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Serious AEF Case Notification Form ADR Monitoring Center* CSR No. ___ Reporting Format No. Name & address of ADR Monitoring center (AMC): Patient Name Age: ___ Sex: Male/Female Father/Husbands Name
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How to fill out serious aefi case notification
How to fill out serious aefi case notification
01
Gather all necessary information about the serious adverse event following immunization (AEFI)
02
Complete the serious AEFI case notification form with accurate and detailed information
03
Include information about the vaccine received, date of vaccination, symptoms experienced, treatment provided, and outcome of the AEFI
04
Submit the completed form to the relevant health authorities or vaccine safety monitoring system
Who needs serious aefi case notification?
01
Healthcare professionals who have identified a serious AEFI in a patient
02
Vaccine manufacturers who need to report serious AEFIs associated with their products
03
Health authorities responsible for monitoring and responding to vaccine safety concerns
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What is serious aefi case notification?
Serious AEFI case notification is a process of reporting any serious adverse events following immunization.
Who is required to file serious aefi case notification?
Healthcare providers and vaccine manufacturers are required to file serious AEFI case notifications.
How to fill out serious aefi case notification?
Serious AEFI case notifications can be filled out online through the designated reporting system or by submitting a paper form.
What is the purpose of serious aefi case notification?
The purpose of serious AEFI case notification is to monitor and track any serious adverse events following immunization to ensure the safety of vaccines.
What information must be reported on serious aefi case notification?
The information that must be reported on serious AEFI case notifications includes details of the adverse event, the vaccine received, patient demographics, and the healthcare provider's information.
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