VAERS

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AcronymDefinition
VAERSVaccine Adverse Event Reporting System (lists hospitalizations or deaths resulting from vaccinations)
References in periodicals archive ?
The Vaccine Adverse Event Reporting System (VAERS), co-managed by CDC and the Food and Drug Administration (FDA), is the national postmarketing safety monitoring system that accepts reports about adverse events that occur after administration of U.
As a result, the Vaccine Adverse Event Reporting System (VAERS), jointly operated by CDC and the U.
The Study: In this retrospective study, researchers looked at data since January, 2014 from the Vaccine Adverse Event Reporting System for cases of babies under nine months of age receiving either the MMR or the MMRV vaccination.
Adverse events associated with vaccines should he reported to the Vaccine Adverse Event Reporting System at https://vaers.
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).
The US Vaccine Adverse Event Reporting System (VAERS), which relies on volunteer reports, is the sole means of tracking negative effects.
In searching the Vaccine Adverse Event Reporting System for rotavirus vaccination administration errors between 2006 and 2013, researchers found 66 reports of problems.
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.