vaccine adverse event recording system

adverse events from vaccines are common but underreported, with less than one percent reported to the food and drug administration (fda). new surveillance methods for drug and vaccine adverse effects are needed. the electronic support for public health – vaccine adverse event reporting system (esp: vaers) project sought to create a generalizable system to facilitate detection and clinician reporting of vaccine adverse events.

every patient receiving a vaccine was automatically identified and for the next 30 days their health care diagnostic codes, laboratory tests, and medication prescriptions were evaluated for values suggestive of an adverse event. a total of 1.4 million vaccine doses (of 45 different vaccines) were given to 376,452 individuals. the team concluded that it is possible to automatically detect adverse events in defined ways, and to electronically report them to vaers.

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,, .

vaers is a national vaccine safety surveillance program created as an outgrowth of the national childhood vaccine injury act of 1986 (ncvia) information about the vaccine adverse event reporting system (vaers), which is a national vaccine safety surveillance program co-sponsored since its creation in 1990, the u.s. centers for disease control and prevention’s (cdc) vaccine adverse event reporting system (vaers) has, .

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