26,041 Deaths 2,448,362 Injuries Following COVID Shots in European Union’s Database

By Brian Shilhavy | Health Impact News | September 29, 2021
The European Union database of suspected drug reaction reports is EudraVigilance, and they are now reporting 26,041 fatalities, and 2,448,362 injuries, following COVID-19 injections.
A Health Impact News subscriber from Europe reminded us that this database maintained at EudraVigilance is only for countries in Europe who are part of the European Union (EU), which comprises 27 countries.
The total number of countries in Europe is much higher, almost twice as many, numbering around 50. (There are some differences of opinion as to which countries are technically part of Europe.)
So as high as these numbers are, they do NOT reflect all of Europe. The actual number in Europe who are reported dead or injured following COVID-19 shots would be much higher than what we are reporting here.
The EudraVigilance database reports that through September 25, 2021 there are 26,041 deaths and 2,448,362 injuries reported following injections of four experimental COVID-19 shots:
- COVID-19 MRNA VACCINE MODERNA (CX-024414)
- COVID-19 MRNA VACCINE PFIZER-BIONTECH
- COVID-19 VACCINE ASTRAZENECA (CHADOX1 NCOV-19)
- COVID-19 VACCINE JANSSEN (AD26.COV2.S)
From the total of injuries recorded, almost half of them (1,176,130) are serious injuries.
“Seriousness provides information on the suspected undesirable effect; it can be classified as ‘serious’ if it corresponds to a medical occurrence that results in death, is life-threatening, requires inpatient hospitalisation, results in another medically important condition, or prolongation of existing hospitalisation, results in persistent or significant disability or incapacity, or is a congenital anomaly/birth defect.”
A Health Impact News subscriber in Europe ran the reports for each of the four COVID-19 shots we are including here. It is a lot of work to tabulate each reaction with injuries and fatalities, since there is no place on the EudraVigilance system we have found that tabulates all the results.
Since we have started publishing this, others from Europe have also calculated the numbers and confirmed the totals.*
Here is the summary data through September 25, 2021.
Total reactions for the mRNA vaccine Tozinameran (code BNT162b2,Comirnaty) from BioNTech/ Pfizer – 12,362 deaths and 1,054,741 injuries to 25/09/2021
- 28,662 Blood and lymphatic system disorders incl. 172 deaths
- 29,569 Cardiac disorders incl. 1,834 deaths
- 277 Congenital, familial and genetic disorders incl. 23 deaths
- 14,027 Ear and labyrinth disorders incl. 9 deaths
- 822 Endocrine disorders incl. 5 deaths
- 16,330 Eye disorders incl. 30 deaths
- 92,590 Gastrointestinal disorders incl. 514 deaths
- 274,633 General disorders and administration site conditions incl. 3,517 deaths
- 1,186 Hepatobiliary disorders incl. 59 deaths
- 10,876 Immune system disorders incl. 65 deaths
- 36,113 Infections and infestations incl. 1,214 deaths
- 13,804 Injury, poisoning and procedural complications incl. 191 deaths
- 26,554 Investigations incl. 387 deaths
- 7,555 Metabolism and nutrition disorders incl. 225 deaths
- 138,223 Musculoskeletal and connective tissue disorders incl. 155 deaths
- 837 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 78 deaths
- 185,082 Nervous system disorders incl. 1,341 deaths
- 1,347 Pregnancy, puerperium and perinatal conditions incl. 39 deaths
- 172 Product issues incl. 1 death
- 19,436 Psychiatric disorders incl. 159 deaths
- 3,605 Renal and urinary disorders incl. 205 deaths
- 24,848 Reproductive system and breast disorders incl. 4 deaths
- 46,177 Respiratory, thoracic and mediastinal disorders incl. 1,443 deaths
- 50,420 Skin and subcutaneous tissue disorders incl. 111 deaths
- 2,007 Social circumstances incl. 15 deaths
- 1,034 Surgical and medical procedures incl. 34 deaths
- 28,555 Vascular disorders incl. 532 deaths
Total reactions for the mRNA vaccine mRNA-1273 (CX-024414) from Moderna – 6,907 deaths and 306,490 injuries to 25/09/2021
- 6,051 Blood and lymphatic system disorders incl. 67 deaths
- 9,283 Cardiac disorders incl. 744 deaths
- 122 Congenital, familial and genetic disorders incl. 3 deaths
- 3,769 Ear and labyrinth disorders incl. 1 death
- 248 Endocrine disorders incl. 2 deaths
- 4,627 Eye disorders incl. 20 deaths
- 26,405 Gastrointestinal disorders incl. 269 deaths
- 82,564 General disorders and administration site conditions incl. 2,617 deaths
- 500 Hepatobiliary disorders incl. 29 deaths
- 2,659 Immune system disorders incl. 11 deaths
- 9,570 Infections and infestations incl. 487 deaths
- 6,759 Injury, poisoning and procedural complications incl. 127 deaths
