TruthArchive.ai - Related Video Feed

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.

The presentation examines the pattern of deployment of toxic vaccine batches using the VAERS dataset. It notes that the Covid vaccine was deployed in batches or lots, each with a number, and the batches are listed in VAERS in the order they were created, with adverse reactions recorded for each batch. A graph was produced with adverse reactions on the vertical axis and the sequence of batches in time on the horizontal axis, showing patterns of deployment in 2021. Each dot represents a batch, and the speaker highlights that about 95% of batches lie close to the x-axis, forming a thick line, with 80% of all batches generating only one or two adverse reaction reports and thus considered harmless. In contrast, the “clouds” and spikes above the x-axis represent toxic batches, with all such dots categorized as toxic. The breakdown given is: - 5% of all batches belong to these clouds and spikes. - The truly toxic batches generate 1,000 to 5,000 adverse reaction reports and are found above a red line, causing harm across every state in the USA where deployed. - These very toxic batches comprise about 0.65% of all batches (roughly one in 200). Total batches deployed in 2021 and recorded in VAERS: 28,330. Eighty percent are harmless (1–2 reports) within the x-axis line; the remaining 20% are more toxic, with the most extreme range up to 5,000 reports. Lesson two asks: “Who did it?” It identifies three companies appearing in VAERS: Moderna, Pfizer, and Janssen (Johnson & Johnson). By filtering VAERS data in Excel, the speaker presents the contributions of each company to the toxic-batch deployment. In the full picture, Moderna accounts for every batch in the first half of the chart except two spikes pre- and post- Moderna, which are attributed to Janssen. Pfizer’s results (from their batches) match the latter half of the chart exactly, suggesting Pfizer appeared to have taken over supply for every USA batch in the latter portion. The deployment is described as carefully compartmentalized, with phases where Janssen, then Moderna, then Janssen again, and then Pfizer dominate in sequence, followed by Moderna exiting and Pfizer continuing. Lesson three describes the purpose behind Moderna’s deployment of toxic batches: Moderna appears to randomly distribute toxic batches, with the intention of harm, possibly to induce fear of a pandemic and justify stronger policies. Janssen’s initial spike is interpreted as a test before Moderna’s deployment. Pfizer is described as carrying out rigorous dosage testing, deploying the most lethal batches systematically and recording effects, and acting as the only company administering batches at that stage to avoid interference from others. Lesson four details the fine art of lethal dosage testing. Pfizer’s deployment is shown as highly clustered in time, forming distinct periods of toxic batches separated by intervals of harmless batches. Toxic batches cluster in discrete ranges (e.g., 3,000–2,500; 2,000–1,500; 1,500–1,000), with abrupt transitions between clusters and harmless periods. Toxicity ranges are not random but follow a stepwise, linear decline across clusters. The speaker concludes that Pfizer deployed highly toxic batches for discrete dosage testing across all states, implying thousands of hospitalizations, injuries, and deaths. The presentation ends by contrasting that 80% of batches are harmless, while a minority exhibit wide toxicity ranges, with claims of systematic, non-random deployment designed for testing, and notes an ironic statement about American exposure to what is described as German-led testing.

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.

Young athletes have experienced cardiac side effects from the shots. However, some people who get the shots have no side effects at all. A study from Denmark found that about a third of the shots have no side effects, while another 70% have mild side effects. The remaining 4.2% of shots in a high-risk batch have more severe side effects. Each vial of the vaccine can vary in its contents, so it's a matter of luck whether someone gets a high-risk injection or not. There is no quality control over the batches, including the amount of messenger RNA or any impurities.

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.

Many labs, including Medicinal Genomics, found DNA contamination in Pfizer and Moderna mRNA vaccines. Regulators like the FDA and EMA admitted to this, but downplayed its significance. The SP 40 sequences omitted by Pfizer are crucial. DNA contamination can cause insertional mutagenesis, as stated in Moderna's patents. Regulatory agencies were deceived and failed to properly address the issue. This poses a serious risk that cannot be ignored.

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 amount of DNA allowed in vaccines was loosened a thousandfold after liability waivers were granted. These limits assumed naked DNA injection, which degrades quickly. However, mRNA vaccines use lipid nanoparticles (LNPs) that also coat contaminating DNA, invalidating the old limits. Studies show DNA levels in the shots are 10 to 100 times higher than the already obsolete limits. The LNPs deliver this DNA directly into cells, changing its persistence and biological impact. Pfizer used a different, more purified product in its trials than what was injected into billions of people. The initial process included a PCR amplification step to reduce DNA background, but this was dropped for mass production due to cost. This resulted in higher levels of background plasmid DNA and potentially E. coli components like endotoxin in the shots, possibly causing anaphylactic reactions. The presence of plasmids has been confirmed, and this process change, documented in the BMJ, is a major violation of manufacturing standards. The EMA requested a new trial after the process change, but the data was never delivered, rendering the original trial data irrelevant.

