About: Vaccine Adverse Event Reporting System

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

system managed by the CDC and FDA that measures harms from vaccines to ascertain whether the risk-benefit ratio is high enough

Attributes	Values
rdf:type	Item
owl:sameAs	Vaccine Adverse Event Reporting System
description	system managed by the CDC and FDA that measures harms from vaccines to ascertain whether the risk-benefit ratio is high enough (en) amerikanisches Meldesystem für Impfstofffehler (de)
rdfs:label	Vaccine Adverse Event Reporting System (de) Vaccine Adverse Event Reporting System (en) Vaccine Adverse Event Reporting System (it) سامانه گزارش عوارض جانبی واکسن‌ها (fa) ワクチン有害事象報告制度 (ja)
skos:prefLabel	Vaccine Adverse Event Reporting System (de) Vaccine Adverse Event Reporting System (en) Vaccine Adverse Event Reporting System (it) سامانه گزارش عوارض جانبی واکسن‌ها (fa) ワクチン有害事象報告制度 (ja)
name	Vaccine Adverse Event Reporting System (de) Vaccine Adverse Event Reporting System (en) Vaccine Adverse Event Reporting System (it) سامانه گزارش عوارض جانبی واکسن‌ها (fa) ワクチン有害事象報告制度 (ja)
Freebase ID	wds:Q7907943-1AB093EA-9E9F-4B33-B925-4B045A9C3FEB
Freebase ID	/m/05w22w
instance of	wds:Q7907943-708e472b-460a-76f1-3a2c-ad58e3fecea3
instance of	medical database
country	wds:Q7907943-7cc48304-4367-d4bd-61bf-e045e737cc1f
country	United States of America
main subject	wds:Q7907943-882d1086-4ba8-7bd1-d2be-9fbdb28cec5a wds:Q7907943-e74ac509-495d-f815-06b8-288d870ef107
main subject	vaccine adverse event vaccine safety
has use	wds:Q7907943-177f87c5-46a8-a927-10da-8c996e86bc12
has use	postmarketing surveillance
short name	wds:Q7907943-8ed13bb6-4b4f-29c1-8c2f-1b6ddc780924
short name	VAERS (en)
skos:altLabel	VAERS (en) アメリカのワクチン有害事象報告システム (ja)
operator	wds:Q7907943-45540019-41fc-4acc-c1ac-ddd87167139f wds:Q7907943-805b61ba-4aa8-b916-9371-5f7f34d41633
official name	wds:Q7907943-fc1b75a2-4373-5bfc-c79c-49896cedae23
official website	wds:Q7907943-ca9a0838-494a-c935-174c-943d0c29ca3c wds:Q7907943-f9d06b4e-4e1a-475d-ed0a-9938871edfae
email address	wds:Q7907943-56138c6b-417e-bbee-522e-98e582a89fa4
operator	Food and Drug Administration Centers for Disease Control and Prevention
official name	Vaccine Adverse Event Reporting System (en)
official website	https://vaers.hhs.gov/indexSpanish.html https://vaers.hhs.gov/
email address	mailto:info@vaers.org
is about of	Vaccine Adverse Event Reporting System https://www.wikidata.org/wiki/Special:EntityData/Q7907943 Vaccine Adverse Event Reporting System https://de.wikipedia.org/wiki/Vaccine_Adverse_Event_Reporting_System https://it.wikipedia.org/wiki/Vaccine_Adverse_Event_Reporting_System https://fa.wikipedia.org/wiki/%D8%B3%D8%A7%D9%85%D8%A7%D9%86%D9%87_%DA%AF%D8%B2%D8%A7%D8%B1%D8%B4_%D8%B9%D9%88%D8%A7%D8%B1%D8%B6_%D8%AC%D8%A7%D9%86%D8%A8%DB%8C_%D9%88%D8%A7%DA%A9%D8%B3%D9%86%E2%80%8C%D9%87%D8%A7
is main subject of	Kawasaki disease after vaccination: reports to the vaccine adverse event reporting system 1990-2007. Data mining in the US Vaccine Adverse Event Reporting System (VAERS): early detection of intussusception and other events after rotavirus vaccination Hypotonic-hyporesponsive episodes reported to the Vaccine Adverse Event Reporting System (VAERS), 1996-1998. Neonatal deaths after hepatitis B vaccine: the vaccine adverse event reporting system, 1991-1998. Recombinant hepatitis B vaccination of neonates and infants: emerging safety data from the Vaccine Adverse Event Reporting System Intussusception among recipients of rotavirus vaccine: reports to the vaccine adverse event reporting system Adverse events in pregnant women following administration of trivalent inactivated influenza vaccine and live attenuated influenza vaccine in the Vaccine Adverse Event Reporting System, 1990-2009. Two-year review of hepatitis A vaccine safety: data from the Vaccine Adverse Event Reporting System (VAERS). The Vaccine Adverse Event Reporting System (VAERS) The epidemiology of fatalities reported to the vaccine adverse event reporting system 1990-1997. Adverse events following administration to pregnant women of influenza A (H1N1) 2009 monovalent vaccine reported to the Vaccine Adverse Event Reporting System Understanding vaccine safety information from the Vaccine Adverse Event Reporting System A case-series of adverse events, positive re-challenge of symptoms, and events in identical twins following hepatitis B vaccination: analysis of the Vaccine Adverse Event Reporting System (VAERS) database and literature review Postmarketing