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One Year Anniversary of President Trump Forcing the FDA to give Emergency Use Authorization to the Pfizer COVID-19 Shot

I am writing this on the eve of the 1 year anniversary, December 11, 2020, of former President Donald Trump pressuring the FDA to give emergency use authorization (EUA) to the Pfizer COVID-19 shots. Moderna's shot was also given an EUA a few days later. Happy Anniversary President Trump! We have created a video to commemorate this most historical day, perhaps the most significant day ever in the history of the United States.

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2,809 Dead Babies in VAERS Following COVID Shots as New Documents Prove Pfizer, the FDA, and the CDC Knew the Shots Were Not Safe for Pregnant Women

The latest data dump into the U.S. Government’s Vaccine Adverse Events Reporting System (VAERS) happened yesterday (12/3/21) and covers data through 11/26/2021. There are now 927,740 cases reported to VAERS following COVID-19 shots for the past 11 months, out of the total of 1,782,453 cases in the entire VAERS database filed for the past 30+ years. In addition, we found 2,809 fetal deaths following COVID-19 shots injected into pregnant and child-bearing women for the past 11 months. By way of contrast, using the exact same search parameters in VAERS, but excluding the COVID-19 shots, we found 2,168 fetal deaths following all FDA-approved vaccines for the past 30+ years. That’s an average of 72 fetal deaths per year following all FDA-approved vaccines for the past 30+ years, compared to what is on pace to be 3064 fetal deaths in 1 year following COVID-19 shots. That is an 80% increase in fetal deaths recorded in VAERS following the COVID-19 shots. And yet, the CDC and FDA continue to recommend these EUA shots for pregnant women and nursing mothers. Not only do they recommend these shots for pregnant women, we now have ample evidence that they have known since earlier this year that these shots are dangerous to pregnant women, and causing fetal deaths. This article will link to publicly available data that shows the CDC, FDA, and Pfizer have known from early on that these shots cause fetal deaths. With all the links to the publicly available data supplied in this article, there is more than enough information to immediately issue arrest warrants for Rochelle Walensky, the director of the CDC, Janet Woodcock, the FDA director, and Albert Bourla, the CEO of Pfizer, for mass murder and crimes against humanity.

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Vaccine Injury Attorney Suing the FDA: FDA Asks Federal Judge to Grant it Until the Year 2076 to Fully Release Pfizer’s COVID-19 Vaccine Data

Attorney Aaron Siri is a Vaccine Injury attorney, one of just a handful of such attorneys in the U.S. Since the passage of the 1986 National Vaccine Injury Compensation law, one cannot sue pharmaceutical companies for vaccine injuries and deaths. A special U.S. Vaccine Court handles all cases with select judges chosen by the U.S. Government, and there only about 100 lawyers in the United States that are even trained to litigate in this special "court." The irony with COVID-19 vaccine injuries and deaths, is that even this very highly specialized and controlled government court will not try vaccine injury cases related to the COVID-19 experimental shots, mainly because they are still under Emergency Use Authorization and not fully approved by the FDA yet. So Aaron Siri's firm is suing the FDA, since there is no avenue in place within the U.S. Judicial system to sue the drug companies, or anyone else for that matter, for damages caused by the experimental COVID-19 "vaccines." We have previously covered Aaron Siri's lawsuit, which represents brave doctors who have chosen to put their careers on the line to dare to expose vaccine deaths and injuries caused by the experimental shots, and these physicians are the plaintiffs. Today, Attorney Siri published an update on his case against the FDA, where he wrote: "The FDA has asked a federal judge to make the public wait until the year 2076 to disclose all of the data and information it relied upon to license Pfizer’s COVID-19 vaccine.  That is not a typo.  It wants 55 years to produce this information to the public. So, let’s get this straight. The federal government shields Pfizer from liability. Gives it billions of dollars. Makes Americans take its product. But won’t let you see the data supporting its product’s safety and efficacy.  Who does the government work for?"

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BOMBSHELL: FDA Allows Whistleblower Testimony that COVID-19 Vaccines Are Killing and Harming People!

