Allegations Against COVID-19 Vaccine Manufacturers

Dear colleagues and supporters, we declare

that Pfizer,

Moderna, BioNTech, Janssen, and

AstraZeneca

and their enablers

willfully withheld and omitted crucial safety and

effectiveness information from patients and

physicians and should be immediately indicted for

fraud. We know that shortly after administration

of these

products, thousands of people have died.

And although correlation isn't causation, reasonable

criterion have been applied to examine the relationship between

injections and the events, and it's absolutely clear-cut

that these are the cause of death.

Mechanistically, the design of these products was

knowingly deficient in a number of ways.

First, they caused the expression in the human

body

of toxic virus spike protein.

Unlike what they told us that it would stay in the injection site,

they

distribute widely around the body.

There is no built-in limit to the amount of toxic spike protein

that can be made or for how long it is made, and that's the

cause of the toxicity.

Turning to the clinical trials, there is evidence of questionable

practices all around. For example, several of the

studies were clearly unblinded while they were ongoing,

contrary to best practice.

And also, in a number of cases, subjects were removed from

the database prior to statistical analysis in a way

that is suggestive of fraud.

We were given blanket assurances time and again by all of the companies

about the benign safety profile of their products.

Even as the products rolled out and in the earliest weeks, they

must have known this was not true.

To add insult to injury, it appears that these products provide little

or no protection from the virus that they sought to protect us

from.

Finally, turning to the non-clinical studies,

my area,

the packages are hugely compromised by omissions

of standard safety studies, which regardless of

regulatory requirements should have been done

because they do impact human safety.

Specifically, so-called ADME tox looking at

distribution. It does leave the injection site,

and they told us it

didn't. They have not conducted complete regul--

reproductive toxicology, without which these should never be

given to pregnant women.

The consistency of the materials being tested in toxicity tests,

and even not all the components have been through toxicity

testing.

And finally, they cannot claim lack of anticipatory

knowledge because the companies and the FDA

knew that products of this type would produce many toxicities.