Posted on 09/13/2022 3:22:13 PM PDT by Qiviut
A data leak suggests the real reason health officials don’t want individual vaccine vials examined by independent scientists is that the vials are all different — and the mRNA in the shots is not intact.
Story at a glance:
A 14-minute video (below) that has been overlooked for nearly two years has now resurfaced, exposing stunning information about the COVID-19 jabs and why health officials don’t want individual vaccine vials examined by independent scientists.
The reason, it turns out, is because the vials are all different — and the mRNA in the shots “is not intact.” Both of these pose potentially serious problems.
In an Aug. 31 Substack article, Steve Kirsch explains:
“Even if you are getting 100% intact mRNA which would be really rare, you’re still not getting anything that resembles the virus. So the efficacy as far as PROTECTING you will be next to nothing.
“However, what it will do very effectively, if you got reasonably intact mRNA, is to cause you significant harm. You are playing a game of chance with your immune system and what is in the bottle.”
The video notes that members of the European Parliament were only allowed to read the contracts with the drug makers after they’d been heavily redacted. Why the heavy-handed secrecy, even toward legislators?
Leaked documents reveal serious quality issues
The finding that the mRNA in the shots was of questionable quality was revealed in a British Medical Journal feature investigation article published in March 2021.
As explained by the author, journalist Serena Tinari, cyber attackers retrieved more than 40 megabytes of Pfizer COVID-19 jab data from the European Medicines Agency (EMA) in December 2020.
The hacked data was subsequently sent to journalists and academics worldwide. It was also published on the dark web. Some of the documents show European regulators had significant concerns over the lack of intact mRNA in the commercial batches sampled.
Compared to the clinical batches, i.e., the shots used in the clinical trial, 55% to 78% of the commercial shots had “a significant difference in % RNA integrity/truncated species.”
In one email, dated Nov. 23, 2020, a high-ranking EMA official noted that the commercial batches failed to meet expected specifications, and that the implications of this RNA integrity loss were unclear. In response to the findings, the EMA sent a list of questions and concerns to Pfizer.
While we do not know if and how the EMA’s concerns were actually addressed and corrected, the EMA authorized Pfizer’s COVID-19 jab Dec. 21, 2020.
According to its public assessment report, “the quality of this medicinal product, submitted in the emergency context of the current (COVID-19) pandemic, is considered to be sufficiently consistent and acceptable.”
Similarly, Health Canada told the Britsh Medical Journal that “changes were made in their processes to ensure that the integrity was improved and brought in line with what was seen for clinical trial batches.” The EMA further tried to deflect concern by claiming some of the leaked documents had been doctored.
As reported by the British Medical Journal:
“EMA says the leaked information was partially doctored, explaining in a statement that ‘whilst individual emails are authentic, data from different users were selected and aggregated, screenshots from multiple folders and mailboxes have been created, and additional titles were added by the perpetrators.’”
Intact mRNA is essential to its effectiveness
Curiously, when the Britsh Medical Journal asked Pfizer, Moderna, CureVac and several regulators to specify the percentage of mRNA integrity considered acceptable, none replied with specifics.
According to the British Medicines and Healthcare Products Regulatory Agency, the FDA and Health Canada, the specification limit on RNA integrity is “commercially confidential.” What we do know — and the EMA has acknowledged — is that intact mRNA is essential for efficacy.
As noted by the Britsh Medical Journal:
“The documents offer the broader medical community a chance to reflect on the complexities of quality assurance for novel mRNA vaccines, which include everything from the quantification and integrity of mRNA and carrier lipids to measuring the distribution of particle sizes and encapsulation efficiency.
“Of particular concern is RNA instability, one of the most important variables relevant to all mRNA vaccines that has thus far received scant attention in the clinical community. …
“RNA instability is one of the biggest hurdles for researchers developing nucleic acid based vaccines. It is the primary reason for the technology’s stringent cold chain requirements and has been addressed by encapsulating the mRNA in lipid nanoparticles.
“‘The complete, intact mRNA molecule is essential to its potency as a vaccine,’ professor of biopharmaceutics Daan J.A. Crommelin and colleagues wrote in a review article in The Journal of Pharmaceutical Sciences late last year.
