vaccine adverse event reporting system


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vaccine adverse event reporting system

,

VAERS

A national surveillance system for monitoring undesirable reactions to administered vaccines.
References in periodicals archive ?
Adverse events following measles, mumps, and rubella vaccine in adults reported to the Vaccine Adverse Event Reporting System (VAERS), 2003-2013.
In 2011, the Vaccine Adverse Event Reporting System committee confirmed a strong temporal relationship between the HPV vaccine administration and the onset of anaphylactic reactions.
It said : "FDA is developing links between CBER s lot distribution database and FDA s Adverse Event Reporting System (FAERS) and Vaccine Adverse Event Reporting System (VAERS) databases.
Two previous studies finding an association, one based on the Vaccine Adverse Event Reporting System and the other on the Vaccine Safety Datalink, reported few vaccinated cases, many of whom had known venous thromboembolism (VTE) risk factors, Nikolai Madrid Scheller and his colleagues at Statens Serum Institut in Copenhagen reported in a research letter (JAMA 2014;312:187-8).
In searching the Vaccine Adverse Event Reporting System for rotavirus vaccination administration errors between 2006 and 2013, researchers found 66 reports of problems.
At least one of these adverse events was present in 74.2% of all the reports by Vaccine Adverse Event Reporting System. (7) In several studies among adults, the most frequent side effect of vaccination was soreness at the vaccination site (affecting 10-64% of patients).
Adverse events following influenza A (H1N1) 2009 monovalent vaccines reported to the vaccine adverse event reporting system, United States, October 1, 2009-January 31, 2010.
The Vaccine Adverse Event Reporting System (VAERS) is a national vaccine safety surveillance program co-sponsored by the Centers for Disease Control and Prevention (CDC) and the Food and
"On its website the FDA advises that adverse events related to biologics be reported via the FDA's MedWatch program or by contacting the Vaccine Adverse Event Reporting System (VAERS) for vaccines.
According to reports from the Vaccine Adverse Event Reporting System (VAERS) (www.vaers.hhs.gov), the frequency of YEL-AVD in US vaccinees was 0.4 per 100,000 doses of vaccine administered (4).
Safety issues have been refuted (Centers for Disease Control and Prevention review of the Vaccine Adverse Event Reporting System [VAERS] database).
There is more: A Vaccine Adverse Event Reporting System (VAERS) was put in place by the government to report vaccine reactions.