- 5,811 Investigations incl. 128 deaths
- 2,944 Metabolism and nutrition disorders incl. 158 deaths
- 38,397 Musculoskeletal and connective tissue disorders incl. 139 deaths
- 369 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 42 deaths
- 53,562 Nervous system disorders incl. 706 deaths
- 583 Pregnancy, puerperium and perinatal conditions incl. 8 deaths
- 62 Product issues incl. 2 deaths
- 5,772 Psychiatric disorders incl. 118 deaths
- 1,772 Renal and urinary disorders incl. 114 deaths
- 4,576 Reproductive system and breast disorders incl. 5 deaths
- 13,315 Respiratory, thoracic and mediastinal disorders incl. 682 deaths
- 16,453 Skin and subcutaneous tissue disorders incl. 62 deaths
- 1,366 Social circumstances incl. 28 deaths
- 1,032 Surgical and medical procedures incl. 71 deaths
- 7,919 Vascular disorders incl. 267 deaths
Total reactions for the vaccine AZD1222/VAXZEVRIA (CHADOX1 NCOV-19) from Oxford/ AstraZeneca – 5,468 deaths and 1,008,357 injuries to 25/09/2021
- 12,160 Blood and lymphatic system disorders incl. 226 deaths
- 17,334 Cardiac disorders incl. 623 deaths
- 163 Congenital familial and genetic disorders incl. 6 deaths
- 11,826 Ear and labyrinth disorders incl. 1 death
- 522 Endocrine disorders incl. 4 deaths
- 17,753 Eye disorders incl. 26 deaths
- 97,985 Gastrointestinal disorders incl. 280 deaths
- 265,482 General disorders and administration site conditions incl. 1,320 deaths
- 866 Hepatobiliary disorders incl. 53 deaths
- 4,104 Immune system disorders incl. 25 deaths
- 26,800 Infections and infestations incl. 347 deaths
- 11,472 Injury poisoning and procedural complications incl. 153 deaths
- 22,152 Investigations incl. 129 deaths
- 11,805 Metabolism and nutrition disorders incl. 77 deaths
- 151,690 Musculoskeletal and connective tissue disorders incl. 76 deaths
- 536 Neoplasms benign malignant and unspecified (incl cysts and polyps) incl. 17 deaths
- 209,576 Nervous system disorders incl. 872 deaths
- 456 Pregnancy puerperium and perinatal conditions incl. 11 deaths
- 164 Product issues incl. 1 death
- 18,858 Psychiatric disorders incl. 50 deaths
- 3,752 Renal and urinary disorders incl. 49 deaths
- 13,707 Reproductive system and breast disorders incl. 2 deaths
- 35,537 Respiratory thoracic and mediastinal disorders incl. 654 deaths
- 46,297 Skin and subcutaneous tissue disorders incl. 40 deaths
- 1,328 Social circumstances incl. 7 deaths
- 1,199 Surgical and medical procedures incl. 24 deaths
- 24,833 Vascular disorders incl. 395 deaths
Total reactions for the COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson – 1,304 deaths and 78,774 injuries to 25/09/2021
- 737 Blood and lymphatic system disorders incl. 32 deaths
- 1,315 Cardiac disorders incl. 129 deaths
- 26 Congenital, familial and genetic disorders
- 687 Ear and labyrinth disorders incl. 1 death
- 47 Endocrine disorders incl. 1 death
- 1,067 Eye disorders incl. 6 deaths
- 7,102 Gastrointestinal disorders incl. 59 deaths
- 20,536 General disorders and administration site conditions incl. 333 deaths
- 98 Hepatobiliary disorders incl. 9 deaths
- 321 Immune system disorders incl. 7 deaths
- 1,943 Infections and infestations incl. 79 deaths
- 743 Injury, poisoning and procedural complications incl. 17 deaths
- 3,998 Investigations incl. 79 deaths
- 465 Metabolism and nutrition disorders incl. 29 deaths
- 12,263 Musculoskeletal and connective tissue disorders incl. 33 deaths
- 37 Neoplasms benign, malignant and unspecified (incl cysts and polyps) incl. 2 deaths
- 16,253 Nervous system disorders incl. 148 deaths
- 26 Pregnancy, puerperium and perinatal conditions incl. 1 death
- 21 Product issues
- 1,059 Psychiatric disorders incl. 11 deaths
- 311 Renal and urinary disorders incl. 15 deaths
- 1,139 Reproductive system and breast disorders incl. 4 deaths
- 2,786 Respiratory, thoracic and mediastinal disorders incl. 148 deaths
- 2,426 Skin and subcutaneous tissue disorders incl. 5 deaths
- 235 Social circumstances incl. 4 deaths
- 572 Surgical and medical procedures incl. 43 deaths
- 2,561 Vascular disorders incl. 109 deaths

Australia Records 10X More Deaths Following COVID-19 Shots than total of ALL Vaccines for Past 20 Years

Source
By Brian Shilhavy | Health Impact News | September 25, 2021
One of our readers contacted me this week with information that the Australian government collects on vaccine injuries on their Department of Health website. Like many countries, Australia maintains a database of adverse reactions for drugs.
The Australian government database for adverse reactions tracks 78 different vaccines for the past 20 years, with a total of 47 deaths following vaccination during the years 2000 through 2020.
