Allergy warning for Pfizer/BioNTech vaccine after UK health workers with allergy history suffer reaction
CNN conveys reports from British physicians who say patients with an allergy history may want to refuse the COVID-19 vaccination.
People with a “significant history of allergic reactions” should not be given the Pfizer/BioNTech coronavirus vaccine, UK health authorities said Wednesday, after two health care workers experienced symptoms after receiving a shot the day before.
The precautionary advice was given after the pair “responded adversely” following their shots on the first day of the mass vaccination rollout in the UK, National Health Service England said Wednesday.
The two staff members — who both carried an adrenaline auto injector and had a history of allergic reactions — developed symptoms of anaphylactoid reaction after receiving the vaccine on Tuesday. Thousands overall were vaccinated in the UK on Tuesday, NHS England told CNN on Wednesday.
“As is common with new vaccines the MHRA [Medicines and Healthcare products Regulatory Agency] have advised on a precautionary basis that people with a significant history of allergic reactions do not receive this vaccination after two people with a history of significant allergic reactions responded adversely yesterday,” said Stephen Powis, the national medical director for NHS England, in a statement. “Both are recovering well.”
The MHRA issued new advice to health care professionals stating that any person with a significant allergic reaction to a vaccine, medicine or food — such as previous history of anaphylactoid reaction, or those who have been advised to carry an adrenaline autoinjector — should not receive the Pfizer/BioNtech vaccine.
The advice also states that vaccines “should only be carried out in facilities where resuscitation measures are available.”
“We are fully investigating the two reports that have been reported to us as a matter of priority,” an MHRA spokesperson said.
“Once all the information has been reviewed we will communicate updated advice,” the spokesperson added.
They advised anyone with a history of a significant allergic reaction due to receive the Pfizer/BioNTech vaccine to speak to the health care professional administering the vaccine.
Pfizer said in a statement that it had been advised by the UK regulator of “two yellow card reports that may be associated with allergic reaction” due to administration of the vaccine.
“As a precautionary measure, the MHRA has issued temporary guidance to the NHS while it conducts an investigation in order to fully understand each case and its causes. Pfizer and BioNTech are supporting the MHRA in the investigation,” the statement said.
“In the pivotal phase 3 clinical trial, this vaccine was generally well tolerated with no serious safety concerns reported by the independent Data Monitoring Committee. The trial has enrolled over 44,000 participants to date, over 42,000 of whom have received a second vaccination.”
Documents released on Tuesday by the US Food and Drug Administration (FDA) said the Pfizer/BioNTech trial data indicated that there were potentially slightly more adverse responses thought to be allergic reactions among the vaccine group compared with the placebo group, at 0.63% compared with 0.51%.
Pfizer’s trial protocol shows that people with a history of severe allergic reaction (e.g., anaphylaxis) “to any component of the study intervention” were not able to take part.
Stephen Evans, professor of pharmacoepidemiology at the London School of Hygiene & Tropical Medicine, told the UK’s Science Media Centre that the increase was only “small” but said there was “a lot of uncertainty around that estimate.”
He said that “some people won’t know if they have hypersensitivity to some constituents of the vaccine.”
He backed the MHRA advice for people who carry an EpiPen to delay having a vaccination until the reason for the allergic reaction has been clarified. But he said the news did not mean the general public should be anxious.
(Read more at CNN)
Who knew that Pfizer/BioNTech could work common allergies and fetal materal into the same vaccination?
Building a vaccine that triggers common allergies while also having markers for fetal material takes a special talent.
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FDA: Death, heart attacks, stroke, blood disorders all possible side effects of COVID vaccine
LifeSiteNews relays information from the FDA: all sorts of blood and heart problems may result from taking the vaccination.
A document drawn up by the Food and Drug Administration (FDA), listing the possible side-effects from a COVID-19 vaccine, includes strokes, encephalitis, auto-immune disease, birth defects, and Kawasaki disease among the potential side-effects to be monitored.
A slideshow presentation compiled by the FDA in October contains an extensive list of possible side effects which are to be monitored in conjunction with administering a COVID-19 vaccine. There is to be both passive and active surveillance of side effects related to the vaccine. Under the former system, the FDA is to partner with the Centers for Disease Control (CDC) to manage the Vaccine Adverse Event Reporting System (VAERS), whereby individuals report adverse side effects to their health care provider.
