Pfizer/BioNTech injections were changed in October 2021 from “toxic and inappropriate as mRNA injections” (purple cap) to “corrected but still toxic and inappropriate" (grey cap)

Check out this brilliant analysis and exposure of wilful malfeasance by the European health regulator – the European Medical Agency (EMA) – I would not be at all surprised to find that it is banned shortly and the good Professor censored and even imprisoned.

Big h/t to kerrylynn

THE PANDORA’s VACCINE on Vimeo

A quick overview:

From kerrylynn: “Prof. Gabriele Segalla (biochemist, specialist in chemistry of micro-emulsions & colloidal systems, author of "Pandora's Vaccine") explains how he believes these injections are killing people (with emphasis on LNPs rather than spike protein) yet are seemingly harmless for others. He also provides proof that Pfizer knew of the dangers. “

My take-aways:

A clear and concise explanation of the causes of various types of clumping, the instability of mRNA delivery, the risks and failures of sucrose buffers and  electrolytes.

The huge bombshells for me were the statements by BioNTech in its 26 November 2019 patent application to the EMA - that Pfizer must have been familiar with (but not necessarily BARDA) - detailing why its mRNA tech should NOT be used as an injectable mRNA treatment.

Just over a year later, in December 2020, the EMA granted emergency use authorisation of the exact same methods, ingredients and technology.

The BioNTech doses of Cominarty were highly unstable and

• had to be transited at 72 degrees C below freezing,

• had to be brought to a 25 degree C room temperature,

• had to be diluted,

• more destabilizing electrolytes had to be added,

• had to be stirred ten times (not shaken) then injected into a 37 degree C arm

meaning the frozen and unstable doses had to traverse a temperature increase of 109 degrees C!!!

Another bombshell – just 10 months after the initial authorization of Cominarty, in October 2021, Pfizer/BioNTech submitted an approval request for a “new and improved” concoction that was intended to correct catastrophic errors in the first version. Version 2 had more stable contents in vials that could be stored in the fridge but still with all the other catastrophic issues with electrolytes and buffers.

Here’s the thing - the EMA immediately approved version 2 of the Pfizer/BioNTech injection but LEFT THE UNSTABLE AND MORE DANGEROUS version 1 concoction on the shelf!!

At the least, the original vials should have been withdrawn and substituted by the new ones – even if that meant a delay of a few weeks to a month before the new (grey top) vials became available.

Pfizer/BioNTech’s original – first – formulation has/had a purple cap, the new formulation has a grey cap.

Just for the first ten months of doses administered in the US and Europe in 2021, we have this:

EU First

Twi thirds of all Pfizer/BioNTech injections were administered before version 2.0

Now the US

The US stopped supplying data on doses by manufacturer to the OWD people 5 months ago. I don’t recall seeing an updated EUA request to the FDA for Version 2 in October 2021 but I may have missed it.

Neither do I recall seeing anything for any other health regulator - UK, Canada, Australia, New Zealand etc either for that matter - do the people injected in other countries even know there was a “new and improved” Cominarty injection available in October 2021 that was less lethal than the original?

Italian law has strict requirements and sanctions against this type of crime. The US has also – but – unlike the US, Italian law is not governed by EUA, the Pentagon and BARDA.

Onwards

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