Vaccines Media Articles
Below are key excerpts of revealing news articles on vaccine controversies from reliable news media sources. If any link fails to function, a paywall blocks full access, or the article is no longer available, try these digital tools.
The payment scheme for people injured by vaccines has cost taxpayers more to run than it has paid out to victims, official figures suggest, fuelling calls for “urgent reform”. The Government has spent more than £25 million since Nov 1 2021 on medically assessing thousands of claims that vaccinations have left people seriously disabled. It is more than the total £23.6 million that since that date has been paid out to 197 victims, with each claim worth £120,000. The Vaccine Damage Payment Scheme (VDPS) was established in 1979 and pays tax-free cash to those deemed to have suffered life-changing injuries as a result of certain vaccinations – including those against Covid-19. It awards a one-off £120,000 tax-free payment to people who have been severely injured, or to the families of those who have died, as a result of a vaccination. The scheme has been heavily criticised for being too slow to assess cases. Victims also claim that the payouts are insufficient and that the threshold claimants must meet to qualify for a payout is too harsh a measure. Kate Scott, whose husband was left with permanent brain damage after taking the AstraZeneca vaccine against Covid-19, criticised the imbalance between the money the scheme costs to run and the sums paid out. Public hearings for the fourth module of the Covid-19 inquiry started in London on Tuesday. It will hear issues around vaccine safety from families of those who suffered side effects from Covid jabs.
Note: The Vaccine Adverse Event Reporting System (VAERS) is a voluntary government reporting system that only captures a portion of the actual injuries. Vaccine adverse event numbers are made publicly available, and currently show 38,264 COVID Vaccine Reported Deaths and 1,658,330 COVID Vaccine Adverse Event Reports. Our Substack dives into the complex world of COVID vaccines with nuance and uncensored investigation.
In December of 2002, Sharyl Attkisson, an Emmy-winning investigative reporter for CBS News, had an unsettling interview with smallpox expert Jonathan Tucker. In a post-9/11 world, with fears of terrorists using a long-eradicated disease like smallpox as a bioweapon, the US was preparing to bring back the smallpox inoculation program. But to Tucker, the very idea was “agonizing,” writes Attkisson. Why? Because it involved “weighing the risk of a possible terrorist use of smallpox ... against the known risks of the vaccine,” Tucker told the author. “A ‘toxic’ vaccine?” She writes. “Didn’t the smallpox vaccine save the world?” But as she soon discovered, it had serious side effects, including a surprisingly high possibility of death. Attkisson witnessed firsthand how deadly the vaccine could be in April of 2003, when a colleague at NBC, journalist David Bloom, died from deep vein thrombosis while on assignment in Iraq. He’d also recently been vaccinated for smallpox, and ... thrombosis was a possible side effect of the inoculation. The majority of scientific studies are funded and even dictated by drug companies. “Studies that could stand to truly solve our most consequential health problems aren’t done if they don’t ultimately advance a profitable pill or injection,” Attkisson writes. “These aren’t necessarily drugs designed to make us well, but ones we’ll ‘need’ for life,” writes Attkisson. Some [drug companies] hire “ghostwriters” to author studies promoting a new drug, exaggerating benefits and downplaying risks, and then paying a doctor or medical expert to sign their name to it. “We exist largely in an artificial reality brought to you by the makers of the latest pill or injection,” she writes. “It’s a reality where invisible forces work daily to hype fears about certain illnesses, and exaggerate the supposed benefits of treatments and cures.”
Note: Top leaders in the field of medicine and science have spoken out about the rampant corruption and conflicts of interest in those industries. For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption from reliable major media sources.
Vaccine adverse effects are real. I know it makes some people uncomfortable to acknowledge this, but alongside the benefits of vaccines, there are cases of profound harm. Recently, the New York Times covered my story: “Thousands Believe COVID Vaccines Harmed Them. Is Anyone Listening?” Sadly, no one is listening yet, and very few people are willing to help. I am a research nurse practitioner who has dedicated my professional career to community health and clinical research, including vaccines. My beliefs are firmly rooted in science. Three years ago, when the COVID-19 vaccine emerged, I stepped forward to receive it. What followed was unexpected and devastating. Within hours I developed tingling along my right arm, which over days radiated across my body. A neurologist and colleague recommended that I proceed with a second dose. With the vaccine mandate from my employer at the top of my mind, I proceeded, against my own medical judgment. After the second dose, my condition rapidly worsened. I developed positional tachycardia, wildly fluctuating blood pressures, internal tremors, electrical zap sensations on my legs, intense right-sided headaches, abdominal pain and severe tinnitus. I struggle to live with all of this and more to this day. Medical gaslighting, coupled with the absence of legal recourse or adequate compensation, compounds the challenges we endure. When I reach out for help, my pleas often fall on deaf ears, or I am disparaged as a misinformed “anti-vaxxer.”