Legal immunity for vaccine producers
And due to a little-known federal law from the 1980s, pharmaceutical companies cannot be sued in court if their vaccines injure or kill someone. Instead, people injured or killed by vaccines (or their relatives) must use the National Vaccine Injury Compensation Program, which was created in 1986. It protects pharmaceutical companies from lawsuits related to vaccine injuries or deaths.
“It was created after lawsuits against vaccine companies and health care providers threatened to cause vaccine shortages and reduce U.S. vaccination rates, which they believed could cause a resurgence of vaccine preventable diseases,” Children’s Health Defense explains.
Children’s Health Defense reports, “According to the vaccine-injured and their loved ones, the program has failed miserably as a litigious, broken system where the injured are up against a government vaccine program, government owned vaccine patents, government health officials who administer the program and government paid attorneys from the Department of Justice. There is no judge, no jury of your peers and no discovery. Claimants feel the system is set up for their claims to fail.”
With the active surveillance, the FDA plans to use the “Biologics Effectiveness and Safety (BEST) System,” with numerous partners. MarketScan, the largest number of the partner companies, has over 250 million patients.
Along with the Center for Medicare & Medicaid Services (CMS), the FDA states that its data can cover “approximately 55 million elderly US beneficiaries >65yrs of age.” It is through using the CMS data that the FDA plans to monitor side-effects from COVID vaccines, based on rapid-cycle analyses.
FDA admits long list of possible negative side-effects
The working list presented has 22 separate entries of “possible adverse event outcomes.”
First on the list is “Guillain-Barré syndrome,” described as “a rare disorder in which your body’s immune system attacks your nerves.” The syndrome has “no known cure” and it mortality rate is “4% to 7%.” In contrast, John Hopkins University estimates that the current percentage of deaths reportedly due to COVID-19 cases in the U.S, is only 1.9%.
“Acute disseminated encephalomyelitis,” a “rare inflammatory condition that affects the brain and spinal cord,” is second on the FDA’s list. Third is “Transverse myelitis,” a neurological disorder which inflames the spinal cord, causing “pain, muscle weakness, paralysis, sensory problems, or bladder and bowel dysfunction.”
Also listed as a possible outcome of a potential vaccine is “Anaphylaxis,” the severe allergic reaction which can lead to anaphylactic shock.
(Read more at LifeSiteNews)
If choosing between contracting a disease that only kills 0.0053% of those who contract it and a vaccine that may cause blood disorders, heart attacks, stroke, or death — I think I will skip the vaccine
This reminds me of the parody commercial for a pharmaceutical that can prevent flatulence, but has the side effects of blindness, searing eye pain, constipation, and sudden death.
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Five questions about the coronavirus vaccine that should scare everyone
LifeSiteNews also reports five questions that the United Kingdom has raised to women before they take the vaccine.
The United Kingdom has announced its approval of the Pfizer coronavirus vaccine. The U.S. is expected to approve a vaccine within weeks, as well.
The U.K.’s government-produced safety instructions indicate that the vaccine should not be used by pregnant or breastfeeding mothers, that it is unknown what effect the COVID-19 mRNA vaccine will have on fertility, and “women of childbearing age should be advised to avoid pregnancy for at least 2 months after their second dose.”
In light of the fact that despots around the world have suggested, some using stronger language than others, that their citizenries will be forcibly vaccinated, or that there should or will be penalties for not receiving the vaccine, one wonders:
- What happens if a woman receives the vaccine and does become pregnant within two months of receiving it? Will she be pressured to abort her child? What impact would such a vaccine have on the baby?
- Will “women of childbearing age” be pressured — or even forced — to go on birth control or forgo pregnancy in order to receive the vaccine, which has been touted as the all-important key to “going back to normal”? In what world would it be considered just or fair to tell women they mustn’t become pregnant so they can receive an optional medical intervention — which has no shortage of side effects and risks — for a disease the vast majority of people survive?
- Will new mothers be pressured to forgo breastfeeding so they can be vaccinated?
