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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.

Data accumulated to the point where meta-analysis studies could be done. These are very comprehensive analyses, and it virtually came back consistently that there was no benefit to risk ratio for taking a messenger RNA vaccine. In fact, it was more dangerous to take a vaccine than it was to contract COVID-19 and be hospitalized with it. This is we're now in 2022 that the status started to come out. The side effects for this essentially gene therapy were so enormous and progressive. It was difficult to fathom. And then finally, a few months ago, some of the detailed biochemistry studies started to appear in the literature. And this sudden flood of messenger RNA, it appears irrespective of what the messenger RNA insert is coding for. Just the sheer amount of number of millions of molecules of messenger RNA entering the cell is creating biochemical

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.

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.

Many people who have received mRNA injections for COVID-19 may die within 3 to 5 years, even with just one dose. These mRNA vaccines were rushed into clinical trials without going through the usual testing phases. Normally, vaccines would go through phase one, phase two, and phase three trials, but these vaccines skipped phase two and went straight to phase three, which involves injecting the entire population. More than 60,000 people have died during these trials, and adverse events such as heart problems and organ failure have been reported. This is a dangerous experiment happening in real time on real people, including children and pregnant women. It is important to be honest and inform people about the risks involved.

In January, a federal judge ordered the CDC to release text entries from a survey where individuals shared their experiences after receiving the COVID vaccine. The first two batches, totaling 780,000 reports from about 523,000 people, revealed numerous health issues, including heart inflammation, facial paralysis, and tinnitus. The data showed a variety of post-vaccination problems, such as miscarriages and seizures. For example, one report described a loss of consciousness and seizure immediately after the injection, while another mentioned a diagnosis of Bell's palsy due to facial numbness and paralysis.

mRNA vaccine recipients may face severe health risks, with predictions of significant mortality within 3 to 5 years. The COVID-19 vaccine trials are described as the most dangerous ever, with more deaths reported in one year than in 30 years of previous vaccine trials. Early treatments for COVID-19, such as vitamin D, hydroxychloroquine, and zinc, were overlooked in favor of vaccines. The mRNA vaccines are still in phase 3 clinical trials, having skipped critical phases, and many adverse events, including heart issues and organ failure, have been documented. The ongoing situation is likened to a large-scale experiment on the population, including vulnerable groups like children and pregnant women, which raises urgent concerns about safety and efficacy.

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.

Insufficient measures were taken to ensure the safety of the vaccine, as important information regarding heart problems was withheld for a couple of years. The speaker mentions that they have previously discussed myocarditis for over two and a half years. A paper by Michels and colleagues revealed 38 deaths, which Pfizer did not disclose during the FDA meeting in December 2020. The deaths were not questioned by the committee or FDA, and had they been fully reported, there would have been a three to four times higher risk of cardiovascular death. With this data, it is unlikely that any FDA panel would have approved the vaccine.

The COVID special committee revealed significant misinformation regarding the mRNA injection. Claims that it saved 20 million lives were exposed as false; that figure actually refers to all vaccines in history, not just the mRNA injection. In reality, it is suggested that the mRNA injections may have contributed to the deaths of 17 million people globally. There is no evidence to support the notion that these injections are safe and effective, as they were never properly tested.

Before the emergency use authorization of the vaccines, significant concerns were already known. The Pfizer technical document revealed that these vaccines caused widespread distribution of the encoded protein in major tissues and were associated with inflammatory reactions due to lipid nanoparticles. It was understood that these nanoparticles could deliver RNA and DNA into cells, and the use of pseudo uridine was intended to enhance the immune response and prolong the product's effectiveness. However, critical investigations regarding potential shedding, reproductive toxicity, and the presence of contaminants were not conducted. These omissions are concerning, especially considering previous FDA regulations that recognized the risks of genotoxicity related to manufacturing processes.

Two years ago, most people would have refused gene or cell therapy, but the pandemic has changed perceptions of innovation. The COVID vaccine is not a traditional vaccine as it doesn't provide immunity or prevent transmission. The Pfizer vaccine wasn't tested for transmission prevention before its release due to the urgency. Vaccinated individuals can still get COVID-19. Countries with rapid mass vaccination have seen increased infections and deaths. A study from the Cleveland Clinic suggests that the more shots received, the higher the risk of getting COVID. Vaccination puts evolutionary pressure on the virus, leading to mutations. Epidemiological analysis shows a significant number of deaths related to the vaccines, with dangerous mechanisms of action and consistency with other fatal conditions. Temporal relation is also evident, with many deaths occurring shortly after vaccination.

There have been unprecedented injuries, disabilities, and deaths from COVID-19 vaccines. By January 22, 2021, 182 deaths were reported to the US vaccine adverse event reporting system. The FDA and CDC, who co-administer the program, lack experience in vaccine campaigns. Pfizer knew about 1,223 deaths within 90 days of their vaccine but kept it confidential. Moderna has not released their data. There are over 34,100 peer-reviewed papers on vaccine injuries, disabilities, and deaths.

