Status and Problems of Adverse Event Reporting Systems in Korean Hospitals [PDF]
Healthcare Informatics Research, 2010 ObjectivesThis study identifies the current status and problems of adverse event reporting system in Korean hospitals. The data obtained from this study will be used to raise international awareness and enable collaborative researches on patient safety ...
Jeongeun Kim +3 more
doaj +9 more sources
A disproportionality analysis of FDA adverse event reporting system events for misoprostol [PDF]
Scientific ReportsMisoprostol was originally used to treat gastric ulcers, and has been widely used in abortion, cervical maturation, induced labour and postpartum hemorrhage. But there are still many undetected adverse events (AEs).
Li Yang, Wenting Xu
doaj +3 more sources
Adverse event reporting systems and safer healthcare [PDF]
Quality and Safety in Health Care, 2009 At the heart of improvement and safety in healthcare is the now-familiar tenet that was espoused decades ago by Demming and paraphrased by Berwick.1 Need we repeat it again? Every defect should lead to improvement processes that make care safer. It is time to deliver on the promise of reporting systems in patient safety.
James B Battles, David Stevens
openalex +4 more sources
Military Healthcare Providers Reporting of Adverse Events Following Immunizations to the Vaccine Adverse Event Reporting System [PDF]
Military Medicine, 2014 We studied military health care provider (HCP) practices regarding reporting of adverse events following immunization (AEFI).A convenience sample of HCP was surveyed to assess familiarity with Vaccine Adverse Event Reporting System (VAERS), AEFI they were likely to report, methods used and preferred for reporting, and perceived barriers to reporting ...
Rongxia Li +7 more
openalex +3 more sources
Assessing taxane-associated adverse events using the FDA adverse event reporting system database
Chinese Medical Journal, 2021 . Background:. Taxanes are an essential class of antineoplastic agents used to treat various cancers and are a fundamental cause of hypersensitivity reactions. In addition, other adverse events, such as bone marrow toxicity and peripheral neuropathy, can
Dong-Hui Lao +4 more
doaj +3 more sources
Musculoskeletal adverse events reported post-hepatitis B vaccination in the vaccine adverse event reporting system [PDF]
Frontiers in Public HealthIntroductionHepatitis B virus (HBV) is a major cause of chronic liver disease. While the hepatitis B vaccine has been proven effective in preventing HBV infection, concerns regarding Events Supposedly Attributable to Vaccination or Immunization (ESAVI ...
Yiqing Sun +4 more
doaj +2 more sources
Adverse events associated with amlodipine: a pharmacovigilance study using the FDA adverse event reporting system [PDF]
Frontiers in Cardiovascular MedicineBackgroundAmlodipine, a widely prescribed clinical medication, is associated with adverse reactions that can impede the proper execution of treatment regimens.
Xingwei Di +6 more
doaj +2 more sources
Adverse event reporting of faricimab: a disproportionality analysis of FDA adverse event reporting system (FAERS) database [PDF]
Frontiers in PharmacologyBackgroundFaricimab is the first and only bispecific antibody approved by the U.S. Food and Drug Administration (FDA) for intravitreal injection. Given its increasingly widespread use in retinal vascular diseases, understanding its adverse events (AEs ...
Chang-Zhu He +5 more
doaj +2 more sources
Comprehensive analysis of adverse events associated with vortioxetine using the FDA adverse event reporting system [PDF]
Frontiers in PharmacologyBackgroundVortioxetine is a novel antidepressant belonging to the class of selective serotonin reuptake inhibitors. This study aims to comprehensively analyze the adverse events (AEs) associated with vortioxetine by analyzing the FDA Adverse Event ...
Liangxia Li +4 more
doaj +2 more sources
Serious Adverse Drug Events Reported to the FDA: Analysis of the FDA Adverse Event Reporting System 2006-2014 Database [PDF]
Journal of Managed Care & Specialty Pharmacy, 2018 Data on adverse drug events (ADEs) observed at the population level provide important evidence regarding the safety of a pharmaceutical product in real-world settings. Recent patterns in serious and fatal ADE reporting have not been documented.To assess recent patterns in serious and fatal ADE reports in the United States.We conducted a retrospective ...
Kalyani Sonawane +2 more
openalex +4 more sources