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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.”

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Health

Airline, journey shares slip after U.S. recommends pause in J&J Covid vaccine

Passengers board an American Airlines flight at Ronald Reagan Washington National Airport in Arlington, Virginia on April 11, 2021.

Andrew Caballero-Reynolds | AFP | Getty Images

Airline and other travel stocks fell Tuesday after U.S. authorities called for a break in using Johnson & Johnson’s Covid-19 vaccine due to rare reports of blood clotting.

The Food and Drug Administration urged states to stop using the single-dose vaccine after six people in the United States developed a rare bleeding disorder after receiving the shot. J&J said that “no clear causal link” was found between the blood clots and the vaccine and that it is working with regulators to assess the problem.

The recommendation comes just as airlines and other travel companies reported an improvement in bookings after coronavirus cases peaked earlier this year and more people were vaccinated.

Delta Air Lines and United Airlines stocks both fell more than 3% in morning trading. American Airlines shares were down about 5%. The Fort Worth-based airline estimated Tuesday that first quarter revenue was 62% lower than in the first quarter of 2019.

American expects a net loss of $ 2.7 billion to $ 2.8 billion for the quarter, excluding state wage support for the sector. The airline said its daily cash use averaged $ 27 million per day for the quarter, including $ 9 million per day in debt and severance payments, down from the previously estimated $ 30 million.

The cruise companies Carnival and Norwegian Cruise Line each gained more than 2%, while Marriott and Hilton both declined more than 1%.

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Business

Pausing J&J Covid vaccine may have far reaching results: Dr. Kavita Patel

Dr. Kavita Patel told CNBC on Tuesday that she believes the Food and Drug Administration’s recommendation that states stop using Johnson & Johnson’s single-shot Covid vaccine is likely to have a lasting impact on the country’s efforts to fight the pandemic.

“This is a devastating blow to this J&J vaccination effort in the US,” said Patel, a family doctor in Washington, DC, in an interview on Squawk Box. She also worked on health initiatives in the Obama administration while serving as director of policy for the Bureau of Interstate Affairs and Public Engagement.

Patel said the supply of Pfizer and Moderna’s two-shot vaccines will not be able to quickly meet the demand caused by the J&J hiatus. This will delay US vaccination efforts, she added.

The FDA recommendation, released Tuesday, came after six people in the US experienced rare and severe blood clotting problems after receiving the J&J vaccine.

In a tweet, the US regulator said its actions were taken “out of caution”.

All six cases occurred in women between the ages of 18 and 48, with symptoms developing six to 13 days after receiving the shot.

So far, J&J has said that there is “no clear causal link” between these rare events and the vaccine. The US drug giant also said it was working with regulators.

While she anticipates that Moderna and Pfizer will at some point be able to “fill some of that void,” said Patel, “it will be some time” before these other vaccine manufacturers have additional doses available in the US

A particular challenge in discontinuing the administration of J & J’s vaccine is that it only requires a single shot, while Moderna and Pfizer’s mRNA vaccines require two doses for complete protection of immunity.

“We just can’t replace it for the next week or three,” said Patel, a medical assistant for NBC News and a non-resident of the Brookings Institution. “This will delay our vaccination efforts.”

To compensate for this, the US could consider reducing second-dose administration to recipients of Moderna and Pfizer vaccines, Patel suggested.

The Chief Medical Officer of the White House, Dr. Anthony Fauci, has spoken out against requests earlier in the pandemic.

The second dose of Moderna is supposed to be given four weeks after the first, while Pfizer is three weeks apart.

“You will hear a renewal for calls to delay that second shot so we can get that many first shots in the arms. It’s not an unreasonable thing to think about now,” said Patel.

“If we postpone the second dose of Moderna or Pfizer for a week or two, it might actually help us fill some of that void faster,” she added.

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Health

Pennsylvania and L.A. Transfer Up Dates for Vaccine Eligibility

The state of Pennsylvania and the city of Los Angeles this week accelerate their plans for broader approval of Covid-19 vaccines as the U.S. nears universal approval for adults.

