ARE BOOSTERS MAKING PEOPLE VULNERABLE TO COVID?
Newly released science is showing that the booster may increase your risk of catching COVID-19. Immune exhaustion and confusion may be to blame.
7 studies that help explain why the vaccinated are getting more infected
Especially the 2nd by Yahi et al; shows the non-neutralizing Abs bind to the virus spike, and enhances infectiousness of virus.
Binds but does not neutralize the virus; “Infection-enhancing anti-SARS-CoV-2 antibodies recognize both the original Wuhan/D614G strain and Delta variants. A potential risk for mass vaccination?”
Dr. Paul Alexander | May 10, 2022
Yahi et al.: so it is the binding to the virus by non-neutralizing Abs that do not eliminate the virus but increases infectiousness… it enhances the infection capability and explains why the vaccinated are getting infected; the non-neutralizing Abs bind to the virus in the upper respiratory tract and drive infection yet binds to the lower respiratory tract and prevents severe disease. This study shows original antigenic sin and ADE…
“our data suggest that the balance between neutralizing and facilitating antibodies in vaccinated individuals is in favor of neutralization for the original Wuhan/D614G strain. However, in the case of the Delta variant, neutralizing antibodies have a decreased affinity for the spike protein, whereas facilitating antibodies display a strikingly increased affinity. Thus, ADE may be a concern for people receiving vaccines based on the original Wuhan strain spike sequence (either mRNA or viral vectors).”
1)Van Egeren et al.: “Risk of rapid evolutionary escape from biomedical interventions targeting SARS-CoV-2 spike protein”
3)An infectivity-enhancing site on the SARS-CoV-2 spike protein targeted by antibodies
4)Lectins enhance SARS-CoV-2 infection and influence neutralizing antibodies
5)Structural insight into SARS-CoV-2 neutralizing antibodies and modulation of syncytia
6)The emergence and ongoing convergent evolution of the SARS-CoV-2 N501Y lineages
Moderna CEO Laments ‘Throwing 30 Million Doses In The Garbage Because Nobody Wants Them’
By Tyler Durden | Zero Hedge | May 24, 2022
Moderna CEO Stéphane Bancel is complaining about having to ‘throw away’ 30 million doses of Covid-19 vaccine because ‘nobody wants them.’
“It’s sad to say, I’m in the process of throwing 30 million doses in the garbage because nobody wants them. We have a big demand problem,” Bancel told an audience at the World Economic Forum, adding that attempts to contact various governments to see if anyone wants to pick up the slack was a total fail.
“We right now have governments – we tried to contact … through the embassies in Washington. Every country, and nobody wants to take them.”
“The issue in many countries is that people don’t want vaccines.”
Bancel’s comments come days after Bloomberg reported that EU health officials want to amend contracts with Pfizer and other vaccine makers in order to reduce supplies.
During a virtual meeting organized by Polish Health Minister Adam Niedzielski, governments shared a joint letter to the EU Commission which reads: “We hope that the discussion with the commission and among member states will allow flexibility in the vaccine agreements,” adding “We are also counting on vaccine producers to show understanding to the exceptional challenges that Poland is facing supporting Ukraine and giving shelter to millions of Ukrainian citizens fleeing the war.”
Some countries are seeking to amend so-called advanced purchase agreements signed with producers, as demand for shots wanes and budgets come under strain from the fallout of the war in Ukraine and the costs of accommodating refugees.
Adjusting deals with suppliers could grant member states the right to “re-phase, suspend or cancel altogether vaccine deliveries with short shelf life,” Estonia, Latvia and Lithuania’s prime ministers wrote in a joint letter to Commission President Ursula Von Der Leyen late last month.
Meanwhile, in a separate letter the health ministry of Bulgaria called for an “open dialog” with the commission and pharmaceutical companies, arguing that the current arrangement forces member states to “purchase quantities of vaccines they don’t need.”
GAIN OF FUNCTION ON POX VIRUSES CONFIRMED
Amazing Polly | May 23, 2022
I cover the US’s leading Orthopox Virus researcher who conducted at least 2 rounds of gain of function research on viruses related to smallpox. Other revelations about bio-terror ‘research’ in here too. Support my work: https://amazingpolly.net/contact-support.php THANKS! References below.
NYT Mousepox Gain of Function: https://www.nytimes.com/2003/11/01/us/bioterror-researchers-build-a-more-lethal-mousepox.html
Buller Says Vaccine for Monkeypox (using smallpox vax) NOT recommended: https://pubmed.ncbi.nlm.nih.gov/17661673
Buller paper on Monkeypox Outbreaks up to 2012: https://pubmed.ncbi.nlm.nih.gov/23626656/
Judicial Watch re James Leduc / Wuhan: https://www.judicialwatch.org/wuhan-lab-fauci-grants/
National Biocontainment Training Center report by Leduc: https://apps.dtic.mil/sti/pdfs/AD1022067.pdf
The Rise of Hepatitis
By Carla Peeters | Brownstone Institute | May 23, 2022
The number of previously healthy children younger than 16 years of age with mysterious hepatitis cases have doubled in two weeks to 450 cases worldwide, including 11 deaths. Most cases have been reported in the UK (160) and the US (currently, 180). In Europe most cases are found in Italy (35) and Spain (22). Over 8-14% of the patients needed liver transplantation. These children will be on lifelong medication. Until now the real cause of a sudden spark in hepatitis is not clear.
Although 50-72% of the cases tested positive with a PCR test for Adenovirus, tissue and liver samples taken in the UK do not show any typical features that might be expected with a liver inflammation due to this virus.
In the UK, 18% of the reported cases tested positive for SARS-CoV-2 virus and three cases had tested positive 8 weeks prior to admission. The most plausible cause of hepatitis traces to a viral origin. Brodin and Aditi hypothesize a SARS-CoV-2 superantigen mediated immune activation in an Adenovirus-sensitized host.
At this point many of the children with hepatitis are too young to be eligible for COVID-19 vaccination. So far, no common environmental exposure has been found.
Jaundice is characteristic for all children with hepatitis, which could have many reasons including toxins and malnutrition. A search into the peer-reviewed scientific literature on the toxicology of nanoparticles, microplastics, disinfectants and hypercapnia/hypoxia, children have been extensively exposed to during the pandemic makes bio corona formation and accumulation of toxic substances a reasonable explanation for disruption of the liver homeostasis.
The capacity for excessive activation of liver inflammatory pathways has been described for these materials prior to the pandemic. Effects of the complex mixture of these materials and associated chemical pollutants presented have not yet been assessed. Understanding how these materials interact with its biological surroundings during long-term and frequent exposure is of utmost importance.