In 2021 for just the 3 COVID-19 vaccines, there have already been a total of 524 deaths recorded following the COVID-19 shots, more than 10X the total for the past 20 years.

And now the Australian government is doing everything they can to lock down the citizens of their country and force them to be injected with one of the COVID-19 shots as a condition for participating in society.
PG&E Charged With Deaths Of 4 In 2020 Wildfire Started By Its Equipment
By Tyler Durden | Zero Hedge | September 24, 2021
Shares of the perennially-troubled PG&E – America’s largest utility whose aging equipment has helped start a rash of deadly wildfires across California – tumbled Friday after the DA in Shasta County hit the company (which just emerged this spring from its second bankruptcy filing in as many decades) with a 31-count indictment, including 11 felonies, and 4 manslaughter charges.
The charges were mostly tied to the 2020 Zogg fire in northern California, where hundreds of homes were destroyed.
During a Friday news conference, Shasta County District Attorney Stephanie Bridgett said her office had determined back in July that PG&E was “criminally liable” for last year’s Zogg Fire, which blazed near the Northern California city of Redding.
“They failed to perform their legal duties. Their failure was reckless, criminally negligent, and resulted in the deaths of four people,” Bridgett said during the briefing.
PG&E’s recent criminal convictions from the last few years, which have been marred by intense wildfire seasons in the West, include pleading guilty last year to 84 counts of involuntary manslaughter tied to the Camp Fire, the 2018 blaze ignited by its long-neglected electrical grid that nearly destroyed the town of Paradise.
It’s also still facing criminal charges from the 2018 Camp Fire in Butte County, the 2019 Kincade Fire in Sonoma County and was on probation from the deadly San Bruno explosion when a 30-inch pipe exploded into flames killing eight people.
Bridgett explained PG&E’s liability thusly: the fire was started because PG&E didn’t remove a tree, which had been marked to be removed in 2013, but never was. A grapevine left in place on that tree caused significant physical defects to its trunk, which ultimately fell on an electrical line during a windstorm on Sept. 27, 2020.
The charges were announced three days before the anniversary of the fire.
“I have determined that we have sufficient evidence to prove beyond a reasonable doubt that the Pacific Gas & Electric Company is criminally liable for their reckless ignition of the Zogg Fire and the deaths and destruction that it caused,” she said at a news conference. “While criminal prosecutions of corporations is rare. One of the primary reasons to charge a corporation criminal is a finding that illegal behavior is widespread and serious. Their failure was reckless and was criminally negligent, and it resulted in the death of four people.”
The indictment counts span from murder to environmental crimes; 20 are misdemeanors.
PG&E said previously the death and destruction caused by the Zogg fire (and all the other fires its equipment has caused) have been “heartbreaking” but that it has resolved civil claims with Shasta County and continues to reach settlements with victims and their families.
“We do not, however, agree with the district attorney’s conclusion that criminal charges are warranted given the facts of this case,” the utility’s statement said after the DA announced her desire to charge the utility this summer.
Of course, the more legal pressure PG&E is facing, the higher the odds that it will simply retreat once again behind bankruptcy protection (what would be its third since 2001) to manage its claims. Though there’s also the threat that its regulator, the Public Utility Board of California, takes over control (something that would probably horrify shareholders).
And, in what’s perhaps the most perverse outcome of all, whatever fines it pays out will be offset by rate hikes borne by its customers, about 16MM people in northern and north-central California. And no matter what happens, next year we’ll get to go through this whole process again since PG&E has already copped to starting more fires this year.
Vaccine effectiveness drops further in the over – 40s, to as low as minus 53%: New PHE report
And That’s a Fact

By Will Jones | The Daily Sceptic | September 24, 2021
It’s official: I am spouting misinformation about the Covid vaccines. Full Fact – the Google, Facebook and George Soros-funded outfit that Ofcom has said it relies on to tell it what to censor regarding COVID-19 – has ‘fact checked‘ my recent piece on PHE data showing negative vaccine effectiveness in August and branded it “incorrect”.
Writer Leo Benedictus – henceforth to be known as the Oracle – takes particular issue with the headline, which he says “falsely claims that a report from Public Health England (PHE) shows the COVID-19 vaccines having ‘negative effectiveness’ in the over-40s”.
“This is not true about the COVID-19 vaccines – nor is it true that the PHE report shows this,” the Oracle declares. Except it is. The data contained in the report is completely clear, and the calculation of unadjusted vaccine effectiveness from that data is straightforward.
According to the Oracle, however, this is not a valid way of estimating vaccine effectiveness. Benedictus quotes the PHE report stating as much – “The vaccination status of cases, inpatients and deaths is not the most appropriate method to assess vaccine effectiveness and there is a high risk of misinterpretation” – and notes that I too quote this. What he fails to acknowledge, though, is that I also examine the reason PHE gives for this claim and counter it.
