Data doodling with C19 mRNA for context for the bombshell of 5 million accumulated Pfizer/BioNTech adverse events over 18 months to June 2022 and 1.5 million for the 6 months to June 2022
A huge story broke out on 15 June 2023 about the recent release of adverse events in the “Pfizer documents”.
These new “Pfizer documents” reported around 5 million cumulative adverse events to 30 June 2022 and 1.5 million for the six months between December 2021 and June 2022.
These “events” should have been reported to VAERS and seem to square with the share of adverse events resulting from doses administered in Europe and the US, as reported to EUDRA and VAERS.
So the scale should not come as a surprise, just the fact that they were not recorded on VAERS.
You may recall that the first post marketing authorization report of around 42,000 GLOBAL adverse events and 1,223 deaths covered the (short) 3 months from mid-December 2920 to end February 2021 for around 70 million doses administered.
70 million administered is my estimate from Our World in Data (OWID) numbers by manufacturer for the US plis EU only; The report shows around 126 million doses shipped worldwide, rather than doses administered worldwide - leading the reader to assume safety percentages using doses shipped, rather than just over hald the doses actually administered.
There has been no particular analysis of any adjustment to adjust for under-reporting to be applied to that first three month post marketing authorization data, which gathered world wide data.
An under reporting factor of 40 results in around 48,000 deaths and over 1.6 million adverse events from 70 million doses administered (35 million receiving the two dose initial series).
Note that from here: Reporting Adverse Events to VAERS | Vaccine Safety | CDC
“Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention.”
The CDC requires reports from manufacturers it regulates from around the world. EUDRA? Not so sure, perhaps just from within the EU? Anyway, there is a risk of double counting, so presumably, adjustments may be made between the CDC and EMA. We have seen the sub-contractors responsible for maintaining the VAERS database, General Dynamics IT, scrubbing some EU data.
Ok, here are some links to the back story on the 5 million adverse events to June 2022 and the 1,5 million from December 2021 to June 2022.
The Conservative Review, Jessica Rose, Karen Kingston, and Aussie17 covered it in their SubStacks below:
Pfizer Appendix 2.2 document compared to VAERS (substack.com)
Pfizer Recorded 5 Million Harmful Outcomes Across 1.5 Million mRNA Injected Victims (substack.com)
Breaking: Shit just hit the fan! - PharmaFiles by Aussie17 (substack.com)
(100) Part 2 of Shit Hitting The Fan! - PharmaFiles by Aussie17 (substack.com)
I will leave the analysis of severe (life altering) and serious (life threatening) to the experts, but I thought I would take a look at the numbers of injections v adverse events over those two time periods (six months and 19 months) just for Europe and the US and compare that to the Phase 3 clinical trial used to forecast adverse events 9yes, clinical trials are an estimated forecast of future outturns!)
I remain somewhat baffled as to why giving two doses to the elderly, weak and malnourished with close to zero left of their immune systems, ny shutting down what’s left for two periods of two weeks for each dose is “therapeutic” when it leaves their body prone to every possible infection or recurrence of disease for a whole month (two x two week periods whilst the body obeys the mRNA instructions to manufacture spike protein)!
Mind you, I am also baffled as to why injecting instructions to produce a spike protein could possibly substitute for, or replace, an immune system, let alone a response from one.
Here are the summary tables of data from the EU and US compared to clinical trials. Apologies for the small print!
First the EU:
Now the US:
The total of EU + US
And a comparison with Pfizer’s Phase 3 clinical trial:
The first metric that leaps out is the deaths per million doses and deaths per million double dosed.
Let’s look at the 6 month period from 31 December 2021 to 30 June 2022 first.
The clinical trial indicated (albeit with low confidence, given the small sample and aborted trial) that 912 people per million injected twice would die – equivalent to 456 deaths per million doses administered.
For the six month period from 31 December 2021 to 30 June 2022, EUDRA shows 122 deaths per million people receiving two doses and VAERS 167 per million receiving two doses (I know, not everyone got two doses over this period, some got one and some three or more).
For the full 18 month period from 31 December 2020 to 30 June 2022, we see that there were 70 deaths per million people double dosed in the EU and 84 in the US.
Note the acceleration in reported deaths per million doses and dosed for the 6 months to June 2022 compared to the first year to 31 December 2021. Almost double the rate of reported deaths for the EU and +60% for the US. Both the EU and US reported deaths are way below the rate indicated by the clinical trial.
