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White Home says states cannot buy Covid vaccine instantly

Ron Klain, former White House Ebola Response Coordinator, speaks during a hearing for the House Subcommittee on Homeland Security in Washington, DC, the United States, on Tuesday, March 10, 2020.

Andrew Harrer | Bloomberg | Getty Images

White House Chief of Staff Ron Klain said Sunday that US states are unable to purchase Covid-19 vaccines directly from manufacturers, as some are trying to do under emergency use approval issued by the Food and Drug Administration to have.

“This vaccine is subject to emergency approval for legal reasons,” Klain told NBC’s Meet the Press when asked about the inquiries. “I don’t think that’s possible.”

The comments come after New York Governor Andrew Cuomo on Monday asked Pfizer CEO Albert Bourla to allow the state to buy vaccines directly from the company, citing the scarcity of supplies.

Pfizer told Cuomo that it would not be able to do so under the terms of his December emergency clearance.

The company said it was open to the idea, but “before we could sell directly to state governments, HHS would need to approve this proposal based on the EUA granted to Pfizer by the FDA.”

The Department of Health and Human Services – still under Republican leadership at the time – accused Democrat Cuomo of trying “to get to the top of the line at the expense of other jurisdictions”.

Klain said he believed governors were “understandably frustrated” with the slow pace of vaccinations to date.

The number of vaccines administered falls far short of projections made under President Donald Trump, although the pace has picked up in recent weeks. President Joe Biden has pledged the US will administer 100 million doses of vaccine in his first 100 days in office.

“We’re going to ramp up production. We’re going to ramp up sales. We’re going to work closely with the governors. We’re going to get this vaccine out to the American people,” Klain said.

The Biden government has urged the federal government to strengthen its role in the manufacture and distribution of Covid-19 vaccines.

TJ Ducklo, a White House spokesman, previously opposed state efforts to buy vaccines direct, saying, “We need to take a national approach to vaccination and make sure states don’t compete against each other as they do with PPE, ventilators and others. ” Testing. “

Ducklo didn’t immediately respond to an email on Sunday. The Department of Health and Human Services also did not immediately respond to a request for comment.

Before Biden took office, other states had asked Trump’s Department of Health and Human Services to allow them to buy vaccines directly from the manufacturer.

The governors of Michigan, Minnesota and Wisconsin – all Democrats – sent a letter on Jan. 15 accusing the Trump administration of botching the introduction of the first vaccine.

“If you cannot or do not want to give us this shipment, we urge you to give us permission to buy vaccines directly so we can distribute them,” wrote the governors.

At least one of those states appears to have been tracking the plan since Biden was inaugurated on Wednesday.

Bobby Leddy, a spokesperson for Michigan Governor Gretchen Whitmer, said in a statement to CBS: “We are confident that President Joe Biden will have a clear national strategy, based on data and science, to help our nation overcome this To help health crisis. ” “”

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Voters extra optimistic about Covid, blame feds for vaccine rollout: NBC ballot

USC School of Pharmacy Assistant Professor Richard Dang (R) gives Ashley Van Dyke a Covid-19 vaccine as a mass vaccination of health care workers is happening on January 15, 2021 at Dodger Stadium in Los Angeles, California.

Irfan Khan | AFP | Getty Images

With President Joe Biden making tackling the Covid-19 crisis his top priority, American voters are a little more optimistic about the pandemic than they were last fall, according to a new poll by NBC News.

Still, many respondents are dissatisfied with the sluggish introduction of the vaccine in the country, and a majority blame the federal government, according to the survey.

Poll results released Thursday showed that 38% of registered voters believe the worst of the health crisis is behind the country, while 44% believe the worst is yet to come. In a poll conducted just before the November elections, those numbers were 25% and 55%, respectively.

In his inaugural address on Wednesday, Biden warned of a difficult battle against the impending coronavirus.

“We are entering what is possibly the toughest and deadliest phase of the virus,” he said.

The country has at least 193,600 new coronavirus cases and at least 3,030 Covid deaths every day, based on a 7-day average calculated by CNBC using data from Johns Hopkins University. New, more infectious strains of the virus have emerged in the United States. At least 406,000 Americans have died from the virus since the pandemic started early last year.

The U.S. has failed to meet its target of vaccinating 20 million people by the end of 2020. Under the administration of former President Donald Trump, just over 14.2 million people had received one or more doses of the Covid-19 vaccine on Wednesday morning, according to the CDC.

While respondents to the NBC survey expressed a slight increase in optimism about the pandemic, more than half of respondents were previously dissatisfied with the introduction of vaccines: 30% said vaccine administration went poorly, while 25% said it was bad that they “didn’t” run too well. “

Another 11% said it was handled “very” well, and 31% said it went “fairly” well.

Among those who said the rollout was below average, 64% primarily blamed the federal government, while 21% blamed the state governments. Another 11% blamed both of them the same.

The answers diverged across the party lines. 79% of Democratic voters who criticized the introduction of the vaccine blamed the federal government. Among Republicans who were dissatisfied with the distribution, 52% blamed states.

The poll polled 1,000 registered voters nationwide from January 10-13. The error rate is plus or minus 3.1 percentage points.

Biden’s plan

Biden plans to accelerate vaccine rollout by increasing funding for local and state officials, creating more vaccination sites, and launching a national awareness campaign, according to his Covid Response Plan released Thursday. Previously, Biden said his government will try to give 100 million vaccine shots in the first 100 days.

His incoming health officials have expressed dismay at the state of the federal vaccine distribution plan.

“What we inherit from the Trump administration is so much worse than we could have imagined,” Jeff Zients, Biden’s Covid Response coordinator, told reporters. “We have to vaccinate as much of the US population as possible to get out of this pandemic, but we don’t have the infrastructure.”

On his first day in office, Biden restored the national security team in charge of global health, safety and biological defense, urged authorities to extend statewide moratoriums on evictions and foreclosures, and urged the Department of Education to put a break on student loan payments and interest to extend.

