Dear Vaccinator Notice of Potential Liability

To: Mr./Mrs.
Pharmacist/Nurse/Doctor/Vaccine Administer
From: Concerned Citizen
Date: June 28, 2021
Re: Informed Consent
NOTICE OF POTENTIAL LIABILITY FOR LACK OF INFORMED CONSENT WHEN ADMINISTERING

COVID-19 VACCINES (“GENE THERAPY”)
I. THE TEN POINTS OF THE NUREMBERG PRINCIPLES

1. The voluntary consent of the human subject is absolutely essential.
2. The experiment should be such as to yield fruitful results for the good of society,
unprocurable by other methods or means of study, and not random and
unnecessary in nature.
3. The experiment should be so designed and based on the results of animal
experimentation and a knowledge of the natural history of the disease or other
problem under study that the anticipated results will justify the performance of the
experiment.
4. The experiment should be so conducted as to avoid all unnecessary physical and
mental suffering and injury.
5. No experiment should be conducted where there is an a priori reason to believe
that death or disabling injury will occur; except, perhaps, in those experiments
where the experimental physicians also serve as subjects.
6. The degree of risk to be taken should never exceed that determined by the
humanitarian importance of the problem to be solved by the experiment.
7. Proper preparations should be made, and adequate facilities provided to protect
the experimental subject against even remote possibilities of injury, disability, or
death.
8. The experiment should be conducted only by scientifically qualified persons. The
highest degree of skill and care should be required through all stages of the
experiment of those who conduct or engage in the experiment.
9. During the course of the experiment the human subject should be at liberty to
bring the experiment to an end if he has reached the physical or mental state where
continuation of the experiment seems to him to be impossible.
10. During the course of the experiment the scientist in charge must be prepared to
terminate the experiment at any stage, if he has probable cause to believe, in the
exercise of the good faith, superior skill and careful judgment required of him that a
continuation of the experiment is likely to result in injury, disability, or death to the
experimental subject.
Any compulsory Covid-19 vaccination requirement is a violation of federal law. I urge you to
advise all vaccine recipients that they have the right to refuse or to take any COVID-19 vaccine.
Any other action is contrary to federal law.
II. Covid-19 Vaccines are Experimental and Require Informed Consent
Covid-19 vaccines are not approved by the FDA. The Covid-19 vaccines are only approved under
an Emergency Use Authorization, for investigational use only.1 Covid-19 vaccines lack requisite
studies and are not approved medical treatment. The FDA’s guidance on emergency use
authorization of medical products requires the FDA to “ensure that recipients are informed to
the extent practicable given the applicable circumstances … That they have the option to accept
or refuse the EUA product …” 2
Title 21, Section 360bbb-3 of the Federal Food, Drug, and Cosmetic Act (the “FD&C Act”) vests
the Secretary of Health and Human Services with the permissive authority to grant Emergency
Use Authorizations (“EUAs”) providing that appropriate conditions designed to ensure that
individuals to whom the product is administered are informed:
1. that the Secretary has authorized the emergency use of the product;
2. of the significant known and potential benefits and risks of such use, and of the extent
to which such benefits and risks are unknown; and
3. of the option to accept or refuse administration of the product, of the consequences, if

