نتایج جستجو برای: adverse event reporting

تعداد نتایج: 485155  

Journal: :the journal of tehran university heart center 0
ahmad sharafi tehran heart center, tehran university of medical sciences, tehran, iran. hamidreza pour-hosseini tehran heart center, tehran university of medical sciences, tehran, iran. arash jalali tehran heart center, tehran university of medical sciences, tehran, iran. mojtaba salarifar tehran heart center, tehran university of medical sciences, tehran, iran. ebrahim nematipour tehran heart center, tehran university of medical sciences, tehran, iran. mohsen shojanasab tehran heart center, tehran university of medical sciences, tehran, iran.

background: controversy persists over the potential benefits/harms of opium consumption in coronary heart disease. this study investigated the association between 12 months' major adverse cardiac events (mace) and pre-procedural opium consumption among patients undergoing percutaneous coronary intervention (pci). methods: retrospectively, 1545 consecutive men who underwent pci between 21 st   j...

Journal: :Journal of child and adolescent psychopharmacology 2006
Andrew D Mosholder Carol A Pamer

OBJECTIVE The aim of this analysis was to delineate trends in spontaneous postmarketing reporting data with antidepressant drugs for adverse events involving suicidal behaviors in children and adolescents. METHODS The U.S. Food and Drug Administration (FDA) Adverse Event Reporting System (AERS) was searched for postmarketing adverse event reports of suicidal thoughts and behaviors occurring i...

Journal: :Pain 2013
Victoria R Cornelius Odile Sauzet John E Williams Salma Ayis Paul Farquhar-Smith Joy R Ross Ruth A Branford Janet L Peacock

High-quality information on the potential benefit and harm of a drug is required for patients and clinicians to make informed treatment decisions and to enable cost-effectiveness modeling to be undertaken. This systematic review describes the collection and reporting of adverse event data as presented in published clinical trials of neuropathic pain for the evaluation of antidepressant or antie...

2014
Mélanie Courtot Ryan R. Brinkman Alan Ruttenberg

BACKGROUND When increased rates of adverse events following immunization are detected, regulatory action can be taken by public health agencies. However to be interpreted reports of adverse events must be encoded in a consistent way. Regulatory agencies rely on guidelines to help determine the diagnosis of the adverse events. Manual application of these guidelines is expensive, time consuming, ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید