[go: up one dir, main page]

An Entity of Type: SocialGroup107950920, from Named Graph: http://dbpedia.org, within Data Space: dbpedia.org

The Vaccine Adverse Event Reporting System (VAERS) is a United States program for vaccine safety, co-managed by the U.S. Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). VAERS is a postmarketing surveillance program, collecting information about adverse events (possible harmful side effects) that occur after administration of vaccines to ascertain whether the risk–benefit ratio is high enough to justify continued use of any particular vaccine.

Property Value
dbo:abstract
  • Das Vaccine Adverse Event Reporting System (VAERS, deutsch Meldesystem für Impfstoffnebenwirkungen) ist ein Meldesystem für Verdachtsfälle unerwünschter Wirkungen von Impfstoffen in den USA. (de)
  • The Vaccine Adverse Event Reporting System (VAERS) is a United States program for vaccine safety, co-managed by the U.S. Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). VAERS is a postmarketing surveillance program, collecting information about adverse events (possible harmful side effects) that occur after administration of vaccines to ascertain whether the risk–benefit ratio is high enough to justify continued use of any particular vaccine. VAERS, the Vaccine Safety Datalink, and the Clinical Immunization Safety Assessment (CISA) Network are tools by which the CDC and FDA monitor vaccine safety to fulfill their duty as regulatory agencies charged with protecting the public. As it is based on submissions by the public, VAERS is susceptible to unverified reports, misattribution, underreporting, and inconsistent data quality. Raw, unverified data from VAERS has often been used by the anti-vaccine community to justify misinformation regarding the safety of vaccines; it is generally not possible to find out from VAERS data if a vaccine caused an adverse event, or how common the event might be. (en)
  • Il Vaccine Adverse Event Reporting System (VAERS) è un programma statunitense per la sicurezza dei vaccini, co-gestito dai centri statunitensi per il controllo e la prevenzione delle malattie Centers for Disease Control and Prevention (CDC) e la Food and Drug Administration (FDA). L'obiettivo principale di questo strumento è quello di individuare eventuali reazioni avverse talmente rare da non essere apparse all'interno dei test clinici. VAERS, il Vaccine Safety Datalink (VSD) e il Clinical Immunization Safety Assessment (CISA) Network sono strumenti mediante i quali il CDC e la FDA monitorano la sicurezza dei vaccini per adempiere al loro dovere di enti regolatori incaricati di proteggere gli individui. Il CDC avverte che non è possibile stabilire una correlazione causa effetto dai dati VAERS, per studi di questo tipo ci si affida al VSD. L'ente europeo incaricato del medesimo compito è l'EudraVigilance, naturalmente possiede le stesse limitazioni dei VAERS. Durante la pandemia di COVID-19, questo database è stato ampiamente utilizzato per condividere disinformazione riguardo ai vaccini. (it)
dbo:wikiPageExternalLink
dbo:wikiPageID
  • 1777037 (xsd:integer)
dbo:wikiPageLength
  • 14115 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID
  • 1116057653 (xsd:integer)
dbo:wikiPageWikiLink
dbp:wikiPageUsesTemplate
dct:subject
gold:hypernym
rdf:type
rdfs:comment
  • Das Vaccine Adverse Event Reporting System (VAERS, deutsch Meldesystem für Impfstoffnebenwirkungen) ist ein Meldesystem für Verdachtsfälle unerwünschter Wirkungen von Impfstoffen in den USA. (de)
  • The Vaccine Adverse Event Reporting System (VAERS) is a United States program for vaccine safety, co-managed by the U.S. Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA). VAERS is a postmarketing surveillance program, collecting information about adverse events (possible harmful side effects) that occur after administration of vaccines to ascertain whether the risk–benefit ratio is high enough to justify continued use of any particular vaccine. (en)
  • Il Vaccine Adverse Event Reporting System (VAERS) è un programma statunitense per la sicurezza dei vaccini, co-gestito dai centri statunitensi per il controllo e la prevenzione delle malattie Centers for Disease Control and Prevention (CDC) e la Food and Drug Administration (FDA). L'obiettivo principale di questo strumento è quello di individuare eventuali reazioni avverse talmente rare da non essere apparse all'interno dei test clinici. L'ente europeo incaricato del medesimo compito è l'EudraVigilance, naturalmente possiede le stesse limitazioni dei VAERS. (it)
rdfs:label
  • Vaccine Adverse Event Reporting System (de)
  • Vaccine Adverse Event Reporting System (it)
  • Vaccine Adverse Event Reporting System (en)
owl:sameAs
prov:wasDerivedFrom
foaf:homepage
foaf:isPrimaryTopicOf
is dbo:wikiPageRedirects of
is dbo:wikiPageWikiLink of
is foaf:primaryTopic of
Powered by OpenLink Virtuoso    This material is Open Knowledge     W3C Semantic Web Technology     This material is Open Knowledge    Valid XHTML + RDFa
This content was extracted from Wikipedia and is licensed under the Creative Commons Attribution-ShareAlike 3.0 Unported License