The FDA held a Vaccine Advisory Committee meeting yesterday (September 17, 2021) to discuss authorizing a third Pfizer COVID-19 "booster shot." There were signs heading into the meeting this week that there could be some fireworks at this hearing, as two top vaccine research scientists at the FDA, Dr. Marion Gruber and Dr. Phillip Kause, the Director and Deputy Director of the Office of Vaccines Research, recently resigned. This followed a report published in The Lancet from 18 officials at the FDA opposing the Biden Administration's plan to start distributing Pfizer "booster shots" later this month (September, 2021) before the FDA had even approved them. To say that there were fireworks at the Vaccine Advisory Committee meeting yesterday might be a gross understatement. The 18 member committee voted 16 to 2 AGAINST approving the booster shots, although later they did give their endorsement on approving them for people 65 and older. During the "open session" part of the meeting, dissenting doctors questioning the Pfizer shots were given a chance to address the public with their concerns, and they presented to the public REAL data about the shots that up until now has been heavily censored.

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After 1,517,211 Injuries and 9,027 Recorded Vaccine Deaths in the U.S. FDA Gives Full Approval to Pfizer COVID-19 Vaccine

After 1,517,211 injuries and 9,027 deaths following the Pfizer COVID-19 vaccines recorded in the U.S. Government's Vaccine Adverse Event Reporting System (VAERS), the FDA today gave full approval to the Pfizer COVID-19 injections for people over the age of 16. Besides the U.S. VAERS, the British Yellow Card reporting system for injuries and deaths following COVID-19 vaccines reports 501 deaths and 293,779 injuries following Pfizer COVID-19 injections. EudraVigilance, the European Union database of suspected drug reaction reports for COVID-19 vaccines, reports 10,616 deaths and 833,498 injuries following Pfizer COVID-19 vaccines. Today is a historic day in the United States, because no pharmaceutical product linked to so many deaths and injuries during its trial period has ever before been approved by the FDA. Just from Europe and the U.S., official government reporting systems list a total of 20,144 deaths and 2,644,488 adverse reactions following Pfizer's injections. We know that these reported numbers, directly from official government health organizations, are severely under-reported, as doctors and other medical personnel are pressured to NOT link these deaths and injuries to the COVID-19 shots. We also know that the same thing is happening in many other countries around the world, as we reported last week that official media sources in Brazil admit that over 32,000 people have died following COVID-19 shots, and one of the approved shots in Brazil is the Pfizer/BioNTech shot. So do you still believe that a worldwide eugenics program in place to reduce the world's population is a "conspiracy theory"?

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FDA Wants to Ban Another Natural Supplement with Success in Treating Symptoms of COVID-19

N-acetyl-L-cysteine (NAC) has been on the market as a supplement for decades—why is the FDA attacking it now? It seems obvious that the FDA is clearing the market of affordable NAC supplements in an effort to eliminate competition for NAC drugs that could be coming to market in the next few years. For starters, a drug company is investigating NAC as a treatment for a rare genetic disorder that damages the myelin sheath, which insulates nerve cells in the brain. But that’s just the beginning. A search through the government’s clinical trials database shows considerable interest from the pharmaceutical industry in NAC. There are 17 trials looking at NAC, in both drug and supplement form, in the treatment of COVID.

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After 300 Million Injections and as Demand Wanes FDA Finally Issues Warning on mRNA COVID-19 Shots for Heart Failure

After injecting Americans with over 300 million doses of one of the mRNA COVID-19 bioweapon shots since December 13, 2020, the FDA has finally agreed to force Moderna and Pfizer to put warning labels on their shots over a "likely association" between the injections and heart problems, which they claim is "rare." The warning comes as the vast majority of Americans who wanted one of the mRNA injections have already been injected, as demand for the shots has decreased to levels seen back in December, just after the shots were given emergency use authorization and were beginning to be rolled out. According to the CDC's latest report published yesterday, June 23, 2021, "318 million doses of COVID-19 vaccines were administered in the United States from December 14, 2020, through June 21, 2021," with only 12 million of those doses being the "J&J/Janssen COVID-19 Vaccine." As we have been reporting throughout the rollout of these non-FDA approved injections, hundreds of cases of people suffering heart problems, including DEATH, have been reported to VAERS, the Government database that tracts adverse reactions to "vaccines."

