Health
Does AstraZeneca Vaccine Stack Up Against Pfizer, J&J and Moderna

Three COVID-19 vaccines have received authorization from the U.S. Food and Drug Administration (FDA) so far: Pfizer’s, Moderna’s, and Johnson & Johnson’s. But a fourth, developed by AstraZeneca and the University of Oxford, could soon be distributed domestically
AstraZeneca’s COVID-19 vaccine is 76% effective against symptomatic coronavirus infections and 100% effective in preventing hospitalization and severe disease, according to an interim analysis of its United States phase 3 trial, which included more than 32,000 people.
Even better, AstraZeneca’s vaccine can be stored at normal refrigerator temperatures, meaning it could be key to reaching people in rural and underfunded areas, one of the most pressing issues in the fight against the novel coronavirus.
Although the vaccine hasn’t been authorized for use in the U.S. yet, here’s what we know about it so far, and how it stacks up against Pfizer’s, Moderna’s, and Johnson & Johnson’s vaccines.
How does the AstraZeneca COVID-19 vaccine work?
AstraZeneca’s vaccine uses adenovirus-vectored technology, a harmless, modified version of a common cold virus that usually spreads among chimpanzees. This altered virus can’t make you sick, but it carries a gene from the novel coronavirus’ spike protein, the portion of the virus that triggers an immune response. This allows the immune system to manufacture antibodies that work against COVID-19, teaching your body how to respond should you become infected.
“It’s used as a Trojan Horse,” says Anna Durbin, M.D., an infectious disease expert at Johns Hopkins Medicine. “The beauty of this is that the genetic material of the spike protein is coming into the body like it would if it were part of the SARS-CoV-2 virus, but you don’t have any of the dangers of [catching] the virus.”
The reason researchers chose a chimpanzee adenovirus is simple: The modified virus needs to be new to the people being vaccinated—otherwise, the body won’t create those all-important, unique antibodies. Johnson & Johnson’s vaccine also relies on similar adenovirus-vectored tech.
The Pfizer-BioNTech and Moderna vaccines, meanwhile, rely on mRNA technology, which essentially introduces a piece of genetic code that tricks the body into producing COVID-19 antibodies, no virus required. Both of these vaccines require two shots spaced about a month apart.
How does AstraZeneca’s vaccine compare to Pfizer’s, Moderna’s, and Johnson & Johnson’s?
Storage and distribution
Johnson & Johnson’s and AstraZeneca’s vaccines are the easiest to transport so far—they can be stored for up to six months between 36°F and 46°F, normal refrigerator temperatures. The Moderna and Pfizer options, meanwhile, must be stored at subzero temps until they’re ready to be used, at -4°F and -94°F, respectively. (mRNA tech is relatively more fragile, meaning it must be kept at much lower temperatures to remain effective and stable.)
Higher storage temperatures could make distribution much easier. “A clinic, a nursing home, or even [regional] health departments may not have freezers that can hold things at -94°F,” says Kawsar Talaat, M.D., an infectious disease doctor, vaccine researcher, and assistant professor in the department of International Health at Johns Hopkins University. Being able to use a typical fridge “allows time for distribution, allows the vaccine time to get to more rural areas, [and allows vaccines] to be kept at a clinic for a longer period of time.”
Cost
The federal government has made all COVID-19 vaccines free to the public, but the U.S. still has to pay for its supply. AstraZeneca’s vaccine is estimated to cost U.S. providers about $4 per dose, per a 2021 BMJ report. Pfizer’s costs about $20 per dose, Moderna’s costs between $25 to $37 per dose, while Johnson & Johnson’s costs about $10 per dose, Forbes reports. These amounts will likely fluctuate as time goes on and the vaccines evolve.
Side effects
All four vaccines’ side effects are similar, including potential injection site pain and flu-like symptoms, including fever, fatigue, headaches, and muscle soreness, which are to be expected as your immune system is primed, especially after a second dose. “Vaccines stimulate the immune system, and you do have some side effects from that,” Dr. Durbin explains. “Symptoms generally last one to two days.”
Overall efficacy
Both Pfizer and Moderna report being about 95% effective against COVID-19 after the second shot in clinical trials. Interim results in a real-world study published by the Centers for Disease Control and Prevention (CDC) found both mRNA options were about 90% effective against SARS-CoV-2 infections. (For comparison, the annual flu shot is usually between 40 and 60% effective.) They also reduce the risk of severe illness even if you do become infected with SARS-CoV-2.
