed the condition within about two weeks of vaccination, and government experts are concerned that an immune system response triggered by the vaccine was the cause. Federal officials said there was broad agreement about the need to pause use of the vaccine while the cases are investigated.

The decision is a fresh blow to Johnson & Johnson. Late last month, the company discovered that workers at a Baltimore plant run by its subcontractor had accidentally contaminated a batch of vaccine, forcing the firm to throw out the equivalent of 13 million to 15 million doses. That plant was supposed to take over supply of the vaccine to the United States from Johnson & Johnson’s Dutch plants, which were certified by federal regulators earlier this year.

The Baltimore plant’s certification by the F.D.A. has now been delayed while inspectors investigate quality control issues, sharply reducing the supply of Johnson & Johnson vaccine. The sudden drop in available doses led to widespread complaints from governors and state health officials who had been expecting much bigger shipments of Johnson & Johnson’s vaccine this week than they got.

United States › United StatesOn Apr. 12 14-day change
New cases 72,286 +6%
New deaths 476 –27%
World › WorldOn Apr. 12 14-day change
New cases 617,202 +22%
New deaths 9,253 +25%

U.S. vaccinations ›

Where states are reporting vaccines given

A Kent State University student getting his Johnson & Johnson vaccination in Kent, Ohio, last week.Credit…Phil Long/Associated Press

Several states quickly followed the call from federal health agencies on Tuesday to pause the administration of Johnson & Johnson’s vaccine after six women in the United States developed a rare disorder involving blood clots within one to three weeks of vaccination.

The states include: Connecticut, Georgia, Illinois, Indiana, Maine, Maryland, Massachusetts, Minnesota, Missouri, New Jersey, Nebraska, New York, Ohio, Oregon, Rhode Island, South Dakota, Texas, Utah, Vermont and Virginia.

CVS and Walgreens, the nation’s largest retail pharmacy chains, also said that they would immediately stop Johnson & Johnson vaccinations. Both companies said they were emailing customers whose appointments would be canceled and would reschedule appointments when able.

Gov. Mike DeWine of Ohio and the state’s chief health official said they were advising all state vaccine providers to temporarily halt use of the single-dose vaccine. Connecticut health officials said they told vaccine providers to delay planned appointments or give an alternative option if they had the supply. New York’s health commissioner, Dr. Howard Zucker, said the state would stop using the Johnson & Johnson vaccine while the Food and Drug Administration and the Centers for Disease Control and Prevention evaluate the safety risks.

The C.D.C.’s outside advisory committee of independent experts has scheduled an emergency meeting for Wednesday.

The White House on Tuesday said that the pause will not have a significant effect on the country’s vaccination campaign, which has accelerated in recent weeks as a rise in new virus cases threatens a fourth possible surge. Many states have already opened vaccination eligibility to all adults and others plan to by next week.

“Over the last few weeks, we have made available more than 25 million doses of Pfizer and Moderna each week, and in fact this week we will make available 28 million doses of these vaccines,” Jeff Zients, the White House Covid-19 response coordinator, said on Tuesday. “This is more than enough supply to continue the current pace of vaccinations of 3 million shots per day.”

As of Monday, 36 percent of the country’s total population has received at least one shot of a vaccine, and 22 percent are fully vaccinated, according to data from the C.D.C.

Even though the reaction to the Johnson & Johnson shot is rare, any questions about the safety of the shots could bolster vaccine hesitancy.

Nearly seven million people in the United States have received Johnson & Johnson shots so far, and roughly nine million more doses have been shipped out to the states, according to data from the C.D.C. The six women who developed blood clots were between the ages of 18 and 48. One woman died and a second woman in Nebraska has been hospitalized in critical condition.

“We are recommending a pause in the use of this vaccine out of an abundance of caution,” Dr. Peter Marks, director of the Food and Drug Administration’s Center for Biologics Evaluation and Research, and Dr. Anne Schuchat, principal deputy director of the C.D.C., said in a joint statement. “Right now, these adverse events appear to be extremely rare.”

“I know there are people who have gotten the vaccine, who are probably very concerned. For people who got the vaccine more than a month ago, the risk to them is very low at this time,” Dr. Schuchat said. “For people who recently got the vaccine within the last couple of weeks, they should be aware to look for any symptoms.”

