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February 09, 2021

Experimental COVID Vaccines: Mounting Deaths Reported in Media and Social Media Continue … Part 4 of 10

Overview:

Deaths and adverse events following COVID vaccines continue to mount. To date, estimated incidence (adjusted for underreporting) of adverse events following each COVID vaccine is now: for every experimental COVID shot given, 1 person in approximately every 26 would report an adverse event (AE); 1 in approximately every 162 to 2,103 would report a serious adverse event (SAE), and 1 in approximately every 579 to 7,519 would report a death (if all AEs, SAEs and deaths were reported). Unheeded warnings from medical specialists to FDA, vaccine manufacturers, and press prove true. Global agencies reverse prior warnings on vaccinating pregnant women despite growing evidence of miscarriage, premature labor, and fetal death. Serious and fatal cardiac adverse events surge worldwide. Widespread violation of medical ethical principle of informed consent. Updated death reports and more, in today’s article.


By Dawn Amittai

Worldwide Administration of Experimental COVID Vaccines Hits 128 Million Doses

vaccines administeredAs COVID vaccination programs continue rolling out worldwide, we have surpassed 100 million doses administered in a total of 73 countries. In the U.S. alone, more than 30 million Americans have had their first shot. See Table 1 for the most recent figures.   

 

The Experimental COVID Vaccines: The Trail of Death and Serious Injuries Continues to Mount…

As of January 29, 2021, CDC’s Vaccine Adverse Event Reporting System (VAERS) currently lists 501 deaths — 404 in the U.S., 48 “foreign” and 49 “unknown” — in their system. An additional 400 deaths have been published by the media through February 7th, 2021. The previous week, VAERS listed 329 deaths following COVIDCOVID Vaccine Deaths by Country-19 vaccines, with an additional 156 published in the media. See Table 2 for the most recent numbers itemized by country.

During this same period — through January 29th — a total of 11,249 adverse events were entered into VAERS, including 1,791 considered serious (see VAERS data reports). As always, keep in mind that these COVID-vaccine related adverse events and deaths reported to the VAERS System are known to represent fewer than 1% of all the actual vaccine adverse events and only 1-13% of serious adverse events/deaths. More accurate figures are obtained by multiplying the number of reported adverse events by 100 (i.e., to account for the fewer than 1% reported), and serious events and deaths by 7.7 and again by 100, to account for the range of 1-13% reported. More accurate numbers, adjusted for under-reporting could be: 1,124,900 adverse events (AEs), 13,791 to 179,100 serious adverse events (SAEs), and 3,857 to 50,100 deaths to date (if all AEs, SAEs, and deaths were reported).

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The distribution of deaths in the U.S. listed by state is displayed in Table 3. California leads the death statistics with 45 fatalities reported to date, Florida is next with 24, followed by New York with 22 reported deaths. Again, fewer than 1% of all the actual vaccine adverse events and only 1-13% of serious events/death are reportedThe CDC also publishes an up-to-date tally of the number of vaccines administered in each state here.table3 vaccine deaths by vaers

The CDC reports that 20,598,212 Pfizer-BioNTech vaccines and 18,336,515 Moderna vaccines have been administered in the U.S. to date. The Pfizer vaccine received its Emergency Use Authorization (EUA) by the FDA on December 11th, one week prior to Moderna’s. This explains why Pfizer continues their lead over Moderna in having administered more vaccines. AstraZeneca’s experimental vaccine was authorized for emergency use in UK on December 30th, and their rollout began first week of January; India’s brand of the AstraZeneca vaccine, Covishield, began administration January 16th in India. Currently, Pfizer’s shot continues its lead in the numbers of deaths following vaccination, as reported by VAERS and the media (see Table 4).

table4 vaccine deaths by manufacturer

Highlighting the Serious Limitations Inherent in the Vaccine Adverse Reporting System (VAERS)

There are many limitations to obtaining accurate up-to-date information from VAERS. First, VAERS website data is almost never current — reported adverse events and deaths are often backlogged, rarely entered in a timely fashion. In fact, the website even details its own limitations: “The number of reports alone cannot be interpreted or used to reach conclusions about the existence, severity, frequency, or rates of problems associated with vaccines… data are subject to limitations of under-reporting, reporting bias, and lack of incidence rates in unvaccinated comparison groups.” VAERS cannot demonstrate causation.  Despite these known limitations, VAERS is the only vaccine adverse event reporting system available to the public.

