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COVID19 Vaccines Safety Surveillance GuidelineIntegrated Addendum to the Third Edition of The Guideline for Surveillance and Response to Adverse Events Following Immunization, EFDA, Addis Ababa, Ethiopia,
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How to fill out covid-19 vaccines safety surveillance

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How to fill out covid-19 vaccines safety surveillance

01
Collect all necessary information on the vaccine recipient such as age, gender, medical history, and any known allergies.
02
Record the specific vaccine received, including manufacturer, lot number, and expiration date.
03
Monitor the recipient for any immediate reactions or side effects after receiving the vaccine.
04
Report any adverse events to the designated surveillance system or health authority.
05
Follow up with the recipient periodically to track long-term effects and overall vaccine safety.

Who needs covid-19 vaccines safety surveillance?

01
Healthcare professionals involved in administering vaccines.
02
Public health officials responsible for monitoring vaccine safety at a population level.
03
Vaccine manufacturers and regulatory agencies interested in post-approval surveillance.
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COVID-19 vaccines safety surveillance refers to the continuous monitoring of vaccine safety after administration to identify any adverse effects or complications that may arise.
Healthcare providers, vaccine manufacturers, and public health agencies are typically required to file COVID-19 vaccines safety surveillance reports.
To fill out COVID-19 vaccines safety surveillance, individuals must complete the required reporting forms, providing detailed information about the vaccinees and any observed adverse events.
The purpose of COVID-19 vaccines safety surveillance is to detect, investigate, and respond to any safety concerns related to the vaccines, ensuring their ongoing safety and effectiveness.
Information that must be reported includes details about the vaccinee, the type of vaccine administered, the date of administration, and any adverse events experienced post-vaccination.
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