COVID Vaccine Problems Media Articles
Below are key excerpts of revealing news articles on COVID vaccine problems 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.
Vaccines that protect against severe illness, death and lingering long Covid symptoms from a coronavirus infection were linked to small increases in neurological, blood, and heart-related conditions in the largest global vaccine safety study to date. The rare events — identified early in the pandemic — included a higher risk of heart-related inflammation from mRNA shots made by Pfizer Inc., BioNTech SE, and Moderna Inc., and an increased risk of a type of blood clot in the brain after immunization with viral-vector vaccines such as the one developed by the University of Oxford and made by AstraZeneca Plc. The viral-vector jabs were also tied to an increased risk of Guillain-Barre syndrome, a neurological disorder in which the immune system mistakenly attacks the peripheral nervous system. More than 13.5 billion doses of Covid vaccines have been administered globally over the past three years. Still, a small proportion of people immunized were injured by the shots, stoking debate about their benefits versus harms. The new research, by the Global Vaccine Data Network, was published in the journal Vaccine last week. Exercise intolerance, excessive fatigue, numbness and “brain fog” were among common symptoms identified in more than 240 adults experiencing chronic post-vaccination syndrome in a separate study conducted by the Yale School of Medicine. The cause of the syndrome isn’t yet known, and it has no diagnostic tests or proven remedies.
Note: 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 that is often discussed by mainstream media as a rare occurrence. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccines from reliable major media sources.
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.
Victims who suffered life-changing injuries from the Oxford-AstraZeneca Covid vaccine say they have faced censorship on social media when trying to discuss their symptoms. The UK-based pharmaceutical giant is being sued in the High Court in a test case by a father-of-two who suffered a significant permanent brain injury as a result of a blood clot after receiving the jab in spring 2021. A second claim is also being brought by the widower and two young children of a woman who died after having the jab. Some who have experienced serious adverse reactions from the AstraZeneca vaccine ... have been given “warnings” on social media websites such as Facebook when trying to talk to one another about their experiences. They say they are being forced to “self censor” and speak in code to avoid having their support groups shut down. In one instance, YouTube attempted to censor a video of testimony given by lawyers to the Covid Inquiry about vaccines, flagging the clip as a violation of its “medical misinformation policy”. UK CV Family, a private Facebook group with 1.2k members for people left injured or bereaved from Covid vaccines, was started in November 2021 by Charlet Crichton after she suffered an adverse reaction from the AstraZeneca jab. Facebook blocked Ms Crichton from commenting at one stage “to prevent misuse” and there were occasions where her account was temporarily banned because her “activity didn’t follow our community standards”.
When the U.S. Government entered into its Covid vaccine agreement with Pfizer, which was acting on behalf of the BioNTech/Pfizer partnership, in July 2020, the agreement encompassed a minimum of 100 million doses of a “vaccine to prevent COVID-19” and a payment of at least $1.95 billion. The Government declared that we were “at war” with a catastrophically dangerous virus. In keeping with the declaration of war, it was a military framework that was used for acquiring the aspirational products that became known as Covid mRNA vaccines. The Government side to the agreement with Pfizer was the Department of Defence (DoD), represented by a convoluted chain of parties, each operating as a subcontractor, or co-contractor, for the next. In fact, agencies governing civilian and public health, like the NIH, NIAID and HHS, do not have the authority to grant certain types of special acquisition contracts, which is why the Covid vaccine contracts had to be overseen by the Department of Defence. Emergency Use Authorisation (EUA) ... is a very special way to authorise a medical countermeasure in very specific types of emergencies. EUA was meant for dire situations of warfare or terrorism, not to protect the entire population from naturally occurring pathogens. For this reason, EUA products do not require the type of legal safety oversight that is applied in civilian contexts by the FDA.
Note: Read how the Department of Defense and the Biomedical Advanced Research and Development Authority allowed vaccine makers to bypass standard safety testing of their products. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccines from reliable major media sources.
