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WEBSITE: www.vaers.hhs.gov E-MAIL: info veers.org FAX: 1-877-721-0366 VACCINE ADVERSE EVENT REPORTING SYSTEM For CDC/FDA Use Only VEERS Number Date Received 24 Hour Toll-Free Information 1-800-822-7967
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What is vaccine adverse event reporting?
Vaccine adverse event reporting is the process of documenting and reporting any negative or unexpected side effects that occur after receiving a vaccine.
Who is required to file vaccine adverse event reporting?
Healthcare providers, vaccine manufacturers, and individuals receiving the vaccine are all required to file vaccine adverse event reporting.
How to fill out vaccine adverse event reporting?
Vaccine adverse event reporting can be filled out online or using paper forms provided by the relevant health authorities. The forms usually require information about the vaccine recipient, the vaccine administered, and details about the adverse event.
What is the purpose of vaccine adverse event reporting?
The purpose of vaccine adverse event reporting is to monitor the safety and effectiveness of vaccines, identify any potential risks or trends, and ensure continuous improvement of vaccine safety.
What information must be reported on vaccine adverse event reporting?
Information such as the vaccine recipient's demographics, medical history, details of the vaccine administered (including lot number and expiration date), description of the adverse event, and any relevant medical interventions must be reported on vaccine adverse event reporting.
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