Pandemic Measures and Liver Toxicity
Early in the pandemic several researchers warned of the unsafe use of facemasks, tests, and disinfectants and their weakening effect on the immune system. Many institutions are starting research on harmful chemicals due to air pollution as they pose a known threat to public health and the economy, representing 10% of global GDP in health costs and 3.75 billion lost working days at the global level in 2060.
Unfortunately, almost no funded research has been started in the area of the safe, cost/benefit use of the mandates. Instead, during the pandemic large amounts of money were spent on less urgent research on non-pandemic related issues.
While Covid-19 was originally thought to be a respiratory infection, various research papers have indicated myocardial inflammation, hepatitis, or neurological experiences independent of severity of Covid-19 and sometimes without evidence of a viral infection. Other researchers found that cardiac damage was more related to clotting and microthrombi were frequent. Almost 25% of people hospitalized develop myocardial injury and many develop arrhythmias or thromboembolic disease.
Lockdowns, with many people experiencing an ongoing state of fear and anxiety and frequent exposure to nanoparticles, microplastics, high CO2 exposure and toxic substances impaired the innate immune system even more.
Furthermore, several studies have indicated a remarkable suppression of the innate immune system after injections with PEGylated lipid nanoparticle (LNP) modified mRNA vaccines. In vivo studies for cytotoxicity and genotoxicity of these vaccines, prior to their release under EUA and being mandated for many people and children, have been neglected.
Unfortunately, more than two years into the pandemic an alarming stage of mysterious rises in infectious and noncommunicable diseases and sudden non-Covid deaths have been reported, even neonatal deaths. The Observer reported one in three people in the UK are experiencing long-term illness.
The Liver Is an Immune Surveillance System
The liver is an important organ responsible for the storage, synthesis, metabolism and redistribution of carbohydrates, fats and vitamins and numerous essential proteins. It is the main detoxification center of the body. A most important organ for generating an effective innate immune response and covering a robust and long-lasting immunity, it works to keep virus, bacteria and excessive inflammations in check.
About 30% of the total blood passes through the liver every minute and is scanned by the mononuclear phagocytic system (MPS) in the liver. The microenvironment in the liver shapes and functions the antigen specific CD4+ T cell population with the capacity for longevity/self-renewal for more than a decade.
High amounts of CD8, Natural Killer T cells, dendritic cells and macrophages (Kupfer cells) in the liver play an important role in the protective innate immune system during injury and infection deciding for tolerance or excessive inflammation. Specific liver cells, hepatocytes, produce 80-90% of the circulating innate immunity proteins in the body including acute phase proteins, complement, bactericidal proteins and more.
Neutrophils, the most abundant leukocytes in the blood, present in the liver perform important functions in inflammation and act as a functional bridge between the innate and adaptive immunity (B cells and T cells) activating antigen specific immune responses.
Homeostatic inflammation is a normal part of a healthy liver. In the complex microenvironment of the liver, the hepatic immune system tolerates harmless molecules while at the same time remaining alert to possible infectious agents, malignant cells or tissue damage. Inflammatory processes are required to rid itself of pathogens, cancer cells or toxic products of metabolic activity. The inflammatory processes are intimately linked to mechanisms that resolve inflammation and promote tissue regeneration.
Excessive and dysregulated inflammatory activity are key drivers of liver pathology, associated with systemic inflammation: chronic infection, autoimmunity and cancer. Mechanisms to resolve liver inflammation are essential to maintain local organ and systemic homeostasis. It is the balance between activation and tolerance that characterizes the liver as a frontline immunological organ. Disrupting this precious surveillance system increases the risk for severe disease and death.
Immune-Liver Disruptors
A possible role of the pandemic measures in excessive inflammation in the human body by immune-liver disruptors is realistic. Independently they may each cause problems of the liver. Serious drawbacks of the measures have become most visible in children, the obese and immunocompromised and the poor.
Nanoparticles (i.e. inhaled graphene oxide, titanium dioxide, Ag from facemasks or swabs) present in the body are cleared from the blood and will preferentially accumulate and sequester in the liver, up to 30-99% from those present in the blood and at much higher quantities as compared to other organs.
Studies in recent years have shown that nanomaterials can modulate and activate neutrophils and other immune cells. Nanomaterials may be considered as a particular case of danger signals that are able to trigger sterile inflammatory responses. Rapid accumulation of nanoparticles in the resident liver macrophages can change the expression of anti-inflammatory genes. Changes of genes related to detoxification and cell cycle have been observed.
Systematically administered nanoparticles may directly interact with circulating erythrocytes leading to erythrocyte aggregation and or hemolysis that is accompanied by hemoglobin release. Surface properties of the nanoparticles are known to play a critical role in nanoparticle-erythrocyte interaction. Most nanoparticles have been known to activate complements by either themselves or through serum proteins. Activation of complements and complement activation pathways could further promote tumor growth.
Nanoparticles develop a specific bio-corona comprising complex and dynamic layers of biomolecules that endow nanoparticles with a new immunological identity.
Studies on polystyrene microplastics (which can be present in facemasks and swabs) showed hepatotoxicity and dysregulation of the lipid metabolism, causing oxidative stress and inflammatory responses. This implicated a potential risk for liver steatosis, fibrosis and cancer and macrophage foam cell formation, a characteristic feature observed during atherosclerosis posing a serious threat to human health.
Another study demonstrated that fish exposed to a mixture of polyethylene with chemical pollutants bioaccumulate the chemical pollutants and suffer liver toxicity and pathology. Moreover 0.1 um microplastics could enter hepatocytes from circulation and result in liver damage even at a low concentration.
Microplastic exposure could induce DNA damage in both nucleus and mitochondria indicating a potential risk of hepatotoxicity and fibrosis. Microplastics are found in the human blood of 80 % of the people tested, in deep lung tissues and human feces.
Covid-19 mRNA vaccines use Acuitas’ PEG (Poly Ethylene Glycol) ylated lipid nanoparticles (LNP). The PEGylated lipids support prolonged circulation and shield the highly inflammatory and cytotoxic effects of the cationic lipids used. If insufficiently shielded by PEG they have been shown to mediate aggregation and interact with and damage the membranes of erythrocytes resulting in hemolysis. PEG content, surface density and conformation of the nanoparticle influence the binding of proteins to a bio corona and the uptake by immune cells.
