Update April 28th, 2021… New USA CDC Data As Of April 28th.3,486 Link
(Update) As of May 21, 2021 the VAERS Data reports 4,406 US deaths. Studies have shown that at best only 10% of adverse vaccine events are recorded in the data base.
3,964 Dead 162,610 Injuries: European Database of Adverse Drug Reactions for COVID-19 “Vaccines”
8,430 DEAD & 354,177 Injuries: European Database Of Adverse Drug Reactions For COVID-19 ‘Vaccines’
Here is what EudraVigilance states about their database:
This website was launched by the European Medicines Agency in 2012 to provide public access to reports of suspected side effects (also known as suspected adverse drug reactions). These reports are submitted electronically to EudraVigilance by national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.
EudraVigilance is a system designed for collecting reports of suspected side effects. These reports are used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorisation in the European Economic Area (EEA). EudraVigilance has been in use since December 2001.
This website was launched to comply with the EudraVigilance Access Policy, which was developed to improve public health by supporting the monitoring of the safety of medicines and to increase transparency for stakeholders, including the general public.
The Management Board of the European Medicines Agency first approved the EudraVigilance Access Policy in December 2010. A revision was adopted by the Board in December 2015 based on the 2010 pharmacovigilance legislation. The policy aims to provide stakeholders such as national medicines regulatory authorities in the EEA, the European Commission, healthcare professionals, patients and consumers, as well as the pharmaceutical industry and research organisations, with access to reports on suspected side effects.
Transparency is a key guiding principle of the Agency, and is pivotal to building trust and confidence in the regulatory process. By increasing transparency, the Agency is better able to address the growing need among stakeholders, including the general public, for access to information. (Source.)
Their report through April 24, 2021 lists 8,430 deaths and 354,177 injuries following injections of four experimental COVID-19 shots
Data From The US VAERS Data Base Recorded 2.9K Deaths well over a month ago. (Video) There have also been allegations of the VAER’s numbers being shaved. (Video) Trunews.com has also made the same allegations and mention in their piece as well that the site is difficult to operate for the layperson.
What follows is an April report on the numbers...
Data released today by the Centers for Disease Control and Prevention (CDC) on the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines revealed steadily rising numbers, but no new trends. VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.
Article by Megan Redshaw from Children’s Health Defense.
Every Friday, VAERS makes public all vaccine injury reports received to the system as of Friday of the previous week. Today’s data show that between Dec. 14, 2020, and March 26, a total of 50,861 total adverse events were reported to VAERS, including 2,249 deaths — an increase of 199 over the previous seven days — and 7,726 serious injuries, up 631 over the same time period.
Of the 2,249 deaths reported as of March 26, 28% occurred within 48 hours of vaccination, 19% occurred within 24 hours and 43% occurred in people who became ill within 48 hours of being vaccinated.
In the U.S., 136.7 million COVID vaccine doses had been administered as of March 26.
This week’s VAERS data show:
- 19% of deaths were related to cardiac disorders.
- 45% of those who died were male, 43% were female and the remaining death reports did not include gender of the deceased.
- The average age of those who died was 77.7 and the youngest death was an 18-year-old.
- As of March 26, 341 pregnant women had reported adverse events related to COVID vaccines, including 104 reports of miscarriage or premature birth.
- Of the 578 cases of Bell’s Palsy reported, 63% of cases were reported after Pfizer-BioNTech vaccinations — almost twice as many as reported (36%) following vaccination with the Moderna vaccine. Seven cases of Bell’s Palsy were reported with Johnson & Johnson (J&J) vaccine (1%).
- There were 2,578 reports of anaphylaxis, with 53% of cases attributed to the Pfizer-BioNTech vaccine, 44% to Moderna and 3% to J&J vaccine, which was rolled out in the U.S. on March 2.
- Using a broadened search for any reference to anaphylaxis in chart notes resulted in 15,193 reports, with 52% of cases attributed to Pfizer’s COVID vaccine, 45% to Moderna and 3% to J&J. With each vaccine, nearly 42% of anaphylactic reports occurred in people aged 17-44.
According to the CDC’s website, “the CDC follows up on any report of death to request additional information and learn more about what occurred and to determine whether the death was a result of the vaccine or unrelated.”
To date, the only information the CDC has published related to the investigation of COVID vaccine-related deaths and how those investigations were conducted is a COVID-19 Vaccine Safety Update via the Advisory Committee on Immunization Practices, published Jan. 27.
An interview in MedPage Today highlighted the shortfalls of the post-marketing surveillance of the COVID vaccine. Aaron Kesselheim, professor of medicine at Harvard Medical School and Brigham and Women’s Hospital in Boston, said we are seeing a lot of spontaneous reporting, a lack of formal post-approval studies because vaccines have only received Emergency Use Authorization and vaccines being given outside the healthcare systems — interfering with the ability to rigorously collect observational data.