Note: This article was written by Shaun Barcavage, a nurse practitioner in New York City. Explore our nuanced, uncensored investigation about this important issue. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccine problems from reliable major media sources.
During his final three years at the US Food and Drug Administration the physician scientist Doran Fink’s work focused on reviewing covid-19 vaccines. But a decade after joining the agency Fink had accepted a job with Moderna, the covid vaccine manufacturer. As he left for the private sector, the FDA’s ethics programme staff emailed him guidelines on post-employment restrictions, “tailored to your situation.” The email, obtained by The BMJ under a freedom of information request, explained that, although US law prohibits a variety of types of lobbying contact, “they do not prohibit the former employee from other activities, including working ‘behind the scenes.’” The legal ability to work “behind the scenes” is enshrined in federal regulations and highlights a “critical, critical loophole” in US revolving door policy. Craig Holman, a government affairs lobbyist for the organisation Public Citizen, told The BMJ that the rules forbid various forms of direct lobbying contact but permit lobbying activity that is indirect. “So, people will leave government service and can immediately start doing influence peddling and lobbying,” Holman explained. “They can even run a lobbying campaign, as long as they don’t actually pick up the telephone and make the contact with their former officials.” A majority of former FDA reviewers take up jobs in industry. Since 2000 every FDA commissioner, the agency’s highest position, has gone on to work for industry.
Note: For more along these lines, see concise summaries of deeply revealing news articles on corruption in government and in Big Pharma from reliable major media sources.
Kansas on Monday sued Pfizer Inc., accusing the pharmaceutical giant of misrepresenting the safety of its Covid-19 vaccine and violating the state’s consumer protection law. The lawsuit was filed by state Attorney General Kris Kobach in Kansas District Court, Thomas County. The suit alleges the drugmaker misled the public when it said it had a safe and effective Covid-19 vaccine. “Pfizer said its COVID-19 vaccine was safe even though it knew its COVID-19 vaccine was connected to serious adverse events, including myocarditis and pericarditis, failed pregnancies, and deaths,” the state wrote in the complaint. The company administered more than 3.5 million vaccine doses in Kansas as of Feb. 7, 2024, according to the lawsuit. The complaint also said Pfizer maintained its own adverse events database, separate from the federal Vaccine Adverse Event Reporting System (VAERS), a national early warning system managed by the Food and Drug Administration and Centers for Disease Control and Prevention to detect possible safety problems in US-licensed vaccines. Pfizer’s database contained cases of adverse events reported spontaneously to Pfizer, cases reported by the health authorities, and cases published in the medical literature, according to the suit. “Pfizer’s adverse events database contained more adverse event data than VAERS because it included both information in VAERS and information not in VAERS,” Kobach wrote.
Note: For more along these lines, see concise summaries of news articles on COVID vaccines from reliable major media sources.
Thousands of Americans believe they suffered serious side effects following Covid vaccination. As of April, just over 13,000 vaccine-injury compensation claims have been filed with the federal government. Only 19 percent have been reviewed. Only 47 of those were deemed eligible for compensation, and only 12 have been paid out, at an average of about $3,600. In a recent interview, Dr. Janet Woodcock, a longtime leader of the Food and Drug Administration ... said she believed that some recipients had experienced uncommon but “serious” and “life-changing” reactions beyond those described by federal agencies. “I feel bad for those people,” said Dr. Woodcock, who became the F.D.A.’s acting commissioner in January 2021. “I believe their suffering should be acknowledged, that they have real problems, and they should be taken seriously.” The government’s understaffed compensation fund has paid so little because it officially recognizes few side effects for Covid vaccines. People who said they had been harmed by Covid shots ... described a variety of symptoms following vaccination, some neurological, some autoimmune, some cardiovascular. All said they had been turned away by physicians, told their symptoms were psychosomatic, or labeled anti-vaccine by family and friends — despite the fact that they supported vaccines. The National Institutes of Health is conducting virtually no studies on Covid vaccine safety, several experts noted.
