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The speaker explains that a series of laws allowed the military to take over vaccine distribution without any clinical trials or safety testing. The safety testing conducted by the pharmaceutical industry was just for show and had no regulatory implications. The FDA, which is responsible for regulating medical products, does not have the authority to regulate these countermeasures. The legal framework being used pretends that these are health products when they are actually in a different legal space.

A bombshell report reveals the Pentagon controlled the COVID-19 program, using shady approval authorizations to shield big pharma from liability. Documents show lack of compliance with good manufacturing practices and deception in clinical trials. The National Security Council treated COVID as an act of war, coordinating with various agencies to keep information secret. The Pentagon ordered countermeasure prototypes, not vaccines, without informed consent. The Biden administration censored lab leak theories. A secret Pandemic Enterprise was formed in 2013 to plan responses. The public was misled about the safety and testing of the injections.

Four companies—Pfizer, Merck, Blackstone, and Sanofi—produce all 72 vaccines and have a history of criminal behavior. Over the last decade, they collectively paid $35 billion in penalties for falsifying science, defrauding regulators, and causing harm. Merck's Vioxx, marketed as a headache pill, led to the deaths of up to 500,000 Americans due to heart attacks, while the company profited despite paying $7 billion in fines. No one was jailed for these actions. It’s difficult to believe these companies, known for dishonesty in other products, are suddenly trustworthy with vaccines. In the U.S., a law passed in 1986 prevents individuals from suing vaccine manufacturers, regardless of negligence or harm caused.

A bombshell report reveals that the Department of Defense controlled the COVID-19 program from the beginning, using shady approval authorizations to shield big pharma from liability. The Pentagon used laws like the PrEP Act, Emergency Use Authorization, and Other Transaction Authority to protect pharmaceutical companies. Documents obtained by a former executive show that the vaccines were not compliant with good manufacturing practices, with extreme variability in adverse events. Clinical trials were deceptive, with subjects and investigators kept in the dark. The National Security Council treated COVID as an act of war, while telling the public it was a health event. The Pentagon's influence extends to multiple agencies, with a secret Pandemic Enterprise formed in 2013. The countermeasures used are prototypes, not fully tested vaccines.

A bombshell report reveals that the Department of Defense controlled the COVID-19 program from the start, using shady approval authorizations to shield big pharma from liability. The Pentagon employed laws like the PrEP Act, Emergency Use Authorization, and Other Transaction Authority to protect pharmaceutical companies and avoid proper clinical trials. Documents obtained by a former pharmaceutical executive, Sasha Lydipova, confirm that the vaccines were not good manufacturing practice compliant, with extreme variability in adverse events. The Pentagon's involvement stems from treating COVID-19 as an act of war, with the National Security Council setting policy. The deception extends to censoring lab leak theories and coordinating efforts across multiple agencies. The public was misled about the nature of the vaccines, which were actually prototypes and not subject to proper testing.

The top agencies leading Operation Warp Speed were the NSA and the Pentagon, not public health agencies like HHS, CDC, or NIH. The vaccines were developed by NIH and manufactured by military tractors, with Pfizer and Moderna being paid to put their names on them. The speaker believes that Operation Warp Speed is not new, as it has been happening since 1980 at Fort Detrick, a bioweapons lab. They claim that the government has been involved in unethical practices, such as injecting the military with HIV in the 1990s.

Maddy DeGary, a participant in Pfizer's COVID-19 vaccine trial for 12 to 15-year-olds, suffered serious injuries post-vaccination. Pfizer initially downplayed her condition as abdominal pain, misleading the FDA. Despite being wealthy, only after an email to FDA officials did Pfizer admit to DeGary's injuries. FDA's response was lackluster, showing no concern for Pfizer's misconduct. The failure to report all adverse events corrupts the trial process, with no repercussions for Pfizer's actions.

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.

In October 2020, the speaker was asked if Operation Warp Speed would use the expanded access use pathway to get on the market. The speaker responded that they would not be using that pathway because it requires an institutional review board (IRB) and informed consent, which they wanted to avoid due to the added complexity. The speaker expressed concern for the lack of informed consent in vaccine injuries and deaths. They mentioned that this scheme was designed to deceive professionals and took years to uncover. Both sides, including FDA staff, CDC staff, pharma staff, management, and lawyers, were aware of what they were doing.

Four companies, Pfizer, Merck, Blackstone, and Sanofi, are responsible for producing all 72 vaccines. However, these companies have a history of criminal activity, collectively paying $35 billion in fines for falsifying science, defrauding regulators, lying to doctors, and causing the deaths of hundreds of thousands of people. For instance, Merck's product, Vioxx, was sold as a headache pill but caused heart attacks and killed around 120,500 Americans. Despite this, they only paid fines and faced no jail time. It is hard to believe that these companies, known for lying and cheating, are honest when it comes to vaccines. The vaccine industry is immune to lawsuits, making it the perfect place for these companies to avoid consequences.

