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Data Mining of the Public Version of the FDA Adverse Event Reporting System

The US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS, formerly AERS) is a database that contains information on adverse event and medication error reports submitted to the FDA. Besides those from manufacturers, reports can be submitted from health care professionals and th...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Sakaeda, Toshiyuki, Tamon, Akiko, Kadoyama, Kaori, Okuno, Yasushi
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Ivyspring International Publisher 2013
Gaiak:
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3689877/
https://ncbi.nlm.nih.gov/pubmed/23794943
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijms.6048
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