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Supplementary Data 1. Questionnaire This is a questionnaire for monitoring adverse reactions after COVID-19 vaccination of Public health doctors of Korean Medicine. To understand the adverse reactions
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How to fill out selected adverse events reported
How to fill out selected adverse events reported
01
Gather all necessary documentation related to the adverse event, such as medical records, lab results, and witness statements.
02
Fill out the adverse event reporting form completely and accurately, including details of the event, patient demographics, and any relevant medical history.
03
Submit the completed form to the appropriate regulatory agency or reporting system as specified by your organization or local regulations.
Who needs selected adverse events reported?
01
Healthcare providers
02
Pharmaceutical companies
03
Medical device manufacturers
04
Regulatory agencies
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What is selected adverse events reported?
Selected adverse events reported are specific incidents of harm or side effects experienced by individuals as a result of a product or service.
Who is required to file selected adverse events reported?
Manufacturers, healthcare providers, and consumers are required to report selected adverse events.
How to fill out selected adverse events reported?
Selected adverse events can be filled out online, through a helpline, or by submitting a written report.
What is the purpose of selected adverse events reported?
The purpose of selected adverse events reported is to track and monitor safety concerns related to products or services.
What information must be reported on selected adverse events reported?
Information such as the date of the event, the affected individual, the product or service involved, and the details of the adverse event must be reported.
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