Like many states, New York had already prepared for a significant drop in its supply of the Johnson & Johnson vaccine after federal officials said that supplies would be limited because of a production issue at a Baltimore manufacturing plant. On Friday, Gov. Andrew M. Cuomo said that New York expected to receive 34,900 Johnson & Johnson shots, a decrease of 88 percent from the previous week.

Dr. Zucker, New York’s health commissioner, said that the state would honor appointments made at state-run mass vaccination sites for the Johnson & Johnson vaccine by giving people the Pfizer-BioNTech vaccine instead. That vaccine requires two doses, and it was not immediately clear how the state would handle the additional strain on its supply.

New Jersey health officials said the state would work with its vaccination sites to help people get appointments for the Pfizer or Moderna vaccine instead. Mayor Bill de Blasio of New York City said that the city would do the same, rescheduling appointments at city-run vaccine sites.

“Every site has been told this morning to stop giving the J&J shots,” he said at a news conference.

The city’s health commissioner, Dr. Dave Chokshi, said that around 234,000 residents have received the Johnson & Johnson vaccine and none had reported any blood clots so far. The city had been relying on the vaccine to inoculate hard-to-reach New Yorkers, including people who are homebound.

Both Mr. Cuomo and Mr. de Blasio received the Johnson & Johnson vaccine at separate appearances last month, which they framed as an effort to boost confidence in that vaccine’s efficacy rate and to address vaccine hesitancy.

Regulators in Europe and elsewhere are concerned about a similar issue with another coronavirus vaccine, developed by AstraZeneca and Oxford University researchers. That vaccine has not been authorized for emergency use in the United States.

Rebecca Robbins contributed reporting.

A box of Johnson & Johnson Covid-19 vaccines shown by a pharmacist in Budapest, Hungary, on Tuesday.Credit…Szilard Koszticsak/EPA, via Shutterstock

Johnson & Johnson on Tuesday said it would delay the rollout of its vaccine in Europe amid concerns over rare blood clots, in another blow to the continent’s ambition to ramp up inoculation campaigns that have lagged behind other countries in the West.

Several countries of the bloc were poised to start administering the vaccine later this week, in what would have been a boost to efforts by the European Union to vaccinate 70 percent of adults by September.

“The safety and well-being of the people who use our products is our number one priority,” Johnson & Johnson said in a statement, adding that it had been reviewing the cases of blood clots detected in the United States with European health authorities.

The first signs of concern in Europe came last week. The European Medicines Agency, the bloc’s drug regulator, said it was investigating reports of four cases of blood clots in people who had received a shot of Johnson & Johnson’s Janssen vaccine in the United States, one of them being fatal. The regulator said it wasn’t clear if there was a link between the vaccine and the clots, adding that it treated the reports as “safety signal” that required further assessment.

Johnson & Johnson started delivering its one-shot vaccine to the bloc on Monday, with some member countries like Spain and Belgium already having received modest quantities of the shot, and preparing for the rollout later in the week. Fifty-five million doses of Johnson & Johnson’s vaccine are expected to be delivered to the European Union by the end of June, and another 120 million later in the year, according to Thierry Breton, the bloc’s top industry official.

On Tuesday, injections of Johnson & Johnson’s single-dose coronavirus vaccine came to a sudden halt in much of the United States on Tuesday after federal health agencies called for a pause in the vaccine’s use following the emergence of a rare blood clotting in six recipients.

All six were women between the ages of 18 and 48 and all developed symptoms within about two weeks of vaccination. One woman died and a second woman in Nebraska has been hospitalized in critical condition.

Nearly seven million people in the United States have received Johnson & Johnson shots so far, and about nine million more doses have been shipped out to the states, according to data from the Centers for Disease Control and Prevention.

Johnson & Johnson’s announcement comes as Europe has been embroiled in a regulatory back-and-forth over another vaccine, AstraZeneca’s. Several countries have restricted the use of the vaccine in younger people, after the European Medicines Agency said there was “a possible link” between blood clots and the vaccine earlier this month, and said it should be listed as a rare side effect.

