We are down to the last 50 pages [of the 4000 he originally requested]. They will not release these. It's been now going close to 2 years. This is what has been provided to us. Do you think there might be some incriminating information in this?

Just like former NIH director Francis Collins Collins told me when I asked about all the deaths being reported on VAERS, [he said], “Senator, people die.” The fact that both of these statements are as true as they are callous highlights the challenge we face in exposing the truth.

I've written 4 [letters on hot-lots] starting in December of 2021. The first letter compared 25,000 lots of COVID vaccine to 22,000 lots of flu vaccine. One COVID lot had 5,297 adverse reactions associated with it. The worst flu lot had a 137. So 5,300 versus 137.

365 COVID lots had more than 100 adverse events. Only 10 flu lots had more than 100. And 80% of the serious adverse events, those with emergency room visits, hospitalization, or death were associated with only 5% of the lots. So, again, to me, I'm from manufacturing. That shows to me a manufacturing process out of control.

[It] took us a year to get some kind of response and, basically, response from the agencies was, “we don't see any variation in lots.”

“Vaccine injuries are rare.” “The benefits outweigh the risk and that the science is clear and overwhelming.” “And anyone challenging this narrative is an is an anti science conspiracy theorist.” In other words, second opinions are not allowed. To me, this attitude is the antithesis of science.

I am amazed at the knowledge mankind has obtained over the millennia. But I would argue that what we don't know vastly exceeds what we do know. So as we pursue truth, we must pursue it with the humility that that reality demands.

I'll be succinct. The SARS CoV 2 modified mRNA based vaccine products were deployed via emergency use authorization without adequate nonclinical and clinical testing and without full disclosure of known patient risk and efficacy data. This violated well established legislatively mandated patient informed consent requirements. The FDA and HHS justified these actions as necessary due to reliance on deeply flawed modeling data indicating that SARS CoV 2 was associated with an infection fatality rate of 3.4%.

Subsequent clinical research experience has revealed a number of problems with the genetic vaccine technology based SARS COV 2 products, which have been marketed as vaccines. In most cases, there has been an effort to obscure or deny facts in public communication by government and pharmaceutical industry representatives.

Doctor Malone, I think one of the things that always bothers me is [that] so much of what we're learning in terms of harms of these vaccine was clearly known before they were rolled out.

Standard operating procedures for analysis of safety signals emergent from VAERS when utilized reveal causal links between the COVID 19 injectable products and the adverse events investigated. Standard operating procedures are not being followed by the owners of the data, namely CDC, HHS, and FDA, and this equates to hiding the millions of people reporting not only adverse events but injuries in the context of the COVID 19 injectable products.

When analyzing the excess death human cost…in 2020, there were approximately 458,000 excess deaths, of which 73% were aged 65 and older and 15 to 64 comprising just 27%. However, in 2021, with the rollout of the “safe and effective vaccine,” there were approximately another 500,000 excess deaths, but a mix shift had occurred from older to younger. In 2021, the 65 plus age category was [only] 57…while the 15 to 64 cohort increased to 43%.

The absolute excess death increase from 2020 to 2021 for the productive working age 15 to 64 was 73% [124,000 to 215,000].

The total excess death since the rollout of the vaccine in the US, including 21, 22, and 23 is approximately 1,100,000. We estimate the economic cost, productive working age people dying at $15,600,000,000 When analyzing disabilities, it's interesting to note that there were no excess disabilities in 2020.

Using the civilian labor force, we have calculated an increase of 2,300,000 individuals with disabilities costing the economy an estimated $77,000,000,000. When analyzing lost work time, which we call injuries, we estimate 28,400,000 individuals are chronically absent resulting in an estimated economic cost of a $135,000,000,000 since 2021…Obviously, the policy cure was undeniably worse than the illness.

This work has been replicated by many labs around the world, and now the FDA, the EMA, and even Health Canada, have admitted to this. The regulatory agents have admitted that Pfizer also omitted the SV40 sequences that are in their vaccine. They've deemed this contamination to be of little consequence, claiming the DNA is of too little concentration to matter or to be containing DNA of no functional consequence. These statements are false and are not supported by any independent testing by these regulators.

After the regulators have admitted to being deceived, they asked the opinion of the party that deceived them how bad was the deception. They shockingly believe the answer they were given, which is that these sequences have no relevance to plasmid manufacturing. As someone who has worked on the Human Genome Project manufacturing millions of plasmids, I can assure you that this is an overt lie. DNA contamination can lead to insertional mutagenesis. This is actually declared in Moderna's own patent regarding the mRNA vaccines.

This is also supported by Lim et al, which speaks to the rate of spontaneous integration in the genome during transfection. We are using transfection after all with LMPs. The SV40 DNA is in fact functional. It is published as a potent gene therapy tool in a nuclear targeting sequence as described by David Dean et al.