Despite achieving high dense surface coatings of PEG, no NP formulation has been developed that can completely resist interaction with blood components. Of concern is that 22-25% of individuals who were never exposed to PEGylated therapeutics were found to have PEG antibodies, which is more than two decades ago. PEG coating can improve the penetration of biological barriers including reducing interactions with tissue extracellular matrix cellular barriers and biological fluids such as mucus leading to improved delivery.
After injection of Moderna LNP very low levels could be detected in the brain, potentially indicating that the mRNA LNP could cross the blood brain barrier and reach the Central Nervous System (CNS). Unfortunately, the potential inflammatory nature of these LNPs was not assessed.
In preclinical studies a strong induction of adaptive immune responses by CD4+ T-cell activation and protective humoral immune responses was found. The synthetic ionizable lipid is speculated to have approximately 20-30 days of half-life in humans. It has been shown that plasma protein absorption occurs very rapidly and that it affects hemolysis, thrombocyte activation, cellular uptake and endothelial cell death. The bio corona formation of the PEGylated nanoparticle may change over time.
The increasing number of side effects and reported high potency for eliciting antibody response may partially stem from the LNP’s highly inflammatory nature characterized by leukocyte infiltration and activation of different inflammatory cytokines and chemokines. Antigen-presenting cells presenting vaccine derived peptides/protein might cause tissue damage and exacerbate side effects, which have been linked to autoimmune diseases.
More severe and systemic side effects after the booster shot might be related to an amplification effect of the adaptive immune response induced by the vaccine resulting in high antibody responses. Neutrophils were found to preferentially internalize PEGylated particles in the presence of human plasma. Also, further studies of complement activation in relation to PEG nanoparticles merit rigorous evaluation for immune safe materials. Observational studies found a greater risk for complications following a positive SARS-CoV-2 test. A study of the University of Lund has indicated by in vitro studies that the BNT162b2mRNA vaccine has a fast take-up into human liver cells. In 6 hours of exposure the RNA was reverse transcribed into DNA.
Sennef et al. describes the disruption of the innate immune system by the Covid-19 mRNA vaccines caused by an impaired interferon signaling, release of large amounts of exosomes containing Spike protein, potential disturbances in regulatory control of protein synthesis and cancer surveillance of and their potential direct link to liver disease (with over 2,000 reports in VAERS December 2021) and other inflammatory diseases. The presence of Spike protein has been detected in the blood and 60 days after mRNA vaccine injection in the lymph nodes.
A functional reprogramming of the innate immune responses after BNT 162b2 injection was also observed by Fohse et al. with a lower response of innate immune cells, while the fungi-induced cytokine responses were stronger. A study on Biovrix by Nguyen et al. demonstrated an impaired lipid metabolism and increased lipotoxicity by the Spike protein. Jiang et al observed that the Spike protein localizes in the nucleus and inhibits DNA damage repair by impeding key DNA repair protein recruitment to a damaged site. A mechanism by which the spike protein might impede the adaptive immunity explaining the potential side effects. Suraswaki et al. stated that the virus itself may dysregulate the innate cellular defenses using various structural and nonstructural proteins.
Taking Back Control of Our Bodies
The European Commission Statement from May 12, 2022, announces to shorten (from 300 to 100 days) the product to market cycle to develop safe and effective vaccines, therapeutics, and diagnostics following the identification of new threats and work to make them widely available.
As discussed, the Covid-19 pandemic measures have shown to be far from safe. All materials are known to interact and bind proteins forming bio corona’s depleting the body of essentials for processes to function properly.
Subtle changes in materials and biological fluids of persons can significantly change the protein composition of the bio corona and can either lead to an excessive inflammation or resilient homeostasis. Especially in children who need more proteins, vitamins and minerals for mental, physical, and immune system development, the accumulation of toxic substances in the liver and formation of bio corona can be a serious threat to health.
At this stage, it is not known whether the mysterious rises in diseases are caused by a virus or an intoxication and/or depletion of essentials that result in impaired signaling routes. The Covid-19 routine diagnostic tests used for mass testing have major flaws which make it impossible to ensure the presence of an infectious virus as a single cause of symptoms.
An increasing number of doctors and researchers agree: the pandemic is over. All pandemic measures need to be halted immediately. The highest priority is lifting the mandates for children. Healthy children always had a very low risk for severe Covid-19 and are protected by a strong robust and long-lasting natural immunity. There is no added value to vaccinate any person with natural immunity. Moreover, the risk for side effects of the mRNA vaccine for children is high. mRNA Covid vaccine accumulates in the liver 30 minutes after it is injected.
Deep investigations on quality, reproducibility and contaminations of the materials of personal protective equipment, facemasks, tests, disinfectants and vaccines, being used with their effects on the human body and the environmental ecosystem need to be prioritized and funded.
During the past two years, the immune system of many people has been harmed and even broken. We need programs to regenerate the liver and immune system so people can face with trust and confidence any possible wave of virus attacks.
Carla Peeters is founder and managing director of COBALA Good Care Feels Better. She obtained a PhD in Immunology from the Medical Faculty of Utrecht, studied Molecular Sciences at Wageningen University and Research, and followed a four-year course in Higher Nature Scientific Education with a specialization in medical laboratory diagnostics and research. She studied at various business schools including London Business School, INSEAD and Nyenrode Business School.
Inclusion, Wokeness, and Davos 2022
By Richard Hugus | May 23, 2022
The picture above is of a sign outside a performing arts theater in Santa Barbara, California. Looks like everyone is welcome. Well, not really. It turns out that if you’re not “vaccinated” you’re not welcome. If you haven’t arrived at the ticket booth with ID and proof of being injected with two doses of an emergency use experimental gene treatment for “covid 19” — a treatment which has no efficacy and is associated with millions of serious injuries and deaths — this #LoveForAll message doesn’t actually apply to you. If you’re not “vaccinated” the only way you can get into the theater now is if you have taken a test proving you don’t have the plague. Don’t want a PCR swab up your nose? Too late for an antigen test? Tough luck. This rainbow venue welcomes EVERYONE, except for carriers of the plague.