The only substantive reason PHE gives that vaccine effectiveness might be underestimated in its data is that “vaccination has been prioritised in individuals who are more susceptible or more at risk of severe disease”. In other words, the high-risk are over-represented in the vaccinated and this skews the sample. I countered that the large majority of the older age groups are now vaccinated so this bias should be very much reduced. Of course, we also need to ask why, if this is supposedly the key confounder of the data presented, we are not also provided with the necessary data on risk categories so that it can be duly quantified and accounted for.
Benedictus reiterates PHE’s claim that vaccine effectiveness should only be estimated via the published studies. However, as I noted in my article, these studies are riddled with serious problems and inconsistencies that bring their findings into question. They are also out of date since they don’t cover the Delta surge, which is the first time the vaccines have really been stress-tested in the U.K.
Benedictus spends half the ‘fact check’ in a bizarre attempt to argue that my vaccine effectiveness calculation is wrong because I used the data PHE itself used for the size of the unvaccinated population. He points out it is different to the ONS figures on this. Er, take that one up with PHE, Leo.
It does seem at times that Benedictus is fact-checking the PHE report rather than my article. At one point he takes the report to task because one of its charts sowed confusion as it “seemed to show for the month in question (August 9th to September 5th) that people in their 40s, 50s, 60s and 70s were more likely to test positive for Covid if they had been vaccinated than if they hadn’t”.
Except the chart didn’t ‘seem’ to show that; it did show that. Again though we are told that this data does “not give a reliable estimate of vaccine effectiveness” because of biases in the samples.
But who defines what makes an estimate of vaccine effectiveness ‘reliable’ enough to be permitted without being labelled false? All vaccine efficacy estimates have limitations arising from the limitations of the data, including those produced by PHE. I was careful to acknowledge the limitations of the estimates I was making, saying they were unadjusted for risk factors – though argued that this shouldn’t matter so much anymore given high coverage. There’s also the point that being high-risk may affect the risk of serious disease and death but there’s no reason to think it will have an impact on infection rates (save for the small number of immuno-compromised).
The unmistakable impression here is of a gatekeeping exercise by the Government and its outriders to ensure it controls the concept of vaccine effectiveness and no one unauthorised is allowed to make an estimate of it. Thus the availability of the data is carefully controlled and we only get a month at a time and without the additional data that would allow us to control for the supposed biases that the report tells us the data includes and which ‘invalidate’ any attempt to make an unauthorised calculation of vaccine effectiveness.
None of this concept-policing does anything to alter the facts, however. In recent weeks reported infection rates have been higher in the double vaccinated than in the unvaccinated for the over-40s. That means that, for this period, (unadjusted) vaccine effectiveness is negative in those age groups.
PHE has published two new reports since my article and in each the unadjusted vaccine efficacy has declined further. Here is the table using data from the latest report, covering August 23rd to September 19th (the related chart from the report itself is above).

It shows that in the two weeks since my article the vaccine effectiveness has dropped further, with unadjusted vaccine effectiveness in the over-40s now hitting as low as minus-53% among people in their 60s. This means that, on this data for this age group, the double vaccinated experienced a 53% higher reported infection rate than the unvaccinated in the past month. And that’s a fact.
Stop Press: Professor Norman Fenton and Professor Martin Neil on the Probability and Risk site have used age-adjusted all-cause mortality to estimate vaccine effectiveness and found that mortality rates are currently higher in the vaccinated than the unvaccinated.
Stop Press 2: Professor David Paton has produced a good Twitter thread responding to one of the more well-informed critics of this (and other) pieces citing the PHE data.
More Than 726,000 COVID Vaccine Injuries Reported to VAERS as CDC, FDA Overrule Advisory Committees’ Recommendations on Third Pfizer Shot
By Megan Redshaw | The Defender | September 24, 2021
Data released Sept. 17 by the Centers for Disease Control and Prevention (CDC) showed that between Dec. 14, 2020 and Sept. 17, 2021, a total of 726,965 adverse events following COVID vaccines were reported to the Vaccine Adverse Event Reporting System (VAERS). The data included a total of 15,386 reports of deaths — an increase of 461 over the previous week.
There were 99,410 reports of serious injuries, including deaths, during the same time period — up 7,887 compared with the previous week.
Excluding “foreign reports” filed in VAERS, 569,294 adverse events, including 6,981 deaths and 44,481 serious injuries, were reported in the U.S. between Dec. 14, 2020 and Sept. 17, 2021.
Of the 6,981 U.S. deaths reported as of Sept. 17, 12% occurred within 24 hours of vaccination, 17% occurred within 48 hours of vaccination and 30% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
In the U.S., 383.6 million COVID vaccine doses had been administered as of Sept. 17. This includes: 220 million doses of Pfizer, 149 million doses of Moderna and 15 million doses of Johnson & Johnson (J&J).

The data come directly from reports submitted to VAERS, the primary government-funded system for reporting adverse vaccine reactions in the U.S.
Every Friday, VAERS makes public all vaccine injury reports received as of a specified date, usually about a week prior to the release date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.
This week’s U.S. data for 12- to 17-year-olds show:
- 20,238 total adverse events, including 1,213 rated as serious and 21 reported deaths. Two of the 21 deaths were suicides.
