Tag: vaers

RFK Jr. slams ‘corruption’ of vaccine injury compensation program, says he’s working to ‘fix’ it

U.S. Secretary for Health & Human Services Robert F. Kennedy Jr. declared that he wants to “fix” the federal Vaccine Injury Compensation Program (VICP) to better serve those who suffer adverse events but has yet to elaborate on how.

On July 28, Kennedy posted to X about the National Childhood Vaccine Injury Act of 1986, which grants vaccine manufacturers general immunity from liability for injuries from their products and instead establishes the VICP through which affected individuals can seek financial compensation under certain circumstances.

“To date, the Vaccine Court has paid out $5.4 billion to 12,000 petitioners. But the VICP no longer functions to achieve its Congressional intent. Instead, the VICP has devolved into a morass of inefficiency, favoritism, and outright corruption as government lawyers and the Special Masters who serve as Vaccine Court judges prioritize the solvency of the HHS Trust Fund, over their duty to compensate victims,” he said.

“The structure itself hobbles claimants. The defendant is HHS, not the vaccine makers; and claimants are therefore facing the monumental power and bottomless pockets of the U.S. government represented by the Department of Justice. Furthermore, most of the Special Masters come from government, legal, or political posts, and typically display an extreme bias that favors the government side. There is no discovery, and the rules of evidence do not apply,” Kennedy added.

“Instead of ‘quickly and fairly’ awarding compensation, Special Masters dismiss over half of the cases. Most of those that proceed typically take 5+ years to resolve, with many languishing for more than 10 years as parents struggle to care for children suffering with often extreme disabilities,” he said.

Keep reading

Everyone Should Be Closely Watching This VAERS Whistleblower Case

A significant COVID-19 accountability case is heading to discovery, establishing critical legal precedents regarding the requirement to report adverse events to the Vaccine Adverse Event Reporting System (VAERS) while receiving federal funding. The COVID jabs have caused harm, including death, to millions, making this a crucial case to watch. Whistleblower Deborah Conrad, a dedicated Physician Assistant, was fired in 2021 by her employer, United Memorial Medical Center (Rochester Regional Health), for purportedly spreading “vaccine misinformation” and “over-reporting” of adverse events following the experimental mRNA COVID-19 injections. But hold on a second—upon examining the entire situation, it appears evident that Deb was, quite simply, “doing the right thing” and reporting adverse events to VAERS.

Nonetheless, Deb was fired in October 2021. She was unexpectedly chaperoned into a conference room, where she was interrogated and then escorted out without due process. Deb and her attorney, Warner Mendenhall, are currently suing Rochester Regional Health for damages, including back pay and civil penalties in violation of the False Claims Act. On June 11, 2025, in a triumph for those who have fought hard throughout the COVID-19 tyranny to protect their patients, the U.S. District Court for the Western District of New York issued a landmark ruling in favor of Deb, denying the hospital’s motion to dismiss the core claims in Deb’s False Claims lawsuit. This move opens the door for Deb’s case to proceed to discovery.

As highlighted by Mendenhall, the court determined that Rochester Regional Health had a significant obligation under its CDC COVID-19 Vaccination Program Provider Agreement to report serious adverse events to VAERS (never mind that the CDC itself looked the other way regarding injuries reported in its V-safe app). Indeed, the hospital’s failure to comply with this requirement—instead literally blocking Deb from reporting serious adverse events after the COVID-19 jab—while continuing to seek federal reimbursement constituted potential fraud against the government. Additionally, the court agreed that the detailed allegations provided by Deb sufficiently met the stringent legal standards for fraud claims, despite her lacking access to internal billing records. Furthermore, the court found that her retaliation claim could proceed, as it was likely she was terminated for attempting to expose the hospital’s non-compliance with adverse event reporting. Mendenhall wrote:

“This ruling is significant beyond just Deborah’s case. It establishes that 1) healthcare providers cannot ignore federal safety reporting requirements while continuing to collect taxpayer money; 2) the False Claims Act can be used to hold institutions accountable for COVID-related misconduct; and 3) whistleblowers who expose these practices have legal protection.