The president has also issued a mask mandate for anyone visiting a federal building or state, or using certain public transportation. Biden launched a 100-Day Masking Challenge that asked Americans to wear face coverings in public for the next 100 days.

Adopting a new Covid aid package will be a challenge for the new Congress and the White House. Democrats have a small majority in both houses of Congress, and Republicans are skeptical about spending increases.

“We have to put politics aside and finally face this pandemic as a nation,” Biden said on Wednesday.

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The Coronavirus Kills Mink. They Might Get a Vaccine.

At least two American companies and Russian researchers are working on coronavirus vaccines against mink. The animals became sick and died in large numbers from the virus, which they also returned to humans in mutated form.

Zoetis, a large New Jersey veterinary drug company with annual sales of more than $ 6 billion in 2019, and Medgene Labs, a small company with about 35 employees in South Dakota, are both testing vaccines in mink. They apply for a license for their products from the US Department of Agriculture.

Both companies said their vaccine technologies are generally similar to Novavax’s for a human vaccine that is in late-stage trials. In this system, insect cells produce the coronavirus spike protein, which is then bound to a harmless virus that invades the body’s cells and trains the immune system to be prepared for reality.

Mink is known to have been infected with SARS-CoV-2, the pandemic virus, in half a dozen countries around the world.

All members of the weasel family are susceptible to infection and to developing some symptoms and passing the virus on, at least to others of their species. This is in part due to the proteins on the surfaces of their cells and the structure of their respiratory systems. Scientists don’t know why minks in particular seem to get very sick, but the overcrowded conditions in farms on farms can cause them to be exposed to higher levels of virus.

The most serious outbreak was in Denmark, where mink breeding was suspended until at least 2022 due to mutations in the virus that appeared in infected mink.

At the end of last autumn Denmark ordered the slaughter of up to 17 million animals. Most of the dead minks were not allowed to be skinned for the fur trade. In average years the country sells up to 17 million pelts, but last year’s decision also killed its breeding population and there are fears that the industry will not recover.

In the United States, on the other hand, according to an industry group, Fur Commission USA, around 275 mostly small mink farms produce around three million skins annually. Thousands of U.S. minks have been infected and died, but states have been addressing the quarantine issue on some farms. The Ministry of Agriculture did not get involved and there was no order to kill mink populations like in Denmark.

Still, mink infections pose a public health threat in the United States. At least two minks that have escaped from farms have tested positive. And a wild mink tested positive. Scientists fear that if the virus spreads to wilder mink or other animals, it could establish itself in natural populations and create a reservoir from which it could possibly emerge in a mutated form to re-infect humans at another time.

So far, the mutations observed in Danish mink have not turned out to be a problem. But mutations in the virus in infected people have produced at least two variants that are more infectious. If a second species, the mink, serves as another breeding ground for the virus, the likelihood of mutation and escape into other animals increases. Consequently, a mink vaccine could have value beyond the industry. And while the Department of Agriculture is not currently considering applications for vaccines for cats and dogs, this is one option companies are considering.

Covid19 vaccinations>

Answers to your vaccine questions

If I live in the US, when can I get the vaccine?

While the exact order of vaccine recipients may vary from state to state, most doctors and residents of long-term care facilities will come first. If you want to understand how this decision is made, this article will help.

When can I get back to normal life after the vaccination?

Life will only get back to normal once society as a whole receives adequate protection against the coronavirus. Once countries have approved a vaccine, they can only vaccinate a few percent of their citizens in the first few months. The unvaccinated majority remain susceptible to infection. A growing number of coronavirus vaccines show robust protection against disease. However, it is also possible that people spread the virus without knowing they are infected because they have mild or no symptoms. Scientists don’t yet know whether the vaccines will also block the transmission of the coronavirus. Even vaccinated people have to wear masks for the time being, avoid the crowds indoors and so on. Once enough people are vaccinated, it becomes very difficult for the coronavirus to find people at risk to become infected. Depending on how quickly we as a society achieve this goal, life could approach a normal state in autumn 2021.

Do I still have to wear a mask after the vaccination?

Yeah, but not forever. The two vaccines that may be approved this month clearly protect people from contracting Covid-19. However, the clinical trials that produced these results were not designed to determine whether vaccinated people could still spread the coronavirus without developing symptoms. That remains a possibility. We know that people who are naturally infected with the coronavirus can spread it without experiencing a cough or other symptoms. Researchers will study this question intensively when the vaccines are introduced. In the meantime, self-vaccinated people need to think of themselves as potential spreaders.

Will it hurt What are the side effects?

The vaccine against Pfizer and BioNTech, like other typical vaccines, is delivered as a shot in the arm. The injection is no different from the ones you received before. Tens of thousands of people have already received the vaccines, and none of them have reported serious health problems. However, some of them have experienced short-lived symptoms, including pain and flu-like symptoms that usually last a day. It is possible that people will have to plan to take a day off or go to school after the second shot. While these experiences are not pleasant, they are a good sign: they are the result of your own immune system’s encounter with the vaccine and a strong response that ensures lasting immunity.

Will mRNA vaccines change my genes?

No. Moderna and Pfizer vaccines use a genetic molecule to boost the immune system. This molecule, known as mRNA, is eventually destroyed by the body. The mRNA is packaged in an oily bubble that can fuse with a cell, allowing the molecule to slide inside. The cell uses the mRNA to make proteins from the coronavirus that can stimulate the immune system. At any given point in time, each of our cells can contain hundreds of thousands of mRNA molecules that they produce to make their own proteins. As soon as these proteins are made, our cells use special enzymes to break down the mRNA. The mRNA molecules that our cells make can only survive a few minutes. The mRNA in vaccines is engineered to withstand the cell’s enzymes a little longer, so the cells can make extra viral proteins and trigger a stronger immune response. However, the mRNA can last a few days at most before it is destroyed.