The most recent deaths involve a 17-year old male (VAERS I.D. 1689212) with cancer who was vaccinated April 17, tested positive for COVID on July 20, was hospitalized and passed away Aug. 29; and a 16-year old female (VAERS I.D. 1694568) who died from a pulmonary embolism nine days after receiving her first Pfizer dose.
Other recent reported deaths include two patients [VAERS I.D. 1655100] who died after their second dose of Pfizer, including a 13-year old female, a 15-year-old boy (VAERS I.D. 1498080) who previously had COVID, was diagnosed with cardiomyopathy in May 2021 and died four days after receiving his second dose of Pfizer’s vaccine when he collapsed on the soccer field and went into ventricular tachycardia; and a 13-year-old girl (VAERS I.D. 1505250) who died after suffering a heart condition after receiving her first dose of Pfizer.
- 3,058 reports of anaphylaxis among 12- to 17-year-olds with 99% of cases
attributed to Pfizer’s vaccine. - 502 reports of myocarditis and pericarditis (heart inflammation) with 494 cases attributed to Pfizer’s vaccine.
- 108 reports of blood clotting disorders, with all cases attributed to Pfizer.
This week’s U.S. VAERS data, from Dec. 14, 2020 to Sept. 17, 2021, for all age groups combined, show:
- 20% of deaths were related to cardiac disorders.
- 54% of those who died were male, 42% were female and the remaining death reports did not include gender of the deceased.
- The average age of death was 72.9.
- As of Sept. 17, 3,726 pregnant women reported adverse events related to COVID vaccines, including 1099 reports of miscarriage or premature birth.
- Of the 2,835 cases of Bell’s Palsy reported, 50% were attributed to Pfizer vaccinations, 42% to Moderna and 8% to J&J.
- 606 reports of Guillain-Barré syndrome, with 39% of cases attributed to Pfizer, 33% to Moderna and 27% to J&J.
- 152,309 reports of anaphylaxis with 42% of cases attributed to Pfizer’s vaccine, 50% to Moderna and 7% to J&J.
- 9,441 reports of blood clotting disorders. Of those, 4,047 reports were attributed to Pfizer, 3,442 reports to Moderna and 1,903 reports to J&J.
- 2,537 cases of myocarditis and pericarditis with 1,608 cases attributed to Pfizer, 825 cases to Moderna and 95 cases to J&J’s COVID vaccine.
© 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
Here’s the skinny on what happened yesterday and today regarding the booster dose
By Meryl Nass, MD | September 23, 2021
Last Friday, FDA’s advisory committee (VRBPAC) voted 16 to 2 against giving a license to a third Pfizer booster shot for everyone age 16 and up.
Although a second vote at Friday’s meeting had not been planned, another question was hastily developed. That question asked whether the vaccine could be licensed for a third booster dose for high risk people under the age of 65. That vote got a unanimous yes.
The panels decisions are not final. The FDA is obliged to take the panels advice into consideration, but it is not required to adopt it. So yesterday, the FDA issued a license for the Pfizer vaccine for the booster dose.
But in doing so, FDA added an additional category of people for the booster dose, a category that had not been included in the Advisory Committee’s vote:
- “individuals 18 through 64 years of age whose frequent institutional or occupational exposure to SARS-CoV-2 puts them at high risk of serious complications of COVID-19 including severe COVID-19.”
This is what I call weasel wording. This statement does not make sense. People whose occupation puts them at high risk of exposure to COVID are no more likely to be at high risk of serious complications or severe COVID-19 than anyone else. They are at higher risk of developing COVID, but not at higher risk of serious COVID.
What FDA did (and you know who did this: Peter Marks, head of CBER and Janet Woodcock, acting Commissioner, are the only people with the authority to come up with this BS) was to take the VRBPAC approval for people with underlying conditions that put them at high risk for severe COVID, and twist it into an approval for all health care workers, staff at schools and colleges, grocery store workers, big box employees, etc.
Why? Because a license is necessary to impose a mandate, that’s why.
It looked like the weasels had won again. However, there was a small hoop left to jump through before any mandates came down.
While FDA determines how a drug or vaccine should be licensed or authorized for use, the CDC’s ACIP committee is the group responsible for creating the recommendations for use of the vaccine in different demographic groups.
And so ACIP did what it never does. It rejected the CDC’s proposal to widen the license for the third dose to all with potential occupational exposures. the ACIP limited their approval to what the FDA advisory committee had voted for last Friday. As CNBC noted,
… Dr. Leana Wen [member of the Council on Foreign Relations and the World Economic Forum], an emergency physician and former Baltimore health commissioner, on Twitter called the CDC panel’s vote to reject boosters more widely a “mistake.”
“Really, we are not allowing healthcare workers, many of whom got vaccinated in back in December, to get a booster? What about teachers in cramped classrooms where masks aren’t required?” she tweeted, adding CDC Director Dr. Rochelle Walensky should overrule the recommendation.
… In a paper published days before an FDA advisory meeting last week, a leading group of scientists said available data showed vaccine protection against severe disease persists, even as the effectiveness against mild disease wanes over time. The authors, including two high-ranking FDA officials and multiple scientists from the World Health Organization, contended in the medical journal The Lancet that widely distributing booster shots to the general public is not appropriate at this time.