We estimate over 500,000 were killed by the shots, millions lost their jobs for refusing them, and Big Pharma received billions for dangerous and experimental treatments. This case reveals a legal pathway to begin holding the system accountable.

The case now moves to discovery, where we will seek the hospital’s internal “vaccination,” treatment, and billing records to uncover the full scope of unreported adverse events, which we believe are in the 1000s in this hospital system alone.”

Incredibly, while successfully managing to submit 160 VAERS reports, Deb’s case involves a shocking 170 serious adverse events that the hospital allegedly stopped her from reporting. Again, under the terms of their vaccine provider agreement and the False Claims Act, 31 U.S.C. §3729, all COVID-19 vaccine providers were legally bound to report adverse events related to the jabs to the Vaccine Adverse Event Reporting System (VAERS). Thus, when Deborah observed several adverse events, including fatalities, following COVID-19 injections in both her own patients and in the patients of her peers, she took the initiative to compile and submit patient reports to VAERS in her spare time.

However, she soon faced pressure from Rochester Regional Health to “dial it back” and was advised to limit her reporting to only her own patients, excluding those treated by other providers. But the hospital didn’t stop there. It further urged her to “toe the company line” by supporting the experimental vaccine to minimize vaccine hesitancy, despite the hospital’s legal duty, again, under its agreement with the CDC in order to receive federal funding during the pandemic, to report vaccine-related injuries.

Keep reading

HHS Secretary RFK Jr. Announces New Vaccine Injury Reporting System More Accurate Than VAERS

The Trump administration will soon unveil a new reporting system for vaccine injuries and adverse reactions improving on the Vaccine Adverse Event Reporting System (VAERS) currently in place, Health and Human Services Secretary Robert F. Kennedy Jr. said.

Speaking to “The Ingraham Angle” on Thursday, RFK said the new system is part of his effort to protect the health of Americans and hold vaccine manufacturers accountable for their products.

Asked if he believed the experimental Covid-19 vaccine or booster jabs were safe, RFK said he couldn’t accurately respond because “We don’t have good data on it, and that is a crime – the fact that we don’t have a surveillance system that actually works.” Kennedy went on to describe the inefficiencies of the current federal Vaccine Adverse Event Reporting System (VAERS), which was intended to compensate vaccine victims who experience debilitating side effects, up to and including death, but has failed to do so adequately. “In 2010, CDC had a surveillance system called the vaccine adverse event reporting system, and it’s supposed to pick up injuries, but CDC did a study of that system in 2010, and that study said – and this is a published study by CDC – that it captures less than one percent of the vaccine injuries. That’s inexcusable.” Kennedy went on to say he’ll implement a new reporting system as has been requested by Congress and multiple health agencies.

Keep reading

How many US VAERS deaths were due to COVID19?

Summary:

  • Daniel (Truth_in_number) on Twitter posted a long thread on VAERS in mid-2023, seemingly based on this comical premise – unlike him, no one else had looked at VAERS extensively1
    • While Daniel did read 120 reports, he hasn’t yet posted the VAERS IDs for them (to the best of my knowledge), so the people who already agree with him are just taking his word in terms of final analysis
  • I refuted most of his central points anyway using large scale text analysis of VAERS reports (for example there are hundreds of reports of sudden death in VAERS, while Daniel claims he did not find any “true” sudden death reports)
  • The one major point he made2 – that 61% of the deaths he read were caused by COVID19 – was much harder to refute till now because it required large scale text analysis of 16000+ reports which did not follow any well defined text pattern
  • I used a recent feature provided by GPT4 to automate this process3, and found that only 39% of 16K deaths even tested positive for COVID19. In other words, less than 39% of US VAERS deaths could actually be due to COVID19, leaving the other 60%+ as potential vaccine induced deaths.

