Brownstone.org

When everyone from the President to your primary care doctor declared loudly and wholeheartedly in December 2020 that the newly FDA-authorized Covid mRNA vaccines were “safe and effective” – what were those claims based on?

In this article, I will review the contractual and regulatory framework applied by the US government to the initial development, manufacture, and acquisition of the Covid mRNA shots. I will use the BioNTech/Pfizer agreements to illustrate the process.

The analysis will show that:

• The Covid mRNA vaccines were acquired and authorized through mechanisms designed to rush medical countermeasures to the military during emergencies involving weapons of mass destruction.

• These mechanisms did not require the application of, or adherence to, any laws or regulations related to vaccine development or manufacturing.

• The FDA’s Emergency Use Authorization for the vaccines was based on clinical trials and manufacturing processes conducted with no binding legal standards, no legally proscribed safety oversight or regulation, and no legal redress from the manufacturer for potential harms. (This last point is being challenged in multiple court cases, so far to no avail.)

TheLibertyDaily.com

It no longer amazes most cognizant Americans to hear that Big Pharma and our own government conspired to promote dangerous “vaccines” to the people. They had their own agendas and saving lives wasn’t among them.

The final batch of Pfizer documents pertaining to Americans 16 and older have been released and they’re as damning as many of us expected. Here’s a breakdown by Twitter user Chief Nerd:

NEW — @ICANdecide Has Received the Final Batch of Pfizer Documents for Ages 16+ and Made Them Available to the Public

See the 🧵 below for observations of particular interest from the 51,893 pages. pic.twitter.com/KyEf7LBKvy

— Chief Nerd (@TheChiefNerd) December 4, 2023

Big Pharma developing a more potent form of experimental gene therapy technology
that will be sold to the public as life-saving 'vaccines.'

TheEpochTimes.com

Infowars.com

When I was looking at the data, which is part of my job, I noticed some discrepancies with the dates of death, people getting people dying within a week of being vaccinated,' says whistleblower.

A database administrator who helped the New Zealand government catalog vaccine recipients has come forward revealing the spike in deaths associated with the Covid-19 jab campaign, which resulted in hundreds dead.

According to the statistician whistleblower, who called himself “Winston Smith,” he worked on a program logging vaccine compensation for providers and was able to pinpoint how deaths began occurring shortly after the vaccine rollout.

TheGatewayPundit.com

Texas Attorney General Ken Paxton has initiated legal action against pharmaceutical giant Pfizer, Inc., citing allegations of deceptive practices related to the company’s COVID-19 vaccine.

The lawsuit asserts that Pfizer engaged in misrepresenting the vaccine’s efficacy, particularly challenging the claim of 95% effectiveness, and accuses the company of trying to stifle public debate on the matter.

Attorney General Paxton accuses Pfizer of violating the Texas Deceptive Trade Practices Act through “false, deceptive, and misleading acts and practices.”

The lawsuit highlights the company’s claims that the vaccine has a 95% efficacy rate against COVID-19 infection, stating that this was based on “relative risk reduction” in Pfizer’s initial short-term clinical trial results

RairFoundation.com

By Maryanne Demasi, PhD
blog.maryannedemasi.com

The recent findings of DNA fragments in the Pfizer and Moderna Covid-19 vaccines has led many to question why the FDA, which is responsible for monitoring the quality and safety of the vaccines, has failed to sound the alarm.

For years, the FDA has known about the risk posed by residual DNA in vaccines. Its own guidance to industry states:

“Residual DNA might be a risk to your final product because of oncogenic and/or infectivity potential. There are several potential mechanisms by which residual DNA could be oncogenic, including the integration and expression of encoded oncogenes or insertional mutagenesis following DNA integration.”

Put simply, the FDA acknowledges the possibility that fragments of DNA left over by the manufacturing process can be incorporated into a patient’s own DNA, to potentially cause cancer.

FreedomFirstNetwork.com

Up until the point when the European Medicines Agency (EMA) granted emergency use authorization (EUA) for the use of Wuhan coronavirus (COVID-19) “vaccines” in children, excess deaths among children throughout Europe were negative, new data shows. Then, once the EUA was granted for the jabs to go into children, excess deaths among children started to soar.

Put a different way, children across Europe were generally safe and healthy all throughout the “pandemic” – except for being forcibly kept away from their friends, in some cases where individual countries enforced stay-at-home and social distancing orders – and only started dying once the government began pushing kids to get jabbed for COVID along with the adults.

NaturalNews.com

So far, the public's response to the latest and greatest Wuhan coronavirus (COVID-19) "vaccines" from Pfizer and Moderna that just received approval and emergency use authorization (EUA) by the Food and Drug Administration (FDA) is overwhelmingly negative, and for good reason: the shots are untested and unsafe.

Almost unbelievably, Newsweek, which just a few years ago was calling for the unvaccinated to be jailed, is calling out the FDA for approving these new so-called "vaccines" without any clinical trials on humans.

According to that report, the new "booster" shots (or whatever you want to call them) were only tested on mice, and on a mere eight of them. If that is not piss-poor "science," then we surely do not know what is.

"These updated boosters will be the first released to the public without any humans involved in the clinical trials, raising questions from some about the efficacy," Newsweek's Nick Mordowanec writes.

Infowars.com

Josh Sigurdson reports on the recent news of Moderna essentially admitting to the Covid “vaccine” causing cancer as Dr. Robert Malone reports the Moderna patent in front of Congress proving a massive coverup operation.

Moderna has recently halted trials of their latest mRNA injection due to myocarditis. Fauci has also recently acknowledged that the injections cause myocarditis in young men “especially.”