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The speaker analyzed the top 10 batches with high death counts and mortality rates. They found that all batches were from Pfizer and had varying mortality rates. The speaker mentioned that the expected mortality rate is 0.75, but these batches had much higher rates. They clarified that the batches included people of all ages and were not specific to any age group. The speaker highlighted batch number 1 with a 21% mortality rate and batch number 71 with a 4% rate. They concluded that the chances of these batches not being a killer are extremely low, with a statistician explaining that it would require dropping 100 billion people to obtain these statistics.

Some batches of the vaccine may have serious side effects or be degraded. The batch number can be checked to see what to expect. Documentation shows that certain batches have more serious adverse effects. Even the best batches from Pfizer and Moderna had a high rate of serious adverse events in the short term, around 1800.

Over 1.6 million adverse event reports have been filed to VAERS for COVID-19 vaccines, with a significant increase in 2021. The underreporting factor is estimated to be around 31 for severe events like hospitalizations and death. The speaker believes the mRNA platform was used to gather data for future gene therapy applications.

I have an internal Pfizer document from a source who reverse-engineered the BioNTech Pfizer SARS COVID-2 vaccine. This document reveals the precise chemical and biological processes used to create an mRNA that contains graphene oxide, a dangerous toxin. Each vaccine contains 15 billion nanoparticles or lipid carrier particles within the mRNA sequence. Once injected, the spike protein binds to blood cells, and graphene oxide begins building a structure, leading to blood clots and heart failure. Patent databases and recovered, deleted Wuhan databases prove that COVID-19 and its vaccines are bioweapons.

The speaker claims Pfizer documents reveal the COVID vaccines didn't work to stop the virus a month after rollout in November 2020. They allege Pfizer knew the third most common side effect was COVID. Within months, Pfizer supposedly needed to hire 2,400 staffers to process adverse event reports. The speaker asserts Pfizer and the FDA knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The speaker states the CDC initially claimed the injection materials stayed at the injection site, but Pfizer knew they biodistributed throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. Pathologist Dr. Robert Chandler allegedly found no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

The FDA allegedly wanted to keep Pfizer's dossier hidden for 55 years, despite knowing about the high number of deaths associated with the vaccine. No safety review board has been called, and there has been no voluntary recall. The large number of deaths is a significant signal, with most occurring within a week of vaccination. There have been reports of blood clots, heart attacks, and fatal cases of myocarditis. The consistency of these adverse events in various systems and literature supports the association. Randomized trials have shown more deaths with Pfizer than with the placebo. The vaccines are believed to be causing deaths in unfortunate individuals due to a combination of factors, including the production of lethal spike proteins.

I am Max Melling, the statistician behind this study, with Viveke as the medical expert. The main result of our study is shown on the screen. It displays the number of adverse effects in each vaccine batch, based on official Danish data created for the study. Some batches are small, while others are large. Normally, a good vaccine would show a nearly perfect line, while a very bad vaccine would have scattered points. However, we observe three almost perfect lines, which is unexpected and suggests a problem with the product. Participants were unable to give informed consent due to the unknown risks. This is a concerning safety signal that requires further investigation.

The speaker analyzed data on the top 10 batches with high death counts and mortality rates. They created a chart showing the batch ID, number of vaccinated individuals, and the number of deaths. The speaker confirmed that all batches discussed were from Pfizer. They specifically mentioned batch number 1, where 711 individuals were vaccinated and 152 of them died, resulting in a 21% mortality rate.

There are four studies indicating significant lot variability in certain batches. Early 2021 batches appeared to be the most dangerous. Some lots are linked to large numbers of adverse events, while others have almost none, essentially being "duds," possibly due to degraded mRNA or manufacturing issues. Some batches decimated people and may be contaminated with high levels of DNA plasmids, mRNA, or even heavy metals. No batch appeared to be the same.

I built and implemented a vaccine payment system called pay per dose. While analyzing the data, I noticed discrepancies in the death dates of people who were vaccinated. As the only database administrator for this system in New Zealand, I have access to unique information. I created a chart displaying the top ten batches with high mortality rates. There are a total of 119 batches in New Zealand, mostly Pfizer. To find specific batch information, there is a website called "Find My Batch." I counted the number of vaccinated individuals and identified the deceased within each batch.