safety surveillance for typhoid fever vaccines from the Vaccine Adverse Event Reporting System, July 1990 through June 2002. Safety of quadrivalent human papillomavirus vaccine (Gardasil) in pregnancy: adverse events among non-manufacturer reports in the Vaccine Adverse Event Reporting System, 2006-2013. The role of the Vaccine Adverse Event Reporting system (VAERS) in monitoring vaccine safety An overview of the vaccine adverse event reporting system (VAERS) as a surveillance system. VAERS Working Group Adverse events after inactivated influenza vaccination among children less than 2 years of age: analysis of reports from the vaccine adverse event reporting system, 1990-2003. A potential signal of Bell's palsy after parenteral inactivated influenza vaccines: reports to the Vaccine Adverse Event Reporting System (VAERS)--United States, 1991-2001 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. Inactivated influenza vaccine (IIV) in children <2 years of age: examination of selected adverse events reported to the Vaccine Adverse Event Reporting System (VAERS) after thimerosal-free or thimerosal-containing vaccine Adverse Events Following Trivalent Inactivated Influenza Vaccination in Children: Analysis of the Vaccine Adverse Event Reporting System Text mining for the Vaccine Adverse Event Reporting System: medical text classification using informative feature selection Internet-based reporting to the vaccine adverse event reporting system: a more timely and complete way for providers to support vaccine safety Analysis of data from the CDC/FDA vaccine adverse event reporting system (1990-2009) on Guillain-Barre syndrome after hepatitis vaccination in the USA. Post-licensure surveillance of quadrivalent live attenuated influenza vaccine United States, Vaccine Adverse Event Reporting System (VAERS), July 2013-June 2014. Guillain-Barre syndrome after vaccination in United States a report from the CDC/FDA Vaccine Adverse Event Reporting System Data mining for prospective early detection of safety signals in the Vaccine Adverse Event Reporting System (VAERS): a case study of febrile seizures after a 2010-2011 seasonal influenza virus vaccine Adverse Events Following Measles, Mumps, and Rubella Vaccine in Adults Reported to the Vaccine Adverse Event Reporting System (VAERS), 2003-2013 Vaccination of yeast sensitive individuals: review of safety data in the US vaccine adverse event reporting system (VAERS). Application of information retrieval approaches to case classification in the vaccine adverse event reporting system Adverse events after Fluzone ® Intradermal vaccine reported to the Vaccine Adverse Event Reporting System (VAERS), 2011-2013. Polyarteritis nodosa reports to the vaccine adverse event reporting system (VAERS): implications for assessment of suspected vaccine-provoked vasculitis. Invasive and in situ cervical cancer reported to the vaccine adverse event reporting system (VAERS). Safety of anthrax vaccine: an expanded review and evaluation of adverse events reported to the Vaccine Adverse Event Reporting System (VAERS). A review of the Vaccine Adverse Event Reporting System database Who is unlikely to report adverse events after vaccinations to the Vaccine Adverse Event Reporting System (VAERS)? Surveillance for safety after immunization: Vaccine Adverse Event Reporting System (VAERS)--United States, 1991-2001. Guillain-Barré syndrome after Gardasil vaccination: data from Vaccine Adverse Event Reporting System 2006-2009. Comment on the contribution by Souayah et al., "Guillain-Barré syndrome after Gardasil vaccination: data from Vaccine Adverse Event Reporting System 2006-2009" Infant immunization with acellular pertussis vaccines in the United States: assessment of the first two years' data from the Vaccine Adverse Event Reporting System (VAERS). Adverse events after anthrax vaccination reported to the Vaccine Adverse Event Reporting System (VAERS), 1990-2007. Causality assessment of adverse events reported to the Vaccine Adverse Event Reporting System (VAERS). The vaccine adverse event reporting system Safety of varicella vaccine after licensure in the United States: experience from reports to the vaccine adverse event reporting system, 1995-2005. Medication errors reported to the vaccine adverse event reporting system (VAERS). Guillain-Barré syndrome after influenza vaccination in the United States, a report from the CDC/FDA vaccine adverse event reporting system (1990-2009).

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