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The Vaccine Adverse Event Reporting System (VEERS) form Version 2.0 (proposed) Tom Shimabukuro, MD, MPH, MBA Immunization Safety Office (ISO) Division of Healthcare Quality Promotion National Center
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How to Fill Out VAERS Form Version 20:

01
Start by downloading the VAERS Form Version 20 from the official website or obtain a physical copy from your healthcare provider.
02
Begin filling out the form by providing your personal information in the designated fields. This includes your name, address, phone number, and date of birth.
03
Next, indicate the vaccine information by specifying the vaccine manufacturer, lot number, and expiration date. If applicable, note the date of vaccination.
04
In the adverse event section, describe any symptoms or reactions you experienced after receiving the vaccine. Be as specific and detailed as possible, including the onset and duration of symptoms.
05
If you sought medical attention following the adverse event, indicate the healthcare provider's information, including their name, address, and any treatment received.
06
Consider attaching any additional documentation or medical records that may support your adverse event report, such as lab results or diagnostic reports.
07
Sign and date the form to verify the accuracy of the information provided.
08
Submit the completed VAERS Form Version 20 to the corresponding authorities either online, by mail, or as directed by the official guidelines.

Who Needs VAERS Form Version 20:

01
Healthcare Providers: Doctors, nurses, and other healthcare professionals involved in administering vaccines are required to fill out VAERS Form Version 20 if any adverse events are observed or reported.
02
Vaccine Recipients or Their Guardians: Individuals who have experienced adverse events or reactions after receiving a vaccine, or their legal guardians, should also complete VAERS Form Version 20 to report any issues.
03
Researchers and Public Health Authorities: VAERS Form Version 20 is essential for researchers and public health authorities as it collects data on vaccine safety and adverse events. This information helps evaluate the safety profile of vaccines and inform future policies and recommendations.
It is crucial to note that filling out VAERS Form Version 20 should be done accurately, honestly, and to the best of your knowledge. Timely reporting of adverse events contributes to the ongoing monitoring and improvement of vaccine safety.
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Vaers form version 20 is the latest version of the Vaccine Adverse Event Reporting System form used to report adverse events following immunization.
Healthcare providers, vaccine manufacturers, and members of the public are required to file Vaers form version 20 when an adverse event following immunization occurs.
Vaers form version 20 can be filled out electronically through the VAERS website or by contacting VAERS to request a paper form.
The purpose of Vaers form version 20 is to collect information on adverse events following immunization to monitor vaccine safety.
Information that must be reported on Vaers form version 20 includes patient demographic information, vaccine information, adverse event details, and reporter contact information.
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