See detailed report at foot of this post. The European database of suspected drug reaction reports is EudraVigilance, which tracks reports of injuries and deaths following the experimental COVID-19 “vaccines.”
These are some of the mechanisms for Covid vaccine-induced deaths and injuries.
This post is a useful primer to the complex multiple dangers. Despite the technical language the post gives us links and some idea of the many potential disasters that may be unfolding from the ‘experimental’ vaccines.
We also post it as a follow up to the widely read Salk Institute exposé HERE. Various pro-vaxxers have denied the suggestion by anti-vakkers that the billions of Spike Proteins in the vaccines could also get into our vascular system, (as they do according to Salk and others, in the actual virus), causing potentially terrible long term injuries, also to the brain. They cite the changes made in the spike proteins in the vaccines to stabilize them for effectivity. Hopefully they are right but even the Nature study or official safety reports make no mention of these changes as safety features, and the vascular connection was unknown or ignored. So we don’t know.. but there is more, much much more…
|Scam of the Century? Covid levels totally Falsified by manipulation of PCR’s CT level.. 3 times now! Edit | Classic Editor ||
Mechanisms of COVID-19 Vaccine Induced Injuries/Deaths
UPDATE 1: I’ve expanded the second half of the article to include many more mechanisms that I’m aware of but didn’t include in the original version.(note: We have put the 2 updates at the foot of the article so as not to scare off readers! With them its really 12 dangers listed.) note: SARS-CoV-2 is the same as Covid-19
A study on UK government’s website, dated Apr 2021, conducted by the ISARIC4C consortium, found that among the hospitalized COVID patients who had ALREADY BEEN VACCINATED, the onset of symptoms is most commonly from the day of vaccination to 3 days after that. The onset is 5x as frequent ON the day of the vaccination as the day BEFORE vaccination! 
The preferred mainstream explanation is blaming behavioural change – they assume that those who had been vaccinated shielded & isolated less. Yet they have no evidence to back that up. Crucially, “No one is suggesting there was a change of behaviour within care homes, except for inviting people in to carry out the vaccinations. However, care homes in every corner of the country saw outbreaks from December”, wrote a rebuttal published in the British Medical Journal.
The other idea offered by some mainstream academics is that going to the vaccination centers itself may be a “super-spreader event” – but again, care homes didn’t fit that bill.
Also, even if these people did contract the virus on the vaccination day, why would more of them have symptom onset on that day and the 3 days immediately after, rather than the usual incubation period of 5 days?
FAR MORE LIKELY are the following mutually non-exclusive mechanisms:
- The rebuttal in the BMJ mentioned above pointed out that both Pfizer and AstraZeneca’s trials had shown white blood cell depletion in the first 3 days post vaccination. The phenomenon is known for other vaccines as well, and there’s at least evidence in children that such transient white cell depletion results in susceptibility to viral infections. In this scenario, an infection previously kept in check by the immune system could become active when response to the vaccine depleted circulating white blood cells.
- The mRNA and DNA vaccines use nanoparticles to enclose the nucleic acids. There has been an accumulating number of studies that found that various types of nanoparticles can interferewith the function of our blood cells, and with the coagulation system, shifting the hemostatic balance, causing deep vein thrombosis (DVT) and disseminated intravascular coagulopathy (DIC), among other serious complications.[8,9] Also, the mRNA vaccine nanoparticles contain PEG-lipid, and the DNA vaccine nanoparticles contain polysorbate 80, both have been known to be allergenic and found responsible for anaphylactic reactions in the past.
- The spike protein of SARS-CoV-2 alone, introduced intratracheally, as well as in in vitro experiments, has been shown to damage lung vascular endothelial cells by downregulating ACE2, and consequently inhibiting mitochondrial function, triggering reactive oxygen species production, increasing glycolysis, and extracellular acidification.[11,4]
- On Dec 9, 2020, BEFORE vaccination rollouts in most countries, Dr. J. Patrick Whelan MD PhD, formerly warned the FDA that, according to multiple lines of evidence, vaccines using SARS-CoV-2 spike protein (including mRNA and DNA vector vaccines) may cause microvascular injury to distant organs including the brain, heart, liver, and kidneys.
