Under-reporting of adverse drug reactions : a systematic review.
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Reporting bias in medical research - a narrative reviewHow drugs get into cells: tested and testable predictions to help discriminate between transporter-mediated uptake and lipoidal bilayer diffusionPatient Participation and the Use of Ehealth Tools for PharmacoviliganceClinical and regulatory perspectives on biosimilar therapies and intended copies of biologics in rheumatologyManaging the incidence of selective reporting bias: a survey of Cochrane review groupsSystematic reviews to ascertain the safety of diabetes medicationsCauses for the underreporting of adverse drug events by health professionals: a systematic reviewBisphosphonates and nonhealing femoral fractures: analysis of the FDA Adverse Event Reporting System (FAERS) and international safety efforts: a systematic review from the Research on Adverse Drug Events And Reports (RADAR) projectInformation and feedback to improve occupational physicians' reporting of occupational diseases: a randomised controlled trialFocus on headache as an adverse reaction to drugsStudy of natural health product adverse reactions (SONAR): active surveillance of adverse events following concurrent natural health product and prescription drug use in community pharmaciesAdverse drug reactions causing admission to a paediatric hospitalMedication monitoring in a nurse-led respiratory outpatient clinic: pragmatic randomised trial of the West Wales Adverse Drug Reaction ProfileValproic acid and fatalities in children: a review of individual case safety reports in VigiBaseRare, serious, and comprehensively described suspected adverse drug reactions reported by surveyed healthcare professionals in UgandaBias in spontaneous reporting of adverse drug reactions in JapanIdentification of Adverse Drug Events from Free Text Electronic Patient Records and Information in a Large Mental Health Case RegisterNurse-Led Medicines' Monitoring for Patients with Dementia in Care Homes: A Pragmatic Cohort Stepped Wedge Cluster Randomised TrialA Retrospective Analysis of Spontaneous Adverse Drug Reactions Reports Relating to Paediatric PatientsAn Interoperability Platform Enabling Reuse of Electronic Health Records for Signal Verification StudiesPharmacovigilance from social media: mining adverse drug reaction mentions using sequence labeling with word embedding cluster featuresBiosimilar Insulins: Basic ConsiderationsMedication incidents in primary care medicine: protocol of a study by the Swiss Federal Sentinel Reporting SystemRecognition and reporting of suspected adverse drug reactions by surveyed healthcare professionals in Uganda: key determinantsThe promotion of data sharing in pharmacoepidemiologyComputing limits on medicine risks based on collections of individual case reportsGeneralized enrichment analysis improves the detection of adverse drug events from the biomedical literatureDictionary construction and identification of possible adverse drug events in Danish clinical narrative textDose-Specific Adverse Drug Reaction Identification in Electronic Patient Records: Temporal Data Mining in an Inpatient Psychiatric PopulationPharmacovigilance Skills, Knowledge and Attitudes in our Future Doctors - A Nationwide Study in the Netherlands.Adverse Drug Reactions in Children: The Double-Edged Sword of Therapeutics.Adverse Health Events Related to Self-Medication Practices Among Elderly: A Systematic Review.Adverse drug event reporting systems: a systematic reviewThrombocytopenia from combination treatment with oseltamivir and probenecid: case report, MedWatch data summary, and review of the literature.Experience of safety monitoring in the context of a prospective observational study of artemether-lumefantrine in rural Tanzania: lessons learned for pharmacovigilance reporting.Data mining of the public version of the FDA Adverse Event Reporting SystemAnaphylaxis associated with gadolinium-based contrast agents: data from the Food and Drug Administration's Adverse Event Reporting System and review of case reports in the literature.Availability of data on adverse reactions to antiretroviral drugs in medical charts according to the Naranjo algorithm: an example of a Brazilian historical cohort.Association of statin use with sleep disturbances: data mining of a spontaneous reporting database and a prescription database.Feasibility and Educational Value of a Student-Run Pharmacovigilance Programme: A Prospective Cohort Study.
P2860
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P2860
Under-reporting of adverse drug reactions : a systematic review.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
@wuu
2006年学术文章
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2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
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2006年學術文章
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name
Under-reporting of adverse drug reactions : a systematic review.
@ast
Under-reporting of adverse drug reactions : a systematic review.
@en
type
label
Under-reporting of adverse drug reactions : a systematic review.
@ast
Under-reporting of adverse drug reactions : a systematic review.
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prefLabel
Under-reporting of adverse drug reactions : a systematic review.
@ast
Under-reporting of adverse drug reactions : a systematic review.
@en
P1433
P1476
Under-reporting of adverse drug reactions : a systematic review.
@en
P2093
Lorna Hazell
Saad A W Shakir
P304
P356
10.2165/00002018-200629050-00003
P577
2006-01-01T00:00:00Z
P6179
1012106416