|Healthcare professionals are encouraged to report any clinically significant adverse event following vaccination to VAERS, even if they are not sure if vaccination caused the event||Vaccine administration errors Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention|
|Cases of observed Multisystem Inflammatory Syndrome• Any adverse event listed in the that occurs within the specified time period after vaccinations• Serious adverse events AEs regardless of causality||Information supplied in the online submission form is transmitted securely to VAERS|
An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine Healthcare providers are strongly encouraged to report to VAERS:• You or your health care provider may be contacted for further information after your report is received.28
|Vaccination administration errors, whether or not associated with an adverse event• The Vaccine Adverse Event Reporting System VAERS accepts all reports, including reports of vaccination errors||Patient information age, date of birth, sex• Persistent or significant incapacity or substantial disruption of the ability to conduct normal life functions;• Online reporting is strongly encouraged|
|Healthcare providers are required by law to report to VAERS:• VAERS is a passive reporting system, meaning it relies on individuals to send in reports of their experiences||Important medical events that may not result in death, be life-threatening, or require hospitalization may be considered serious when, based upon appropriate medical judgment, they may jeopardize the patient and may require medical or surgical intervention to prevent one of the outcomes listed above|
Knowingly filing a false VAERS report is a violation of Federal law 18 U.