Are the Vaccines Being Systematically Distributed to Cause Large Amounts of Deaths in the U.S.? | Professional Data Analysts Think It May

“This is a worldwide experiment. It’s intentional.”

Dr. Jane Ruby shares with Stew Peters and their viewers the shocking implication that the vaccines being sent out may be distributed to certain countries by a specific design; to initiate large numbers of disabilities outside of the U.S., and large amounts of death within the U.S.

At least according to the data being compiled of the certain batch/lot numbers that are contributing to the highest amount of vaccine adverse reactions.

This data was assessed by a team that includes:

Mike Yeadon – Ex Head of Respiratory Research at Pfizer UK

Alexandra Latypova – researcher – analyst – Biotech CEO

Craig Paardekooper – researcher – computer programmer – author

Jessica Rose – researcher – analyst – government consultant

Walter Wagner – consultant on pharma compliance and legal affairs

Source: howbad.info/background

For clarity reasons, I want to add that the howbad.info website does state that they gathered all of their information from the U.S. VAERS database. So one would have to consider that this may not take into account many of the adverse events of vaccines that are being distributed to other foreign-speaking countries (China, Germany, Israel, Russia, Africa, etc., etc., etc.)

It is not specifically clear from this interview where the outside-of-the-US data is coming from. It could have been from the hackers that Dr. Jane Ruby mentioned, or specifically from the US VAERS database; but again, it is not verified. When there is further information, I will try and update this post with the new findings.

Please keep all of this in mind and keep a discerning eye out through all of the research presented. Using critical thinking and asking additional questions should always be approached when coming across new data.

Many thanks to all of those involved for their continued research and investigation into these incredibly important matters, and the groups/individuals involved for helping to share and spread these messages.

Full transcript below. Some embellishment has been added for emphasis.

Stew Peters: “Well Happy New Year and welcome back to the Stew Peters Show. We hope that all of you had a great Christmas season with your families, despite the best efforts of Tony Fauci and the Biden junta to make it a miserable time. But that’s what sets us apart from them. We can feel real love and real joy.

Still, it’s a dangerous world out there, and the enemies of the American people will be just as committed to destroying us in 2022, as they were in ’21. And that means more masking, more restrictions, more vaccine mandates.

Dr. Jane Ruby joins us for her first segment of the year. She says that she has the receipts to prove that vaccine toxicity varies by batch, which we’ve covered before, but now it’s possible to find out if the shot that you’re being pressured to take is from one of these tainted, and deadly, batches.”

Dr. Jane Ruby: “Yes, Happy New Year’s, Stew.

Um, sorry to start out with such bad news. But what we’ve learned is, after I spent 3 hours in an interview with these analysts who have actually taken the previous work of toxicity in lot numbers to a whole new level, what they’re telling us is that this is a worldwide human experiment, it’s intentional, and there’s a subplot to this. That there is an attack on the American people.

What they basically told me is that all 3 companies: Pfizer, Moderna, and Johnson&Johnson, which is essentially Janssen, are testing; they’re actively testing. And it’s worse than what we thought. Because there’s evidence that these companies are intentionally deploying toxic batches.

They’ve also identified what they call “supertoxic” batches. And they’ve released these lot numbers. And I felt it was like an emergency to get this to the American people, and the people of the world.

I want to show you what they found, on – in terms of most dangerous lots. And when we’re done with this segment, I urge everyone to go to howbad.info, where you can check the lots, and you can know which lots are deadly and dangerous, uh, before – if you’re thinking or on the fence of getting any of these bioweapon injections.

When you look at the first column here for Pfizer, I want you to know that the most deadly, dangerous lot will begin with EW. E like Edward, W like winning. EW. Second to that is F like Frank, A like apple. And then F like Frank, C like Charlie. Sorry I don’t know the military terms for that.”

Credited to: howbad.info/Stew Peters Show

Dr. Jane Ruby (cont. @2:28): The most harmful lot for children, under this EW, FA, FC, was something identified; the whole lot number is EW01A2 [editor’s note: could not verify this specific lot id in the howbad.info website] But you could go to howbad.info and look up… the company, and put your lot number in.