Note: Explore our nuanced, uncensored investigation about this important issue. While mainstream narratives emphasize how rare these injuries are, the numbers speak for themselves. The Vaccine Adverse Event Reporting System (VAERS) is a voluntary government reporting system that only captures a portion of the actual injuries. Vaccine adverse event numbers are made publicly available, and currently show 1,640,416 COVID vaccine injury reports, 37,647 COVID Vaccine Reported Deaths, and 216,757 COVID Vaccine Reported Hospitalizations.
Long COVID as it’s commonly known is a serious and poorly understood problem. But there is also growing evidence that the COVID vaccine could cause a similar disease. We are critical care physicians with the FLCCC Alliance (the Front Line COVID-19 Critical Care Alliance) who have treated COVID patients throughout the pandemic. One of us recently opened a private practice focused on patients with long COVID. In two years, the practice has evaluated and treated over 1,000 individuals. Approximately 70 percent of these patients said their reported symptoms occurred in the minutes, hours, days and weeks after COVID vaccination, as opposed to after COVID infection. This could be tied to a new condition that’s flown under the radar until recently. This syndrome, dubbed “long vax,” is just starting to make its way into the medical literature. Dr. Harlan Krumholz at the Yale School of Medicine published a survey of 241 patients who described post-COVID vaccination symptoms of exercise intolerance, excessive fatigue, numbness, brain fog and neuropathy, a nervous system disorder that can cause pain, tingling sensations, numbness or weakness. Long COVID patients were excluded from the study. The concern is that our findings, Krumholz’s study, and any reports of adverse events from COVID-19 vaccination, will be subject to the same institutional censorship we saw throughout the pandemic.
Note: We've documented the growing public backlash against the COVID vaccine, including landmark lawsuits. Vaccine adverse event numbers are made publically available through the Vaccine Adverse Event Reporting System (VAERS), and currently show 1,630,913 COVID vaccine injury reports, 37,231 COVID Vaccine Reported Deaths, and 214,906 COVID Vaccine Reported Hospitalizations.
Finances at the vaccine manufacturer Moderna began to fall almost as quickly as they had risen, as most Americans resisted getting yet another COVID booster shot. In a September call aimed at shoring up investors, Moderna’s then-chief commercial officer, Arpa Garay, attributed some of the hesitancy pummeling Moderna's numbers to uninformed vaccine skeptics. What Garay hinted at during the call, but didn’t disclose, was that Moderna already had a sprawling media operation in place aimed at identifying and responding to critics of vaccine policy and the drug industry. Internal company reports and communications ... show that Moderna has worked with former law enforcement and public health officials and a drug industry-funded non-governmental organization called The Public Good Projects (PGP) to confront the “root cause of vaccine hesitancy” by rapidly identifying and “shutting down misinformation.” Part of this effort includes providing talking points to some 45,000 healthcare professionals “on how to respond when vaccine misinformation goes mainstream.” PGP routinely sent Excel lists of accounts to amplify on Twitter and others to de-platform, including populist voices such as ZeroHedge. The messages also suggested emerging narratives to remove from the platform. The growing network these efforts rely on shows the growth of what has been called the censorship industrial complex.
Note: Learn more about Moderna's misinformation department. For more along these lines, see concise summaries of deeply revealing news articles on pharmaceutical industry corruption and media manipulation from reliable sources.
The recent findings of DNA fragments in the Pfizer and Moderna Covid-19 vaccines has led many to question why the FDA, which is responsible for monitoring the quality and safety of the vaccines, has failed to sound the alarm. For years, the FDA has known about the risk posed by residual DNA in vaccines. Its own guidance to industry states: “Residual DNA might be a risk to your final product because of oncogenic and/or infectivity potential. There are several potential mechanisms by which residual DNA could be oncogenic, including the integration and expression of encoded oncogenes or insertional mutagenesis following DNA integration.” Put simply ... fragments of DNA left over by the manufacturing process can be incorporated into a patient’s own DNA, to potentially cause cancer. A recent preprint paper ... analysed batches of the monovalent and bivalent mRNA vaccines. The authors found “the presence of billions to hundreds of billions of DNA molecules per dose in these vaccines. Using fluorometry all vaccines exceed the guidelines for residual DNA set by FDA and WHO.” For the Pfizer product, the higher the level of DNA fragments found in the vaccine, the higher the rate of serious adverse events. Pfizer’s vaccine used in the clinical trials (PROCESS 1) was manufactured differently to the vaccine that was injected into the wider population (PROCESS 2). This switch from PROCESS 1 to PROCESS 2 is what introduced the plasmid DNA impurities.
