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AstraZeneca Covid vaccine will likely be Thailand’s ‘principal’ shot: Well being minister

A health worker holds a box of the AstraZeneneca vaccine at the Bamrasnaradura Institute for Infectious Diseases in Nonthaburi Province on the outskirts of Bangkok.

Chaiwat subprasome | SOPA pictures | LightRocket via Getty Images

The coronavirus shot developed by AstraZeneca and Oxford University will be Thailand’s “main vaccine” as the country seeks to revitalize its crucial tourism sector, the Thai health minister told CNBC on Monday.

Renewed safety concerns over the AstraZeneca-Oxford shot led countries such as Germany and the Netherlands to stop using the vaccine for those under the age of 60.

Before these final steps, several countries – including Thailand – suspended the use of the AstraZeneca vaccine after blood clots were reported in some people who received the shot. However, many lifted their suspension after the World Health Organization announced that a review of the available data found that the vaccine’s benefits outweigh the risks.

In Thailand, more than 150,000 people have been vaccinated with the AstraZeneca vaccine and the percentage of people who experienced side effects is considered “very low,” said Anutin Charnvirakul, the country’s deputy prime minister and health minister.

Anutin told CNBC’s Street Signs Asia that Thailand is waiting for further deliveries of the vaccine from AstraZeneca, which are expected to take place in June. In addition to the AstraZeneca vaccine, Thailand is also using one developed by China’s Sinovac Biotech, the minister said.

Almost 250,000 people have received Covid vaccines in Thailand since late February, Anutin said.

Attracting foreign visitors

Compared to many countries around the world, Thailand has reported relatively few Covid cases and deaths. Official data showed the country had confirmed more than 29,000 infections and 95 deaths as of Sunday.

However, the tourism-dependent economy was hit hard, shrinking 6.1% year over year in 2020 as countries restricted travel to avoid the spread of Covid-19, according to the Office of the National Council for Economic and Social Development to slow down.

Thailand is stepping up efforts to restart its tourism industry, including introducing vaccines in “significant” numbers in popular destinations like Phuket and Koh Samui, Anutin said.

“We want to make sure that our people are safe, that is our top priority. Once our people are safe, we believe that our guests, namely tourists or business people, would definitely come to visit our country,” he said Minister.

To attract visitors, Thailand has cut the quarantine period for foreigners entering the country from this month. The country is also striving to waive quarantine requirements for vaccinated foreign visitors to its largest holiday island, Phuket.

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Pfizer says shot is 100% efficient in children ages 12 to 15

A nurse, Cindy Mendez, wearing a protective mask, holds a syringe containing a dose of Pfizer-BioNTech COVID-19 vaccine during the coronavirus disease (COVID-19) pandemic at NYC Health + Hospitals Harlem Hospital in the Manhattan neighborhood of New York City. New York, February 25, 2021.

Jeenah Moon | Reuters

Pfizer said on Wednesday that its Covid-19 vaccine was 100% effective in a study in adolescents ages 12-15.

Albert Bourla, CEO of Pfizer, said the company hoped to submit the new data on the vaccine, which was being developed in partnership with German drug maker BioNTech, “as soon as possible” to the Food and Drug Administration and other regulatory agencies that children in the age group can get vaccinated before the next school year.

“We share the urgency to expand our vaccine approval to younger populations and are encouraged by clinical trial data from adolescents 12-15 years of age,” Bourla said in a press release.

The study enrolled 2,260 participants in the United States. 18 confirmed Covid-19 infections were observed in the placebo group and no confirmed infections were observed in the group that received the vaccine, the company said. This resulted in a vaccine effectiveness of 100%. The shot is also well tolerated, with side effects generally the same as in adults.

The company also said the vaccine produced a “robust” antibody response in children that outperformed that in a previous study of 16-25 year olds.

Vaccinating children is critical to ending the pandemic, say public health officials and infectious disease experts. The nation is unlikely to achieve herd immunity – if enough people in a given community have antibodies to a given disease – until children can be vaccinated, experts say.

According to the government, children make up around 20% of the US population. According to experts, between 70% and 85% of the US population must be vaccinated against Covid to achieve herd immunity and some adults may refuse to get the shots.

Dr. Scott Gottlieb, a former FDA commissioner, said he expected it would take the U.S. agency about a month to review the new data. If the FDA process goes well, the vaccine could be available to children between the ages of 12 and 15 by the fall, he told CNBC’s Squawk Box.

Isaac Bogoch, an infectious disease specialist who served on various data and security monitoring bodies, described the results as “wonderful news”. This is a “big step forward” in protecting more people from the virus and making schools safer for children.

“We are talking about improving the safety of youth activities such as youth sports and art, as well as after-school activities for youth,” he said.

Pfizer’s vaccine has already been approved for use in the United States in people aged 16 and over. Clinical studies testing the vaccine in children whose immune systems may react differently than adults had yet to be completed.

The Chief Medical Officer of the White House, Dr. Anthony Fauci, speaking to a House committee earlier this month, said the U.S. could vaccinate older children against Covid-19 starting this fall, while elementary school-age children may get their shots early next year.