I think 2 things happened. The propaganda that the vaccines still prevent serious disease while perhaps not preventing mild disease stood in the way of approving boosters to prevent mild disease. Why give a potentially dangerous booster to prevent a cold? It doesn’t make sense.
Second, everyone on those committees knew that if the vaccine’s third dose did get approved for a huge swath of the general public, it would be mandated for themselves in no time. A third dose would have been required for every member of both FDA’s and CDC’s advisory committees. I don’t think they were ready for that. And maybe they weren’t ready for the resistance from those who took the 2 shots thinking they were done… and now, it seems they could get into a situation where they could be fired for not having a third dose. What about more and more doses?
Or maybe the large demonstrations in Australia and Europe were influencing those advisory committee members…
Facebook and Instagram delete Project Veritas vaccine video for “misinformation” that could cause “harm”
By Cindy Harper | Reclaim The Net | September 21, 2021
Facebook and its subsidiary Instagram have removed a new video from the undercover reporting operatives Project Veritas under its “misinformation” policy.
“We encourage free expression, but we don’t allow false information about COVID-19 that could contribute to physical harm,” the Facebook message shared with Project Veritas read.

Facebook didn’t specifically state which part of the video caused them to decide to delete it.
The video in question featured a whistleblower from the Health and Human Services Department (HHS), registered nurse Jodi O’Malley, making allegations that the federal government were underreporting the side effects of the COVID-19 vaccines.
In the video, O’Malley was discussing with Dr. Maria Gonzales, an ER doctor, who alleges that not all patients suffering from heart inflammation after taking the vaccine are being reported. “But now, they [the government] are not going to blame the vaccine,” Dr. Gonzales said of a patient who had suspected myocarditis.
On hearing of Facebook and Instagram removing the video, O’Keefe made another video sharing the news of the deletion of the video. “We’ve just learned that Facebook and Instagram have taken down this video, and we have a screenshot here which we received from Instagram… It says ‘your post goes against our community standards on misinformation that could cause physical harm.”
O’Malley disputed that the video contained any misinformation. “All I did was just record it,” O’Malley said. “I recorded their statements and I recorded the actual diagnosis, right, now they’re telling the physician the diagnosis [of the] patient is misinformation.”
The deletion of users’ posts based on Facebook’s policy on removing content about “COVID-19 that could contribute to physical harm” was first reported around April of 2021 and is often used on posts that question the safety of the COVID-19 vaccines.
Nearly 15,000 Deaths, More than 700,000 Injuries Reported to VAERS Since Dec. 2020 COVID Vaccine Rollout in US
By Megan Redshaw | The Defender | September 20, 2021
Data released Sept. 17 by the Centers for Disease Control and Prevention (CDC) showed that between Dec. 14, 2020 and Sept. 10, 2021, a total of 701,561 adverse events following COVID vaccines were reported to the Vaccine Adverse Event Reporting System (VAERS). The data included a total of 14,925 reports of deaths — an increase of 419 over the previous week.
There were 91,523 reports of serious injuries, including the reports of deaths, during the same time period — up 3,352 compared with the previous week.
Excluding “foreign reports” filed in VAERS, 559,462 adverse events, including 6,756 deaths and 43,073 serious injuries, were reported in the U.S. between Dec. 14, 2020 and Sept. 10, 2021.
Of the 6,756 U.S. deaths reported as of Sept. 10, 12% occurred within 24 hours of vaccination, 17% occurred within 48 hours of vaccination and 31% occurred in people who experienced an onset of symptoms within 48 hours of being vaccinated.
In the U.S., 378.2. million COVID vaccine doses had been administered as of Sept. 10. This includes: 216 million doses of Pfizer, 148 million doses of Moderna and 15 million doses of Johnson & Johnson (J&J).

The data come directly from reports submitted to VAERS, the primary government-funded system for reporting adverse vaccine reactions in the U.S.
Every Friday, VAERS makes public all vaccine injury reports received as of a specified date, usually about a week prior to the release date. Reports submitted to VAERS require further investigation before a causal relationship can be confirmed.
This week’s U.S. data for 12- to 17-year-olds show:
- 19,827 total adverse events, including 1,169 rated as serious and 19 reported deaths. Two of the 19 deaths were suicides.
The most recent death involves one report of two patients [VAERS I.D. 1655100] who died after their second dose of Pfizer, including a 13-year old female.
Other recent reported deaths include a 15-year-old boy (VAERS I.D. 1498080) who previously had COVID, was diagnosed with cardiomyopathy in May 2021 and died four days after receiving his second dose of Pfizer’s vaccine on June 18, when he collapsed on the soccer field and went into ventricular tachycardia; and a 13-year-old girl (VAERS I.D. 1505250) who died after suffering a heart condition after receiving her first dose of Pfizer.
- 2,972 reports of anaphylaxis among 12- to 17-year-olds with 99% of cases
attributed to Pfizer’s vaccine. - 488 reports of myocarditis and pericarditis (heart inflammation) with 481 cases attributed to Pfizer’s vaccine.
