Criminal FDA Authorizes Pfizer and Moderna Bivalent Booster COVID Injections for Babies 6 Months Old to 4 Years

The criminal FDA today gave an emergency use authorization for the deadly new Bivalent COVID shots for babies as young as 6 months old. There were no advisory committee meetings to discuss this, just a review of the documentation provided by the companies who supply the shots, Pfizer and Moderna. We can trust them, right? Just a reminder, these Bivalent shots were just authorized last September, and it was the first time in history that the FDA authorized a "vaccine" without any completed testing done on humans. All three drug companies that have EUA COVID vaccines in the U.S., Pfizer, Moderna, J&J, have former FDA Commissioners working for them. Keeping the COVID Plandemic active by declaring it to be a continuing "National Emergency," the FDA is pushing to the limits just what they can do under the cover of "emergency use" which means the drug manufacturers can effectively use the American public as their laboratory, since going through the proper FDA approval channels to get a new vaccine to market on average takes about 10 years. Since these Bivalent booster shots were authorized 3 months ago, there have been 10,547 reported cases of harm to the U.S. Government's Vaccine Adverse Events Reporting System (VAERS), including 90 deaths. They were authorized to be injected into children between the ages of 5 and 11 in October, and there are now 1,151 reports of harm done to children in VAERS. And just a reminder, less than 1% of vaccine injuries are ever reported to VAERS. And as of today, the FDA has authorized them to be injected into babies as young as 6 months old. The politicians in Washington D.C. will not do anything about this, even though Senator Ron Johnson had another meeting this week in D.C. to testify about these facts. This is like the 4th or 5th time Senator Johnson has done this. And what has been the result? The FDA continues to authorize more shots. Parents continue to ignorantly harm their children with experimental gene therapy shots. Not a single Governor has the courage to stop these shots, and neither does anyone in Washington D.C.  Big Pharma owns them all. So you're on your own. Do your research. Share this with others.

425 Different Tests for COVID Still Have Emergency Use Authorizations from the FDA in Third Year of “Pandemic”

Almost 2 years ago, on May 5, 2020, we published an article reporting that not a single test being used to allegedly detect the COVID-19 virus was approved by the FDA, and that the ones that were granted emergency use authorizations (EUAs) were admitted to be unreliable by the FDA and the pharmaceutical manufacturers. I included testimony from a reader of Health Impact News who had 43 years of experience in Clinical Diagnostics and was appalled that our nation was being locked down over an alleged virus for which there was no accurate test. Fast forward now 2 years to today, and the only thing that has changed over these faulty tests is that now there are a lot more of them that have been given EUAs, and still none of them have been granted FDA approval. We have previously reported on how the CDC withdrew their EUA request on certain PCR tests at the end of 2021 because they claimed that some of these COVID tests could not distinguish between an influenza virus, or a COVID-19 virus. We have also previously reported how the CDC changed how they reported deaths at the end of 2020, because the statistics at the end of the year were not showing excess deaths in the year the COVID "pandemic" started, and they added about 400,000 deaths to make COVID appear to be a serious killer virus, which then hid the real increase in deaths that occurred in 2021 after the COVID-19 vaccines were rolled out. This is the biggest scam in the history of the world, as the flu disappeared in 2020 and still remains absent here in 2021, because there just are not enough sick people dying to inflate both flu and COVID numbers. And the real tragedy that this corruption has caused, besides the fact that the COVID-19 vaccines are destroying people's lives, is that this group of upper respiratory symptoms that used to be called "influenza" but is now called "COVID-19" is very easily treatable, by either using older drugs that are generally safe such as Ivermectin, or even natural products such as high-dose Vitamin C IV treatment. But to make sure these existing treatments do not interfere with the new vaccines and drugs that have been given EUAs by the FDA, the FDA has issued 215 warning letters for "Fraudulent Coronavirus Disease 2019 (COVID-19) Products" to protect the pharmaceutical industry and their EUA products "by pursuing warning letters, seizures, injunctions or criminal prosecutions against products and firms or individuals" that dare to defy the FDA by using unauthorized products to actually heal people.

