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Since May 2020, Remdesivir has been linked to a 30% death rate among patients receiving the drug for 5 to 10 days in hospitals. In New York, 26.9% of Medicare-aged patients who received Remdesivir died. The Cardiovascular Toxicology Journal found in October 2020 that Remdesivir is cardiotoxic and can cause death of heart cells. Despite this, the FDA and NIH continue to approve and recommend Remdesivir as the only drug for hospitalized COVID-19 patients. The World Health Organization published in April of last year that Remdesivir leads to increased acute kidney failure compared to other drugs. Shockingly, the FDA recently authorized the use of Remdesivir for newborns and children up to 18 years old.

In April 2020, BioNTech and Moderna called mRNA injections experimental gene therapy. Publicly traded pharmaceutical executives admit they deceived the public by labeling them as vaccines to increase acceptance. They suggest these injections turn people into bioweapons factories and could lead to addiction to gene editing technologies. Pseudouridine, a cancer promoter, was added to shots, potentially increasing cancer risk by 400%. The pharmaceutical industry may have a financial interest in promoting these injections. This could make people customers of an industry with a history of harming citizens since 1604.

Speaker 0 described a guest whose 18-year-old daughter was injected with Pfizer and developed cancer. He stated that he has sat across numerous people who lost their children to these injections, with some deaths immediate and others gruesome, and that these people must testify to lawmakers and others recounting their stories repeatedly. He framed this as a massive crime that needs to stop. He asserted that the FDA was fully aware that these injections would cause cancer, citing published guidance documents. He claimed that the FDA regulates the industry and, in 2015 and 2013 (and even more recently), wrote extensive guidance documents explaining to manufacturers developing mRNA products that they must study risks, including cancer, death, fertility issues, blindness, strokes, and cardiovascular issues. He said these risks were documented as regulatory knowledge and that manufacturers were told they had to study these risks and exclude them. He also claimed that studying these risks in healthy volunteers was not allowed because it was considered unethical. He contrasted this with 2020, stating that “all of a sudden, all of this is solved,” calling it a joke, and that this period raised his suspicions, prompting him to investigate independently. He concluded by describing the situation as a premeditated crime in which regulators knew, and that the military conducted a “fake exercise” to capture all these pharmaceutical companies and compel them to create these weapons.

At home, it is recommended to treat viral replication by giving remedies like zinc and hydroxychloroquine, ivermectin, which reduce the spread of the disease. However, the protocol followed was different. No treatment was given until hospitalization, where ventilators and Remdesivir were used. It is known that Remdesivir can be harmful, as it caused side effects in Ebola patients. The drug was manipulated and made standard of care, leading to kidney failure, heart failure, and organ collapse in COVID-19 patients. The deaths during the pandemic were often attributed to kidney failure, which was caused by Remdesivir, not the virus itself.

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.

Since May 2020, Remdesivir has been linked to a 30% death rate among patients receiving the drug in hospitals for 5 to 10 days. In New York, 26.9% of Medicare-aged patients who received Remdesivir died. The Cardiovascular Toxicology Journal found in October 2020 that Remdesivir causes heart cell death and is cardiotoxic. However, the FDA and NIH continue to approve and recommend Remdesivir as the only drug for hospitalized COVID-19 patients, despite the World Health Organization's report in April of last year that it causes increased acute kidney failure. Shockingly, the FDA recently authorized the use of Remdesivir for newborns and children up to 18 years old.

Since May 2020, remdesivir may result in at least 30% death in hospitalized patients who receive it for five to ten days. CMS data for Medicare patients in New York showed 26.9% of those who received remdesivir died. In October 2020, the cardiovascular toxicology journal found remdesivir causes death of heart cells, is cardiotoxic, and can lead to cardiac arrest. Despite this, in December 2020, the NIH, with Anthony Fauci, updated guidelines listing remdesivir as the only FDA-approved drug for hospitalized Americans, even though the WHO published data in April of last year that it increases acute kidney failure compared to other drugs used to treat COVID-19. As of January 21st of this year, the FDA extended emergency use authorization, making remdesivir the only authorized medication that can be administered intravenously to newborns to 18-year-olds for COVID-19.

Before the pandemic, Dr. Fauci tested Remdesivir in an Ebola trial in Africa alongside four other drugs. However, the institutional review board (IRB), responsible for ensuring safety in clinical trials, intervened and removed Remdesivir from the trial due to its high fatality rate. Ebola typically kills 53% of those infected, but Remdesivir was causing even more deaths. It seems illogical to then administer this drug to individuals with a disease that has a much lower infection fatality rate of 1%. This decision appears questionable, but unfortunately, there is a history of similar actions being taken.

