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RIVERS Collaboration For Vaccine Adverse Events Reporting Functional and Process Recommendations of the American Immunization Registry Association (AIR) Vaccine Safety and Registry Community (VASE)
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How to fill out iis-vaers collaboration:

01
Start by accessing the IIS-VAERS collaboration platform.
02
Once you have logged in, select the option to create a new entry or report.
03
Provide the required information, such as the patient's name, date of birth, and contact details.
04
Indicate the type of vaccine or immunization administered.
05
Include the date, time, and location of the vaccination.
06
Specify any adverse reactions or side effects experienced by the patient.
07
Provide any additional relevant details, such as previous medical conditions or allergies.
08
Review the information entered for accuracy and completeness.
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Submit the form or report to complete the process.

Who needs iis-vaers collaboration:

01
Healthcare professionals who administer vaccines and immunizations can benefit from using the IIS-VAERS collaboration platform. It allows them to report adverse events and monitor vaccine safety.
02
Public health agencies and authorities utilize the IIS-VAERS collaboration to collect data on adverse effects and detect any potential trends or patterns that may emerge.
03
Researchers and scientists interested in vaccine safety and surveillance can access the IIS-VAERS collaboration platform to analyze the reported data and contribute to ongoing studies in the field.
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The IIS-VAERS collaboration is a partnership between Immunization Information Systems (IIS) and the Vaccine Adverse Event Reporting System (VAERS) to enhance vaccine safety monitoring and reporting.
Healthcare providers, public health agencies, and vaccine manufacturers are required to participate in the IIS-VAERS collaboration.
To fill out the IIS-VAERS collaboration, healthcare providers can input vaccine adverse event reports into their state's IIS system which is then shared with the VAERS system.
The purpose of the IIS-VAERS collaboration is to improve vaccine safety monitoring, detect adverse events following vaccination, and facilitate reporting to the appropriate authorities.
Information reported on the IIS-VAERS collaboration includes patient demographics, vaccine type and lot number, healthcare provider information, and details of any adverse events experienced post-vaccination.
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