“Who doesn’t love LOVE?” Apparently, the state of North Carolina doesn’t. The founder of Insist On Love For All which makes and sells the $60 sign displayed above, took a trip to Asheville, North Carolina a few years ago and was impressed by signs “embracing diversity.” Says Insist On Love’s founder,
shop owners started displaying these signs over two years ago [2018] to encourage tourism following the passage of the controversial House Bill 2 in North Carolina, which requires certain public bathrooms to be designated for use by males or females based on their biological sex. “The signs in Asheville moved me. Love is the only weapon we can use to fight hate . . . “
In this case, “hate” was displayed by 1) the idea that men and women should have separate bathrooms, 2) the idea that men (or men who think they’re women) don’t have a right to walk into women’s bathrooms, and vice versa, 3) the fact that other sexes besides male and female have not been acknowledged, and 4) the fact that the state of North Carolina thus discriminated against all those who don’t have male/female privilege. There is also the ‘hate’ involved in the unwillingness of North Carolina to provide separate bathrooms for a theoretically unlimited number of other genders. Unless #LoveForAll is somehow a front for a consortium of plumbing supply companies (this would actually be comforting news), there is nothing left for us to conclude but that ‘love’, as the term is being used here, is indeed a weapon, not to fight hate, but to fight reason. ‘Love’ is now a buzzword in a well-established “diversity and inclusion” narrative sent down from academic critical theory to the progressive left to the mainstream media to the culture at large. Has there ever been a time when good things have been so twisted into their opposite? This is not about love or inclusion. This is shallow virtue signaling by people who have been swallowed up by a political machine designed to turn cultural norms upside down, not for the purpose of bringing needed change, but for the purpose of creating chaos and a loss of rationality, after which new supposed norms can just be lifted into place.
“All sexual orientations”, cited in the sign, is also a topic at the current May 22-28 Davos forum, where “resilience through equity” and “inclusivity” for the “LGBTQI+ community” is on the formal agenda. Do the corporate bosses, social engineers, and preening politicians at this forum really care about equality, or are they just using the brand to create the upheaval necessary to bring in fantastic profits and power? The answer is obvious. The agenda is exclusion, not inclusion; fascism, not liberalism. Their plan is for the majority of humanity, gay or straight, to be excluded from their rights, autonomy, and independence, while the bosses enjoy their wealth and slave labor. Like #LoveForAll, everyone is welcome in the Great Reset except those who believe there are only two sexes — that is, just about everybody since the beginning of human history. Everyone is welcome in virtue-signaling countries, corporations, and institutions except those who choose not to accept a medical intervention also never heard of before in human history — that of altering the human genome on the pretext of defeating a virus. In other words, everyone is welcome except those who have chosen not to go insane. The insanity is called wokeness. Wokeness is nothing but a tool being used to effect a very ugly and very ambitious power grab. When the job is done, everyone duped into thinking they were fighting for the victims of oppression and equality for all will be swatted away like flies.
The would-be gods at Davos brought us their own version of the Apocalypse — plague, war, famine, and death became covid, Ukraine, food shortages, and vaccines. Do such people even remotely care about racial prejudice and gender dysphoria? No. They either massively exploited or completely made up these issues to create disorder. Indeed, their eugenicist predecessors had certain, ahem, opinions about people with disabilities, sexual deviants, and racial groups which they know can’t be mentioned in polite society today. So they went the other way. Not believing in God, the Davos elite see themselves as gods. The further this delusion takes them, the harder they will fall. There will also come a time of reckoning for the collaborators in this program — those who, wittingly or not, aided this monstrosity. Galling self-righteousness, ignorance, and hypocrisy were the least of the crimes in this class. The ones higher up — those who made the plans, gave the orders, and knew what they were doing — face a reckoning that perhaps we do not have words for. It may be a regular new round of guillotining such as we have seen before in history. Or it may be that this time wickedness has gone so far it will have to be ended forever. Prospects for the Davos crew do not look good.
FDA Dumps More Pfizer Documents: Why Were So Many Adverse Events Reported as ‘Unrelated’ to Vaccine?
By Michael Nevradakis, Ph.D. | The Defender | May 17, 2022
The latest release of Pfizer-BioNTech COVID-19 vaccine documents raises questions about how frequently adverse events experienced by clinical trial participants were reported as “unrelated” to the vaccine.
The 80,000-page document cache released May 2 by the U.S. Food and Drug Administration (FDA) includes an extensive set of Case Report Forms (CRFs) from Pfizer trials conducted at various locations in the U.S.
The documents also include the “third interim report” from BioNTech’s trials conducted in Germany (accompanied by a synopsis of this report and a database of adverse events from this particular set of trials).
The FDA released the documents, which pertain to the Emergency Use Authorization (EUA) of the vaccine, as part of a court-ordered disclosure schedule stemming from an expedited Freedom of Information Act (FOIA) request filed in August 2021.
Public Health and Medical Professionals for Transparency, a group of doctors and public health professionals, submitted the FOIA request.
Adverse events during Pfizer vaccine trials in the U.S. usually reported as ‘unrelated’ to vaccination
Pfizer conducted a series of vaccine trials at various locations in the U.S., including the New York University Langone Health Center, Rochester Clinical Research and Rochester General Hospital (Rochester, New York) and the J. Lewis Research, Inc. Foothill Family Clinic (Salt Lake City, Utah).
The Pfizer documents released this month by the FDA included a series of CRFs for patients who suffered some type of adverse event during their participation in the COVID-19 vaccine trials.
As the documents reveal, despite the occurrence of a wide range of symptoms, including serious cardiovascular events, almost none were identified as being “related” to the vaccine.
Such serious yet “unrelated” adverse events included:
- Acute asthma exacerbation
- Aortic aneurysm (listed as a pre-existing condition)
- Appendicitis (requiring hospitalization)
- Atrial defibrillation
- Cardiac arrest and acute respiratory failure, requiring hospitalization, sustained by a patient who then was “lost” (could not be located for continued participation in the trial)
- Chest pain (requiring hospitalization, later listed as cardiac ischemia)
- Coronary artery occlusion (listed as both serious and life-threatening)
- Injuries sustained from a fall
- Intermittent non-cardiac chest pain (requiring hospitalization)
- Left breast cancer (listed as a pre-existing occult malignancy)
- Neuritis (peripheral nerve Injury), listed as “unrelated” to the vaccine but related to the blood draw during vaccination
- Pulmonary embolism and bilateral deep venous thrombosis
- Respiratory failure (requiring hospitalization)
- Right ureteropelvic junction obstruction (requiring hospitalization, listed as congenital)
- Small bowel obstruction, listed as “unplanned,” and a panic attack
Of the CRFs found in the documents released this month, only one adverse event is clearly specified as being related to the vaccination: a participant who suffered from psoriatic arthritis, with no prior history of the condition.
In addition, several CRFs indicated exposure during pregnancy (see here and here), or during a partner’s pregnancy (see here and here). However, the documents provided do not appear to have provided any follow-ups regarding any outcomes or potential adverse events for the participants, their partners or their newborn babies once born.
