Informed Consent

The FDA says “Informed consent is more than just a signature on a form, it is a process of information exchange that may include, in addition to reading and signing the informed consent document, subject recruitment materials, verbal instructions, question/answer sessions and measures of subject understanding.”

However, what we’re finding with experimental COVID-19 vaccines is that our public health agencies appear to be unconcerned with such trivialities as “informed consent”. In fact, many people around the world have been deprived of the knowledge that they are participating in a medical experiment, as that inconvenient fact is often omitted altogether.

Fact-checkers have even attempted to assert that Nuremberg conventions are not applicable to COVID-19 vaccines, because “they are not ‘experimental,'” despite the fact that long-term trial data does not exist.

COVID-19 vaccines “are not experimental,” but “real world data on the safety of COVID-19 shots for children is just weeks away.”

Not only are mRNA vaccines ‘experimental,’ there is no data supporting the use of continued mRNA boosters – Pfizer reportedly had a sample size of less than 30 people prior to getting the boosters ‘approved’. The data on the use of mRNA vaccines and perpetual boosters on children is almost non-existent, and there have been no long term studies evaluating how children injected with these mRNA cocktails now will fare in six months, still yet six years. They appear to be using us—and our children—as guinea pigs.

We hold it to be self-evident that this is wrong. We cannot allow it to continue.

Stunningly, flying in the face of the principle of informed consent, some of these vaccines were rolled out to people with blank drug information inserts. The AP, diligently performing their role as spokespeople for Big Pharma, explains away the blank inserts:

AP’S ASSESSMENT: Missing context. The paper insert states that it was intentionally left blank and that FDA-authorized fact sheets are available electronically, according to a J&J representative. This is intended to ensure vaccinators and consumers refer to the most up-to-date information about the vaccine during the FDA’s emergency use authorization, the representative said.

Read that again – the drug information inserts were intentionally left blank. Just Google it if you want the most up-to-date information, we’re told. When has this ever been acceptable in the history of FDA ‘approved’ medications? Never before in human history have the pharmaceutical companies been given a blank check to inject “all the people of the world” with a concoction rushed out at “warp speed” and mandated in the blink of an eye. And the FDA would like us to wait decades for FOIA data relating to the EUA process. What are they trying to hide?

The FormerFedsGroup is trying to find out. While we do that, we are providing resources that can help you ensure that your family, your neighborhood, your doctors and your community are aware of the nature of this experiment – the greatest scientific experiment ever carried out in human history. Once everyone is aware of how far wrong things have gone and we have their attention, we aim to unite the people under a common banner, and put an end to The Great Experiment. After that, we must hold those who have perpetuated this evil to account.

FDA produces first 91+ pages of Pfizer’s Covid-19 vaccine documents. It reveals that Pfizer, after just 2 ½ months of vaccine use, received 25,957 reports of “Nervous system disorders.” Only 54 years, 11 months to go for the remaining pages… https://t.co/I4c7F45Nqy

— Aaron Siri (@AaronSiriSG) November 20, 2021

Malicious and powerful forces can append their lies to the truth, but where the people are informed, they will see through it, and set things right.

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www.ncbi.nlm.nih.gov

Informed consent: Issues and challenges - PMC

Informed consent is an ethical and legal requirement for research involving human particip...

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