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.

A peer-reviewed paper confirms Pfizer's mRNA vaccine is contaminated with DNA and SV40 enhancers, considered dangerous. Pfizer used bacterial plasma DNA during mass production, leading to contamination with spike protein genes, antibiotic resistance markers, and SV40 enhancers. Researchers found 4-5 times more DNA than the safe limit. The DNA fragments could integrate into the human genome due to the SV40 enhancer. Injected vaccine samples caused super strong kidney cells to produce spike protein, excreted via exosomes, potentially spreading body-wide. The vaccines were toxic to these cells, causing pathological changes. The DNA, tucked into lipid nanoparticles, could integrate into the human genome, turning the jab into accidental gene therapy. The SV40 enhancer drags DNA into the nucleus. The study suggests the inclusion of SV40 enhancers was deliberate, not accidental, and scrubbed from regulatory paperwork. Experts theorize this contamination could be linked to an explosion of turbo cancers. The study concludes mRNA shots should be suspended until safety is determined. Another study found vaccine spike protein expressed in cerebral arteries of stroke patients for up to 17 months, accompanied by an autoimmune response.

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.

A peer-reviewed paper confirms Pfizer's mRNA vaccine is contaminated with dangerous DNA and SV40 enhancers. During production, bacterial plasmid DNA led to contamination with spike protein genes, antibiotic resistance markers, and SV40 enhancers. Researchers found four to five times more DNA than the safe limit; these DNA fragments could integrate into the human genome due to the SV40 enhancer. Experiments showed the vaccines were toxic to cells, causing pathological changes and spike protein production, potentially spreading body-wide via exosomes. The DNA contamination, tucked into lipid nanoparticles, could lead to unintended gene therapy. The SV40 enhancer, deliberately added but removed from regulatory paperwork, raises questions about Pfizer's intentions. Experts theorize this contamination could be linked to an increase in "turbo cancers," coinciding with Pfizer's acquisition of a cancer drugmaker. An epidemiologist noted the study found DNA from the manufacturing process way over regulatory limits, including the cancer-promoting SV40 promoter enhancer and spike-producing DNA. A separate study found vaccine spike protein expressed in cerebral arteries of stroke patients for up to seventeen months, potentially contributing to autoimmune responses. There are now 11 independent reports that have found, DNA contamination within these shots of up to 60000% above regulatory limits.

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.

Pfizer and Moderna used two processes to create their vaccines. Initially, they used PCR to amplify and create the DNA for clinical trials. However, when they received approval, they needed to produce billions of copies, so they used circular bacterial DNA plasmids. Unfortunately, this led to contamination with junk DNA. Researchers in Ontario, Canada tested 27 mRNA vials from 12 different lots and found billions to hundreds of billions of DNA molecules per dose, exceeding FDA and WHO guidelines by 188 to 509 times. This is a significant amount, far beyond what is considered acceptable.

There is significant DNA contamination found in vaccines, with evidence from multiple researchers in Germany, Japan, and the U.S. Regulatory bodies like the FDA and EMA acknowledge this contamination but downplay its significance, relying on Pfizer's assurances. The clinical trials used cleaner DNA, but the mass-produced vaccines did not undergo the same purification, leading to increased background DNA and endotoxin levels. Regulators received a plasmid map missing crucial annotations, suggesting manipulation. Claims about expired vials and PCR methods used to measure contamination have been challenged, with evidence showing that Moderna's vaccines are cleaner. Regulators are allowing different measurement standards for RNA and DNA, raising concerns about transparency and integrity in the regulatory process.

Pfizer and Moderna vaccines use two processes. The first process involves using PCR to amplify and create DNA for clinical trials. Once approved, they use circular bacterial DNA plasmid to replicate billions of mRNA DNA sample copies. However, this resulted in contaminated vaccines with junk DNA. A study found DNA fragments in Pfizer and Moderna vaccines in Ontario, Canada. Researchers tested 27 mRNA vials from 12 different lots and discovered billions to 100 billions of DNA molecules per dose, exceeding FDA and WHO guidelines by 188 to 509 times. This is a significant amount, far beyond what is acceptable.

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.

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.