In some instances, while the CRFs claimed the adverse events suffered by patients were not related to the vaccine, their cause was unspecified, simply indicated as “other,” while in another case, a participant’s “unplanned” small bowel obstruction and panic attacks were listed as being unrelated to the vaccination despite no relevant medical history pertaining to the SAEs (severe adverse events) in question.
Did Pfizer hide critical information from regulators?
It is difficult to draw concrete conclusions about any specific case from the data provided by CRFs and vaccine trial summaries.
However, what raises eyebrows is the very large number of adverse events — often serious and often requiring the hospitalization of the patients involved — that were determined to be “unrelated” to the administration of the COVID vaccine.
Previously released Pfizer documents also included discrepancies in the recording of adverse events.
According to investigative journalist Sonia Elijah, these discrepancies include:
- Trial participants were entered into the “healthy population” but were, in actuality, far from healthy.
- SAE numbers were left blank.
- Barcodes were missing from samples collected from trial participants.
- The second vaccine dose was administered outside the three-week protocol window.
- New health problems were dismissed as “unrelated” to the vaccination.
- A remarkable number of patients with an observation period of exactly the same duration — 30 minutes, with very little variety in observation times and raising questions as to whether patients were adequately observed or were put at risk.
- Oddities pertaining to the start and end dates of SAEs – for instance, a “healthy” diabetic suffered a “serious” heart attack on October 27, 2020, but the “end” date for this SAE is listed as the very next day, even though the patient was diagnosed with pneumonia that same day.
- Impossible dating: in the aforementioned example of the patient who sustained a heart attack and pneumonia, the individual in question later died, but the date of death is indicated as the day before the patient was recorded as having gone to a “COVID ill” visit.
- Unblinded teams, who were aware of which patients received the actual vaccine or a placebo, were responsible for reviewing adverse event reports, potentially leading to pressure to downplay COVID-related events in the vaccinated, or to indicate that adverse events were related to the vaccine.
- Other adverse events were indicated as “not serious” despite extensive hospital stays, of up to at least 26 days in the case of one patient who suffered a fall which was classified as “not serious,” yet facial lacerations sustained as a result of the fall were attributed to hypotension (low blood pressure).
Many of these practices seem to appear in the trial-related documents released this month.
Medical and scientific experts who spoke to The Defender expressed similar concerns about what this month’s tranche of documents reveals, and addressed cases of “disappearing” adverse events.
Brian Hooker, chief scientific officer for Children’s Health Defense, remarked:
“I’m most concerned about ‘disappearing’ patients. One cannot conduct a valid trial and simply omit the results that they don’t like!
“With the stories about Maddie de Garay and Augusto Roux surfacing, I have to wonder how many other participants were dropped in order to hide vaccine adverse events/effects.
“If you look at the data in VAERS [Vaccine Adverse Event Reporting System], COVID-19 vaccines are the most dangerous ever introduced into the population.”
Dr. Madhava Setty, a board-certified anesthesiologist and senior science editor for The Defender, said:
“The ‘unrelated’ label the investigators use to divert attention from AEs [adverse events] is a powerful point that stands on its own. We haven’t pushed back on this enough.
“Equivalently, we can say that the meager and short-lived benefit of these shots is also ‘unrelated’ using their ‘standards.’ On what grounds can they say that their product is preventing infection (which it isn’t anymore), or death (marginally)?
“They cannot have it both ways. They cannot claim a benefit through short-term outcomes while denying that side effects of any kind are related to their product.
“That’s the whole point of doing a trial. You cannot prove causation, only statistically significant correlation.”
Setty provided further context for his remarks in an April 2022 article for The Defender and in a March 2022 presentation, in which he discussed the number of these adverse events and how Pfizer swept them away (timestamp 24:00).
In Setty‘s view:
“There’s a high likelihood of malfeasance going on. [Pfizer whistleblower] Brook Jackson says the PIs [principal investigators] were unblinded. If true, it would make it very easy for the investigators to bump up the AEs in the placebo group while ignoring some of the AEs in the vaccine group.
“Pfizer claims that 0.5% of placebo recipients suffered a serious adverse event compared to 0.6% in the vaccine group. This is how these events were obscured.”
The extant body of evidence indicates Pfizer “is hiding critical information from regulators,” Setty said:
“The clincher is in the memorandum to the VRBPAC [Vaccines and Related Biological Products Advisory Committee] (Table 2, efficacy populations), where they show us that five times more people in the vaccine group were pulled out of the trial than the placebo within seven days of their second shot for ‘important protocol deviations.’
“In a trial that big the chances that could have happened coincidentally is infinitesimally small (less than 1 in 100,000).
“Moreover, months later, the same thing happened in the pediatric trial (Table 12). This time, six times more children were pulled from the trial after their second dose.
“There are, of course, procedural differences when administering a placebo versus the mRNA vaccine, but why didn’t it happen after the first dose as well?
“Mathematically, that is about as close as you can get to eliminating any ‘shadow of doubt.’ With a formal allegation by a trial coordinator that states the same thing [referring to whistleblower Brook Jackson], we can be assured Pfizer is hiding critical information from regulators.”
BioNTech trials in Germany claim few adverse events ‘related’ to vaccine
The BioNTech trial in Germany tested various dosages of two COVID-19 vaccine formulas, labeled BNT162b1 and BNT162b2 — the latter granted EUA by the FDA.
The latest cache of Pfizer documents suggests a pattern, similar to the one in the U.S. trials, of not reporting adverse events as related to the vaccine.
According to the third interim report, dated March 20, 2021, among trial participants who were administered the BNT162b2 candidate vaccine granted EUA in the U.S.:
- 87% of younger participants reported solicited local reactions, and 88% reported solicited systemic reactions, with 10% reporting solicited systemic reactions of Grade 3 or higher.
- 87% of younger participants experienced “mild” solicited local reactions, and 35% experienced “moderate” solicited local reactions.
- 88% of younger participants experienced “mild” solicited systemic reactions, and 38% experienced “moderate” solicited systemic reactions. As stated in the report:
“The most frequently reported solicited systemic reactions of any severity were fatigue (n=40, 67%), followed by headache (n=32, 53%), malaise (n=24, 40%), and myalgia (n=23, 38%). The remaining symptom terms were less frequent.
“For nausea, headache, fatigue, myalgia, chills, arthralgia and malaise each symptom was assessed as severe in <10% of participants.”
- 43% of younger participants reported a total of 51 unsolicited TEAEs (treatment-emergent adverse events, referring to conditions not present prior to treatment or that worsened in intensity after treatment) within 28 days of the first or second dose, nine of which were deemed to be “related” to the vaccination. One participant in this category sustained a TEAE assessed as Grade 3 or higher, but “which was assessed as not related by the investigator.”