Moderna, which also has a US-approved vaccine, announced on March 16 that it has started testing its shot in children under the age of 12. Moderna started a study in December testing children ages 12-17.

Johnson & Johnson plans to test its single-shot vaccine in infants and even newborns after it was first tested in older children, according to the New York Times.

Pfizer announced last week that it had started a clinical trial testing its Covid-19 vaccine in healthy children aged 6 months to 11 years.

In the first phase of this study, the company will determine the preferred dosage level for three age groups – between 6 months and 2 years, 2 and 5 years, and between 5 and 11 years. The children will initially receive a dose of 10 micrograms of the vaccine before gradually moving to higher doses, according to the company. Participants also have the option of ingesting 3 micrograms doses.

Pfizer said Wednesday it plans to apply to the FDA for an amendment to its current emergency approval to include adolescents ages 12-15. All participants in the study will be monitored for two more years after their second dose, the company said.

Pfizer and BioNTech plan to submit the data for scientific review.

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Germany suspends use of AstraZeneca’s Covid shot for the under-60s

Medical syringes and small figures of people can be seen in front of the AstraZeneca logo displayed on a screen. On Saturday March 26th 2021 in Dublin, Ireland.

NurPhoto | NurPhoto | Getty Images

Germany has stopped using the coronavirus vaccine developed by AstraZeneca and Oxford University in the under 60s due to renewed concerns over reports of blood clots.

The move comes after the country’s medicines agency found 31 cases of a rare type of blood clot in a small number of people immunized with the coronavirus vaccine made by the Anglo-Swedish drug maker. The suspension is likely to deal another blow to the vaccine’s reputation.

What happened?

Initially, some regions suspended the use of the shot on Tuesday due to concerns about a possible link to rare but serious forms of blood clots. However, it was announced on Tuesday that the entire country will no longer distribute the vaccine to anyone under the age of 60 after the country’s independent vaccine committee known as STIKO recommended it.

The committee said in a statement on Tuesday that “after several consultations, the majority of the STIKO, with the help of external experts, decided to only recommend the Covid-19 AstraZeneca vaccine to people aged 60 and over.”

This decision was based “on the currently available data on the occurrence of rare but very severe thromboembolic side effects. This side effect occurred 4 to 16 days after vaccination, mainly in people (under) 60 years of age,” it said.

Regarding the question of giving the second dose of vaccine to younger people who have already received a first dose of the AstraZeneca vaccine, the German vaccine committee announced that it would issue guidelines on the matter by the end of April.

Germany’s Paul Ehrlich Institute, a federal agency and medical regulator, told CNBC that there have been 31 cases of blood clots in the cerebral veins – a condition known as sinus vein thrombosis or cerebral venous sinus thrombosis – reported as part of a spontaneous admission.

Out of that number, thrombocytopenia (a condition characterized by abnormally low blood platelet levels) has also been reported in 19 cases. In nine of these cases, those affected died.

All but two of the 31 cases concerned women between the ages of 20 and 63, while the two men affected were 36 and 57 years old, according to the Paul Ehrlich Institute.

It added that it “continues to examine and evaluate all incoming case reports and actively participate in the relevant discussions at EMA, the European Medicines Agency, where case reports from all EU Member States are evaluated.

To put the numbers in context: By Monday, almost 2.7 million people in Germany had received a first dose of the AstraZeneca vaccine, 767 people had received a second dose, according to the German health department, the Robert Koch Institute.

Hit AstraZeneca

“Everything is based on a principle and that is trust,” said Merkel at a press conference, reported Reuters. “Trust arises from the knowledge that every suspicion is counted in every individual case.” The 66-year-old Chancellor added that she would also be ready to receive the AstraZeneca vaccine “when it is my turn,” reported Deutsche Welle.

Still, the German move is sure to cause AstraZeneca more pain and confuse the public and worry about the vaccine.

AstraZeneca has already suspended its shot in a handful of European countries before the EMA and World Health Organization reviewed the vaccine’s safety data and concluded that it was “safe and effective” and that the benefits outweigh the risks.

The EMA said at the time, however, that it could not rule out a connection between the shot and the blood clots, which at least occur regularly in the general population. Enough concerns have been raised for Canada to suspend use of the vaccine in those under 55 due to fears of a possible association with blood clots.

However, clinical and real world data has shown the vaccine to drastically reduce Covid cases, hospital stays and deaths. The vaccine is a key part of vaccination programs in the UK and other countries and is viewed as an inexpensive vaccine that is easy to transport and store.

Drugmaker defends himself

Many scientists and the UK government have defended the shot, claiming it had saved thousands of lives.

In a statement to CNBC, AstraZeneca said that international regulators had determined that the benefits of the sting significantly outweighed any possible risks.

It said it continues to analyze its database of tens of millions of records for the vaccine to understand “whether these very rare cases of thrombocytopenia-related blood clots are more common than would naturally be expected in a population of millions of people “.