The SV40 promoter DNA is also known to bind to the tumor suppressor gene known as p53.

We've applied these vaccine system cancer cell lines and have evidence that it enters the cell and can survive several cell divisions. We have preliminary evidence, although this requires replication in other labs, that this DNA can integrate into the genome. We found 2 spike sequence integration events in ovarian cancer cell lines of CAR 3 into chromosome 12 and 19 very recently. Since these vaccines were expected to only contain mRNA, they were never assessed for genotoxicity studies. These studies were therefore being conducted as guinea pig US citizens as we witnessed an unprecedented rise in cancer drug sales since the vaccines rolled out.

It is time for our representatives to repeal or review the PDUFA Act of 1992.  This act allows regulators to defray the cost of regulation by accepting payments directly from the companies they regulate. Over half of the FDA's budget is sourced through this act.

Federal rules requiring ingredient transparency date all the way back, believe it or not, to 1862 [and] it's the whole reason the FDA was started in 1906. Prior to COVIDsRNA injections, the FDA had approved 4 different RNA based products. Onpattro, shown here, was the 1st RNA product approved back in 2018…as you can see by looking at this label, Onpattro prominently details the exact structure, milligram strength, and molecular weight. Highlighted in green at the very top, you'll see it specifies [what its] lipid nanoparticles are engineered for.

In contrast to the previous labels I've shown, here is the official FDA label for COVID RNA injections. As you can see just looking at it, it details a lot less information. We don't [even] have the structure.

Of note, in pharmacology, even very minor deviations in any molecular structure can mean the difference between a drug and a poison…The lack of transparency means that scientists can't use modeling to test lipid nanoparticles for safety receptor specificity or analyze inequality [in batches of those products].

Unfortunately, around 70% of the 127 page document that explains the methodology to perform quality control on RNA injections are redacted much like the document I've shown here.

I worked with parents in congress to secure safety and informed consent provisions in the National Childhood Vaccine Injury Act of 1986. It was an historic law, the first official acknowledgment by government that federally licensed and state mandated vaccines can and do injure and kill some children. In January, my eyewitness perspective of how and why child vaccine victims and their parents were betrayed after that law was passed 38 years ago, was featured in a 2 hour conversation I had on the Highwire.

I encourage everyone to watch it and learn how parents trusted that the 5 years of work we put into that 1986 act to successfully secure life saving, informing, recording, reporting, and research provisions in it, and to protect the legal right of vaccine victims to sue vaccine manufacturers for product design defects, and to sue negligent doctors for medical malpractice, and to create an expedited, more just, less traumatic federal vaccine injury compensation system alternative to a lawsuit were all destroyed by congressional amendments, by federal health agencies, and the US Supreme Court after that law was passed. Following that betrayal of trust, Congress directed federal agencies to create lucrative public private business partnerships with the pharmaceutical industry, a business deal that has broken America's public health system.

By the way,I became aware of you from that excellent documentary which I would also recommend. What struck me about [it] is back then in 1982 through 1986, you could talk about these things. You could advocate for your child who's vaccine injured.  You weren't ostracized. You were actually welcomed here in the senate by people like Senator Hatch and Senator Kennedy and you got this [law] signed by Ronald Reagan.

I never imagined when I began this work in 1982 that the day would come when I would not be able to exercise freedom of thought and conscience in the country I love. And I thank you for allowing me to exercise that right today.

In 1962, children received 5 vaccine doses, and in 1986, the schedule expanded to 25 doses of 5 different vaccine formulations. Shortly after the passage of the 1986 National Childhood Vaccine Injury Act, the law was amended to essentially erect a liability shield protecting vaccine manufacturers, and the schedule expanded dramatically. By 2023, 73 doses of 16 different vaccine formulations were given to children up to age 18. [As we discovered through lawsuits] the FDA approved these formulations individually only with minimal and inadequate safety testing, and the CDC has never tested the cumulative effect of the vaccine schedule on childhood health outcomes.

Since [proper trials] are really the only way to establish that a pharmaceutical product is safe, it is misinformation to state that the vaccines are safe.

However, independent researchers have assessed the outcomes of vaccinated versus unvaccinated children.

This [study] demonstrates that vaccinated children were at least twice as likely to be diagnosed with developmental delays, ear infections, and gastrointestinal disorders.

[In this study] a control group of over 1800 unvaccinated children recruited from 46 different states in the US were compared to the national average rates of the listed disorders…For each of the autoimmune, neurodevelopmental, and other disorders considered, the unvaccinated group fares much better with incidence rates between 4-20 times lower than their vaccinated counterparts.

The CDC has a database called the vaccine safety data link. It's over 10,000,000 individuals with 2,000,000 children from 10 participating HMOs.  I would say that within that database, there were at least 10,000 unvaccinated children that can be studied.