Zoetis produces many vaccines for farm animals as well as dogs and cats. For pets, vaccines are made against infectious respiratory diseases in dogs, feline leukemia viruses, and others. The company began work on an animal vaccine in February at the start of the pandemic.

“When we saw the first case of dog infection in Hong Kong, we immediately followed up our normal procedures for developing a vaccine against emerging infectious diseases,” said Mahesh Kumar, senior vice president, Global Biologics, Zoetis. “We have decided to prepare a vaccine for dogs and cats.”

However, upon news of mink infections, the company reached out to the US Department of Agriculture and obtained permission to test the vaccine in mink. In the past, it took several months from testing to approval of other vaccines.

Dr. Kumar pointed out that coronavirus veterinary vaccines are common, for example for avian infectious bronchitis. The disease was first identified in the 1930s and a number of companies make vaccines.

Medgene, an early-stage small company, began work on coronavirus vaccine technology for animals in response to a devastating disease affecting pigs in China in 2013, the epidemic swine diarrhea virus. Mark Luecke, the company’s chief executive officer, said that as soon as the news of the pandemic became known last year and the coronavirus was identified and its genetic sequence described, a team “immediately started work on a vaccine that is for animals is suitable “.

Not knowing which animals would be susceptible, the company began testing it on mice, as it usually does with vaccine developers. When mink was found to be particularly vulnerable, the company contacted people in the mink industry and began testing the virus. Mr Lücke said it should be feasible to produce it this spring pending licensing.

Outside the US, other researchers are also working on mink vaccines. Researchers in Russia and Finland are tracking animal vaccines that could be used on mink and other animals.

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Pfizer to provide as much as 40 million Covid vaccine doses to Covax international program

A nurse prepares the Pfizer BioNTech Covid-19 vaccine on January 10, 2021 at a vaccination center in Sarcelles near Paris.

ALAIN JOCARD | AFP | Getty Images

Pfizer will deliver up to 40 million doses of its coronavirus vaccine to a global alliance that aims to provide coronavirus vaccines to poor nations, the head of the World Health Organization said on Friday.

The agreement will enable Covax – together with the WHO – to deliver vaccine doses to the participating countries from February, said WHO Director General Tedros Adhanom Ghebreyesus during a press conference. Tedros added that until an emergency is approved, the program expects 150 million doses of AstraZeneca’s vaccine to be available for distribution in the first quarter of this year.

The Covax program aims to provide 2 billion doses of Covid-19 vaccines to participating countries, which include low- to middle-income countries, by the end of this year. The Pfizer BioNTech vaccine requires two vaccinations spaced weeks apart, suggesting the deal would only cover 20 million people.

Tedros said the deal would allow other countries with supplies of Pfizer’s vaccine to donate them to the program. The WHO chief criticized wealthy nations for signing supply agreements with drug manufacturers for their starting doses of Covid-19 vaccines to stockpile supplies from poorer nations.

“This is not only important for COVAX, it is also an important step forward for equitable access to vaccines and an essential part of the global effort to fight this pandemic. We will only be safe everywhere if we are safe everywhere,” so Dr. Seth Berkley, CEO of Gavi, the Vaccine Alliance, said in a statement.

Albert Bourla, CEO of Pfizer, said during the press conference that the company will make the vaccine doses available to Covax and poorer countries for a fee. Pfizer was the first company to receive a global list of emergency uses for its vaccine from the WHO, allowing other countries to expedite their regulatory approval processes to begin administering the vaccine.

Bourla said the company will help ship the cans, which require ultra-cold storage and special handling, to low-income countries. UNICEF, which is helping with the dispensing of the cans, previously warned that some of the world’s poorest countries could face the challenge of storing and managing the shots upon arrival.

The program’s contract with Pfizer increases supply agreements to a total of just over 2 billion doses, but negotiations for an additional supply continue. The goal, according to Covax, is to immunize healthcare and other frontline workers as well as some high-risk individuals from the first quarter of this year.

The agreement follows the United States’ decision to remain a member of WHO under President Joe Biden. The new administration will also join the Covax program, a move the Trump administration opposed last year.

“I couldn’t escape the temptation to say that I’m very happy that this press conference is taking place on the day the United States rejoins the WHO organization. I think it’s a symbolic, great day for us,” Pfizer boss Bourla said at the meeting.

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Pfizer says its Covid vaccine trial for youths ages 12 to 15 is totally enrolled

Walgreens pharmacist Jessica Sahni will hold the vaccine against Pfizer BioNTech coronavirus disease (COVID-19) at the New Jewish Home in New York on December 21, 2020.

Yuki Iwamura | Reuters

Pfizer said it had fully enrolled its Covid-19 vaccine study in children ages 12-15, an important step before the vaccine could be used in that age group.

The study, an extension of the study used to support the company’s emergency approval for the vaccine in people aged 16 and over, enrolled 2,259 children between the ages of 12 and 15, Pfizer told CNBC on Friday. The entry on a government clinical trial website has been updated to determine that subjects are no longer being recruited.

The vaccine developed with German partner BioNTech was approved in December for people aged 16 and over. Studies in younger age groups are needed to ensure the correct dose as well as safety and effectiveness in these different groups, said Dr. Evan Anderson, a pediatrician at Emory University School of Medicine.

“I am very uncomfortable sending my children back to school where, despite the school’s best efforts, there is a real risk of getting Covid-19,” Anderson told CNBC in October.

While children are less affected by Covid-19 than adults, they still catch the virus and get sick. Some even died. According to a report from the American Academy of Pediatrics and the Children’s Hospital Association, more than 2.5 million cases of Covid-19 in children were reported as of Jan. 14, about 13% of all cases.

“Children can still get sick and die from Covid-19,” said Dr. Paul Offit, director of the Vaccine Education Center and an infectious disease doctor at Philadelphia Children’s Hospital. “In the past year, as many children died of Covid-19 as of influenza. And we recommend an influenza vaccine for children.”

