CHD: 5 Questions Fauci and FDA Need to Answer on Pfizer and Moderna COVID Vaccines

Another day, another story about a healthcare worker suffering a “severe allergic reaction” after receiving Pfizer’s COVID vaccine — this time, in New York. The report follows the news Children’s Health Defense (CHD) has been covering about similar severe reactions, first in the UK, then in Alaska and Illinois.

In light of these events, and because CHD previously warned the U.S. Food and Drug Administration (FDA) officials and Dr. Anthony Fauci, director of the National Institute for Allergy and Infectious Diseases (NIAID), about the potential for the Pfizer and Moderna vaccines to cause anaphylactic reactions, we have some questions we’d like Fauci and the FDA to answer.

They are:

1. Why didn’t the FDA’s Center for Biological Evaluation and Research require Moderna and Pfizer-BioNTech to conduct immunogenicity testing on their COVID-19 vaccines for anti-drug antibodies as recommended in the agencies’ own guidelines for drug development during clinical trials?

In January 2019, the U.S. Department of Health and Human Services, FDA, Center for Drug Evaluation and Research, and Center for Biologics Evaluation and Research issued a document, “Immunogenicity Testing of Therapeutic Protein Products — Developing and Validating Assays for Anti-Drug Antibody (ADA) Detection: Guidance for Industry.”

The document, described as providing “recommendations to facilitate industry’s development and validation of essays for the assessment of the immunogenicity of therapeutic protein products during clinical trials,” clearly acknowledges the existence of anti-drug antibodies, such as polyethylene glycol (PEG), in humans. …

2. Why does the FDA seem surprised by the recent reports of life-threatening anaphylactic reactions after the agency approved emergency use of two mRNA COVID-19 vaccines that contain polyethylene glycol?…

3. Why did FDA officials not acknowledge the valid and scientifically supported concerns regarding the use of PEG in COVID-19 vaccines when CHD first notified them in September? …

4. Why did the FDA abandon its regulatory authority to the pharmaceutical companies developing COVID-19 vaccines?…

5. Will FDA and NIAID now require mRNA vaccine manufacturers to conduct assessments of the immunogenicity of the pegylated lipid nanoparticles used in their COVID-19 vaccines, and will they also consider pre-screening of all mRNA vaccine recipients for the presence and titers of anti-PEG antibodies? …

https://childrenshealthdefense.org/defender/fauci-fda-pfizer-moderna-covid-vaccines/?itm_term=home

I know the answer to the last question and you do too.   Are you outraged yet?  They’re playing with people’s lives, including children.   They know damn well this thing can be treated with conventional methods, probably more effectively and certainly more safely than any vaccine.   But treatment isn’t the point is it, and PEG is only a distraction from the deeper question of what exactly this concoction will do to people over time, which is the whole purpose for which they invented and released the virus in the first place.

Fearmongering by Gates Raises Question of Staged Bioattack in USA

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