How the Criminal FDA Protects Big Pharma by Controlling the Media

The British Medical Journal (BMJ) has released a video of whistleblower Brook Jackson, who was a regional director employed by Ventavia Research Group in Texas in 2020 to monitor the Pfizer COVID-19 vaccine trials. When she observed the data from the trials being handled improperly, she recommended they stop enrolling people in the trials. But her employer did not agree, so she reported them to the FDA. She thought that the FDA would take action to correct this fraud, but instead, her employer fired her shortly after she contacted the FDA. Brook Jackson learned the hard way that the FDA does not protect the public, but the pharmaceutical industry. Not only did the FDA not respond to her reporting, they did not even bother to investigate the site where the alleged infractions occurred. So she took her story to the British Medical Journal (BMJ), who ended up publishing it because she backed up everything she was reporting with solid facts and information. But when the article in the BMJ was shared on Facebook, the Facebook fact checkers marked it as fake news. This is a common tactic that the FDA has done historically, by controlling the media to cover up the crimes of Big Pharma.

FDA Committee Rubber Stamps Pfizer’s Plan to Inject 28 Million Children 5 to 11-Years-Old

I was going to have the headline to this article state that the FDA rubber stamped the Biden Administration's plans to vaccinate 28 million children with the Pfizer COVID shot, but let's stop pretending and state what is obvious to everyone: Pfizer is calling the shots in the White House regarding COVID-19 vaccine policy. Unsurprisingly, the FDA Advisory Committee today voted 17-0 to approve the experimental Pfizer COVID-19 injection for children ages 5 to 11. The panel was made up of industry insiders, including the infamous pediatrician, Paul Offit, who has stated that he believes an infant can easily be injected with 10,000 vaccines at one time. He is the pharma-controlled corporate media's go-to "doctor" spokesperson when it comes to childhood vaccines. Another doctor on the committee that was considering whether these shots were safe enough to give to young children stated: "We're never gonna learn about how safe the vaccine is until we start giving it, and that's just the way it goes." The FDA collected comments from the public regarding whether or not the Pfizer shots should be recommended to be given to children age 5 through 11, and according to Steve Kirsch, the Executive Director of the Covid-19 Early Treatment Fund, they counted over 139,470 comments posted AGAINST giving authorization to the shots, and could only find ONE comment in favor of the shots. Dr. Jessica Rose's excellent analysis of the VAERS data was also presented to the FDA Advisory Committee, which we have previously published here on Health Impact News. So the FDA Advisory Committee was not lacking for real scientific data, but in the end Pfizer's voice was the only one that mattered, because they have the ability to destroy the lives and careers of these FDA doctors who do not do what they are told. And now they are going to try to also destroy the lives of America's children.

All 3 FDA-Authorized COVID-19 Vaccine Companies Employ Former FDA Commissioners

Have an experimental drug that needs rapid authorization from the FDA in order to be sold to the masses? Looking to siphon billions of dollars from the U.S. taxpayer for your newfound pharmaceutical product? In today’s America, you can buy yourself a former FDA commissioner, and use the public-sector private-sector revolving door system of corruption to impose your will on the American public, and make a windfall for your executives and shareholders in the process. That appears to be the exact strategy utilized by Johnson & Johnson, Pfizer, and the company that founded Moderna, which have rostered a series of former top ranking government officials into top positions in their respective organizations.

Systemic Corruption at FDA Reported

We have long documented many cases of FDA-approved killer drugs and agency interference in a person’s right to natural medicine (and much of this information and more is collected in our new FDA Death Meter website). But when the FDA’s own scientists send a letter to Congress exposing outrageous cases of retaliation against those refusing to sign off on unsafe, unproven, ineffective products, it’s clear the corruption at the FDA is far-reaching and thoroughly entrenched. Pressure to approve dangerous drugs and devices is coming from top managers with ties to big business. Can you imagine working in an atmosphere where the honest employee fears the dishonest employee, and not the other way around? How can anyone trust the FDA’s claims that a particular food or drug or medical device is safe to eat or put in or on your body, when the former director of the agency, Margaret Hamburg, has been accused of racketeering?