COVID-19 Shots Debunked
From Pfizer Pfraud . . .
- Go here for additional information and to download a flyer with some of this information in PDF format.
PLEASE SHARE THE FOLLOWING VIDEO LINKS:
Defeat the Mandates — Live from Grand Park, April 10, 2022
- The Doctors of Front Line Covid Critical Care Alliance, the Unity Project & the Global Covid Summit
- View about 30 minutes from 1:57:30 to 2:48:30
Do infants and young children need or benefit from Covid-19 shots? You decide.
Over 75% of all children have already been exposed to SARS-CoVi-2 and have developed natural immunity.
- Efficacy = the power to produce an effect
- Placebo = an inert or innocuous substance used especially in controlled experiments testing the efficacy of another substance
- Shot = a medical or narcotics injection
- Vaccine = an antigenic preparation of a typically inactivated or attenuated pathogenic agent (such as a bacterium or virus)
- Gene Therapy = the insertion of usually genetically altered genes into cells especially to replace defective genes in the treatment of genetic disorders
- Bamboozle = to deceive by underhanded methods; to confuse, frustrate, or throw off thoroughly or completely
- Fraud = intentional perversion of truth in order to induce another to part with something of value or to surrender a legal right; an act of deceiving or misrepresenting
- Pfraud = fraud conducted by Big Pharma Co. Pfizer, Inc..
- Big Pharma Financial Liability for making and distributing any of the above = $0
- Big Pharma Profit Opportunity is unprecedented, so it seems to be full-steam ahead, no matter what the data show . . . FOR MORE $$$ !!!
- Pfizer gross profit for the quarter ending March 31, 2022 was $15.677B, a 51.34% increase year-over-year.
- Pfizer gross profit for the twelve months ending March 31, 2022 was $55.785B, a 57.66% increase year-over-year.
- Pfizer annual gross profit for 2021 was $50.467B, a 52.16% increase from 2020
The evidence from Jan 2019 to the present, overwhelmingly shows that the FDA, CDC, Big Pharma, Hospitals and far too many medical doctors have combined forces to bamboozle the US population about known effective treatments against SARS-CoVi-2 (the virus) and COVID-19 (the illness) — being propopents of some and opponents of others in order to maximize their profit opportunities — while ignoring their Hippocratic oath (an oath embodying a code of medical ethics usually taken by those about to begin medical practice; to first, do no harm).
The Nuremberg Code is a set of ethical research principles for human experimentation created by the court in U.S. v Brandt, one of the Subsequent Nuremberg trials that were held after the Second World War. The Nuremberg principles are a set of guidelines for determining what constitutes a war crime, including Principle VI: Crimes against humanity:
Murder, extermination, enslavement, deportation and other inhumane acts done against any civilian population, or persecutions on political, racial, or religious grounds, when such acts are done or such persecutions are carried on in execution of or in connection with any crime against peace or any war crime. Leaders, organizers, instigators and accomplices participating in the formulation or execution of a common plan or conspiracy to commit any of the foregoing crimes are responsible for all acts performed by any persons in execution of such plan.
Ten points of the Nuremberg Code
The ten points of the Nuremberg code were given in the section of the judges’ verdict entitled “Permissible Medical Experiments“:
- The voluntary consent of the human subject is absolutely essential. This means that the person involved should have legal capacity to give consent; should be so situated as to be able to exercise free power of choice, without the intervention of any element of force, fraud, deceit, duress, overreaching, or other ulterior form of constraint or coercion; and should have sufficient knowledge and comprehension of the elements of the subject matter involved as to enable him to make an understanding and enlightened decision. This latter element requires that before the acceptance of an affirmative decision by the experimental subject there should be made known to him the nature, duration, and purpose of the experiment; the method and means by which it is to be conducted; all inconveniences and hazards reasonably to be expected; and the effects upon his health or person which may possibly come from his participation in the experiment. The duty and responsibility for ascertaining the quality of the consent rests upon each individual who initiates, directs, or engages in the experiment. It is a personal duty and responsibility which may not be delegated to another with impunity.
- 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.
- 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.
- The experiment should be so conducted as to avoid all unnecessary physical and mental suffering and injury.
- 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.
- 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.
- Proper preparations should be made and adequate facilities provided to protect the experimental subject against even remote possibilities of injury, disability, or death.
- 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.
- 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.
- 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.