Although the CDC and U.S. Food and Drug Administration (FDA) have various systems in place to monitor the safety of vaccines, they are not “up and running” and do not have adequate resources behind them, Kesselheim said.
According to Kesselheim, there’s essentially nobody keeping track of COVID adverse reactions in the U.S. and no long-term safety data, but emphasized that this new mRNA technology is “extremely effective and extremely safe.”
On March 8, The Defender contacted the CDC with questions about reported deaths and injuries related to COVID vaccines. We provided a written list of questions about how the CDC conducts investigations into reported deaths, the status of investigations on deaths reported in the media, if autopsies are being done and the standard for determining whether an injury is causally connected to a vaccine.
We also inquired about whether healthcare providers are reporting all injuries and deaths that might be connected to the COVID vaccine, and what education initiatives are in place to encourage and facilitate proper and accurate reporting.
It took the CDC 22 days to respond to our repeated inquiries. When someone did, the person told us the agency had never received the questions — even though the employees we talked to several times said their press officers were working through the list of questions and were reviewing the email we sent. We provided the questions again yesterday, and requested a response by April 7.
Dr. Peter McCullough, in a 32-minute interview with journalist Alex Newman, said if this were any other vaccine it would have been pulled from the market by now for safety reasons.
McCullough holds the honor of being the most cited medical doctor on COVID-19 treatments at the National Library of Medicine, with more than 600 citations. He has testified before Congress and won numerous awards during his distinguished medical career.
Between Dec. 14 and April 23, there were 3,544 deaths reported to the CDC’s Vaccine Adverse Event Reporting System [VAERS], along with 12,619 serious injuries.
One might expect these numbers would trigger an exhaustive investigation from the U.S. Food and Drug Administration. But the opposite has occurred. According to McCullough, the government has taken what amounts to a passing glance at the alarming numbers and dismissed them with a bare minimum of scrutiny.
“A typical new drug at about five deaths, unexplained deaths, we get a black-box warning, your listeners would see it on TV, saying it may cause death,” McCullough said. “And then at about 50 deaths it’s pulled off the market.”
The U.S. has a precedent for this. In 1976 during the Swine Flu pandemic the U.S. attempted to vaccinate 55 million Americans, but at that point the shot caused about 500 cases of paralysis and 25 deaths.
“The program was killed, at 25 deaths,” McCullough said.
Compare that type of response to the government’s reaction to much higher reported death numbers related to the Moderna and Pfizer shots and the contrast is alarming, McCullough said, especially when the shots have not even been granted full FDA approval and are only being allowed on the market under an Emergency Use Authorization.
“In the U.S. today [as of late March] we have approximately 77 million people vaccinated for COVID and we have 2,602 deaths reported, so it’s unprecedented how many deaths have accrued,” he said.
“Then on March 8 the CDC announced on their website with very little fanfare, that they had reviewed about 1,600 deaths with unnamed FDA doctors and they indicated not a single death was related to the vaccine,” he added. “I think that was concerning in the academic community.”
McCullough said he knows from first-hand experience that doing a thorough investigation into 1,600 potentially vaccine-related deaths would have taken months to complete.
“I have chaired and participated in dozens of data safety monitoring boards and sat on those committees and I can tell you that this type of work would have taken many months to review all the labs, the death certificates and all the circumstances of an event. It is impossible for unnamed regulatory doctors without any experience with COVID 19 to opine that none of the deaths were related to the vaccine.”
Previous studies, including one from Harvard University, estimate that only 1 to 10 percent of all vaccine-related deaths get reported to VAERS. So in all likelihood, there are more people dying than even gets reported, yet the FDA can’t come up with a single death related to the Moderna and Pfizer shots.
“Reporting a death requires a healthcare worker to enter it into the system,” he said. And if the death does not occur within the normal 15-minute monitoring period they often go unreported. Most deaths occur within 72 hours of the shot. “They pile up on day one, two and three,” he said.
As a matter of comparison: There are 20 to 30 deaths reported every year to VAERS related to the flu shot. That’s with 195 million receiving flu shots. Compare that to the COVID shot, which resulted in 2,602 reported deaths through 77 million vaccinations.
That’s a stunningly high ratio of deaths to vaccinations, the highest for any vaccine in U.S. history, and yet no major media outlet has launched an investigation. Independent journalists and researchers such as Alex Newman, Robert F. Kennedy Jr. and Leo Hohmann have been ruthlessly censored.
“So the U.S. government has made a decision, along with the stakeholders – the CDC, NIH, FDA, Big Pharma, World Health Organization, Gates Foundation – they have made a commitment to mass vaccination as the solution to the COVID pandemic and we are really going to be witness to what’s going to happen in history. We’re sitting on, right now, the biggest number of vaccine deaths, there’s been tens of thousands of hospitalizations, all attributable to the vaccine, and going strong.”
McCullough testified before the U.S. Senate on Nov 19, 2020.
“I estimated at that time we could have saved half of the lives lost,” he told Newman. “There are now current estimates that we are up to about 85 percent of all lives lost could have been saved with something called sequenced oral multi-drug therapy.”