VAERS is a passive reporting system with low awareness. Even though medical doctors are legally required to report any post-vaccination reactions to VAERS, a CDC-funded study at Harvard Pilgrim found fewer than 1% of all the actual vaccine adverse events and only 1-13% of serious events/death are reported. More accurate figures are obtained by multiplying the number of reported adverse events by 100, and serious events and deaths by 7.7.

Illustrating the Mounting Deaths and Serious Adverse Events Following Experimental COVID Vaccines

Using data provided by Bloomberg’s COVID-19 Vaccine Tracker, we obtained the total number of vaccine doses administered to Americans by January 29th — the most recent date VAERS uploaded reports to their system — and calculated the estimated incidence of adverse events and deaths reported by VAERS per the number of vaccines administered (see Table 5). To date estimated incidence (adjusted for underreporting) for every experimental COVID shot given, 1 person in approximately every 26 would report an adverse event (AE); 1 person in approximately every 162 to 2,103 would report a serious adverse event (SAE), and 1 person in approximately every 579 to 7,519 would report a death  if all AEs, SAEs, and deaths were reported. 

 

Revisiting the Use of Experimental COVID Vaccines in Pregnancy

Last week we touched upon the deeply troubling issue of the use of experimental COVID vaccines during pregnancy. We reported that neither the Pfizer or the Moderna COVID vaccines have been tested on pregnant women, yet the World Health Organization (WHO) issued the recommendation that “… based on what we know about this kind of vaccine, we don’t have any specific reason to believe there will be specific risks that would outweigh the benefits of vaccination for pregnant women.” Again, this raises the question, how did they arrive at that conclusion? This week, Dr. Fauci declared “…there have been “no red flags” from 10,000 pregnant women who have had the COVID-19 vaccine in the US.”Fauci No Red Flags

Considering that a simple search of VAERS data on pregnant women who received at least one of these experimental mRNA vaccines, turns up more than a dozen showing premature labor, miscarriages, and fetal deaths, do these not qualify as “red flags” Dr. Fauci?  Why, even a glance at *Twitter this week brought a sad story of an MD who had a 14-week pregnancy when she took one of these vaccines, and joyfully tweeted (see Tweet), “14 weeks pregnant and fully vaccinated! [*injuries and deaths reported on social media are unconfirmed]. I got the #CovidVaccine to protect myself, my baby, my family, my patients, and my community! When it’s available to you, I encourage you to do the same!” Just one week later, she tweeted, “…and it’s with a heavy heart that I tell my #MedTwitter family that I’ve suffered a miscarriage at 14 ½ weeks…” No red flags, Dr. Fauci? Really? How can our health “authorities” be missing such easily observable, critical evidence? How can we trust their recommendations, and put our lives and that of our precious loved ones in their hands?

Following Dr. Fauci’s announcement, Dr. Sherry Tenpenny, a triple-board certified osteopathic medical doctor and an expert on the potential adverse impact of vaccines on health, tweeted a critical point: “Remember that these injections are not approved for anyone under 16, so how it is ok for babies in utero?” Excellent question, Dr. Tenpenny! And for that matter, do we have any idea of the potential effects these emergency-authorized, experimental, mRNA vaccines might have on the developing fetus? There has simply not been sufficient time — with the warp speed development of these brand-new technology vaccines and their hasty rollout — to obtain critical short-term safety data… let alone long-term! So, how can we have any idea what we might be seeing — if and when these vaccine-exposed babies are born?

Unheeded Warnisara beltran mdngs from Medical Specialists on COVID Vaccines Part I: Focus on Cardiac-Related Complications

