OBJECTIVES This study investigated the impact of television news coverage on total adverse event reporting rates 1 month before and after the bulletins during a medication health scare. We further investigated whether individual side effects mentioned in each bulletin were reflected in the adverse event reports following the coverage. DESIGN A retrospective pre-post observational study. SET...

background: the most common types of medical error are medication errors (mes) which defined as any preventable event that may be caused by an inappropriate medication usage and lead to an adverse drug reaction (adr) event in patients. in recent years, different approaches have been proposed to reduce mes, one of which is reporting adrs. the present study was designed to assess the knowledge, a...

BACKGROUND Spontaneous Reporting Systems [SRS] are critical tools in the post-licensure evaluation of medical product safety. Regulatory authorities use a variety of data mining techniques to detect potential safety signals in SRS databases. Assessing the performance of such signal detection procedures requires simulated SRS databases, but simulation strategies proposed to date each have limita...

Background The development of behavioral addictions (BAs) in association with dopamine agonists (DAs, commonly used to treat Parkinson's disease) has been reported. A recent report presented data that these associations are evident in the US Food and Drug Administration's (FDA) Adverse Event Reporting System (FAERS), a database containing information on adverse drug event and medication error r...

Background: Voluntary hospital reporting systems are potentially valuable sources of information about medical errors and adverse events. This study examined the extent and variation in the reporting of medication errors and adverse drug events in a voluntary hospital incident reporting system. Methods: A retrospective analysis of received incident reports of potential and preventable adverse d...