Updated: Dec 31, 2020
Healthcare providers are required BY LAW to report adverse reactions to vaccines!
According to the CDC, they are required to report an adverse event listed in the ‘VAERS Table of Reportable Events Following Vaccination’ and any adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine.
VAERS is the Vaccine Adverse Event Reporting System put in place in 1990. It is a reporting system that has been estimated to account for less than 1% of vaccine injuries.
"Adverse events from drugs and vaccines are common, but underreported. Although 25% of ambulatory patients experience an adverse drug event, less than 0.3% of all adverse drug events and 1-13% of serious events are reported to the Food and Drug Administration (FDA). Likewise, fewer than 1% of vaccine adverse events are reported."
Easily search through VAERS data using this tool: https://www.thearkivist.net/openvaers
(OpenVAERS is built from the HHS data. There are over 757,000 complaints listed as of December 31, 2019.)
Read manufacturer package inserts here: https://www.vaccinesafety.edu/package_inserts.htm