For under Pfizer for adults, the most toxic, deadly batches begin with E like Edward, N like Nancy. And then second to that is E like Edward, R like Robert.

Under Moderna, they found under for all ages, adults and – I don’t believe they have a young child authorization yet, but their toxic, deadly batches end in 20A – Alpha. They’re supertoxic.

Under Moderna, have, in the middle section, they got very clever. Uh, Pfizer coded their lot numbers – all companies coded their lot numbers, with – so that they would know where the most toxic batches are. And I’m going to share with you why that’s important in a little bit. But Moderna took it a step further with a little cleverness, because they embedded their code, for their most toxic amount, either in dose or, or chemical composition, under the letters – in the middle of that lot number, J, K like kite, L like love, M like Mary.

The analysts were a team that included the well-known Dr. Michael Yeadon, Craig Paardekooper, from Africa, a woman named Alexandra Latypova, who’s in California, our well-known Jessica Rose, that we’ve interviewed on the Stew Peters Show before, and another analyst named Walter Wagner.

Look. This EW lot for children, anything that starts with EW, is responsible for almost – watch this – all adverse events in children, all ER visits, all hospitalizations, all life-threatening events, disabilities, and all deaths. This is serious.

And here’s the kicker, Stew. All of these deadly lots that we’re going to show you, are already in circulation, remembering that there could be up to 1.5 million doses per lot. This quantification is set by each company. And the way they know that, is because they have looked at the companies and they’ve gotten into their systems to see how the companies have laid this out.

They made the assertion, Stew, that – and this was shocking – that what these companies are doing is they’re exporting disability as defined by the VAERs system itself, out to Europe. Ex-USA. And what they’re doing is they’re, they’re exporting, if you will, death – more death, more lethal doses, in the United States.

Now let me, let me share with everyone, there’s another chart I want to show you with a scatter plot. It’s called Pfizer batches. And when Pfizer batches, their batch codes, rather, were arranged alpha-numerically, along the X-axis, the following patterns emerged. And you can see these dots, these vertical dots, represent batch numbers. And again, there’s that EW. You can see the green stack of dots. Those are children’s doses. Even though the company claims that the amount is less than the adult dose, supposedly, we have no idea what’s in there.”

Credited to: howbad.info/Stew Peters Show

Dr. Jane Ruby (cont. @5:54): “They are actively testing… – Stew, I’m gonna tell you something. They are conducting what we call lethal dose studies.

Now in pharmaceutical drug development, lethal dose studies looks at how much you need to cause death. And obviously, we – they’re not done in humans. In people. They’re always done in animals, although they’ve slowed down in recent years because people have become concerned, even though they’re rats and mice, lower forms, they’ve become concerned about the cruelty to animals. But they’re never done in people.

And what’s happening here, is they are, basically, from the analysis, these analysts tell us that these 3 companies are actively – RIGHT NOW – conducting lethal dose studies.

Let me explain lethal dose. They take the highest amount of chemical, in terms of dosage and composition. And what they do is, they determine, the leth- what lethal amount to test half the population. It’s one of the means to assess acute toxicity prior to going into human studies. Um, and like I said, it has been largely fazed out. They are – they are conducting it without informed consent, it’s against all ethical and regulatory rules. In other words, we believe these companies are just proceeding with impunity, because there is nothing stopping them.

I want to also show people something. Before we get to a little bit of a larger look at the lot numbers and what’s happening, and how these analysts are so sure that this is not by randomization; this is not by chance. I want to take a look at the parts of a Moderna batch – code.

I mentioned earlier that Moderna got a little more complex and clever. Remember, these companies, we now know, are actually embedding into their lots, a code to tell them which doses, which lots, are toxic, which ones are causing disabilities, and what types of disabilities. I mean, this is absolutely outrageous.

When you look at the parts of the Moderna batch code, you see here this number. It’s 011, the letter L like love, 20A. 20A. As we mentioned before, in the first chart I showed, is the most lethal, that, you know, is the most lethal batch of lot codes in the Moderna program right now. And remember, all of these numbers I’m going to show you, are from the middle of November up until as late as December 16, of just a couple of weeks ago.