“‘Even a minor degradation reaction, anywhere along a mRNA strand, can severely slow or stop proper translation performance of that strand and thus result in the incomplete expression of the target antigen.’”
For an effective product, mRNA integrity needs to be 100%. Considering how ineffective the jabs are, it seems fair to question whether lack of mRNA integrity might be to blame. We also do not know whether nonintact mRNA might be harmful.
As noted by Kirsch, “Unstable mRNA means the spike protein … could collapse, making the whole process useless to support immunity, but still dangerous in terms of damage to cells. So, you get all the risk and no benefit.”
While our public health agencies claim fragmented RNA poses no health risk, just how do they know that? The leaked documents revealed they specifically did not have an answer to that question, and no research into the matter has been published, that I’m aware of.
Fragmented RNA may produce incomplete spike proteins
In May 2021, Stephanie Seneff, Ph.D., a senior research scientist at MIT for over five decades, published an excellent paper in which she highlighted several potential dangers of the COVID-19 jabs, including the unknown hazard of injecting fragmented RNA.
That same month, I interviewed her about her concerns. You can find that interview in “COVID Vaccines May Bring Avalanche of Neurological Disease.”
In her paper, Seneff noted:
“The EMA Public Assessment Report … describes in detail a review of the [Pfizer] manufacturing process … One concerning revelation is the presence of ‘fragmented species’ of RNA in the injection solution.
“These are RNA fragments resulting from early termination of the process of transcription from the DNA template.
“These fragments, if translated by the cell following injection, would generate incomplete spike proteins, again resulting in altered and unpredictable three-dimensional structure and a physiological impact that is at best neutral and at worst detrimental to cellular functioning.
“There were considerably more of these fragmented forms of RNA found in the commercially manufactured products than in the products used in clinical trials. The latter were produced via a much more tightly controlled manufacturing process. …
“While we are not asserting that non-spike proteins generated from fragmented RNA would be misfolded or otherwise pathological, we believe they would at least contribute to the cellular stress that promotes prion-associated conformational changes in the spike protein that is present.”
Kirsch points out that the EMA also expressed concern over visible particles in the vials, which the Britsh Medical Journal did not follow up on. “Is it still a problem?” Kirsch asks. That’s a good question, and the answer is probably yes.
But even worse is that we have absolutely no idea what these incomplete spike proteins are doing, none, zero, nada. It has never been directly examined. For that matter efforts to evaluate, and complications of the jab, have been consciously suppressed as have following simple metrics such as increases in all-cause mortality.
Deaths dismissed and side effects misclassified
The leaked EMA documents also showed that Pfizer dismissed all deaths in its trial as “unrelated to the vaccine,” even though no proper investigation was ever conducted.
We now have additional evidence of this — just like the court-ordered FOIA documents showed what Pfizer did in their U.S. trials. At least they are consistent in implementing their fraud.
As reported by Children’s Health Defense (CHD) back in June, Freedom of Information Act (FOIA) documents, released by court order, reveal Pfizer classified nearly all severe reactions in its trials as unrelated to the shot, even in cases where the health problems in question are extremely difficult to dismiss as anything other than a direct effect of the shot:
“The latest release by the U.S. Food and Drug Administration (FDA) of Pfizer-BioNTech COVID-19 vaccine documents reveals numerous instances of participants who sustained severe adverse events during Phase 3 trials. Some of these participants withdrew from the trials, some were dropped and some died. …
“The CRFs [case report forms] included in this month’s documents contain often vague explanations of the specific symptoms experienced by the trial participants. They also reveal a trend of classifying almost all adverse events — and in particular severe adverse events (SAEs) — as being ‘not related’ to the vaccine. …
“The many serious adverse events — and several deaths — recorded during the Phase 3 trials are also apparent in a separate, massive document exceeding 2,500 pages, cataloging such adverse events.
“This document lists a wide range of adverse events suffered by trial participants classified as toxicity level 4 — the highest and most serious such level. However, not one of the level 4 (most severe) adverse events listed in this particular document is classified as being related to the vaccination.”
As just one example, a teenage girl got the shot Sept. 11, 2020, and in mid-November 2020 was diagnosed with right lower extremity deep vein thrombosis, which we now know is a potential side effect of the jab.