A bombshell report reveals that the Department of Defense controlled the COVID-19 program from the beginning, using shady approval authorizations to shield big pharma from liability. The Pentagon used laws like the PrEP Act, Emergency Use Authorization, and Other Transaction Authority to protect pharmaceutical companies and avoid proper clinical trials. Clinical trial subjects and investigators were deceived, and informed consent was not required. The National Security Council treated COVID-19 as an act of war, while telling the public it was a health event. The Pentagon's influence extended to agencies like the FDA and NIH. A secret Cabal called the Pandemic Enterprise was formed in 2013 to discuss countermeasures with strict confidentiality. The so-called vaccines were actually prototypes ordered by the Department of Defense, and people were not informed of this. Safety testing and animal trials were skipped, violating regulations.

It turns out that the manufacturers did not do due diligence to ensure these were safe products before they were released onto the American market. And throughout 2021 to 2024, the drug companies essentially ran the pandemic response. Judicial Watch, America's first legal, were able to obtain some documents. They didn't want to release it. Pfizer, they wanted a seventy year moratorium on the clinical data from the trials, which from the start showed these never prevented infection, never prevented disease transmission. And there's no good clinical data to ever show it reduced the severity of disease. The CDC in response, I don't know what's wrong with that once fine agency, but they've become a supplicant of big pharma. No. The paper's been torn to shreds by epidemiologists. It was based against a computer model and against an idea where you have the peak and it comes down and then it goes back up again.

Pfizer knew within three months of rollout that 1,225 people had died. By April 2021, Pfizer was aware that minors' hearts were being damaged by the injection, with warnings coming from the Israeli health ministry and a pediatric group. Email chains, obtained through FOIA requests, show this information was sent to Dr. Fauci, Dr. Walensky, the President, and White House staffers. A "freak out conference" ensued, allegedly to plan how to lie to the American people, resulting in a 17-page redacted script. The claim is that in April and May 2021, authorities stated that pericarditis and myocarditis in young men and teenagers were transient, mild, and rare, despite allegedly knowing otherwise. This was followed by a summer-long propaganda campaign using influencers and TikTok personalities to encourage young people to get injected.

A bombshell report reveals that the Department of Defense controlled the COVID-19 program from the beginning, using shady approval authorizations to shield big pharma from liability. The Pentagon used laws like the PrEP Act, Emergency Use Authorization, and Other Transaction Authority to protect pharmaceutical companies and avoid proper clinical trials. The documents obtained by Sasha Lydipova, a former executive of a pharmaceutical contract resource organization, show that the vaccines were not good manufacturing practice compliant and had extreme variability in adverse events. The Pentagon's involvement was part of treating COVID as an act of war, with the National Security Council setting policy. The deception extended to censoring lab leak theories and keeping the public in the dark.

In 2018, the World Health Organization changed the definition of vaccine adverse events, only considering those already established in published clinical literature. This conveniently allows Pfizer and Moderna to claim no adverse events from genetically modified injections. The definition change occurred just before the pandemic, suggesting a plan. This information is not widely known, as it is censored by mainstream media. Most people avoid asking the question of whether we want to be a submissive and tyrannized population or live in freedom. The reality is that we are currently a docile and compliant humanity. Pharmaceutical companies are responsible for more deaths than the military-industrial complex, and they will control and limit our freedoms.

We found that the FDA lied about a maternal rat study that was testing the safety of mandating a vaccine to pregnant women. In every litter, individual pups had horrible bone deformities. This signal was extremely prominent. Moderna submitted the rat study, as they were required to do. The FDA then lied about the study results by claiming there were no problems. It was a huge enterprise in lying.

Indian tribal girls were allegedly used as guinea pigs for an untested vaccine by two American farmer giants. The HPV vaccine was administered to over 24,000 girls without proper study or informed consent. Some girls suffered severe injuries, seizures, and even death. The Gates Foundation denied any involvement in clinical trials, but the Indian parliament formed a task force and eventually kicked out the foundation. However, an American organization continues to operate in India. The manipulation of media and public opinion by political leaders and pharmaceutical companies is concerning. Additionally, a study found that over 490,000 children in India developed paralysis from a Gates-supported oral polio vaccine. The truth about these incidents persists despite attempts to bury the story.

At the outset, a process was approved by the FDA for emergency use authorization. However, it was later discovered that the approved process was swapped out for one containing contaminants like DNA and a cancer-causing substance. Pfizer redacted 800 pages of the manufacturing process, hiding the fact that a carcinogen was included. This lack of transparency led to no informed consent and potential harm to individuals. The vaccine rollout included a trial with a 2.4 times higher adverse event rate, including the presence of a carcinogen.

Over 100 million Americans were required to get vaccinated due to job mandates. The government claimed vaccines were safe and effective, but data showed vaccinated people could still carry the virus. Despite promises of freedom, there have been 1 million adverse events reported from COVID-19 vaccines, with only 11 compensated cases. Big Pharma has immunity from liability for vaccine injuries.

