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Adverse Event Profiles of Platinum Agents: Data Mining of the Public Version of the FDA Adverse Event Reporting System, AERS, and Reproducibility of Clinical Observations

Objective: Adverse event reports (AERs) submitted to the US Food and Drug Administration (FDA) were reviewed to confirm platinum agent-associated adverse events, and to clarify the rank-order of these drugs in terms of susceptibility. Methods: After a revision of arbitrary drug names and the deletio...

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Dettagli Bibliografici
Autori principali: Sakaeda, Toshiyuki, Kadoyama, Kaori, Okuno, Yasushi
Natura: Artigo
Lingua:Inglês
Pubblicazione: Ivyspring International Publisher 2011
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3167097/
https://ncbi.nlm.nih.gov/pubmed/21897761
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