Results 21 to 30 of about 519,396 (228)

Adverse Effects of Cholinesterase Inhibitors in Dementia, According to the Pharmacovigilance Databases of the United-States and Canada. [PDF]

, 2015
This survey analyzes two national pharmacovigilance databases in order to determine the major adverse reactions observed with the use of cholinesterase inhibitors in dementia.
Abagyan, Ruben, Ali, Thibault B, Chen, Winston Yuchen, Reilly, Brian M, Schleret, Thomas R   +4 more
core   +3 more sources

Adverse drug event reporting systems: a systematic review [PDF]

British Journal of Clinical Pharmacology, 2016
AimAdverse drug events (ADEs) are harmful and unintended consequences of medications. Their reporting is essential for drug safety monitoring and research, but it has not been standardized internationally. Our aim was to synthesize information about the type and variety of data collected within ADE reporting systems.MethodsWe developed a systematic ...
Chantelle, Bailey, David, Peddie, Maeve E, Wickham, Katherin, Badke, Serena S, Small, Mary M, Doyle-Waters, Ellen, Balka, Corinne M, Hohl   +7 more
openaire   +2 more sources

Antipsychotics and Torsadogenic Risk: Signals Emerging from the US FDA Adverse Event Reporting System Database [PDF]

, 2013
Background: Drug-induced torsades de pointes (TdP) and related clinical entities represent a current regulatory and clinical burden. Objective: As part of the FP7 ARITMO (Arrhythmogenic Potential of Drugs) project, we explored the publicly available US ...
A Bate, A Clarke, A Pariente, AK Chung, Ariola Koci, B Darpo, BJ Drew, C Meyer-Massetti, DM Roden, DW Hough, E Poluzzi, E Poluzzi, E Poluzzi, E Raschi, E Raschi, Edoardo Spina, Elijah R. Behr, Elisabetta Poluzzi, Emanuel Raschi, EP Puijenbroek van, ER Behr, F Ponti De, F Ponti De, F Rani, Fabrizio De Ponti, GC Alexander, GK Isbister, H Verdoux, J Nielsen, J Papay, K Jolly, K Titier, LC Wittkampf, LS Schneider, Miriam Sturkenboom, NP Tatonetti, P Kannankeril, P Manu, P Vigneault, RC Owens Jr, RR Shah, S Dhillon, S Hennessy, S Kongsamut, S Leucht, SM Straus, Ugo Moretti, W Crumb, W Crumb, WA Ray, WA Ray, WJ Crumb Jr, WP Stephenson, Y Suzuki   +53 more
core   +4 more sources

Digital Drug Safety Surveillance: Monitoring Pharmaceutical Products in Twitter [PDF]

, 2014
Background: Traditional adverse event (AE) reporting systems have been slow in adapting to online AE reporting from patients, relying instead on gatekeepers, such as clinicians and drug safety groups, to verify each potential event.
Bao, Wenjie, Brownstein, John S., Dasgupta, Nabarun, Filice, Ross, Freifeld, Clark C., Kass-Hout, Taha, Menone, Christopher M.   +6 more
core   +3 more sources

Methods for Detecting and Measuring Adverse Hospital Events [PDF]

Iranian Journal of Public Health, 2005
Introduction: An adverse event is defined as an unexpected event such as a patient fall, a drug reaction or an infection, which leads to patient injury and is caused by healthcare management rather than patient own diseases.
A Baba-Akbari Sari, TA Sheldon   +1 more
doaj   +1 more source

Assessment of Reye’s syndrome profile with data from the US Food and Drug Administration Adverse Event Reporting System and the Japanese Adverse Drug Event Report databases using the disproportionality analysis

SAGE Open Medicine, 2020
Objectives: Reye’s syndrome is a rare and potentially fatal illness that is defined as encephalopathy accompanied by liver failure. The aim of this study was to assess Reye’s syndrome profiles by analyzing data from the spontaneous reporting system ...
Kiyoka Matsumoto, Shiori Hasegawa, Satoshi Nakao, Kazuyo Shimada, Ririka Mukai, Mizuki Tanaka, Riko Satake, Yu Yoshida, Fumiya Goto, Misaki Inoue, Hiroaki Ikesue, Kazuhiro Iguchi, Tohru Hashida, Mitsuhiro Nakamura   +13 more
doaj   +1 more source

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, Michael M, McNeil, Susanne, Pickering, Michael R, Pemberton, Laurie L, Duran, Limone C, Collins, Michael R, Nelson, Renata J M, Engler   +7 more
openaire   +2 more sources

Contributory factors in surgical incidents as delineated by a confidential reporting system [PDF]

, 2018
Background Confidential reporting systems play a key role in capturing information about adverse surgical events. However, the value of these systems is limited if the reports that are generated are not subjected to systematic analysis.
Kapur, N, Lawton, R, Mushtaq, F, O’Driscoll, C, Smith, FCT, Wilkins, D   +5 more
core   +1 more source

A logic programming approach to medical errors in imaging [PDF]

, 2011
Background: In 2000, the Institute of Medicine reported alarming data on the scope and impact of medical errors calling the public attention. One solution to this problem is the adoption of adverse event reporting and learning systems that can help to ...
Alves, Victor, Brandão, Paulo, Nelas, Luís, Neves, José, Rodrigues, Susana Isabel Magalhães da Rocha   +4 more
core   +1 more source

Adverse event profiles of solvent-based and nanoparticle albumin-bound paclitaxel formulations using the Food and Drug Administration Adverse Event Reporting System

SAGE Open Medicine, 2019
Objectives: Paclitaxel is a highly effective antitumor agent with notable adverse events, including hypersensitivity reactions, peripheral neuropathy, arthralgia, myalgias, and neutropenia.
Misa Naganuma, Kohei Tahara, Shiori Hasegawa, Akiho Fukuda, Sayaka Sasaoka, Haruna Hatahira, Yumi Motooka, Satoshi Nakao, Ririka Mukai, Kouseki Hirade, Tomoaki Yoshimura, Takeshi Kato, Hirofumi Takeuchi, Mitsuhiro Nakamura   +13 more
doaj   +1 more source