- Will Catholic bishops tell women they ought to forgo pregnancy so they can be vaccinated? The Catholic bishops of California say they are committed “to promoting and encouraging COVID-19 vaccinations in the communities we serve.” If they will tell women to forgo childbearing, at least temporarily, so they can receive the shot, how will that be squared with Church teaching that children are the primary end of marriage and contraception is intrinsically evil?
- According to the U.K. government’s guidelines, which will presumably be similar to Pfizer vaccine guidances in other countries, pregnant women shouldn’t receive the shot. Will unvaccinated pregnant women be discriminated against because of this, and denied access to airlines and other spaces?
The fact that these questions even need to be asked is chilling (not as chilling as the vaccine itself, which bizarrely has to be stored at -70°C — colder than Antarctia).
(Read more at LifeSiteNews)
These are all good questions, even for those who are not Christian
Considering that many people want to keep their bodies pure, knowing that this vaccine will cause issues with to-be-pregnant women, pregnant women, and nursing women can be useful.
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Should we be concerned about “ethical” vaccines?
For those who look at the ethical side of vaccinations, Celebrate Life Magazine points out the dilemma created by vaccines.
To address the coronavirus (COVID-19) pandemic, Congress directed $10 billion to project Operation Warp Speed to develop vaccines, therapeutics, and diagnostics—so-called countermeasures. While the public health community and media laud the ambitious goal of producing enough vaccine for every person in the US by January 2021, other people have expressed concern that rapid development of a coronavirus vaccine might take shortcuts with proper safety testing. Indeed, 50 percent of Americans would not receive a coronavirus vaccine when one becomes available, and another 25 percent aren’t sure.
Historically, vaccine development can take 10 years or longer, which may explain why many Americans, parents especially, lack trust in a coronavirus vaccine developed under such a hasty timeline.
Perhaps more people have experienced or learned of adverse safety issues with other vaccines and are suspicious of claims by government and vaccine manufacturers that vaccines are “safe and effective.”
Considering that coronavirus has a 99.8 percent recovery rate—similar to annual influenza—one could even question the need for a vaccine. Additionally, new coronavirus vaccines may be only 50 percent effective, similar to a yearly flu shot.
Are “ethical” vaccines really ethical?
Another concern for people of faith is news that experimental coronavirus vaccines could be produced using tissue derived from aborted babies. In addition to future coronavirus vaccines, several vaccines used for other diseases can be designated as “unethical” because their production methods use tissues derived from aborted human fetuses to cultivate vaccine viruses. Children of God for Life has meticulously documented such vaccine origins. Its founder, Debra Vinnedge, was prominently featured in Meredith Wadman’s 2017 book The Vaccine Race, which offers a detailed history of vaccines developed using aborted human fetal tissue.
If a vaccine is not derived from aborted fetal tissue, can it then be termed “ethical” and thus appropriate for administration to entire populations? Unfortunately, vaccines may be considered unethical for reasons beyond the use of fetus-derived tissue. After many years of vaccine research, I have found abundant evidence of corruption and unethical practices within drug companies and the government public health community.
Use of the term “ethical” to describe vaccines ignores the mandatory nature of vaccines and the potential for severe vaccine adverse effects, regardless of how the vaccines were made.
For example, within minutes of birth, babies are injected with the vaccine for hepatitis B—a disease of promiscuous homosexuals, heterosexuals, and intravenous drug abusers. This is a so-called “ethical” vaccine because it’s not derived from aborted human fetuses. But is it ethical to inject all babies with a lifestyle-disease vaccine?
In addition, pre-teens are injected with an HPV (human papillomavirus) vaccine with the unproven goal of preventing cervical cancer. Infection with certain high-risk types of HPV—a sexually transmitted disease—can cause cancer of the cervix, genital areas, or throat. Cervical cancer is commonly related to early sex with multiple partners or to having a male sexual partner who has had multiple sexual partners. The HPV vaccine is another so-called “ethical” vaccine because it’s not derived from aborted human fetuses. But is it ethical to inject pre-teen girls and boys with a lifestyle-disease vaccine?
Furthermore, mandating vaccines is a blatant violation of medical informed consent—a basic tenet of ethical medical practice. With numerous vaccines currently mandated for work, school, college, and daycare—and soon a coronavirus vaccine likely added to the list when marketed—the potential for harm increases.
Are vaccines totally safe?