- 106 reports of blood clotting disorders, with all cases attributed to Pfizer.
This week’s U.S. VAERS data, from Dec. 14, 2020 to Sept. 10, 2021, for all age groups combined, show:
- 20% of deaths were related to cardiac disorders.
- 54% of those who died were male, 42% were female and the remaining death reports did not include gender of the deceased.
- The average age of death was 72.9.
- As of Sept. 10, 3,650 pregnant women reported adverse events related to COVID vaccines, including 1076 reports of miscarriage or premature birth.
- Of the 2,783 cases of Bell’s Palsy reported, 50% were attributed to Pfizer vaccinations, 42% to Moderna and 8% to J&J.
- 593 reports of Guillain-Barré syndrome, with 39% of cases attributed to Pfizer, 33% to Moderna and 27% to J&J.
- 149,681 reports of anaphylaxis with 42% of cases attributed to Pfizer’s vaccine, 51% to Moderna and 7% to J&J.
- 9,260 reports of blood clotting disorders. Of those, 3,968 reports were attributed to Pfizer, 3,376 reports to Moderna and 1,866 reports to J&J.
- 2,452 cases of myocarditis and pericarditis with 1,545 cases attributed to Pfizer, 806 cases to Moderna and 93 cases to J&J’s COVID vaccine.
© September 20, 2021 Children’s Health Defense, Inc. This work is reproduced and distributed with the permission of Children’s Health Defense, Inc. Want to learn more from Children’s Health Defense? Sign up for free news and updates from Robert F. Kennedy, Jr. and the Children’s Health Defense. Your donation will help to support us in our efforts.
More Evidence Emerges That Long Covid Is A Load Of Bollox
By Richie Allen | September 17, 2021
The Office for National Statistics (ONS) has suggested that more than half of those who believe that they have so-called long covid, may just be suffering from normal bouts of ill health.
The ONS looked at 27,000 people who tested positive for covid. Three different methods were used to estimate the prevalence of long covid. One analysis found that 5 per cent reported at least one symptom 12 to 16 weeks after their infection.
But, the ONS found that 3.4 per cent of people who didn’t have covid reported the same long covid symptoms.
According to The Telegraph :
Kevin McConway, emeritus professor of applied statistics at The Open University, said: “That’s not all that much less than the 5.0 per cent for the infected people, which does show that having one or more of these symptoms isn’t uncommon regardless of Covid-19.”
Long Covid symptoms are fever, headache, muscle ache, weakness/tiredness, nausea/vomiting, abdominal pain, diarrhoea, sore throat, cough, shortness of breath, loss of taste and loss of smell.
The ONS said however, that these symptoms are common in the general population.
The long covid fairy-tale is coming apart at the seams. Earlier this month, University College London produced a study that concluded that the danger of long covid to children had been wildly exaggerated.
Dr Michael Absoud, honorary reader at the department of women and children’s health at King’s College London told The Telegraph :
“The ONS are to be congratulated for engaging with clinicians and scientists to review their methodology and provide updated estimates on post-Covid symptoms. The ONS first published the approach in April 2021, and reported a 12-week prevalence of long Covid in 14 per cent. This has now been revised down to 3 per cent in the latest estimate.”
The ONS and University College London are to be congratulated for doing their jobs. Long covid was invented to encourage uptake of covid jabs. Covid itself (if it exists) is a mild respiratory illness, dangerous only to the very elderly and those with underlying health conditions.
Knowing that covid itself wasn’t enough to send folks rushing to the jabbatoirs, they needed to come up with something else to convince them that covid was far more serious. Long covid was perfect. They attributed so many common symptoms to it, that anyone at anytime could claim to be suffering from it.
I called it bollox last year. Scientists are calling it bollox today.
Hospital Beds Are Filling Up — With Children. But It’s Not What You Think
By Dr. Joseph Mercola | September 13, 2021
Children with nowhere else to go because of the nature of their illness occupy a third of acute-care hospital beds in England. In the midst of the COVID-19 pandemic, these children are suffering from mental health and neurological problems.
Some have violent or self-harming behavior; others have severe neurodevelopment disorders. Still others are there due to an eating disorder. Yet, despite their individual needs, many have no specific psychiatric diagnosis.
And, without a diagnosis, they don’t qualify for a bed in a true psychiatric ward, even when they are so violent that they become a danger not only to themselves, but to everyone around them. What this means is these children end living at a regular hospital, sometimes for months.
What’s even more concerning is that since the pandemic began, the number of children in these beds has increased dramatically.
In the U.S., “children’s hospitals around the country say they have seen a meteoric rise in the number of children who need mental health help,” CNN said. “Several children’s hospitals said the supply of inpatient psychiatric beds has been so short, they’ve had to board kids in their emergency departments — sometimes for weeks.”
SOURCES:
Czech Republic might have to destroy 45,000 AstraZeneca doses as demand for the jab nosedives
RT | September 13, 2021
Prague might have to dispose of thousands of AstraZeneca’s Covid-19 vaccine doses as they expire next month. The demand for the jab recommended only to those over 60 years old due to possible side-effects remains low.
