Another Damning EU Vaccine Safety Report

Part 1 of my analysis of the Periodic Safety Update Report #3 (PSUR #3) for the Pfizer-BioNTech Covid-19 mRNA vaccine, covering the 6-month period of 19 December 2021 through to 18 June 2022, focused on the disturbing pregnancy and lactation cases. Part 2 of the report focuses on the tragic child deaths. 

Firstly, a comparative look at the data in PSUR #3 revealed similar findings in 1st PSUR, apart from a significant 55% increase in the number of case reports and a 36% increase in the number of adverse events recorded. The following similarities were found in both sets of data: three times the number of cases were reported for women; the age group most affected was for 31-50-year-olds; one-third of all cases were classified as serious and a significantly high percentage of cases were classified with outcomes as either unknown or not recovered. 

An Overview of the Data

  • 508,351 cases (individuals) suffering from 1,597,673 adverse events
  • Three times the number of cases were reported for women than men
  • 1/3 of all cases were classified as serious
  • 3,280 deaths reported 
  • 60% of cases were reported with either outcome unknown or not recovered
  • 92% of cases did not have any comorbidities
  • Highest number of cases occurred in the 31-50 year age group
  • Germany had the highest recorded number of cases (22.5% of all reported worldwide 
  • cases)

Germany had the highest number of recorded cases, a total of 114,573, which accounted for 22.5% of all worldwide cases for that 6-month period. It is worth noting that from December 2020 through to June 2022, a staggering 323,684 individual reports of suspected Covid-19 vaccine side effects were received by The Paul-Ehrlich-Institut, an Agency of the German Federal Ministry of Health. Yet, despite this large number, Karl Lauterbach, Germany’s Minister for Health, known for his pro-lockdown and pro-vaccine stance, made the unsubstantiated claim that the “vaccine was without side effects” in August 2021.

However, earlier this year, Lauterbach made a surprising U-turn in a TV interview, where he stated, “These unfortunate cases [of Covid-19 vaccine adverse effects] are heart-breaking and every victim is one too many…” Only recently, the first lawsuit against BioNTech was filed in Germany, by the law firm, Rogert and Ulbrich, with the plaintiff seeking damages due to an injury, allegedly caused by the German vaccine manufacturer’s mRNA product. 

Keep reading

The Department of Defense Continues to Hypocritically Deny Military Service Members Medical and Religious Exemptions for Vaccines

For service members whose careers survived the now-rescinded COVID-19 military “vaccine” mandate, many are becoming increasingly concerned about all vaccines, which include the flu vaccine.

Objections, including those based on religious grounds, about the safety, efficacy, testing, and research of the injections they once agreed to receive are on the rise.

The Gateway Pundit spoke to Daniel Schmid, Liberty Counsel’s Associate Vice President of Legal Affairs. “Many military members have sincere religious objections to certain immunizations, either because of their connections to aborted fetal cells or because they just have other religious convictions,” Mr. Schmid said. “There’s a federal statute called the Religious Freedom Restoration Act (RFRA), as well as the First Amendment, which entitles them to protection for those religious beliefs,” he explained.

Upon the 2021 implementation and enforcement of COVID immunizations, thousands of service members were reluctant to take the vaccine—and many sought religious accommodation. According to Mr. Schmid, these requests should have been reviewed by a chaplain and then sent up the chain of command for serious individual consideration. However, he said, most requests for religious accommodation were “denied in mass.” The appeals of service members were also overwhelmingly denied.

Members of the military who refused to comply with the now-rescinded COVID-19 vaccine mandate faced a variety of punitive actions, including letters of reprimand, dishonorable discharges, and more. At the same time, COVID-19 injections were being “billed as 100 percent safe and effective, and they clearly are not.”

As service members began to learn more about the COVID-19 vaccine, he said, the conversations often steered toward the use of aborted fetal cells in vaccine testing and research, as well as the toxicity of the “gene altering” injection and its associated adverse health effects. According to a 2020 Moderna, Inc. report by the Securities and Exchange Commission, “mRNA is considered a gene therapy product by the FDA.” The Gateway Pundit has widely reported the vaccine’s adverse health effects.

Keep reading

Insurance Data Showing the U.S. Excess Death Crisis Slides Behind a $10,000 Paywall

The Society of Actuaries has put up a five-figure paywall for access to new reports on covid mortality that in the past have revealed shocking rates of above-normal, or “excess,” deaths. 

In a post on its website, the SOA—a national source of risk data for life insurers—said it will charge $10,000 for four updates of post-pandemic deaths through next February.  

“This new series of group life mortality quarterly reports and data are only available for purchase,” SOA communications manager, Michael Nowak, confirmed in an email. Previous reports—which showed young workers dying at far higher excess rates than senior citizens—are still available on the SOA website, he said, and new, less-technical ones will be released to the public at an unspecified time.

Some industry watchers suggested the non-profit society, whose members pays dues, may be trying to develop a new business model. But it also may be attempting to extract itself from the contentious and politically charged issue of excess deaths and, moreover, what is causing them.  