any, of refusing administration of the product, and of the alternatives to the product
that are available and of their benefits and risks. 1
The right to avoid the imposition of human experimentation is fundamental, rooted in the
Nuremberg Code of 1947, has been ratified by the 1964 Declaration of Helsinki, and further
codified in the United States Code of Federal Regulations. In addition to the United States
regarding itself as bound by these provisions, these principles were adopted by the FDA in its
regulations requiring the informed consent of human subjects for medical research. It is unlawful
to conduct medical research, even in the case of an emergency, unless steps are taken to secure
informed consent of all participants. 3
Vaccine administers, such as yourself, Mr./Mrs. (doctor, nurse, pharmacist, misc. health care
worker) have an obligation to inform participants of the adverse events and death which has
occurred from these Covid-19 vaccines.
• “potential benefits and risks” of the Covid vaccines, AND
• Of “the extent to which such benefits and risks are unknown;” AND
• “of the option to accept or refuse administration of the product,” AND
• “of the alternatives to the vaccine that are available and of their benefits and risks.” 1
III. Vaccine Administers have Duty to Inform Recipients of Known and Unknown Risks
of the Covid-19 Vacines
• Based on VAERS as of June 16, 2021, there have been 5,993 deaths reported, 4 and
358,379 adverse events related to the Covid-19 vaccines. 5
• By comparison, from July 1, 1997, until December 31, 2013, VAERS received 666 adult
death reports for all vaccines. 6
• In 1976, the US government halted the rollout of the experimental swine flu vaccine for
25 deaths after 55 million people were inoculated.
• The FDA and these pharmaceutical companies allow children 12 years and older to receive
this vaccine, however children were never studied in this trial. Never before in history
have we given medications that were not FDA approved to people who were not initially
studied in the trial. There were no trial patients under the age of 18! They’re
extrapolating the data from adults down to children and adolescents. This is not
acceptable. Children are not little adults. Children have 99.997% survivability from the
covid.
• The CDC’s Advisory Committee is meeting in June to address the higher number of
observed than expected myocarditis/pericarditis cases in 16–24-year-olds.” 7 This is
inflammation of the heart. There is no such thing as a “mild case” of heart inflammation.
• Brain injuries after the COVID-19 vaccines are increasingly being reported. Search the
federal government VAERS Database for any diagnostic term such as “dementia” or
“Bell’s Palsy” or “brain bleeding,” sadly the numbers are rising daily. 8
• A study published by the renowned Cleveland Clinic in Ohio indicates that natural
immunity acquired through prior infection with COVID-19 is stronger than any benefit
conferred by a Vaccine. People that have had Covid in the past and are now recovered,
have a much stronger (10-20x) 6 antibody response to the vaccine. The response is much
too strong and overwhelms the person's health system. Medical studies show severe side
effects post vaccination in those persons with prior infection of Covid, including life-
threatening harm to plaintiffs. 9 10 Health professionals have never blanket administered
vaccines without checking for titers first (Hep B, MMR, Varicella, etc.). You must exclude
vaccinating persons who already had the infection for which the inoculation is being
considered. 11
• Pregnant persons were not studied in the initial Covid-19 vaccine trials. As such, the
risks/benefits are unknown. The mere fact that there are unknown risks needs to be
communicated to each vaccine recipient.
Please consider this an official notice that you may be personally liable for injuries sustained by
individuals from these vaccines should you refuse to inform your vaccine recipients of these
risks. Any pressure, coercion, or threat of reprisal constitutes reckless endangerment and has a
reasonable expectation of causing personal injury resulting in damages. Throughout world
history, “I just did my job” has never been a defense to forced medical experimentation (or
medicine intentionally lacking informed consent).
1 Title 21, Section 360bbb-3 of the Federal Food, Drug, and Cosmetic Act (the “FD&C Act”)
2
https://www.fda.gov/media/97321/download
3
21 CFR § 50.24
4
https://vaers.hhs.gov/data.html
5
https://www.openvaers.com/covid-
data?fbclid=IwAR1LBbvL_banBKlvSBDZh7VJsvTYvKyZzzdcJFq5bqc_xAu0LOlOvVXNyZQ
6
Exhibit 5. Pedro L. Moro, Jorge Arana, Mria Cano, Paige Lewis, and Tom T. Shimabukuro, Deaths Reported to the
Vaccine Adverse Event Reporting System, United States, 1997-2013, VACCINES, CID 2015:61 (September 2015).
7
https://childrenshealthdefense.org/defender/cdc-teens-vaccinated-pfizer-moderna-higher-risk-heart-
inflammation/
8
https://wonder.cdc.gov/vaers.html June 2, 2021
9
https://www.news-medical.net/news/20210511/Severe-COVID-19-linked-to-genetic-clotting-predisposition.aspx
10
https://www.medrxiv.org/content/10.1101/2021.05.04.21256617v1.full.pdf
11
https://www.cdc.gov/vaccines/covid-19/hcp/answering-questions.html

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Dear Vaccinator Notice of Potential Liability

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To: Mr./Mrs.

NOTICE OF POTENTIAL LIABILITY FOR LACK OF INFORMED CONSENT WHEN ADMINISTERING

I. THE TEN POINTS OF THE NUREMBERG PRINCIPLES

II. Covid-19 Vaccines are Experimental and Require Informed Consent

3. of the option to accept or refuse administration of the product, of the consequences, if

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