Both Johnson & Johnson and AstraZeneca use the same technology, prompting concerns that the blood clots reported in recipients of both vaccines could be the same rare, yet sometimes fatal side effect.

The agency stopped short of advising to curb the use of the vaccine in 27 member countries, saying that it was up to the national authorities to decide who should receive which vaccine, which resulted in a patchwork of different national regulations.

France and Belgium have restricted its use for those older than 55, and Germany, Italy and Spain, for those over 60. Some other countries, such as Poland, which rely heavily on AstraZeneca in their national rollouts, decided to go ahead with AstraZeneca’s vaccine.

Students line up for vaccines at Oakland University on Friday in Rochester, Mich. Coronavirus cases in the state have continued to rise in recent weeks.Credit…Emily Elconin for The New York Times

The virus is again surging in parts of the United States, but it’s a picture with dividing lines: ominous figures in the Northeast and Upper Midwest, but largely not in the South.

Experts are unsure what explains the split, which doesn’t correspond to vaccination levels. Some point to warmer weather in the Sun Belt, while others suspect that decreased testing is muddying the virus’s true footprint.

The contours of where the virus is resurgent can be drawn around one figure: states that are averaging about 15 new cases a day for every 100,000 people. The 23 states — including Alabama, Mississippi and Arkansas — that have averaged that or fewer over the past week seem to be keeping cases relatively low, according to a New York Times database. Nationally, the country is averaging 21 new cases per 100,000 people.

In the 27 states above that line, though, things have been trending for the worse. Michigan has the highest surge of all, reporting the most drastic increase in cases and hospitalizations in recent weeks. Illinois, Minnesota and others have also reported worrisome increases.

Nationally, reported cases in the United States are growing again after a steep fall from the post-holiday peak in January. In the past two weeks, new confirmed cases have jumped about 11 percent, even though vaccinations picked up considerably, with an average of 3.2 million doses given daily.

Some Southern states, like Alabama and Mississippi, are lagging in vaccinations. Only about 28 percent of people in each state have received at least one shot, according to a New York Times vaccine tracker. Still, case counts continue to drop in both states.

Health experts say cases are rising in the Northeast and Upper Midwest for several reasons, including pandemic fatigue, the reopening of schools and the resumption of youth sports.

Hospitalizations tend to follow the trend line in cases by a few weeks, and have been rising in some states, most notably in Michigan.

Officials are also concerned about the spread of more contagious virus variants, especially B.1.1.7, first identified in Britain. The variant is now the leading source of new coronavirus infections in the United States, the director of the Centers for Disease Control and Prevention said last week.

Just why those factors might affect some states more than others is hard to pinpoint, experts say.

Dr. David Rubin, the director of PolicyLab at the Children’s Hospital of Philadelphia, said warmer weather in Southern states and California was probably playing a role, because it allows people to gather outdoors, with less risk of transmission.

New case reports have fallen by about 11 percent in Georgia over the past two weeks. And in Alabama, new cases are down roughly 29 percent, with a 17 percent decline in hospitalizations.

Some experts say, though, that reduced testing in some states could be obscuring the true picture. Testing in Alabama, for instance, has started to dip, but the share of tests that come back positive has remained high, at 11.1 percent, compared with a nationwide average of 5.1 percent, according to data compiled by Johns Hopkins University.

“People who are symptomatic and go to their provider are going to get a test,” said Dr. Michael Saag, the associate dean for global health at the University of Alabama at Birmingham, but “the desire for people to go get tested just because they want to know what their status is has dropped off dramatically.”

Still, Dr. Saag said, there is probably not a hidden spike in cases in Alabama right now, since hospitalizations in the state remain low.

People sitting near the Dome of the Rock at the Aqsa Mosque compound, Islam’s third holiest site, in the old city of Jerusalem on Monday.Credit…Ahmad Gharabli/Agence France-Presse — Getty Images

Millions of Muslims on Tuesday began celebrating a second Ramadan in the middle of the pandemic, although in many countries the first day of the holy month offered the promise of a Ramadan with fewer restrictions than last year.

Mosques across the Middle East and other parts of the world were closed for prayer last year, and lockdowns prevented festive gatherings with friends and family. In Jerusalem, for instance, the Old City was largely empty and the Aqsa Mosque compound was closed to the public, as coronavirus cases were surging.

