VAERS-excessDeaths2021
A shout out to Hervé Seligmann
A very impressive graphical analysis by my new friend Hervé! Hervé is a very accomplished PhD and savvy analytics guy. His papers can be found on researchgate.net HERE. A mutual friend whom I will keep anonymous reached out to me saying he had a friend and colleague that wanted to confirm some VAERS data retrospectively like what VAERS data looked like at a previous point in time? When this particular friend comes calling I will jump quickly as he is a good guy and did appear at a Sen. Ron Johnson Roundtable once or twice. At first it started out with a simple request like do I have the downloadable files from a particular point in 2021 or 2022? What got interesting is when I demonstrated how the purposeful delay in publishing reports (throttling) might make a material difference especially if you’re analyzing deaths from 2021, as those are still being published “new” today!
Herve was cool! The man is down to earth and easy to talk to, I took him on nearly a four hour carpet ride into my dashboards. The short story is, when we discussed my formulary for Relative Lot Toxicity, I said it’s probably worth doing the same calculations but at the state and country level. I will assume that most people know already states like Tennessee and Kentucky are at the top of list with most DEATHS in VAERS. Or that South Dakota is technically #1 when factoring in population size. I have many images and downloadable spreadsheets you can find at my website or by starting HERE. But what about Michigan? Have you seen the crazy amount of Hospitalization reports Michigan has compared to all other states, it’s astonishing!
Anyhow, when I thought people were fed up looking at or talking about VAERS, along comes Hervé to show me smart people are still walking around the gates of Jericho, so I will too. I knew I was not alone. I created a new page on my website HERE basically called Adverse Events RVU by States and Foreign. The new page has various viewable pdf’s you can scroll and see how states and countries stack up to each other in relation to their RVU. Here is a few views with domestic and foreign comingled and by themselves.:
Thank You Hervé for finally giving Kid Fresh a seat at the dinner table! God Bless.
My creative juices are flowing, I can see a geo map added to my dashboard, like the one I made here:
Then there also are other adverse drug reaction reporting systems, such as (to my knowledge) SAVAERS (VAERS South Africa), the Yellow Card system in the UK, WHO's VigiAccess, the Canadian government website, the Therapeutic Goods Administration Australia (TGA) website, Signalement-sante.gouv.fr, the New Zealand government's official reporting system, the Noti-FACEDRA reporting system in Central America and VARR-PH in the Philippines.
Do we know anything about databases in Russia or China? We keep hearing about the numerous adverse vaccine reactions in Russia and China that occur there.
Dear Welcome the Eagle 88, Dear Albert,
The other day I looked at all the adverse effects of "vaccines" for people under 18.
It was shocking to see the number of adverse effects increase by a thousand-two every year or two. We never analyzed this before, never asked questions.
Personally, I was never against "vaccinations", in fact, I tried to stay up to date with all of them. Not anymore... Now I actually rely ONLY on SCIENCE, not dogma!
ALL THESE INJECTIONS ARE HARMFUL! None of these "vaccines" are needed or safe. They are effective to create patients for life because of these toxins: I will give a SIMPLE EXPLANATION OF THE FACT THAT YES, ALL "VACCINES" CAN CAUSE AUTISM and ALL OTHER ADVERSE EFFECTS, INCLUDING DEATH: Aluminum, nanotechnology (carbon-based materials, quantum dots, CNTs, graphene, etc.), mercury, etc. - are all toxic. Twenty-two adverse effects of C-19 "vaccines": https://www.fda.gov/media/143557/download page 16: “FDA Safety Surveillance of COVID-19 Vaccines: DRAFT Working list of possible adverse event outcomes ***Subject to change*** -Guillain-Barré syndrome -Acute disseminated encephalomyelitis -Transverse myelitis -Encephalitis /myelitis/encephalomyelitis/meningoencephalitis/meningitis/encephalopathy -Convulsions/seizures -Stroke -Narcolepsy and cataplexy -Anaphylaxis -Acute myocardial infarction -Myocarditis/pericarditis -Autoimmune disease -Deaths -Preganacy and birth outcomes -Other acute demyelinating diseases -Non-anaphylactic allergic reactions -Thrombocytopenia -Disseminated intervascular coagulation -Venous thromboembolism -Arthritis and arthralgia/joint pain -Kawasaki disease -Multisymptom Inflammatory Syndrome in Children -Vaccine enhanced disease” As well as a long list: https://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf (dated February 28, 2021) p. 30 Reissue_5.3.6 Postmarketing Experience.pdf" https://outraged.substack.com/p/common-denominator-for-adverse-effects are caused by TOXICITY