- TEAEs among younger participants included hypoaesthesia, lymphadenopathy, heart palpitations, external ear inflammation, blepharitis, toothache, non-cardiac chest pain, cestode infection, oral herpes, tonsillitis, neck pain, insomnia, anosmia and dysmenorrhea.
- No unsolicited treatment-emergent serious adverse events (TESAEs) or deaths were reported among younger participants, but one discontinued participation due to moderate nasopharyngitis.
- One younger participant “discontinued due to a moderate AE (nasopharyngitis).”
- 86% of older participants reported solicited local reactions, with 6% reporting solicited local reactions of Grade 3 or higher, 78% reporting “mild” solicited local reactions and 36% reporting “moderate” solicited local reactions.
- 72% of older participants reported solicited systemic reactions, with 11% of these participants sustaining solicited systemic reactions of Grade 3 or higher, 69% sustaining “mild” solicited reactions and 36% sustaining “moderate” solicited reactions.
- 33% of older participants reported a total of 20 unsolicited TEAEs, four of which were determined to be “related” to the vaccination. Among older participants, 8% reported a TESAE of Grade 3 or higher, with “one event assessed as related by the investigator.”
- One older participant was reported to have sustained a “not related TESAE” (an ankle fracture).
- TESAEs among older participants included back pain, chest pain, facial injury, increased lipase, increased amylase, muscle spasms, musculoskeletal pain, tendon pain, orthostatic intolerance, renal colic, seborrhoeic dermatitis and “painful respiration.”
Among trial participants who received the BNT162b1 candidate vaccine (not granted EUA):
- 86% of “younger participants” reported solicited (expected) localized reactions (remaining in one part of the body), with 18% reporting Grade 3 or higher solicited local reactions, 86% of younger participants reporting “mild” solicited local reactions and 54% reporting “moderate” solicited local reactions.
- 92% of younger participants reported solicited systemic reactions (spreading to other parts of the body), with 44% reporting Grade 3 or higher solicited systemic reactions, 90% reporting “mild” solicited systemic reactions and 74% experiencing “moderate” solicited systemic reactions.
The report states:
“The most frequently reported solicited systemic reactions of any severity were fatigue (n=68, 81%), headache (n=66, 79%), myalgia (n=51, 61%), malaise (n=50, 60%), and chills (n=47, 56%). The remaining symptom terms were less frequent.
“For nausea, vomiting, diarrhea, myalgia, arthralgia and fever each symptom was assessed as severe in ≤10% of participants.”
- 45% of younger participants reported a total of 83 unsolicited (unexpected) TEAEs within 28 days of receiving the first or second dose.
A total of 51 of these unsolicited TEAEs were reported as “related” to the vaccination, while 2% of participants sustained Grade 3 or higher TEAEs (four in total), “of which three events were assessed as related by the investigator.”
No unsolicited TESAEs or deaths were reported in this category.
- According to the report, among younger participants, TEAEs included:
“‘General disorders and administration site conditions’ reported by 9 participants (11%),” including influenza-like illness and injection site hematoma.
“‘Nervous system disorders’ reported by 10 participants (12%),” including presyncope, hyperaesthesia, paraesthesia, and headache.
“‘Respiratory, thoracic and mediastinal disorders’ reported by 9 participants (11%),” including cough and oropharyngeal pain.”
Other symptoms included back pain, musculoskeletal chest pain, cervicobrachial syndrome, taste disorder, sleep disorder, depression, hallucination, dysmenorrhoea, pruritus and pityriasis rosea, while one participant required the excision (removal) of a papilloma.
- One younger participant discontinued participation in the trial, “due to a moderate AE (malaise),” while another participant discontinued participation “due to dose-limiting toxicity.”
- 83% of “older participants” reported solicited local reactions, but none were reported as Grade 3 or higher, while 83% of solicited local reactions were “mild” and 42% were “moderate.”
- 92% of older participants reported solicited systemic reactions, with 28% of participants experiencing Grade 3 or higher solicited systemic reactions, 89% experiencing “mild” solicited systemic reactions, and 61% experiencing “moderate” solicited systemic reactions.
According to the report:
“The most frequently reported solicited systemic reactions of any severity were headache (n=29, 81%), fatigue (n=27, 75%), myalgia (n=18, 50%), and malaise (n=18, 50%). The remaining symptom terms were less frequent.”
- 36% of participants reported a total of 24 unsolicited TEAEs within 28 days of the first or second dose, nine of which were assessed as “related” to the vaccination.
Of the participants in this category, 11% reported TEAEs of Grade 3 or higher (four events in total), with one of these events assessed as “related” to the vaccination.
- TEAEs reported by older participants included oropharyngeal pain, nasopharyngitis, bladder dysfunction, sleep disorder, musculoskeletal pain and musculoskeletal chest pain, pollakiuria, migraine, syncope and alopecia.
- One older participant receiving the BNT162b1 candidate sustained a TESAE (syncope), and there were no deaths in this category.
Of note, none of the participants for either vaccine candidate were pregnant, which raises questions about recommending and administering the vaccine to pregnant women despite the absence of any clinical trial data.
As the documents show, a wide range of adverse effects were reported, including cardiovascular and nervous system conditions, most of which were determined to be unrelated to the vaccination itself.
Michael Nevradakis, Ph.D., is an independent journalist and researcher based in Athens, Greece.
© 2022 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
South Australia introduces prospect of jail time for breaking strict Covid restrictions
By Dan Frieth | Reclaim The Net | May 20, 2022
The state government of South Australia is about to introduce the harshest penalties in the nation, and some of the most severe in the world, for those breaking Covid restrictions.
The regulations, which are coded in the Public Health Act, mandate that citizens that break isolation rules or fail to abide by vaccine passport and mask mandates are subject to a fine of $20,000 or two years in prison.
Businesses that are in noncompliance with the law face an even bigger fine of $75,000. The law is expected to pass Parliament this week and applies to those who break Covid regulations in high-risk settings. Upon passage, regulations codified in the Public Health Act would take effect on June 30.
The tough regulations have drawn sharp criticism from some members of South Australia’s Parliament and civil liberties groups. Despite this disapproval, Premier Peter Malinauskas, a Labour Party member, says that the new law is necessary to protect the state’s most vulnerable residents. Continuing, Malinauskas adds that Australia is in a stage of the pandemic where governments need to once again conduct basic services in a normal manner, thus necessitating the codification of Covid laws.
Those who oppose the new law not only criticize its tough penalties but how it was passed by Parliament.