Note: Watch a fascinating interview with Dr. Ryan Cole, who discusses DNA contamination in the COVID vaccines and its concerning links to the rise in cancers and autoimmune diseases. Although you need a subscription to watch the full video, the full transcript is accessible. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and COVID vaccines from reliable major media sources.
The Vaccine Adverse Event Reporting System (VAERS) ... collects reports of symptoms, diagnoses, hospital admissions, and deaths after vaccination. VAERS is supposed to be user friendly, responsive, and transparent. However, investigations by The BMJ have uncovered that it’s not meeting its own standards. Not only have staffing levels failed to keep pace with the unprecedented number of reports since the rollout of covid vaccines but there are signs that the system is overwhelmed. In the face of an unprecedented 1.7 million reports since the rollout of covid vaccines, VAERS’s staffing was likely not commensurate with the demands of reviewing the serious reports submitted, including reports of death. While other countries have acknowledged deaths that were “likely” or “probably” related to mRNA vaccination, the CDC—which says that it has reviewed nearly 20,000 preliminary reports of death using VAERS (far more than other countries)—has not acknowledged a single death linked to mRNA vaccines. In November 2022, React19, an advocacy group of some 30,000 people who have experienced prolonged illness after covid vaccination, reviewed 126 VAERS reports among its ranks. 22% had never been given a permanent VAERS ID number and 12% had disappeared from the system entirely. The BMJ has found that the FDA and CDC essentially maintain two separate VAERS databases: a public facing database, containing only initial reports; and a private, back end system containing all updates and corrections—such as a formal diagnosis, recovery, or death.
Note: Vaccine adverse event numbers on VAERS are made publically available here, and only capture a portion of the actual vaccine injuries. Albert Benavides is a VAERS researcher who recently wrote a comprehensive Substack piece investigating the corruption and dysfunction of the VAERS system, including how the VAERS system even deleted dead Pfizer Trial patients. Another excellent article explores these concerning implications from the perspective of cardiologists, physicians, and science researchers.
On April 27, 2021, then-director of the CDC, Rochelle Walensky stated, “we have not seen any reports” of post-vaccination myocarditis, but this was a false statement. When Walensky claimed to have “not seen any reports,” there were dozens of reports in the US Vaccine Adverse Event Reporting System (VAERS). “The CDC,” notes [journalist Zachary] Stieber, “was warned by Israel on Feb. 28, 2021, about a ‘large number’ of myocarditis cases after Pfizer COVID-19 vaccination. Internally, the warning was designated as ‘high’ importance and set off a review of US data.” The Israeli Ministry of Health requested a joint meeting with the Food and Drug Administration (FDA) and the CDC to respond to this trend. “The Israeli National Focal Point is noticing a large number of reports of myocarditis, particularly in young people, following the administration of the Pfizer vaccines,” the email stated. Even when more information about myocarditis became public, [Walensky's] agency continued to downplay the risks. Stieber also found that the CDC’s V-Safe self-reporting system did not include a category for myocarditis reports. To this day, the CDC has not released complete, updated data on myocarditis. The agency’s cover-up of adverse cardiac events has had profound consequences and represents a major breach of trust and abuse of authority. Due to the higher risks of myocarditis after Moderna, Sweden, Norway, Finland, Germany, and France suspended the use of the Moderna vaccine for people under 30 two years ago.
Note: When current and former FDA advisers and academics asked the FDA to improve COVID vaccine labeling given the significant risk of severe vaccine injuries, the agency denied almost every single request. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and coronavirus vaccines from reliable major media sources.
