نتایج جستجو برای: adverse event reporting

تعداد نتایج: 485155  

Journal: :journal of pharmaceutical care 0
maryam etminani-isfahani department of clinical pharmacy, school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran sarah mousavi department of clinical pharmacy and pharmacy practice, faculty of pharmacy and pharmaceutical sciences, isfahan university of medical sciences, isfahan, iran amin rakhshan school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran mehrdad assarian school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran leila kuti department of clinical pharmacy, school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran kaveh eslami department of clinical pharmacy, school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, iran

background: adverse drug reactions (adrs) are one of the leading causes of morbidity and mortality and contribute to excessive health care costs. detection and reporting of adrs could decrease these consequences. the present study was designed to assess the knowledge, attitude and practice (kap) of pharmacy students towards adrs monitoring and reporting. methods: a questionnaire was prepared to...

2015
Thibault B. Ali Thomas R. Schleret Brian M. Reilly Winston Yuchen Chen Ruben Abagyan Andrea Cavalli

This survey analyzes two national pharmacovigilance databases in order to determine the major adverse reactions observed with the use of cholinesterase inhibitors in dementia. We conducted a statistical analysis of the Food and Drug Administration Adverse Event Reporting System (FAERS) and the Canada Vigilance Adverse Reaction Database (CVARD) concerning the side effects of cholinesterase inhib...

2017
Lindsay M Gorrell Roger M Engel Reidar P Lystad Benjamin T Brown

BACKGROUND Reporting of adverse events in randomized clinical trials (RCTs) is encouraged by the authors of The Consolidated Standards of Reporting Trials (CONSORT) statement. With robust methodological design and adequate reporting, RCTs have the potential to provide useful evidence on the incidence of adverse events associated with spinal manipulative therapy (SMT). During a previous investig...

2018
Megumi Horibe Yuuki Hane Junko Abe Toshinobu Matsui Yamato Kato Natsumi Ueda Sayaka Sasaoka Yumi Motooka Haruna Hatahira Shiori Hasegawa Yasutomi Kinosada Hideaki Hara Mitsuhiro Nakamura

Aim Postpartum depression is a mood disorder that commonly affects women during the early postpartum period. The objective of this study was to analyse the association of postpartum depression with drugs (including contraceptive devices and implants) with spontaneously reported adverse events reported in the US Food and Drug Administration Adverse Event Reporting System database. Design Retro...

Journal: :Healthcare policy = Politiques de sante 2009
Rishma Walji Heather Boon Joanne Barnes Zubin Austin G Ross Baker Sandy Welsh

Herbal products are readily available over the counter in health food stores and are often perceived to be without risk. The current Canadian adverse event reporting system suffers from severe underreporting, resulting in a scarcity of safety data on herbal products. Twelve health food store personnel in the Greater Toronto Area were interviewed about their responses to herbal product-related a...

2011
Ingrid Christiaans-Dingelhoff Marleen Smits Laura Zwaan Sanne Lubberding Gerrit van der Wal Cordula Wagner

BACKGROUND Patient record review is believed to be the most useful method for estimating the rate of adverse events among hospitalised patients. However, the method has some practical and financial disadvantages. Some of these disadvantages might be overcome by using existing reporting systems in which patient safety issues are already reported, such as incidents reported by healthcare professi...

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