CDC reports 4434 deaths “among people who received a COVID-19 vaccine”, Insufficient Informed Consent, Why FDA should not authorize vaccines for children
“Why are we vaccinating healthy adults when 81 percent of Covid-19 cases are mild and there is a 99 percent survival rate. Why are we testing vaccines on children who are minimally impacted by the disease?”…Citizen Wells
“it is my sincere hope that this public letter might stimulate FDA, Pfizer and Moderna leaders to think critically and quickly about the immunological danger the COVID-19 vaccine might pose to those persons naturally infected by SARS-CoV-2 — most especially to those infected who are recently convalescent, asymptomatic carriers, the elderly and frail or those with significant cardiovascular risk factors.”...Dr. Hooman Noorchashm
“VAERS received 4,434 reports of death (0.0017%) among people who received a COVID-19 vaccine.”...CDC May 11, 2021
From the CDC May 11, 2021.
“Over 259 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through May 10, 2021. During this time, VAERS received 4,434 reports of death (0.0017%) among people who received a COVID-19 vaccine.”
Patients are not being properly informed to make a decision weighing the costs and benefits of receiving the vaccine.
Informed Consent legal definition:
“Consent of a patient or other recipient of services based on the principles
of autonomy and privacy; this has become the requirement at the center of
morally valid decision making in health care and research. Seven criteria
define informed consent: (1) competence to understand and to decide,
(2) voluntary decision making, (3) disclosure of material information,
(4) recommendation of a plan, (5) comprehension of terms (3) and (4),
(6) decision in favor of a plan, and (7) authorization of the plan.
A person gives informed consent only if all of these criteria are met.
If all of the criteria are met except that the person rejects the plan,
that person makes an informed refusal.”
From the CDC.
“For each COVID-19 vaccine authorized under an Emergency Use
Authorization (EUA),the Food and Drug Administration (FDA)
requires that vaccine recipients or their caregivers are
provided with certain vaccine-specific EUA information to
help make an informed decision about vaccination. This is
accomplished by providing an EUA Fact Sheet for Recipients
Patients are not being informed, warned of the deaths that have occurred and serious injuries after vaccinations.
Therefore, minimally, all vaccinations should be halted until this is fixed and more information is available.
From The Defender May 11, 2021.
“Why FDA Should Not Authorize COVID Vaccines for Kids, Teens
The authors (two physicians and a professor) argue that Emergency Use Authorization for mass child vaccination presents a different balance of risks and benefits than it did for adults.”
“Pfizer has requested the FDA amend the existing EUA for its vaccine to allow eligibility for children aged 12 to 15, and further clinical trials of COVID-19 vaccines, including for younger children, are underway. Unlike for adults, however, the likelihood of severe outcomes or death associated with COVID-19 infection is very low for children, undermining the appropriateness of an EUA for child COVID-19 vaccines.”