According to the CRF, her condition was due to a bone fracture that occurred before the date of her injection — a determination that seems questionable at best.
What’s the cause behind the ‘bad batch’ phenomenon?
The “bad batch” phenomenon may also be indicative of quality problems. Independent investigations have revealed that some lots of the shots are associated with very severe side effects and death, whereas other lots have very few or no adverse events associated with their use.
According to howbadismybatch.com, a site that matches up vaccine lot codes with reports in the VAERS system, approximately 5% of the lots are responsible for 90% of all adverse reactions. Some of these batches have 50 times the number of deaths and disabilities associated with them, compared to other lots.
Another website that basically does the same thing is WelcomeTheEagle’s VAERS Dashboard. A video explaining how to use the dashboard can be found on Bitchute.
However, an even deeper dive into this data suggests random quality issues are not the problem. In the video above, Reiner Fuellmich, cofounder of the German Corona Investigative Committee, and Dr. Wolfgang Wodarg, a former member of the German parliament, discuss this “smoking gun” evidence.
According to Fuellmich and Wodarg, the lot-dependent data suggests vaccine makers may be conducting secret experiments within the larger public trial. In other words, they appear to be doing lethal-dose testing on the public.
The tipoff that these “hot” batches are not caused by intermittent poor manufacturing is the fact that they’re being released in a coordinated fashion.
Wodarg argues that the evidence for this is very clear from the data. Basically, the vaccine manufacturers are coordinating their lethal-dose experiments so that they’re not all releasing their most toxic lots at the same time, or in the same areas. This avoids detection through clustering.
New boosters will not undergo additional testing
Considering the multitude of open questions surrounding the safety of the original COVID-19 shots, the fact that new, reformulated boosters will not require any additional testing whatsoever is beyond disturbing.
In the “Friday Roundtable” video above, Dr. Meryl Nass, Toby Rogers, Ph.D., Aimee Villella McBride, Polly Tommey and Brian Hooker, Ph.D., discuss the FDA’s decision to allow vaccine makers to reformulate their COVID-19 shots without additional testing, in perpetuity.
As noted by Rogers, Pfizer’s bivalent booster against Omicron variants BA.4 and BA.5 was tested on a total of eight mice, and only to check antibody levels. Moderna also used mice to ascertain antibody responses, but has not disclosed the number of mice used.
That’s the extent to which these shots were tested. The original COVID-19 jabs are the most dangerous drugs ever released to the public, and these newer boosters may turn out to be even worse.
As explained by Rogers, the shots “imprint” your immune system to respond only to the antigen in the shot, while simultaneously impairing your immune system so that it’s less capable of protecting you against other pathogens.
Another term for this process is “original antigenic sin.” It essentially explains why those who are jabbed are getting infected and sicker than those who avoided the jabs.
Rogers predicts we’ll be faced with a winter of severe illness and death among those who have gotten the jabs. All the rest of us can do is stand back, avoid the shots at all costs and “let the mainstream system self-destruct.” Hopefully, he’s correct in his other prediction, which is that the vast majority of Americans will reject these boosters.
Great stuff.
I still think the overall creation is AI it's too complex for most anyone to put it all together. It's an extremely sophisticated plan/OP to screw with humans on a broad scale and accomplish probably a dozen purposes.
The key purpose would be what Lieber is doing:
create a super solider, a cyborg.
....................................
Here's Malones latest:
Cyborgs as just the beginning.
After looking into Malone I am coming to believe that this guy trys to play all sides and so far has been wildly successful.Will he be able to keep it up? Hard to say.
..........................
Human Cyborgs are Just the Beginning.
The USG Administrative State believes that Human Augmentation is ‘Imperative’
Robert W Malone MD, MS
Sep 14
DownloadCCDC CBC-TR-1599, Cyborg Soldier 2050: Human/Machine Fusion and the Implications for the Future of the DOD
The Office of the Under Secretary of Defense for Research and Engineering (Alexandria, VA) established the DOD Biotechnologies for Health and Human Performance Council (BHPC) study group to continually assess research and development in biotechnology.
The BHPC group assesses scientific advances for improved health and performance with potential military application; identifies corresponding risks and opportunities and ethical, legal, and social implications; and provides senior leadership with recommendations for mitigating adversarial threats and maximizing opportunities for future.