So when you look at this numbers, 011L20A, what you’re looking at in the 011, is the temporal batch order. So how it’s being developed over time, and deployed by the company. The L is the concentration – it determines, it tells the company the toxicity and number of adverse reactions. And then the 20A is qualitative. It’s the ingredient. In either 20A, which was the most highly toxic of their batch lots, or 21A came up as well.

So this is their clever scheme to – this is not a matter of, you know, throwing this out. You know. We’re going to try this new technology and we’re getting, with impunity, we’re going to see what the safety issues come- The reason they’re not concerned about safety issues is because this is an a priori design. This is designed ahead of time to send out toxic batches and then to gather their information.

I – so anyway, let’s move on to – there’s just so much information that I learned from these analysts. They told me – “

Stew Peters: “And how did these – how did these analysts know that these are coming from Pfizer, Moderna, Johnson&Johnson?”

Dr. Jane Ruby: “Because, first of all, they, they told me that they were informed by professional hackers, that this is big news – nobody else has broken this. That these professional hackers got into Pfizer, and Moderna systems, and they were able to verify the lots.

Dr. Paardekooper has a list of all the Moderna batches deployed so far. And Moderna also has a web tool – this’ll probably disappear after the Stew Peters Show airs, it has a web tool for checking the expiration dates for batches. And these computer guys hacked Moderna’s website, and got the entire list of Moderna batches with a full list of batch codes. And they did the same for Pfizer.

I just want to make something really clear. This exporting death to the USA and exporting disability to EU, what they found was that the Mo- for example, in the Moderna analysis, there were 10 times the death rate in the United States, than in the EU, and in the Moderna group, there were 10 times more disabilities in the EU group, compared with the USA.

So this, this is – all 3 companies are using their lot numbers to label… they’re looking – and when a researcher does an a priori study, they’re testing concentrations. Remember I told you it was a dose finding study? But this dose finding range is much higher than just testing, you know, a therapeutic group of range to find out what works. This is lethal dose testing at its finest.

And we’re gonna talk about this more, Stew, I know we’re limited on time, but it was really important. It’s what’s most important is that before you let your child get in line for these bioweapon shots, if you don’t believe anything we’ve said, at least ask them for the lot number and if it starts with EW or EN.

Just before we close out, there’s a list I want to show you of batch codes with highlights. These batch codes are in a perfect mathematical series, Stew. And what this tells us is, if it was random, you see these highlighted EN lot numbers? These are all thousands, 2 or 3 thousand deaths and disabilities per these batches, but look at how it drops. It drops immediately down to 37, 25, 23. The subsequent batch numbers.”

Credited to: howbad.info/Stew Peters Show

Dr. Jane Ruby (cont. @12:05): If this was random, it would not just drop off so sharply like that. You’re going to hear more from these analysts, you’re going to hear more and more – But you are empowered now to look up if you’ve had one of these shots, you can look up your lot number… Please don’t take anymore of this. This is not going to stop.

Stew Peters: “Yeah. There’s just absolutely no reason why anybody should have their kid in line to take these bioweapons. But before knowing what we know now, you subjected yourself or your young ones to these injections, and you want to know, now you have these lot numbers, which you can find at stewpeters.tv.

You’re right, I am out of time, I gotta go. Dr. Jane Ruby, thank you so much. Happy New Year. And, I mean, this is unbelievable. [Dr. Jane Ruby: “Thank you. We’ll continue.”] So yeah. This is going to go away though. This search function’s going to go away.

And thanks to these hackers, as well, [Dr. Jane Ruby: “Yes. Bravo.”] and for your time in investigating and being inside of that meeting. Dr. Jane Ruby, thank you so much. God bless you.” [Dr. Jane Ruby: “Thank you Stew.”]

Fact checking is extremely important. I want to reiterate not to take everything at face value; no matter what you read, where you read it from, or who you hear it from. And to be clear, do not rely on “fact checking” websites to give you accurate information either. These are just as likely, (if not even more likely…), to feed false information and false debunking accounts to manipulate the reader. Please take everything into consideration before adhering to a certain narrative – and always keep your mind open to other possibilities.