Most states and US territories have already extended access to those over the age of 16. Others, including Massachusetts, New Jersey, Oregon, and Washington state, have plans for universal adult access in the next few days. All states are expected to be there by Monday, a deadline set by President Biden.

Some states have local eligibility differences, including Illinois, where Chicago didn’t join a statewide expansion that began Monday.

California as a whole has set Thursday as the date, but Los Angeles Mayor Eric Garcetti said Sunday that all residents 16 and over in his city, the second largest in the country, would be eligible two days earlier. In Pennsylvania, Governor Tom Wolf said Monday that all adults there would be eligible on Tuesday, six days earlier than previously planned.

“We need to further accelerate the introduction of the vaccine, especially as the number of cases and hospitalization rates have increased,” Wolf said in a statement.

The extended authorization did not always bring immediate access. The demand for vaccinations continues to outpace supply in much of the country, and people are striving to book tight appointments as soon as they become available. And the supply of Johnson & Johnson’s single-dose vaccine will be extremely limited until federal regulators approve production at a Baltimore manufacturing facility with a pattern of quality control errors, the White House pandemic response coordinator said Friday.

“We ask for your patience as we continue to expand our operations, receive more doses, and enter this new phase of our campaign to end the pandemic,” Garcetti said.

More than 119 million people – or more than a third of the US population – have now received at least one dose of a Covid-19 vaccine, according to the Centers for Disease Control and Prevention. The nation administers an average of 3 million doses per day.

Two of the three vaccines approved for use in the United States – those made by Moderna and Johnson & Johnson – are approved for use in adults. The third from Pfizer-BioNTech is approved for use by people aged 16 and over. The company would like to expand this area to young people between the ages of 12 and 15. No vaccine has yet been approved for use in younger children.

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Business

Covid variant from South Africa was capable of ‘break by means of’ Pfizer vaccine in Israeli research

An Israeli health worker from Maccabi Healthcare Services prepares to deliver a dose of the Pfizer BioNtech vaccine in Tel Aviv on February 24, 2021.

Jack Guez | AFP | Getty Images

The coronavirus variant, first discovered in South Africa, may evade some of the protection provided by the Pfizer BioNTech vaccine, according to a new Israeli study that has not yet been peer-reviewed.

Researchers from Tel Aviv University and Clalit, the largest health organization in Israel, examined nearly 400 people who had tested positive for Covid-19 after receiving at least one dose of the vaccine. They compared it to the same number of people who were infected and not vaccinated.

The researchers found that the prevalence of the South African variant known as B.1.351 was about eight times higher in patients who received two doses of the vaccine than in those who were not vaccinated. The data, released online over the weekend, suggest that B.1.351 may “break through” the vaccine’s protection better than the original strain, the researchers in the study wrote.

“Based on patterns in the general population, we would have expected only one case of the South African variant, but we saw eight,” Professor Adi Stern, who led the research, told The Times of Israel. “We can say it’s less effective, but more research is needed to see exactly how much.”

CNBC asked Pfizer to comment on the study.

The new data comes as public health officials are increasingly concerned that highly contagious variants, studies have shown can reduce the effectiveness of vaccines, could slow global advances in the pandemic.

Last month, CDC Director Dr. Rochelle Walensky issued a terrible warning, telling reporters that she feared the United States was facing “impending doom” as variants spread and daily Covid-19 cases rise again, threatening to move more people to the US send hospital.

“I’m going to stop here, I’m going to lose the script, and I’m going to think about the recurring feeling I have before the impending doom,” she said on March 29, so much promise and potential where we are and so much reason to Hope, but right now I’m scared. “

Israel launched its national vaccination campaign in December, prioritizing people aged 60 and over, healthcare workers, and people with comorbid illnesses. By February, it was the world leader in vaccinations, vaccinating millions of its citizens against the virus.

In January, Pfizer and the Israeli Ministry of Health signed a collaboration agreement to monitor the real effects of its vaccine.

The researchers found that the study’s main limitation was sample size. B.1,351 only made up about 1% of all Covid-19 cases, they said. B.1.1.7, the variant first identified in Great Britain, is more common.

As the variants spread, drug manufacturers tested whether a third dose would offer more protection.

