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I have a chart that shows the CDC and FDA's own numbers on adverse events. Despite social media censorship, these are the true numbers. Over 28 years of reporting, Ivermectin, Hydroxychloroquine, and Dexamethasone are shown to be safe drugs. However, since the COVID pandemic, remdesivir and the COVID vaccines have had adverse events. Our response to COVID has been a failure, with 4% of the world's population but supposedly 16% of the deaths. The VAERS system has recorded 1,600,000 adverse events from the COVID vaccines alone.

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.

Behind the scenes communications from the BC Centre for Disease Control revealed that COVID-19 vaccines were 16 times more dangerous than flu shots for children. The data was manipulated before being released to the public, omitting comparisons to flu vaccines and downplaying serious adverse events. This lack of transparency raises concerns about health regulators withholding vital information from the public.

Deaths in multiple countries increased after COVID-19 vaccine rollouts, with 17 million deaths linked to vaccines. All-cause mortality rose in countries post-vaccine deployment, with peaks during booster rollouts. The report found no evidence of COVID-19 vaccines saving lives, showing increased deaths with age and no beneficial effects. Countries like India, Australia, Canada, Israel, and the US experienced similar trends, with excess deaths coinciding with vaccine campaigns. In the US, 160,000 excess deaths occurred in the 25-64 age group during a vaccine surge. Share this information to help others make informed decisions about COVID-19 vaccines. Stay healthy.

The speaker discusses safety signals from VAERS data related to COVID-19 vaccines, highlighting a high number of adverse events and deaths. They question why these issues are not being addressed properly by authorities. Comparisons are made to past vaccine withdrawals due to adverse events. The speaker emphasizes the significant increase in adverse event reporting for COVID-19 vaccines, especially in children. They also mention specific criteria being met to establish causality. In conclusion, they criticize the lack of adherence to standard procedures by CDC, HHS, and FDA in addressing vaccine-related injuries.

The Dutch paper reveals a 36% higher risk of serious adverse events in the Pfizer vaccine group compared to the placebo. Despite this, the public was misled about the safety and effectiveness of the vaccines. Adverse reactions like stroke and heart attack were downplayed, making it difficult to link them to the vaccines. The truth is slowly coming to light, exposing the deception by big pharma, governments, and the media. Those responsible may face consequences in the future.

One in thirty-five recipients of the booster vaccine had vaccine-associated myocardial injury. This level of adverse reaction is described as off the scale in healthcare. The speaker suggests that promoting the vaccine in places like New Zealand is unethical. The speaker believes this risk level would only be acceptable if the alternative was certain death, and otherwise, it is complete madness.

Speaker 0 states that the study confirms suspicions from the past five years that common sense has deteriorated in the population. The study analyzed the VAERS system from the 1990s to 2024 and examined PRRs (proportional reporting ratios), which measure how many more adverse events occur with the COVID shots compared to the flu shot or other vaccines. It reports 8686 safety signals of neuropsychiatric adverse events, with some up to 3,000 times higher than the flu shot. The safety signal threshold defined by CDC/FDA for PRRs is greater than two, and all reported signals exceeded this threshold. The listed conditions include schizophrenia, dementia, Alzheimer's, cognitive impairment, strokes, brain clots, homicidal tendencies, homicidal behavior, and psychosis, described as people hallucinating and brain damage. The speaker notes that this large number of safety signals aligns with a recent study indicating that people who had strokes showed toxic spike protein production in their brains for up to seventeen months after vaccination, which the speaker suggests explains the observed deterioration in cognitive function.

In an 18-month period, ACC in New Zealand paid out $7,560,000 for COVID vaccine injuries, with only 1,664 out of 4,156 claims accepted. This is significantly higher than the typical annual payments for vaccine injuries in 2018 and 2019, which were around $146,000. The high bar for acceptance raises concerns about the safety of COVID vaccines compared to previous years.

In 2022, Australia had over 10 million COVID cases, with over half the country infected despite vaccination efforts. The excess deaths in 2021 were higher than expected, and there were over 140,000 reported vaccine injuries, three times higher than previous years. The TGA, responsible for monitoring vaccine injuries, ignores these signals. The head of the organization, Professor Skerritt, has a conflict of interest as it is funded by Big Pharma. The chief health officer, Professor Brendan Murphy, hadn't read the non-clinical report on the Pfizer vaccine and made incorrect statements about it. The law in Australia states that vaccination cannot be coerced and individuals must be properly informed about the vaccine's contents.

A whistleblower provided access to 5 million confidential New Zealand government vaccination records. Analysis showed that the mortality rate in New Zealand increased for 5 months after vaccination, regardless of the time of year. The rate of mortality increase also rose with each subsequent booster. The chances of this excess being random and not caused by the experimental vaccines were calculated at 1 in 100 billion. The speaker requested the government to suspend the mRNA vaccines to prevent further harm. However, Speaker 1 disagreed, stating that over 120,000 deaths were prevented by COVID vaccines in England. The report mentioned by the first speaker has been debunked globally, as adverse events after vaccination do not necessarily mean they were caused by the vaccine.

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.

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.

The Australian government is accused of suppressing COVID vaccine adverse reactions and deaths. Excess deaths in 2022 are around 26,000, but no questions are being asked. Doctors are not reporting adverse effects or deaths, with only 14 deaths officially attributed to the vaccine out of over 1,000 reported. Doctors fear losing their livelihoods if they report accurately. The spike in deaths after COVID was attributed to the vaccine, leading to anger over the situation.

