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Do Your Part to Report Vaccine Adverse Events
Only about 1 percent of adverse vaccine reactions are reported to the FDA.

The Vaccine Adverse Event Reporting System (VAERS) is a national passive reporting system that accepts reports from the public on events associated with vaccines licensed in the United States. VAERS data are monitored toβ€”

  • Detect new, unusual, or rare vaccine adverse events
  • Monitor increases in known adverse events
  • Identify potential patient risk factors for particular types of adverse events
  • Identify vaccine lots with increased numbers or types of reported adverse events
  • Assess the safety of newly licensed vaccines

Approximately 30,000 VAERS reports are filed annually, with 10–15% classified as serious (causing disability, hospitalization, life-threatening illness or death). Anyone can file a VAERS report, including health care providers, manufacturers, and vaccine recipients or their parents or guardians.

Since the system is passive, most adverse events are never reported.

According to Dr. David Kessler, former head of the Food and Drug Administration (FDA), "Only about 1 percent of serious events [adverse drug reactions] are reported to the FDA." Thus, it is entirely possible that millions of people are adversely affected by mandatory vaccines every year.”

Applying this reality to the actual VAERS reports, there may be as many as 3,000,000 adverse events per year with 450,000 considered serious (causing disability, hospitalization, life-threatening illness or death).

This passive system is the primary tool the Center for Disease Control and Prevention (CDC) and FDA use to monitor safety of vaccines. Unless health professionals and the public do a better job of reporting ALL adverse events, the harm done by vaccines can never be fully understood, documented and ultimately stopped.

The VAERS form requests the following information: the type of vaccine received, the timing of vaccination, the onset of the adverse event, current illnesses or medication, past history of adverse events following vaccination, and demographic information about the recipient.

Reporting an adverse event could not be any simpler.



Click on the image above to be taken to the Vaccine Adverse Event Reporting System online event reporting form.

Alternatively, you can download the form, which after being completed is postage pre-paid back to the VAERS program. The form is available here:

Vaccine Adverse Event Reporting System Form

If you are a health professional, I would suggest that you print out multiple copies of this form and have them available to give to your practice members. You should familiarize yourself with the form and if necessary, review the steps to complete and return the form with your patients.

Most lay persons are unaware this system even exists. Many medical doctors and nurses that I have spoken with, while acknowledging that they are legally bound to report adverse events, inform me that they have never used the system.

It is up to you and me to help document the harm being inflicted by these chemicals. We must be vigilant in our efforts to inform individuals of the inherent risks associated with vaccines, as well as any chemical intervention intended to restore, improve or maintain health.

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