What if I told you one in 50 people who took a new medication had a “medically attended adverse event” and the manufacturer refused to disclose what exactly the complication was — would you take it? And what if the theoretical benefit was only transient, lasting about three months, after which your susceptibility goes back to baseline? And what if we told you the Food and Drug Administration cleared it without any human-outcomes data. That’s what we know about the new COVID vaccine the Biden administration is firmly recommending. COVID vaccines are very different from flu vaccines. COVID vaccines have higher complication rates, including severe and life-threatening cardiac reactions. Flu shots have a 50-plus-year safety record whereas COVID vaccines have been associated with a serious adverse event rate of one in 5,000 doses, according to a German study by the Paul-Ehrlich-Institut. Another study, published last year in the medical journal Vaccine, estimated the rate of serious adverse events to be as high as one in 556 COVID vaccine recipients. And for young people, the incidence of myocarditis is six to 28 times higher after the vaccine than after infection, even for females, according to a 2022 JAMA Cardiology study. That’s one of the reasons a study that we and several national colleagues published last year found that college booster mandates appear to have resulted in a net public health harm.
Note: The above was written by Marty Makary, MD, a professor at the Johns Hopkins School of Medicine. Anecdotals is a powerful documentary that follows the lives of many people who stepped up to get vaccinated for themselves or the greater good, yet whose lives changed drastically as a result. Instead of having their stories of vaccine injuries heard and seen, they were discredited and abandoned by the medical system and our media systems.
The Centers for Disease Control and Prevention (CDC) V-safe website quietly stopped collecting adverse event reports with no reason or explanation. The V-safe website simply states: “Thank you for your participation. Data collection for COVID-19 vaccines concluded on June 30, 2023.” If you go there today, V-safe directs users to the FDA’s VAERS website for adverse event reporting, even though officials continually derided VAERS as “passive” and “unverified.” VAERS and V-safe are mutually exclusive safety collection databases operated by the FDA and CDC, respectively. According to the FDA Vaccine Adverse Event Reporting System (VAERS) database, mRNA “vaccines” have been named the primary suspect in over 1.5 million adverse event reports, of which there are >20,000 heart attacks and >27,000 cases of myocarditis and pericarditis just in the USA alone. VAERS reports represent fewer than 1 percent of vaccine adverse events. Based on VAERS and previous V-safe findings, adverse events from mRNA shots in the USA alone could be considered a humanitarian crisis. Despite those alarming clinical findings, the CDC has concluded that collecting new safety reports is somehow no longer in the interest of America’s public health. Existing data from the V-safe site showed around 6.5 million adverse events/health impacts out of 10.1 million users, with around 2 million of those people unable to conduct normal activities of daily living.
Note: For more along these lines, see concise summaries of deeply revealing news articles on government corruption and coronavirus vaccines from reliable major media sources.
In 2013, the National Vaccine Program Office of the U.S. Department of Health and Human Services (HHS) commissioned an update of earlier findings on the lack of evidence to support claims that the Centers for Disease Control and Prevention (CDC) infant/child vaccination schedule was safe. The Institute of Medicine (IOM) committee [was] charged with producing the update. The lack of information on the overall safety of the vaccination schedule was so compelling that the committee then recommended HHS incorporate the study of the safety of the overall childhood immunization schedule into its processes for setting priorities for research, “recognizing stakeholder concerns, and establishing the priorities on the basis of epidemiological evidence, biological plausibility, and feasibility.” The IOM also recommended the CDC use its private database, the Vaccine Safety Datalink (VSD), to study the overall health effects of the vaccination schedule using retrospective analyses. Ten years later, the CDC has yet to do such a comparison study, even though it is sitting on a vast repository of data in the VSD, which include comprehensive medical records for more than 10 million individuals and 2 million children. The VSD also contains records for a significant number of unvaccinated children, yet the CDC refuses to compare the health outcomes of vaccinated children to completely unvaccinated children. The CDC also prohibits VSD outside researchers from accessing the VSD data.
Note: Read more about how HHS was in violation of the “Mandate for Safer Childhood Vaccines” as stipulated in the Vaccine Injury Compensation Act. For more along these lines, see concise summaries of deeply revealing news articles on vaccines from reliable major media sources.
