نتایج جستجو برای: adverse event reporting
تعداد نتایج: 485155 فیلتر نتایج به سال:
Pharmacovigilance is a method of quick detection and reporting, of adverse drug reactions and adverse drug events after drug is in clinical use, thus preventing major drug events. Ignorance of physicians in developing world, about reporting adverse drug reaction is a big roadblock to pharmacovigilance. This cascades into many problems e.g.; increased lab to clinic interval, increased premarketi...
Abstract The U.S. Food and Drug Administration (FDA) approved the first chimeric antigen receptor T‐cell therapy, tisagenlecleucel, in August 2017. We sought to describe adverse events (AEs) reported FDA Adverse Event Reporting System (FAERS) for tisagenlecleucel post‐marketing period. searched FAERS reports identify patients treated with between 30, 2017‐August 31, 2019. reviewed individual re...
BACKGROUND Dietary supplements are used by >50% of the adult population in Japan, and adverse events related to these products have been reported with their increased use. Thus, an efficient system to gather and report data on these adverse events is essential. To date, however, reporting has been limited. The aim of this study was to address this deficiency by exploring the routine reporting p...
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