But instead, the government and its “stakeholders” in Big Pharma chose to focus on vaccines. At the same time, news organizations were recruited to present only one side of the vaccine story.
Mainstream outlets have agreed to not allow any news critical of the shots to reach the American people. This corrupt collusion falls under the Trusted News Initiative, a global collaboration signed onto by Big Tech social-media giants and many of its corrupt corporate media “partners.”
The partners signed onto the Trusted News Initiative to date are: Associated Press, AFP; BBC, CBC/Radio-Canada, European Broadcasting Union (EBU), Facebook, Financial Times, First Draft, Google/YouTube, The Hindu, Microsoft, Reuters, Reuters Institute for the Study of Journalism, Twitter, The Washington Post. The New York Times has also participated in the past.
Reporting facts related to the dark side of the experimental mRNA vaccines is considered “dangerous disinformation” by the globalist media elites behind the Trusted News Initiative.
Dr. McCullough describes ‘whitewash of historic proportions‘
“So I think this was effectively a scrubbing, like we’ve seen elsewhere. There is a Trusted News Initiative, which is very important for Americans to understand, this was announced Dec. 10, and this is a coalition of all the major media and government stakeholders in vaccination, where they are not going to allow any negative information about vaccines to get into the popular media because they’re concerned about vaccine hesitancy, that if Americans got any type of fair, balanced coverage on safety events then they simply would not come forward and get the vaccine.”
“The Trusted News Initiative is really troublesome,” he continued, “because we’re now at record numbers of deaths, they continue to occur every day.”
Confirming a LeoHohmann.com report from earlier this month, McCullough said the Johnson & Johnson vaccine, while it does have issues with blood clots, is actually the safest of the three vaccines now being offered to Americans.
“In my professional opinion, the safest vaccine on the market was the J&J vaccine. And that was pulled for very rare blood-clotting events. We had seven million people vaccinated but the estimates are for the other two vaccines available, the blood-clotting rates are probably 30 times that of J&J, and these others are going strong.”
McCullough suggested that there is an incestuous relationship between the U.S. government and certain elements within Big Pharma, which causes regulators to look the other way when confronted with safety issues.
“A lot of Americans don’t understand how tight these stakeholders are. Keep in mind the NIH [National Institutes of Health] is a co-owner of the Moderna patent, so they have a vested financial interest in keeping these vaccines going,” he said.
More than 15 months into the COVID nightmare, the evidence is beginning to suggest the U.S. government colluded from the outset with the Gates Foundation, CDC, FDA, the United Nations World Health Organization and Big Pharma to make the vaccines the central focus of the global COVID response effort. They started promoting the vaccines before they were even out of clinical trials, McCullough said, which is against U.S. regulatory law.
More reports of high death counts
LeoHohmann.com has been getting reports that confirm Dr. McCullough’s warning that harmful events caused by the vaccine are being covered up by the medical establishment, the government, the legacy media and social-media giants Google, Facebook and Twitter.
A physician with a practice in the Kansas City area told LeoHohmann.com that of a recent 500-person sampling of nursing-home patients who received the COVID injection, 22 died within 48 hours. That represents an astonishing 4.4 percent death rate. Most people in the Kansas City area nursing homes are receiving the Pfizer shot, he said.
“I can’t prove they all died of the vaccine, all I can prove is it happened within 48 hours,” the physician told LeoHohmann.com.
“The requirements are they only need to be monitored for 15 minutes. So we are never going to know the real numbers,” he said. “If it happens outside of that 15-minute window it’s going to be impossible to prove… If the FDA approves this then God help us.”
The Kansas City physician requested his name not be revealed for fear that he could lose his medical license.
A Canadian doctor, Dr. Charles Hoffe, recently broke his silence and went public in defiance of a gag order, blowing the whistle on how “Moderna shots killed, disabled patients.”
McCollough said the government has never placed a focus on treating sick patients, choosing instead to focus on the WHO recommended strategy of social distancing, lockdowns, masking and vaccines. If the strategy had focused instead on a regimen that includes a multi-drug treatment of early onset symptoms, tens of thousands of lives could have been saved, he said.
In a December 2020 paper, A Guide for Home-Based COVID-19 treatment: Step by step doctor’s plan that could save your life, McCullough prescribes a four-pronged strategy that includes contagion control, early home treatment, late-stage treatment and lastly vaccination.
“I talked about the four pillars, with the first pillar being contagion control [wearing masks and lockdowns]. We’ve spent a lot of time on that. But really the missing pillar, if we would have spent our time focusing on sick patients, that would have had the highest public-health value.
“But what happened in the U.S. was we developed a game plan …that we were going to promote the importance of social distancing as part of contagion control and just have the population wait for a vaccine. There have been no updates on treatment, not outpatient, not inpatient. We don’t hear anything about sick patients. All we heard was about masking, lockdowns and wait for a vaccine.”