There was no pandemic, as all-cause mortality data did not increase, and the WHO fraudulently declared one. An inappropriate PCR test was used, giving the false impression of a novel disease. People were mistreated via mass ventilation, sedatives and respiratory depressants in care homes, and denial of antibiotics, leading to deaths from bacterial pneumonia. Since there was no pandemic, experimental medical interventions were unnecessary. It is impossible to rapidly invent, test, and manufacture a complex biomedical product; the fastest record was six years. What was done was the advancement of intentionally toxic materials, rushed and injected into people, resulting in millions of deaths. The lie of a pandemic was maintained to inject billions with an intentionally dangerous substance, resulting in 17 million deaths so far.

Ralph Barrick, the inventor of coronavirus and developer of Remdesivir, a drug used to treat COVID, had a hand in both. However, Remdesivir had a high kill ratio of 53% and was pulled by the World Health Organization for Ebola treatment. Despite this, in 2020, Anthony Fauci and others decided to use Remdesivir on COVID patients, knowing it would cause deaths. This was premeditated murder, with the criminals sitting next to President Donald Trump. There are other individuals involved as well. Efforts are being made by courageous sheriffs and DAs to compile evidence of the deaths caused by Remdesivir and take legal action to end these felonies.

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.

In 2018, remdesivir had a high kill rate in Ebola trials, making it unethical for use in Africa. Despite this, it was chosen in 2020 to treat COVID. The financial interests behind promoting certain drugs during the pandemic raise concerns about justice. The same group linked to eugenics influences these decisions, which is troubling.

Patients are dying not from COVID, but from treatments like remdesivir causing organ failure. One person's mother died after being given remdesivir against their wishes, leading to organ shutdown. There was a financial incentive for hospitals to admit patients and put them on ventilators, resulting in unnecessary treatments and deaths.

I recently heard stories of people losing their children to Pfizer injections, some experiencing immediate or gruesome deaths. The FDA knew about potential risks like cancer from as far back as 2013, but suddenly in 2020, these concerns were ignored. This seems like a premeditated crime, with regulators aware of the dangers. Military involvement in pushing these products is suspicious.

Multiple studies, including one by the WHO, show that Remdesivir actually increases the risk of death. It's concerning that the federal government incentivizes hospitals to prescribe this toxic drug by offering a 20% bonus on the entire hospital bill for Medicare patients. Remdesivir costs around $3,000 per course. On the other hand, Ivermectin, as mentioned by Dr. Kory, reduces the risk of death by about 50%. Unfortunately, clinicians still use the wrong drug, Dexamethasone, in the wrong dose and for the wrong duration of time, simply because the NIH recommends it. The NIH and other agencies have disregarded multiple FDA-approved drugs that are both cost-effective and safe.

In 2018, remdesivir was considered unethical for Ebola clinical trials in Africa due to a 53% kill rate, higher than Ebola's typical mortality. Despite this, it was chosen to treat COVID in April and May 2020, with Anthony Fauci and Deborah Burke advocating for its use despite the World Health Organization's ethical concerns. The speaker claims that a conflict of interest exists because the same entities that financially benefit from promoting certain products are declaring the pandemic. These entities are allegedly linked to the Eugenics office at Carnegie Mellon in 1913 and the establishment of the World Health Organization in 1953. The speaker expresses concern about the influence of eugenics on these decisions.

An experimental drug called remdesivir will be responsible for people's deaths. People diagnosed with COVID-19 in the hospital died between day one and day nine, specifically on day nine of a ten-day remdesivir treatment. Dr. Anthony Fauci claimed in May 2020 that remdesivir was found safe and effective in a drug trial in Africa a year earlier (02/2019), and hyperlinked the study in a memo to hospitals. However, in that trial, remdesivir killed 53% of people, and the safety board suspended its use at month six, deeming it too deadly and toxic for Ebola patients. Dr. Anthony Fauci and his department at the NIH funded the Ebola trial in Africa in 02/2019. Therefore, Fauci lied to Congress and the American people by claiming the drug was safe and effective against Ebola, when the safety board had deemed it too deadly and pulled it from the trial.

