Tag: vaccines

Woman With Vaccine Injury in Clinical Trial Sues AstraZeneca

An American woman who suffered an injury from AstraZeneca’s COVID-19 vaccine sued the company on May 13, alleging the company breached a contract by not paying for the medical care she requires to deal with the injury.

“They left us no choice,” Brianne Dressen, a preschool teacher in Utah, told The Epoch Times in an email.

Ms. Dressen has paid tens of thousands of dollars to drugs to treat the nervous system disorder and other issues she’s experiencing, according to the complaint, filed in federal court in her home state.

Ms. Dressen chose to participate in AstraZeneca’s clinical trial in 2020 because she wanted to help the company develop its COVID-19 vaccine. The consent form she signed stated in part that AstraZeneca would “cover the costs of research injuries” and “pay the costs of medical treatment.”

“With these reassurances should something go wrong, Bri signed the form, rolled up her sleeve, and let the drug company inject the experimental product into her arm. Her mind was at peace, as Bri believed she was doing the right thing for her country, her students, and her family,” the suit states.

Ms. Dressen soon started experiencing problems, including blurred vision, tinnitus, and vomiting. She later became extremely sensitive to light and suffered spikes in her heart rate.

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CDC forced to release V-safe data, which includes over 780,000 reports of adverse reactions to Covid-19 shot

Reports of Covid-19 shot-related health problems, which were collected and kept hidden by the U.S Centers for Disease Control and Prevention (CDC) for several years, have now been published and reveal serious immune and brain dysfunction symptoms, include heart inflammation and death. Information on about 780,000 reports of adverse events following Covid shots were gathered and stored in the CDC’s special V-safe monitoring system that enabled Covid shot recipients to report adverse events via a cell phone text message.

V-safe is a smart-phone based surveillance system that allows users to access web-based surveys monitoring Covid shot adverse events and report reaction symptoms via a text message to federal health officials.

In the weeks after getting a Covid shot, V-safe users receive daily text messages asking about their health status. The messages contain a link to V-safe that allows users to answer follow-up questions including a checkbox of 12 symptoms, as well as enter a description of adverse events in a text message of not more than 250 characters.

According to a Jan. 13, 2024 article in The Epoch Times, CDC officials have collected approximately 7.8 million text responses from Covid shot recipients through V-safe. 

Previously, the CDC denied the public access to the V-safe reports and instead reported studies alleging that the data collected showed the shot was safe.

V-safe data released in 2022 from another lawsuit shows that between eight to ten million people, or 25 percent of responders reported reactions to Covid shots that were serious enough to require them to miss school, work or other normal activities or required medical attention or a hospital visit.

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Emails Reveal Fauci Ignored Early Reports Of Injuries Caused By COVID-19 Vaccine

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.”

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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. 

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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.

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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. 

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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.

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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.

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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.”

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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.

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