A New Zealand man was recently arrested after allegedly illegally accessing COVID-19 vaccine data from the country's health agency. Barry Young, 56, a former IT employee at Te Whatu Ora, the country's health agency, was arrested and accused of illegally obtaining COVID-19 vaccine data and sharing it on the internet. Young appeared on Infowars, where he was interviewed by ... Alex Jones. "I just looked at the data and what I was seeing, since the rollout, it just blew my mind. I was just seeing more and more people dying that shouldn't have been dying. It was just obvious," Young told Jones. The incident comes as COVID-19 vaccine skeptics have continued to question the efficacy of the inoculation. Texas Attorney General Ken Paxton recently announced that he was suing vaccine manufacturer Pfizer "for unlawfully misrepresenting the effectiveness of the company's COVID-19 vaccine and attempting to censor public discussion of the product." During the interview with Infowars, Young explained that he had suspicions about the COVID-19 vaccine in New Zealand since its rollout. "I want people to analyze this, I want people to look at it...we need to open it up and the government needs to have an inquiry about it. Just bring it to the public's attention," Young said.
Note: U.S.-based genomics scientist Kevin McKernan had uploaded Barry Young's data onto a file hosting service, MEGA, only to have his whole account deleted by MEGA overnight. For more along these lines, see concise summaries of deeply revealing news articles on COVID vaccine problems from reliable major media 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 Moderna misinformation reports, reported here for the first time, reveal what the pharmaceutical company is willing to do to shape public discourse around its marquee product. The mRNA COVID-19 vaccine catapulted the company to a $100 billion valuation. Behind the scenes, the marketing arm of the company has been working with former law enforcement officials and public health officials to monitor and influence vaccine policy. Key to this is a drug industry-funded NGO called Public Good Projects. PGP works closely with social media platforms, government agencies and news websites to confront the “root cause of vaccine hesitancy” by rapidly identifying and “shutting down misinformation.” A network of 45,000 healthcare professionals are given talking points “and advice on how to respond when vaccine misinformation goes mainstream”, according to an email from Moderna. An official training programme, developed by Moderna and PGP, alongside the American Board of Internal Medicine, [helps] healthcare workers identify medical misinformation. The online course, called the “Infodemic Training Program”, represents an official partnership between biopharma and the NGO world. Meanwhile, Moderna also retains Talkwalker which uses its “Blue Silk” artificial intelligence to monitor vaccine-related conversations across 150 million websites in nearly 200 countries. Claims are automatically deemed “misinformation” if they encourage vaccine hesitancy. As the pandemic abates, Moderna is, if anything, ratcheting up its surveillance operation.
Note: Strategies to silence and censor those who challenge mainstream narratives enable COVID vaccine pharmaceutical giants to downplay the significant, emerging health risks associated with the COVID shots. For more along these lines, see concise summaries of deeply revealing news articles on corporate corruption and the disappearance of privacy from reliable major media sources.
An FDNY firefighter says he was forced to retire on half his salary after the city-mandated COVID-19 vaccine left him with permanent heart damage. O’Brian Pastrana now wants a judge to award him a more lucrative disability pension, which would pay three-quarters of his final salary tax-free, according to court papers. Pastrana, 37, got the jab in October 2021 because the city required it, and had an immediate allergic reaction, including swollen lips, chills and body aches. Despite three trips to the emergency room, he claims he was forced to get the second Pfizer shot a month later. “I thought I was going to die after that second dose,” Pastrana [said], adding he was again rushed to the ER after the second shot. By February 2022, the married father of two was diagnosed with myocarditis, which results in potentially fatal inflammation of the cardiac muscle, and was nearly in heart failure, court records show. The heart condition is a rare side effect of the vaccine, according to the Centers for Disease Control and Prevention. Pastrana was then told he could never be a firefighter again, and forced to retire in March after over a decade on the job. “I was completely blindsided,” he wrote in a statement to the court. The FDNY Uniformed Firefighter Association called his injury “totally avoidable.” The city “held his job over his head and forced him to choose between a vaccine that he did not want, and feeding his family,” Andrew Ansbro, the union’s president, said.