He cited evidence that while “the coronavirus replicates almost exclusively in the septal capillary endothelial cells of the lungs and the nasopharynx”, “viral lysis and immune destruction of those cells releases viral capsid proteins (or pseudovirions) that travel through the circulation and bind to ACE2 receptors in these other parts of the body…… that not only damages the microvascular endothelium but also induces the production of many pro-inflammatory cytokines”. He cited evidence that the brain tissues of those that died from COVID were found to have pseudovirions (spike, envelope, and membrane proteins) without viral RNA, in the endothelia of cerebral microvessels, and that injecting just the S1 spike subunit in mice led to neurologic signs.
- On Jan 26, 2021, Dr. Hooman Noorchashm emailed the FDA regulators, Pfizer leaders and the press, to deliver “a warning and a, nearly certain, prognostication”, that anyone who has had a recent COVID infection (irrespective of whether they are symptomatic or convalescent) can be expected to have viral antigens in the endothelial lining of their blood vessels, and that vaccine triggered antigen specific immune response will target those antigens, and therefore those tissues, and cause tissue inflammation and damage. In other words, the vaccines will cause vasculature damage and blood clots in the lungs, as well as damage in the vasculature of the brain, heart, liver, kidney etc., anywhere residual viral antigens from a recent infection may be found.
It’s relevant with regard to what Dr. Noorchashm is warning about, to note that Pfizer’s clinical trial protocol (on page 41) explicitly excluded anyone who has had COVID-19 from enrolment.
- Another point specifically about the mRNA and DNA vaccines encoding the spike protein, is raised by Dr. Sucharit Bhakdi, who was for over 2 decades the head of the Institute of Medical Microbiology and Hygiene, University of Mainz, and Editor in Chief of Medical Microbiology and Immunology.
He warned that a large part of the injected mRNA or DNA-containing nanoparticle packets encoding the spike protein will reach local lymph nodes, and through there, into blood circulation. In the lymph nodes, when they’re taken up by lymphocytes which then express the spike protein, those cells will be targeted for destruction by other lymphocytes, (likely accounting for the white blood cell depletion mentioned in #1 above). The lymphocytes thus activated will multiply and swarm out of the lymph nodes to seek out more S protein antigen. They’ll attack any muscle cells where the S protein is presented (muscle swelling, pain).
The nanoparticles that get into the bloodstream will be trapped there. Some will fuse with blood cells, but most will be taken up by endothelial cell lining the smallest of veins where blood flows really slow. The expression and presentation of the S protein by these microvascular endothelial cells attracts and activates platelets, which induces clotting. These cells also produce trash during spike protein production, which he says will be placed outside the cell, and attracts killer lymphocytes to attack the presenting endothelial cells, damaging the vascular lining, causing inflammation, and clotting.
- Many have been pointing out from the beginning, the very real danger of Antibody Dependent Enhancement of Disease (ADE), that any SARS-CoV-2 vaccine may cause. All attempts to develop a vaccine against the closest human coronavirus, SARS-CoV, had failed in the past two decades, when vaccinated animal models got more severe disease and died, upon challenge with the actual virus. All SARS-CoV-2 vaccines clinical trials have simply not had enough observation time to allow such a deadly consequence to become apparent, before the vaccine rollouts were rushed worldwide – and we’re already seeing the beginning of the onslaught! [13-15]
- The SARS-CoV-2 spike protein has also been found to contain high sequence similarity to 4 human proteins essential for embryonic development, including Syncytin-1 and Syncytin-2, since February 2020. This lead Dr. Wolfgang Wodarg and Dr. Michael Yeadon (Pfizer’s former chief scientific officer) to write an urgent petition on Dec 1, 2020, to the European Medicines Agency, to halt the vaccine rollout due to the possibility that antibodies against the S protein in vaccinated women may attack these proteins, preventing the formation of a placenta, and rendering them infertile. Like all the other warnings, it was completely ignored.