The Johnson & Johnson vaccine is about 66% effective at preventing symptomatic COVID-19, and 85% effective against the severe form of COVID-19 that can lead to hospitalization and death, per the FDA. The company’s phase 3 trial also reported no COVID-19-related deaths and no COVID-19 cases requiring medical intervention after 28 days in vaccinated participants.
Interim results from AstraZeneca’s United States trial report that the vaccine is 76% effective against symptomatic COVID-19 infection after two doses spaced four weeks apart; it’s 100% effective against severe illness and hospitalization. Based on a previous study, the AstraZeneca vaccine might become even more effective with doses spaced further than four weeks apart; more research is needed to confirm the significance of this finding, however.
Efficacy against variants
Pfizer’s and Moderna’s trials were done before highly infectious coronavirus variants became widespread; both companies are currently doing more testing to see how their respective vaccines stack up; a third booster dose will be necessary for renewed protection. So far, Pfizer maintains that it has “not seen any evidence that the circulating variants result in a loss of protection,” while Moderna says initial data shows its vaccine “provides neutralizing activity against variants of concern.”
Johnson & Johnson’s global phase 3 trial was completed amid the spike in variants. Its study found that the vaccine’s efficacy dropped in South Africa, presumably due to the B.1.351 variant that has dominated the region. That said, it still provided worthwhile protection in South Africa: 64% efficacy after 28 days, which is in-line with the annual flu shot’s protection.
South African research on the AstraZeneca vaccine, conducted in roughly 2,000 people, found an under-25% efficacy against mild and moderate illness from B.1.351, failing to meet the threshold for approval. As a result, South Africa stopped offering the AstraZeneca vaccine to its citizens, instead pivoting to Johnson & Johnson.
Does the AstraZeneca vaccine cause blood clots?
First approved in the United Kingdom on December 30, AstraZeneca’s COVID-19 vaccine received World Health Organization (WHO) approval in February and has since expanded to much of Europe, Asia, and Africa. But sporadic reports of a rare blood clotting disorder called cerebral venous sinus thrombosis (CVST) hindered the vaccine’s rollout, which was temporarily paused by 13 European nations and Thailand in mid-March.
However, both the European Medicines Agency (EMA) and the WHO insist that the vaccine is safe, citing under 30 reported cases of serious blood clots among 20 million people given the AstraZeneca vaccine across Europe. In its review, the EMA noted that it is unclear if the events are related, and more research is needed to confirm direct causation.
Johnson & Johnson’s COVID-19 vaccine, the only adenovirus-vectored option offered in the U.S., was also temporarily paused in the U.S. in April following rare reports of CVST. Part of the reason for the pause, Dr. Durbin explains, is making sure that healthcare providers are prepared to treat these blood clots and to inform people of the risks—however slight—of complications.
“The thought is [incidents of CVST] have something to do with the adenovirus vector that’s being used to deliver that spike protein genetic material,” Dr. Durbin says. These cases are so rare that most experts believe that there is a “host component, something about the people who got the clotting disorder that’s different from people who didn’t.”
Right now, Dr. Durbin explains, more research is needed before drawing any conclusions about what might cause these rare blood clotting incidences following the AstraZeneca and Johnson & Johnson vaccines. These issues were missed in clinical trials, she says, because they’re so exceedingly rare. No increased likelihood of blood clotting was found among participants in AstraZeneca’s United States trial.
Which COVID-19 vaccine is the best?
“The best vaccine is the one that’s offered the day you go in for your appointment,” says Andrew Thomas, M.D., chief clinical officer at The Ohio State University Wexner Medical Center. “All of the [available] vaccines are incredibly effective. They’re all safe.”
Each vaccine that has received FDA authorization has been proven to decrease severe illness, hospitalization, and death, the worst outcomes of COVID-19. Although the AstraZeneca vaccine hasn’t yet been approved in the U.S., research suggests it has those same effects in the places where it’s being distributed.
“The best vaccine is the one that’s offered the day you go in for your appointment.”
“If all you got from COVID-19 was a head cold, we wouldn’t be concerned,” Dr. Durbin says. “That’s what these vaccines are doing: They’re preventing that severe disease that is paralyzing healthcare systems around the world.”
But remember: Vaccines aren’t a silver bullet. They must be combined with masks, hand-washing, and social distancing to work as effectively as possible, per the CDC. No matter which COVID-19 vaccine becomes available to you first, you can feel confident in its ability to protect you, as long as you continue being cautious until positive cases, hospitalizations, and deaths are significantly reduced nationwide.
