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Health.NSW.gov.auCOVID19 vaccine: Enhanced surveillance and adverse event reporting guidelines Last updated 24 May 2021 AEF reporting flow chart updated to reflect the latest ATARI advicePurpose of
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Begin by gathering all relevant information regarding the adverse event, including the date it occurred, any symptoms experienced, and any treatments given.
02
Fill out the appropriate form or documentation provided by the relevant regulatory authority or organization. This may include details such as patient information, adverse event details, and any relevant medical history.
03
Be sure to accurately and thoroughly document all information, including any potential causes or contributing factors to the adverse event.
04
Submit the completed adverse events report to the appropriate authority or organization as soon as possible.

Who needs adverse events of special?

01
Healthcare professionals such as doctors, nurses, and pharmacists who encounter adverse events in their patients.
02
Pharmaceutical companies and manufacturers who need to document and report adverse events related to their products.
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Regulatory authorities and agencies responsible for monitoring and evaluating adverse events to ensure public safety.
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Adverse events of special refer to incidents or occurrences that are outside of the norm and may have serious consequences.
Healthcare providers, manufacturers, and distributors are required to file adverse events of special.
Adverse events of special should be filled out with detailed information about the incident, including date, time, location, and individuals involved.
The purpose of adverse events of special is to ensure that incidents are properly documented and investigated to prevent future occurrences.
Information such as the nature of the incident, any injuries or damages, and any actions taken as a result must be reported on adverse events of special.
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