U.S. forces. At the direction of the BHPC Executive Committee, the BHPC study group conducted a year-long assessment entitled “Cyborg Soldier 2050: Human/Machine Fusion and the Impact for the Future of the DOD”. The primary objective of this effort was to forecast and evaluate the military implications of machines that are physically integrated with the human body to augment and enhance human performance over the next 30 years.
(All this wreaks of what dr. Charles Lieber has been doing in China for over 20 years. Who knows how far he has gotten.We do know he has 66 patents in this field)
This report summarizes this assessment and findings; identifies four potential military-use cases for new technologies in this area; and assesses their impact upon the DOD organizational structure, warfighter doctrine and tactics, and interoperability with U.S. allies and civil society.
.......................
Documents leaked from the EMA confirms why we aren't allowed to analyze the vaccine vials.
It's like rolling the dice for what you get in your vial.
Both the FDA and EMA knew this but kept this out of the public view because if it were known, nobody would take the vaccines.
Steve Kirsch,P> Aug 31
One of my readers has been trying to get my attention for 8 months on the EMA data leak that happened nearly 2 years ago.
He recently posted this substack article documenting his attempts to get visibility on what the EMA document leak revealed.
The gem in the article is this video which was posted 18 months ago that few people have seen. The video is just 14 minutes long and is very well done. The findings are all consistent with what I and others have long suspected: the vials are all different.
(The first time I read this I was thinking this is not done by humans this is AI crap and I still think that)
The key finding is the reason they won't let anyone analyze the vials: mRNA is not intact. The BMJ wrote about this on March 10, 2021 [my comments are in brackets]:
On Nov 23, 2020, EMA knew about the quality control issues with severely compromised mRNA integrity (ranging from 78% to 55%). [It's supposed to be 100% if you want an effective vaccine.]
Just two days later, a source in the US said the lots were now “back at around 70-75%, which leaves us cautiously optimistic that additional data could address the issue.”
(this shows that Pfizer Moderna the rest all play with the mix no one ever knows what they are getting)
“The complete, intact mRNA molecule is essential to its potency as a vaccine,” professor of biopharmaceutics Daan J.A. Crommelin and colleagues wrote in a review article in The Journal of Pharmaceutical Sciences late last year.”
The BMJ asked Pfizer, Moderna, and CureVac, as well as several regulators, what percentage mRNA integrity they consider acceptable for vaccines against covid-19. None offered any specifics.(that should tell you all you ever need to know right there--the fix is in,its a huge con) [“Wow, that's really comforting. ”]
The EMA told The BMJ that the levels of truncated mRNA “and the amounts of a potential protein produced by the truncated mRNA would be too low to constitute a safety risk.” [uh… how does the EMA know that exactly?]
Health Canada told The BMJ that Pfizer had conducted investigations into the root cause of reduced integrity in the commercial vaccine batches, and “changes were made in their processes to ensure that the integrity was improved and brought in line with what was seen for clinical trial batches.” Health Canada said the three agencies subsequently determined that “there was no concern with the RNA integrity or any other product specifications.” [Whew! Now I'm relieved! No data on the new levels produced. If you can't trust Pfizer, who can you trust?]
In general, the BMJ wasn't happy about anything they heard from the regulators. They were basically stonewalled in their requests.
The fact that it's illegal for anyone to analyze the vials (they are government property) doesn't help inspire confidence at all.
Even if you are getting 100% intact mRNA which would be really rare, you're still not getting anything that resembles the virus. So the efficacy as far as PROTECTING you will be next to nothing. However, what it will do very effectively, if you got reasonably intact mRNA, is to cause you significant harm. You are playing a game of chance with your immune system and what is in the bottle. (this is the key to the entire scam no one ever knows what they are getting.With that in mind its hard to make a case against the mfg. much less do any relevant research into what they are doing with over 2,000 different vaccines each one a little bit and sometimes a lot different)
The video highlights some of the things we learned from the EMA data breach:
The EMA claims the documents were manipulated to make them look bad, but won't say how they were manipulated. I'm not buying the EMA story at all.
The Members of the European Parliament (MEP) weren't allowed to read the contracts with the vaccine makers (only heavily redacted versions). Again, if you can't trust Pfizer and the EMA, who can you trust?