- Yet another treachery with the spike protein is its potential ability to cause prion disease, both by the protein, and by the mRNA for it contained in Pfizer and Moderna vaccines. I will make a separate post of this.
- As if all that isn’t bad enough, some scientists (e.g., Dr. Judy Mikovits) have stated that vaccinated people may shed microRNAs (miRNA) derived from the genetic vaccines, which could explain the many adverse health effects that unvaccinated people around those vaccinated are reporting (especially many women reporting abnormal and extremely heavy menses, even spontaneous abortions). She says these miRNAs can spread through air, and easily taken in by another person, as she’s worked on formulating therapeutic miRNA for aerosolized delivery.
Update 3: A peer reviewed paper from MIT published in Apr 2021, confirmed their earlier pre-print version published Dec13, 2020, that “Reverse-transcribed SARS-CoV-2 RNA can integrate into the genome of cultured human cells and can be expressed in patient-derived tissues”. Their results are “consistent with a LINE1 retrotransposon mediated, target-primed reverse transcription and retroposition mechanism.”
Even though with infection of SARS-CoV-2 virus, they detected only subgenomic sequences derived mainly from the 3′ end of the viral genome integrated into the DNA of the host cell,in the case of mRNA vaccines, given that we’re told the S protein gene is the only gene encoded by the mRNA, which by default is near the 3’ end, and was given a poly(A) tail and various other features to stabilize it, and given that tens of billions of copies of this mRNA are injected in one dose, it seems to me that there’s a good chance similar reverse transcription and retrotransposition of the S protein gene – the MOST PATHOGENIC gene of this entire virus – could really occur, as many scientists have warned from the beginning.
Once integrated into the genome, the host could express the S protein in the long term, which would trigger persistent autoimmune response, causing attack on the cells it has integrated into.
Update 2: Here’s yet another way that making our own cells express the spike protein via the genetic vaccines can lead to disaster: causing cells expressing the spike protein and cells that have ACE2 receptor on their surface to conglomerate, forming something called a “multinucleated syncytia”: “Proteins that mediate fusion between viral and cellular membranes can in some cases also do so between cells that express the viral fusion protein and those that express the viral receptor. For instance, cells expressing the HIV-1 envelope glycoprotein gp160 can form multinucleated syncytia with cells expressing the HIV-1 receptors CD4 and CCR5”. The 2003 Nature paper went on to demonstrate that “293T cells transfected with ACE2, but not those transfected with human immunodeficiency virus-1 receptors, formed multinucleated syncytia with cells expressing S protein (of SARS-CoV-1)”.
So indeed, the spike protein that the vaccines contain or encode for, is alone sufficient to cause COVID symptoms (and deaths in severe cases), and have numerous medium to long term potentially serious consequences. Only criminal governments would have rushed it ahead and imposed it on the world with utter deceit.
Maggie Zhou received her PhD from the University of Wisconsin – Madison in 1997, and worked as a computational biologist for a number of years. She is currently an independent seeker of truth.
originally published in https://stateofthenation.co/?p=66690
Related in this Category
- Scientists challenge health officials on vaccinating people who already had COVID
- Mass COVID-19 Vaccination Site Shut Down After Adverse Reactions Reported
- Former Pfizer VP: ‘Your government is lying to you in a way that could lead to your death.’
- COVID-19 Vaccine ‘Possibly’ Linked to Rare Blood Clots: EU Agency
- Vaccine expert calls on WHO to immediately halt all coronavirus mass vaccinations
- see also Disappearing adverse reactions..Covid levels totally Falsified by manipulation of PCR’s CT level..