Some 55,000 doses of the vaccine manufactured by Anglo-Swedish company AstraZeneca and shipped to the Czech Republic are set to expire by the end of October, Czech radio station IROZHLAS reported. While some 10,000 of them are expected to be used to administer second doses, the remaining batches might have to be incinerated if the demand for the jab fails to shoot up.
So far, it has been hitting rock bottom. According to the data cited in the report, only 36 people have chosen AstraZeneca for their first dose in September, and a total of 774 people have been vaccinated with it so far.
In the span of July and August, only about 1,200 of those newly vaccinated opted for AstraZeneca’s vaccine, a tiny fraction of some 860,000 people who applied for their first dose within that period.
Some 14,000 doses of AstraZeneca’s vaccine were thrown away in the past month alone due to the lack of interest from the public, Czech media reported.
The apparent lack of popularity has been blamed on the fact that the Czech health ministry recommends AstraZeneca and Johnson&Johnson’s Covid-19 vaccines only to those older than 60 years since June. The precaution was introduced after the vaccines were suspected of causing potentially deadly blood clots detected in some younger people after they received the jab. Although the cases are reported to be rare, several countries, including the Czech Republic, limited or halted the use of the vaccine.
Spokesman for the Czeh Ministry of Health, Daniel Köppl, admitted that the government expects that not all outstanding doses could be used before time runs out. And while Prague has donated over 200,000 of doses, including that of AstraZeneca, to other countries before, this time the batches can’t be salvaged due to legal hurdles, he told the outlet over the weekend.
The problem is that the unused doses have already been delivered and distributed across the country. “The law does not allow us to donate these vaccines, because the moment they are removed from the controlled distribution chain, they are expected to be used. They cannot be passed on,” Köppl said.
So far, some 55 percent of the eligible Chezh population have been fully vaccinated, while the authorities set 75% vaccination rate as their target.
Red Cross issues warning to stop blood plasma donations from vaccinated people
Natural News | September 2, 2021
If you took a Wuhan coronavirus (Covid-19) “vaccine,” the American Red Cross will not accept blood plasma donations from you due to the inherent toxicity issues caused by the injection.
As it turns out, convalescent plasma should only be collected from the unvaccinated who still have clean blood that has not been contaminated with deadly spike proteins and other chemicals that threaten to kill those who receive blood transfusions.
Thanks to “Operation Warp Speed,” there is now a massive shortage of pure blood in the United States that has not been tainted with genetic modifications and other damage. Mass vaccination, in other words, is effectively killing people who desperately need unvaccinated blood but cannot find it.
A now-archived document from the American Red Cross explains that anyone who takes “any type of COVID vaccine” is “not eligible to donate convalescent plasma” because of the serious risks involved.
“One of the Red Cross requirements for plasma from routine blood and platelet donations that test positive for high-levels of antibodies to be used as convalescent plasma is that it must be from a donor that has not received a COVID-19 vaccine,” the document explains.
Scientifically speaking, it is critical for those receiving donor blood to have sufficient antibodies directly related to their own immune systems. Tainted blood from vaccinated people does not qualify.
“This is to ensure that antibodies collected from donors have sufficient antibodies directly related to their immune response to a COVID-19 infection and not just the vaccine, as antibodies from an infection and antibodies from a vaccine are not the same.”
Red Cross discontinues convalescent plasma donation program entirely after FDA rule change
The U.S. Food and Drug Administration (FDA) apparently thinks differently about vaccinated blood.
A new document on the Red Cross website now explains that because the FDA “allows people who have received a COVID-19 vaccine to donate dedicated COVID-19 convalescent plasma,” the Red Cross has decided to discontinue its convalescent plasma donation program entirely.
“The FDA allows people who have received a COVID-19 vaccine to donate dedicated COVID-19 convalescent plasma within six months of their infection of the virus, based on data that antibodies from natural infection can decline after six months however, the Red Cross has discontinued our convalescent plasma collection program,” the new document explains.
In other words, it would appear as though the Red Cross is not comfortable continuing to collect and administer convalescent plasma from people who took the jab, even though the FDA claims that doing so is completely safe.
This type of thing is par for the course for the FDA, which rarely promotes policies that benefit actual human beings. The agency really is nothing more than an extension of Big Pharma that does whatever is necessary to keep the profits flowing – even at the expense of human life.
“The antibodies naturally produced by covid infection actually work,” wrote one commenter at Citizen Free Press.
“The antibodies artificially produced by covid vaccines do not work as well, and actually wipe out the natural covid antibodies. This is why vaccinated people are increasingly becoming significantly ill with covid.”
Another commenter wrote that the Red Cross is denying that it does not accept convalescent plasma from vaccinated people, even though the document on its website claims otherwise.
“The FDA says that you can donate convalescent plasma within six months of infection, even if you’ve been vaccinated,” this person wrote, calling it a “legal lie.”
“But the Red Cross guidelines prohibit them from using convalescent plasma if the individual has been vaccinated.”
The latest news about the how Chinese Virus injections contaminate a person’s blood can be found at ChemicalViolence.com.
Sources for this article include:

