Pfizer and Moderna Trial Data Shows a Higher Risk of Serious Adverse Events Among Vaccinated Participants, a New Study Finds

peer-reviewed study published two days ago found that both the Moderna and the Pfizer vaccine trial data appeared to have a negative benefit/harm ratio.  One of the authors of the paper is Peter Doshi, an associate editor of the British Medical Journal.

Using a prespecified list of adverse events of special interest (“AESI”) identified by the Brighton Collaboration, the study found a higher risk of serious AESI in the mRNA COVID-19 vaccine group relative to placebo in both the Pfizer and Moderna adult phase III trials.

“These results raise concerns that mRNA vaccines are associated with more harm than initially estimated at the time of emergency authorisation,” the study authors wrote.

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War Zone: New Pfizer Data Reveal Horrifying Rates of Miscarriage

Since the rollout of the experimental COVID shots, U.S. health officials have adamantly claimed the shots are safe for pregnant women, and have been urging all pregnant women to get the jab “to protect themselves and their babies.” To this day, the U.S. Centers for Disease Control and Prevention recommends the COVID shot for:1

“… people who are pregnant, breastfeeding, trying to get pregnant now, or might become pregnant in the future.”

The CDC further recommends:2

“People who are pregnant should stay up to date with their COVID-19 vaccines, including getting a COVID-19 booster when it’s time to get one.”

And claims:3

“Evidence continues to build showing that:

  • COVID-19 vaccination during pregnancy is safe and effective.
  • There is currently no evidence that any vaccines, including COVID-19 vaccines, cause fertility problems in women or men.”

All the while, they’ve had Pfizer data showing the shots cause shocking rates of miscarriage which, adding insult to injury, have been blatantly miscategorized as a “recovered/resolved” adverse effect.4 Who in their right mind would consider DEATH a resolved side effect unless they had a depopulation agenda in mind all along?

I don’t see how this could be described as anything but a criminal cover-up. The only reason we know any of this is because U.S. District Judge Mark Pittman ordered the U.S. Food and Drug Administration to release Pfizer documents at a rate of 55,000 pages per month. The FDA and Pfizer had asked to release the documents at a pace of 500 pages per month, which meant it would take 75 years to disclose them all.5

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FDA to Authorize New COVID Booster for Omicron – But No Human Trials, Only Mice

The ‘Emergency Use Authorization’ canard seems to be the key tool which Big Pharma and Big Government use to run their confidence trick on a largely unsuspecting public. More fast-tracked ‘testing’ means more mass experimentation on the general population.

When it comes to the vaccine business, the hundreds of millions spent by industry lobbyists continues to pay massive dividends. Despite the fact that there is no discernible COVID-19 ‘pandemic’ anywhere, operatives embedded in corrupt institutions like the FDA are continuing to push the false premise that the world in stuck in a perpetual state of emergency, thereby justifying any and every half-baked measure and legal loophole – all designed to push products which are either being subsidized or directly purchased by government. That’s why business is still booming.

So let the ‘game of variants’ begin again.

It’s the same oil script being trotted out by the usual suspects…

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Nate Silver: ‘Liberal elites’ pressured Pfizer to delay vaccine until after 2020 election

Nate Silver claimed “liberal public health elites” pressured Pfizer to delay fast-track approval of its COVID-19 vaccine until after the 2020 presidential election — thus denying then-President Donald Trump a political win before voters headed to the polls.

The number-crunching data journalist reacted to an article by Politico that cited a House report that claimed the Trump administration sought to expedite approvals for both vaccines and “unproven treatments” for COVID-19.

“‘Trump pushed for vaccine approvals too fast’ is the worst possible critique of the Trump administration’s COVID policy,” Silver, founder of the Disney-owned FiveThirtyEight political news and analysis website, tweeted.

“That probably saved a lot of lives. If anything approval should have been faster.”

In a subsequent tweet, Silver wrote that “liberal public health elites” pushed Pfizer to “change its original protocols” that govern its authorization of vaccines so that the decision would be put off until after Election Day two years ago.

Silver noted that Pfizer’s decision “had the convenient side-effect of delaying any vaccine announcement until after the election” and that the story “deserves more scrutiny.”

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DC Mayor Says No Virtual Learning, Giving Unvaccinated Black Teens Zero Alternative Options 

The District of Columbia does not appear to have a contingency plan for unvaccinated students, who are banned from attending schools in person this fall after the first twenty days, according to comments made by Washington, D.C. Mayor Muriel Bowser Thursday. 

During a press conference, Bowser, a Democrat, admitted there are no alternative options, including virtual learning, for students who cannot attend school due to the District’s vaccine mandate, meaning unvaccinated children will effectively be left without an education.  

Over 40% of blacks ages 12-17 are not vaccinated, according to city data. 

The Daily Signal asked Bowser what the plan was for unvaccinated students. Washington, D.C. public schools start Monday.  

Bowser responded “They can go to school on Monday. But they need to get their vaccinations… and their families will be alerted as to the dates.” 