- See widely read Salk Institute exposé HERE.
Detailed breakdown of EudraVigilance report up to May 22 2021
A Health Impact News subscriber in Europe ran the reports for each of the four COVID-19 shots we are including here. This subscriber has volunteered to do this, and it is a lot of work to tabulate each reaction with injuries and fatalities, since there is no place on the EudraVigilance system we have found that tabulates all the results.
Since we have started publishing this, others from Europe have also calculated the numbers and confirmed the totals.*
Here is the summary data through May 22, 2021.
Total reactions for the experimental mRNA vaccineTozinameran (code BNT162b2,Comirnaty) from BioNTech/ Pfizer: 5,961 deaths and 452,779 injuries to 22/05/2021
- 13,531 Blood and lymphatic system disorders incl. 59 deaths
- 9,828 Cardiac disorders incl. 735 deaths
- 71 Congenital, familial and genetic disorders incl. 4 deaths
- 5,468 Ear and labyrinth disorders incl. 3 deaths
- 183 Endocrine disorders
- 6,266 Eye disorders incl. 14 deaths
- 41,214 Gastrointestinal disorders incl. 216 deaths
- 128,031 General disorders and administration site conditions incl. 1,909 deaths
- 327 Hepatobiliary disorders incl. 27 deaths
- 4,802 Immune system disorders incl. 31 deaths
- 13,948 Infections and infestations incl. 648 deaths
- 4,821 Injury, poisoning and procedural complications incl. 81 deaths
- 10,374 Investigations incl. 221 deaths
- 3,354 Metabolism and nutrition disorders incl. 120 deaths
- 65,326 Musculoskeletal and connective tissue disorders incl. 71 deaths
- 250 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 15 deaths
- 81,748 Nervous system disorders incl. 616 deaths
- 279 Pregnancy, puerperium and perinatal conditions incl. 7 deaths
- 88 Product issues
- 7,978 Psychiatric disorders incl. 94 deaths
- 1,342 Renal and urinary disorders incl. 93 deaths
- 1,570 Reproductive system and breast disorders incl. 3 deaths
- 18,597 Respiratory, thoracic and mediastinal disorders incl. 697 deaths
- 21,101 Skin and subcutaneous tissue disorders incl. 53 deaths
- 663 Social circumstances incl. 9 deaths
- 160 Surgical and medical procedures incl. 10 deaths
- 11,459 Vascular disorders incl. 225 deaths
Total reactions for the experimental mRNA vaccine mRNA-1273(CX-024414) from Moderna: 3,365 deaths and 72,596 injuries to 22/05/2021
- 1,335 Blood and lymphatic system disorders incl. 22 deaths
- 2,045 Cardiac disorders incl. 370 deaths
- 12 Congenital, familial and genetic disorders incl. 2 deaths
- 718 Ear and labyrinth disorders
- 37 Endocrine disorders incl. 1 death
- 997 Eye disorders incl. 4 deaths
- 6,305 Gastrointestinal disorders incl. 108 deaths
- 20,774 General disorders and administration site conditions incl. 1,480 deaths
- 129 Hepatobiliary disorders incl. 8 deaths
- 691 Immune system disorders incl. 4 deaths
- 2,392 Infections and infestations incl. 183 deaths
- 1,292 Injury, poisoning and procedural complications incl. 63 deaths
- 1,743 Investigations incl. 77 deaths
- 816 Metabolism and nutrition disorders incl. 64 deaths
- 9,149 Musculoskeletal and connective tissue disorders incl. 62 deaths
- 77 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 11 deaths
- 12,314 Nervous system disorders incl. 339 deaths
- 83 Pregnancy, puerperium and perinatal conditions
- 11 Product issues
- 1,375 Psychiatric disorders incl. 51 deaths