“We will continue to work with the German authorities to answer any questions,” he added.

The drug company stressed that “tens of millions of people around the world have received our vaccine. The vast amounts of data from two large clinical datasets and real evidence demonstrate its effectiveness and reinforce the role the vaccine can play in this public health crisis.”

Germany had previously not given the vaccine to people aged 65 and over because there was insufficient data on its effectiveness in this age group. However, when more data emerged showing it was safe and effective, it reversed that policy.

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Three Ladies Working to Vaccinate Kids Shot Useless in Afghanistan

KABUL, Afghanistan – Three health workers, all women working for the government’s polio vaccination campaign, were shot dead Tuesday in Jalalabad, eastern Afghanistan, local officials said just weeks after three television women were killed in the same city .

The women, all in their twenties, were working in the busy city near the border with Pakistan when they were gunned down in two separate attacks.

Semin, 24, and Basira, 20, who like many Afghans had only one name, were shot dead by two armed men when they entered a house in Jalalabad to vaccinate the children living there, the governor’s office said.

The two walked door-to-door in the city, a practice that the Taliban have banned in areas under their control in the past.

It was Semin’s first vaccination campaign; said Ahmad Faisal Nizami, the victim’s cousin. She was recently married and trained as a teacher.

Negina, 24, who was in charge of the polio vaccination campaign that began in Afghanistan on Monday, was shot dead elsewhere in the city about an hour later.

No group immediately took responsibility for the murders.

Taliban spokesman Zabihullah Mujahid denied any involvement in the incident in a WhatsApp message.

Afghanistan, which recorded 56 cases of polio in 2020 according to the Global Polio Eradication Initiative, is one of two countries where the disease has not been eradicated, trailing Pakistan.

Around the same time as Tuesday’s shooting, there was an explosion at the city’s regional hospital, officials said outside the compound where the vaccines are stored. There were no victims, but the windows were broken.

The recent killings – part of a wave of targeted attacks that often singled out women, journalists, professionals, activists and doctors – came at a difficult moment for Afghanistan as the Taliban have made steady military gains and those considered to be with the Afghans work together, relentlessly attack government. In addition, the remnants of the Islamic state operating in the region have focused on carrying out less large-scale bombings and smaller but targeted attacks.

The United States has yet to say definitively whether it will meet the May 1 withdrawal deadline for all American forces. This emerges from an agreement the Trump administration signed with the Taliban in February 2020.

“My niece Basira was a poor girl,” said Haji Moqbel Ahmad, a tribal elder in Jalalabad, who added that the woman had not previously been threatened. “She was shot while she was doing her job.”

A vaccination worker since her youth, Basira had been signed up for a five-day vaccination campaign for which she would receive less than $ 30.

The month began with the murder of three women who worked for a television station in Jalalabad. A TV and radio presenter from the same station was shot in the same way in December. The Islamic State took responsibility for both incidents.

The New York Times documented the deaths of at least 136 civilians and 168 security personnel in such targeted killings in 2020, more than in almost any other year of the war. Until 2021 there has been no reprieve from the same type of violence.

The Taliban are exerting increasing pressure on the government and society and claiming dominance as stuttering, intermittent negotiations are taking place to resolve the Afghan conflict.

Jalalabad is one of the hardest hit cities. One day after the murders of television workers, a doctor was killed there by a roadside bomb.

Ross Wilson, the U.S. ChargĂ© d’Affaires in Kabul, condemned the murders Tuesday.

“Such attacks are a direct violation of Afghans’ dream of building better lives for their children,” Wilson wrote on Twitter. “My deepest condolences to the families of the victims as we seek justice,” he wrote. “The attack on vaccines is as heartless as it is inexplicable.”

Humanitarian aid organizations were also outraged. Henrietta Fore, Managing Director of Unicef, issued a statement calling victims “courageous vaccines that have been at the forefront of efforts to fight the spread of polio and protect the children of Afghanistan from this disabled disease”.

Zabihullah Ghazi reported from Jalalabad and Fahim Abed from Kabul, Afghanistan.

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All the problems and issues the shot has confronted

The Covid vaccine Petra Moinar prepares syringes with the AstraZeneca vaccine before it is administered on March 8, 2021 at the Battersea Arts Center in London, England.

Chris J Ratcliffe | Getty Images News | Getty Images

AstraZeneca’s Covid shot, dubbed the “Vaccine for the World”, has had high hopes since its inception. However, unlike other coronavirus vaccines, the shot developed by AstraZeneca and the University of Oxford has been plagued from problem to problem.

AstraZeneca’s problems began almost as soon as preliminary trial data was released and have continued ever since.

The drug maker “seems to be having a real PR problem in the US and Europe,” Sunaina Sinha Haldea, managing partner of Cebile Capital, told CNBC on Thursday, warning that its “PR problem is raising confidence in the vaccine outdoors could undermine “the UK”

Here is a timeline of all the issues that AstraZeneca has encountered over the past year:

November 2020 – process data dispute

AstraZeneca released an interim clinical trial analysis showing that its Covid vaccine has an average of 70% effectiveness in protecting against the virus. The result was initially welcomed by the global community, which was already supported by positive results for the recordings by Moderna and Pfizer-BioNTech.