Fair use disclaimer: Some of the links from this article are provided from different sources/sites to give the reader extra information and cite the sources, but does not necessarily mean that I endorse the contents of the site itself. Additionally, I have tried to provide links to the contents that I used from other sites as an educational and/or entertainment means only; if you feel that any information deserves further citation or request to be clarified, please let me know through the contact page.

Featured image by hakan german from Pixabay

Federal Lawsuit Seeks Immediate Halt of COVID Vaccines, Cites Whistleblower Testimony Claiming CDC is Under-Counting Vaccine Deaths

America’s Frontline Doctors addressing the fraudulent use of the EUA for COVID vaccines.

All Global Research articles can be read in 51 languages by activating the “Translate Website” drop down menu on the top banner of our home page (Desktop version).

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America’s Frontline Doctors filed a motion to stop the use of Emergency Use Authorization (EUA) COVID vaccines for anyone under 18, anyone with natural immunity or anyone who hasn’t received informed consent.

America’s Frontline Doctors (AFLDS) filed a motion July 19, seeking immediate injunctive relief in Alabama Federal District Court to stop the use of Emergency Use Authorization (EUA) COVID vaccines — Pfizer/BioNTech, Moderna and Johnson & Johnson (J&J) — for three groups of Americans.

According to a press release, AFLDS is asking to immediately stop administration of experimentalCOVID vaccines in anyone 18 and younger, all those who have recovered from COVID and acquired natural immunity, and every other American who has not received informed consent as defined by federal law.

The 67-page motion requests the judge issue a preliminary injunction pursuant to § 360bbb–3(b)(1)(C) for the following reasons:

  • There is no emergency, which is a prerequisite to issuing EUA and EUA renewals for COVID vaccines.
  • There is “no serious or life-threatening disease or condition.”
  • Vaccines do not diagnose, treat or prevent SARS-CoV-2 or COVID.
  • Known and potential risks of the vaccine outweigh their known and potential benefits.
  • There are adequate, approved and available alternatives to vaccines.
  • Healthcare professionals and vaccine candidates are not adequately informed.

The authors of the motion attached a declaration by a whistleblower who came forward alleging deaths occurring within 72 hours of receiving a COVID vaccine are significantly under-reported in the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Events Reporting System (VAERS) maintained by the U.S. Food and Drug Administration (FDA).

As of July 9, reported deaths in the VAERS totaled 10,991. Of those, 4,593 occurred within 72-hours of vaccination.

The whistleblower — a computer programmer who developed more than 100 distinct healthcare fraud algorithms, and who has expertise in healthcare data analytics that allows her to access Medicare and Medicaid data obtained by the Centers for Medicare and Medicaid Systems (CMS) — filed a sworn statement under penalty of perjury alleging the actual number of COVID vaccine-related deaths is closer to 45,000.

 

The whistleblower alleged that VAERS, while extremely useful, is under-reported by a conservative factor of at least five.

In her statement, she said:

“On July 9, 2021, there were 9,048 deaths reported in VAERS. I verified these numbers by collating all of the data from VAERS myself, not relying on a third party to report them. In tandem, I queried data from CMS medical claims with regard to vaccines and patient deaths, and have assessed that the deaths occurring within 3 days of vaccination are higher than those reported in VAERS by a factor of at least 5. This would indicate the true number of vaccine-related deaths was at least 45,000. Put in perspective, the swine flu vaccine was taken off the market which only resulted in 53 deaths.”

AFLDS said the findings were shocking, and informed consent is impossible when safety data is not accurate.

In a press release, AFLDS said:

“It is unlawful and unconstitutional to administer experimental agents to individuals who cannot make an informed decision as to the true benefits and risks to the vaccine on an independent basis. They must be of an age or a capacity to make informed decisions and have been provided with all of the risk/benefit information necessary to make an informed decision.”

One of the named plaintiffs, Deborah Sobczak, the mother of a 15- and 17-year-old, said in the press release:

“My child will not be the subject of an experiment. What kind of monsters are we allowing to control us? Perfectly healthy children have developed heart inflammation, brain bleeding and even died! I have had enough. I am not sacrificing my child so a pharmaceutical company can experiment on her. This madness has to stop.”

