Experimental COVID Vaccines: Mounting Deaths Reported in Media and Social Media
By Dawn Amittai
Growing List of Deaths
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. 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 below serve as anecdotes that may soon establish a pattern. Following this initial coverage, Children’s Health Defense – California Chapter will continue to update this article with newly reported deaths that occur after COVID vaccination.
Death is one of the side effects being monitored by the Food and Drug Administration, per this list of vaccine adverse events from their October 22, 2020 meeting:
More than a dozen deaths have been reported in the media to date. Gregory Michael, a “very healthy 56-year old” physician died after being injected with the Pfizer COVID vaccine, according to a post by his wife on Facebook. “The love of my life, my husband Gregory Michael MD an obstetrician that had his office in Mount Sinai Medical Center in Miami Beach died the day before yesterday due to a strong reaction to the COVID vaccine.”
A 41-year old healthcare worker in Portugal at Porto’s IPO Cancer Hospital, a mother of two without “any illness or health complication” was found dead in bed two days after taking the Pfizer vaccine. Four long-term care residents in Israel, two in Norway, two in Denmark, and one in Sweden died shortly after taking the Pfizer experimental vaccine. These deaths are all detailed in Table 1 below.
Through December 30, 2020, thirteen U.S. deaths have been reported after COVID vaccination to the Vaccine Adverse Event Reporting System (VAERS), mostly among nursing home patients. There are almost 4,000 total COVID vaccine reactions reported to VAERS so far, including 140 reports for serious adverse events. A CDC-funded study at Harvard Pilgrim concluded that “fewer than 1% of vaccine adverse events are reported” to VAERS, a passive reporting system. Therefore, it is reasonable to multiply any reported events by 100 to approximate the actual number of deaths and adverse events after any vaccination. In fact, the COVID vaccine injury rate, based on the December Advisory Committee on Immunization Practices meeting is 1 in 43. Note that all approved COVID vaccines require two doses, so these data are mostly based on one dose. In the trials, the second dose was much more reactogenic, so we expect the serious injury rate to be much higher after the second dose.
The highly anticipated coronavirus vaccines began their rollout for use in the middle of December 2020. Although these vaccines have been touted by our health authorities and vaccine manufacturers as being “safe and effective,” questions are now being raised as to the reality of these claims. After all, these vaccines have been developed at “warp speed.” Clinical trials take a minimum of 8 to 10 years to complete. In contrast, these COVID-19 vaccines have been developed in less than one year, and have been authorized for use by the FDA’s emergency use authorization (EUA).
Under an EUA, the FDA is essentially allowing the emergency use of an investigational medical product. In other words, the Moderna and Pfizer-BioNTech coronavirus vaccines remain experimental. They do not have full licensure — this requires 8 to 10 years. They have only been authorized on an emergency basis, to be distributed in the U.S. for use in individuals 18-years of age and older. This fact — that they are investigational only — may not be well known by the public, as the media continues to erroneously publish that the “FDA has approved” these vaccines. Additionally, these vaccines are a brand new technology with known complications — and we can certainly anticipate numerous unforeseen complications as well.
In fact, today there are about a dozen vaccines in use in the United States and another 66 have been withdrawn, most for safety issues, such as LymeRix, RotaShield and DTP. These fully licensed vaccines were judged as safe with government approval. This shows a vaccine withdrawal rate of 73%. If three-quarters of fully licensed vaccines are withdrawn, the chances of a warp speed experimental vaccine being withdrawn are far higher.
As these non-fully licensed COVID vaccines are now being rapidly administered — first to healthcare personnel and long-term care facility residents — we are just beginning to see the fallout. Experimental shots are being given as part of unprecedented, large-scale global vaccination campaigns, and we are already seeing their fatal consequences. To date, a total of about two dozen death within hours or days after COVID vaccine administration have been reported by the media or to VAERS.
An additional 26 deaths have occurred shortly after a COVID vaccine (see Table 2 below) — however, more documentation is not yet available. In a nursing home in Auburn New York where there had not been any prior COVID infections, 24 deaths occurred just 7 days after 80% of the residents were given COVID vaccines; the casualties are being attributed to COVID infection. There is a high likelihood that these fatalities are not “coincidental” but instead are vaccine-related.
Below is an overview of the deaths reported in the media and in social media to date:
Table 1: REPORTED DEATHS FROM EXPERIMENTAL COVID VACCINES
Location: PA, USA
Cause: Heart Attack
For a complete list of Table 1, please click this link
Table 2: SUSPICIOUS DEATHS FOLLOWING EXPERIMENTAL COVID VACCINES
Location: Ohio, USA
Twitter post – awaiting announcement in news
Location: TN, USA
Location: NY, USA
For the most part, these deaths — as well as innumerable vaccine injuries generating emergency room visits and hospitalizations — are commonly being classified as “unrelated to the vaccine” despite the fact that the FDA is anticipating many known adverse event outcomes, including death. For example, acute myocardial infarction (i.e., sudden heart attack) and deaths are listed on the FDA’s “Working list of possible adverse event outcomes.”
However, when a 75-year old Israeli man died from a heart attack a few hours after receiving Pfizer’s vaccine, health authorities stated it was “unrelated to the shot.” It is not made clear how medical authorities immediately came to such a critical conclusion without an investigation. This has also been the case with innumerable vaccine injuries generating emergency room visits and hospitalizations.
It’s important to remember that manufacturers have no liability for vaccine injuries or deaths from any of these experimental COVID vaccines. This lack of liability is clearly stated in the Public Readiness and Emergency Preparedness Act (PREP Act), enacted by Congress in February 2020. If the new technology in COVID-19 vaccines injures or kills us or our loved ones, vaccine manufacturers have blanket indemnity. They cannot be sued for any injury or death caused by their experimental COVID vaccines.
In the U.S., the only possibility for compensation for casualties from these investigational products is to file a claim with the Countermeasures Injury Compensation Program (CICV), which Congress created to cover these matters related to pandemics. Sadly, according to CNBC the CICV “…is difficult to use and rarely pays. Attorneys say it has compensated less than 6% of the claims filed in the last decade.” This is not good news for those irreparably harmed, and financial compensation does not help someone recover nor bring a loved one back to life.
Clearly, the track record for these experimental COVID vaccines does not demonstrate that they are as ”safe” as our medical authorities are proclaiming. What about their effectiveness? Will they stop transmission of the virus to others? Will they prevent COVID infection? Will they reduce morbidity and mortality? In a featured article in British Medical Journal (BMJ) on October 21, 2020, associate editor of this peer-reviewed journal, Peter Doshi, explained, “None of the trials currently underway are designed to detect a reduction in any serious outcome such as hospital admissions, use of intensive care, or deaths. Nor are the vaccines being studied to determine whether they can interrupt transmission of the virus.” He further clarified, “These trials have been designed to reduce symptomatic COVID of any severity.” In fact, Dr. Anthony Fauci, Director of the National Institute of Allergy and Infectious Diseases (NIAID), supported the World Health Organization (WHO) admission that health officials actually do not know if COVID-19 vaccines can prevent infection or the spread of the virus to others after getting vaccinated.
This leads us to the obvious question: If the COVID vaccines are not proving to be safe, and they are unable to prevent transmission of the virus or COVID-19 infection, does the potential benefit —reducing the severity of symptomatic COVID-19 infection — outweigh the risk of vaccine injury or death? And, will the disabilities and deaths experienced by COVID vaccine recipients actually be fewer than those caused by COVID-19 infection? Time will tell. As always, Children’s Health Defense – California Chapter supports fully informed consent and no medical mandates.