Upon further examination, it became clear that the 70% figure came from the combination of the analyzes of two separate dosage regimens within the experiments. One dosing regimen showed 90% effectiveness when subjects received half a dose followed by a full dose at least a month apart. The other showed 62% effectiveness when given two full doses at least one month apart.

AstraZeneca admitted that the half-dose regimen was a mistake, but described it as a “useful mistake” and a “coincidence”. However, it has been criticized by US experts, and AstraZeneca’s chance announcement of the bug was arguably the start of its reputational problems.

January 2021 – delivery dispute

In early January, the UK began rolling out the AstraZeneca-Oxford University vaccine. It had an added bonus for the country: the majority of its cans would be made in the UK.

It wasn’t long, however, before a dispute over supplies with the European Union began after reports that the drug maker was failing to make its contracted supplies to the bloc.

A very public dispute over contracts erupted, sparking a history of bitter relations between the EU and the UK and the Anglo-Swedish drug maker. The EU has made waves suggesting AstraZeneca is rerouting supplies from the UK to the block

January 2021 – Effectiveness in disputes over 65 years of age

90 year old Margaret Keenan is greeted by staff as she returns to her ward after becoming the first patient in the UK to receive the Pfizer / BioNtech COVID-19 vaccine at the University Hospital Coventry, UK December 8, 2020.

Jacob King | Reuters

March 2021 – Dispute over blood clots

Late March 2021 – US data dispute

AstraZeneca worries continued this week – even though they started at a high level for the drug maker. On Monday, the results of a large U.S. study showed the vaccine was safe and highly effective, raising hopes that it could soon seek U.S. approval for the shot.

However, on Tuesday, a US health agency announced that AstraZeneca may have included “out of date” information in its study results, casting doubts about published efficacy rates.

AstraZeneca responded that the numbers released Monday were “based on a pre-determined interim analysis with a February 17th data deadline,” saying it would share its primary analysis within 48 hours of the most recent efficacy data.

On Wednesday, the company released updated Phase 3 trial data for its Covid-19 vaccine, showing that its vaccine is 76% effective – slightly lower than the 79% rate published on Monday.

What’s next for AstraZeneca?

The problems facing AstraZeneca could continue as EU leaders virtually meet on Thursday to discuss possible vaccine export bans that could hit the drug maker. However, the EU and the UK said on Wednesday that they wanted to find a “win-win” solution to the supply problem.

The negative coverage of AstraZeneca has led some viewers (and certainly the UK media) to point out that post-Brexit, the vaccine has become a target for negative sentiment in Europe directed against the UK. It has also been suggested that the shot could be the victim of vaccine nationalism in the US, where competing shots came from Moderna and Pfizer-BioNTech (although BioNTech is a German company).

Regardless of the underlying causes, AstraZeneca’s reputation has been badly damaged.

As Shore Capital health analysts said in a note Thursday, “Any confusion about results can quickly turn into concerns about the safety and effectiveness of vaccines, even if those concerns are not based on solid evidence.”

The AstraZeneca vaccine was “particularly badly affected by confusion about the data reported. Importantly, this confusion can lead to an erosion of trust in vaccines, which are proven, life-saving drugs.”

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Free With Your Covid Shot: Beer, Arcade Tokens and Krispy Kreme Doughnuts

The benefits of vaccination against Covid-19 – namely, protection against a dangerous virus – should be obvious at this stage of the pandemic.

If that’s not enough, consider swag.

Companies in the U.S. and beyond are offering free merchandise and other items to people receiving Covid shots. The perks include free rides, donuts, cash, arcade tokens, and even marijuana.

Behavioral motivation experts say offering incentives isn’t necessarily the most effective or inexpensive way to increase vaccine intake. But that hasn’t stopped the freebies from piling up.

In Cleveland, Market Garden Brewery is offering 10-cent beers to the first 2021 people to show a Covid-19 vaccine certificate. “Yes, you read that right,” says the brewery on its website. “Ten cents.”

At the greenhouse at Walled Lake, a Michigan medical marijuana dispensary, anyone aged 21 and over who is receiving a Covid vaccine can pick up a pre-rolled joint by the end of the month.

Chobani offers free yogurt at some vaccination sites. And Krispy Kreme said Monday that for the rest of the year, anyone with evidence of Covid-19 vaccination would be given one glazed donut a day.

As vaccinations accelerated in the United States, “We made a decision, ‘Hey, we can support the next act of joy.” When you come by, show us a vaccination card and pick up a donut anytime you want, any day, ”company executive director Michael Tattersfield told Fox News.

The Krispy Kreme initiative has nothing to do with the “vaccinated donuts” that were sold by a bakery in Germany last month and are garnished with plastic syringes that dispense a sweet lemon-ginger amuse-bouche. Nor does it entitle vaccinated Americans to endless donuts, as Mr. Tattersfield seemed to imply in his Fox News interview – only one a day, as the company notes on its website.

