VAERS Reporting Requirements for COVID-19 VaccinesĪs of August 2022, there are four vaccines available to protect against COVID-19 disease:
Guidance on reporting vaccination errors is available if you have additional questions. VAERS accepts all reports, including reports of vaccination errors. Please report clinically important adverse events that occur after vaccination of adults and children, even if you are not sure whether the vaccine caused the adverse event. Vaccine manufacturers are required to report to VAERS all adverse events that come to their attention. Any adverse event that occurs after the administration of a vaccine licensed in the United States, whether it is or is not clear that a vaccine caused the adverse event.Healthcare providers are strongly encouraged to report to VAERS: An adverse event listed by the vaccine manufacturer as a contraindication to further doses of the vaccine.Any adverse event listed in the VAERS Table of Reportable Events Following Vaccination that occurs within the specified time period after vaccinations.Healthcare providers are required by law to report to VAERS: Anyone can submit a report to VAERS, including parents and patients.
The Vaccine Adverse Event Reporting System (VAERS) is a passive reporting system, meaning it relies on individuals to send in reports of their experiences. Click here for VAERS reporting requirements for healthcare providers administering COVID-19 vaccines
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