DBpedia 2016-04

Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Adverse_Event_Reporting_System> ?p ?o }

Showing triples 1 to 36 of 36 with 100 triples per page.

Adverse_Event_Reporting_System abstract "The Adverse Event Reporting System (AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) post-marketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses AERS to monitor for new adverse events and medication errors that might occur with these marketed products.".
Adverse_Event_Reporting_System wikiPageExternalLink research.php.
Adverse_Event_Reporting_System wikiPageExternalLink AdverseDrugEffects.
Adverse_Event_Reporting_System wikiPageExternalLink medwatch-online.htm.
Adverse_Event_Reporting_System wikiPageID "31085244".
Adverse_Event_Reporting_System wikiPageLength "3474".
Adverse_Event_Reporting_System wikiPageOutDegree "13".
Adverse_Event_Reporting_System wikiPageRevisionID "684002064".
Adverse_Event_Reporting_System wikiPageWikiLink Category:Food_and_Drug_Administration.
Adverse_Event_Reporting_System wikiPageWikiLink Category:Government_databases_in_the_United_States.
Adverse_Event_Reporting_System wikiPageWikiLink Causality.
Adverse_Event_Reporting_System wikiPageWikiLink Center_for_Biologics_Evaluation_and_Research.
Adverse_Event_Reporting_System wikiPageWikiLink Center_for_Drug_Evaluation_and_Research.
Adverse_Event_Reporting_System wikiPageWikiLink Epidemiology.
Adverse_Event_Reporting_System wikiPageWikiLink Food_and_Drug_Administration.
Adverse_Event_Reporting_System wikiPageWikiLink Health_professional.
Adverse_Event_Reporting_System wikiPageWikiLink MedDRA.
Adverse_Event_Reporting_System wikiPageWikiLink MedWatch.
Adverse_Event_Reporting_System wikiPageWikiLink Medical_error.
Adverse_Event_Reporting_System wikiPageWikiLink Postmarketing_surveillance.
Adverse_Event_Reporting_System wikiPageWikiLink Regulation.
Adverse_Event_Reporting_System wikiPageWikiLinkText "Adverse Event Reporting System".
Adverse_Event_Reporting_System subject Category:Food_and_Drug_Administration.
Adverse_Event_Reporting_System subject Category:Government_databases_in_the_United_States.
Adverse_Event_Reporting_System hypernym Database.
Adverse_Event_Reporting_System type BiologicalDatabase.
Adverse_Event_Reporting_System type Drug.
Adverse_Event_Reporting_System type Agency.
Adverse_Event_Reporting_System type Drug.
Adverse_Event_Reporting_System comment "The Adverse Event Reporting System (AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) post-marketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses AERS to monitor for new adverse events and medication errors that might occur with these marketed products.".
Adverse_Event_Reporting_System label "Adverse Event Reporting System".
Adverse_Event_Reporting_System sameAs Q4686710.
Adverse_Event_Reporting_System sameAs m.0ggbgcx.
Adverse_Event_Reporting_System sameAs Q4686710.
Adverse_Event_Reporting_System wasDerivedFrom Adverse_Event_Reporting_System?oldid=684002064.
Adverse_Event_Reporting_System isPrimaryTopicOf Adverse_Event_Reporting_System.