vaers reporting system

the .gov means it’s official.federal government websites often end in .gov or .mil. the https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. the vaccine adverse event reporting system (vaers) is a national vaccine safety surveillance program co-monitored by the food and drug administration (fda) and the centers for disease control and prevention (cdc).




although extensive studies are needed prior to use under an emergency use authorization (eua) or licensure (approval), post-marketing research and surveillance are necessary to identify rare safety issues that may only be detected following vaccination in a much larger and more diverse population. some events may occur coincidentally after the administration of a vaccine while others may in fact be caused by a vaccine. as a result, if a safety signal is found in vaers, further studies can be conducted in safety systems such as the cdc’s vaccine safety datalink (vsd), or the clinical immunization safety assessment (cisa) project.

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 vaers is the national vaccine safety monitoring system that accepts reports of adverse events after vaccination. the system can quickly detect potential the information in this database contains reports received from 1990 to the present. data can be searched by the following: age, event category, gender,, .

anyone can report a post-vaccination health issue to the vaccine adverse event reporting system—which anti-vaccination activists often vaers is a national vaccine safety surveillance program created as an outgrowth of the national childhood vaccine injury act of 1986 (ncvia) the vaccine adverse event reporting system (vaers) is a valuable tool for post-marketing safety surveillance (monitoring after a product has, .

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