Offit also pointed out that children can suffer from a disease related to Covid-19 called multisystem inflammatory syndrome, “which can be debilitating”.

According to the Centers for Disease Control and Prevention, as of Jan. 8, there were 1,659 cases of the syndrome in children named MIS-C and 26 related deaths. There were a total of 78 deaths from Covid-19 in children under 4 years old and 178 in children between 5 and 17 years old, according to CDC data, although those numbers do not explain all deaths from the United States

Children compete for class at PS 361 on the first day of returning to class during the coronavirus disease (COVID-19) pandemic in the Manhattan neighborhood of New York City, New York, United States, on December 7, 2020.

Carlo Allegri | Reuters

Pfizer declined to say when it expected results from the study, which would depend on the observed infection rate, to compare the rates in the placebo group with those who received the vaccine. With infection rates higher in the US since the fall – the 7-day average of daily cases now stands at 187,500, according to a CNBC analysis of the Johns Hopkins University data – vaccine effectiveness studies have shown their ads are getting faster.

However, enrollment for adolescent studies has been slower than hoped, at least for Moderna’s study in children ages 12-17, Moncef Slaoui, chief advisor to Operation Warp Speed, the Trump administration’s vaccine effort, said at their last meeting on Dec. January.

By then, around 800 children had been included in the study for over a month, of which around 3,000 were needed. Moderna’s vaccine was approved for people aged 18 and over in December, weeks after its teenage study began. Pfizer lowered the age of his trial to 12 years in October.

“While enrollment was lower during the holiday season, we expect an increase in the new year as planned,” said Moderna spokeswoman Colleen Hussey on Friday. “We are on track to provide updated data by mid-2021.”

AstraZeneca, whose vaccine developed by Oxford University is in late-stage trials in the US and approved in the UK, told CNBC Friday that it plans to continue UK trials in a new protocol for children ages 5-18 from the coming months. “”

Johnson & Johnson, whose results are expected in the third phase in adults, said it was in talks with regulators about including pediatric populations in its development plan. The same technology used for the Covid-19 vaccine was found to have been used in vaccines given to more than 200,000 people, including people over 65, infants, children, HIV-positive adults, and pregnant women .

Typically, vaccine trials are conducted in younger age groups after they have been shown to be safe and effective in older groups. The manufacturers of Covid-19 vaccines have indicated that they will follow this plan here as well.

Moderna’s chief executive Stephane Bancel said earlier this month the company is unlikely to have data on children ages 11 and younger who would include a lower dose before next year. He said he expected data for children 12 years and older could be available before September.

U.S. public health officials such as White House Chief Medical Officer Dr. Anthony Fauci, said they hope that by fall 75% to 80% of the US population could be vaccinated so life can return to some form of normal.

About 78% of the US population, or 255 million people, are over 18 years old, according to a CNBC analysis of the census data. Another 25 million people are between 12 and 17 years old.

Fauci did not immediately respond to a query about the need to include children in vaccinations in order to meet his goal of 75% to 80% coverage.

“It is important that all children are vaccinated, and manufacturers cannot conduct these trials fast enough,” Angela Rasmussen, virologist and subsidiary at the Georgetown Center for Global Health Science and Safety, told CNBC on Friday. “The more people of all ages are vaccinated, the better.”

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Pfizer Will Ship Fewer Covid-19 Vaccine Vials to Account for ‘Additional’ Doses

However, the federal health authorities that manage the government’s syringe contracts told the FDA that more than 70 percent of the sites are using more efficient syringes and that more syringes can be bought or made according to another person who is aware of the situation.

Still, Pfizer’s attempts to pressurize the FDA worried some health officials, especially since the company itself originally calculated the vials contained five doses. If an extra dose could be extracted, it would mean the vaccine supply could be stretched, protecting more Americans from the virus. On the other hand, too few specialty syringes would mean the government could pay for wasted doses.

In early January, the debate was resolved after a “standard and customary legal review process,” said an FDA spokeswoman. On January 6, in a change to the emergency approval, the FDA officially changed the vaccine datasheet to specify six doses.

“Syringes and / or needles with low dead volume can be used to extract six doses from a single vial,” says the new US bulletin. It also warned, “If standard syringes and needles are used, there may not be enough volume to extract a sixth dose from a single vial.”

In a statement, an FDA spokeswoman said the agency considered several factors in approving Pfizer’s request, including the availability of the specialty syringes, the fact that other health officials had made a similar decision, and that the change would vaccinate Americans faster.

Pfizer and the federal government have agreed to keep track of which locations receive the syringes and other equipment needed to extract the extra dose, and that the company will not bill the US for six doses per vial for locations without these devices. According to a person familiar with the negotiations who was not allowed to speak because the conversations are confidential.

Beginning next week, the number of Pfizer vaccines the federal government will allocate to each state could be based on the assumption that each vial contains six doses, according to a federal official with no legal capacity to discuss the matter. The CDC and the Department of Health and Human Services did not discuss when they could do the shift until Friday afternoon.

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Pfizer Will Ship Fewer Vaccine Vials to Account for ‘Further’ Doses

In December, pharmacists made the happy discovery that they could squeeze an extra vaccine dose out of Pfizer vials that were supposed to contain only five.

Now, it appears, the bill is due. Pfizer plans to count the surprise sixth dose toward its previous commitment of 200 million doses of Covid vaccine by the end of July and therefore will be providing fewer vials than once expected for the United States.

And yet, pharmacists at some vaccination sites say they are still struggling to reliably extract the extra doses, which require the use of a specialty syringe.

“Now there’s more pressure to make sure that you get that sixth dose out,” said Michael Ganio, the senior director for pharmacy practice and quality at the American Society of Health-System Pharmacists.

For weeks, Pfizer executives pushed officials at the Food and Drug Administration to change the wording of the vaccine’s so-called emergency use authorization so that it formally acknowledged that the vials contained six doses, not five.