In a promotion called “Tokens for Poke’ns,” Up-Down, a chain of bars with vintage arcade games, is offering free tokens worth $ 5 to guests who present a completed vaccination card. Up-Down, with six locations in five states of the Midwest, expands the offering to guests who visit within three weeks of the final ingestion.

Up-Down’s communications manager David Hayden said he got the idea while sitting in an observation room after receiving his own vaccine.

“It’s something we’ve been expecting for so long,” he said, adding that the token giveaway was a way to give customers something different to look forward to after vaccination.

Cleveland Cinemas, an Ohio cinema chain, is offering free 44-ounce popcorn at two locations to anyone who presents a vaccination card by April 30th.

To encourage younger people to get vaccinated, Tel Aviv city set up a mobile vaccination clinic in a bar last month and offered free beer and non-alcoholic peach juice to those who received a shot, The Times of Israel reported.

Showing cards for so many promotions can cause wear and tear. To protect the cards from damage, Staples offers to laminate them for free after customers have received their final dose. The promotion runs until May 1st.

Some vaccination benefits flow from companies to their employees. Tyson Foods, Trader Joe’s, and others pay for the time it takes to get vaccinated, while Kroger pays them a $ 100 bonus.

Other incentives are aimed at people in vulnerable groups. For example, Uber has agreed to offer seniors, key workers and others in countries in North America, Europe and Asia 10 million free or discounted trips to help them access vaccination centers.

“Governments like these initiatives because they help them get more vaccines in more guns,” said Chris Brummitt, a spokesman for the company in Singapore.

That may be true, but the science of getting people to vaccinate is complex.

“Behavioral nudges,” based on scientific observations, could be a cheaper way to convince people to get the Covid-19 vaccine than direct incentives, said Hengchen Dai, professor of management at the University of California at Los Angeles .

In a recent study, Ms. Dai and her colleagues found that text messages can encourage people to receive influenza vaccinations. The most effective texts were framed as a memento to preserve recordings that were already reserved for the patient. They also resembled the type of communication patients expect from healthcare providers.

Jon Bogard, a PhD student at UCLA who contributed to the study, said policy makers should be cautious about incentives as they can sometimes backfire. One problem is that the campaigns are expensive, he said. Another reason is that people who receive gunshots might see a huge incentive as a sign that “vaccines are riskier than they actually are”.

A better alternative, Bogard said, might be to hand out “low personal value, high social value” items – such as stickers and badges – that convey a greater sense of “social motivation and accountability”.

There seems to be no shortage of such loot swirling around the world’s hospitals and vaccination clinics.

“Protected!” says a button that patients receive at a vaccination center in Hong Kong. It shows a cartoon syringe fist poking a masked doctor.

At a small league ballpark in Hartford, Connecticut, people who are shot can pick up a sticker that reads “I got my Covid-19 shot” featuring the home team’s mascot, a goat.

If you are not satisfied with the vaccine-style equipment at your local clinic, there are numerous options available to purchase online.

A badge – “I have my Fauci ouchi” – pays homage to America’s most famous doctor, Dr. Anthony S. Fauci.

“Thank you, science,” says another.

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U.S. well being consultants attempt to ease Covid vaccine fears as AstraZeneca’s shot faces overview in Europe

A photo illustration of the AstraZeneca COVID-19 vaccine in the Copes pharmacy in Streatham on February 4, 2021 in London, England.

Dan Kitwood | Getty Images

Medical experts in the US are trying to allay fears that Covid-19 vaccines may be unsafe after several European countries suspended AstraZeneca’s shot after reports of blood clots in some recipients.

On Tuesday, Sweden, Latvia and Lithuania became the youngest countries to join a growing list of nations to stop using the AstraZeneca Oxford shot because of blood clot problems. Germany, France, Italy and Spain said Monday they would also stop administering the shot.

The European Medicines Agency, which assesses drug safety for the EU, convened a meeting on Thursday to review the results. So far it has been claimed that the benefits of the shot in preventing hospitalizations and death still “outweigh the risk of side effects.” The World Health Organization agreed and on Wednesday urged countries to keep using AstraZeneca’s shots.

Without the results of the upcoming European Medicines Agency meeting, it’s hard to tell if the vaccines are causing the reported blood clots, US medical experts told CNBC, but the drug giant already has a PR mess on its hands. Some doctors in the US fear that European nations are reacting prematurely to political pressure and safety concerns, and extensive efforts will be required to restore confidence in the vaccine when it is approved online.

“This vaccine is now a problem,” said Dr. William Schaffner, epidemiologist and professor of preventive medicine at Vanderbilt University, told CNBC in a telephone interview.

“I think if the vaccine is cleared – not guilty – there will have to be a significant public relations effort in Europe and around the world to restore confidence in this vaccine,” he said.

No red flags in the US

While the AstraZeneca vaccine has not yet been approved for use in the U.S., White House Chief Medical Officer Dr. Anthony Fauci informed lawmakers on Wednesday that there will likely be enough safety and efficacy data to get dosing approval in April.