- 468 Renal and urinary disorders incl. 40 deaths
- 175 Reproductive system and breast disorders incl. 1 death
- 3,513 Respiratory, thoracic and mediastinal disorders incl. 306 deaths
- 3,726 Skin and subcutaneous tissue disorders incl. 23 deaths
- 259 Social circumstances incl. 9 deaths
- 235 Surgical and medical procedures incl. 26 deaths
- 1,925 Vascular disorders
Total reactions for the experimental vaccine AZD1222/VAXZEVRIA (CHADOX1 NCOV-19) from Oxford/AstraZeneca: 2,489 deaths and 655,534 injuries to 22/05/2021
- 7,200 Blood and lymphatic system disorders incl. 100 deaths
- 9,748 Cardiac disorders incl. 311 deaths
- 103 Congenital, familial and genetic disorders incl. 2 deaths
- 6,740 Ear and labyrinth disorders
- 217 Endocrine disorders incl. 2 deaths
- 10,591 Eye disorders incl. 8 deaths
- 69,826 Gastrointestinal disorders incl. 116 deaths
- 178,037 General disorders and administration site conditions incl. 685 deaths
- 396 Hepatobiliary disorders incl. 20 deaths
- 2,409 Immune system disorders incl. 9 deaths
- 13,832 Infections and infestations incl. 163 deaths
- 5,870 Injury, poisoning and procedural complications incl. 46 deaths
- 13,474 Investigations incl. 50 deaths
- 8,405 Metabolism and nutrition disorders incl. 35 deaths
- 104,075 Musculoskeletal and connective tissue disorders incl. 25 deaths
- 222 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 6 deaths
- 141,437 Nervous system disorders incl. 388 deaths
- 156 Pregnancy, puerperium and perinatal conditions incl. 3 deaths
- 76 Product issues
- 12,272 Psychiatric disorders incl. 21 deaths
- 2,264 Renal and urinary disorders incl. 20 deaths
- 3,327 Reproductive system and breast disorders
- 21,237 Respiratory, thoracic and mediastinal disorders incl. 278 deaths
- 29,750 Skin and subcutaneous tissue disorders incl. 14 deaths
- 582 Social circumstances incl. 4 deaths
- 498 Surgical and medical procedures incl. 15 deaths
- 12,790 Vascular disorders incl. 168 deaths
Total reactions for the experimental COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson: 369 deaths and 15,281 injuries to 22/05/2021
- 145 Blood and lymphatic system disorders incl. 10 deaths
- 264 Cardiac disorders incl. 34 deaths
- 8 Congenital, familial and genetic disorders
- 77 Ear and labyrinth disorders
- 5 Endocrine disorders incl. 1 death
- 191 Eye disorders incl. 2 deaths
- 1,302 Gastrointestinal disorders incl. 11 deaths
- 3,619 General disorders and administration site conditions incl. 97 deaths
- 38 Hepatobiliary disorders incl. 2 deaths
- 51 Immune system disorders
- 245 Infections and infestations incl. 8 deaths
- 209 Injury, poisoning and procedural complications incl. 6 deaths
- 1,134 Investigations incl. 23 deaths
- 104 Metabolism and nutrition disorders incl. 10 deaths
- 2,368 Musculoskeletal and connective tissue disorders incl. 12 deaths
- 12 Neoplasms benign, malignant and unspecified (incl cysts and polyps)
- 3,051 Nervous system disorders incl. 48 death
- 7 Pregnancy, puerperium and perinatal conditions
- 8 Product issues
- 181 Psychiatric disorders incl. 3 deaths
- 69 Renal and urinary disorders incl. 4 deaths
- 62 Reproductive system and breast disorders
- 637 Respiratory, thoracic and mediastinal disorders incl. 29 deaths
- 324 Skin and subcutaneous tissue disorders incl. 1 death
- 39 Social circumstances incl. 2 deaths
- 214 Surgical and medical procedures incl. 20 deaths
- 917 Vascular disorders incl. 46 deaths