by Dr. Joseph Mercola, public domain

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(Dec. 19, 2021) — 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.

No, People Are Not Filing Fake Reports

A common attempt to explain away the VAERS data by so-called fact checkers is to say that it’s unreliable because anyone can file a report. This is pure hogwash. Yes, anyone can file a report, but there are penalties for filing a false report, and the filing is time-consuming and exacting. We can be quite certain there’s no over-reporting going on.

It takes on average 30 minutes to fill out a report, and the system is set up in such a way that you cannot save anything until you get to the very end. Even worse, each page will time out after an allotted period of time, forcing you to start from the beginning if you take too long to fill in the details.

“This probably frustrates enough people that they don’t start again,” Rose says. Indeed, the cumbersomeness of the website itself has often been cited as a reason for why doctors don’t report adverse events. Doctors don’t have the time to do it, and most patients don’t know they can file on their own. As noted by Rose:

“[VAERS] is probably one of the best adverse event data collection systems in the world, but it’s completely lamentable. It’s antiquated … Nonetheless … it’s a way to detect safety signals that weren’t detected during premarket testing or clinical trials.

And it is functioning that way, because there are many, many safety signals [about the COVID jabs] being thrown out by the data. For example, everyone’s heard of myocarditis … which is one of the safety signals being thrown off in VAERS. And so, we’ve learned that it happens in young people, more so in boys.”

One explanation for this gender discrepancy has to do with androgens. Testosterone has been shown to facilitate entry of the spike protein into cells by activating a specific enzyme. This could help explain why men, who have higher testosterone levels, are getting myocarditis at much higher rates than women.

Most Lethal ‘Vaccines’ in Medical History

Rose continues:

“I implore everybody to do this … [VAERS] is very accessible. Just go to their website and download the CSV files. You can play with it in Excel, or use whatever is compatible with the CSV file. The OpenVAERS system is even easier to use.

There are three separate files that you can download for the domestic data set, which includes the individual’s data, the symptoms or adverse events that they reported (and it can be up to 15 different types), and the injection data …

You can merge them so that, as per [each] VAERS ID, you have a lot more information … That’s what I did. All you have to do is count the number of adverse events that have occurred in 2021. In the context of the COVID-19 products, exclude all the other vaccines to isolate the signal, and compare the number of adverse events to the total number of adverse events reported in every single year going back 30 years.

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.”

Can Causation Be Established?

While the U.S. Food and Drug Administration and Centers for Disease Control and Prevention outrageously deny that a single death can be attributed to the COVID jabs, it’s simply impossible to discount 19,532 deaths5 (8,986 in the U.S. territories alone6) reported as of November 26, 2021. As noted by Rose:

“It’s not even statistically plausible to say that not one death out of 10,000 was caused [by the shot]. It’s not scientific to say that … Those people, not 100% of them would have died anyway? That’s not how life works.”

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