The speaker analyzed the top 10 batches with high death counts and mortality rates. They found that all of these batches were from Pfizer. The mortality rates ranged from 21% to 4%. The speaker explained that these batches included people from all age groups and vaccination centers, so it wasn't specific to one age group. They mentioned that the chances of these results occurring naturally by chance are extremely low, indicating that the vaccine may be causing deaths. They estimated that to obtain these statistics, they would have had to vaccinate 100 billion people, while they currently have data for 2.2 million individuals.

The speaker analyzed the top 10 batches with high death counts and mortality rates. They found that all of these batches were from Pfizer. The mortality rates ranged from 21% to 4%. The speaker explained that these batches included people from all age groups and vaccination centers, so it wasn't specific to one age group. They stated that the chances of these results occurring naturally by chance are extremely low, suggesting that the vaccine may be causing deaths. They estimated that to obtain these statistics, they would have had to vaccinate 100 billion people, while they have only vaccinated 2.2 million.

According to the speaker, Pfizer documents reveal that one month after the vaccine rollout in November 2020, Pfizer knew the vaccines didn't stop COVID and identified vaccine failure. Within months, the company allegedly needed to hire 2,400 staffers to process adverse event reports. The speaker claims Pfizer knew in May 2021 that the vaccines caused heart damage in 35 minors within a week of injection, but this information wasn't shared with parents until August 2021. The speaker alleges that the CDC initially stated the injection materials stayed in the injection site, but Pfizer knew these materials biodistribute throughout the body within 48 hours, settling in the brain, liver, adrenals, spleen, and ovaries. The speaker asserts that there is no mechanism for the body to eliminate lipid nanoparticles from the ovaries, leading to accumulation with each injection.

The speaker analyzed the top 10 batches with high death counts and mortality rates. They found that all batches were from Pfizer and had varying mortality rates. The speaker mentioned that the normal mortality rate is 0.75%, while the batches ranged from 4% to 21%. They clarified that the batches included all age groups and were not specific to one age group. The speaker highlighted that the chances of these batches not being a killer were extremely low, with odds of 100 billion to 1. They emphasized that statistically, there is no chance that the vaccine is not causing deaths.

The speaker discusses a paper from Denmark that reveals a significant variation in suspected adverse reactions to the Pfizer vaccine. The data shows a 1,000-fold difference in incidence depending on the batch of vaccines administered. This information is currently gaining popularity.

Key points: "the vials that were in fact approved are not the vials that were given to the public." The clinical trial used "process one that used PCR to make the DNA that was going to then turn into the RNA to make the spike protein." After the trial, "they switched" to a production process that "manufactured this DNA in E. Coli," introducing endotoxin risk. "There are these plasmids that have additional DNA that were not present in the actual clinical trial." Sequencing found mixtures, including "expired" and samples that had "been tapped into." Regarding Pfizer, "the Pfizer vaccines actually had a component that was not disclosed to the regulators." "The plasmid map on the right is what was disclosed to the EMA" with "no mention of the SV40 components" now "inside this DNA sequence." "The plasma on the left is what we actually found," with components not disclosed to regulators nor to patients. Monovalent Pfizer; prior ones were the bivalent vaccines from Moderna and Pfizer.

Four studies are cited as showing significant lot variability in the vaccine batches. The speaker notes that the variability is substantial across lots, with some batches from the early 2021 period appearing to be the most dangerous. They state that some lots are linked to large numbers of adverse events, while other lots are linked to no adverse events at all, describing these as “duds.” According to the speaker, these problematic batches may result from several issues: the mRNA being degraded, or the cold-chain failure such as being left out of the refrigerator for too long, or problems in the manufacturing process that rendered the batch ineffective. The implication is that these dud batches were not manufactured properly. The speaker emphasizes that some of these batches had devastating effects on individuals. They further claim that these batches were probably contaminated with high levels of DNA plasmids from the manufacturing process, extremely high levels of mRNA, and even heavy metal contamination. The range of issues is described as broad, indicating multiple types of contamination or quality problems in different batches. The overall assertion is that not a single batch appears to be the same as another; there is clear heterogeneity across batches, with some batches causing major adverse events and others causing none.

