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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.

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Revolving door: You are free to influence us “behind the scenes,” FDA tells staff leaving for industry jobs
2024-07-01, The BMJ (Formerly British Medical Journal)
https://www.bmj.com/content/386/bmj.q1418.short

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 Sues Pfizer Over Covid-19 Vaccine’s Safety, Efficacy
2024-06-17, Bloomberg
https://news.bloomberglaw.com/health-law-and-business/kansas-sues-pfizer-over...

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 Believe Covid Vaccines Harmed Them. Is Anyone Listening?
2024-05-03, New York Times
https://www.nytimes.com/2024/05/03/health/covid-vaccines-side-effects.html

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: 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. Explore our nuanced, uncensored investigation about this important issue.


Is it long COVID or long vax? Does the government want to know?
2024-03-06, The Hill
https://thehill.com/opinion/healthcare/4512451-is-it-long-covid-or-long-vax-d...

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.


Moderna Surveillance Operation Targeted Independent Media Voices
2024-01-16, Lee Fang on Substack
https://www.leefang.com/p/moderna-surveillance-operation-targeted

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.


FDA Shuts Down Enquiries about DNA Contamination in Covid Vaccines
2023-11-28, Brownstone Institute
https://brownstone.org/articles/fda-shuts-down-enquiries-about-dna-contaminat...

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.


Is the US’s Vaccine Adverse Event Reporting System broken?
2023-11-10, The BMJ (Formerly British Medical Journal)
https://www.bmj.com/content/383/bmj.p2582

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.


CDC Covered Up COVID Vaccine Myocarditis
2023-10-03, Public on Substack
https://public.substack.com/p/cdc-covered-up-covid-vaccine-myocarditis

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, FinlandGermany, 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.


The real data behind the new COVID vaccines the White House is pushing
2023-09-14, New York Post
https://nypost.com/2023/09/14/the-real-data-behind-the-new-covid-vaccines-the...

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.


CDC Now Refusing New COVID Vaccine Adverse Event Reports in Its V-Safe Program
2023-08-24, Brownstone Institute
https://brownstone.org/articles/cdc-refusing-new-covid-vaccine-adverse-event-...

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.


10 Years After HHS Asked CDC to Study Safety of Childhood Vaccine Schedule, CDC Hasn’t Produced It
2023-08-21, Children's Health Defense
https://childrenshealthdefense.org/defender/vax-unvax-hhs-cdc-safety-childhoo...

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.


Covid Censorship Proved to Be Deadly
2023-07-07, Wall Street Journal
https://www.wsj.com/articles/covid-censorship-proved-to-be-deadly-social-medi...

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.


Robert F. Kennedy Jr. Tops Biden And Trump In New Favorability Poll
2023-06-14, Forbes
https://www.forbes.com/sites/maryroeloffs/2023/06/14/robert-f-kennedy-jr-tops...

2024 Democratic presidential contender Robert F. Kennedy Jr.–an environmental lawyer with anti-vaccine views and a strong family dynasty at his back–has higher favorability numbers than either President Joe Biden or former President Donald Trump, according to a new poll by The Economist and YouGov. Kennedy Jr. was viewed favorably by 49% of respondents and unfavorably by just 30%, leaving him with a net rating of 19 points–higher than any other candidate in the poll, which surveyed 1,500 adult respondents from June 10 to 13. Biden had a negative 9-point net favorability rating, with 52% of respondents viewing him somewhat or very unfavorably while 45% have very or somewhat favorable impressions, and Trump had a negative 10-point net rating, with 53% viewing him unfavorably and 43% favorably. Kennedy Jr. announced he would challenge Biden for the 2024 Democratic nomination in April, joining a largely empty field. He is the son of assassinated former attorney general and 1968 presidential candidate Robert F. Kennedy, and the nephew of former President John F. Kennedy. Previously known as an environmental lawyer, he has become known in recent years for promoting dubious claims. A collection of tech moguls have gotten behind Kennedy Jr. in recent weeks, including former Twitter CEO Jack Dorsey, Social Capital founder Chamath Palihapitiya and venture capitalist David Sacks. Billionaire Twitter owner Elon Musk hosted him for a Twitter Spaces discussion earlier this month.

Note: Robert F. Kennedy Jr. has an up-hill battle to climb, given the massive propaganda campaign against him. This is especially relevant regarding his stance on vaccines, due to the "Illusion of Consensus" in biomedical science about vaccine issues. In reality, the vaccine issue is complex, very political and easy to distort. Furthermore, Kennedy Jr. is challenging entrenched power in a big way. Read a compelling summary of his bestselling book, The Real Anthony Fauci: Bill Gates, Big Pharma, and the Global War on Democracy and Public Health.