People injured by the COVID-19 vaccines are suing the federal government, claiming the federal program they're forced to pursue compensation through is an opaque and unconstitutional "kangaroo court" that unjustly rejects almost all claims it receives. React19, a patient group of the vaccine injured ... is one of several plaintiffs challenging the constitutionality of the Countermeasures Injury Compensation Program (CICP). The other plaintiffs are all individuals whose compensation claims were rejected by the CICP, despite many having diagnoses from their doctors that the severe injuries they experienced within a few hours or days of receiving a COVID-19 vaccine were a result of the vaccine. Their lawsuit was filed in October. The CICP is currently the only avenue through which those with a COVID-19 vaccine injury can seek compensation. A mix of federal law and pandemic-era emergency declarations bar the vaccine injured from suing vaccine manufacturers in civil court. Those with a COVID-19 vaccine injury are also prohibited from pursuing compensation through the standard Vaccine Injury Compensation Program (VICP). People must file a CICP claim within one year of vaccination. "Most of us don't know what's wrong with us for over a year if we can ever get a diagnosis," says [legal affairs director for React19 Christopher] Dreisbach, who himself suffered a COVID-19 vaccine injury. "So many ... don't even know the program even exists." The CICP was first authorized in 2005 by a piece of war-on-terror legislation intended to encourage companies to produce emergency countermeasures to a bioweapons attack or a similar disaster by shielding them from lawsuits.
The U.S. was in a fit of Covid panic during Thanksgiving week two years ago. By month’s end, Pfizer’s stock-market value had surpassed $300 billion, up 50% from the start of the pandemic. Moderna’s shares had soared by more than 1,000% over the same period. In 2022 Pfizer became the first pharmaceutical company to book more than $100 billion in annual sales owing to government purchases of its vaccines and antiviral pill. Fast-forward to today. The pandemic is over. Demand for Covid vaccines and treatments has plunged. Pfizer’s total revenue has fallen more than 40% since last year. Earlier this month the company took a $5.5 billion write-off on its Covid products owing to “lower-than-expected demand.” Only 14% of American adults have received the latest updated booster shots. The jabs’ greatest benefit was in providing political leaders with the courage to lift destructive lockdowns and mask mandates. The vaccines were supposed to be a two-shot-and-done regimen, not blockbuster medicines that rung up tens of billions of dollars in sales every year with government support. Statins and diabetes medicines prevent heart attacks, but the government doesn’t run ads urging Americans to use Lipitor or Ozempic. The government’s vaccine boosterism ... has increased public cynicism toward pharmaceutical companies. Drug makers can dine out on any given medicine only for so long before needing to cook up another pharmaceutical bonanza.
The Justice Department has just posted a new jobs ad — it’s looking for eight new attorneys to defend the federal government in vaccine injury cases. Presumably, the hiring spree is in anticipation of a surge of COVID vaccine lawsuits, as people who were forced by government mandates to take the jab, and suffered serious side effects as a result, try to extract compensation from a system that is stacked against them. “The office is currently expanding to address workload created by an increase in cases filed under the Vaccine Act,” reads the ad posted by the Torts Branch of the DOJ on the USAJobs website. The recruitment drive comes on the heels of a little-noticed lawsuit filed in Louisiana last month by six vaccine-injured plaintiffs against the federal government. The suit aims to overturn the legal immunity that pharmaceutical giants like Pfizer and Moderna enjoy on their COVID shots. Meanwhile, almost 13,000 Americans who claim the COVID vaccine caused them or their dead loved ones adverse reactions ... remain in limbo after doing what they were told was “the right thing”: heeding government mandates to submit to the jab. The unaccountable, understaffed government tribunal that presides over the so-called Countermeasures Injury Compensation Program (CICP), for vaccines administered under emergency measures, is a “kangaroo court,” says the lawsuit filed by attorney Aaron Siri, partner at New York firm Siri & Glimstad.
Note: Learn about the legal landmark case in the UK alleging significant injuries and damages from the AstraZeneca COVID vaccine. For more along these lines, see concise summaries of revealing news articles on government corruption and coronavirus 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.