In a previous article I mentioned that LLMs can be used to extract cause of death from a VAERS report.

Keep reading

RSV Vaccine Now Killing Babies — VAERS Reports

At least two infants died after they were mistakingly given Pfizer’s respiratory syncytial virus (RSV) vaccine along with Nirsevimab, a monoclonal antibody injection approved for infants that’s meant to prevent RSV.

A 29-day-old premature girl died after receiving an RSV shot meant for the elderly, according to the Vaccine Adverse Event Reporting System (VAERS).

“According to the mother, the patient departed the clinic at 1 pm after the vaccine was administered. Subsequently, the patient took a nap and at approximately 8 pm, the father observed that the patient was not breathing. The parents attempted CPR but it was unsuccessful,” the VAERS report said. “Shortly thereafter, the parents called both ambulance and police assistance. Upon the paramedics” arrival, the patient had already deceased; The causes of death are unknown, An autopsy is presently in the process of being investigated. The mother has not yet reported the exact cause of death, information was given via a telephone call.”

A 27-day-old boy also received the RSV shot, which resulted in a similar fate.

“Her son was only 27 days old and received the vaccine at doctor”s office and he passed away right there; Her son was only 27 days old and received the vaccine at doctor”s office and he passed away right there; This is a spontaneous report received from a Consumer or other non HCP. A 27-day-old male patient received rsv vaccine prot.subunit pref 2v (ABRYSVO), as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient”s relevant medical history and concomitant medications were not reported,” the VARES report said. “The following information was reported: DEATH (death, medically significant), outcome “fatal”, PRODUCT USE ISSUE (non-serious), outcome “unknown” and all described as “Her son was only 27 days old and received the vaccine at doctor”s office and he passed away right there”. The date and cause of death for the patient were unknown. It was not reported if an autopsy was performed. The information on the batch/lot number for rsv vaccine prot.subunit pref 2v, rsv vaccine prot.subunit pref 2v will be requested and submitted if and when received.; Reported Cause(s) of Death: Her son was only 27 days old and received the vaccine at doctor”s office and he passed away right there.”

Keep reading

98% of PE reports involve COVID shots

Pulmonary embolism (PE) occurs when a blood clot moves into the lungs and it is dangerous. Using reports in the VAERS database dating back to 1990, about 15,000 reports of PE have accrued over the past 34 years.

But when filtering them down to just those reports which involved COVID shots, you find that almost 98% of all PE reports involved COVID shots.

This majority is even more striking when one realizes that COVID shots make up just below 10% of all shots given in 34 years. Due to 98% of all PE reports involving COVID shots, you would have thought that government regulators would have warned the public about it. You would think that they would have a duty (legal obligation) to do so.

Keep reading

A new study finds that covid injections cause tinnitus

There’s a new paper on the loose that supports what many of us have been stating as fact for years: tinnitus is caused by the covid-19 injections.

The paper was published in Frontiers in Pharmacology on 22 May 2024 and is entitled ‘Covid-19 vaccination-related tinnitus is associated with pre-vaccination metabolic disorders’.1 The paper demonstrates a causal link between tinnitus and covid-19 injections using a survey on 398 cases of covid-19 injection-related tinnitus, and 699,839 covid-19 injection-related reports in the VAERS from 2021.

They found 7 main things:

  1. tinnitus report frequencies for Pfizer, Moderna and Janssen vaccines in VAERS are 47, 51 and 70 cases per million full vaccination;
  2. the symptom onset was often rapid;
  3. more women than men reported tinnitus and the sex difference increased with age;
  4. for 2-dose vaccines, the frequency of tinnitus was higher following the first dose than the second dose;
  5. for 2-dose vaccines, the chance of worsening tinnitus symptoms after the second dose was approximately 50%;
  6. tinnitus was correlated with other neurological and psychiatric symptoms; and,
  7. pre-existing metabolic syndromes were correlated with the severity of the reported tinnitus.

