Coronavirus Vaccine Problems News StoriesExcerpts of Key Coronavirus Vaccine Problems News Stories in Major Media
This comprehensive list of coronavirus vaccine problems news stories is usually updated once a week. Explore our full index to revealing excerpts of key major media news stories on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.
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 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.
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.
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.
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.
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.
George Garvey, along with several other individuals (collectively, Petitioners) are former NYC Department of Sanitation workers who got fired for their failure to get vaccinated or obtain an approved exemption. They filed a lawsuit pursuant to Article 78 of the New York Civil Practice Law and Rules. They sued NYC, the NYC Department of Health and Mental Hygiene, the NYC Department of Sanitation, the NYC Commissioner of the NY Department of Health and Mental Hygiene and the Mayor of NYC (collectively, Respondents). Judge Ralph J. Porzio issued an order essentially dismissing the Respondent’s arguments and accepting most of the Petitioners’ arguments. The order commanded that all terminated Petitioners be reinstated on October 25, 2022 and collect back pay from their date of termination. The court held that the vaccination mandate was unlawful. First, it was arbitrary and capricious. The court ... argued that it treated similarly situated people differently without providing evidence to support the unequal treatment. Athletes, performers and artists could be exempted from the vaccination requirement, but the Petitioner could not. The court noted that the Petitioners could continue working while their exemption requests were being processed. Therefore, the court felt that the vaccination mandate was never about public safety. Because if it was, any unvaccinated workers would have immediately been placed on leave until a decision concerning their requests for a coronavirus vaccine exemption.
Elon Musk said he had 'major side effects' from his second Covid-19 booster shot that left him feeling like he 'was dying'. Musk, 51, took to Twitter to share his experience of the Covid-19 vaccine in response to a retweet of a poll that said 7 percent of adults claimed they experienced major side effects from the Covid vaccine. The Twitter and Tesla CEO said the second booster 'crushed me'. Musk also shared that his younger cousin, who he said was in 'peak health', had to be hospitalized after his jab suffering from myocarditis. 'I had major side effects from my second booster shot. Felt like I was dying for several days. Hopefully, no permanent damage, but I dunno,' Musk tweeted over the weekend. He added: 'And my cousin, who is young & in peak health, had a serious case of myocarditis. Had to go to the hospital.' Myocarditis is an inflammation of the heart and is named as a possible, but very rare, side effect of Covid-19 vaccinations. A large study published in JAMA Network of more than 192 million people who received Covid vaccines found there were 1,626 cases of myocarditis - a rate of 8.5 cases per million people (0.000845 per cent). Many people have reported side effects from Covid shots, including headaches, a temperature, fatigue and injection site soreness, but in most cases the symptoms only last a few days. When asked why he had gotten the second booster, Musk said that it was not his choice but because it was a requirement fly to Germany.
Note: Explore a list of recent news articles we've summarized that reveal how vaccine-induced myocarditis is not as rare as we're told to believe. For more along these lines, see concise summaries of deeply revealing news articles on coronavirus vaccine problems from reliable major media sources.
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.
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.
Life insurance actuaries are reporting that many more people are dying – still – than in the years before the pandemic. Among working people 35 to 44 years old, a stunning 34% more died than expected in the last quarter of 2022, with above-average rates in other working-age groups, too. “COVID-19 claims do not fully explain the increase,” a Society of Actuaries report says. There was an extreme and sudden increase in worker mortality in the fall of 2021 even as the nation saw a precipitous drop in COVID-19 deaths. In the third quarter of 2021, deaths among workers ages 35-44 reached a pandemic peak of 101% above ... the three-year pre-COVID baseline. In two other prime working-age groups, mortality was 79% above expected. In the year ending April 30, 2023 ... at least 104,000 more Americans died than expected. In the U.K., 52,427 excess deaths were reported in that period; in Germany, 81,028; France, 17,731; Netherlands, 10,418; and Ireland, 2,640. The actuarial reports can only speculate on the factors causing these deaths, including oft-cited delayed health care, drug overdoses and even weather patterns. But the question remains: What explains this ongoing wave of excess deaths? Life insurance data suggests something happened in the fall of 2021 in workplaces, especially among white-collar workers. These are people whose education, income level and access to health care would predict better outcomes.