The distinction was critical: Pfizer’s contract with the federal government requires that it be paid by the dose.

At one point, Pfizer executives lashed out at the top federal vaccine regulator over the government’s reluctance to budge on the request, according to people familiar with the discussions who were not authorized to discuss them.

On Jan. 6, Pfizer got what it wanted. The F.D.A. changed the language in its fact sheet for doctors to confirm that the vials contain a sixth dose. The change mirrors similar labeling updates by the World Health Organization and the F.D.A.’s counterpart in the European Union.

Company officials, including the chief executive, Dr. Albert Bourla, have said that the sixth dose allows Pfizer to stretch its supply of scarce vaccine even further — it was one factor, for example, in the company’s new estimates that it will be able to manufacture two billion doses for the world this year, instead of the 1.3 billion it had originally planned.

A Pfizer spokeswoman, Amy Rose, said the company would “fulfill our supply commitments in line with our existing agreements — which are based on delivery of doses, not vials.”

When Pfizer first began shipping the vaccines in mid-December, it said that each vial contained enough liquid for five doses. But pharmacists in hospitals across the country soon noticed that the vials held enough for a sixth — and sometimes a seventh — dose. The discovery prompted a flurry of excitement and confusion, with some pharmacists throwing out the extra vaccine because they did not have permission to use it.

But they were soon advised by the F.D.A. that they could use those extra doses, which could be extracted with a so-called low dead volume syringe that is designed to cut down on wasted medication and vaccines.

Suddenly, it seemed as if the 100 million doses of vaccine that Pfizer has promised to the United States by the end of March would stretch to as much as 120 million — a welcome development given the scarcity of Covid-19 vaccines and the coronavirus pandemic’s mounting death toll.

But Pfizer insisted that those doses be counted toward its existing contract. It can now sell vials the United States had been expecting to other countries, or charge the United States for them in future deals. That could threaten the wave of good publicity that the company has enjoyed since developing a highly effective vaccine at record speed.

“Pfizer will make a lot of money from these vaccines, and the U.S. government assumed a lot of the upfront risk in this case, so I’m not sure why Pfizer didn’t just continue to fill their supply as planned, even if it meant oversupplying a little,” said Dr. Aaron S. Kesselheim, a professor of medicine at the Brigham and Women’s Hospital and Harvard Medical School, who studies drug prices.

Covid-19 Vaccines ›

Answers to Your Vaccine Questions

If I live in the U.S., when can I get the vaccine?

While the exact order of vaccine recipients may vary by state, most will likely put medical workers and residents of long-term care facilities first. If you want to understand how this decision is getting made, this article will help.

When can I return to normal life after being vaccinated?

Life will return to normal only when society as a whole gains enough protection against the coronavirus. Once countries authorize a vaccine, they’ll only be able to vaccinate a few percent of their citizens at most in the first couple months. The unvaccinated majority will still remain vulnerable to getting infected. A growing number of coronavirus vaccines are showing robust protection against becoming sick. But it’s also possible for people to spread the virus without even knowing they’re infected because they experience only mild symptoms or none at all. Scientists don’t yet know if the vaccines also block the transmission of the coronavirus. So for the time being, even vaccinated people will need to wear masks, avoid indoor crowds, and so on. Once enough people get vaccinated, it will become very difficult for the coronavirus to find vulnerable people to infect. Depending on how quickly we as a society achieve that goal, life might start approaching something like normal by the fall 2021.

If I’ve been vaccinated, do I still need to wear a mask?

Yes, but not forever. The two vaccines that will potentially get authorized this month clearly protect people from getting sick with Covid-19. But the clinical trials that delivered these results were not designed to determine whether vaccinated people could still spread the coronavirus without developing symptoms. That remains a possibility. We know that people who are naturally infected by the coronavirus can spread it while they’re not experiencing any cough or other symptoms. Researchers will be intensely studying this question as the vaccines roll out. In the meantime, even vaccinated people will need to think of themselves as possible spreaders.

Will it hurt? What are the side effects?

The Pfizer and BioNTech vaccine is delivered as a shot in the arm, like other typical vaccines. The injection won’t be any different from ones you’ve gotten before. Tens of thousands of people have already received the vaccines, and none of them have reported any serious health problems. But some of them have felt short-lived discomfort, including aches and flu-like symptoms that typically last a day. It’s possible that people may need to plan to take a day off work or school after the second shot. While these experiences aren’t pleasant, they are a good sign: they are the result of your own immune system encountering the vaccine and mounting a potent response that will provide long-lasting immunity.

Will mRNA vaccines change my genes?

No. The vaccines from Moderna and Pfizer use a genetic molecule to prime the immune system. That molecule, known as mRNA, is eventually destroyed by the body. The mRNA is packaged in an oily bubble that can fuse to a cell, allowing the molecule to slip in. The cell uses the mRNA to make proteins from the coronavirus, which can stimulate the immune system. At any moment, each of our cells may contain hundreds of thousands of mRNA molecules, which they produce in order to make proteins of their own. Once those proteins are made, our cells then shred the mRNA with special enzymes. The mRNA molecules our cells make can only survive a matter of minutes. The mRNA in vaccines is engineered to withstand the cell’s enzymes a bit longer, so that the cells can make extra virus proteins and prompt a stronger immune response. But the mRNA can only last for a few days at most before they are destroyed.

Pfizer’s accounting for the extra dose is already creating controversy in Europe, where some countries — like Belgium — say they have had to cancel vaccination appointments after discovering that Pfizer is sending them fewer vials. “It’s linked to the sixth dose,” Sabine Stordeur, an official overseeing vaccination efforts in Belgium, told the newspaper Le Soir. “It’s still a private company, so one shouldn’t be surprised.”