The mRNA is unstable, even at the required temperatures because light, movement (like shipping it to a destination), and any temperature variation disrupts it.
Unstable mRNA means the spike protein (which was artificially propped up) could collapse making the whole process useless to support immunity, but still dangerous in terms of damage to cells. So you get all the risk and no benefit.(more bottom line stuff here!!
The mRNA integrity was better in the clinical trial than commercial batches. But don't assume that the vaccine worked in the trials since the trials were heavily gamed to produce favorable outcomes, mostly by excluding people with weak immune systems from the vaccine group (this is why there were 5X the number of exclusions in the vax group). So you're looking at a vaccine which likely does absolutely nothing except make people believe they are protected. This mind control works quite well.(more bottom line stuff here--its all mind control)
People bought the story for over a year before they realized they were getting infected at the same rate as people who didn't get the vaccine.
The mRNA integrity varied between countries.
Pfizer never told anyone that the commercial vaccines had lower mRNA integrity than the vaccines used in the trials. This is unethical, bordering on fraud.
The EMA tried to cover it up. Instead of protecting the public and making Pfizer look bad, the EMA basically covered up the problem.
Pfizer never told the public or governments about the risks associated with mRNA integrity. If it wasn't for the leak, we'd never have known. But it's all OK because the drug companies are exempt from any liability. The patient takes all the risk here, not the drug companies.
EMA was concerned about visible particles in the vials. The BMJ never investigated that. Is it still a problem? I don't think anyone cares to know the answer to that.
The deaths in the trials are all dismissed as “unrelated to the vaccine” without doing the proper analysis.
There should be an investigation into these issues, but the governments are not going to expose their own fraud since it would be too embarrassing so nothing will happen.
Summary
This video summarizing the leaked EMA documents constitutes yet more evidence that the vaccines confer no benefits, only risk.
However, like everything else, it will be ignored by the authorities.
However, this is important information for the public to know about how they(the public) are being manipulated into taking a useless vaccine.
NOBODY is calling for any quality control here.
Have you ever seen a study where the authors collect vials randomly and sequence them? It's not going to happen. Not in my lifetime.
Fuellmich: “I believe it’s the right time ..... it’s the body count .... people cannot look away any more”. Not a direct quote, but close.
Skip to about the 10 minute mark, that’s when the interview gets more intense/informative .....
Dr. Reiner Fuellmich SPEAKS out on Vaxx Genocide: GLOBAL Class Action Lawsuit For Pfizer and Moderna, Nuremburg 2.0
https://rumble.com/v1jyjft-dr.-reiner-fuellmich-speaks-out-on-vax-genocide-global-class-action-lawsuit.html
++++++++++++++++++
I’m pretty much out of (publicly acceptable) words to describe what is going on ... REALITY, not The Regime/Enemedia bubble they would have us believe we live in, boils down to democide, genocide, absolute evil.
Death and injury are starting to appear in my circle of acquaintances, friends & has impacted a close family member (someone I would have a hard time living without) in a life-threatening way (survival or death: still to be determined). Being a “realist” with eyes wide open, I could see this was coming and now it is here ...”in my grill” as SKB likes to say. I don’t know how to describe how I feel other than to say I am “internally screaming” ... not a good state to be in, frankly. “Accountability” and “justice” that would be somewhat satisfactory for me, has to be at an eye for an eye level.
For some hopefully not many its too late.
Also, it appears a few enlightened souls are figuring out how to counter some of these attacks by what could be described as the soldiers of evil.
In addition, I have mentioned it before but it pays to remind people that whomever created this monster immune system killer likely created a true vaccine for it as well. It would be rare if they didn't. One that can transcend the many varieties of the bio-weapon. It's likely one exists. The key could be the counter to what all the various bio-weapons have in common.
Giving up is not in our DNA and there are far more of us than there are of them.
RNA polymerase inaccuracy underlies SARS-CoV-2 variants and vaccine heterogeneity
BYW, there are also issues about inappropriate administration, subcutaneous vs intramuscular. Pre-approved federally registered CoupFlu vaccinators who don't know the difference and/or are too cheap to use longer needles when required.
And then there are the adjuvants....
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