Nowak would not grant my request to interview an SOA official who recently told a trade publication that deaths in young insured adults in 2023 were still far above normal. “Very important information in our reports we’ve been studying,” the official told me before our communication was cut off.  

Moreover, in an email, Nowak included an advisory, writing, “Please know that the SOA Research Institute data and reports on COVID-19 mortality does not validate any claims made to suggest a causal relationship between COVID-19 vaccines and mortality.”   

I had not asked about such a relationship.

The society’s primary job is to help insurers set rates based on the likelihood of injury and death, an indisputably technical and costly task. But because it is considered an unbiased source of trend information, its reports have also helped define the pandemic toll on working-age, insured people. While SOA has the right to use its reports as it sees fit, their loss would be a blow to pandemic information.  

In six articles published in mainstream venues, Dr. Pierre Kory, president emeritus of FLCCC Alliance, and I have used Society of Actuaries findings to call attention to the unheralded problem of excess deaths in America. In the first nine months of 2023, 158,000 more Americans died than normal, fifty times the toll in the World Trade Center attacks and more than in every U.S. military conflict since the Vietnam War. 

Keep reading

More than 30 Babies Mistakenly Vaccinated with Pfizer or GSK’s RSV Shots

At least 34 babies were mistakenly given the respiratory syncytial virus (RSV) vaccine and one of those babies was hospitalized according to a study published today in Pediatrics.

Researchers from the Centers for Disease Control and Prevention (CDC) analyzed data from the Vaccine Adverse Event Reporting System (VAERS) for the RSV vaccines, which are not approved for children.

The researchers found 27 reports of the Pfizer RSV vaccine (Abrysvo) and seven reports of the GSK RSV vaccine (Arexvy) mistakenly administered to children under 2 between Aug. 21, 2023, and March 18, 2024.

“While rare, vaccine administration errors are known to occur and may increase after a new vaccine or product is introduced,” Dr. Pedro Moro, lead author of the study, told MedPage Today.

Both vaccines were first approved in May 2023 for people ages 60 and older. Pfizer’s Abrysvo was approved in August 2023 for pregnant mothers during part of their third trimester, targeting RSV prevention in babies.

Keep reading

Whistleblower Exposes Internal Email Suggesting Pfizer Offered “Separate and Distinct” COVID-19 Vaccines to Employees

A whistleblower from Pfizer has leaked an internal email indicating that the pharmaceutical giant offered a “separate and distinct” COVID-19 vaccine to employees at its Pearl River research site in Rockland County, New York, InfoWars reported.

The email, dated January 2021, reassures  Pfizer employees that the vaccine supply for this internal program would not affect the doses committed to national governments worldwide.

According to the leaked document, site-essential workers were identified to receive these exclusive vaccinations.

According to the whistleblower, there was a widespread belief among employees that they were receiving vaccines that were different from those distributed to the public.

“I know we employees at Pfizer were receiving different vaccines and/or placebos, and this was the word around my site when I worked there,” the whistleblower told Infowars.

Keep reading

Fauci Ignored Early Reports of Vaccine Injuries, Emails Obtained by CHD Reveal

Dr. Anthony Fauci knew COVID-19 vaccines were causing serious injuries within days of the vaccines’ rollout in December 2020, according to documents obtained by Children’s Health Defense (CHD). However, he didn’t respond to emails from people who described their injuries and asked for help — and he didn’t warn the public.

The 300-page tranche of documents released on April 21 relates to correspondence between the National Institutes of Health (NIH) and people who contacted the agency about adverse events they experienced after receiving the COVID-19 vaccine.

CHD requested the documents via a Freedom of Information Act (FOIA) request in November 2022. On April 12, 2023, CHD sued the NIH to obtain the records after the NIH failed to respond to the FOIA request.

As part of an October 2023 settlement, the NIH agreed to produce up to 7,500 pages of documents at a rate of 300 per month.

Dr. Joel Wallskog is a Wisconsin orthopedic surgeon who stopped practicing medicine after being injured by Moderna’s COVID-19 vaccine. He told The Defender the documents prove public health officials, including Fauci, “were well aware of the avalanche of adverse events that were occurring early in 2021.”

“No communication was made about these adverse events to the public,” said Wallskog, now co-chairman of React19, a nonprofit representing vaccine injury victims. “This prevented the public from receiving informed consent.”

Wallskog said that while the emails “are heartbreaking,” Fauci “was too busy to respond to Americans pleading for help.”

Keep reading

AstraZeneca withdraws Covid vaccine worldwide

AstraZeneca pharmaceutical company has announced the withdrawal of its Covid-19 vaccine from global markets, claiming the drug has been sidelined by alternatives.

The development comes after the drug manufacturer recently admitted that the vaccine can cause potentially fatal blood clots in rare cases.

In a statement on Wednesday, cited by multiple media outlets, a spokesperson for AstraZeneca said multiple variants of the vaccine had been developed since the start of the pandemic, leading to a decline in demand for Vaxzevria, which is no longer being manufactured or developed. A spokesman also cited independent estimates claiming that “over 6.5 million lives were saved in the first year of use alone and over 3 billion doses were supplied globally.”

