نتایج جستجو برای: adverse event reporting
تعداد نتایج: 485155 فیلتر نتایج به سال:
Mortality and oral anticoagulants in the Food and Drug Administration Adverse Event Reporting System
OBJECTIVE Determine the degree of congruence between several measures of adverse events. DESIGN Cross-sectional study to assess frequency and type of adverse events identified using a variety of methods. SETTING Mayo Clinic Rochester hospitals. PARTICIPANTS All inpatients discharged in 2005 (n = 60 599). INTERVENTIONS Adverse events were identified through multiple methods: (i) Agency f...
OBJECTIVE Case reports showing that proton-pump inhibitors (PPIs), omeprazole and esomeprazole, can cause hypomagnesaemia have been accumulating since 2006. In this study, the reports submitted to the Adverse Event Reporting System (AERS) of the US Food and Drug Administration (FDA) were evaluated to assess omeprazole and esomeprazole in terms of susceptibility to hypomagnesaemia. METHODS Aft...
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