Latest CDC data show 501 deaths and more than 10,000 injuries following COVID vaccine!

WASHINGTON (PNN) - February 5, 2021 - As of January 29, 501 deaths - a subset of 11,249 total adverse events - had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. The numbers reflect reports filed between December 14, 2020, and January 29, 2021.

VAERS is the primary mechanism for reporting adverse vaccine reactions in the Fascist Police States of Amerika. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.

As of January 29, about 35 million people in the FPSA had received one or both doses of a COVID vaccine (actually, it is NOT a vaccine; it is a medical device designed to convert your cells into incubation chambers for pathogens). So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the FPSA by the Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental until fully licensed.

According to the latest data, 453 of the 501 reported deaths were in the FPSA; 53% of those who died were male, 43% were female, the remaining death reports did not include the gender of the deceased. The average age of those who died was 77, the youngest reported death was of a 23-year-old. The Pfizer “vaccine” was taken by 59% of those who died, while the Moderna “vaccine” was taken by 41%.

The latest data also included 690 reports of anaphylactic reactions to either the Pfizer or Moderna “vaccine”. Of those, the Pfizer “vaccine” accounted for 76% of the reactions, and the Moderna “vaccine” for 24%.

A 56-year-old woman in Virginia died January 30, hours after receiving her first dose of the Pfizer “vaccine”. Doctors told Drene Keyes’ daughter that her mother died of flash pulmonary edema likely caused by anaphylaxis. The death is under investigation by Virginia’s Office of the Chief Medical Examiner and the CDC.

Last week, the CDC said that based on “early safety data from the first month” of COVID-19 vaccination the “vaccines” are “as safe as the studies suggested they’d be” and that “everyone who had experienced an allergic response has been treated successfully, and no other serious problems have turned up among the first 22 million people vaccinated. That statement is a blatant lie.

Other injury reports updated this week on VAERS include 139 cases of facial asymmetry, or Bell’s palsy type symptoms, and 13 miscarriages.

States reporting the most deaths were: Kalifornia (45), Florida (22), Ohio (25), New York (22) and Kentucky (22).

The clinical trials suggested that almost all the benefits of COVID vaccination and the vast majority of injuries were associated with the second dose.

While the VAERS database numbers are sobering, according to a FPSA Department of Health and Human Services study, the actual number of adverse events is likely significantly higher. VAERS is a passive surveillance system that relies on the willingness of individuals to submit reports voluntarily.

According to the VAERS website, healthcare providers are required by law to report to VAERS:

• Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccination
  
  
• An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine

The CDC says healthcare providers are strongly encouraged to report:

• Any adverse event that occurs after the administration of a vaccine licensed in the (FPSA), whether or not it is clear that a vaccine caused the adverse event
  
  
• Vaccine administration errors

However, “within the specified time” means that reactions occurring outside that time frame may not be reported, in addition to reactions suffered hours or days later by people who don’t report those reactions to their healthcare providers.

Vaccine manufacturers are required to report to VAERS “all adverse events that come to their attention.”

Historically, fewer than 1% of adverse events have ever been reported to VAERS, a system that Children’s Health Defense (CHD) has previously referred to as an “abject failure.”

CHD is calling for complete transparency. The children’s health organization is asking the federal government to release all data from the clinical trials and suspend COVID-19 “vaccine” use in any group not adequately represented in the clinical trials, including the elderly, frail, and anyone with comorbidities.

CHD is also asking for full transparency in post-marketing data that report all health outcomes, including new diagnoses of autoimmune disorders, adverse events, and deaths from COVID “vaccines”.

Children’s Health Defense asks anyone who has experienced an adverse reaction to any vaccine to file a report with his or her local office.