The U.S. negotiations come at a particularly harrowing time, as the Biden administration is said to be discussing the purchase of a third round of 100 million doses of Pfizer’s vaccine later in the year. The country is racing to vaccinate as many people as possible before more contagious virus variants become widespread, potentially spurring a wave of new hospitalizations and deaths.

Pfizer’s efforts to capitalize on the discovery were for weeks camouflaged in a bureaucratic language dispute. Before Christmas, Pfizer approached F.D.A. officials requesting a formal change to its fact sheet so that it said each vial contained six doses of vaccine instead of five. But regulators instead suggested the phrase “up to six doses,” depending on what kinds of needles and syringes were used to extract the vaccine.

After the F.D.A. signed a new fact sheet with that more cautious language, Pfizer approached F.D.A. officials again, saying it was crucial to say “six doses.” The company suggested altering the language to indicate that low dead volume syringes should be used. At one point, Pfizer executives lashed out at Dr. Peter Marks, the top vaccine regulator at the F.D.A., according to two people who heard about the exchange but were not authorized to discuss it.

An F.D.A. spokeswoman disputed that characterization of the exchange and said it was “constructive.”

Ms. Rose, the Pfizer spokeswoman, said that “in a situation of limited vaccine supply amidst a public health crisis, our intent with this label change is to provide clarity to health care providers, minimize vaccine wastage, and enable the most efficient use of the vaccine.”

In late December, federal health officials sought to figure out whether there were enough of the specialized syringes to justify the shift. Officials at the Centers for Disease Control and Prevention said they were uncertain whether the supply was sufficient, according to a person familiar with the conversations.

But federal health officials who manage the government’s contracts for syringes told the F.D.A. that more than 70 percent of the sites were using the more efficient syringes and that more could be easily bought or manufactured, according to another person knowledgeable about the situation.

Still, Pfizer’s attempts to pressure the F.D.A. unsettled some health officials, especially since the company itself originally calculated that the vials contained five doses. If an extra dose could be extracted, that would mean the vaccine supply could be stretched, protecting more Americans from the virus. On the other hand, too few of the specialty syringes would mean the government could end up paying for wasted doses.

By early January, the debate was resolved after a “standard and usual legal review process,” an F.D.A. spokeswoman said. On Jan. 6, in an amendment to the emergency authorization, the F.D.A. formally changed the vaccine’s fact sheet to specify six doses.

“Low dead-volume syringes and/or needles can be used to extract six doses from a single vial,” the new U.S. fact sheet read. It also warned, “If standard syringes and needles are used, there may not be sufficient volume to extract a sixth dose from a single vial.”

Pfizer and the federal government have agreed to track which sites are receiving the syringes and other equipment needed to extract the additional dose, and that the company will not charge the United States for six doses per vial at sites that don’t have that equipment, according to a person familiar with the negotiations who was not authorized to speak because the talks are confidential.

Beginning as soon as next week, the number of Pfizer vaccines that the federal government allocates to each state could be based on the assumption that each vial contains six doses, according to a federal official not authorized to discuss the matter. The C.D.C. and the Department of Health and Human Services were discussing as recently as Friday afternoon when they might make the shift.

Pharmacists around the country are still reporting that they don’t have the right supplies to reliably extract extra doses, said Erin Fox, the senior pharmacy director for drug information and support services at the University of Utah.

She said Pfizer deserved credit for developing the vaccine, but “it isn’t fair to people that can’t access the right syringe and needle combination to be able to get that sixth dose out.”

The contracts for low dead volume syringes are managed by the Department of Health and Human Services’ Biomedical Advanced Research and Development Agency. A spokeswoman for the agency said the federal government had procured enough of the syringes for the Pfizer vaccine currently available and was working with the company to “track current inventory and future deliveries of these specific syringes for Pfizer and continually comparing them to projected delivery of doses from Pfizer.”

Dr. Fox said that McKesson, the distribution company that has contracted with the federal government to deliver vaccination supplies, is still sending kits that contain only enough supplies for five doses per vial.

A McKesson spokesman said the company began sending out kits that account for the sixth dose this week.

Jen Psaki, the White House press secretary, said on Thursday that the Biden administration might use the Defense Production Act to accelerate production of the specialized syringes in order to increase supply, suggesting that the federal government is uncertain whether it will have enough in the future.

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Health

CDC modifications Covid vaccine steerage to OK mixing Pfizer and Moderna pictures

Syringe containers for the Covid-19 vaccines from Pfizer BioNtech and Moderna Inc. in Tucson, Arizona, USA, on Friday, January 15, 2021.

Cherry Orr | Bloomberg | Getty Images

The Centers for Disease Control and Prevention have tacitly changed their guidelines for Covid-19 vaccine shots, stating that it is now okay to mix Pfizer and Moderna shots in “exceptional situations” and that it is in Okay, wait up to six weeks to get the second shot. Two-dose immunization from both companies.

While Pfizer and Moderna’s vaccines, both of which use messenger RNA technology, were approved 21 and 28 days apart, the agency now says that under new guidelines, you can get both shots as long as they’re at least apart 28 days administered will be published on its website Thursday.

Although “every effort” should be made to ensure that a patient receives the same vaccine, in rare situations “any available mRNA COVID-19 vaccine can be administered with a minimum of 28 days between doses” – if supply Is limited or the patient does not know what vaccine they originally received, the CDC says in new guidelines.

The CDC says the two products are not interchangeable, admitting that they hadn’t yet investigated whether their new recommendations would alter the safety or effectiveness of either vaccine.

The agency said health care providers should give patients a vaccination card detailing when they received their first shot and what type of shot it was to ensure patients know which shot to receive the second time. The agency also recommends providers to record the patient’s vaccination information on their medical records and on the government vaccination information system.

Both companies need two doses to achieve maximum protection against the coronavirus. While both shots should be administered according to the guidelines originally recommended, the CDC said the second dose of both companies’ vaccine could be delayed for up to six weeks if necessary.

