The U.S. Vaccine Adverse Event Reporting System (VAERS) is among the best adverse event data collection systems in the world, but it’s antiquated and difficult to use. Still, it’s a good way to detect safety signals that weren’t detected during premarket testing or clinical trials
There are unmistakable, unprecedented safety signals in VAERS for the COVID shots. While the U.S. Food and Drug Administration and Centers for Disease Control and Prevention claim no deaths can be attributed to the COVID jabs, it’s impossible to discount 8,986 deaths in the U.S. territories alone, reported as of November 26, 2021
The estimated underreporting factor for COVID jab injuries in VAERS is between 31 and 100, so the actual death toll in the U.S. could be anywhere from 278,500 to 898,600
There’s a strong safety signal for female reproductive issues and for heart inflammation (myocarditis) in young men and boys. VAERS data show an inverse relationship between myocarditis and age, with youths being more frequently affected than older men
VAERS data are being deleted without explanation. Each week, about 100 or so reports are routinely deleted, so there are now thousands of inexplicably missing reports
Jessica Rose, Ph.D., a research fellow at the Institute for Pure and Applied Knowledge in Israel, has taken a deep-dive into the U.S. Vaccine Adverse Events Reporting System (VAERS), and in this interview she shares the details of what she’s finding.
VAERS, despite flaws and drawbacks, is one of the greatest tools we have to evaluate vaccine safety. It was implemented as a consequence of the 1986 National Childhood Vaccine Injury Act. While vaccine companies were given blanket immunity against liability for adverse reactions under this law, VAERS was created to collect injury reports in a centralized database so that the post-marketing safety of childhood vaccines could be monitored.
The system was actually launched in 1990, so we have three decades’ worth of data to compare trends against. Granted, vaccine injuries are notoriously underreported. Investigations have found only 10%1 to as little as 1%2,3 of injuries are reported.
When it comes to the COVID jab specifically, calculations4 by Steve Kirsch, executive director of the COVID-19 Early Treatment Fund, suggest injuries are underreported by a factor of 41. But despite that and other shortcomings, VAERS can still provide valuable information about a given vaccine.
Rose is a computational biologist with postdoc degrees in molecular biology and biochemistry. While a native Canadian, she did her postgraduate training in Israel, where she still lives. When her dream of surfing in Australia were dashed due to the COVID-19 outbreak, she decided to start writing code for statistics and graphics, and as the pandemic wore on, she applied those programming skills to the VAERS database.
There’s absolutely zero comparison. The average number of adverse event reports for the past 10 years is ~39,000, and that includes the adverse event report data for all of the vaccines combined. There are a lot of them …
So we’re looking at about 39,000 total adverse events per year [on average for all vaccines], as opposed to 675,942 [adverse events post COVID jab] in the domestic dataset alone [Editor’s note: Please note that all data are as of the day of the interview and have not been updated prior to publication]. And this does not include the underreporting factor …
We see the same trend when we isolate standalone adverse events like death. There are over 10,000 [post COVID jab] deaths reported now in the domestic dataset alone, not including the underreporting factor, and in the previous 10 years, the average was 155 deaths for the entire year for all the products combined. This is over 6,000% increase in reporting for deaths.
So, the question I’ve been posing to the FDA, the CDC and whoever wants to listen to me is, ‘What’s the cut-off number?’ Because you kind of think of death as being the worst outcome in terms of adverse events in the context of a vaccine or a biological product.
I think there are worse things than death personally. But most people think death is pretty bad. So that’s why I always talk about death in this context. What’s the cut-off number here? How many people have to die in order for these products to be deemed unsafe? So that’s basically all you have to do in VAERS. I mean, you can stop there. You don’t have to look at anything else. But there’s so much more.”
What that means is that when you hear us say these numbers, you have to multiply them by 41, if you want to go with Steve’s estimate, or 31, in the case of mine. Mine is the most conservative estimate. I took Pfizer’s Phase 3 clinical trial data that they presented to the FDA.
There were over 18,000 participants in the drug group and the placebo groups, and there were a certain percentage of individuals in each arm that succumbed to a severe adverse event, which includes death, hospitalization, visit to the ER, a life threatening adverse event, disability or birth defect.
So, 0.7% of people in the drug arm succumbed to a severe adverse event according to their data. I used that rate, and multiplied it by the number of people who had been injected with one shot of Pfizer on a certain date, August 10, and that number becomes your expected number of people that would succumb to a severe adverse event based on their data.
So, you take that number and divide it by the number of reports of severe adverse events, and you get a multiplication factor, an underreporting factor. When you use that base dataset, the Pfizer Phase 3 clinical trial data, you get 31. Ronald Kostoff has also published a paper in Toxicology Reports, and his estimate is 100, I believe.