OF THESE SUBSTANCES AND OXIDATIVE DAMAGE THEY CAUSE. THERE IS ONLY ONE COMMON DENOMINATOR FOR ALL THESE ADVERSE EFFECTS OF C-19 INJECTION: IT IS OXIDATIVE STRESS OR MORE PRECISELY OXIDATIVE DAMAGE. OXIDATIVE STRESS/DAMAGE IS ASSOCIATED WITH ALL OF THESE ADVERSE EFFECTS. OXIDATIVE STRESS/DAMAGE UNDERLIES ALL OF THESE ADVERSE EFFECTS. THE TOXICITY OF THE COMPONENTS OF THESE INJECTIONS CAUSES THIS! https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921264/ Many recent studies have found a link between ASD and elevated oxidative stress, which may play a role in its development. ASD is caused by oxidative stress in several ways, including protein post-translational changes (e.g., carbonylation), abnormal metabolism (e.g., lipid peroxidation), and toxic buildup [e.g., reactive oxygen species (ROS)]. Conclusion Many studies have demonstrated that oxidative stress plays a crucial part in the disease process of ASD because ASD cases have greater levels of oxidative stress and decreased antioxidant capability. The active use of biomarkers to monitor ASD patients' physiological status is helpful for disease diagnosis, intervention, and treatment. https://www.nature.com/articles/s41398-020-01135-3 Abstract There is increasing awareness that oxidative stress may be implicated in the pathophysiology of autism spectrum disorder (ASD). Conclusions The results from this study showed that blood GSSG, MDA, homocysteine, SAH, nitric oxide, and copper concentrations were significantly increased, whereas GSH, tGSH, GSH/GSSG, tGSH/GSSG, SAM/SAH, methionine, cysteine, vitamins (B9, B12, D, and E), and calcium concentrations were significantly reduced in children with ASD. Due to the consistent and large ESs for the associations between glutathione metabolism markers, vitamin D, and ASD, they have the potential to be used as diagnostic markers for ASD. Therefore, future investigations into oxidative stress markers as potential early diagnosis and therapeutic target of ASD are necessary. https://www.frontiersin.org/articles/10.3389/fpsyt.2022.813304/full Conclusion Many studies have demonstrated that oxidative stress plays a crucial part in the disease process of ASD because ASD cases have greater levels of oxidative stress and decreased antioxidant capability. The active use of biomarkers to monitor ASD patients' physiological status is helpful for disease diagnosis, intervention, and treatment. We mainly summarize the most recent research progress in the field of ASD oxidative stress biomarkers in this review. etc. The same is true for C-19 "vaccines." Not only are these adverse effects related to oxidative stress, but the nanotechnology/graphene used in these injections has exactly this mechanism of toxicity: https://particleandfibretoxicology.biomedcentral.com/articles/10.1186/s12989-016-0168-y GRAPHENE TOXICITY/TOXICITY OF NANOTECHNOLOGY With more than 6,000 scientific studies on the toxicity of graphene and its applications, including biological applications, today we already know the mechanism of graphene toxicity, which causes oxidative stress, DNA damage, inflammatory response, apoptosis, autophagy and necrosis. Acute oxidative stress often leads to the formation of blood clots, organ failure, strokes and many other injuries, including death. Graphene toxicity can cause acute inflammatory response and chronic injury by interfering with the normal physiological functions of vital organs. Studies on the risks of graphene in the brain show that graphene application leads to harmful effects on the development of brain tissue, and abnormal ultrastructure has been observed in the brain. Graphene shows toxicity in the central nervous system and toxicity in the reproductive and developmental systems. In animal studies, pregnant mice had miscarriages at all doses, and most pregnant mice died when given a high dose late in pregnancy, and offspring development was delayed during lactation. The high dose reduces milk production and delays offspring development. Developmental toxicity of graphene causes structural abnormalities, growth retardation, behavioral and functional abnormalities and even death. Graphene causes lung damage with infiltration of inflammatory cells, pulmonary edema and formation of granulomas in the lungs. Graphene causes cytotoxic effects and damage to mitochondria, leads to inflammation, causes DNA damage, reduces cell adhesion and causes apoptosis, or cell death. Graphene inserts itself between the base pairs of double-stranded DNA and disrupts the flow of genetic information at the molecular level, which is the main reason for its mutagenic effect. It is hemotoxic, cytotoxic, cardiotoxic, neurotoxic, and harmful to the reproductive system. The sharpened edges of graphene cause physical destruction. (Toxicity of graphene-family nanoparticles: a general review of the origins and mechanisms | Particle and Fibre Toxicology | Full Text (biomedcentral.com)