The updated guidelines come as some cities and counties across the country cancel vaccination appointments because they don’t have as many doses as they originally expected.

Wayne County, Michigan, for example, said last week it would be a priority to make sure people who got their first shot get their second shot on time. But the county said it had to cancel nearly 1,400 appointments for people to get their first shot.

“The intent is not to suggest people do something else, but rather to give clinicians flexibility in exceptional circumstances,” said Jason McDonald, a CDC spokesman, in an email to CNBC.

Dr. Nancy Messonnier, director of the CDC’s National Center for Immunization and Respiratory Diseases, was asked on Friday about the interval at which the two shots should be administered.

“The data we have is of a two-dose vaccine on the recommended schedule of 21 or 28 days,” she said at a virtual event hosted by Harvard TH Chan School of Public Health and National Public Radio . “At this point in time, we at CDC agree with what the FDA says, and the FDA has made it very clear that we should be using the approved regimen.”

“It’s firmly ingrained in science and the evidence available, and doing anything else would not follow science and possibly not allow us to really get the full potential of these vaccines,” she added. “For now, from the CDC’s point of view, we think it has to be two doses on the recommended schedule.”

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Russia’s Sputnik vaccine will get its first approval within the EU, UAE

A medical worker fills a syringe with the Gam-COVID-Vac vaccine (under the brand name Sputnik V) in Butovo, in southern Moscow.

Sergei Savostyanov | TASS | Getty Images

DUBAI, United Arab Emirates – Russian vaccine Sputnik V Covid-19 saw a number of improvements on Thursday as Hungary and the United Arab Emirates became the first countries in the European Union and the Gulf region to register the emergency shot.

Hungary’s decision was confirmed by President Viktor Orban’s spokesman, who said that if the country agrees to a shipping agreement with Moscow, it will be the first EU country to receive the vaccine. This is because the country’s cases have fallen from a high of more than 6,000 a day in early December to below 2,000 a day.

“This decision is very important as it shows that over 90% of the vaccine’s safety and efficacy is valued by our partners in Hungary,” said Kirill Dmitriev, head of the Russian Direct Investment Fund, in a statement.

The EU drug regulator has not yet approved the Russian stab, although Chancellor Angela Merkel gave Sputnik further hope on Thursday, suggesting that the German vaccine regulator could advise Russia on steering the EU approval process. The RDIF has submitted Sputnik for EU registration and expects its review in February.

UAE approval comes amid a dramatic surge in infections

The UAE approval comes amid a record spike in cases in the little Gulf Sheikh, which excelled internationally by welcoming tourists and fully reopening its economy by late summer last year.

Confirmed coronavirus cases have more than tripled in about three weeks, prompting Emirati authorities to suspend unnecessary hospital surgery and “entertainment” activities in their busy hotels and restaurants just days after the country gave assurances that the virus was under Control was to fail.

The UAE’s daily number of cases hit a record high of 3,529 on Thursday, well above neighboring Gulf states, where registered infections are below 500 per day.

A man from the Emirates wearing a protective mask walks at al-Barsha Health Center in the Gulf of Dubai on December 24, 2020.

GIUSEPPE CACACE | AFP via Getty Images

Sputnik V will be the third vaccine to be used in the United Arab Emirates after China’s Sinopharm vaccine and the Pfizer BioNTech vaccine developed in the US and Germany were released to the public in December. The country of around 10 million people is running the second fastest national vaccination campaign in the world after Israel per capita, according to the government, and aims to vaccinate half of the country’s population by the end of March.

“The decision is part of the UAE’s comprehensive and integrated efforts to ensure a higher level of prevention,” the country’s health ministry said in a statement on Thursday about Sputnik’s approval. “The study results have demonstrated the vaccine’s effectiveness in eliciting a strong antibody response to the virus, its safety to use and its compliance with international safety and efficacy standards.”

Lack of late-stage experimental data

The approvals came despite detailed research data not yet published on the results of the phase 3 human vaccine study. The capital of the United Arab Emirates, Abu Dhabi, began phase 3 testing for Sputnik V earlier this month but has not released any data on it. 1,000 volunteers in the emirate have received their first dose, according to RDIF.

Sputnik V, which according to its developer, the Gamaleya Research Institute, is 91% effective after two doses, has been used across Russia for months. Scientists expressed concern about what many have described as the rush to launch the vaccine, which gave the green light for mass use in Russia ahead of the completion of Phase 3 trials.

As the first step in the largest vaccination campaign in Argentina’s history, first line health workers are receiving the Russian Sputnik V vaccine against the coronavirus.

Patricio Murphy | SOPA pictures | LightRocket | Getty Images

Analysis of the phase 1 and phase 2 studies of the vaccine was published in The Lancet in September, which found that the initial results did not show any significant negative side effects, but further studies were required.

“The results of the Phase III clinical trials are expected to be published shortly,” according to the official Sputnik V.

Prior to Thursday’s announcements, it had been approved for emergencies in nine countries and territories outside Russia – Algeria, Argentina, Bolivia, Belarus, Serbia, Venezuela, Paraguay, Turkmenistan and the Palestinian Territories.

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U.S. Vaccine Provide: What to Know

The demand for vaccines is growing rapidly as the US grapples with a record death rate from Covid-19 and the threat of new, more contagious variants. After a slow start in December, many states and cities have rapidly accelerated vaccine delivery, expanded access to larger populations, and established mass testing sites.

But now there’s a new wrinkle: some mayors and governors say they have run out of vaccines available and have had to cancel appointments.

The Biden government has promised to revise the country’s volatile vaccination efforts, but there is only so much it can do to increase the supply available.

Here’s what you need to know.

There are simply not enough doses of approved vaccines to meet the huge demand. And that probably won’t change in the next few months.

The two approved vaccine companies, Moderna and Pfizer, each have promised to make 100 million doses of vaccine available to the United States by the end of March, or enough to give 100 million people the two needed vaccinations.