On July 4, U.S. District Judge Terry Doughty temporarily blocked numerous federal agencies and the White House from collaborating with social-media companies and third-party groups to censor speech. Discovery in Missouri v. Biden exposed relationships among government agencies and social-media firms and revealed an additional layer of university centers and self-styled disinformation watchdogs and fact-checking outfits. Elon Musk's release of some of Twitter's internal files revealed that up to 80 Federal Bureau of Investigation agents were embedded with social-media companies. The agents mostly weren't fighting terrorism but flagging wrongthink by American citizens, including eminent scientists who suggested different paths on Covid policy. The U.S. government spent $6 trillion to buoy its shuttered economy, and most people got Covid anyway. Excess mortality in most high-income nations was worse in 2021 and 2022 than in 2020, the initial pandemic year. Sweden, which didn't have a lockdown, performed better than nearly every other advanced nation. Hiding these realities has become more difficult in the internet age. The information explosion has allowed more people to spot quickly the mistakes of officials. Those in charge feel threatened. Digital censorship is their response to this crisis of authority. True, misinformation is rampant online. But it was far worse before the internet, when myths could persist for centuries.
Note: For more along these lines, see concise summaries of deeply revealing news articles on the government corruption and media manipulation from reliable sources.
Current Food and Drug Administration (FDA)-approved labels for the Pfizer and Moderna COVID-19 vaccines are obsolete, misleading and out of touch with regulators elsewhere. Take the ongoing uncertainty over whether vaccines reduce viral transmission. We asked the FDA to clarify in labeling that there isn't substantial evidence that mRNA vaccines reduce viral transmission. The FDA also failed to warn about the documented risk of sudden death, even though myocarditis is now a well-recognized side effect, particularly among young men. To support adding "sudden death" to product labeling, we pointed to multiple autopsy studies on lethal vaccination-associated myocarditis. We asked the FDA to add seven adverse event types to product labeling: multi system inflammatory syndrome in children (MIS-C), pulmonary embolism, sudden cardiac death, neuropathology and autonomic disorders, decreased sperm concentration, heavy menstrual bleeding and detection of vaccine mRNA in breast milk. Current and former FDA advisers and academics from around the country ... tried to fix this problem by asking the FDA to make critical changes to official product labels. But four months later, in a 33-page response letter, the agency denied almost every single request. In doing so, the FDA failed to follow the lead of regulators elsewhere. We cited the European regulator's addition of heavy menstrual bleeding to product information as a potential vaccine adverse reaction. The FDA's response was a sophisticated version of "who cares!"
Note: Explore a deeper look into why medical experts are calling for more accurate COVID-19 vaccine labeling. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and coronavirus vaccines from reliable major media sources.
Thousands of people say they've developed tinnitus after they were vaccinated against Covid. Shaowen Bao, an associate professor in the physiology department of the College of Medicine at the University of Arizona, Tucson, believes that ongoing inflammation, especially in the brain or spinal cord, may be to blame. Bao, a longtime tinnitus sufferer and a representative of the American Tinnitus Association's scientific advisory board, has studied tinnitus for more than a decade. A Facebook group of people who developed tinnitus after getting a Covid vaccine convinced Bao to look into the possible link. One man told Bao that he couldn’t hear the car radio over the noise in his head while driving. Along with ringing in their ears, participants reported a range of other symptoms, including headaches, dizziness, vertigo, ear pain, anxiety and depression. Significantly more people first developed tinnitus after the first dose of the vaccine, compared with the second. This suggests "that the vaccine is interacting with pre-existing risk factors for tinnitus. If you have the risk factor, you will probably get it from the first dose," Bao said. As of Sunday, at least 16,183 people had filed complaints with the Centers for Disease Control and Prevention that they'd developed tinnitus, or ringing in their ears, after receiving a Covid vaccine. [Vaccine expert Dr. Gregory] Poland, who was stricken with tinnitus after he received his Covid vaccines two years ago, suggested that the CDC remains "unconcerned" about these reports of tinnitus.