The Oxford-AstraZeneca Covid-19 vaccine has been branded “defective” in a multi-million pound landmark legal action that will suggest claims over its efficacy were “vastly overstated”. The pharmaceutical giant is being sued in the High Court in a test case by Jamie Scott, a father-of-two who suffered a significant permanent brain injury that has left him unable to work as a result of a blood clot after receiving the jab in April 2021. A second claim is being brought by the widower and two young children of 35-year-old Alpa Tailor, who died after having the jab made by AstraZeneca. The test cases could pave the way for as many as 80 damages claims worth an estimated £80 million over a new condition known as Vaccine-induced Immune Thrombocytopenia and Thrombosis (VITT) that was identified by specialists in the wake of the AstraZeneca Covid-19 vaccine rollout. In the months following the rollout, the potential serious side effect of the AstraZeneca jab was identified by scientists. Following this, it was recommended it no longer be given to the under-40s in the UK because the risk of receiving the jab outweighed the harm posed by Covid. Official figures ... show at least 81 deaths in the UK are suspected to have been linked to the adverse reaction that caused clotting in people who also had low blood platelets. Victims and their lawyers question the Government’s monitoring of the rollout and point out that ... Germany suspended the vaccine’s use for the under 60s at the end of March 2021.
Note: In the US, when current and former FDA advisers and academics asked the FDA to improve COVID vaccine labeling given the 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 coronavirus vaccines from reliable major media sources.
Executives at the largest insurance companies in the United States are alarmed that teenagers, young and white-collar Americans in the prime of life are inexplicably dying at a record pace, causing a “monumental outflow” of death claims. According to an Oct. 26 report in InsuranceNewsNet, U.S. insurance companies expected higher-than-normal payouts from excess deaths during the COVID-19 pandemic. Insurers saw death benefits rise 15.4% in 2020, the biggest one-year increase since the 1918 Spanish flu epidemic, followed by a record $100.28 billion — nearly double the historic norm — in total death benefits paid out by the industry in 2021. CDC numbers ... show the death rate for Americans ages 15-45 rose 20-24% above normal in 2020, and soared in 2021, to a nearly 30% death increase for 15-year-olds and a more than 45% increase for 45-year-olds. CDC data reported in August showed that Americans in the period January-May 2023 were still dying at abnormally high rates with the pandemic long over. Dr. Pierre Kory ... who treats long COVID and vaccine-injured patients in his practice, called on insurance companies to work with media and governments and investigate the powerful evidence that countless deaths and disabilities are temporally linked to the COVID-19 mRNA vaccines. Kory cited the more than 1 million COVID-19 vaccine-linked injuries, disabilities and more than 30,000 deaths reported ... to the Vaccine Adverse Event Reporting System (VAERS).
Note: Mentioned in this article is critical care physician Dr. Pierre Kory, who recently published an in-depth explanation on the link between COVID-19 mRNA vaccines and excess death among American youth. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
Nearly a quarter of Americans believe someone they know died from COVID-19 vaccine side effects, and even more say they might be willing to become plaintiffs in a class-action lawsuit against vaccine makers. The latest Rasmussen Reports national telephone and online survey finds that 24% of American Adults say they know someone personally who died from side effects of the COVID-19 vaccine. Sixty-nine percent (69%) don’t know anyone who died from being vaccinated against the virus. (To see survey question wording, click here.) Forty-two percent (42%) say that, if there was a major class-action lawsuit against pharmaceutical companies for vaccine side effects, they would be likely to join the lawsuit, including 24% who say it’s Very Likely they’d join such a lawsuit. Forty-seven percent (47%) aren’t likely to join a class-action lawsuit against vaccine makers, including 25% who say it’s Not At All Likely. Another 11% are not sure. The survey of 1,110 American Adults was conducted on October 26 and 29-30, 2023 by Rasmussen Reports. The margin of sampling error is +/- 3 percentage points with a 95% level of confidence. Nearly half (47%) say they know someone personally who died from the COVID-19 virus, while 49% don’t know anyone who died from the virus, which became a pandemic in the United States in 2020. Among those who say someone they know died from the COVID-19 virus, 41% also say they know someone who died from side effects of the COVID-19 vaccine.
