Professor Yeadon is a former VP at Pfizer Professor Yeadon was so distressed by the way the UK government has pandered to the vaccine lobby that he
wrote an open letter to Matt Hancock, the Secretary of State for Health and Social Care of United Kingdom.
This is the sentence in the letter that jumps out at me because he is addressing the new lipid nanoparticle delivery system (brand new) used in
creating the Pfizer mRNA vaccine “ Several of the vaccine candidates utilise novel technology which have not previously been used to create
vaccines. There is therefore no long term safety data which can be pointed to in support of the notion that it’s reasonable to expedite development
& to waive absent safety information on this occasion.”
Dr Yeadon’s letter to the UK Health Minister reads:
“Dear Mr. Hancock,
I have a degree in Biochemistry & Toxicology & a research based PhD in pharmacology. I have spent 32 years working in pharmaceutical R&D, mostly in
new medicines for disorders of lung & skin. I was a VP at Pfizer & CEO of a biotech I founded (Ziarco – acquired by Novartis). I’m knowledgeable
about new medicine R&D.
I have read the consultation document. I’ve rarely been as shocked & upset.
All vaccines against the SARS-COV-2 virus are by definition novel. No candidate vaccine has been in development for more than a few months.
If any such vaccine is approved for use under any circumstances that are not EXPLICITLY experimental, I believe that recipients are being misled to a
criminal extent.
This is because there are precisely zero human volunteers for whom there could possibly be more than a few months past-dose safety information. My
concern does not arise because I have negative views about vaccines (I don’t), Instead, it’s the very principle that politicians seem ready to
waive that new medical interventions at this, incomplete state of development- should not be made available to subjects on anything other than an
explicitly experimental basis. That’s my concern.
And the reason for that concern is that it is not known what the safety profile will be, six months or a year or longer after dosing.
You have literally no data on this & neither does anyone else.
It isn’t that I’m saying that unacceptable adverse effects will emerge after longer intervals after dosing. No: it is that you have no idea what
will happen yet, despite this, you’ll be creating the impression that you do.
Several of the vaccine candidates utilise novel technology which have not previously been used to create vaccines. There is therefore no long term
safety data which can be pointed to in support of the notion that it’s reasonable to expedite development & to waive absent safety information on
this occasion.
I am suspicious of the motives of those proposing expedited use in the wider human population. We now understand who is at particularly elevated risk
of morbidity & mortality from acquiring this virus.
Volunteers from these groups only should be provided detailed information about risk / benefit, including the sole point I make here. Only if informed
consent is given should any EXPERIMENTAL vaccine be used.
I don’t trust you. You’ve not been straightforward & have behaved appallingly throughout this crisis.
You’re still doing it now, misleading about infection risk from young children. Why should I believe you in relation to experimental vaccines?
Dr. Michael Yeadon
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