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Criminal FDA Authorizes Emergency Use for Pfizer’s mRNA Injections on 12-15 Year-olds – Up to State Governors to Save the Nation’s Children

As expected, the FDA granted emergency use authorization to Pfizer's experimental COVID mRNA shots to be injected into children between the ages of 12 and 15 today. The FDA is a criminal organization comprised of medical professionals with ties to Big Pharma who are serving the pharmaceutical industry, and not the public. None of the COVID-19 injections given emergency use authorization were done so legally. Many scientists and doctors have protested, and even filed official complaints against the FDA, because there are already effective treatments for COVID-19, making an emergency use authorization unnecessary. In addition, the current injections for COVID-19 do not meet the legal definition of a "vaccine," but are an entirely new class of injections that inject an operating system into your body and works directly with your DNA. Many young people aged 16 to their early 20s have already died and been seriously injured following the Pfizer injections, and we have covered their stories here on Health Impact News. There is a eugenic agenda here to reduce the world's population, and for those young girls in the 12 to 15 year age range whose parents allow them to get this experimental injection, most if not all of them will probably become infertile and never be able to bear children, if they survive the shots. Governors can stop this at the State level, and refuse to adopt the FDA Guidelines.

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FDA Whistleblower Claims the FDA is Not Properly Inspecting Plants where Vaccines are Manufactured, Mainly Merck Who Will Begin Producing COVID Experimental Vaccines

After it was recently announced that Merck & Co. would take over producing some of the experimental COVID "vaccines" for Johnson and Johnson, an FDA whistleblower has now stepped forward to reveal that the FDA is not properly examining production facilities where these experimental COVID shots are being produced. This is just another routine incident that highlights the incestuous relationship between Big Pharma and government health regulatory agencies like the FDA and the CDC, which primarily work for the pharmaceutical industry to maximize their profits, and are not very concerned about public health at all. Most of the people appointed to these government agencies come out of the pharmaceutical industry, and then return there once they are finished working for agencies like the FDA and the CDC. Merck is now set to join the ranks of pharmaceutical companies producing experimental COVID injections that have a long history of criminal activity. We have previously reported how Pfizer is notorious for previously having the largest criminal settlement with the Department of Justice, and Johnson and Johnson also has a very long criminal rap sheet ranging from their baby powder causing cancer, to flawed hip replacements and multiple product recalls that have harmed millions. So now faced with manufacturing problems in producing enough of the experimental COVID injections, they are turning to another criminal organization to help them, Merck. Merck's vaccines historically have probably killed and maimed more people than any other vaccine manufacturer, and they are still embroiled in lawsuits to this day over some of their vaccines, mainly the measles, mumps, and rubella (MMR) vaccine, and their HPV vaccine, Gardasil. And now they are slated to use a plant to help produce the Johnson and Johnson experimental COVID shots, where employees are deliberately soiling their clothes with blood, urine and feces because they don't want to take the time to use the restrooms and go through the entire sterilization process again, and the FDA is overlooking this. And yet the vast majority of the public remains religiously pro-vaccine and are rushing out to get experimental injections produced by criminal pharmaceutical companies and regulated by criminal government regulatory agencies that are supposed to be overseeing them. The reduction of the world's population is in full swing now, and the pro-vaccine masses are the first ones to be culled.

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Unlike UK, U.S. FDA Allows Pregnant and Nursing Women to Receive Experimental Pfizer COVID Vaccine

The U.S. FDA has given emergency use authorization (EUA) to the experimental Pfizer COVID mRNA vaccine, a type of vaccine that has never before been authorized for use in humans. The FDA's EUA for the Pfizer COVID vaccine follows an emergency use authorization in the U.K. about 10 days ago. Both governments have issued guidelines for the new vaccines, one set of guidelines for doctors and healthcare providers who will administer the vaccine, and a shorter set of guidelines for "recipients" who plan on taking the vaccine. Even though these guidelines cover the same vaccine from the same company (Pfizer), there are notable differences. The UK guidelines, issued by the UK Department of Health and Social Care and the Medicines & Healthcare products Regulatory Agency, give strict warnings to doctors NOT to give the vaccine to women who are pregnant or nursing, or to women planning on becoming pregnant, with a warning about potential infertility issues. However, the U.S. FDA's guidelines contain no such warning.

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