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WHO Library CataloguinginPublication Data Global manual on surveillance of adverse events following immunization. 1.Immunization Programs. 2.Adverse Drug Reaction Reporting Systems. 3.Vaccination
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How to fill out monitoring vaccine safety and

01
Collect data on vaccine adverse events from healthcare providers, pharmaceutical companies, and patients
02
Analyze the data to identify any patterns or trends in adverse events following vaccination
03
Report any findings to relevant regulatory authorities and public health agencies
04
Implement surveillance systems to track vaccine safety over time
05
Conduct research studies to further investigate potential safety concerns

Who needs monitoring vaccine safety and?

01
Healthcare providers
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Pharmaceutical companies
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Regulatory authorities
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Public health agencies
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Patients
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Monitoring vaccine safety is the process of collecting, analyzing, and interpreting data regarding the safety of vaccines to detect any potential safety issues or adverse effects.
Healthcare providers, vaccine manufacturers, and certain public health professionals are required to file reports related to vaccine safety monitoring.
To fill out a monitoring vaccine safety report, one must provide detailed information about the adverse event, including patient demographics, details of the vaccine administered, and a description of the event that occurred.
The purpose of monitoring vaccine safety is to ensure vaccines are safe for public use and to identify any potential risks associated with vaccinations for prompt investigation and action.
Information that must be reported includes the type of vaccine, patient information (age, gender), details of the adverse event, date of administration, and any relevant medical history.
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