If an adult or child is killed or injured by a vaccine, federal law—the National Childhood Vaccine Injury Act of 1986—prohibits the person from suing the drug company that made the vaccine. Despite the government’s narrowing criteria for injured parties to collect on vaccine death or injury, the taxpayer fund has paid out more than $4 billion to vaccine victims and their families. If vaccines are safe, why must drug companies be protected from lawsuits?
When recipients of a new coronavirus vaccine are killed or injured, they or their families will be prohibited from suing the vaccine makers. Since new COVID-19 vaccines are termed “countermeasures,” they are covered under the federal Countermeasures Injury Compensation Program. Described as a government “black hole” process with no transparency or accountability, the CICP appears to lack sufficient funding, reflected in its less than 10 percent payout rate for mostly H1N1 swine flu vaccine injury claims and limited one-year statute of limitations. Since the program began reviewing claims in 2010, it has received 485 claims, yet only 39 people have received compensation, prompting one critic to portray this as “the right to file and lose.”
In congressional hearings leading to passage of the NCVIA, which gave lawsuit immunity to drug companies for vaccine injuries and death, Dr. Martin Smith, then president-elect of the American Academy of Pediatrics, compared children harmed by vaccines to military soldiers in combat. Dr. Smith stated: “This country does, and it should, provide compensation and continuing care for its soldiers who are injured in the defense of their country. It has been and is the contention of the [AAP] that the children of this nation are also soldiers in the defense of this country against disease.”
This means the government is telling you to risk sacrificing your children instead of giving drug companies incentive to develop safer vaccines. In his testimony to Congress, polio vaccine pioneer Dr. Jonas Salk expressed concerns that the NCVIA would remove “the incentive for manufacturers and the scientific community to improve existing vaccines.” In recent years, adults have also been encouraged to receive an ever-increasing number of vaccines.
When vaccines are mandated and the federal government (through taxes) pays the vaccine liability costs for drug companies, these companies have no incentive to make safer products or improve existing products.
Moreover, the Department of Health and Human Services has ignored directives under the 1986 NCVIA to report every two years to Congress how the agency has improved vaccine safety. In a Freedom of Information lawsuit in 2018, the HHS revealed that it had never submitted a single biennial safety report in 30 years. In the meantime, HHS promotes and funds a growing vaccine schedule with little apparent concern for the safety of currently licensed vaccines.
In their goal to achieve 100 percent vaccination rates, drug companies and government public health authorities withhold and distort an unconscionable amount of information. Common practices include inflating disease incidence data to mislead the public into thinking a disease is more common than it really is and minimizing reports on a vaccine’s adverse reactions.
(Read at Celebrate Life Magazine for the rest of the article and the footnotes)
Ok. This goes deep into the vaccinate/not vaccinate debate. Still, it is good to consider.
If you don’t occasionally review your beliefs, you will not know how to defend them.
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YouTube bans LifeSite over video of Bp. Strickland refusing to take corona vaccine
LifeSiteNews reports that YouTube has banned LifeSiteNews due to a video where Bishop Strickland discussed why he would not take the abortion-tainted vaccine.
YouTube has once again censored LifeSiteNews, this time for an episode of The Bishop Strickland Show in which Bishop Joseph Strickland of Tyler, Texas discussed why he will not be receiving an abortion-tainted coronavirus vaccine.
The episode of the bishop’s was labeled “medical misinformation.” LifeSite will appeal the decision, which suspends our YouTube account that boasts more than 200,000 subscribers for two weeks.
The last time LifeSiteNews was banned from YouTube – less than a month ago – it was a one-week suspension of our account. That censorship came almost immediately after LifeSite uploaded audio of a Canadian doctor slamming lockdowns and discussing the ineffectiveness of masks.
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No matter what happens with our YouTube channel, or what censorship we face on any platform, LifeSiteNews will always report the truth – as is our duty as journalists. And we will continue to provide our followers with information about life, faith, family, and freedom.
(Read more at LifeSiteNews)
While corornavirus may be a real disease, the media (and social media companies) use it to manipulate
For whatever reason there is in promoting this vaccine, media wants to push us all into being obedient drones. Just as we have all been pushed into wearing masks, keeping out of gatherings, and doing the things that make us individuals — the media and other Democrats want to force us into compliance (while they ignore any restrictions).
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