VAERS accepts reports of adverse events that occur following vaccination. Anyone, including Healthcare providers, vaccine manufacturers, and the public can ...
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Each compressed file contains the three CSV files listed for a specific data set. Last updated: May 3, 2024. ( * Data contains VAERS reports processed as of: 04 ...
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Reports of all possible associations between vaccines and adverse events (possible side effects) are filed in VAERS. Therefore, VAERS collects data on any ...
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Important: If you are experiencing a medical emergency, seek immediate assistance from a healthcare provider or call 9-1-1. CDC and FDA do not provide ...
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What adverse events should healthcare providers report to VAERS after COVID-19 vaccination? · Vaccine administration errors, whether or not associated with an ...
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VAERS is the national vaccine safety monitoring system that accepts reports of adverse events after vaccination. The system can quickly detect potential ...
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A. Anaphylaxis or anaphylactic shock (3 days). B. Brachial neuritis (28 days). C. Shoulder Injury Related to Vaccine. Administration (2 days).
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The VAERS database contains information on unverified reports of adverse events (illnesses, health problems and/or symptoms) following immunization with US- ...
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VAERS is co-sponsored by the Centers for Disease Control and Prevention (CDC), and the Food and Drug Administration (FDA), agencies of the U.S. Department of ...
What will I need to fill out the report? Patient information (age, date of birth, sex); Vaccine information (brand name, dosage); Date, time, and location ...
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