But that doesn’t mean that those 200 million cans are lying in a factory warehouse somewhere waiting to be shipped. Both companies produce the cans at full capacity and jointly dispense between 12 and 18 million cans per week.

As of Wednesday, nearly 36 million doses of the Pfizer and Moderna vaccines had been distributed to state and local governments. However, only about 16.5 million shots were given to patients.

However, if the local health authorities are better able to handle the distribution of vaccines, they will ultimately catch up with the limited supply. Some local officials, including those in New York City, said they had already reached this point and canceled appointments because they said they didn’t have enough.

Vaccine experts and the companies themselves have stated that applying the Defense Production Act will not add much to supply, at least in the short term, although any little bit could help. This is because production facilities are already full or almost full and there is a global race to develop vaccines that use a limited amount of resources.

Despite criticism of the Trump administration for not using the Defense Production Act more aggressively to stimulate production of test supplies and protective equipment, it used the act many times to give vaccine manufacturers priority access to suppliers of raw materials and equipment.

In a plan released Thursday, the Biden government announced that it would continue to use the law to increase supplies needed to make vaccines, as well as other materials needed to immunize tens of millions of people. Although the plan was few in detail, one example cited is to increase production of a special syringe that can squeeze six doses out of Pfizer vials that were originally supposed to contain five.

There are no vaccine reserves to speak of. For the most part, vaccines are shipped every week when they are made. (The exception is a small emergency supply that the Biden government has announced will continue.)

Last week, Alex M. Azar II, the outgoing Secretary for Health and Human Services, caused confusion when he announced that the federal government would release a reserve of vaccine doses. Many states have been told that an influx of vaccines is on the way that will allow more people to be vaccinated.

In his press conference, Mr Azar urged states to open their vaccination guidelines, saying they moved too slowly to use the doses they had already received. As a result, several governors, including Andrew M. Cuomo of New York, changed admissions rules to allow people 65 and older to have the vaccine.

However, last Friday, senior administration officials made it clear that all of those reserve doses were already earmarked as booster shots for people who had received the vaccine, and that Mr Azar was just setting out the logical extension of a distribution policy established by federal officials in December when supplies began. The release of the reserve doses would go to people who needed their second dose, not new groups of people who received their first shot.

In the future, Azar said, the government will switch to a new model: instead of sticking to a reserve of booster shots, every weekly shipment from the manufacturers would include doses for new people as well as second doses for those due for their booster shots. President Biden repeated this policy when he announced his vaccination schedule last week.

The Biden Administration

Updated

Jan. 21, 2021, 8:45 p.m. ET

Federal officials previously said they worked with states to find out who received a vaccine and when they were due for their booster shots, three weeks later for the Pfizer vaccine, and four weeks later for the Moderna vaccine.

They said that each weekly delivery gives priority to people who need their second dose that week, and what is left is used to vaccinate new people.

However, the plan relies on federal and state governments working together to specify exactly who has received a vaccine and what is needed from week to week. Many state governments have complained that they do not have the resources to carry out the vaccine distribution plan and the next few weeks will show how well the system works.

Biden’s new administration has vowed to revise the distribution to the states to give local officials more transparency on how much vaccine to expect in hopes of allowing states to better plan.

No, that probably won’t happen.

Last week, Michigan Governor Gretchen Whitmer asked the federal government for permission to buy 100,000 doses of vaccine directly from Pfizer. And on Monday, Mr. Cuomo wrote a letter to Pfizer asking the state to buy vaccines direct.

Pfizer and Moderna supplies have been fully drawn for at least the first quarter of this year, meaning a replacement vaccine is unlikely to be sold to individual states.

Additionally, the emergency approvals for the Pfizer and Moderna vaccines provide for the federal government to oversee distribution.

In a statement, a Pfizer spokeswoman said the company is “open to working with the US Department of Health on a distribution model that will allow as many Americans as possible to get access to our vaccine as soon as possible.” However, she noted that “before we can even think about direct sales to state governments, HHS would have to approve the proposal.”

A state official said Tuesday that the governor felt it was important to exhaust all of his options, no matter how unlikely they might be, and pointed to his efforts in March to buy fans direct from manufacturers – which sparked a bidding war between states he later criticized the federal government for refueling.

However, advisors to the Biden government have indicated that they are not in favor of such a move. On Monday, Dr. Celine Gounder, a pandemic advisor to Mr Biden during his change of presidency, said that if states could do separate deals, it would cause more problems than it would solve.

In an interview on CNBC, Dr. Gounder’s earlier criticism from Mr. Cuomo for bidding on ventilators. “I think this kind of approach to vaccine allocation will frankly lead to the same situation that he himself criticized last spring,” she said.

Yes, most likely.

At least three other vaccines are in late-stage clinical trials, and the success of any of those vaccines could mean millions more doses for US citizens by spring.

Johnson & Johnson is expected to announce the results of its vaccine study every day. If this is successful, the first doses could be available in the US by February. Although early production of the vaccine has lagged, the company has signed a contract to deliver 100 million doses of its single-dose vaccine by the end of June.

Results of studies with two-dose vaccines from AstraZeneca and Novavax could also be published by March and April. AstraZeneca has an agreement with the US government to supply 300 million doses and Novavax to supply 110 million doses.

Additionally, both Pfizer and Moderna state that their factories are adding and expanding capacity every week. They have signed contracts to deliver an additional 100 million doses of their vaccines each during the second quarter of this year.

It’s still not clear, though conservative, that there could be enough vaccines by the summer.

With no other vaccines approved, the United States has signed contracts with Pfizer and Moderna for a total of 400 million doses to be dispensed by the summer, or enough for 200 million people.

That’s pretty close to the American population of 260 million adults (the vaccines aren’t yet approved for children, although studies are ongoing).

But if other vaccines prove safe and effective – which experts believe is likely – millions of people could be vaccinated faster, possibly by late spring.