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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.

I was fired after 31 years as an ER doctor for questioning the need for vaccination in those with natural immunity. Pfizer's hidden biodistribution studies reveal the vaccines spread throughout the body, causing various side effects due to the spike protein reaching all organs.

I was fired after 31 years as an ER physician for questioning the need for vaccination in those with natural immunity. Pfizer's biodistribution studies revealed that the COVID vaccines spread throughout the body, causing a wide range of side effects due to the spike protein reaching all organs.

Every day, just the 1% of the cells of your DNA that gets replicated stretches from here to the sun four times. If you're to line it up end by end, that's very hard to conceptualize. But it should give you a little bit of humility before you go and start monkeying with it with these vaccines that can actually alter your DNA. And that's what I'm gonna show you. Is that the vaccines had a DNA contamination in them that didn't tell you about that could in fact alter your genome. Alright? These people are vibe coding your genome. And this is a major attack surface to the human gene pool because if this thing starts to alter the lifespan of people, it's going to part you with your Bitcoin. You're gonna end up spending money in a fiat system that has no controls, has no liability, and ends up oftentimes inducing mandates to get what it wants done. Many people had have peer have gone and replicated this work. It happened on Twitter. It did not happen very quickly in the peer review system. The peer review system kinda kicked it out. Some of these papers have now been peer reviewed, but it took years for them to come to this conclusion. Now, the FDA, the EMA and the TGA have all admitted that this mistake has happened. How did it happen? There's a big bait and switch. Pfizer actually ran the trial of 22,000 people on the process on the left and after they got to the trial, they then switched to the process on the right and didn't retrial the drug. And in doing so, they left a tremendous amount of excess DNA behind in the product. So all of the vaccine efficiency numbers you've heard in the news are flawed. They're not real because that's not what actually went into the trial. What went to the public was actually something that came out of this process too. It's published now in the BMJ that this fraud happened and no one has yet been prosecuted for it. So what did they leave in there? What they left in there was something we know from the polio scandal. If you're not familiar with the polio scandal, that polio vaccines were also contaminated with something known as SV40 and it created a massive cancer wave. Now the whole virus isn't in these vaccines, but there is a very curious part of this called the SV40 region that Pfizer intentionally removed from the disclosure that they gave to the FDA. So the FDA has admitted that this SV40 material is in there. They did not spell this out to the regulators. The regulators did not find them and they're actually running cover for them saying this DNA is too little consequence to matter, it's too small, and it's not functional. But we know it's functional because Dean et al has published that this piece of DNA drives DNA straight to the nucleus. It gets used in gene therapy vectors.

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.

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 found blank inserts in vaccine information and a redacted 148-page study on myocarditis after COVID vaccination. There's a cover-up involving CDC, FDA, and other agencies worldwide. Pfizer withheld safety data for 55 years, revealing 1,223 deaths and 1,200 new adverse events post-vaccination. The FDA failed to regulate and disclose information on genetic transfer technology vaccines.

Willem Engel, a pharmaceutical scientist and human rights activist, discusses the concerns and safety issues surrounding COVID vaccines. He criticizes the spread of misinformation by governments and the lack of accurate registration of vaccine risks. He questions the validity of informed consent when crucial information is not shared with the public. Another speaker highlights the patterns of adverse reactions in different vaccine batches, suggesting that informed consent was impossible due to the unknown risks associated with each batch. The statistician presents data showing three distinct patterns of adverse reactions in different vaccine batches, indicating a concerning safety signal. The speakers call for the withdrawal of vaccine marketing authorizations and accountability for the alleged mishandling of the vaccination campaign.

Global governments and health authorities are ignoring the data that I see, suggesting a cover-up. I believe the vaccines are the cause, but I'm open to other explanations. This is a massive mistake for humanity, as we have administered this experimental vaccine to 5 billion people without proper human testing. The 28-day trial seems fraudulent, and I suspect data fraud at Pfizer.

I'm a doctor and scientist who has worked with the NHS and the World Health Organization. I sent an urgent report to the MHRA stating that the COVID vaccines were unsafe and causing harm. The yellow card scheme showed 250,000 adverse event reports and 1,253 deaths associated with the vaccines. The MHRA responded, suggesting that some reports may be coincidental. Since then, the Vigi access database has recorded over 5,000,000 reports of COVID vaccine harms, injuries, and deaths. These vaccines are genetic therapies, not safe or effective. Trust me, I am a scientist and doctor.

I was fired as an ER doctor for questioning the need to vaccinate those with natural immunity. Pfizer's hidden biodistribution studies revealed their vaccines spread throughout the body, causing a wide range of side effects due to the spike protein reaching every organ.

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.

I'm Philippe Boucalt, a cancer genomics researcher at the University of South Carolina. I've sequenced the DNA in the Pfizer vaccine and found that it contains fragments of DNA. This DNA could potentially cause rare but serious side effects, such as cardiac arrest and future cancer risks. The regulatory process that allowed this contamination is concerning. The DNA could integrate into long-lived somatic cells and potentially cause autoimmune attacks or disrupt tumor suppressors. To produce the vaccine, they cloned the PCR product into a plasmid vector, which led to the contamination. We can easily measure the amount of this substance in the vaccine and should conduct further studies to understand its implications. The FDA should require Pfizer to remove the DNA from the vaccine.

