Pfizer has about 1,000 more full-time employees than CDC doing "vaccine surveillance," British Medical Journal estimates. House COVID subcommittee expresses concern.

JustTheNews.com

Federal public health agencies are reportedly withholding the most accurate and up-to-date reports of vaccine injury from the public, allegedly to protect privacy. Patients don't necessarily see it that way, and it's not clear the feds told Congress.

The Vaccine Adverse Events Reporting System, jointly managed by the CDC and FDA, has a secret "back end" privy only to regulators, an FDA official told advocates of VAERS reform nearly a year ago, according to a British Medical Journal investigation published Friday.

"Anything derived from medical records by law" cannot be included in the "front end system" accessible to the public, Narayan Nair, director of the Division of Pharmacovigilance, allegedly told advocates.

by Jon Rappoport
Blog.nomorefakenews.com

I’ve described how the major clinical trials of the COVID vaccine are designed to prevent nothing more than a cough, or chills and fever [1] [2].

The whole plan to gain FDA approval of the vaccine is a stark fraud.

Now let’s move on to the next con: how to make it seem the vaccine is a roaring success.

Brief background: My readers know I’ve presented a complete case to show the SARS-CoV-2 virus was never proved to exist in the first place [3] [4] [5] [6] [7] [8] [9] [10]. So the whole idea of a vaccine is a non-sequitur, an absurdity. Likewise, the PCR test for “the virus” is a fraud on several levels [11]:

For example, the number of “cycles” for which the test is set is a key factor. Each cycle is a huge amplification of the tissue sample taken from the patient.

When you blow up that tissue sample above 34 cycles, you get gigantic numbers of false-positive results, even by the standards of the test. Fauci has admitted it. I’ve pointed out that FDA guidelines nevertheless recommend doing the test at up to 40 cycles. This alone explains reports of “rising COVID case numbers.”

Let’s say Pfizer and then Moderna win FDA approval to release their vaccines in the US. With the military doing the logistics of shipping, millions of doses move out, and soon, an extraordinary number of Americans are lining up to take the shot.

After a suitable period of time, the elite medical planners will change the way the PCR test is done. The number of cycles will be drastically reduced. That order will go out to labs in the US.

What does this mean? It means that far fewer positive test results will occur.

Therefore, the trend of “new COVID cases” will stop rising. It will level off, and then it will fall.

This rigging will be heralded as proof that that vaccine is producing a victory over the virus.

DailySkeptic.org

Sudden deaths were twice as high in the vaccine group of the original Pfizer clinical trial than in the placebo group, researchers have found, reigniting concerns about the safety of the novel mRNA drug.

The worrying finding comes from new analysis of the data from the original randomised controlled trial (RCT) of the vaccine which were released as part of legal action in Texas.

Researchers at the Health Advisory and Recovery Team (HART) found that there were four additional sudden deaths in the vaccine group than in the placebo group, all of which occurred after the first 60 days. Many assurances of vaccine safety assume that any harms will be seen within 28 days of vaccination, meaning signals after 60 days would be missed.

TheGatewayPundit.com

In a heart-wrenching incident, Melody Rain Palombi-Malmgren, a 15-month-old girl, tragically passed away two days after receiving routine vaccinations. Her mother, Katherine Palombi, recalls the shock and sorrow of losing a child who was the epitome of joy and health.

On October 17, during a routine 15-month well-visit at the Herbert Kania Pediatric Group in Warwick, New York, Melody received three vaccines, News12 Westchester reported.

Just two days later, she suddenly stopped breathing and suffered cardiac arrest despite exhibiting no warning signs.

TheGatewayPundit.com

Korean pharmaceutical company GC Biopharma has announced it has applied for approval of its GC1109 recombinant anthrax vaccine to the Korean Ministry of Food and Drug Safety.

According to GC Biophrama “GC1109 contains protective antigen (PA) as its active pharmaceutical ingredients produced by recombinant DNA technology which delivers 2 types of proteins that comprise anthrax toxin, namely, lethal factor (LF) and edema factor (EF), into cells.”

GC Biopharma in a press release revealed the reason they’re creating the vaccine is “in order to prepare against potential bioterrorism.”

If approved the ‘GC1109’ will be the world’s first recombinant anthrax vaccine.

In this short video, Naomi Wolf exposes the fact that Pfizer hid Covid jab trial death statistics because it would show that their deadly cocktail was not safe nor was it effective.  The accurate data showed the experimental jabs were worthless and dangerous.  Had they reported the information accurately they could have never obtained the emergency use authorization they needed to reap BILLIONS in profits.

Gavi, the Vaccine Alliance is investing more than $600 million to reach its goal of vaccinating 86 million girls in low- and middle-income countries by 2025. The alliance is funded in large part by the Bill & Melinda Gates Foundation.

ChildrensHealthDefense.org

An international campaign — funded in large part by the Bill & Melinda Gates Foundation — to inject tens of millions of young girls with the human papillomavirus (HPV) vaccine is drawing fire from critics who allege the vaccine will cause far more harm than good.

Claiming the initiative will avert “over 1.4 million future deaths,” Gavi, the Vaccine Alliance announced it is investing more than $600 million to reach its goal of vaccinating 86 million girls in low- and middle-income countries by 2025.

The Gates Foundation co-founded Gavi and is one of its four permanent board members. UNICEF, the World Bank and the World Health Organization (WHO) — whose second-largest donor is Gates — hold the other permanent seats.

The Clinton Health Access Initiative also sits on the board.

James Lyons-Weiler, Ph.D., a critic of the global HPV vaccine campaign, suggested mass vaccination will cause a devastating number of serious side effects among young girls, even though there are still no studies showing the HPV vaccine prevents cancer, despite claims to the contrary by vaccine makers and public health officials.

TheEpochTimes.com

A new preprint study up for peer review finds billions of residual DNA fragments in the COVID-19 mRNA vaccine vials.

"In our study, we measured DNA copies of spike, ori (origin of replication), and SV40 enhancer genes," he told The Epoch Times. "The loads of SV40 enhancer-promoter, ori, and virus spike in Pfizer are up to 186 billion copies per dose."

JustTheNews.com

The FDA repeatedly told the public that an antiviral with a sterling safety record, ivermectin, should not be used to treat COVID-19 because it was also prescribed, at higher dosages, to livestock.

The agency didn't appear to show the same concern about correctly dosing the new single-shot mRNA COVID vaccines and is now scrambling to educate healthcare providers not to give children adult-strength jabs even while denying that overdosing is a safety risk.

Its demonization of cheap, widely available antivirals to treat SARS-CoV-2 infections in higher-risk populations looks increasingly shortsighted, with two new peer-reviewed studies on hydroxychloroquine's effectiveness when combined with azithromycin, a common antibiotic.

Jeffery Jaxen joins the Highwire to expose the fact that the vaccine that was jabbed into the arms of BILLIONS around the world was not the formulation used in the so-called clinical trials.  What they actually injected into people was a horrific contaminated cocktail.