“If you can get a vaccine, get vaccinated,” Dr. Durbin says. “[Take] whatever vaccine that you can get to help us get out of this pandemic.”
Disclaimer:
This article is accurate as of press time. However, as the COVID-19 pandemic rapidly evolves and the scientific community’s understanding of the novel coronavirus develops, some of the information may have changed since it was last updated. While we aim to keep all of our stories up to date, please visit online resources provided by the CDC, WHO, and your local public health department to stay informed on the latest news. Always talk to your doctor for professional medical advice.
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Health
Report Causes Pfizer Stock to Climb Approximately $1 Billion Acquired by Starboard

(VOR News) – According to a rumor that activist investor Pfizer Starboard Value has taken a holding in the struggling pharmaceutical business that is expected to be worth around one billion dollars, the stock of Pfizer (PFE) is on the increase in premarket trading on Monday.
This comes after the report was made public. The report was made available to the general public following this. Starboard Value was successful in moving forward with the acquisition of the position.
Starboard is said to have approached Ian Read, a former chief executive officer of Pfizer, and Frank D’Amelio, a former chief financial officer, in order to seek assistance with its goals of boosting the performance of the company, according to the Wall Street Journal. Read and D’Amelio are both former Pfizer executives.
The purpose of this is to facilitate the accomplishment of its objectives, which include enhancing the overall performance of the firm.
In their previous jobs, D’Amelio and Read were chief financial officers.
It is stated in the report that the hedge fund is of the opinion that Pfizer, which is currently being managed by Albert Bourla, who succeeded Read as Chief Executive Officer (CEO) in 2019, does not demonstrate the same level of mergers and acquisitions (M&A) discipline that Read did. Bourla took over for Read in 2019. Read was succeeded by Bourla in the year 2019.
Pfizer, a multinational pharmaceutical conglomerate, has made substantial investments in the acquisition of more companies that are involved in the research and development of cancer medicines.
These businesses have been acquired for billions of dollars. The biotechnology company Seagen, which was acquired by Pfizer in the previous year for a price of $43 billion, is included in this category. One of the businesses that can be classified as belonging to this category is Seagen.
In spite of the fact that the S&P 500 Index experienced a 21% increase in 2024.
No major trading occurred in Pfizer stock that year.
Due to the fact that the demand for Pfizer’s COVID-19 vaccines fell after the firm reached its pandemic peak in 2021, the share price of the corporation has decreased by over fifty percent since that time.
This drop has occurred ever since the company’s shares reached their maximum peak, which was during the time that this decline occurred. Not only have they not changed at all, but they have also remained essentially stable. This is in contrast to the S&P 500, which has gained 21% since the beginning of this year.
Recently, the corporation was forced to take a hit when it decided to recall all of the sickle cell illness medications that it had distributed all over the world.
Fears that the prescription could lead patients to experience severe agony and possibly even death were the impetus for the decision to recall the product. In spite of the fact that Pfizer’s stock is increasing by almost three percent as a result of the news that followed the company’s decision, this is the circumstance that has come about.
SOURCE: IPN
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Health
New Study Reveals Drinking Soda Pop Increases the Risk of Stroke

A recent report from global research indicates that excessive consumption of coffee or soda pop is associated with an increased risk of stroke, although the intake of black and green tea is correlated with a reduced risk. Excessive consumption of soda pop or coffee warrants caution!
Recent research indicates that it may substantially elevate the risk of stroke.
Consuming four cups of coffee daily elevates the risk of stroke, according to studies, although ingesting 3-4 cups of black or green tea daily typically offers protection against stroke. Additionally, consume more coffee; it may reduce your risk of mortality.
Recent findings from global research studies co-led by the University of Galway and McMaster University, alongside an international consortium of stroke researchers, indicate that soda, encompassing both sugar-sweetened and artificially sweetened variants such as diet or zero sugar, is associated with a 22 percent heightened risk of stroke. The risk escalated significantly with the consumption of two or more of these beverages daily.
Stroke Risk Fizzy Drinks and Soda Pop
The correlation between fizzy drinks consumption and stroke risk was most pronounced in Europe, the Middle East, Africa, and South America. Women exhibit the most elevated risk of stroke from bleeding (intracranial hemorrhage) associated with fruit juice beverages. Consuming over 7 cups of water daily diminishes the likelihood of stroke due to a clot.