Note: For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
The death of a psychologist after his Oxford-AstraZeneca Covid-19 jab was due to "unintended complications of the vaccine", an inquest has ruled. Stephen Wright, an NHS employee in south-east London, died 10 days after his first dose in January 2021, senior coroner Andrew Harris found. Dr Wright, 32, suffered a blood clot to the brain after receiving the vaccine. His wife Charlotte has been trying to get the "natural causes" wording on her husband's death certificate changed. She is pursuing legal action against the pharmaceutical company. At London Inner South Coroner's Court, Mr Harris described it as a "very unusual and deeply tragic case". Dr Wright suffered from a combination of a brainstem infarction, bleed on the brain and "vaccine-induced thrombosis", the inquest heard. His condition rapidly worsened, but the nature of the bleed meant he was unfit for surgery. After the inquest, Mrs Wright ... said: "It was made clear that Stephen was [previously] fit and healthy and that his death was by vaccination of AstraZeneca. For us, it allows us to be able to continue our litigation against AstraZeneca. This is the written proof." Speaking about the coroner's ruling, mother-of-two Charlotte Wright said: "It provides relief but it doesn't provide closure. I think we're only going to get that when we have an answer from AstraZeneca and the government." From May 2021, the AZ jab was no longer offered to adults under 40 after it became clear the vaccine carried [a] risk of blood clots which could be fatal.
Note: Dr. Wright's death is one of many tragedies related to the COVID-19 vaccine, as revealed in a powerful documentary that follows the lives of people significantly harmed by the vaccine, yet were discredited and abandoned by the medical system and our media systems. A recent analysis report estimates that in 2022 alone, out of 148 million people, the mass COVID-19 inoculations injured 26.6 million, disabled 1.36 million, and caused 300,000 excess deaths, with an estimated economic cost of nearly $150 billion. For more along these lines, explore revealing news articles on coronavirus vaccines from reliable major media sources.
A doctor died from a rare reaction to the AstraZeneca Covid jab in one of the first rounds of vaccinations, a coroner has ruled. Dr Stephen Wright, 32, an NHS clinical psychologist and frontline health worker, suffered from a combination of a brainstem infarction, bleed on the brain and vaccine-induced thrombosis, an inquest at London’s Southwark coroner’s court heard. He was in one of the earliest groups of people to be given the jab, and died 10 days after it was administered. After the inquest, Wright’s widow, Charlotte, said she is considering legal action against AstraZeneca and the government. She remembered Wright as “the most amazing husband” and a good father to their sons, and said it was a relief to have a “black and white” conclusion. Medical experts told the court nothing could be done to save Wright. Dr Mark Howard, a consultant pathologist and medical examiner at King’s College hospital, said scientists and medical experts were not aware of the vaccine’s possible deadly side effects when Wright received the jab as it was so early in its rollout, but even at later stages there would have been no way of predicting this “rare and unintended consequence”. He said: “Stephen was a very fit, young and healthy man in January 2021. It is a truly tragic and very rare complication of a well-meant vaccination. It’s not fully understood why this happens. It’s an idiosyncratic reaction. The circumstances arise in a very small number of people.”
Note: An excellent documentary reveals how mild to severe reactions to vaccines were more common than was being told. Anecdotals follows the lives of many people who stepped up to get vaccinated for themselves or the greater good, yet were greatly harmed by the vaccine. Instead of having their stories heard and seen, they were discredited and abandoned by the medical system and our media systems. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
Dr. Peter Gøtzsche is a well known Danish physician with four decades of research experience, publishing 97 papers in the “big five” (BMJ, Lancet, JAMA, Annals of Internal Medicine, and New England Journal of Medicine) and 19 Cochrane reviews. He is a co-founder of the Cochrane Collaboration. Gøtzsche, along with ... Maryanne Demasi, PhD, have published a new paper titled “Serious harms of the COVID-19 Vaccines: A Systematic Review.” It’s been a task for academics to look into this phenomenon given the fact that vaccine manufacturers and drug regulators never allowed independent researchers to examine the raw trial data, forcing transparency advocates to sue the FDA for access to the documents. The adenovirus vector vaccines increased the risk of venous thrombosis and thrombocytopenia. (Authorities have responded by suspending the use of AstraZeneca’s vaccine across many European countries, and in the US, regulators have advised restricted use of Janssen’s vaccine). The mRNA-based vaccines increased the risk of myocarditis, with a mortality of about 1-2 per 200 cases. It was more common in younger males. We found evidence of serious neurological harms, including Bell’s Palsy, Guillain-Barré syndrome, myasthenic disorder and stroke, which are likely due to an autoimmune reaction from mRNA and adenoviral vector vaccines. Severe harms, i.e. those that prevent daily activities, were underreported in the randomized trials.
Note: For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
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