But a large degree of normalcy was back on Tuesday: The Old City’s narrow alleys were crowded, sweet shops were preparing Ramadan desserts, clothing stores were open and the Aqsa compound was welcoming worshipers.

“Last year, I felt depressed and I didn’t know how long the pandemic would last,” said Riyad Deis, a co-owner of a spice and dried fruit shop in the Old City, while selling whole pieces of turmeric and Medjool dates to a customer. “Now, I’m relaxed, I have enough money to provide for my family and people are purchasing goods from my shop — it’s a totally different reality.”

The enthusiasm of some didn’t mean the Ramadan would go as normal. Across several countries in the Middle East, the authorities imposed limitations on customs and festivities, requiring that mosques enforce social distancing and telling worshipers to bring their own prayer rugs and to wear face masks.

In Dubai, Saudi Arabia and Egypt, taraweeh, the optional extra prayers that worshipers can observe at night, were capped at half an hour. No one will also be allowed to spend the night in a mosque, as is common during the last 10 days of Ramadan.

Mosques around the region were also prohibited from serving the fast-breaking meal of iftar or the predawn meal of suhoor. Though Muslims could still gather for those meals with friends and family, the authorities asked them to limit those gatherings this year.

In Jerusalem, Omar Kiswani, the director of Al Aqsa Mosque, said he was overjoyed that the compound was open to worshipers, but still urged caution.

“These are times of great happiness — we hope the blessed Aqsa Mosque will return to its pre-pandemic glory — but these are also times of caution because the virus is still out there,” Mr. Kiswani said.

In Egypt, government officials and prominent television hosts linked to the authorities warned Egyptians of a third wave of infections as Ramadan approached, hinting that another curfew or other lockdown restrictions could be imposed if cases rose.

“If you want the houses of God to remain open,” Nouh Elesawy, an official who oversees mosques at the Egyptian Ministry of Endowments, said earlier this month, “adhere to the precautionary procedures and regulations.”

The Ramadan restrictions may hit the hardest in poor neighborhoods, where residents depend on iftar banquets usually sponsored by wealthy individuals or organizations. For those people, feasting and Ramadan gifts are likely to be rarer, with tourism still at a trickle and many small businesses still suffering from the economic effects of the pandemic.

In Lebanon and Syria, the pandemic has worsened economic crisis that will likely squeeze people’s ability to enjoy the holy month, more than the governments’ limited restrictions aimed at curbing the spread of the coronavirus.

In Syria, where experts say the official infection and death numbers for Covid-19 are far below the reality, the government has few restrictions in place. Worshipers will even be allowed to stand in line inside of mosques to pray together after breaking their fast, the Syrian Ministry of Religious Affairs said.

In Lebanon, which emerged recently from a strict lockdown, shops and restaurants can operate regularly during the day but must offer only delivery service during a nighttime curfew from 9:30 p.m. to 5 a.m.

Global Roundup

Administering a coronavirus vaccine to a frontline worker in New Delhi, last week.Credit…Rebecca Conway for The New York Times

India said on Tuesday that it would fast-track the approval of vaccines in use in other countries, a move aimed at rapidly increasing the country’s vaccine supply as it battles what is currently the world’s biggest coronavirus outbreak.

The Indian government said that it would grant emergency authorization to any foreign-made vaccine that had been approved for use by regulators in the United States, the European Union, Britain or Japan, or by the World Health Organization. The move had been recommended by a panel of Indian scientists and eliminates a requirement for drug companies to conduct local clinical trials.

“The decision will facilitate quicker access to such foreign vaccines” and encourage imports of materials that would boost India’s vaccine manufacturing capacity, the government said in a statement.

Earlier on Tuesday, India’s top drug regulator granted emergency approval to Sputnik V, the Russian-made vaccine, adding a third vaccine to the country’s arsenal on the same day that health officials recorded 161,736 new coronavirus infections in 24 hours.

It was the seventh straight day that India has added more than 100,000 cases, according to a New York Times database. Only the United States has seen a faster rise in infections during the pandemic.