In February, Pfizer and BioNTech announced that they were testing a third dose of their Covid-19 vaccine to better understand the immune response against new variants of the virus.

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Health

Germany well being minister requires lockdown, considers Russian vaccine

On Tuesday, January 12, 2021, a health care worker will take care of a Covid 19 patient in the intensive care unit of the Robert Bosch Hospital in Stuttgart. Chancellor Angela Merkel warned that Germany would face tough lockdown measures until the end of March if the authorities do not contain a rapidly spreading variant of the coronavirus.

Bloomberg | Bloomberg | Getty Images

LONDON – Germany got one step closer to the nationwide lockdown on Friday when Chancellor Angela Merkel sought to standardize the restrictions across the various states.

“The Infection Protection Act is being changed to give the state the necessary power,” said a government spokesman in Berlin on Friday.

The law update is expected to be approved by lawmakers next week, and a lockdown could be imposed shortly thereafter.

Earlier on Friday, German health officials said they were concerned about the rising coronavirus infections in the country and said a nationwide lockdown was needed to end the ongoing third wave.

Germany has faced high rates of Covid infection since last October, and despite an improvement in February, the number of new cases has increased since the end of March.

“Many citizens recognize the need to break this wave with additional measures, and the majority are in favor of stricter rules. A lockdown is needed to break the current wave,” said German Health Minister Jens Spahn at a press conference on Friday.

This third wave of the coronavirus is putting pressure on the country’s health system at a time when regional and federal governments are arguing over what to do.

“The number of intensive care patients is increasing far too quickly. Doctors and nurses have been under constant stress for months and rightly sound the alarm,” said Spahn.

“We have to break the third wave as quickly as possible. That means: reduce contacts and reduce mobility. This is the only way to prevent further increases.”

The country reported over 30,000 new Covid cases on Wednesday and around 26,000 on Thursday.

German officials disagreed on the right approach to dealing with emerging cases, while citizens were frustrated with the different regimes between different regions.

Federal Finance Minister Olaf Scholz told CNBC earlier this week: “If we could come to similar measures in all locations, this would help a lot and make it more understandable.”

The German health authorities are pushing for an increase in vaccinations in the country, which has already paid off. On Thursday, the daily vaccination count approached 720,000 compared to around 317,000 a week ago, according to the Ministry of Health.

“I think we’re going to a situation where by the end of this month it will be 4 to 5 million doses a week,” Scholz told CNBC.

Sputnik V.

At the press conference on Friday, the Minister of Health confirmed that, according to Reuters, contract negotiations are currently taking place for the purchase of the Sputnik V vaccine developed in Russia. Spahn added that there is still a question mark over whether these vaccines would be available in the coming months.

The European Medicines Agency started evaluating the Russian shot in early March and will decide whether to recommend it for use in the 27 EU member states. Although the regulator is using an urgent method to verify the effectiveness of Sputnik V, it is unclear when final approval could come.

German authorities previously announced they would consider using the Russian vaccine if the EMA concluded that the shot was effective in preventing the Covid-19 virus.

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World News

My Household’s International Vaccine Journey

On February 22nd, Mom wrote that she and Dad had booked an appointment on March 11th to take their first recordings, followed by the second dose in April. A day later, she reported that Dad hadn’t pressed the button to confirm the appointment in the online booking system and had lost the slots.

The next week they texted again: They had gone to a private clinic where Sinovac recordings were handed in. After a short wait, they received the vaccine. On April 2nd, they announced that they had received their second dose of Sinovac and were feeling fine. Mom complained that even though they had an appointment, they “still have to wait half an hour”.

Our responses were more enthusiastic.

“Great news,” I wrote.

“Yay!” Pui-Ying texted him, followed by solemn emojis.

“Congratulations!” Said Pui Ling.

Pui-Ying moved to Malawi with her family in 2016 to work as a doctor and conduct clinical studies on children’s health. Resources at the Queen Elizabeth Central Hospital where she works have been limited. When Madonna’s charity funded the construction of a new children’s wing in the hospital, which opened in 2017, it was big news.