Around the world, reports of people dying shortly after receiving the COVID-19 vaccines have been pouring in — from Norway, UK, Germany, India, Gibraltar and more — where sudden death has occurred within hours or days of getting the shot. Tragic reports have just come in from Italy of 3 young hospital healthcare workers dying from untimely heart attacks or sudden cardiac arrest, shortly after receiving experimental Pfizer mRNA COVID injections. A 45-year-old doctor “iitalian medical deadn the prime of his life and in perfect health” dropped dead from a heart attack, a 42-year-old surgical technician was found dead in bed from a heart attack, and a 39-year-old nurse dies from sudden cardiac arrest.  Are these startling, untimely deaths not cause for alarm? The journalist went on to comment, “We are just supposed to believe that these 3 young hospital workers all died of cardiac arrest from ‘natural causes’ despite no pre-existing conditions, and that this has nothing to do with the experimental Pfizer mRNA COVID injections.” Do an equal number of young people die of cardiac arrest in the days leading up to their COVID vaccine administration?  If cardiac arrest in young healthy people is normal, we would see this before their first vaccine appointment as well. Why could we not have anticipated these catastrophic events? Sadly, it turns out that there have been a number of medical specialists who have been sounding warnings to our health regulatory agencies, precisely predicting these consequences.

In early December 2020, J. Patrick Whelan, M.D. PhD, a pediatric specialist caring for children with multisystem inflammatory syndrome, expressed his concerns in a warning letter to the FDA about the Moderna and Pfizer COVID vaccines: “I am concerned about the possibility that the new vaccines aimed at creating immunity against the SARS-CoV-2 spike protein (including the mRNA vaccines of Moderna and Pfizer) have the potential to cause microvascular injury to the brain, heart, liver, and kidneys in a way that does not currently appear to be assessed in safety trials of these potential drugs.” After citing research to validate his concerns, he concluded, “While there are pieces to this puzzle that have yet to be worked out, it appears that the viral spike protein that is the target of the major SARS-CoV-2 vaccines is also one of the key agents causing the damage to distant organs that may include the brain, heart, lung, and kidney. Before any of these vaccines are approved for widespread use in humans, it is important to assess in vaccinated subjects the effects of vaccination on the heart…” This warning letter was posted by the FDA on December 8, 2020. Clearly, these concerns have not yet been heeded by the FDA or any other U.S. public health agency for that matter

Similar concerns are now being echoed by Hooman Noorchashm, M.D., Ph.D., a physician-scientist specialist in cardiothoracic surgery, who wrote a warning letter to FDA regulators, Pfizer leaders and the press on January 26th. His primary concern is that those patients who have had a recent COVID-19 infection and receive a COVID vaccine, are likely to suffer from autoimmune attacks along the ACE-2 receptors (i.e., ACE-2 is a protein on the surface of many cell types whereby the SARS-CoV-2 virus enters the body to cause infection) present in the heart, and in the microvasculature of the brain, liver and kidney. When the immune system attacks those tissues, it causes inflammation, which can lead to clot formation, and result in heart attack, stroke, and so on. Dr. Noorchashm warned, “As an immunologist with a good understanding of how antigen specific immune responses could cause organ and tissue specific damage, I am recommending to you, as our lead FDA regulators, not to gloss over the real possibility that vaccinating persons with pre-existing SARS-CoV-2 viral antigens in their tissues could cause that subset of people grave harm — and especially the frail with cardiovascular disease.

Lyn Redwood, RN, MSN, director and president emerita of Children’s Health Defense followed by issuing a plea to the FDA and CDC to protect the health of Americans by convening emergency meetings to review these concerns, and issue new guidelines for vaccine administration to address them. She cautioned, “Ignoring these valid and scientifically supported warnings from leading physicians may result in hundreds of millions of people suffering potentially deadly injuries or permanent damage following vaccination.” As mounting evidence of their predictions is revealed by the alarming numbers of deaths we are now seeing after these experimental vaccines are administered, why are these warnings and pleas from our medical experts being ignored by our regulatory agencies and vaccine manufacturers? Why even a simple search of VAERS — with all its inherent limitations — reveals a large number of cardiac-related events and deaths just up through the data entered into their system by January 29th. cardiac vaers

A VAERS search for serious and fatal cardiac-related events revealed 140 serious cardiac adverse events and 77 cardiac events resulting in death. These reports include people of all age groups, even in those aged 17-44 (see Table 6). Keep in mind that these are only those cases entered into VAERS by January 29th, and that these likely represent fewer than 1% of all the actual vaccine adverse events and only 1-13% of serious events/death. Some examples of individual cases are: 