The AstraZeneca vaccine was rolled out in early 2021, shortly after the Covid-19 outbreak was declared a pandemic by the World Health Organization. AstraZeneca voluntarily withdrew its market authorization for the vaccine in the EU last March, with the European Medicines Agency confirm.

Shortly after the rollout, AstraZeneca found itself at the center of controversy after numerous Western countries suspended the use of its vaccine over fears that it may have caused some patients to develop blood clots. However, EU health officials at the time insisted that the benefits of the inoculation still outweighed the risks.

Keep reading

Systematic Review Reveals Many COVID-19 Vaccine Recipients Experienced New-Onset Psychosis

Individuals who took COVID-19 vaccines were found to have later suffered from psychosis, with Pfizer and AstraZeneca shots linked to most of the cases.

The peer-reviewed systemic review, published in the Frontiers in Psychiatry journal on April 12, examined cases of new-onset psychosis among people who took the vaccines. Psychosis refers to symptoms that occur when an individual has difficulty differentiating between reality and fantasy, with hallucinations and delusions being two key types. The review looked at 21 articles describing 24 cases of psychosis symptoms following vaccination. The researchers concluded that “data suggest a potential link between young age, mRNA, and viral vector vaccines with new-onset psychosis within 7 days post-vaccination.”

Collecting data on vaccine-related psychiatric effects is crucial for prevention, and an algorithm for monitoring and treating mental health reactions post-vaccination is necessary for comprehensive management.”

Out of the 24 cases, 13 were female. The median age of participants was 36 years. Twenty-two patients (91.2 percent) had no specific history of somatic illness and comorbidities.

In 33.3 percent of the cases, administration of the Pfizer mRNA vaccine “potentially induced adverse psychiatric events,” the study said. The viral vector AstraZeneca vaccine was linked to psychotic symptoms in 25 percent of cases.

In 45.8 percent of incidences, psychotic symptoms were reported after the first shot and in fifty percent after the second dose.

“Almost all reviewed cases (95.8 percent) presented with psychotic symptoms, such as hallucinations (visual, auditory, olfactory, and tactile) and delusions (mostly persecutory and delusions of reference).”

The most common form of hallucination was auditory, experienced in 54.2 percent of the cases, while visual hallucinations were experienced by 12.5 percent of patients.

“Motor disturbances, such as increased or decreased motor activity and bizarre behavior, were mentioned in 83.3 percent of cases. In 3 (12.5 percent) cases, a suicidal attempt was described.”

The psychotic symptoms mostly lasted for a period of one and two months.

The patients were treated using various methods including antipsychotics and steroids, but only 12 out of the 24 made a full recovery. The remaining suffered from “residual symptoms such as decreased emotional expressions, low affect, or residual psychotic symptoms.”

Keep reading

Moderna Stops New mRNA Vaxx Trials after High Rate of Side Effects

The phase 1 trial of Moderna’s new mRNA HIV vaccine has been halted after a high rate of “puzzling skin side effects” were reported.

The new vaccine requires a series of mRNA shots to be delivered, but an “unusually high percentage of recipients developed rashes, welts or other skin irritation,” according to Science magazine.

“We are taking this very seriously,” Carl Dieffenbach told Science. Dieffenbach heads the Division of AIDS at the National Institute of Allergy and Infectious Diseases, which funded the phase 1 trial.

It’s unclear at this stage whether the problem is caused by the “cumulative effect from multiple mRNA shots,” the genetic background of the recipients or the HIV sequence.

Different versions of this vaccine have already been tested, but in every instance skin problems occurred at a worryingly high level. In one study, 11 out of 60 recipients ended up developing some form of skin problem.

Keep reading

Service Members Are Waiting For Congress and Department of Defense to Acknowledge That the COVID-19 Shot Mandate Was Unlawful and Harmful

House Armed Service Committee (HASC) Republicans announced on X this morning that service members and military families will be prioritized in the FY2025 National Defense Authorization Act (NDAA).

For many, last year’s NDAA was an abject disappointment, failing to recognize Defense Secretary Lloyd Austin’s 2021 shot mandate was unlawful. It remains to be seen whether this year’s version will call a spade a spade or hide behind similar weak language.

One thing is certain: Thousands of service members, veterans, and their supporters will be watching, laser-focused on the statement made by HASC. Earlier this year, 231 active service members and veterans signed the Declaration of Military Accountability (DMA)—an open letter seeking accountability over the harm caused by the implementation and enforcement of the now-rescinded COVID-19 shot mandate. Nearly 34,000 others, including civilians, have pledged their support alongside the original signatories of the letter.

Brad Miller, a former U.S. Army lieutenant colonel who previously served as a battalion commander in the 101st Airborne Division, is one of the original signatories of the DMA and a voice for accountability. In October 2021, after nearly 19 years of honorable service, he was unjustly relieved of command for refusing the jab.

For service members like Miller, Congress, and DOD must acknowledge the unlawfulness and harmful effects of the once-mandated COVID-19 injection.

Keep reading