Researchers observed that numerous items advertised as fruit juice are derived from concentrates and have added sugars and preservatives, potentially negating the advantages often associated with fresh fruit and instead elevating stroke risk.
Fruit juice beverages were associated with a 37 percent heightened risk of stroke resulting from bleeding (intracranial hemorrhage). Consuming two of these beverages daily increases the risk thrice.
Consuming over four cups of coffee daily elevates the risk of stroke by 37 percent, although lower consumption levels do not correlate with stroke risk. Conversely, tea consumption was associated with an 18-20 percent reduction in stroke risk. Additionally, consuming 3-4 cups daily of black tea, such as Breakfast and Earl Grey varieties, excluding green and herbal teas, was associated with a 29 percent reduced risk of stroke.
Consuming 3-4 cups of green tea daily was associated with a 27 percent reduction in stroke risk. Notably, the addition of milk may diminish or inhibit the advantageous effects of antioxidants present in tea. The lower risk of stroke associated with tea consumption was negated for individuals who added milk.
Disclaimer: This article is intended solely for informational reasons and should not be considered a replacement for professional medical counsel. Consistently consult your physician regarding any inquiries pertaining to a medical problem.
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Health
Following a Diagnosis of Breast Cancer, What Else Should You Know?

(VOR News) – Even though breast cancer affects one in eight American women, receiving a diagnosis can make a woman feel isolated.
Experts in breast cancer from the American College of Physicians (ACS) advise patients on how to manage their disease so that they may better cope with this awful information.
First, the kind and stage of breast cancer dictates the course of your care.
In addition to immunotherapy and chemotherapy, there are various surgical options available for the treatment of breast cancer.
Women of African descent are disproportionately affected by triple-negative breast cancer, an extremely aggressive form of the disease that has never proven easy to treat.
According to the American Cancer Society, pembrolizumab (Keytruda), an immunotherapy, has been shown to be helpful when combined with chemotherapy and is currently the recommended course of treatment for certain combinations of triple-negative breast cancer.
In her presentation, Dr. Katharine Yao said, “It’s really important that the patient and physician discuss the patient’s preferences and values when deciding what type of treatment to pursue and that they have an honest, individualized discussion with their care team.”
She is currently responsible for developing breast cancer treatment recommendations for more than 575 hospitals and institutions nationwide in her role as chair of the American College of Surgeons’ National Accreditation Program for Breast Institutions (NAPBC).
Yao, vice chair of research at Endeavor Health NorthShore Hospitals in New York, pointed out that each decision made about a patient’s treatment plan should take her preferences and diagnosis into consideration.
She ought to think about whether she would prefer a mastectomy—a surgical procedure that involves removing the entire breast with or without reconstruction—or a lumpectomy, which involves a surgical procedure that spares part of the breast tissue.
She stated that “the breast cancer you have may be very different from the breast cancer you hear about in your neighbor, colleague, or friend” in a press release issued by the American Cancer Society (ACS).
“Consider that while discussing breast cancer with others.”
Throughout your journey, it is critical that you look after your emotional health because having breast cancer may have a detrimental impact on your mental health.
“Getting a cancer diagnosis does not mean that everything in your life stops to be normal.” Director of the Fellowship in the Diseases of the Breast program at the Winthrop P. Rockefeller Cancer Institute at the University of Arkansas and state head of the American Cancer Society Commission on Cancer for Arkansas, Dr. Daniela Ochoa She thinks adding the burden of a cancer diagnosis and treatment to all the other pressures in life may be taxing.
“Managing stress and emotional health is vital component of a treatment plan.”
Ochoa recommends clinically trained psychologists and social workers who have assisted people in coping with cancer to anyone receiving treatment. Learning coping techniques might also be facilitated by joining cancer support groups or cancer wellness initiatives.
Breast cancer specialists say your care team is crucial.
The American Cancer Society (ACS) defines comprehensive care as having support at every stage of the procedure from surgeons, oncologists, patient navigators, nurses, social workers, psychologists, and other specialists.
After receiving a breast cancer diagnosis, women should see a surgeon or medical oncologist to explore their options; nevertheless, treatment shouldn’t be discontinued after just one appointment or after surgery is over.
Additionally, you can ask trustworthy friends or family members to accompany you to appointments and aid you with research or notes. They could serve as a network of support for you.
Yao stated in his talk that “one of the most important things is that patients should search out a team they have confidence in, that they trust will have their back when they need it, and a team they feel they can get access to and that will help them when they are in need.”
SOURCE: MP
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