Canadian Government Data: The Rate of SERIOUS Post-Vaccine Adverse Events per Person Is 1 in 3,444!

COVID-19 vaccines have the highest rate of serious injury of all the vaccines circulating in Ontario

According to the latest Canadian Government data, the SERIOUS adverse events rate per person is 1 in 3,444.

Knowing that less than 10 percent of adverse effects are reported, it’s not difficult to imagine what the real numbers would look like.

The data breakdown and analysis brought to us by Knowledge Acquisition and golden pup :

Knowledge Acquisition @KnowledgeAcqui1

A look at ⚡️SERIOUS ⚡️post-vaccine adverse events in Canada 🇨🇦, nation wide. Serious Adverse Events: 9,241 People Vaccinated: 32,443,713 The rate is provided per dose. But, a per person rate is more useful. The rate of serious AE's per person is 1 in 3,444. 🧵

Knowledge Acquisition @KnowledgeAcqui1

This rate is comparable to the myocarditis rate among young males in Ontario. Only this is all serious adverse events, across the entire population. Clearly, we are seeing events other than just myocarditis.

Knowledge Acquisition @KnowledgeAcqui1

In Ontario, there are a large number of adverse events in the 'Other Severe or Unusual' category. Could this be what we are seeing in the federal roll up data? With so many 'Other' events, surely some are repeated enough to be worthy of their own category?

Knowledge Acquisition @KnowledgeAcqui1

Myocarditis risk in ON is concentrated among young males. Overall AE risk is concentrated among females. And, look at the age rates. Are the bulk of the serious events we see from the federal data concentrated among middle aged women?

COVID-19 vaccines have the highest rate of serious injury of all the vaccines circulating in Ontario

golden pup @Golden_Pup

COVID-19 Vaccine Adverse Events in Ontario (Apr 25 - May 8) - 203 new adverse events reported - 10 more hospitalizations - 5 more cases of myocarditis/pericarditis - 81 more Other Severe or Unusual Events Source: publichealthontario.ca/-/media/docume…

golden pup @Golden_Pup

When interpreting this data, please note that even though this is a bi-weekly report, adverse events can be reported up to 6 weeks following a dose. Here is the temporal criteria for reporting from Public Health Ontario. Note that all COVID-19 vaccines are non-live.

golden pup @Golden_Pup

More info on "Other Severe or Unusual Events" Source: health.gov.on.ca/en/pro/program…

golden pup @Golden_Pup

COVID-19 vaccines have the highest rate of serious injury of all the vaccines circulating in Ontario. publichealthontario.ca/en/data-and-an…

And of course, the most compelling are the testimonies of real people whose loved ones, friends, and coworkers have been injured or killed by the poison.

I see several such posts on Twitter daily and it is truly heartbreaking…

thirdEYEcyclops 👑 @wytewzrdz

It's happening now. My cousin just turned 41 and died of a heart attack. Friends 21 yr old son died in his sleep. Many others I know coming down with shingles, hepatitis, strokes & heart issues. I don't know how they're going to explain this all away.

THEY are not going to bother explaining anything. They are busy prepping the herd for the next extermination phase.

“The Pandemic is not over….The Pandemic is not over…The Pandemic is not over”

Wittgenstein @backtolife_2022

‘Global COVID-19 Summit’

“Moderna expects stronger vaccine sales in the second part of the year as governments order more shots to get ready for fall inoculation campaign”

Wittgenstein @backtolife_2022

Jimmy Dore - worrisome...

Related articles:  

A Public Health Emergency in Canada: The Rate of Change in Excess Millennial Deaths Can’t Be Explained by a Sudden Rush of Suicides, Overdoses, Cancers

Vaccine Democide: Terrifying Data From Group Life Mortality Survey and Recent MIT Study

Pfizer Data Fraud? The Pfizer Documents Show Major Anomalies in Clinical Trial Enrollment Data

Dr. Michael Yeadon: THIS MUST STOP! Pfizer Documents Show FDA Knew of Death Risk

Moderna SEC Filing: We May Be Delayed or Prevented From Receiving Full Regulatory approval. Unexpected Safety Issues Could Significantly Damage Our Reputation and That of Our mRNA Platform

BioNTech 2022 SEC Filing: We May Not Be Able To Demonstrate Sufficient Efficacy or Safety of Our COVID-19 Vaccine. Significant Adverse Events Could Delay or Prevent Regulatory Approval

mRNA "Vaccines" Are Gene Therapy. May cause Undesirable Side Effects That Could Delay Or Prevent Their Regulatory Approval According To BioNTech SEC Filing

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