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This document is a reporting form for healthcare providers and patients to report adverse events following vaccination as required by law.
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How to fill out vaccine adverse event reporting
How to fill out Vaccine Adverse Event Reporting System
01
Visit the Vaccine Adverse Event Reporting System (VAERS) website.
02
Click on the 'Report an Event' option to access the reporting form.
03
Fill out the required fields, including your contact information and the details of the vaccine received.
04
Provide information about the adverse event, including the date of the event, symptoms experienced, and any medical treatment received.
05
Indicate any additional relevant medical history or other vaccines taken around the same time.
06
Review all provided information for accuracy.
07
Submit the completed report through the website.
Who needs Vaccine Adverse Event Reporting System?
01
Healthcare providers who observe adverse events after vaccination.
02
Patients or caregivers who experience or witness adverse events post-vaccination.
03
Public health officials who monitor vaccine safety.
04
Researchers conducting studies on vaccine safety and efficacy.
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How to access VAERS data?
VAERS data is accessible by downloading raw data in comma-separated value (CSV) files for import into a database, spreadsheet, or text editing program, or by using the CDC WONDER online search tool.
What is the vaccine adverse event reporting system?
The Vaccine Adverse Event Reporting System (VAERS) is the nation's early warning system that monitors the safety of FDA-approved vaccines and vaccines authorized for use for public health emergencies. The system accepts and analyzes reports of possible adverse events after vaccination and is co-managed by CDC and FDA.
What government agencies oversee VAERS?
VAERS is co-managed by the Centers for Disease Control and Prevention (CDC) and the U.S. Food and Drug Administration (FDA). VAERS accepts and analyzes reports of adverse events (possible side effects) after a person has received a vaccination.
What does AEFI stand for?
An adverse event following immunization (AEFI) is an unwanted or unexpected health effect that happens after someone receives a vaccine, which may or may not be caused by the vaccine.
What are the types of AEFI for reporting?
Types of AEFI for Reporting For purpose of reporting, AEFIs can be minor, severe and serious. Common, self-limiting reactions, usually occur within a few hours of injection and resolve after short period of time and pose little danger. Examples: pain, swelling at injection site, fever, irritability, malaise etc.
What should be reported to AEFI?
Healthcare providers should report: any significant (or rare and unexpected) AEFIs in both children and adults. any vaccine reaction that requires assessment by a healthcare provider. any vaccine reaction that has affected a family's confidence in future immunisation.
How to view VAERS data?
VAERS data is accessible by downloading raw data in comma-separated value (CSV) files for import into a database, spreadsheet, or text editing program, or by using the CDC WONDER online search tool.
What is AEFI reporting?
An adverse event following immunization (AEFI) is defined as any untoward medical occurrence following immunization which does not necessarily have a causal relationship to the vaccine. The adverse event may be any unfavourable or unintended sign, abnormal laboratory finding, symptom or disease.
Is VAERS a passive reporting system?
VAERS is a passive surveillance system, meaning it relies on people sending in reports of their experiences after vaccination.
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What is Vaccine Adverse Event Reporting System?
The Vaccine Adverse Event Reporting System (VAERS) is a national system for monitoring the safety of vaccines in the United States, designed to detect potential safety concerns by collecting and analyzing reports of adverse events following vaccination.
Who is required to file Vaccine Adverse Event Reporting System?
Healthcare providers are required by law to report any adverse events they observe after vaccination, while anyone can file a report, including patients, parents, or guardians.
How to fill out Vaccine Adverse Event Reporting System?
Reports can be filled out online through the VAERS website or by submitting a paper form. Required details include information about the vaccine, the individual vaccinated, and a description of the adverse event.
What is the purpose of Vaccine Adverse Event Reporting System?
The primary purpose of VAERS is to monitor vaccine safety, detect possible safety signals, and assess whether vaccines are causing adverse events, thus ensuring public confidence in vaccination programs.
What information must be reported on Vaccine Adverse Event Reporting System?
Information that must be reported includes the patient's demographics, details about the vaccination, any adverse events or symptoms experienced, and the date of the incident.
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