When asked if the suspension of AstraZeneca in European countries could create anxiety among Americans taking other vaccines, Fauci reiterated that the shots will undergo rigorous clinical trials and verified by an independent safety oversight body before they become widespread.

“The whole process is both transparent and independent and we are explaining this to people and taking the time to address their hesitation without being confrontational,” Fauci told lawmakers during a hearing with the House Committee on Energy and Trade.

This isn’t the first time Fauci has stressed the safety of the current vaccines amid AstraZeneca’s suspension. The infectious disease expert told MSNBC in an interview on Tuesday that scientists in the US are carefully examining the side effects of vaccine recipients, even after they have been authorized and used.

For example, medical experts were concerned about reports of severe allergic reactions – or anaphylaxis – in people vaccinated with Pfizer and Moderna’s shock. However, these cases seem rare, he said, even though the nation has distributed at least one shot to 73 million adult Americans – more than 28% of the population.

“So far there are no safety signals that turn out to be red flags and you need to monitor these things very carefully,” said Fauci of the vaccines currently in use in the US

Dr. Francis Collins, director of the National Institutes of Health, told Reuters in an interview published Monday that he was “fairly reassured” by statements from European regulators that the problems might arise randomly.

“I was a bit surprised that so many countries decided to stop vaccine administration, especially at a time when the disease is so incredibly threatening even in most of those countries,” Collins later told CNN on Wednesday and added that he has no access to the “primary data that may have led to an alert”.

More data needed

Unwanted medical problems like blood clots occur regardless of whether people are vaccinated or not. The problem scientists are now trying to determine is whether the vaccines were the culprit, Schaffner said.

“We knew in the beginning when we started vaccinating that since we are targeting older adults, medical events would only occur every day in this population, even without vaccines,” Schaffner told CNBC.

“It is possible that if you were vaccinated on Monday, certain medical events could occur on Tuesday, Wednesday, Thursday and Friday,” he said. “The question is, did the vaccine speed up, fail, or cause these events?”

For its part, AstraZeneca said in a statement on Sunday that of the more than 17 million people in the EU and UK who have received a dose of the Oxford AstraZeneca vaccine, fewer than 40 cases of blood clots have been reported to date Week.

The pharmaceutical company said that 15 events involving deep vein thrombosis and 22 events involving pulmonary embolism were reported among those vaccinated in the EU and the United Kingdom. These numbers suggest that adverse events occur less often than expected in the general population, not higher.

“I don’t think this is real, but I am very concerned because this is the vaccine we all count on worldwide,” said Dr. Carlos del Rio, a professor of medicine at Emory University’s medical school, told CNBC in a telephone interview, he added that the shot costs less than its competitors. However, Del Rio noted that without the data it is difficult to determine whether the suspensions are appropriate.

“This requires extensive damage control,” said del Rio.

Politics could be the problem

There are some concerns that the issue with AstraZeneca’s vaccine could be more political. A dangerous time also comes: some European nations are battling another wave of new Covid-19 infections, even when vaccines are used.

So far, the introduction of vaccines in the EU has been slow compared to other countries such as the US and UK

“It is a major concern that Europe just doesn’t have that many people vaccinated,” said Dr. Ezekiel Emanuel, former Covid advisor to President Joe Biden, told CNBC on Tuesday. “It’s another reason we need to be concerned about the Covid situation in other countries, not just the US.

The suspensions follow a public dispute between the EU and AstraZeneca in January when the drug company said it was forced to cut its initial dose supply for the block. Several European countries also initially declined to recommend the shot to residents over 65 as there was insufficient evidence that it was effective before that decision was reversed.

“It may be that … governments are trying to respond to people’s concerns about the vaccine, not necessarily the data,” said Emanuel, a bioethicist and oncologist who served as vice provost on global initiatives at the University of Pennsylvania acts.

“Actions don’t necessarily follow data. They follow more emotional responses to things like this,” he said.

– CNBC’s Sam Meredith, Holly Ellyatt and Silvia Amaro contributed to this report.

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Extra EU international locations halt AstraZeneca shot as EMA opinions uncomfortable side effects

An Army health worker prepares a dose of Covishield, AstraZeneca / Oxford’s Covid-19 coronavirus vaccine from the Indian Serum Institute at an Army hospital in Colombo on January 29, 2021.

Sign S. Kodikara | AFP | Getty Images

LONDON – Two other countries decided on Tuesday to suspend use of the AstraZeneca vaccine in Europe amid blood clot concerns as regulators conducted a new side effects review.

Sweden and Latvia announced Tuesday morning that they are suspending the rollout of the AstraZeneca vaccine developed with Oxford University. Portugal, Luxembourg and Slovenia decided to stop using the shot on Monday evening. Earlier in the day, Germany, France, Italy and Spain also joined the group of nations that stopped using the vaccine.

So far, 13 countries in the European Union have made this decision, while a few others have stopped using individual lots of the AstraZeneca vaccine. Austria first decided last week after the death of a 49-year-old woman who received this vaccine to stop using a certain batch of AstraZeneca shots.