Students get 20 days to provide their vaccination certificate. The Office of the State Superintendent of Education for D.C. announced that “all students must have up-to-date immunization certification on file with the school within the first 20 school days or they will not be allowed to attend school or school activities until the immunization certification is secured by the school.” 

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Company Linked to CIA Now Making mRNA for Moderna’s Reformulated COVID Booster Shots

Last September, it was quietly announced that a company called National Resilience (often referred to simply as Resilience) would begin manufacturing the mRNA for Moderna COVID-19 vaccine products.

Under the terms of the multi-year agreement, “Resilience will produce mRNA for the Moderna COVID-19 vaccine at its facility in Mississauga, Ontario, for distribution worldwide.”

National Resilience was founded relatively recently, in November 2020, and describes itself as “a manufacturing and technology company dedicated to broadening access to complex medicines and protecting biopharmaceutical supply chains against disruption.”

It has since been building “a sustainable network of high-tech, end-to-end manufacturing solutions with the aim to ensure the medicines of today and tomorrow can be made quickly, safely and at scale.”

It further plans to “reinvent biomanufacturing” and “democratize access to medicines,” namely gene therapies, experimental vaccines and other “medicines of tomorrow.”

In pursuit of those goals, the company announced it would “actively invest in developing powerful new technologies to manufacture complex medicines that are defining the future of therapeutics, including cell and gene therapies, viral vectors, vaccines and proteins.”

It was founded with the reported intention “to build a better system for manufacturing complex medicines to fight deadly diseases” as a way to improve post-COVID-19 “pandemic preparedness.”

The company initially marketed its manufacturing capabilities as “the Resilience platform,” and offers principally “RNA Modalities,” including RNA development for vaccines, gene editing and therapeutics; and “Virus Production,” including viral vectors, oncolytic viruses (i.e. a virus engineered to preferentially attack cancer cells), viruses for use in vaccine development and gene-edited viruses for unspecified purposes.

It is worth noting that, to date, many controversial “gain-of-function” experiments have justified modifying viruses for the same purposes as described by National Resilience’s Virus Production capabilities.

In addition, National Resilience offers product formulations and other modalities, such as biologics and cell therapies, to its clientele and the “Virus Production” of its website has since been removed.

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The CDC (Finally) Admitted the Science on Natural Immunity. Why Did It Take so Long?

In August 2021 Science Magazine, a peer-reviewed academic journal of the American Association for the Advancement of Science, highlighted groundbreaking research out of Israel that upended the public health establishment.

The research, which relied on a database enrolling some 2.5 million Israelis and was led by Tal Patalon, head of the KSM Research and Innovation Center at Maccabi Healthcare Services, and deputy Sivan Gazit, found that previous infection from Covid-19 conferred considerably stronger and longer-lasting protection against the Delta variant than vaccines.

“The newly released data show people who once had a SARS-CoV-2 infection were much less likely than never-infected, vaccinated people to get Delta, develop symptoms from it, or become hospitalized with serious COVID-19,” Science staff writer Meredith Wadman noted.

Wadman also noted that the research showed that “never-infected people who were vaccinated in January and February were, in June, July, and the first half of August, six to 13 times more likely to get infected than unvaccinated people” who had previously had Covid.

“It’s a textbook example of how natural immunity is really better than vaccination,” Charlotte Thålin, a physician and immunology researcher at Danderyd Hospital and the Karolinska Institute, told Science.

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Unusual Toxic Components Found in COVID Vaccines, ‘Without Exception’: German Scientists

A group of independent German scientists found toxic components—mostly metallic—in all the COVID vaccine samples they analyzed, “without exception” using modern medical and physical measuring techniques.

The Working Group for COVID Vaccine Analysis says that some of the toxic elements found inside the AstraZeneca, Pfizer, and Moderna vaccine vials were not listed in the ingredient lists from the manufacturers.

The following metallic elements were found in the vaccines:

  • Alkali metals: caesium (Cs), potassium (K)
  • Alkaline earth metals: calcium (Ca), barium (Ba)
  • transition metals: cobalt (Co), iron (Fe), chromium (Cr), titanium (Ti)
  • Rare earth metals: cerium (Ce), gadolinium (Gd)
  • Mining group/metal: aluminum (Al)
  • Carbon group: silicon (Si) (partly support material/slide)
  • Oxygen group: sulphur (S)

These substances, furthermore, “are visible under the dark-field microscope as distinctive and complex structures of different sizes, can only partially be explained as a result of crystallization or decomposition processes, [and] cannot be explained as contamination from the manufacturing process,” the researchers found.

They declared the findings as preliminary.

The findings “build on the work of other researchers in the international community who have described similar findings, such as Dr. Young, Dr. Nagase, Dr. Botha, Dr. Flemming, Dr, Robert Wakeling, and Dr. Noak,” Dr. Janci Lindsay, Ph.D., a toxicologist not involved in the study, told The Epoch Times.

“The number and consistency of the allegations of contamination alone, coupled with the eerie silence from global safety and regulatory bodies, is troublesome and perplexing in terms of ‘transparency’ and continued allegations by these bodies that the genetic vaccines are ‘safe,’” Lindsay added.

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