So, whenever you’re talking about the underreporting factor, I think you should talk about it in terms of a range, because each adverse event is going to have their own [underreporting factor] …
I think if people actually knew the reality of what was going on, they would decide very quickly, right now, never to go near these things. This isn’t hearsay. It’s not conjecture. The clinical trials are garbage, and there’s no safety data. I’m not just saying this — it’s very reflective in all of these adverse event data collection systems all over the world.
They’re all saying the same thing, the Yellow Card [system in the U.K.], the U.S. [VAERS], Australia’s [system9]. They’re all saying the same thing. As an example, myocarditis and young boys. You know, it’s not something that you can ignore. There’s a reason why this is happening. It’s because the [shots] are not safe.”
So, she set out to either confirm or deny whether reports were going missing each week, as data sets are updated weekly. She’s been downloading all the data sets since January 2021, which put her in the unique position of being able to compare the different sets, because when the data set is updated, the old data is overwritten.
Now, there are valid reasons for deleting a VAERS ID. One reason would be if both the doctor and the patient file a report. The two reports then need to be combined, and the ID number of one of the duplicated reports is erased. However, what Rose found is that reports are indeed being deleted that shouldn’t be. She explains:
“The way I was determining if entries, if their IDs, were disappearing was by finding out which VAERS IDs didn’t show up in the next update, because you would assume that every single ID that got into the system would stay in the system. And so, the next update would have that data set and a little more, but that’s not how it works.
There are removals every single week, and they’re not explained. There’s no explanation for these. So, the first thing I did when I found this — and it was over 1,000 [missing IDs] — was to check if a high proportion of these deleted reports were deaths. It wasn’t anything overly suspicious, something like 18%.
Then I checked severe adverse events, then I checked children, because this is a big one that’s happening now. A lot of babies are going missing in VAERS, and they shouldn’t be there [since the COVID shots aren’t being given to babies yet], which is probably why they’re being removed.
So, there wasn’t anything overtly suspicious about the nature of the [missing] IDs. But that’s not even the point. These are people who trusted in these products, and listened to people who are telling them they are safe and effective. They were healthy. They went out and got the shots.
Some of them suffered an adverse event, some of them died. These reports got filed to VAERS, and then they got removed. That’s atrocious. I’m not speculating here, either. This is what is happening. They went through this horrifying experience, which no human should be going through, and then they got disappeared. I don’t even know what the word for that is. It’s appalling.”
At the time she looked into this, there were approximately 5,570 reports with a metric code indicating that the product was given to a patient of inappropriate age. In fact, it was the most frequently occurring adverse event type among young children.
“So, there were so-called medical professionals injecting children without confirming their age,” she says, “and then those children suffered adverse reactions in the thousands. And this doesn’t include the underreporting factor. Some of them died. In the 5- to-11 age group, two of them died. One was 11, one was 13, and the timeframe between the death and the injection in one of the kids was five days, in the other it was one day.
So, this was in close temporal proximity. The part that’s even more disturbing than that is that … something like 60 children had died between the ages of zero and 18, and 38% of those children were under 2. [The next week] that percentage went down to 30%. I’m like, wait now, that was late last week. What happened to them?
There are these enormous inconsistencies in the data. Here’s another one. I have about 100 different files that contain algorithms that run code for specific things, like I have a kid’s file, a cancer file, a prion disease file. So, I run them all with the updated data.
Myocarditis is one of them. And there was this big chunk of data for the 50- to 75-year-olds pertaining to myocarditis reports last week, and this week, it’s one-half. It’s staggeringly obvious that something’s very different in the data. The absolute number of reports went up, but it seems to have shifted somehow.
There could be a plausible explanation. But the fact is there’s no reference at all as to how this data is being shifted around. There’s no record. So, we as the public, have no idea what’s actually going on. All we can say with absolute certainty is that something is going on.”
The CD8+ T cells are the killer cells. These cells are in charge of killing virally infected cells, so they’re very important in the context of a viral infection. One of these studies showed that in people post injection, the gene profiles were very different for CD positive T cells.
If we’re talking about going beyond immune dysregulation, if we’re talking about immune dysfunction, if we’re talking about certain immune cells being depleted, that could be a possible reason why you’re seeing a reemergence of a latent viral species, possibly. We’re also seeing cancer resurgences.
Another paper that came out shows that there might be problems in the realm of double-stranded DNA repair. There are two enzymes (BRCA and 53BP1) that have been reported to be impaired that are very important in repairing double stranded DNA breaks, and if you have an impairment of essential proteins that are meant to repair double stranded DNA breaks, you have serious problems.
One of those problems is proliferation of cells. So, whenever you get a certain type of exposure to a virus, say a cold or a flu virus, and it gets the better of you so your acquired immune system kicks in, you get these swollen glands. That is actual populations of T cells proliferating.
