This article already has been archived at Mercola.com
Lymerick

By Dr. Joseph Mercola
Global Research, November 26, 2023
Mercola 25 November 2023

The Vaccine Adverse Events Reporting System (VAERS) does not meet its own standards, and safety signals are not being addressed

Before the COVID pandemic, VAERS received an average of 60,000 adverse event reports after vaccination each year. In the first year of the rollout of the experimental gene therapies against COVID (2021), reports skyrocketed to 1 million. By the end of October 2023, the number of reports associated with the COVID shots was 1,605,764, and nearly 1 in 5 of those reports involves a “serious” adverse event

The U.S. Food and Drug Administration and the Centers for Disease Control and Prevention, which share responsibility for VAERS, insist these data in no way reflect a potential problem with the COVID shots

Filing a VAERS report is a time-consuming process. It can take several hours for a trained medical professional to fill out a single report, and this is time that cannot be billed to anyone. As a result, side effects, including deaths, are massively underreported

VAERS has a public front end and a private back end that public users aren’t allowed to see. The public database only contains the initial reports. Corrections and updates on outcomes go into the private-facing end. As a result, we have no idea how many of the injuries have resulted in death after an initial report was filed. The death count we see when we look at VAERS is the number of reports filed where death was the reason for filing the report in the first place. This “dual system” can leave the public with the false impression that deaths are less common than they are. We also don’t know how many injuries end up progressing and resulting in permanent disability, or how many of them resolve

SNIP