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Protected B When CompletedREPORT OF ADVERSE EVENTS FOLLOWING IMMUNIZATION (AEF) INSTRUCTIONS: For more complete instructions and definitions, refer to the user guide at: https://www.canada.ca/en/publichealth/services/immunization/reportingadverseeventsfollowingimmunization/userguidecompletionsubmissionaefireports.html
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How to fill out adverse events following immunization

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How to fill out adverse events following immunization

01
Obtain the proper adverse events following immunization form
02
Fill out the individual's personal information
03
Provide details of the immunization received
04
Document the date and time of the immunization
05
Record details of the adverse event experienced by the individual
06
Include any additional relevant information
07
Submit the completed form to the appropriate healthcare provider or authority

Who needs adverse events following immunization?

01
Healthcare providers
02
Vaccine manufacturers
03
Public health authorities
04
Individuals who have experienced adverse events following immunization
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Adverse events following immunization, also known as AEFI, are any unfavorable medical occurrences that follow the administration of a vaccine.
Healthcare providers, vaccine manufacturers, and patients or their caregivers may be required to file adverse events following immunization depending on the reporting requirements of the specific jurisdiction.
Adverse events following immunization can typically be filled out using specific reporting forms provided by public health authorities or through online reporting portals.
The purpose of adverse events following immunization is to monitor and investigate any potential safety concerns associated with vaccines to ensure they remain safe and effective for the population.
Information that may need to be reported on adverse events following immunization includes the type of vaccine administered, the date of administration, the symptoms experienced, and any pre-existing medical conditions.
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