Referring to the law as a “backroom deal,” Adelaide Advertiser of the Liberal Party condemned it as a way for Malinauskas to quickly incarcerate rule breakers. The Law Society of South Australia also criticizes the law as being overly vague.
The group’s head, Justin Stewart-Rattray, says that the act fails to provide an adequate definition of what constitutes a close contact. Examining Australian regulations since the start of the pandemic, Stewart-Rattray points out that the definition of close contact has changed several times throughout the crisis.
Given how unclear the law is, Stewart-Rattray says that enforcement could be too wide, leading to rampant abuse of power and loss of rights for accused citizens.
Why the World should be very concerned about New Zealand under the Jacinda government
By Guy Hatchard | Waikanae Watch | May 19, 2022
The New Zealand government relies upon a science body known as Te Punaha Matatini (Centre for Science in Society) whose work is funded directly by the office of the Prime Minister and cabinet.
Yesterday, Te Punaha Matatini published a 21-page document entitled “The Murmuration of Information Disorders” (see attached release from the Science Media Centre) designating those opposed to the government’s pandemic policies as violent right wing insurrectionists planning the weaponised storming of parliament and the execution of public servants, academics, journalists, politicians, and healthcare workers.
This is an utterly false characterisation worthy of the worst excesses of historical propaganda.
This 21-page document, represented to the public as a scientific paper, contains not a single discussion of the scientific concerns being raised in opposition to government pandemic policy.
It omits for example analyses of the government’s own official figures which show that the vaccinated are more vulnerable to infection, hospitalisation, and death than the unvaccinated, a fact that has been deliberately hidden from the public.
Prime Minister Jacinda Ardern introduced yesterday’s Te Punaha Matatini report with the words:
“One day it will be our job to try and understand how a group of people could succumb to such wild and dangerous mis- and disinformation. And while many of us have seen that disinformation and dismissed it as conspiracy theory, a small portion of our society have not only believed it, they have acted upon it in an extreme and violent way that cannot stand. We have a difficult journey in front of us to address the underlying cause.”
Since when do reasonable scientifically-based questions asked of the government in good faith constitute violent insurrection?
I am tempted to think that Ardern could just as well be talking about her own government. The Prime Minister and the social scientists(?) working at Te Punaha Matatini might do well to read the New York Times, (although they probably don’t do so because the official policy of the New Zealand government is to discourage any information that is not sanctioned and edited by themselves).
A NYT article on 10 May 2022 entitled “Emergent Hid Evidence of Covid Vaccine Problems at Plant” reports that
“Emergent BioSolutions, a longtime government contractor hired to produce hundreds of millions of coronavirus vaccine doses, hid evidence of quality control problems from Food and Drug Administration inspectors in February 2021 — six weeks before it alerted federal officials that 15 million doses had been contaminated.”
A reasonable observer might conclude that early (and later) concerns being voiced about vaccine safety were justified, but the New Zealand government is far from reasonable.
A succession of scientific papers published in reputable journals during recent weeks (which we and many others have reported extensively and communicated directly to the government) have in fact fully justified concerns about safety and efficacy, but unbelievably our government is in denial and still moving ahead with propaganda advertising of their mRNA vaccination agenda for all ages and, as today’s Te Punaha Matatini report shows, labelling any opposition as a conspiracy with violent aims.
How Did the Transformation of the NZ Government Come About?
New Zealand has a small population of 5 million, but it has been used to trial new products in order to gauge what the public reaction and acceptance might be in bigger markets overseas. Never more so than during the pandemic. Take up of the Pfizer mRNA Covid vaccination has reached up to 95% of the eligible population.
This has been achieved through a transformation in the style of government, media control, science funding, intellectual standards, and international relations unprecedented in the western world, along with the coercion of draconian employment mandates and the pursuit of dissenters through compliant courts.
This has been engineered under the leadership of a person with a bachelor’s degree in communication who grew up in a strict rural Mormon household and cut her political teeth under the Blair administration in London. In keeping with her upbringing and education, Ardern is a leader who is sure she is right and is prepared to enforce her orthodoxy against all opposition and reason.
Her international perspective is one of unquestioning acceptance of the authority and right to rule of global institutions. Her top confidant and mentor Helen Clark, former NZ Labour Prime Minister, is closely associated with this outlook. Ardern recounts that she begins her day with a discussion with Clark over breakfast.
Like Ardern, Clark is renowned for her iron fist management style. She ruffled feathers at the United Nations Development Programme, which she led from 2009 to 2017, reportedly undermining human rights and supporting China’s Belt and Road initiative.
On 9 July 2020 the World Health Organization (WHO) appointed Clark as co-chair of a panel reviewing the WHO’s handling of the COVID-19 pandemic and the response of governments to the outbreak. The Independent Panel for Pandemic Preparedness and Response (IPPR) examined how the outbreak occurred and how future pandemics can be prevented.
Nothing says more about the overt global agenda of Ardern and Clark than this 11 May 2022 statement of the New Zealand government:
“The establishment of a pandemic treaty/instrument was a key recommendation of the Independent Panel for Pandemic Preparedness and Response and is one of New Zealand’s foremost global health priorities”
Like China, New Zealand’s fading international reputation for successful management of the pandemic was actually built on a single policy—control the borders, restrict entry, and impose lengthy quarantine.
The Current Situation in New Zealand is Deeply Concerning
Ardern controls the media and the science dialogue through a mixture of government funding and exclusion of dissent. The government has spent big on saturation advertising advising complete safety and efficacy of the Pfizer vaccine, and continues to do so.
It has instituted funding of cultural groups, GPs, and commercial organisations who promote vaccination. The level of funding is so generous that it has distorted prior long standing economic and political relationships.
So far the government has spent on the order of $100 billion on the pandemic in addition to normal expenditure. To put this in stark perspective, that is equal to the total annual government budget prior to the pandemic—more than $20,000 for every man, woman, and child. This is borrowed money which will have to be repaid through increased taxation of an already struggling population.
We Have No Constitution in New Zealand, the Power of the Government Is Absolute.
The control that Ardern’s government exercises over the courts, government agencies, parliament, media, independent regulators, and over the vast majority of the population is staggering and rigidly enforced. Dissenting medical professionals are excluded from practicing and in some cases prosecuted also. They are also mercilessly hounded and vilified by bought mainstream media.
In an atmosphere of strict government control, more worrying aspects of information control have emerged. In some cases noted by my scientific colleagues, policy and pronouncements that they have demonstrated are in conflict with published research have disappeared from the public record.