“The benefits still outweigh the risks.”

The European health authority has insisted that “the benefits of the AstraZeneca vaccine in preventing Covid-19, with the associated risk of hospitalization and death, outweigh the risks of side effects”.

In a statement on Monday, the European Medicines Agency said it would “look further into the information” and called an extraordinary meeting on Thursday on the subject. The institution then reiterated its position during a press conference on Tuesday.

“There is currently no evidence that vaccination caused these conditions,” said Emer Cooke, director of the European Medicines Agency. “The benefits still outweigh the risks, but this is a serious problem and requires serious and detailed scientific assessment. We are currently involved in that.”

She added, “We are concerned that this could affect vaccine confidence … but our job is to make sure the products we approve are safe.”

Of course, we need speed, not just for the economy, but above all for the health of our citizens, but at the same time we need security.

Paolo Gentiloni

EU commissioner for the economy

The World Health Organization has urged nations to continue their vaccination campaigns with the AstraZeneca vaccine and Oxford University.

A number of EU countries have spoken out in favor of the shot. In Belgium, Health Minister Frank Vandenbroucke said on Monday that interrupting use was “irresponsible”. While the authorities in the Czech Republic have also announced that they will continue to administer the vaccine.

Outside the EU, Canada, Australia and the UK have also joined forces to support AstraZeneca.

According to the European Center for Disease Prevention and Control, more than 6 million doses of the AstraZeneca shot have been administered in the EU to date.

AstraZeneca announced on Sunday that of the 17 million people vaccinated in the EU and the UK, 15 had deep vein thrombosis events and 22 cases of pulmonary embolism. This is based on data received as of March 8th.

“This is much less than expected to occur naturally in a general population of this size and it is similar to other approved Covid-19 vaccines,” the company said in a statement.

Concerns about the vaccine could jeopardize the EU’s goal of vaccinating 70% of the adult population by the end of the summer. The AstraZeneca vaccine has proven popular in Europe so far because it is cheaper than its competitors and easier to store. This could then possibly delay the economic recovery in the region.

“Of course we need speed, not only for the economy, but above all for the health of our citizens, but at the same time we need security,” said Paolo Gentiloni of the European Commission at a press conference on Monday.

He added that the precautionary measures were “justified” and that the EMA review should “keep our EU citizens safe”.

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Docs react as EU international locations droop shot

A healthcare worker prepares a syringe with the dose of AstraZeneca Covid-19 in Coria City Hospital, Spain.

Gustavo Valiente | SOPA pictures | LightRocket via Getty Images

LONDON – Health professionals are disappointed and confused about the numerous suspensions of the coronavirus vaccine developed by AstraZeneca and Oxford University. They warn that there is not enough data to justify these decisions.

Germany, France, Italy and Spain joined a rapidly growing list of European countries on Monday that are stopping use of the vaccine as a precautionary measure after reports of blood clots.

Other countries such as Austria have temporarily stopped using certain lots of the Oxford-AstraZeneca vaccine. Thailand became the first Asian nation on Friday to stop using the shot because of safety concerns.

The UK, Canada and Australia, which continue to use the vaccine, are among the countries trying to reassure citizens about its benefits.

The World Health Organization, the European Medicines Agency and the International Society on Thrombosis and Hemostasis have recommended that countries continue to use the Oxford-AstraZeneca vaccine.

There is still no evidence of data to really justify these decisions.

Michael Head

Senior Research Fellow in Global Health at the University of Southampton

“The decisions made by France, Germany and other countries look amazing,” said Dr. Michael Head, Senior Research Fellow in Global Health at the University of Southampton, UK

“The data we have suggests that the number of blood clot-related adverse events is the same (and possibly fewer) in vaccinated groups compared to non-vaccinated populations,” he continued.

“Pausing the introduction of a vaccine during a pandemic has consequences. This creates delays in protecting people and a possible delay in vaccine due to people who have seen the headlines and are understandably concerned. There is still no evidence of data that really justify these decisions, “added Head.

WHO experts will meet on Tuesday to review the safety of the shot.

The European Medicines Agency, which also evaluates the drug’s safety, says there is no evidence that it causes blood clots and believes the benefits of the vaccine “continue to outweigh the risks”.

What did AstraZeneca say?

More than 17 million people in the European Union and the United Kingdom have received a dose of the Oxford AstraZeneca vaccine. As of last week, fewer than 40 cases of blood clots had been reported, AstraZeneca said in a statement.

The pharmaceutical company said that 15 events involving deep vein thrombosis and 22 events involving pulmonary embolism were reported among those vaccinated in the EU and the United Kingdom.

“This is much less than expected to occur naturally in a general population of this size, and it is similar to other approved COVID-19 vaccines,” said AstraZeneca.

The EMA has also said that the data available so far showed that the number of blood clots in vaccinated people is no higher than in the general population.

A bottle of the AstraZeneca vaccine.