If you have stunted proliferative capacities, or if you have an impairment of that process, you don’t have an immune system if it happens in T cell and B cell populations …
So, in addition to the hyperinflammation that the spike protein seems to be inducing all over the body, there’s this immune function impairment. That’s really scary to me. [It’s something] we need to investigate and absolutely another reason why these rollouts should stop right now.”
“The Truth About COVID-19” exposes the hidden agenda behind the pandemic, showing the countermeasures have nothing to do with public health and everything to do with ushering in a new social and economic system based on totalitarian, technocracy-led control. So, it’s not misinformation they fear. It’s the truth they want to prevent from spreading. Pick up a copy of this best-selling book today before it’s too late.
Big Pharma’s Five Major Minions that Everyone, Vaxxed or Unvaxxed, Must Oppose
This is not an “anti-vaxxer” article, per se. It’s a call for everyone to wake up to the nefarious motives behind vaccine mandates, booster shots, and condemnation of freedom.
The worst kept secret in world history SHOULD be that the unquenchable push for universal vaccinations against Covid-19 has little if anything to do with healthcare and everything to do with Big Pharma’s influence over the narrative. Unfortunately, that secret has stayed firmly hidden from the vast majority of people because of the five major minions working on behalf of Big Pharma.
What’s even worse is the fact that Big Pharma’s greed is merely a smokescreen to hide an even darker secret. We’ll tackle that later. First, let’s look at the public-facing ringleaders behind the vaccine push, namely Big Pharma. But before we get into their five major minions, it’s important to understand one thing. This is NOT just an article that speaks to the unvaccinated. Even those who believe in the safety and effectiveness of the vaccines must be made aware of agenda that’s at play.
Let’s start with some facts. The unvaccinated do NOT spread Covid-19 more rampantly than the vaccinated. Even Anthony Fauci acknowledged the viral load present in vaccinated people is just as high as in the unvaccinated. This fact alone should demolish the vaccine mandates as it demonstrates they have absolutely no effect on the spread of the disease. But wait! There’s definitely more.
This unhinged push to vaccinate everyone defies science. Those with natural immunity may actually have their stronger defenses against Covid-19 hampered by the introduction of the injections which fool the body into creating less-effective antibodies. Moreover, the push to vaccinate young people is completely bonkers. The recovery rate for those under the age of 20 is astronomical. Children neither contract, spread, nor succumb to Covid-19 in a statistically meaningful way. What they DO succumb to more often than Covid-19 are the adverse reactions to the vaccines, particularly boys.
All of this is known and accepted by the medical community, yet most Americans are still following the vaccinate-everybody script. It requires pure cognitive dissonance and an overabundant need for confirmation bias to make doctors and scientists willingly go along with the program. Yet, here we are and that should tell you something.
Before I get to the five major minions of of Big Pharma, I must make the plea for help. Between cancel culture, lockdowns, and diminishing ad revenue, we need financial assistance in order to continue to spread the truth. We ask all who have the means, please donate through our GivingFuel page or via PayPal. Your generosity is what keeps these sites running and allows us to expand our reach so the truth can get to the masses. We’ve had great success in growing but we know we can do more with your assistance.
Who does Big Pharma control? It starts with the obvious people, the ones who most Americans believe are actually behind this push. Our governments at all levels as well as governments around the world are not working with Big Pharma. They are working for Big Pharma. Some are proactive as direct recipients of cash. Others may oppose Big Pharma in spirit but would never speak out because they know anyone who does has no future in DC.
This may come as a shock to some, but it’s Big Pharma that drives the narrative and sets the agenda for the “experts” at the CDC, FDA, WHO, NIH, NIAID, and even non-medical government organizations.
Most believe it’s the other way around. They think that Big Pharma is beholden to the FDA for approval, but that’s not exactly the case. They need approval for a majority of their projects, but when it comes to the important ones such as the Covid injections, Big Pharma is calling the shots. They have the right people in the right places to push their machinations forward.
That’s not to say that everyone at the FDA is in on it. Big Pharma only needs a handful of friendlies planted in leadership in order to have their big wishes met. We have seen people quitting the FDA in recent weeks for this very reason. The same can be said about the other three- and five-letter agencies. Too many people in leadership have been bribed, bullied, or blackmailed into becoming occasional shills for the various Big Pharma corporations. Some have even been directly planted by Big Pharma. That’s the politics of healthcare and science that drives such things as Covid-19 “vaccines.”
With that said, our content may be reproduced and distributed as long as it has a link to the original source and the author is credited prominently. We don’t mind you using our content as long as you help out by giving us credit with a prominent link. If you feel like giving us a tip for the content, we will not object!
JD Rucker – EIC @jdrucker
***
This article has been archived by Conspiracy Resource for your research. The original version from Based Underground can be found here.