The government tracked vaccine side effects through the VAERS system and the new v safe system for COVID-19 vaccines. V safe required all Americans to sign up and report any adverse events after vaccination. Around 7.7% of the 10 million participants sought medical care within the first 6 months, with over 70% needing emergency or urgent care. The CDC published 40 studies based on this data.

In November 2022, Medsafe discontinued regular reports on adverse events following COVID injections in New Zealand. They acknowledged that the reporting system captures only a small fraction of the actual number of adverse events. By that time, Medsafe had received 65,000 adverse event reports, suggesting that around 1.3 million New Zealanders experienced adverse events. Among these reports, there were 3,688 serious cases, nearly 6,000 for young people aged 5 to 19, and 184 deaths. The numbers of adverse events and deaths following COVID injections far exceed those from other vaccines. Similar trends are observed globally, with thousands of deaths and millions of adverse event reports for COVID vaccines. The impact on individuals and families is significant and unprecedented.

Following a subpoena to HHS, a timeline reveals that on 02/28/2021, Israeli health officials notified the CDC of myocarditis reports, especially in young people, after the Pfizer vaccine. On April 12, a DOD consultant raised concerns to the CDC and FDA about monitoring cardiac adverse events, stating, "If you do not ask, you will not see it." In mid-April 2021, CDC officials discussed myocarditis safety signals with mRNA vaccines based on DOD and Israeli data but didn't immediately warn the public. By April 2021, VAERS reported 2,926 worldwide deaths within 30 days of injection, with 46% occurring on days zero, one, or two. The speaker claims that when he raised this issue, he was censored. From May 17-21, 2021, CDC officials discussed a formal health warning on myocarditis, noting underreporting to VAERS. On May 24, officials asked if VAERS was signaling for myopericarditis and were told yes for ages 16-24. From May 25-27, the CDC updated Pfizer and Moderna but not the public. On May 26, the FDA didn't concur with the warning, and the CDC and FDA decided to nix it, publishing less formal clinical considerations instead. An FDA official raised concerns about even posting those. The CDC then edited clinical considerations, removing advice to restrict patients with myocarditis from rigorous activity.

We are generating real-time data on mRNA vaccines, which have been in development for years due to side effects. Pfizer and Moderna used the pandemic to accelerate their development. The collaboration with BioNTech on flu led to the quick rollout of the mRNA vaccine. Clinical trials skipped phases, causing uncertainty. Concerns arise about vaccine distribution and the need for booster shots. Politics play a role in decision-making.

The speaker questions how many people injected with mRNA products knew they weren't receiving a traditional vaccine, suggesting many, including medical professionals, are unaware due to the perception of conspiracy. The speaker claims there was a sufficient safety signal in VAERS to halt the rollout in January, citing almost 90,000 VAERS entries and nearly 700 deaths within the first month. They state that historically, products causing over 50 deaths have been pulled from the market. The speaker questions why the CDC, HHS, and FDA aren't investigating this data.

According to Pfizer documents, one month after the vaccine rollout in November 2020, Pfizer knew the vaccines didn't stop COVID and identified vaccine failure. Internal documents showed COVID was the third most common side effect. Within months, Pfizer hired 2,400 staffers to process adverse event reports. By May 2021, Pfizer and the FDA knew the vaccines caused heart damage in 35 minors within a week of injection, but this wasn't disclosed to parents until August 2021. The CDC initially claimed the injection materials stayed in the injection site, but Pfizer knew the materials biodistribute throughout the body within 48 hours, settling in the brain, liver, adrenals, and spleen. In women, they accumulate in the ovaries, and there's no known mechanism for the body to eliminate the lipid nanoparticles from the ovaries.

As of February 2024, the number of reports for COVID-19 vaccines in VAERS is significantly higher than all other vaccines combined since 1990. The government was not fully prepared for this overwhelming influx of reports. They had to quickly reassign people and hold numerous meetings to increase their capacity to review these reports.

Pfizer knew their failed coronavirus modifications were dangerous, causing heart issues and death in animals. There is extensive literature, including patents and scientific publications, showing that they knew the heart was the target. The mRNA shots using pseudo uridine were known to generate tumors and rapid cancers. Remdesivir, with a 53% mortality rate, was chosen by the FDA as a COVID treatment, despite being deemed unethical by the World Health Organization due to its high death rate. The definition of adverse events was changed to exclude any causal link, allowing them to deny any negative effects. Data on these injections won't be published for another four and a half years.

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.

Many recent conspiracy theories have proven true. The claim that mRNA injections saved 20,000,000 lives was debunked as it actually referred to all vaccines, not just mRNA. In reality, mRNA injections may have caused 17,000,000 deaths worldwide. These injections were not properly tested, contradicting claims of safety and effectiveness.

None of the vaccines, including the COVID vaccine, have undergone proper testing. No childhood vaccine has completed a placebo-controlled clinical trial with sufficient duration and power to confirm its safety before being administered to millions of children in America. This is not an opinion; it can be verified by anyone visiting the FDA website, where the package inserts and clinical trial documents are available for review.

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.