Even rare court rulings in favour of caution have been rapidly bypassed by simply passing new laws without debate. Court rulings about mandates have also been openly flouted, as happened when the military vaccine mandate was ruled illegal. With the support of the government, the military said the courts had no jurisdiction over its operation and went ahead anyway.
Ardern has introduced her policies in such a dedicated, persuasive, secretive, and complete way that almost the whole population of New Zealand has complied. They have accepted limitations on medical choice, judicial protections, human rights, press freedom, freedom of information, privacy, employment conditions and opportunities, standard of living, and social interaction.
Ardern’s successful efforts to persuade the population that government should be your only source of truth, have all but negated any of the longstanding mechanisms of government accountability. A majority of the population have all but concurred with Ardern that the unvaccinated may be safely blamed for every government failing and omission; and for all Covid case loads, hospitalisations, and deaths contrary to all evidence.
The opposition parties have apparently accepted that they will in future go about their business using the same Ardern doctrines and techniques. Accordingly they have failed to sound the alarm, investigate Covid science publishing deeply, or oppose draconian legislation. They have joined Ardern in labelling peaceful protest as unacceptable and illegal.
Ardern on the Global Stage
Ardern is about to deploy her international political capital to promote the globalisation of her policies and outlook. Her public persona can be deceptively mesmerising. You should be worried.
The world’s economy also has no constitution. So far Ardern appears to be happy to allow it to be controlled by global economic predators. Pfizer has been uncritically promoted by her, and the notion of WHO control over New Zealand’s sovereign rights is being welcomed with open arms. It fits with her strict hierarchical perspective.
Ardern may be viewed by naive foreign governments as a pandemic success story unfairly criticised in her own country. Stop for a moment and consider that she is about to lend her support to the promotion of a new world order on the global stage using her trademark persuasive techniques of propaganda, coercion, and control of information.
VAERS Data Show New Deaths, Injuries After COVID Vaccines, As CDC Signs Off on 3rd Shot for Kids 5-11
By Megan Redshaw | The Defender | May 20, 2022
The Centers for Disease Control and Prevention (CDC) today released new data showing a total of 1,268,008 reports of adverse events following COVID-19 vaccines were submitted between Dec. 14, 2020, and May 13, 2022, to the Vaccine Adverse Event Reporting System (VAERS).
VAERS is the primary government-funded system for reporting adverse vaccine reactions in the U.S.
The data included a total of 28,141 reports of deaths — an increase of 173 over the previous week — and 230,364 serious injuries, including deaths, during the same time period — up 1,887 compared with the previous week. There were 6,859 additional total adverse events reported to VAERS over the previous week.
Excluding “foreign reports” to VAERS, 817,538 adverse events, including 12,961 deaths and 82,544 serious injuries, were reported in the U.S. between Dec. 14, 2020, and May 13, 2022.
Foreign reports are reports foreign subsidiaries send to U.S. vaccine manufacturers. Under U.S. Food and Drug Administration (FDA) regulations, if a manufacturer is notified of a foreign case report that describes an event that is both serious and does not appear on the product’s labeling, the manufacturer is required to submit the report to VAERS.
Of the 12,961 U.S. deaths reported as of May 13, 16% occurred within 24 hours of vaccination, 20% occurred within 48 hours of vaccination and 59% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
In the U.S., 581 million COVID-19 vaccine doses had been administered as of May 13, including 343 million doses of Pfizer, 219 million doses of Moderna and 19 million doses of Johnson & Johnson (J&J).
Every Friday, VAERS publishes vaccine injury reports received as of a specified date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.
Historically, VAERS has been shown to report only 1% of actual vaccine adverse events.
U.S. VAERS data from Dec. 14, 2020, to May 13, 2022, for 5- to 11-year-olds show:
- 10,745 adverse events, including 279 rated as serious and 5 reported deaths.
- 22 reports of myocarditis and pericarditis (heart inflammation).The CDC uses a narrowed case definition of “myocarditis,” which excludes cases of cardiac arrest, ischemic strokes and deaths due to heart problems that occur before one has the chance to go to the emergency department.The Defender has noticed over previous weeks that reports of myocarditis and pericarditis have been removed by the CDC from the VAERS system in this age group. No explanation was provided.
- 43 reports of blood clotting disorders.
U.S. VAERS data from Dec. 14, 2020, to May 13, 2022, for 12- to 17-year-olds show:
- 31,572 adverse events, including 1,824 rated as serious and 44 reported deaths. VAERS reported 44 deaths in the 12- to 17-year-old age group last week.
- 64 reports of anaphylaxis among 12- to 17-year-olds where the reaction was life-threatening, required treatment or resulted in death — with 96% of cases attributed to Pfizer’s vaccine.
- 651 reports of myocarditis and pericarditis with 639 cases attributed to Pfizer’s vaccine.
- 168 reports of blood clotting disorders with all cases attributed to Pfizer.
U.S. VAERS data from Dec. 14, 2020, to May 13, 2022, for all age groups combined, show:
- 20% of deaths were related to cardiac disorders.
- 54% of those who died were male, 41% were female and the remaining death reports did not include the gender of the deceased.
- The average age of death was 73.
- As of May 13, 5,527 pregnant women reported adverse events related to COVID-19 vaccines, including 1,732 reports of miscarriage or premature birth.
- Of the 3,622 cases of Bell’s Palsy reported, 51% were attributed to Pfizer vaccinations, 40% to Moderna and 8% to J&J.
- 880 reports of Guillain-Barré syndrome, with 42% of cases attributed to Pfizer, 30% to Moderna and 28% to J&J.
- 2,291 reports of anaphylaxis where the reaction was life-threatening, required treatment or resulted in death.
- 1,707 reports of myocardial infarction.
- 13,972 reports of blood-clotting disorders in the U.S. Of those, 6,266 reports were attributed to Pfizer, 4,989 reports to Moderna and 2,679 reports to J&J.
- 4,194 cases of myocarditis and pericarditis with 2,570 cases attributed to Pfizer’s, 1,427 cases to Moderna’s and 183 cases to J&J’s COVID-19 vaccines.
Children’s Health Defense (CHD) asks anyone who has experienced an adverse reaction, to any vaccine, to file a report following these three steps.
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The Mysterious Death of UN Secretary General Dag Hammarskjold
By Lisa Pease | Consortium News | September 16, 2013
More than a half century ago, just after midnight on Sept. 18, 1961, the plane carrying UN Secretary-General Dag Hammarskjöld and 15 others went down in a plane crash over Northern Rhodesia (now Zambia). All 16 died, but the facts of the crash were provocatively mysterious. … continue
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