I can confirm and corroborate almost every single one of these points using only VAERS data, and in science, reproduction is ESSENTIAL. It is staggering how many (percentage-wise) peer-reviewed studies cannot be replicated.

1. Tinnitus report frequencies for Pfizer, Moderna and Janssen vaccines in VAERS are 47, 51 and 70 cases per million full vaccination. (NB: these rates are for 2 doses.)

Keep reading

Clot-related adverse events in VAERS 60 days out from last shot

When we wrote up the updated myocarditis paper1, we had an idea to include examples of individuals who had succumbed to myocarditis many months after their last injection of COVID-19 injectable product, as per their reports to VAERS. In both cases included our paper, the product was Pfizer. As you can see in Figure 1 below, a 15-year-old boy had a diagnosis of idiopathic myocarditis that resulted in death 358 days after his first, and last, Pfizer injection.

This is shocking enough, and these are only two examples. These late occurrences of myocardial incidents left me thinking about the long-term effects of these modified mRNA COVID-19 products.

I was more recently prompted to examine clot-related adverse events (AEs) in VAERS, since the lipid nanoparticles (LNPs) are suspected to be – along with the spike protein – a root cause of hemagglutination. I gave a talk about all things LNP to Doctors for COVID Ethics last year, and you can watch that here. I think they disrupt the zeta potential of red blood cells, as does the spike protein.23

Keep reading

Novel Robust Methodology for VAERS Analysis Reveals Very High Risk of Myocarditis and Pericarditis Following Dose 2 and Dose 3: #PathogenicPriming

A new study published in the Journal of Evidence-Based Medicine by Daoyuan Lai and colleagues, a team of researchers from the University of Hong Kong, has made significant strides in understanding the safety of COVID-19 mRNA vaccines, particularly in relation to myocarditis risk after vaccination. The study may also represent a watershed moment in the methodology used to assess causality using VAERS data.

The study, which focuses on the rare but concerning risk of myocarditis following the administration of COVID-19 mRNA vaccines, introduces a novel approach to analyzing vaccine safety data that could transform how we monitor vaccine adverse events.

The study analyzed data from the US Vaccine Adverse Event Reporting System (VAERS), a resource that has been used to monitor post-vaccination adverse events. Recognizing the limitations of data in VAERS, including potential underreporting and the absence of a control group, the team employed a modified version of the Self-Controlled Case Series (SCCS) method. This innovative approach allowed for more accurate detection and quantification of myocarditis risk following the second and third doses of mRNA COVID-19 vaccines.

Keep reading

Alarming Revelation: Government Data Unveils Astounding 143,233% Spike in Deadly Cancer Cases Tied to COVID Vaccines

Cancer begins when genetic changes interfere with the normal replication and replacement of cells in the body. Cells start to grow uncontrollably and may form a tumour. It is the No. 2 leading cause of death in the United States.

Unfortunately, it appears the disease may be on the rise thanks to the experimental Covid-19 injections. Because official U.S. Government data confirms the risk of developing cancer following Covid-19 vaccination increases by a shocking 143,233%.

The Centers for Disease Control (CDC) hosts a Vaccine Adverse Event Reporting System (VAERS) which contains historical data on adverse reactions reported against every vaccine that has been administered in the United States of America.

A quick search of the CDC VAERS database on the number of cancer cases reported as adverse reactions to the Covid-19 injections since they were first rolled out in the USA, reveals that from December 2020 up to 5th August 2022, a total of 2,579 adverse events related to cancer were made in just 1 year and 8 months.

But performing a similar search of the VAERS database on the number of cancer cases reported as adverse events to all other available vaccines between 2008 and 2020, a period of 13 years, reveals there were just 791 adverse events related to cancer.

Keep reading