Turning to injuries/adverse events, If we make the leap that only severe and serious events are reported to EUDRA and VAERS, we see that for the clinical trial, 18,200 per million people double dosed suffered these type of injuries, compared to 19,440 for the last 6 months for the EU and 7,441 for the US.
Over the full 18 month period, we see a rate of adverse events/injuries pf around 7,700 for the EU and around 4,400 per million people double dosed for the US compared to that 18,300 indicated by the aborted clinical trial.
Still a huge rise in reporting rates for adverse events. Reporting rates for injuries for the EU leapt from a rate of 5,800 for calendar year 2021 to 19,440 for the six months to 30 June 2022. For the US, 2021 calendar year reported adverse events were 3,850 per million people double dosed compared tp 7,441 for the six months to 30 June 2022.
Okay, we know the numbers are dubious – so there are no actual numbers that we can access to come up with data which is accurate and complete.
Here is the background work and references to source material.
For ease, I categorised the data as a six month period, from 31 December 2021 to 30 June 2022 and a cumulative 18 month period from 31 December 2020 to 30 June 2022.
Let’s start with the number of injections administered in the EU over those periods by manufacturer and compare that to adverse events reported to the EU’s European Medicines Agency (EMA) equivalent of VAERS – EUDRA.
The only site that I have found that even makes the attempt at decrypting the EUDRA database is Vaccine Impact - - It is a mammoth task, with that site relying on the assistance of one of the websites intrepid readers to decrypt. I was not able to replicate the numbers produced!
I have exchanged a few emails with the helpful EMA team, but really it is NOT like Brer Rabbit asking Brer Fox to throw him into the briar patch as a punishment AT ALL! I also had to pretend to be from Northern Ireland to even get as far as submitting the initial data enquiry. The team at the EMA does not collect much of the data that would be helpful to analyse – for reassurance or challenge.
To give you some idea of the work required to get data from EUDRA, here’s a few links.
European database of suspected adverse drug reaction reports - Eudravigilance (adrreports.eu)
Here is a link to Pfizer AE’s as currently stated on EUDRA.
Oracle BI Interactive Dashboards - DAP (europa.eu)
If you click the tiny icon in the top right hand corner, you can export to Excel.
Ok. Number of injections by manufacturer at 31 December 2021 and 30 June 2022 compared with US doses – but not any others from e.g. South America, Canada or Australia
EU doses by manufacturer From here:
COVID-19 vaccine doses administered by manufacturer, European Union (ourworldindata.org)
US doses from manufacturer here:
COVID-19 vaccine doses administered by manufacturer, United States (ourworldindata.org)
Adverse events reported to EUDRA to December 2021 – Scroll down the page for granular detail per manufacturer per event.
In total, to 31 December 2021, the large image on the link shows 36,257 dead and 3,244,062 injuries, through I January 2022.
The link shows a breakdown for Pfizer/BioNTech as below:
“Total reactions for the mRNA vaccine Tozinameran (code BNT162b2, Comirnaty) from BioNTech/ Pfizer: 16,471 deaths and 1,546,829 injuries to 01/01/2022”
In total to 30 June 2022, the large image on the link shows 46,160 dead and 4,823,724 injurie3s through 1 July 2022
The link shows a breakdown for Pfizer/BioNTech as below:
Total reactions for the mRNA vaccine Tozinameran (code BNT162b2,Comirnaty) from BioNTech/ Pfizer: 21,746 deaths and 2,387,920 injuries to 02/07/2022
Adverse events reported to VAERS from here and here:
VAERS Summary for COVID-19 Vaccines through 12/31/2021 – VAERS Analysis
VAERS Summary for COVID-19 Vaccines through 7/1/2022 – VAERS Analysis
31 December 2021 Pfizer deaths = 14,251, Adverse events = 569,584. Doses = 300,486,092
30 June 2022 Pfizer deaths = 18,937, Adverse events = 778,629, Doses = 352,959,331
The sharp-eyed amongst you will have spotted the 300 million doses above compared to the 296 million shown for data from OWID – one day’s difference in doses administered?
These numbers can be compared to the Pfizer Phase III clinical trial outcomes, which, although aborted with two out of the six months trial period remaining, should at least, not suffer from any under reporting.
The COVID-19 Inoculations - More Harm Than Good FINAL Video & Print (canadiancovidcarealliance.org)
Onwards
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The numbers are catastrophic, how is this information not readily available to everyone to see. I have sent things like this to my sister but she refuses to read it, she's had 4 jabs, as has the rest of her family. Thank you for trying to wake people up to the truth.
So it is levelling off for 2023? Let’s hope this doesn’t get lost in history now.