Note: For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
Anti-vaccine advocates have recently made allegations against the Pfizer COVID-19 vaccine in hopes that the charges may hurt the drug manufacturer. In a series of posts on X (formerly Twitter), Steve Kirsch expressed concern over reports that Pfizer's vaccine was contaminated, saying that the Food and Drug Administration (FDA) "is now at a crossroads." "Either they admit that they knew about the plasma contamination, and failed to disclose that to the public and to the outside committees, or they can claim that they didn't know about it in which case Pfizer is liable. But we have the Pfizer documents that were given to the FDA so we know what the FDA got," Kirsch wrote. "I seriously doubt there's any disclosure of SV40 contamination. That means we have an adulterated vaccine and the FDA has to remove it from the market until the adulteration is fixed. If the FDA doesn't do that, they should face criminal prosecution for endangering the public, and not following the law." (SV40 refers to simian virus 40.) In his posts, Kirsch also references an incident in Michigan where a judge ruled that the manufacturer of the COVID-19 medication Remdesivir was no longer protected by the federal Public Readiness and Emergency Preparedness (PREP) Act after a man filed a lawsuit against the manufacturer. The man filed the suit after suffering strokes and an amputation following treatment with the drug, Remdesivir, which was contaminated with glass particles.
Note: While the data is still being uncovered, read an in-depth, scientific investigation into vaccine contamination, including concerns that Pfizer hid this contamination from regulators. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccines from reliable major media sources.
Pfizer-BioNTech delayed reporting vaccine-associated deaths among BNT162b2 clinical trial participants until after the U.S. Food and Drug Administration (FDA) issued an Emergency Use Authorization (EUA) for the product. The vaccine makers also failed to account for a large number of subjects who dropped out of the trial. Together, these strategies kept regulators and the public ignorant of a 3.7-fold increase in cardiac deaths among subjects who received the vaccine, according to analysis in the International Journal of Vaccine Theory, Practice, and Research. Investigators looked at each of the 38 deaths occurring between July 27, 2020, the start of phase 2/3 of the Pfizer-BioNTech vaccine trial, and March 13, 2021, the end date culminating in Pfizer-BioNTech’s 6-month interim report. This trial phase involved 44,060 subjects. Half received a dose of BNT162b2, half got a placebo. The trial was unusual because at week 20 after the FDA issued the EUA for the vaccine, trial subjects in the placebo group were allowed to switch to the vaccinated group and receive their first BNT162b2 shot. Of 20,794 unblinded placebo subjects in the Pfizer trial, 19,685 received at least one dose of BNT162b2. After 33 weeks the data revealed no significant difference between deaths in the vaccinated and placebo groups for the initial 20-week placebo-controlled portion of the trial. 79% of relevant deaths were not recorded in time to be included in Pfizer’s regulatory paperwork.
Note: Read our recent essay on Big Pharma corruption to further explore the significant harms associated with the COVID vaccine. For more along these lines, see concise summaries of deeply revealing news articles on Big Pharma corruption and coronavirus vaccines from reliable major media sources.
Kangaroo court. That’s how plaintiffs lawyers in a federal lawsuit ... describe the obscure U.S. government tribunal charged with adjudicating claims for compensation by thousands of people who say they suffered serious injuries from COVID-19 vaccines. The lawsuit ... alleges that the Countermeasures Injury Compensation Program (CICP) violates the 5th and 7th amendments of the U.S. Constitution by failing to provide “basic due process protections, transparency, and judicial oversight.” The plaintiffs — eight people who say they experienced debilitating side-effects from the COVID-19 vaccine, as well as React 19, a nonprofit organization for people who claim vaccine-related injuries, want to stop the government from forcing their claims into the CICP until due process safeguards are added. Those include the right to review evidence, obtain discovery, present expert witnesses and appeal adverse decisions. Vaccine makers Pfizer, Moderna and Johnson & Johnson, which have been indemnified by the government and are not named in the suit, also did not immediately respond to requests for comment. The plaintiffs blame the COVID vaccine for causing a wide range of ailments including Bell’s palsy, blood clots in the brain, vertigo, vascular inflammation, chronic fatigue syndrome, small fiber neuropathy, heart palpitations and more. Four plaintiffs have filed claims for compensation with the CICP but have been told there is “no timeline” for adjudicating their cases.
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.
Important Note: Explore our full index to key excerpts of revealing major media news articles on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.