We tried to improve COVID vaccine labeling – the FDA said 'no thanks'
2023-06-09, The Hill
https://thehill.com/opinion/healthcare/4037145-we-tried-to-improve-covid-vacc...

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.


Possible links between Covid shots and tinnitus emerge
2023-04-23, NBC News
https://www.nbcnews.com/health/health-news/covid-vaccine-side-effects-tinnitu...

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.


Psychologist's death due to AstraZeneca Covid vaccine reaction
2023-04-19, BBC News
https://www.bbc.com/news/uk-england-london-65321937

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.


Doctor died from rare reaction to AstraZeneca Covid jab, UK coroner rules
2023-04-19, The Guardian (One of the UK's Leading Newspapers)
https://www.theguardian.com/world/2023/apr/19/doctor-died-from-rare-reaction-...

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.


Renowned Medical Researcher & Colleague Publish Systematic Review of Serious Harms From COVID-19 Vaccines
2023-04-04, The Pulse
https://www.thepulse.one/p/renowned-medical-researcher-and-colleague

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.


New Research Shows Pfizer’s mRNA Vaccine Can Instruct Cells To Produce ‘off-target’ Proteins
2023-01-30, The Pulse
https://www.thepulse.one/p/new-research-shows-pfizers-mrna-vaccine

Since the rollout of mRNA COVID-19 vaccines, experts and academics from around the world have been raising numerous short-term and long-term safety concerns. One of these deals with the spike protein that the human cell is instructed to generate as a result of the shot, and how it differs from the spike protein that’s generated from a natural infection. A “pseudouridine” molecule has been added to the mRNA to give it a longer half-life than normal mRNA. Therefore, the production of spike protein within the cell, of those who have been vaccinated, is not being turned off. This is concerning because multiple studies have shown that the vaccine induced spike protein can leak outside of the cell and enter into the blood- stream. This is one possible mechanism of action in which vaccine injuries are occurring. During an autopsy of a vaccinated person who had died after mRNA vaccination, it was found that the vaccine disperses rapidly from the injection site and can be found in nearly all parts of the body. Looking into these concerns is important to figure out why so many COVID vaccine injuries around the world have been reported compared to previous vaccines. Approximately 50 percent of vaccine injuries reported to the Vaccine Adverse Events Reporting System (VAERS) in the last 30 years have all been from COVID products. Concerning autopsy results have also been published. It’s quite clear something very serious about these shots is and has been ignored.

Note: VAERS only captures a portion of vaccine injuries and deaths. Vaccine adverse event numbers are made publically available, and currently show 2,579,111 COVID vaccine injury reports and 37,100 COVID Vaccine Reported Deaths (out of 47,290 Total Reported Deaths from all vaccines). Read our in-depth report about this concerning trend, and how the VAERS system presents an incomplete picture of vaccine injuries. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccines from reliable major media sources.


FDA vaccine advisers 'disappointed' and 'angry' that early data about new Covid-19 booster shot wasn't presented for review last year
2023-01-11, CNN News
https://www.cnn.com/2023/01/11/health/moderna-bivalent-transparency/index.html

Some vaccine advisers to the federal government say they're "disappointed" and "angry" that government scientists and the pharmaceutical company Moderna didn't present a set of infection data on the company's new Covid-19 booster during meetings last year when the advisers discussed whether the shot should be authorized and made available to the public. That data suggested the possibility that the updated booster might not be any more effective at preventing Covid-19 infections than the original shots. US taxpayers spent nearly $5 billion on the new booster, which has been given to more than 48.2 million people. "I was angry to find out that there was data that was relevant to our decision that we didn't get to see," said Dr. Paul Offit, a member of the Vaccines and Related Biological Products Advisory Committee, a group of external advisers that helps the FDA make vaccine decisions. The data that was not presented to the experts looked at actual infections: who caught Covid-19 and who did not. It found that 1.9% of the study participants who received the original booster became infected. Among those who got the updated bivalent vaccine ... a higher percentage, 3.2%, became infected. A 22-page FDA briefing document given to the advisers did not mention this infection data. Dr. Jerry Weir, director of the Division of Viral Products at the FDA's Office of Vaccines Research and Review, also did not mention the infection data in his presentation to the advisers.

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.


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