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VAERS was established in 1990, the Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in U.S. licensed vaccines. VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA) People can file their own VAERS report online at Vaers.hhs.gov The Vaccine Adverse Event Reporting System (VAERS) is a passive reporting system, meaning it relies on individuals to send in reports of their experiences. Anyone can submit a report to VAERS, including parents and patients. Also,…mehr

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Produktbeschreibung
VAERS was established in 1990, the Vaccine Adverse Event Reporting System (VAERS) is a national early warning system to detect possible safety problems in U.S. licensed vaccines. VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA) People can file their own VAERS report online at Vaers.hhs.gov The Vaccine Adverse Event Reporting System (VAERS) is a passive reporting system, meaning it relies on individuals to send in reports of their experiences. Anyone can submit a report to VAERS, including parents and patients. Also, healthcare providers are required by law to report side effect to VAERS:

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Autorenporträt
I, SABELL, am a Freelance Researcher. I have been a researcher for 20 years. I research vaccine side effects resulting from the Influenza vaccines and Covid-19 mRNA Vaccines. I feel manufacturers of vaccines could do a better job with their products if people would stop complaining on social media and file a VAERS report regarding their side effects. Manufacturers need this valuable feedback. I would like to thank the various U.S. Governmental Agencies and Worldwide Medical Journals for their total transparency regarding vaccine ADR's: CDC, FDA, NIH, PubMed, VAERS, and many more.