The speaker states: "We found circulating Pfizer mRNA in his exosomes three point six years after his last shot, and we also found plasmid DNA from the manufacturing process SV40 ORI segments, as well as the spike expression segments in his skin, in his Grover's disease area. He developed this skin disease after the shots." They add: "We also found vaccine spike protein and no nucleocapsid in this skin area as well." The speaker emphasizes timing: "Three point six years after his last shot, he suffered from myocarditis, pulmonary embolism, multisystem vaccination syndrome, neurological adverse events as well." They conclude: "And so the fact that we are finding this material forty three months after the last shot means we were lied to completely." The speaker claims: "We were told it would stay in the arm, it would degrade within weeks, that was wrong and we expect lawsuits to begin to flood in."

A recent study suggests that Pfizer may have excluded known deaths in the vaccine arm of its clinical trial from its data filing with the FDA in 2020. The study also found that trial subjects vaccinated with Pfizer's COVID-19 vaccine experienced a significant increase in cardiovascular deaths compared to placebo controls. This information was not disclosed by Pfizer when the FDA was evaluating the vaccine for emergency use. Additionally, researchers identified instances where Pfizer attributed potential vaccine-associated deaths to other causes, undermining vaccine safety data. The data presented to the FDA prior to the authorization of Pfizer's vaccine did not include all the deaths that occurred during the trial. The speaker raises concerns about the prioritization of profit over lives and warns against trusting Big Pharma.

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.

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.

The Pfizer vaccine may contain DNA in addition to mRNA, according to a scientist who sequenced the vaccine in his lab. He obtained empty vials from a colleague and found DNA in them. This DNA could potentially cause serious side effects and integrate into the genomic DNA of cells, leading to long-term effects. The scientist is concerned about the regulatory process that allowed this to happen and warns of the risks of genome modification and autoimmune attacks. While the risk of cancer is believed to be rare, it is not zero. Further investigation is needed to determine the extent of these risks.

I analyzed data showing a consistent 1.3 mortality gap between Moderna and Pfizer vaccines, with Moderna being 30% more likely to cause death. Pfizer reduced its active ingredient dosage due to toxicity concerns. The medical community must address this issue to maintain credibility. I reached out to a journal editor to review the data, which could potentially damage the reputation of health authorities and regulators.

The Pfizer vaccine contains not only mRNA but also plasma DNA from the vector used in its production. I sequenced samples from two batches of the vaccine in Colombia and found this DNA, which raises concerns about potential health risks. This DNA could integrate into the genomic DNA of cells, leading to permanent changes. Such integration poses theoretical risks, including autoimmune responses and cancer, depending on where the DNA inserts itself in the genome. While these risks may be rare, they warrant investigation to understand their implications better.

The Pfizer vaccine is contaminated with plasma DNA, not just mRNA. This DNA is the DNA vector used as the template for the in vitro transcription reaction. This was discovered by sequencing vials of Pfizer vaccine from Colombia. It's surprising that there's any DNA in there. The speaker is alarmed about the possible consequences of this, including rare but serious side effects like death from cardiac arrest. Mixing DNA with a lipid complex allows it to enter cells and become a permanent fixture. This is a real hazard for genome modification of long-lived somatic cells, like stem cells, and could cause a sustained autoimmune attack. There is also a very real theoretical risk of future cancer in some people. The risk is not zero and it may be high enough that we ought to figure out if this is happening or not.

A Pfizer whistleblower has revealed documents indicating over 158,000 reports of adverse reactions from December 2020 to February 2021, including serious issues like spontaneous abortions. This raises concerns about the intentional release of the vaccine and the knowledge of its potential to cause severe health problems, including heart attacks and infertility. The FDA's efforts to keep these documents hidden for 75 years suggest awareness of these dangers. The continued availability of the vaccine is alarming, especially considering that other vaccines have been removed for far fewer adverse cases. Those involved in this situation must be held accountable.

I spent 9 months researching the Pfizer vaccine with whistleblowers and scientists. Trials showed a 1 in 800 risk of serious harm from the vaccine, higher than COVID hospitalization rates. Other vaccines were pulled for less harm. Serious harm included hospitalization, disability, and life-changing events, with 40% related to clotting disorders.

I, along with six colleagues, wrote a letter to the European Medicines Agency (EMA) expressing concerns about the COVID vaccines. The EMA's response revealed shocking facts. They admitted that the vaccines were only approved for individual immunization, not for controlling or preventing infections. The EMA emphasized the lack of data on contagiousness and stated that repeated exposure to the virus could increase the risk of infection, even for the unvaccinated. The government's campaigns promoting vaccination to protect others were unauthorized and based on false information. The EMA also highlighted the importance of carefully considering safety information before administering vaccines. The mass vaccination efforts were in direct contradiction to the approved use of the vaccines. The EMA expected reports of side effects, but the government failed to report them, endangering lives. The vaccination campaign should be halted immediately.