India has administered about 105 million domestically produced vaccine doses for a population of 1.3 billion, but it is widely believed that the country needs to scale up inoculations rapidly because other measures have failed to control the virus. Many states have reimposed partial lockdowns and weekend curfews. In the country’s financial hub, Mumbai, health officials are racing to erect field hospitals as facilities report shortages of oxygen, ventilators and coronavirus testing kits.

And there is the risk of a superspreading event with the gathering of millions of Hindu pilgrims for the annual Kumbh Mela festival on the banks of the Ganges River, where the authorities say they are powerless to enforce social distancing.

India’s outbreak is reverberating worldwide as its pharmaceutical industry — which was supposed to manufacture and export hundreds of millions of doses of the AstraZeneca vaccine — is keeping most supplies at home. The approval of the Sputnik vaccine, whose first doses are expected to be available for use in weeks, offers hope that India could speed up its inoculation drive.

But it is unclear at this stage whether India will be able to procure significant quantities of other vaccines, including the Pfizer, Moderna and Johnson & Johnson shots in use in the United States. Major Western nations have accumulated much of the global supply of those vaccines and manufacturers are struggling to meet the surging demand.

India will import millions of Sputnik doses from Russia and then begin manufacturing the vaccine domestically, officials said. More than 850 million doses will be made, with some intended for export, Kirill Dmitriev, chief executive of the Russian Direct Investment Fund, a sovereign wealth fund that has financed the vaccine’s development, said in an interview with India’s NDTV channel.

“India is a vaccine-manufacturing hub and our strategic partner for production of Sputnik V,” Mr. Dmitriev said.

India has more than 13.6 million confirmed coronavirus cases, the second most after the United States, and 171,058 deaths, the fourth highest toll.

In other news around the world:

  • Japan has begun vaccinating 36 million people over age 65, the first time shots have been made available to the public during the country’s slow vaccine rollout. Officials said that 1,139 people nationwide had received doses on Monday, and that doses to cover all Japanese above the age threshold would reach municipal health facilities by the end of June. Although Japan has weathered the pandemic better than most countries, the pace of its vaccination effort, which until now had only covered 1.1 million frontline medical workers, has sparked public criticism and raised questions about readiness for the Tokyo Summer Olympics in just over three months.

  • Scotland on Tuesday moved forward plans to loosen its coronavirus lockdown, a day after the British government eased many restrictions in England. New rules beginning Friday will permit Scots to meet outdoors in groups of up to six adults from six households. The current rules restrict travel and set the maximum group size at four, from two households. Restrictions on shops and outdoor service in pubs, now relaxed in England, are scheduled to remain in Scotland until April 26.

  • Austria’s health minister resigned on Tuesday, citing personal health problems that he said have been exacerbated by the grueling job of helping lead the country’s response to the pandemic. “It feels like it has not been 15 months, but 15 years,” the minister, Rudolf Anschober, said in a statement. Mr. Anschober, 60, was appointed in January last year, as a Green party minister in a Conservative-led coalition, and has been one of the main faces of Austria’s coronavirus response. “In the worst health crisis in decades, the republic needs a health minister who is 100 percent fit. That is not currently me,” he said.

  • France will suspend all flights to and from Brazil, because of growing worries about the virus variant spreading there. “We see that the situation is getting worse” in Brazil, Prime Minister Jean Castex told lawmakers. The country previously permitted essential travel from Brazil, subject to testing and isolation requirements.

  • The World Health Organization on Monday evening called on governments to suspend the sale of live wild mammals in food markets to help prevent the emergence of new diseases. “Traditional markets, where live animals are held, slaughtered and dressed, pose a particular risk for pathogen transmission to workers and customers alike,” the agency said in a statement. Animals are the source of more than 70 percent of emerging infectious diseases in humans, it said. Early in the pandemic, Chinese officials suggested that the coronavirus outbreak might have started at a market. But W.H.O. experts said in a report last year that the role of animal markets in the story of the pandemic was still unclear.

Chancellor Angela Merkel, center, at a cabinet meeting in Berlin on Tuesday. Her government’s proposal on coronavirus restrictions would place half the country over the threshold for lockdown.Credit…Pool photo by Andreas Gora

BERLIN — Chancellor Angela Merkel’s government moved a step closer on Tuesday to securing the right to force restrictions on areas where the coronavirus is spreading rapidly, overriding state leaders reluctant to take action.

