The Vaccine Adverse Event Reporting System is a United States program for vaccine safety, co-managed by the U.S. Centers for Disease Control and Prevention and the Food and Drug Administration.
VAERS accepts reports on a wide range of adverse events, including but not limited to allergic reactions, fever, pain at the injection site, swelling, or more severe events. By collecting diverse adverse events data, VAERS can capture the full spectrum of possible vaccine-related effects.
Not all reported adverse events are necessarily caused by vaccines. VAERS collects information on any adverse events that occur after vaccination, regardless of whether a causal relationship is established. This allows for comprehensive monitoring and subsequent investigations to determine the true causality.
VAERS encourages healthcare providers, vaccine manufacturers, and individuals to report any adverse events they suspect are related to vaccination. By involving multiple stakeholders, VAERS captures a broader perspective on vaccine safety.
VAERS maintains strict protocols to ensure data quality and accuracy. The system verifies and investigates reports, conducts follow-ups, and collaborates with healthcare professionals and other reporting sources to gather additional information when necessary. These rigorous measures help maintain the reliability and integrity of VAERS data.
You can download the datasets on the VAERS.HHS.Gov website.
The data on VaxInsights is regularly updated to provide users with the most current information. We strive to ensure that our visualizations and analysis reflect the latest vaccine adverse events data reported to VAERS.
VaxInsights offers customization options, allowing you to tailor the visualizations to your specific requirements. You can select specific vaccines, adverse event categories, demographic filters, and time periods to explore the data and uncover insights relevant to your work.
Yes, the visualizations on VaxInsights are interactive, enabling users to zoom in, hover over data points for detailed information, and apply filters in real-time. This interactivity enhances your ability to explore the data, identify patterns, and gain deeper insights into vaccine adverse events.
Public health professionals can leverage VaxInsights to conduct comprehensive surveillance of vaccine adverse events, identify potential safety concerns, and inform public health interventions. The visualizations aid in risk assessment, resource allocation, and the implementation of targeted strategies to optimize vaccine safety and public health outcomes.
Vaccine manufacturers can utilize VaxInsights to monitor and evaluate the safety profiles of their products. By exploring adverse events data, manufacturers can identify potential signals, assess the real-world impact of their vaccines, and inform post-marketing surveillance efforts. These insights aid in continuous product improvement and ensuring the safety and efficacy of their vaccines.