Igor Petyx | KONTROLAB | LightRocket via Getty Images

Europe’s caution regarding the drug has exacerbated the problems of the battered vaccination campaign in the region and comes at a time when the German health department has warned that a third wave of coronavirus infections has already begun.

Dr. Stephen Griffin, associate professor in the University of Leeds School of Medicine, said the news that many countries in Europe had suspended the introduction of the Oxford-AstraZeneca vaccine was “disappointing”.

“With many European countries currently experiencing a resurgence of SARS-CoV2 infections and still lagging behind on adoption, the importance of continuing vaccination programs and the harm done by people having access to one should not be underestimated Vaccine denied will do. ” even the worst-case scenarios probably outweigh the odds, if at some point a connection to the coagulation disorders is found, “said Griffin.

“It should also be noted that nationwide gestures like these inevitably create hesitation or a more extreme sentiment towards vaccines and further undermine vaccination efforts,” he added.

How does the vaccine work?

The Oxford AstraZeneca vaccine is designed to prevent coronavirus in people aged 18 and over. It’s made up of an adenovirus that has been modified to contain the gene to make a protein from SARS-CoV-2, the virus that causes Covid-19. Therefore, the vaccine does not contain a virus and cannot cause Covid.

The most common side effects of the shot are typically mild or moderate and get better within a few days after vaccination.

In late clinical studies, the AstraZeneca Oxford shot was found to have an average of 70% effectiveness in protecting against the virus.

“We are carefully reviewing the reports, but the evidence available does not suggest that the vaccine is the cause,” said Dr. Phil Bryan, Vaccine Safety Director for the UK Medicines and Health Products Regulatory Agency.

“Blood clots can occur naturally and are not uncommon. In the UK, more than 11 million doses of the AZ vaccine have now been given and the number of blood clots reported after the vaccine is no more than the number that would have occurred naturally in the UK of the vaccinated population, “he continued.

“We are working closely with international colleagues to understand the global safety experience of COVID-19 vaccines and to share safety data and reports quickly. People should still get their COVID-19 vaccine when prompted,” said Bryan.

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Biden to announce Merck will assist make Johnson & Johnson’s shot

President Joe Biden will announce Tuesday that pharmaceutical company Merck will help manufacture the Covid-19 vaccine from Johnson & Johnson, a senior administrative official who has been confirmed to NBC News.

The decision is made as the administration is working to ramp up production of J & J’s single-shot vaccine. Senior government officials said Sunday the US government will ship J & J’s entire inventory of 3.9 million cans this week, adding that supply would be “uneven” over the following weeks. Another 16 million doses are expected by the end of the month.

Under the agreement, Merck will deploy two facilities in the US for J & J’s vaccine, the Washington Post previously reported. One will make the vaccine and the other will provide “fill-finish” services when the vaccine is put into vials.

Officials began scouring the country for additional manufacturing capacity after discovering in the early days of the government that J&J had fallen behind in vaccine production, according to NBC. They soon sought a deal with Merck, which abandoned plans to develop its own Covid vaccine in January after a clinical study showed its shots were ineffective.

J&J declined to comment on the deal with CNBC. In a statement, Merck said it was “unwavering in our commitment to contribute to the global response to the pandemic and prepare us to deal with future pandemics”.

The Washington Post reported the news earlier.

Biden is expected to make the announcement from the White House on Tuesday afternoon.

The Food and Drug Administration on Saturday approved J & J’s vaccine for use in people aged 18 and over. Unlike Pfizer and Moderna vaccines, patients with the single dose of J&J do not need to take a second dose and can be stored at refrigerator temperature for months.

In comparison, Pfizer’s vaccine must be stored in ultra-cold freezers that keep between minus 112 and minus 76 degrees Fahrenheit. However, the FDA recently allowed the company to store its vaccine for two weeks at temperatures commonly found in pharmaceutical freezers. Moderna vaccine must be shipped at 13 to 5 degrees above zero Fahrenheit.

The New York Times first reported in January that unexpected delays in manufacturing would result in decreased primary care of J & J’s medication if it were given emergency approval.

The Chief Medical Officer of the White House, Dr. Anthony Fauci said last month he was “disappointed” with the number of doses J&J originally expected, adding that the federal government had assumed there would be “significantly more”. The New Jersey-based company has signed a contract with the United States to supply 100 million cans by the end of June.

“It can take June, July and August to get everyone vaccinated,” Fauci told CNN on February 16. I don’t think anyone will disagree that this will be good by the end of summer and we’ll get into early fall. “

At the time, Bidens Covid Tsar Jeff Zients said the federal government was “doing everything it can to work with the company to expedite the delivery schedule”.

This is not the first partnership between two drugmakers to help improve vaccine supply.

In late January, French drug maker Sanofi announced it would help fill and package millions of doses of Pfizer’s two-shot vaccine to meet demand. Moderna has a partnership with the Swiss company Lonza, which makes most of the medicines for the company’s vaccine.

The Biden government has also announced that it is using the Defense Equipment Act to improve supplies of Pfizer’s vaccine.