The staff was scarce even before the coronavirus, said Pui-Ying. When the pandemic broke out, the hospital opted for a weeklong, weeklong routine to reduce staff exposure to Covid-19 while ensuring there were enough healthcare professionals working at all times. Masks, gloves and other protective equipment were rare.

In pediatrics, Pui-Ying and her colleagues have set up a “breathing zone” for children with Covid-19. It was essentially a two-room ward with about a dozen beds in the main room. The second room, which was an isolation unit, had space for four children.

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Health

Analysts level to promising pipeline regardless of Covid vaccine jitters

A healthcare worker prepares to inject a vaccine against AstraZeneca coronavirus disease (COVID-19).

Eloisa Lopez

The AstraZeneca Covid-19 vaccine controversy has sparked some investor concerns about its stock, according to Jefferies – but it’s not all bad news for the UK pharmaceutical company.

Australia, the Philippines and the African Union have either contained or abandoned proposed Oxford-AstraZeneca University coronavirus purchases due to possible links to blood clots.

This came after UK health and vaccine regulators issued a change to guidelines on Wednesday on who should get the shot, suggesting that those under 30 should be given an alternative vaccine. Both UK and European Medicines Regulators (MHRA and EMA, respectively) have stressed that the benefits of the sting still outweigh the risks, but EU leaders have yet to agree on a common policy on the shots.

In a research report earlier this week, Jefferies Research Analyst Peter Welford said he received a pushback from customers because he recently decided to buy AstraZeneca’s shares to buy based on the “noise” about the vaccine .

This is despite the fact that the company has promised that the vaccine will be non-profit making for the “duration of the pandemic” and that it will be offered to low- and middle-income countries on a permanent basis.

The overall risk of blood clots has been estimated at around one in 250,000 and British policymakers and health experts have rushed to defend the vaccine in recent days.

Welford noted that, despite the company’s “notable successes” in gaining regulatory approval and accelerating the manufacture of its profitable vaccine, safety concerns expressed in Europe “are of paramount concern to many generalists.”

“We see FDA emergency use approval and UK / EU dose distribution agreements as key to moving the debate beyond the COVID-19 vaccine, despite concerns that it will be a distraction for management,” he explained.

The vaccine has been approved for use in the UK, Europe and other countries, and hundreds of millions of doses have been ordered from countries around the world. However, no emergency permit has yet been issued in the United States

Jefferies thought outside the box and upgraded AstraZeneca to buy in mid-March. He noted its “compelling growth profile within the EU pharmaceuticals industry” and its relative discount based on the expected strategic benefits of the $ 37 billion acquisition of Alexion Pharmaceuticals in the third quarter.

Welford defended the move by highlighting that 15 times the company’s estimated price-earnings ratio by 2022 – a mechanism for determining whether a company’s stock is fairly valued – is similar to its peers despite its “leading growth profile” .

Promising pipeline

AstraZeneca was trading on the London Stock Exchange on Friday at £ 7,337 a share and Jefferies has set a price target of £ 8,850. In Wednesday’s research note, Welford again pointed to several catalysts in the pipeline that could drive stocks higher in the coming months.

The phase 3 study data for the breast cancer treatment enhertu is expected to be available in the second half of 2021, along with possible approvals for the anifrolumab drug for the treatment of lupus. Jefferies is also anticipating approvals for the asthma drug tezepelumab in the first half of 2022 after “impressive” phase three data and a long delayed approval for the anemia candidate Roxadustat in the second half of 2021. Updated first and second phase data from Lung cancer datopotamab is also expected soon.

In a recent announcement, Damien Conover, Director of Healthcare Equity Research at Morningstar, said of AstraZeneca, “The strong overall innovation that has come from the vaccine and pipeline strengthens our beliefs in the company’s vast moat.”

He added that AstraZeneca had “made progress in addressing areas of unmet medical need” and forecast that data from the company’s Phase 3 trial of Farxiga treatment for conserved heart failure would likely lead to approval of the drug.

Conover rated anifrolumab as a “higher regulatory risk”, while roxadustat was rated as a “medium risk” and tezepelumab as a “lower risk”.