Note: Critical care physician Dr. Pierre Kory, one of the co-authors of this article, recently published an in-depth explanation on what he believes is behind the excess death among American youth, and why it wasn’t mentioned in the USA Today article. For more along these lines, see concise summaries of deeply revealing news articles on health from reliable major media sources.
National Institutes of Health scientists raked in more than $325 million in royalties from Chinese and Russian entities — as well as pharmaceutical companies — over more than a decade, according to a new report. Former NIH director Dr. Francis Collins and former National Institutes of Allergy and Infectious Diseases (NIAID) director Dr. Anthony Fauci were among the thousands of government whitecoats who took the cash between September 2009 and October 2020, the taxpayer watchdog OpenTheBooks.com revealed. Several of those royalties came from companies that in turn received federal contracts and grants, prompting concerns about conflicts of interest. Unredacted documents obtained by the group through the Freedom of Information Act (FOIA) show at least 34 Chinese companies are licensing NIH technologies initially funded by US taxpayers. Some of those licensing fees came from the Wuhan Institute of Biological Products Co. Ltd., a subsidiary of the Chinese government-owned pharmaceutical company Sinopharm, which produced a COVID-19 vaccine. In 2016, the biological products company moved its headquarters next to the Wuhan Institute of Virology, where risky “gain-of-function” research funded by the US government may have led to the outbreak of the pandemic. The late Dr. Robert Chanock, the former head of the NIAID’s laboratory of infectious diseases, and Dr. Jeffrey Cohen, his successor, were just a few of the virologists on the take from the Wuhan-based company.
Many of 4000 social media posts secretly censored by government during the height of the Covid-19 pandemic contained factual information and reasonable arguments rather than misinformation, new documents reveal. Digital posts released after Freedom of Information applications show the censored information shared facts such as the ineffectiveness of vaccines in preventing Covid-19 infection and transmission or argued against measures such as mask mandates and lockdowns. For instance, the then Coalition government sought the removal of an Instagram post in April 2021 that claimed "Covid-19 vaccine does not prevent Covid-19 infection or Covid-19 transmission". That statement clearly was accurate yet the official intervention via the Home Affairs Department claimed it breached Instagram's community guidelines because it was "potentially harmful information" that was "explicitly prohibited" by the platform. An April 2021 tweet was challenged because it claimed "Covid-19 was released or escaped from Wuhan laboratory in China and that it was funded by the US government". The Home Affairs Department claimed this was "explicitly prohibited" under Twitter's rules because it might "invoke a deliberate conspiracy by malicious and/or powerful forces", yet American intelligence agencies have found the most likely source of the virus was the Wuhan Institute of Virology, and it has been revealed that some work at the laboratory was funded by the US.
Note: The Journal of the American Medical Association (JAMA) recently published a study that tracked the spread of COVID-19 'misinformation' during the course of the pandemic. Despite significant evidence pointing to the likelihood that COVID leaked from a lab and the unprecedented collusion between the Biden administration and tech giants to remove politically unfavorable views on social media, this JAMA study stated that these claims were inaccurate. How do we stay open to debate, instead of silencing voices with legitimate concerns and labeling it as misinformation? For more along these lines, see concise summaries of deeply revealing news articles on government corruption and media manipulation from reliable sources.
