Adverse drug reaction reporting among health care workers at Mulago National Referral and Teaching hospital in Uganda [PDF]
, 2015 Background: Adverse Drug Reactions (ADRs) are an important contributor to patient morbidity and hospitalisation in Uganda. Under-reporting of ADRs may increase medicine-induced morbidity and mortality among patients.
Katusiime, Barbara +2 more
core +2 more sources
Integrating pharmacovigilance into the routine of pharmacy department: experience of nine years [PDF]
Farmacia Hospitalaria, 2019 Objective: To describe our pharmacovigilance program and to analyze the reported adverse drug reactions. Method: Observational longitudinal study conducted from 2008 to 2016.
Ariadna Pérez-Ricart +4 more
doaj +1 more source
Bayesian model selection in logistic regression for the detection of adverse drug reactions [PDF]
, 2015 Motivation: Spontaneous adverse event reports have a high potential for detecting adverse drug reactions. However, due to their dimension, exploring such databases requires statistical methods.
Marbac, Matthieu +2 more
core +2 more sources
Focusing on the System Barriers to Widespread Reporting of Adverse Drug Reactions
Oncology Times, 2003 Rabiya S. Tuma
openalex +2 more sources
Delayed angioedema during therapy with angiotensin-converting enzyme inhibitors [PDF]
Vojnosanitetski Pregled, 2011 Introduction. Angiotensin-converting enzyme inhibitors are leading cause of drug-induced angioedema, with incidence of 0.1 to 0.2%. The angioedema is not of immune nature; in predisposed individuals it is caused by accumulation of vasoactive mediators
Janković Slobodan M. +1 more
doaj +1 more source
Views of healthcare professionals to linkage of routinely collected healthcare data : a systematic review [PDF]
, 2013 Peer reviewedPublisher ...
Bond, C +4 more
core +2 more sources
Nurses' reporting of suspect adverse drug reactions: a mixed-methods study
Annali dell'Istituto Superiore di Sanità, 2015 OBJECTIVE: To assess nurses' knowledge, attitudes and practices (KAP) towards spontaneous adverse drug reactions (ADRs) reporting. METHODS: The mixed-method study was conducted following a quanti-qualitative sequential approach: a survey (using a KAP ...
Alessia De Angelis +4 more
doaj +1 more source
Cadernos de Saúde Pública, 2021 : The U.S. Food and Drug Administration (FDA) has stated that the prescription of remdesivir should be cautious for patients with estimated glomerular filtration rate (eGFR) < 30 and some studies reported risk of adverse renal events.
Nayara Aparecida de Oliveira Silva +3 more
doaj +1 more source
System of adverse drug reactions reporting: What, where, how, and whom to report?
Indian Journal of Critical Care Medicine, 2015 Sir, The continuous progress in medical and pharmaceutical sciences has made the availability of pharmaceutical products in the Indian market to prevent and control of several disease conditions. Irrespective of the benefits associated with the use of medicines adverse effects associated with them has emerged the challenges of monitoring Adverse ...
Gyanendra Nath Singh +3 more
openaire +3 more sources
South African Journal of Industrial Engineering, 2018 Since 2010, pharmaceutical organisations have begun to provide drug patents in sub-Saharan Africa through the UN Medicine Patent Pool. This initiative allows any pharmaceutical manufacturer to access these patents and manufacture the drugs, thereby ...
Huysamen, Biance +2 more
doaj +1 more source