There is no emergency warranting EUA of COVID vaccines, plaintiffs allege

According to the complaint, the U.S. Department of Health and Human Services (HHS) secretary, named as one of the defendants in the lawsuit, declared on Feb. 4, 2020, pursuant to § 360bbb–3(b)(1)(C), that SARS-CoV-2 created a “public health emergency.”

This initial emergency declaration has been renewed repeatedly and remains in force today — a necessary legal prerequisite for the issuance of vaccine EUAs, the complaint states. EUA allowed the mass use of the vaccines by the American public before the completion of the standard regimen of clinical trials and FDA approval.

Plaintiffs allege the emergency declaration and its multiple renewals are illegal because there is no underlying emergency. Using HHS COVID death data, SARS CoV-2 has an overall survivability rate of 99.8% globally, which increases to 99.97% for persons under the age of 70. This is consistent with the seasonal flu, the complaint states.

Plaintiffs argue HHS deliberately inflated COVID case data

Plaintiffs allege HHS’ data is deliberately inflated. On March 24, 2020, HHS changed the rules applicable to coroners and others responsible for producing death certificates and making “cause of death” determinations exclusively for COVID.

The rule change states: “COVID-19 should be reported on the death certificate for all decedents where the disease caused or is assumed to have caused or contributed to death.”

According to the complaint, HHS statistics showed 95% of deaths classified as “COVID-19 deaths” involved an average of four additional comorbidities. Plaintiffs claim the CDC knew the rules for coding and selection of the underlying cause of death would result in COVID being the underlying cause more often than not.

Plaintiffs said the actual number of COVID cases is also far lower than the reported number due to emergency use of polymerase chain reaction (PCR) tests, which are used as a diagnostic tool for COVID. The PCR tests are themselves experimental products, authorized by the FDA under separate EUAs. The package inserts state PCR tests should not be used to diagnose COVID.

The complaint alleges the way in which the PCR tests are being administered knowingly guarantees an unacceptably high number of false positive results.

COVID vaccine risks undisclosed and under-reported, lawsuit says 

AFLDS medico-legal researchers analyzed the accumulated COVID vaccine risk data and found migration of the pathogenic SARS-CoV-2 spike protein in the body. Yet vaccines were authorized without any studies demonstrating where the spike proteins traveled in the body following vaccination, how long they remain active and what effect they have, the complaint states.

AFLDS researchers analyzed VAERS and discovered an increased risk of death from COVID vaccines. The database indicated vaccine deaths in the first quarter of 2021 represented a 12,000% to 25,000% increase in vaccine deaths, year-on-year.

From 2009 to 2019, there were 1529 reported deaths associated with all vaccines reported to VAERS, according to the motion. In the first quarter of 2021, there were more than 4,000 reported deaths with 99% of all reported vaccine deaths in 2021 attributed to the COVID vaccine. Only 1% were attributed to other vaccines in the system.

Plaintiffs also disclosed evidence of reproductive harm, vascular disease, autoimmune disease, neurological damage and they highlighted an increased risk of harm for children with COVID vaccines to support their position.

Why the secrecy around V-Safe data?

The complaint called attention to the secrecy of the CDC’s V-Safe system — a parallel system used to track reported adverse events via a smartphone app controlled exclusively by the CDC.

Plaintiffs raised concerns that information in V-Safe exceeds that in VAERS. They claim VAERS is inaccurate because it potentially includes fewer than 1% of all vaccine adverse events, and the federal government is failing to provide data from other monitoring sources such as V-Safe, CMS and the military.

Plaintiffs stated informed consent cannot be given without understanding the risks. They said they can’t help but wonder why HHS would fail to disclose to the public critical information related to risk from it’s reporting systems, “particularly in light of the fact that they have had the time and resources to study and extend the authorizations on the vaccines, build an enormous vaccine marketing machine and roll out vaccine clinics all over the nation.”

The lawsuit was filed by several law firms, including RENZ Law. The complaint and whistleblower declaration can be read here.

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Megan Redshaw is a freelance reporter for The Defender. She has a background in political science, a law degree and extensive training in natural health.

Featured image is from CHD