I recently met someone whose 18-year-old daughter developed cancer after receiving the Pfizer vaccine. I've heard from many parents who lost children to these injections, some experiencing immediate and horrific deaths. They repeatedly share their stories with lawmakers, highlighting a significant crime that must end. The FDA was aware of the potential cancer risks associated with these vaccines, as outlined in guidance documents from 2013 and 2015. These documents instructed manufacturers to study risks like cancer, fertility issues, and cardiovascular problems, and deemed it unethical to test on healthy volunteers. Yet, by 2020, these concerns were seemingly overlooked. This raises serious suspicions about the intentions behind the vaccine rollout, suggesting a premeditated crime where regulators and the military may have colluded with pharmaceutical companies.

Technology was proven unsafe long before 2021. The COVID-19 vaccines contain lipid nanoparticles that carry synthetic DNA into various organs, risking genomic instability, cancers, autoimmune diseases, and hereditary disorders. Contamination levels are far above permissible limits, and we're seeing evidence in patients. Cancer-free patients are relapsing with aggressive cancers post-vaccination, including unusual and rapid tumor growth. There's a rise in blood cancers too. The vaccines also contained endotoxin, which causes shock and can lead to death. The lab-leak possibility was dismissed without investigation, leading to devastating lockdowns. The "safe and effective" mantra was a lie; these injections have caused unprecedented harm. Ethical principles were ignored, and informed consent was violated. These mRNA gene therapies shouldn't have been used on anyone. We must halt distribution, monitor cancer trends, develop testing, and research vaccine-related conditions.

In 2018, remdesivir had a high kill rate in Africa, making it unsuitable for Ebola trials. Yet, in 2020, it became the top choice for treating COVID-19. Despite objections from the World Health Organization, Anthony Fauci and Deborah Birx endorsed its use. The issue lies in allowing those with financial interests to dictate pandemic responses, potentially influenced by eugenics ideologies.

Remdesivir, also known as "run death is near," played a key role in creating the illusion of a deadly pandemic. Doctors were told COVID-19 causes pneumonia and kidney failure. The hospital protocol involved renal and internal medicine consults, screening patients for kidney issues due to remdesivir's potential kidney damage. They monitored kidney function and were supposed to stop the drug if function declined. Remdesivir-induced kidney injury led to fluid buildup, often misdiagnosed as COVID-19 pneumonia. This, followed by ventilation and more drugs, became a deadly cycle. The increase in acute kidney injury deaths coincided with the rollout of the new tech bonus and later, the vaccine rollout in 2021, with unvaccinated patients possibly targeted for these protocols.

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.

Patients were desperate for ivermectin as their loved ones died, but the focus shifted to remdesivir, a previously failed Ebola drug. By November 2020, the World Health Organization advised against its use, citing ineffectiveness and potential kidney and liver damage. The European Society of Critical Care supported this stance. Despite the warnings, the U.S. Health and Human Services incentivized hospitals with a 20% bonus for administering remdesivir, leading to widespread use. It failed to reduce mortality and caused serious injuries, with some patients dying as a result. In May 2022, the WHO reaffirmed its initial decision, stating that remdesivir should never have been used.

Speaker 0: Remember that in 02/2018, remdesivir, one of my favorite targets, remdesivir was too unethical to put into Ebola clinical trials in Africa because it had a fifty three percent kill rate published in medical journals. Ebola doesn't have a fifty three percent kill rate, but it was chosen in April and May 2020 to be the drug of choice to treat COVID. This drug was too unethical to use in an African clinical trial because it was killing fifty three percent of the people that it was given to. And we had Anthony Fauci, Deborah Burke sitting next to the president going, we need to use remdesivir despite the fact that the World Health Organization said it was unethical to use it. Here's the problem. The problem is as long as the financial interest that dictates what product is going to be promoted is the one making the declaration of the pandemic, We have no possibility for accountability. We have no possibility for justice. And what we do is we allow people who were formed out of the Eugenics office, Carnegie Mellon in 1913, that same group of people that were the same group of people that established the World Health Organization in 1953, that same group of people are the ones who are making this decision. And I don't know how you feel about Eugenics, but I have a problem with it.

I've stated since May 2020 that remdesivir will result in at least 30% death in those who receive it in the hospital. I had data pulled for Medicare patients in New York, and found that 26.9% of those who received remdesivir died. As of October 2020, the cardiovascular toxicology journal found that remdesivir causes death of heart cells and can lead to cardiac arrest. Yet, in December, the NIH decided to update all guidelines for treatment drugs allowed for COVID-19, and remdesivir was the only FDA-approved drug for hospitalized Americans, despite the WHO publishing that it causes increased acute kidney failure. As of January of this year, the FDA extended an emergency use authorization, making remdesivir the only authorized medication that can be administered to newborns to 18-year-olds.