  • 23-year-old male in NY: “Patient developed 104.4 temp approximately 48 hours after being given the vaccine. I treated him with antibiotics, IV fluids, cooling methods. CXR does show a new right perihilar infiltrate. However, his fever came down within the next 24-48 hours. Unfortunately, he suffered a cardiac arrest on 1/21/21 in the early morning and expired.”
  • 56-year-old male from Florida: “Cardiac arrest within 1 hour Patient had the second vaccine approximately 2 pm on Tuesday Jan 12th He works at the extended care community and was in good health that morning with no complaints. He waited 10-15 minutes at the vaccine admin site and then told them he felt fine and was ready to get back to work. He then was found unresponsive at 3 pm within an hour of the 2nd vaccine. EMS called immediately worked on him 30 minutes in field then 30 minutes at ER was able to put him on life support yet deemed Brain dead 1-14-21 and pronounced dead an hour or so later.”
  • 58-year-old female from Washington: “Vaccine received at about 0900 on 01/04/2021 at her place of work, Medical Center, where she was employed as a housekeeper. About one hour after receiving the vaccine she experienced a hot flash, nausea, and feeling like she was going to pass out after she had bent down. Later at about 1500 hours she appeared tired and lethargic, then a short time later, at about 1600 hours, upon arrival to a friend’s home she complained of feeling hot and having difficulty breathing. She then collapsed, then when medics arrived, she was still breathing slowly then went into cardiac arrest and was unable to be revived.”
  • 49-year-old female from Alabama: “Patient suffered a cardiac arrest and was unable to give details about her symptoms. Per husband, patient did not complain of any symptoms after vaccine administration. She began seizing without warning which was complicated by cardiac arrest of uncertain etiology.”

A final example from the news this past week, is the story of a perfectly healthy 19-year-old Israeli, now in the ICU after developing endocarditis following Pfizer’s experimental COVID vaccine. Right after his second dose, “…he experienced an accelerated heartbeat, along with shortness of breath and sharp pains that were radiating down his left arm, according to Terem’s Dr. Badarnih Bahaa. “Blood tests diagnosed endocarditis — heart inflammation, a condition predicted by Drs. Whelan and Noorchashm in their warning letters — which, if left untreated can lead to dangerous heart rhythms and death. The news reported, “It has still not been confirmed with certainty that the inflammation was developed as a side-effect to the vaccination…” As expected, health authorities chalk these life-threatening events up to “coincidence,” despite multiple warnings to the FDA by esteemed medical specialists. To further erode trust in our federal regulators, it is crystal clear that the FDA has been and remains fully aware of the potential for these serious and even fatal cardiac events following experimental COVID-19 vaccines — and yet vehement denials continue. A review of the FDA’s “Working list of possible adverse event outcomes” from their Vaccines and Related Biological Products Advisory Committee October 22, 2020 Meeting Presentation reveals acute myocardial infarction (i.e., heart attack) and myocarditis/pericarditis (i.e., inflammation of various heart tissues) in their list of known possible adverse event outcomes (see below).

fdaCOVID19 Vaccines

Why the surprise? Where is the evidence of truth in the incessantly parroted narrative, “COVID vaccines are safe and effective?” Is this not a violation of the medical ethical principle of informed consent, when the public is denied access to the truth that they are potentially dangerous and even lethal? And to top that off, the survival rate for a previously healthy 19-year-old young man — if he contracted COVID-19 illness — is 99.997%.  Had this young man been provided full informed consent — i.e., had he been advised of the potential life-threatening risks of these experimental shots as well as the 99.997% chance of survival should he acquire COVID-19 illness — do you think he would have chosen to take this vaccine?

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This article contains a growing list of deaths that occurred after the experimental COVID vaccine was administered. The death reports are culled from the media and from social media, as well as from the CDC’s Vaccine Adverse Event Reporting System (VAERS).  Injuries and deaths reported on social media are unconfirmed. Although the deaths are temporally related to the COVID vaccination, Children’s Health Defense – California Chapter cannot claim the COVID vaccine definitively caused the deaths. That said, the symptom patterns and timing are highly suspicious, and tend to follow patterns of adverse events widely recognized to occur after other vaccinations. The death reports serve as anecdotes that may soon establish a pattern. Children’s Health Defense – California Chapter is providing regular updates on newly reported deaths that occur after COVID vaccination. As always, Children’s Health Defense – California Chapter supports fully informed consent and no medical mandates. This is not medical advice. Please share this information with, and consult, your doctor.