Ms. Merkel and her ministers approved a legislative proposal that would make it easier for the national government to enforce lockdowns and other limits on movement in regions where infection levels pass a set threshold. At current levels, it could lock down more than half of the country.

Under Germany’s decentralized leadership structures, the 16 state leaders have been meeting regularly with the chancellor to agree on nationwide coronavirus response policies. But with different regions experiencing different rates of infection, some state leaders have been reluctant to enforce the agreed limitations, leading to confusion and frustration among many Germans.

“I believe this amendment is as important as it is an urgent decision about how to proceed in the coronavirus pandemic,” the chancellor told reporters after meeting with her ministers.

Parliament still has to debate and approve the proposal, which would take the form of an amendment to the Protection Against Infection Act, and that process is expected to begin this week.

“We are in a situation where an emergency mechanism is necessary,” Ralph Brinkhaus, the leader of the Christian Democratic Union in Parliament, told reporters, before a meeting of his party lawmakers to discuss the amendment.

Under the proposed amendment, the federal government could force stores and cultural institutions to close and enforce limits on the number of people allowed to meet up in any region where infections surpass 100 new cases per 100,000 residents over a period of seven days.

More controversially, the law would also allow Ms. Merkel’s government to order that schools and day care centers close if the number of new infections reaches more than 200 per 100,000 inhabitants. Schools fall under the jurisdiction of the states, and local leaders are reluctant to relinquish that control.

Germany has registered more than three million infections and more than 78,700 deaths from Covid-19 since the virus began moving through the country last spring. It recorded 10,810 new cases of infection on Tuesday, bringing the national rate of infection to more than 140 per 100,000.

The number of patients in intensive care is expected to hit a record this month, as the country struggles to vaccinate enough people to get ahead of the spread of the highly contagious B.1.1.7 variant.

Vaccinations at a mosque in London earlier this month. Britain’s program has reached over 32 million people, more than half the adult population.Credit…Andrew Testa for The New York Times

Britain has now offered vaccinations to everyone in the country age 50 and older, the government announced late on Monday, and is extending its program to another age group, the latest sign that the national rollout is continuing at pace.

On Tuesday, the authorities opened vaccinations to anyone 45 or older, yet the announcement came with a small hiccup: The website for the country’s National Health Service crashed for a short time after the younger cohort was invited to book appointments online.

The new step in the country’s vaccine rollout comes as the authorities eased several restrictions in England on Monday after months of stringent lockdowns, with pubs and restaurants opened for drinks and dining outside, and nonessential shops once again opening their doors.

Prime Minister Boris Johnson called the moment a “hugely significant milestone” and in a statement thanked those involved with the vaccine rollout. Mr. Johnson said the country was on track to offer all adults a vaccination by the end of July. More than 32 million people across Britain have received their first dose of one of the vaccines, according to government data.

The government said it had also already offered vaccinations to every health or care worker, and to everyone with a high-risk medical condition.

England has also began rolling out the Moderna vaccine, which will be offered as an alternative alongside the Pfizer BioNTech vaccine for those under 30, instead of AstraZeneca’s, which has been the mainstay of Britain’s program so far.

There have been concerns about a possible link between the AstraZeneca vaccine and very rare blood clots, and last week British regulators said an alternative should be provided for younger people. Potential infection still poses much greater risks than any vaccine side effect for all those over 30, they said, and could do so for younger people if cases surged again.

“The Moderna rollout marks another milestone in the vaccination program,” Stephen Powis, the medical director of the National Health Service, said in a statement. “We now have a third jab in our armory.”

The vaccination program, he added, “is our hope at the end of a year like no other” as he encouraged people to book their appointments.

But despite the hopeful vaccine news and the return to public life, the country is still battling new cases of the virus, and a cluster in two London neighborhoods of a worrisome variant first discovered in South Africa has prompted mass testing. Health workers have gone door to door to urge residents to get tested, even if they are not showing symptoms, as dozens of cases have emerged. Similar measures were carried out elsewhere in the city earlier this month.

Studies have shown that the variant contains a mutation that diminishes the vaccines’ effectiveness against it. Dr. Susan Hopkins, the chief medical adviser for the country’s test and trace campaign, said the cluster of cases in parts of South London was “significant.”

