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Federal Whistleblower Reveals 45,000 People Have Died from the COVID-19 “vaccines”


U.S. FDA Data Publicly Shows More Than 11,000 Americans Dead from COVID ‘Vaccines’


By:  David Deschesne

Fort Fairfield Journal, July 28, 2021

   Data from the U.S. Food & Drug Administration’s Vaccine Adverse Event Reporting System (VAERS) shows that as of July 16, 2021 there have been 11,405 deaths in the U.S. collectively attributed to the various experimental COVID-19 ‘vaccines’ in circulation since late December of 2020.1 

   However, Ohio Attorney, Thomas Renz recently revealed he had a sworn deposition from a federal whistleblower who stated the number of deaths from the COVID-19 ‘vaccines’ is actually 45,000.2  He recently filed a lawsuit in federal court based upon this information.  “We know from this sworn declaration that there have been at least 45,000 deaths from this vaccine,” said Renz in a recent press conference.  “There have been 45,000 deaths based on how many people died within three days of the vaccine in just one system that’s reporting to the federal government.  There are reportedly around ten or eleven systems that are reporting deaths and injuries to the government.  How many have really died?  And why are they covering it up?”

   Renz is also currently working with Maine attorney, Ron Jenkins in a lawsuit against Governor Janet Mills, Dr. Nirav Shah and others within the Maine government for their malfeasance during the contrived COVID-19 scare of 2020.

   Members of the establishment, left-wing news media are failing to report these death numbers even though they were fixated on the artificially elevated COVID-19 death numbers all last year with daily up-to-the minute updates.

   Two of the three ‘vaccines’ are actually an experimental gene therapy from Moderna and Pfizer/BionTech which have never been tried before in humans.  The third is an experimental adenovirus vector vaccine from Johnson & Johnson.

   None of the so-called COVID-19 ‘vaccines’ have been approved as safe and effective by the FDA, but were granted “Emergency Use Authorization” due to the excessive and irresponsible hype by the leftist media and governments surrounding the purported SARS-CoV-2 outbreak last year.

   SARS-CoV-2, which causes a disease referenced as COVID-19, was found as early as last Fall to have a fatality rate similar to seasonal flu among the frail, elderly population with multiple health issues and adults who are obese with other multiple health issues.  Children and adults of all ages who are otherwise in good physical condition and in reasonably good health either do not suffer symptoms of COVID-19 at all, or they may have a fever, cough and other flu like symptoms for a few days before fully recovering and obtaining natural immunity to the disease.

   The greater than 99% survival rate of those who do catch SARS-CoV-2 has not stopped the media’s and government’s marketing push for the purported vaccines.  The marketing propaganda has gone to almost clownish levels as governments are offering sweepstakes winnings, free hunting and fishing licenses, and in some cases free video game consoles, gift cards or even cash for those who volunteer to participate in the experimental vaccines’ ongoing medical trials.

   The FDA’s VAERS data is a voluntary system which compiles statistics from people who have received adverse effects from any vaccine.  In the case of a death, the family or deceased’s physician can submit the information to the FDA.  Past statistical analyses of the VAERS shows that only between 1 and 10 percent of the people who suffer an adverse event (or death) from a vaccine actually bother to voluntarily submit that information to the FDA.  In this case, the number of deaths from the COVID-19 vaccines could be tens of thousands more than the data currently shows.

   As of July 16, the VAERS shows deaths in the following age groups:


under 3 years   3

12-17 years      12

17-44 years      313

44-65 years      1,187

65-75 years      1,505

75+ years         4,083

unspecified age           4,302


  A document from the FDA’s Vaccines and Related Biological Products Advisory Committee, dated October 22, 2020 - three months before the experimental vaccines were released to the general public under Emergency Use Authorization - explains the criteria for the monitoring of the experimental COVID-19 “vaccines”3

   The document states that the “FDA and CDC have weekly and bi-weekly coordination meetings on VAERS and Pharmacovigilance activities between CBER OBE and OBE Division of Epidemiology (DE) and CDC Immunization Safety Office.”

 “CBER DE Physicians will be reviewing the serious adverse event reports from VAERS for COVID-19 vaccines –review of individual reports, death reports, conduct aggregate analyses, case-series, etc.

FDA will utilize statistical data-mining methods to detect disproportional reporting of specific vaccine-adverse event combinations to identify [Adverse Events] that are more frequently reported.”

   The FDA document also mentions a list of potential side effects of the COVID-19 vaccines as;


Guillain-Barré syndrome

Acute disseminated encephalomyelitis

Transverse myelitis

Encephalitis/myelitis/encephalomyelitis/ meningoencephalitis/meningitis/ encepholapathy



Narcolepsy and cataplexy


Acute myocardial infarction


Autoimmune disease


Pregnancy and birth outcomes

Other acute demyelinating diseases

Non-anaphylactic allergic reactions


Disseminated intravascular coagulation

Venous thromboembolism

Arthritis and arthralgia/joint pain

Kawasaki disease

Multisystem Inflammatory Syndrome in Children

Vaccine enhanced disease


   There have been over 200,000 adverse events from the experimental COVID-19 vaccines in the U.S. alone since their roll-out.

   Joe Biden recently announced that he would be sending a large cadre of federal agents door-to-door to every home in the U.S. to try to sell vaccine-hesitant people on the vaccines and convince them to participate in the medical trials.  The COVID-19 vaccines have still not been approved, so everyone who has accepted one has unwittingly volunteered to be part of the medical experiment surrounding those concoctions.

   Vaccine manufacturers have been granted complete immunity from lawsuits for any of the vaccine-related deaths or long-term side effects that may result from the experimental vaccines.  So, anyone who experiences an adverse event which requires hospitalization, such as heart attack or blood clotting, will likely be required to pay for those costs by themselves or through their health insurance.