I am one of the scientists involved in a study on the safety and dependency of vaccine batches. We found three types of side effects: mild, severe, and even death. These adverse effects were present in the initial batches, which may have been changed during production or transportation. Patients were not informed of the risks and some received poor-quality batches. The Vice President of Pfizer admitted to building the plane while flying, and we have shown that one wing has fallen off. There is a safety issue that the European Medicines Agency (EMA) and national institutions should have addressed and informed the public about. Our study also suggests a potential link between certain cancers and different vaccine batches. We have observed increased mortality rates in European countries since May 21st. The EMA should have reacted to these findings and halted vaccinations or at least withdrawn the problematic batches. As a concerned citizen and doctor, I expected more action from the EMA. Thank you.

The speaker discusses the severe damage caused by multiple doses of a certain substance, suggesting that taking it once is enough. They mention leaked documents from Pfizer and Moderna, revealing different lot numbers and formulations. The FDA's role is to ensure uniformity and safety across the country, but the speaker claims that different concentrations and ingredients were used, resulting in varying effects. Some lots were found to be 5000% more lethal than others. The speaker suggests that this variation was intentional to prevent clear correlation and discourage people from realizing they were being poisoned.

There are four studies that show lot variability, significant lot variability. The early twenty twenty one batches were actually the most dangerous it appeared. Some lots are linked to large numbers of adverse events, while some lots are linked to no adverse events really at all. And they're basically batches called duds. Right? Probably the mRNA is degraded or it's been left out of the refrigerator for too long or the manufacturing process was a bust and it wasn't manufactured properly. Thankfully right for those individuals. But, yeah, some of these batches, they just decimated people and they're probably contaminated with high levels of DNA plasmids from a manufacturing process, extremely high levels of mRNA, even heavy metal contamination has been detected in these batches. So all sorts of things. But, yeah, really no batch appeared to be the same.

I am one of the scientists involved in a study on the safety and dependency of vaccine batches. We found three types of side effects: mild, severe, and even death. These adverse effects were present in the initial batches, which were later changed, possibly due to Pfizer altering the product or during transportation. Patients were not informed of the risks and some received poor-quality batches. The study also reveals a safety issue that both Pfizer and regulatory institutions should have addressed. Pfizer had already informed the European Medicines Agency (EMA) about the safety problem in August 2021. Our data from Sweden indicates that this is a European issue, not just a Danish one. We are concerned about long-term side effects and their potential links to cancer and increased mortality rates. The EMA should have taken action based on the data and informed the public. The vice-president of Pfizer's statement about building the plane while flying is apt, as we have shown that one wing has fallen off.

Approximately 15% of people are injured by COVID-19 vaccines, with around 2.5% experiencing heart damage. The pharmaceutical industry suggests that not all vaccine vials are the same. It has been discovered that 80% of deaths from Pfizer vaccines come from 30% of the lots, while 80% of deaths from Moderna vaccines come from 20% of the lots. These lots may have varying concentrations of genetic material and contaminants, affecting their quality. This issue is currently receiving significant attention.

Pfizer has been forced to release previously secret documents, including FDA approval packages, due to court orders and successful FOIA requests. These documents reveal that Pfizer tested different versions of their vaccine during preclinical and clinical trials, which goes against FDA guidance. The different versions included modified RNA, unmodified RNA, self-amplifying RNA, and Spike protein alone. Surprisingly, all these versions were tested under the same investigational new drug number, despite FDA guidance stating that multiple versions should have their own individual numbers. Additionally, the toxicity of the mRNA active ingredient in the COVID-19 vaccines was never studied. This raises concerns about the regulatory process and the lack of safety testing.

The speaker analyzed the top 10 batches with high death counts and mortality rates. They found that all of these batches were from Pfizer. Batch number 1 had 711 vaccinated and 152 deaths, resulting in a 21% mortality rate. The expected mortality rate is 0.75%. These batches included all age groups, not specific to one age group. Other batches in the top 10 had mortality rates of 17%, 15%, and 4%. The speaker concludes that the chances of these batches not being a killer are extremely low, with odds of $100,000,000,000 to 1.

These batches are different. So yep. So so many people, nobody even really got the same product. The quality control was so bad. Some people got a tiny dose of the mRNA. Some people got a massive dose depending on the batch. And you can check your batch at howbadismybatch.com, which uses the Vaccine Adverse Events Reporting System, and it'll tell you how many people died from this batch, how many reports of blood clots were there from my batch? So that's an important tool you can use to see, what the possible risks you you you might face, regarding your injection.