“It’s really important people in the local area play their part in stopping any further spread within the local community,” she said in a statement.

Pacific Palace, a dim sum restaurant on a commercial strip in the Sunset Park section of Brooklyn, has seen revenue plunge.Credit…Victor J. Blue for The New York Times

More than a year after the coronavirus first swept through New York, the streets of Sunset Park in southern Brooklyn reflect the pandemic’s deep and unhealed wounds intertwined with signs of a neighborhood trying to edge back to life.

The sidewalks are filling with shoppers and vendors. More businesses are welcoming customers. But owners still struggle to pay rent and keep their enterprises afloat, while many workers laid off after the city locked down last year remain without jobs.

And while the rate of vaccination in New York has increased significantly, the coronavirus still percolates through this densely packed neighborhood. The ZIP code that includes Sunset Park had the highest rate of positive cases in Brooklyn in early April, nearly double the citywide rate. Some residents have expressed skepticism about the vaccines, spooked by false information circulated over TikTok and other social media.

Adding to the stress is a spate of hate crimes and violence against people of Asian descent in New York and around the country, fed in some cases by racist claims that Asian-Americans are responsible for spreading the virus.

About a third of the residents in Sunset Park have received at least one dose of the vaccine, roughly the same level as the city overall, according to the city health data. But local leaders say they want to push that number much higher.

Kuan Neng, 49, the Buddhist monk who founded Xi Fang Temple on Eighth Avenue, said that people had come to him in recent weeks to express concerns over vaccines.

“Why do I need to do that?” is a common refrain, according to Mr. Kuan, followed by: “I’m healthy now. The hard times are over, more or less.”

“Many people want to delay and see,” Mr. Kuan said, himself included.

The owner of the Cinerama Dome in Hollywood and 15 other movie theaters said it would not reopen after the pandemic.Credit…Kate Warren for The New York Times

ArcLight Cinemas, a beloved chain of movie theaters based in Los Angeles, including the Cinerama Dome in Hollywood, will permanently close all its locations, Pacific Theaters announced on Monday, after the pandemic decimated the cinema business.

ArcLight’s locations in and around Hollywood have played host to many a movie premiere, in addition to being favorite spots for moviegoers seeking out blockbusters and prestige titles. They are operated by Pacific Theaters, which also manages a handful of theaters under the Pacific name, and are owned by Decurion.

“After shutting our doors more than a year ago, today we must share the difficult and sad news that Pacific will not be reopening its ArcLight Cinemas and Pacific Theaters locations,” the company said in a statement.

“This was not the outcome anyone wanted,” it added, “but despite a huge effort that exhausted all potential options, the company does not have a viable way forward.”

Between the Pacific and ArcLight brands, the company owned 16 theaters and more than 300 screens.

The movie theater business has been hit particularly hard by the pandemic. But in recent weeks, the majority of the country’s largest theater chains, including AMC and Regal Cinemas, have reopened in anticipation of the slate of Hollywood films that have been put back on the calendar, many after repeated delays because of pandemic restrictions. A touch of optimism is even in the air as a result of the Warner Bros. movie “Godzilla vs. Kong,” which has generated some $70 million in box office receipts since opening over Easter weekend.

Still, the industry’s trade organization, the National Association of Theater Owners, has long warned that the punishing closures were most likely to affect smaller regional players like ArcLight and Pacific. In March, the Alamo Drafthouse Cinema chain, which operates about 40 locations across the country, announced that it had filed for Chapter 11 bankruptcy protection but would keep most of its locations operational while it restructured.

That does not seem to be the case for Pacific Theaters, which, according to two people with knowledge of the matter, fired its entire staff on Monday.

The reaction to ArcLight’s closing around Hollywood has been emotional, including an outpouring on Twitter.

