نتایج جستجو برای: spontaneous reporting
تعداد نتایج: 205546 فیلتر نتایج به سال:
Adverse drug reactions (ADRs) are considered as one of the leading causes of death among hospitalized patients. Thus reporting of adverse drug reactions become an important phenomenon. Spontaneous adverse drug reaction reporting form is an essential component and a major tool of the pharmacovigilance system of any country. This form is a tool to collect information of ADRs which helps in establ...
BACKGROUND There is a limited guidance for outcome reporting for cardiac arrest trials. This review was conducted to explore the degree of variation and identify trends in outcome reporting. METHODS Randomised controlled trials enrolling patients with cardiac arrest (2002-2012) were identified by applying a search strategy to four databases. Titles, abstracts and short-listed studies were ind...
Detection of adverse drug reactions (ADRs) in hospitals provides an important measure of the burden of drug related morbidity on the healthcare system. Spontaneous reporting of ADRs is scare and several obstacles to such reporting have been identified formerly. This study aimed to determine the role of clinical pharmacy residents in ADR reporting within a hospital setting. Clinical pharmacy res...
IntRoductIon An adverse drug reaction (ADR) is unintended injuries caused by the drug at normal doses during normal use.[1] ADR monitoring is a long‐term work of medical institutions. Medical institutions at all levels have their corresponding requirements of reporting ADRs.[1] On December 12, 2010, the National Health and Family Planning Commission of the People’s Republic of China issued the ...
PURPOSE We developed an adverse events (AEs) reporting form for Korean folk medicine. METHODS The first version of the form was developed and tested in the clinical setting for spontaneous reporting of AEs. Additional revisions to the reporting form were made based on collected data and expert input. RESULTS We developed an AEs reporting form for Korean folk medicine. The items of this form...
OBJECTIVES To analyse an Italian database of spontaneous reporting of suspected adverse drug reactions in order to compare the safety profile of amoxicillin and amoxicillin/clavulanic acid. METHODS Data were retrieved from the spontaneous reports collected by six Italian regions (the GIF database) from January 1988 to June 2005. Drug utilization data were also available for the two drugs. The...
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