Evidence that nine million adverse events are missing from VAERS – and probably held on a “secret server” at the CDC – until the CDC pays General Dynamics IT more money

The above table is what is on VAERS for deaths and harms from C19 injections made by US makers of C19 mRNA (plasmid DNA) injections.

DEAFENING SILENCE BY ALL!!!! Still no coverage of the massive non-disclosure of adverse event reports caused by C19 injections made by US manufacturers OUTSIDE THE US (substack.com)

The IS administered 677 million doses manufactured by Pfizer, Moderna, JnJ and Novavax.

I estimated that 8 times that number, around 6 billion doses were administered OUTSIDE the US. So, unless overseas doses (doses ex-US) were different, the same rate of adverse events should have been reported from overseas, into VAERS.

The regulatory agencies in each country are supposed to report injuries to the US manufacturer who in turn is supposed to report to VAERS.

Now every country has an adverse event reporting system, but leading countries do.

By subtracting the total adverse events (LHC) from the US numbers (RHX) we get 1.6 million less 1 million = just 500,000.

I do not have up to date numbers for the EU and UK, but these two jurisdictions alone had these numbers of adverse events for Pfizer and Moderna injections.

50,663 DEAD and 5,315,063 Injured Following COVID-19 Vaccines in European Database of Adverse Reactions - Vaccine Impact

For the EU, more than a year ago, back in February 2023, there were 1.6 million adverse events reported and more than 47,000 fatalities.

Back then there had been almost 820 million doses injected in nthe EU (around a billion ow).

COVID-19 vaccine doses administered by manufacturer, European Union (ourworldindata.org)

Now for the UK. From here - updated 8 March 2023, so also a year ago, covering data to 23 November 2022:

ARCHIVED - Coronavirus vaccine - summary of Yellow Card reporting - GOV.UK (www.gov.uk)

“Up to and including 23 November 2022, the MHRA received and analysed 177,925 UK Yellow Cards from people who have received the monovalent or bivalent COVID-19 Vaccine Pfizer/BioNTech. These reports include a total of 511,776 suspected reactions (i.e., a single report may contain more than one symptom). The first report was received on 9 December 2020.”

And this:

“Up to and including 23 November 2022, the MHRA received and analysed a total of 47,045 UK reports of suspected ADRs to the monovalent and bivalent COVID-19 Vaccine Moderna. These include a total 151,628 suspected reactions (a single report may contain more than one symptom). The first report was received on 7 April 2021.”

Dor the period up to 23 November 2022, the UK’s Yellow Card system had received more than 663,000 adverse event reports.

So, just European Medica Agencies EUDRA system plus the UK’s Yellow card system, we have more than 2,2 million reports of adverse events.

Compare that to the 600,000 adverse event reports for overseas (ex-US) reports showing on VAERS!!!

All the adverse event reports from Japan, Australia, Canada South Kora et al who have adverse event reporting systems of with some degree of sophistication, need to be added to this umber for the UK and EU from a year to 15 months ago. Those countries that don’t have such systems – well maybe a proxy of the average for other countries can be used.

Assuming that around 6 billion doses made by US manufacturers were used outside the US , and, the harms were proportional to the harms suffered inside the US from 677 million doses, I guesstimate that an additional 8.4 million adverse events should have been reported to VAERS  from outside the US – lifting the ex-US total to 9 million and the overall total to 10 million.

The AstraZeneca shot was mostly made under license in India by the Serum Institute – around 2 billion doses. The adverse events from AZN shots are excluded from this article as AZ is not a US manufacturer and was not granted a EUA for its shots.

Lastly, just a speculative observation, - around 70-75% of injections did not result in harms. The remaining 25-30% did – of all those injected 4-7% (one in 14 to 1 in 25) suffered severe (life altering) or serious (life threatening) injuries.

Just for the Pfizer and Moderna shots – using a lower total number of 6 billion shots injected worldwide by these two manufacturers, the implication is that 240 million people have suffered serious events out of 420 million serious adverse events.

Eve if the umber of overseas injections was lifted to 9 million and the total adverse events to 10 million, the under-reporting of severe adverse events would be around 42.

Remember, the adverse events will only be processed from the CDC’s “secret server” at the rate at which the CDC pays its sub-contractor. General Dynamics IT.

It is no coincidence that the number of deaths for the US and ex-US are around 18,500, despite there being almost ten times the injections administered outside the US as inside.

Onwards!

Please subscribe ten bucks a month or annually for 100 bucks. You can also donate via Ko-fi – any amount from three bucks upwards. Ko-fi donations here: https://ko-fi.com/peterhalligan