In the message described, Speaker 0 highlights a key claim: the CDC and FDA were fully aware of the masking phenomenon within their empirical Bayesian analysis. The speaker emphasizes that this awareness was part of the information being conveyed in a letter to Bobby Kennedy. The central issue raised is not about general safety signals, but about the timing of deaths relative to vaccination. The speaker notes a concern that began earlier, stating that back in October there were discussions with Mike Eden about these injections. The concern is tied to what was observed in the data, specifically that “early on in March and April” the data appeared to be "screaming at us" when looking at thousands of deaths. The speaker provides a concrete statistic: “forty six percent of those deaths were occurring on the day of vaccination than one or two days.” The speaker then updates the figure, saying that they are “up to almost thirty nine thousand deaths” in total, and adds that “Twenty four percent of those deaths occurred on the day of vaccination or within one or two days.” The speaker asserts that this information “has been available month by month by month since about March, April 2021,” yet alleges that “the federal officials are still not acknowledging it.” Instead of acknowledging these signals, the speaker claims officials point to other metrics, stating they “go to these, you know, PRR, the proportional reporting ratios, or a more sophisticated” approach. The claim continues that when PRRs were showing safety signals, officials reacted as if, “oh, we're not using those. We're using empirical Bayesian analysis. They set the trigger.” In summary, the transcript presents a narrative in which the CDC and FDA are described as being aware of a masking phenomenon identified through empirical Bayesian analysis, with specific, alarming timing data linking a significant proportion of deaths to the day of vaccination or the following couple of days. The speaker contends this information has been publicly accessible on a monthly basis since early 2021, but accuses federal officials of not acknowledging it and of favoring a different analytic framework (PRR) or of claiming to use empirical Bayesian analysis after the fact, implying that the trigger for safety signals was set within that framework. The overall emphasis is on the alleged discrepancy between available data and official acknowledgment, as well as the choice of analytic methods used to interpret safety signals.

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.

The speaker expresses concern that only 5% of adverse reactions are reported in the database, suggesting it's just the tip of the iceberg. Another speaker reassures that the vaccine is safe and there is no evidence of it causing deaths. Prior to the COVID vaccine rollout, an average of 1500 adverse event reports were received annually for all vaccines in New Zealand, resulting in one or fewer reported deaths per year.

The speaker claims that based on the number of vaccine doses administered worldwide, they have calculated the toxicity of the vaccine and believe it would have killed 17 million people. They also mention a correlation between booster rollouts and an increase in all-cause mortality, which they observe in multiple countries. Another speaker adds that typically, deaths increase in winter and decrease in summer, but during the COVID vaccine campaign, there are spikes in mortality right after vaccine campaigns, even in the summer. They note this pattern globally, including in the Southern Hemisphere. This phenomenon is described as unusual and unprecedented.

Australia has administered over 60 million vaccine doses to over 20 million people. Despite this, governmental health authorities have chosen not to monitor new or emerging cancer trends, and have failed to make post-vaccination cancer trend data publicly available, which is a critical oversight. Given the massive contamination levels of rogue residual DNA in the Australian vials, we must expect an ongoing rise in cancers and other genetic disorders in Australia. This is a potential long-term health crisis. This matter must be taken seriously. We must advocate for immediate public health responses and monitoring of these trends. Without action, Australians are vulnerable to preventable diseases that may devastate families and strain our healthcare system. These gene-based vaccines should never have been considered. The technology had never been proven to be effective in preventing coronavirus infections and was unsafe long before 2021.

Australia has administered over 60 million vaccine doses to more than 20 million people, yet health authorities have not monitored cancer trends post-vaccination. The lack of publicly available data on these trends raises concerns about public health oversight. Given the contamination levels of residual DNA in the vaccines, there is a potential for an increase in cancers and genetic disorders, posing a long-term health crisis. Immediate public health responses are necessary to monitor these trends and protect Australians from preventable diseases that could overwhelm the healthcare system. The use of gene-based vaccines raises questions, as their effectiveness in preventing coronavirus infections had not been proven, and safety concerns existed prior to their use in 2021.

Over the past 10 years, the number of adverse events and deaths from COVID products has far surpassed those from all other vaccines combined. This is a concerning trend that affects people of all age groups, not just the elderly. The data, owned by the FDA and CDC, is normalized to the number of doses administered, and it clearly shows a significant increase in adverse events, particularly among children and young adults. The use of bivalent shots has been disastrous, with severe adverse events and even deaths reported soon after their administration. Babies as young as 0 to 4 years old were injected with these vaccines before they were officially authorized. The data also suggests a potential link between syncope (fainting) and myocarditis diagnoses, particularly in the 25 to 39 age group. Younger individuals are filing more reports, indicating that they are more affected by these adverse events.

The speakers express concern that only a small percentage of adverse reactions to vaccines are reported. Despite this, they assure viewers that the COVID vaccine is safe. They highlight that prior to the COVID vaccine rollout, an average of 1500 adverse event reports were received each year for all vaccines in New Zealand, resulting in one or fewer reported deaths annually.

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.

The speaker discusses the increase in mortality rates after the vaccine rollout in Australia. They point out a peak in mortality during the country's summer, which coincides with the sudden rollout of the third dose of the vaccine. The same pattern is observed in different states of Australia. The speaker then mentions a vaccine equity program in Mississippi, where the most vulnerable people were vaccinated. This program resulted in a significant increase in cumulative doses given and a corresponding peak in mortality rates for individuals aged 25 to 64 in poor states across the United States, such as Alabama.

The speakers express concern about the limited reporting of adverse reactions to vaccines. They mention a report suggesting that only 5% of adverse reactions are recorded in the database. Despite this, they assure viewers that the COVID vaccine is safe. They highlight that prior to the COVID vaccine rollout, the average number of adverse event reports for all vaccines in New Zealand was 1500 per year, with one or fewer deaths reported annually.