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Alberta Health Adverse Events Following Immunization Data Submission and Response Guidelines Adverse Events Following Immunization Data Submission and Response Guidelines Version 6.5 September 2016
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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 necessary forms: Start by obtaining the appropriate forms for reporting adverse events following immunization. These forms can typically be obtained from the healthcare provider, vaccine manufacturer, or the local health department.
02
Provide accurate identification details: Begin by providing accurate identification details about the person experiencing the adverse event. This includes their full name, date of birth, contact information, and any other relevant identifiers.
03
Describe the adverse event: Clearly describe the adverse event experienced following immunization. Include details such as the date and time of the event, the specific vaccine administered, and any symptoms or reactions observed.
04
Include medical history: Provide any relevant medical history information about the individual experiencing the adverse event. This may include previous immunizations, allergies, existing medical conditions, or medications being taken.
05
Provide contact information: Include contact information for the person reporting the adverse event. This allows for follow-up communication or additional information if needed.

Who needs adverse events following immunization:

01
Healthcare professionals: Healthcare professionals, including doctors, nurses, and pharmacists, need adverse events following immunization reports to monitor the safety and effectiveness of vaccines. This information helps in identifying any potential side effects or adverse reactions.
02
Vaccine manufacturers: Vaccine manufacturers require adverse events following immunization reports to ensure the safety and quality of their products. By analyzing these reports, they can identify any patterns or potential issues with their vaccines.
03
Public health agencies: Public health agencies at the local, national, and international level rely on adverse events following immunization reports to conduct vaccine safety surveillance. This information helps in monitoring vaccine safety on a broader scale and implementing necessary interventions if needed.
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