Comparing adverse event rates of oral blood glucose-lowering drugs reported by patients and healthcare providers: a post-hoc analysis of observational studies published between 1999 and 2011.

Background: Non-serious symptomatic adverse drug events (ADEs) affect the real benefit-risk ratio of a drug. Currently, such ADEs are quantified in different ways, often using reports from a healthcare provider or patients, resulting in large variations in estimated rates. Several studies showed tha...

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Detalles Bibliográficos
Publicado en:Drug Safety Vol. 34; no. 12; pp. 1191 - 1203
Autores principales: Hakobyan L, Haaijer-Ruskamp FM, de Zeeuw D, Dobre D, Denig P, Hakobyan, Liana, Haaijer-Ruskamp, Flora M, de Zeeuw, Dick, Dobre, Daniela, Denig, Petra
Formato: research Journal Article
Publicado: Springer Nature 2011
Acceso en línea:Ver este registro en EBSCOhost