Neither do they they publish the results [discovered from that data], nor do they let any independent scientist in to look at that information. [That’s] because [they know] the bloated vaccination schedule is responsible is in part responsible for the epidemic of chronic disorders that we see in children in the United States.

Every one of the childhood vaccines has a similar [lengthy] list of [severe] side effects. Though they are considered rare, how rare is it when you multiply roughly 50 potential side effects 72 times, which is the total number of doses given to a child by the time they're 18. The revelations from the recent study of the COVID vaccine explains what we have been saying for years. Vaccines are not completely safe, and [though] those side effects are rare. What happens when you add them altogether?

These [abhorrent] policies [e.g., the vaccine mandates] were justified via claims about the vaccine’s effectiveness and safety. Now recent research published in major medical journals reveals that these claims were highly exaggerated…we have found in the studies varying definitions of fully vaccinated and unvaccinated. And, generally, what we find with the term fully vaccinated is that they are ignoring COVID cases, COVID infections, in the partially vaccinated…that effect was found to be up to 48% using data from Pfizer's trial as an example.

We can't be sure what the actual exaggeration is because we aren't supplied with all the data. So it's impossible to actually know. But it looks like there are huge exaggerations of effectiveness because of what you could call manipulation of the data. So if these [omitted COVID cases] were included, or if even just some of these were included, we could have an effectiveness of the vaccines of around 10%...[which]is well below the 50% required for approval. Furthermore, looking to safety in the clinical trials, adverse effect counting windows are again incredibly short.

If the news reporters did their jobs instead of reporting propaganda, this fraud would have been exposed from the outset.

Censorship is what actually caused these deaths. It was the lie that assured us it was safe when it wasn't, and it still isn't

In America, it's much worse. The vaccine companies are allowed to sponsor the news directly…To a visiting Canadian, the news here looks like one big ad for pharmaceutical products. It's a bit of a culture shock when you turn on the TV. There wouldn't even be a US newscast without Pharma ads. So the reporters on your newscasts are all conflicted.

They can't bite the hand that feeds them. They can't possibly investigate the most important stories of our time.

It appears that the reporters are actually colluding with their sponsors to break FDA advertising laws.  FDA law requires them to conspicuously describe the known risks of any pharmaceutical product [which news anchors promoting vaccines never do.

The good news is no one believes the TV news anymore. Only 15% of Canadians, 15%, are getting the boosters.

[The media has] now canceled lunchtime news hours. It's canceled weekend newscasts. After these reporters are laid off, we'll only be left with the trusted favor of the trusted faces of our favorite news anchors, delivering the propaganda of the day, instead of the news of the day. But when those trusted faces are telling us lies, they're like a super weapon aimed directly at us. The news anchors are now the finger on the trigger in that game of Russian roulette.

When the news is poisoned, so is Democracy…most every other country is letting this happen, but where goes America, so goes the world. You have a unique role in setting the moral tone for Western democracies.

So I respectfully recommend that the senate investigate the role of American television news networks, including with pharmaceutical advertisers to skirt the FDA laws that require them to declare the known risks of a pharmaceutical product. This investigation should extend to any reporters, news anchors, editors, and executives who lied to their audience about the safety of the COVID vaccines.

[Johnson] Now I kind of want to ask you, I describe my eyes being opened up, certainly during COVID to a number of things…Can you just describe your [red pill] journey here?

[Weinstein] Well, I think we are all on a similar journey. I did not think that I was naive 7 years ago, and then I learned that I had been very naive and I keep learning that lesson. Each new discovery reveals that I was missing something that was right in front of me, and I think that's actually the hallmark of the exact pattern I'm describing.

We are a party having probably 10% of the votes we got in the parliament in 2020, and we, from the very beginning of this pandemic, we decided that the rights of the people to decide if they accept, or [do not accept receiving] an experimental drug should be respected.

When the European Union started behaving like the USSR with those commissars coming to us and mister Barnier came to Romania. This gentleman was the commissioner for internal affairs of the European Union and pushed us, pushed the Romanian parliament to vote [for COVID vaccine mandates].

But in Romania the problem they face is that we are 40 years after a communist dictatorship, 30, 34 years after a communist dictatorship. And it's in our genes to distrust the government because we knew every time a communist government is saying anything or is directing anything, we knew that's a lie, that's something that we should not trust or we should not follow.

We did everything in the book that we could to stop that and we stopped it. And, as a consequence to that, the Romanian rate of vaccination was probably less than half of what the other European countries experienced or United States, Canada and Australia [experienced]. And, therefore we can compare now the low rate and the excess mortality. And that's the best proof I can bring to the table is the fact that having a relationship between a low rate of vaccination and low excess mortality, which is right there you see it on the, Romania is the last country on the right which means we have negative excess mortality while all the other countries in Europe have positive excess mortality.