Speaker 0: I find information like this, you know, inserts for the vaccine. Paper's there, and there's nothing printed on it. I find that very interesting, disheartening, disgusting, and lots of other words, but then it gets better. It just keep wait. There's more. It just keeps happening. The CDC redacts every single word of a 148 page study on a myocarditis after COVID vaccination. So I asked research to print the study for me. 148 pages. The entire thing is redacted. What good does a study do if there's nothing there? Then I wanna know, wait, what might have been there that they needed to redact it? That's even scarier. Speaker 1: We're witnessing an active cover up of a colossal consumer product safety debacle that is is basically affecting the entire world. Mhmm. So in The United States, our CDC, National Institutes of Health, and the FDA are actively involved in a cover up. And the same is occurring in The UK with the MHRA, Europe with European medicine agencies, and Australia with the Therapeutic Goods Administration. Something is going on that's very big. Each one of these companies that puts out a product has an obligation to produce ninety days of safety monitoring after their product comes out. It's a regulatory dossier. If somebody has a problem with the new product and they call the company like Pfizer, Pfizer has to report, write down what happened, and they have to collate that in a report and produce it and make it publicly available. When it came to ninety days with Pfizer, the first vaccine that came out, remember Pfizer was approved 12/10/2020. Pfizer didn't produce the report. And then people started asking, well, what's happening with your vaccine? And Pfizer would not disclose what happened. And then it went to court. And the lawyer for the FDA stepped in and said they don't wanna release Pfizer's dossier for fifty five years. Mhmm. Oh. Fifty five years. And the the the plaintiff pushed. And finally, slowly, the Pfizer dossier came out. Pfizer recorded one thousand two hundred and twenty three deaths with their product within ninety days of release. People were calling Pfizer in desperation watching their family members die after taking the vaccine. Pfizer recorded over twelve hundred new adverse events, new problems that doctor Boden has talked to you about that we are grappling with the entire time. But the point is our FDA worked to cover this up. The FDA should be regulating this company. FDA should have been having at least monthly meetings and fully disclosing what was going on with these novel vaccines, which are a genetic transfer technology platform.

Maddy DeGary, a participant in Pfizer's 12-15 year old COVID-19 vaccine trial, suffered serious injuries post-vaccination. Pfizer misrepresented her condition as "functional abdominal pain" to the FDA. Despite efforts to bring attention to her true injuries, the FDA showed little concern and failed to hold Pfizer accountable for withholding information. This lack of transparency undermines the integrity of the trial process.

Vaccines are not subjected to true placebo-controlled trials before licensure. The DDP vaccine was pulled in the US due to lawsuits against drug companies. Wyeth, now Pfizer, requested full immunity from liability for all vaccines from the Reagan administration in 1986, threatening to leave the vaccine business. The company claimed they were losing $20 in downstream liability for every dollar of profit. When asked to make vaccines safe, they responded that "vaccines are unavoidably unsafe." This phrase is in the statute granting them immunity and was cited in the Brusowitz Supreme Court case. The industry obtained immunity by convincing the president and Congress that vaccines are unavoidably unsafe.

We were deceived with false information about the safety and effectiveness of these products. The claim that they would remain at the injection site and lymph nodes was proven false. The modified RNA in these products was said to only last a short time, but we now know it remains active in the body for weeks or even months. We were also manipulated into believing that we all needed to be vaccinated for everyone to be safe, using illegal tactics like coercion and enticement. These lies were used to justify the deployment of these experimental products, which aimed to establish a profitable vaccine platform technology.

The COVID-19 vaccines were rolled out under a series of laws that allowed the military to take over distribution, bypassing typical clinical trials and safety testing. The FDA's involvement was a "pretend authorization," as their mandate is to regulate interstate commerce of medical products, not countermeasures. The Department of Defense is fully in charge of the development, clinical trials, manufacturing, and distribution of the vaccines, utilizing "other transaction authority" (OTA), initially intended for NASA and weapons procurement. The vaccines are purchased under OTA as demonstration products, exempting them from FDA and CDC authority. Pharmaceutical companies were brought in largely for branding purposes, while the military oversaw manufacturing and distribution through military contractors.

Vaccine manufacturers are uniquely protected from design defect claims, unlike manufacturers of other products like planes, cars, and drugs. This immunity was granted in 1986 through the National Childhood Vaccine Injury Act because manufacturers of the three routine childhood vaccines (MMR, Polio, and DTP) faced excessive liability and potential bankruptcy due to harm caused by their products. Instead of requiring safer products, Congress granted immunity, allowing manufacturers to continue selling vaccines regardless of potential harm. This immunity extended to all future routine childhood vaccines. Consequently, the CDC schedule has expanded from 3 injections in the first year of life in 1986 to 29 today. Pharmaceutical companies developing these vaccines know they won't be liable for injuries. Unlike typical drug trials, vaccine trials often lack placebo controls (except for the COVID-19 vaccine), have short safety review periods (days, weeks, or up to six months), and are underpowered, making it difficult to confirm product safety.