Following a recent opinion written from the Department of Justice claiming that federal law permits mandating an emergency use vaccine, non-profit Informed Consent Action Network’s attorneys issued a response disputing the conclusion in this opinion.

On July 26, 2021, at the request of the White House, the DOJ’s Acting Assistant AG released an opinion claiming the Food, Drug and Cosmetic Act, Section 564 permits mandating an emergency use vaccine. Section 564 states that for all emergency use products, i.e. unlicensed medical products, individuals must be informed of “the option to accept or refuse administration of the product.” 

ICAN counsel’s response explains why the DOJ’s conclusion that an unlicensed medical product can be mandated runs contrary to the text of Section 564, its statutory framework, the history surrounding its passage, and its consistent interpretation by the FDA, CDC, DCO, and other federal agencies. 

It is also illogical for Congress to provide in Section 564 that individuals must be informed of “the option to accept or refuse administration of the product” but permit expelling an individual from school, employment, or the military if they refuse.

“The Department of Justice is supposed to blindly enforce the law, without political persuasion.  This DOJ opinion written for the White House falls far short of this fundamental responsibility to the American people,” says Del Bigtree, founder of ICAN, Emmy Award winner and host of the online weekly investigative news program “The HighWire With Del Bigtree.”

“The long-standing principal that no individual should be coerced or unduly influenced to accept an unlicensed medical product should not be abandoned based on the political needs of the day,” Bigtree says. “Whatever short term gain the President and the DOJ believe will be achieved by casting aside this fundamental protection pales in comparison to the harm likely to result in the future, if not from this product, but from others, by permitting mandating people to receive unlicensed medical products.”

ICAN’s response requests that the DOJ officials that drafted the opinion reconsider their interpretation and guidance regarding Section 564 and revise it, and that the DOJ fulfill its duty by enforcing this provision which prohibits mandates of an EUA product, rather than casting this important right aside.

“We live in an unprecedented time, making it all the more important to hold tight to the principles that we have learned from history,” Bigtree says.

READ THE PRESS RELEASE HERE:
https://www.einpresswire.com/article/548512480/informed-consent-action-network-s-attorneys-challenge-doj-mandatory-vaccine-opinion?r=pabnzgloZIZNKZYRuw

Jefferey Jaxen

Jefferey Jaxen is a health journalist and featured in his weekly segment, ’The Jaxen Report’, on The HighWire. As an investigative journalist, researcher, and compelling writer, Jefferey serves as Lead editor of The HighWire News and Opinion Team.

Other Headlines

Coronavirus

Yale Study Finds Post-Vaccine Syndrome Shares Symptoms with Long COVID

A preprint study from Yale University researchers examined a condition known as post-vaccination syndrome. The study included 42 individuals with PVS and 22 without. Researchers observed elevated levels of spike proteins in the PVS group for 36 to 709 days because the time that lapsed since the last vaccination varied between participants. It is aContinue reading Yale Study Finds Post-Vaccine Syndrome Shares Symptoms with Long COVID

More news about Coronavirus

Health & Nutrition

Jury Slams Bayer With Nearly $2.1B Verdict Over Glyphosate Cancer Claims

A Georgia jury has ruled against Bayer in which a plaintiff claimed his use of Roundup caused his non-Hodgkin’s Lymphoma. The nearly $2.1 billion verdict is the largest payout the biotechnology company has paid out, as 60,000 lawsuits are still pending. The verdict includes $65 million in compensatory damages and $2 billion in punitive damages.Continue reading Jury Slams Bayer With Nearly $2.1B Verdict Over Glyphosate Cancer Claims

More news about Health & Nutrition

Vaccines

RFK Jr. Halts COVID-19 Oral Vaccine Trial for 90 Days, Ends Flu Vaccine Ad Campaign

HHS Secretary Robert F. Kennedy Jr. paused a clinical trial funded by the Biomedical Advanced Research and Development Authority (BARDA) for a COVID-19 oral vaccine made by Vaxart. Kennedy said, “While it is crucial that the Department [of] Health and Human Services (HHS) support pandemic preparedness, four years of the Biden administration’s failed oversight haveContinue reading RFK Jr. Halts COVID-19 Oral Vaccine Trial for 90 Days, Ends Flu Vaccine Ad Campaign

More news about Vaccines

Science & Tech

23andMe Files for Chapter 11 Bankruptcy; Genetic Data of 15 Million Users at Risk of Sale

The genetic data of 15 million people will soon be for sale as 23andMe has filed for Chapter 11 bankruptcy. The attorneys general for California and New York issued consumer alerts to advise consumers to take action to protect their data. New York AG Rob Bonta said “There’s health insurance companies that are interested inContinue reading 23andMe Files for Chapter 11 Bankruptcy; Genetic Data of 15 Million Users at Risk of Sale

More news about Science & Tech

Environment

Bayer Seeks Capital Raise to Cover Roundup Lawsuit Settlements

Bayer continues to face struggles related to its acquisition of Monsanto and the flagship product Roundup, which currently has 67,000 pending cases alleging the herbicide has caused serious health conditions. So far, Bayer has paid out $10 billion to settle cases and has $5.9 billion set aside to resolve the pending cases. Sources told ReutersContinue reading Bayer Seeks Capital Raise to Cover Roundup Lawsuit Settlements

More news about Environment

Policy

Peter Marks Resigns From FDA As HHS Fires 10,000 Employees In Reorganization Effort

Dr. Peter Marks, an FDA official involved in Operation Warp Speed, has resigned from his position as director of the Center for Biologics Evaluation and Research (CBER). Marks started his career at the FDA as deputy director of the CBER in 2012 and has been the director since 2016. CBER is tasked with ensuring biologicalContinue reading Peter Marks Resigns From FDA As HHS Fires 10,000 Employees In Reorganization Effort

More news about Policy