A little-known federal agency called BARDA dedicated to countering "health security threats" was responsible for conducting the quality review of every COVID-19 vaccine dose administered in the U.S., Sasha Latypova reported on her Substack. But BARDA, the Biomedical Advanced Research and Development Authority, which has a "militarized" purpose according to Latypova, is not subject to the same regulations as typical pharmaceutical manufacturers, distributors or regulatory agencies. "The public was told these vaccines are made by Pfizer and Moderna and rigorously approved by the FDA," [said Latypova]. That ... would mean that the "consumer protections we expect from pharmaceutical products, medical devices and even food ... we expect them to be in place." But in fact, countermeasures contracts made available through Freedom of Information Act (FOIA) requests ... and U.S. Securities and Exchange Commission disclosures show the U.S. Department of Defense (DOD) and BARDA contracts with the pharmaceutical companies were structured such that these protections weren't required. The contracts also specified that manufacturers and federal agencies were protected by the Public Readiness and Emergency Preparedness (PREP) Act, which shields "covered persons" – such as pharmaceutical companies, or the DOD/BARDA – from liability for injuries sustained from "countermeasures," such as vaccines ... administered during a public health emergency.
Note: Sasha Latypova is a former pharmaceutical industry executive who now specializes in uncovering fraud in pharmaceutical research, development, and manufacturing. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and coronavirus vaccines from reliable major media sources.
Public health leaders like Rochelle Walensky and Anthony Fauci make false claims, or contradict themselves repeatedly, on subjects related to the pandemic response, while leading scientists, like Peter Hotez in the US and Christian Drosten in Germany, are equally susceptible to such flip-flops and lies. All of these figures publicly and aggressively promoted anti-public health policies, including universal masking, social distancing, mass testing and quarantining of healthy people, lockdowns and vaccine mandates. All the top pro-lockdown scientists and public health experts – in perfect lockstep – suddenly started (and continue to this day) to misread studies and advocate policies that they had claimed in the past were unnecessary. The public health experts were not responsible for pandemic response policy. The military-intelligence-biodefense leadership was in charge. The most startling switch was the replacement of the public health agencies by the National Security Council and Department of Homeland Security at the helm of pandemic policy and planning. As part of the secret switch, all communications – defined in every previous pandemic planning document as the responsibility of the CDC – were taken over by the National Security Council under the auspices of the White House Task Force. The CDC was not even allowed to hold its own press conferences!
Note: Read more about how the national security state was involved in COVID public health policies. For more along these lines, see concise summaries of deeply revealing news articles on government corruption and the coronavirus from reliable major media sources.
Thousands of Covid-19 vaccine injury allegations have been submitted to the federal government and are unlikely to be reviewed any time soon without intervention by the Biden administration and Congress, according to attorneys whose potential clients feel they have nowhere to turn. Appendicitis, cognitive difficulty, abdominal pain, and abnormal heart rhythm are just some of the Covid vaccine-related injuries cited by the 8,208 individuals who have filed requests for benefits with the Health and Human Services Department's Countermeasures Injury Compensation Program. The CICP has reached only 749 decisions on claims related to Covid treatments, with four cases resulting in compensation. Now, with the public health emergency officially over, attorneys say it's time for the administration and Congress to move Covid vaccine injury claims to a program they say is better suited for addressing them. But doing so would require lawmakers to tackle some much-needed reforms. "It doesn't have the infrastructure yet," Renee Gentry, director of the Vaccine Injury Litigation Clinic at the George Washington University, said of the ... Vaccine Injury Compensation Program. Even half of the Covid caseload "would double the size of the vaccine program. It would come to a crashing halt." "A lot of these people have devastating injuries, and they need at least a fair shot at compensation," Gentry said.
Note: Although significant evidence reveals how COVID vaccines harmed more people than what was announced by US government agencies, the FDA recently refused to improve COVID vaccine safety labeling despite calls from current and former FDA officials. For more along these lines, watch a powerful documentary that follows the lives of people significantly harmed by the vaccine, yet were discredited and abandoned by the medical and media establishment.
Important Note: Explore our full index to revealing excerpts of key major media news stories on several dozen engaging topics. And don't miss amazing excerpts from 20 of the most revealing news articles ever published.