“In the longer term, we are encouraged by the robustness of the early-stage pipeline and the opportunities to develop combinations with Farxiga appear well-positioned to address several major cardiometabolic indications where unmet medical needs remain high,” said Conover. He added that Morningstar also remains bullish on AstraZeneca’s cancer drugs pipeline.

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Business

U.S. states face steep decline in J&J vaccine

Vials labeled “COVID-19 Coronavirus Vaccine” and syringe can be seen in front of the displayed Johnson & Johnson logo in this illustration dated February 9, 2021.

Given Ruvic | Reuters

Johnson & Johnson is reducing shipments of its single-dose Covid-19 vaccine next week by 86% as it grapples with manufacturing issues at a large Baltimore facility.

The government allocated just 700,000 J&J shots to the states next week, up from 4.9 million the week before. This is based on data from the Centers for Disease Control and Prevention.

J&J is awaiting regulatory approval for a facility in Baltimore operated by Emergent BioSolutions Inc and is working with the U.S. Food and Drug Administration to obtain approval.

Workers at the Baltimore plant mixed the ingredients for the J&J and AstraZeneca vaccines a few weeks ago, resulting in around 15 million J&J doses being ruined. The Biden administration hired J&J to manufacture vaccines at the factory and stopped producing the AstraZeneca vaccine there.

Once approved, J&J could dispense up to eight million doses a week, White House Covid-19 coordinator Jeff Zients said during a news conference on Friday. And the company remains on track to deliver 100 million cans by the end of May.

Michigan Governor Gretchen Whitmer has urged the Biden administration to increase vaccines in her state, which is grappling with the country’s worst outbreak. Michigan is expected to receive 17,500 J&J cans next week, an 88% decrease from the previous week.

The government said it will continue to assign shots based on population and has no plans to increase doses to more affected states as it cannot predict where infections might rise next.

“There are tens of millions of people across the country in every state and county who have not yet been vaccinated,” Zients said Friday. “And the fair and just way to distribute the vaccine is based on the adult population by state, tribe and territory. That is how it was done, and we will continue to do it.”

“The virus is unpredictable. We don’t know where the next surge in cases might be,” he added.

New York Governor Andrew Cuomo said in a statement Friday that the state will only receive 34,900 doses, an 88% decrease from the previous week.

“As has been the case since our vaccination efforts began, the X-Factor is supply, supply, supply, and like any other state, our Johnson & Johnson dose allocation will be significantly lower next week,” said Cuomo.

In California, the J&J grant will decrease from 572,700 to 67,600. Florida from 313,200 to 37,000; and Texas from 392,100 to 46,300.

Some states have also temporarily suspended J&J vaccinations in certain facilities after people suffered side effects. The Georgia Department of Health stopped all recordings in one location after reactions occurred in eight people, and other locations in North Carolina and Colorado also stopped giving doses due to reactions.

However, according to a statement from the North Carolina Department of Health and Human Services, the CDC has found no safety issues or cause for concern regarding the J&J doses. The Colorado Department of Public Health and Environment also said there was “nothing to worry about.”

“After reviewing each patient’s symptoms, analyzing other vaccinations from the same vaccine lot, and speaking with the CDC to confirm our results, we are confident that there is no cause for concern,” said Dr. Eric France, chief medical officer of the department’s officer, said in a statement.

The J&J vaccine was the third vaccine approved in the United States, after vaccines from Pfizer and Moderna. According to CDC data, the company shipped nearly 15 million cans in the US on Friday night.

The US delivers an average of 7 million vaccine doses per day over a seven-day period. One in five Americans is now fully vaccinated, according to the CDC.

The rate of new Covid cases and deaths in the US has fallen dramatically since the winter summit, when hundreds of thousands of new infections and thousands of deaths were reported daily.

According to the Johns Hopkins University, the 7-day average of new cases in the US was 67,000 on Saturday. This is comparable to the upswing that hit the nation last summer. The US reports an average of 982 deaths daily.

New infections are increasing in 23 states as the more infectious variant first identified in Great Britain has become the dominant strain. US President Joe Biden has urged states to grant vaccine appointments to all adults by April 19 as the nation struggles to immunize as many people as possible, people as good as the virus mutates.