Devastating. Too many losses to process. It’s just too much… At some point when I’m less upset, I’ll tell you guys a funny story about my first time meeting Quentin Tarantino in the lobby of Hollywood Arclight. https://t.co/cFypJxEk4L

— Lulu Wang (@thumbelulu) April 13, 2021
Firefighters at the site of COVID-19 hospital Matei Bals, after a fire broke out in one of its buildings in Bucharest, Romania, in January.Credit…Robert Ghement/EPA, via Shutterstock

Three people infected with the coronavirus died at a hospital in Bucharest on Monday evening after the oxygen supply stopped functioning, according to the authorities, the latest incident involving oxygen failure, which in many countries has driven up the virus death toll.

It was also another fatal setback for Romania’s ageing and overwhelmed health care system, which has suffered two fires in Covid-19 wards in recent months, killing at least 15 people.

Ventilators shut down at a mobile intensive care unit set up at the Victor Babes hospital in Bucharest after oxygen pressure reached too high a level, the country’s health authorities said in a statement, depriving patients of a vital supply. In addition to the three patients who died, five others were evacuated and moved to other facilities in the city.

Romania has recorded its highest rate of Covid-19 patients in intensive care units since the pandemic began, and on Sunday Prime Minister Florin Citu said that there were just six intensive care beds available across Romania, out of nearly 1,600.

Intensive care units in Hungary and Poland have also been at risk of being overwhelmed, as much of Eastern Europe has struggled to cope with a third wave of infections across the continent. Some Hungarian hospitals have sought medical students and volunteers to assist in Covid-19 wards, giving training to those without previous medical experience.

The mobile unit struck by the oxygen problem on Monday had only been in operation since Saturday, and it has epitomized long-running concerns over the country’s fragile health care system. In January, five patients died and a further 102 were evacuated from a different hospital in Bucharest after a fire broke out. In November, 10 patients hospitalized with the coronavirus died after a fire broke out in a hospital in the northeastern city of Piatra Neamt.

Romania’s spending on health care is among the lowest in the European Union, with just over five percent of gross domestic product allocated toward it, compared with 10 percent on average among other countries of the bloc.

More than 25,000 people who tested positive for the virus have died in Romania, and the authorities have closed schools and kindergartens throughout April as part of an extended Easter holiday.

The authorities have so far administered more than 3.5 million vaccine doses, in a population of about 19 million.

Alisa Stephens, a biostatistician at the University of Pennsylvania in Philadelphia, had to manage work and taking care of her children after the city went into lockdown last year.Credit…Hannah Yoon for The New York Times

Studies have found that women in academia have published fewer papers, led fewer clinical trials and received less recognition for their expertise during the pandemic.

Add to that the emotional upheaval of the pandemic, the protests over structural racism, worry about children’s mental health and education, and the lack of time to think or work, and an already unsustainable situation becomes unbearable.

Michelle Cardel, an obesity researcher at the University of Florida, worries that this confluence of factors could push some women to leave the sciences.

“My big fear is that we are going to have a secondary epidemic of loss, particularly of early career women in STEM,” she said.

Female scientists were struggling even before the pandemic. It was not unusual for them to hear that women were not as smart as men, or that a woman who was successful must have received a handout along the way, said Daniela Witten, a biostatistician at the University of Washington in Seattle.

Women in academia often have little recourse when confronted with discrimination. Their institutions sometimes lack the human resources structures common in the business world.

Compounding the frustration are outdated notions about how to help women in science. But social media has allowed women to share some of those concerns and find allies to organize and call out injustice when they see it, said Jessica Hamerman, an immunologist at the Benaroya Research Institute in Seattle.

In November, for example, a study on female scientists was published in the influential journal Nature Communications suggesting that having female mentors would hinder the career of young scientists and recommending that young women seek out male help.

The response was intense and unforgiving: Nearly 7,600 scientists signed a petition calling on the journal to retract the paper — which it did on Dec. 21.

The study arrived at a time when many female scientists were already worried about the pandemic’s effect on their careers, and already on edge and angry with a system that offered them little support.

Alisa Stephens found working from home to be a series of wearying challenges. Dr. Stephens is a biostatistician at the University of Pennsylvania, and carving out the time and mental space for that work with two young children at home was impossible.

Things eased once the family could safely bring in a nanny, but there was still little time for the deep thought Dr. Stephens had relied on each morning for her work.

Over time, she has adjusted her expectations of herself. “Maybe I’m at 80 percent as opposed to 100 percent,” she said, “but I can get things done at 80 percent to some extent.”