To ensure ethical treatment of human research subjects, the United States Department of Health and Human Services codified the Common Rule in Part 46 of Title 45 of the Code of Federal Regulations. These regulations are enforced by Institutional Review Boards (IRBs). In 1966, the International Covenant on Civil and Political Rights was adopted by the United Nations, and after enough nations had ratified the Covenant, it came into force on March 23, 1976. Article Seven prohibits experiments conducted without the “free consent to medical or scientific experimentation” of the subject. As of September 2019, the Covenant had 173 states parties.
In 2021, the CDD changed its definitions . . . why?
Note the text
removed added, below.
- vaccination = “the act of introducing a vaccine into the body to produce
immunityprotection to a specific disease.”
- vaccine = “
a product that stimulates a person’s immune system to produce immunity to a specific disease” to “a preparation that is used to stimulate the body’s immune response against diseases.”
Facts about Pfizer and Moderna shots
- Pfizer and Moderna COVID-19 shots are NOT FDA APPROVED for children in these age groups. These injections contain man-made genetic materials that have received Emergency Use Authorization only.
- There is NO information on the co-administration of the COVID-19 shots with other childhood injections.
- It is likely that additional boosters will be recommended/required, whether or not they are necessary.
- The shots that are authorized for use in children 6 months through 4 years of age includes the same mRNA and lipids, but different inactive ingredients compared to the shots that have been studied in clinical trials.
- The FDA authorized these shots for emergency use in children ages 6 months to 4-5 years on the basis of a theory known as “immuno-bridging.” Ask anyone pressuring you to give your child these shots to explain immuno-bridging to you.
- In 2021, the CDC changed the definition the term “vaccine” — from a shot that stimulates a person’s immune system to produce immunity to a shot that merely offers some form of protection.
- The shots are experimental gene therapies that have received only Emergency Use Authorization.
- The shots have NOT been shown to prevent COVID-19 disease.
- The shots have NOT been shown to prevent or reduce rates of hospitalization.
- They shots have NOT been shown to prevent death due to COVID-19.
Consequences of your decisions
- Pfizer and Moderna and whoever actually injects children with these shots are legally protected from liability for any harm that your child may suffer due to the ingredients in these shots.
- As a parent, YOU are morally responsible for any and all harm that your child may suffer due to your decision.
- As a parent, YOU are financially responsible for any hospitalization and long term care for your child, should they suffer an adverse reactions to the shots.
- DO NOT ALLOW ANYONE TO COERCE OR BULLY YOU. THERE IS NO MANDATE. ASK QUESTIONS. DEMAND ANSWERS. BE FULLY INFORMED. MAKE YOUR OWN DECISION.
Consider this data published by Big Pharma
Pfizer COVID-19 Shots for 6-23 months (3 mcg)
- Purported Vaccine Efficacy after three doses: +14%
- Purported Vaccine Efficacy after one dose: -29.7%
- One of the vaccine recipients suffered a febrile seizure and needed to be hospitalized.
- 98 of 1027 participants who received the Pfizer shots were diagnosed with COVID-19.
- Over 2/3 of the vaccine group dropped out and only 277 children completed the clinical trial.
Pfizer COVID-19 Shots for 2-4 years (3 mcg)
- Purported Vaccine Efficacy after three doses: +32%
- Purported Vaccine Efficacy after one dose: -32.5%
- 127 of 1673 participants who received the Pfizer shots were diagnosed with COVID-19.
- Over 2/3 of the vaccine group dropped out and only 481 children completed the clinical trial.
- ZERO of placebo recipients were hospitalized or died.
Moderna COVID-19 Shots for 6-23 months (25 mcg)
- Purported Vaccine Efficacy Efficacy: 31.5 to 50.6%
- The Moderna shots deliver 8x more MRNA than Pfizer and show a higher rate of adverse effects.
- Shot recipients were 500% more likely to suffer Severe Adverse Events than the placebo group.
- 38.5% (678/1761) of the children who received Moderna shots suffered an adverse event that required medical attention.
- % of children who experienced crying (68%), pain (46%), loss of appetite (32%), sleepiness (37%), fever (14%)
Moderna COVID-19 Shots for 2-5 years (25 mcg)
- Purported Vaccine Efficacy: 36.8 to 46.4%
- The Moderna shots deliver 8x more MRNA than Pfizer and show a higher rate of adverse effects.
- Shot recipients were were 342% more likely to suffer Severe Adverse Events than the placebo group.
- 33% (1002/3031) of the children who received the Moderna shots suffered an adverse event that required medical attention.
- % of children who experienced pain (71%), crying (55%), fatigue (48%), loss of appetite (31%), fever (17%)