The past, present and perhaps future of pharmacovigilance: homage to Folke Sjoqvist

scientific article

The past, present and perhaps future of pharmacovigilance: homage to Folke Sjoqvist is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/S00228-013-1486-8
P698PubMed publication ID23640186
P5875ResearchGate publication ID236662185

P2093author name stringNicholas Moore
P2860cites workPower and weakness of spontaneous reporting: a probabilistic approachQ68101463
Adverse Drug Reaction Monitoring ProgramQ68278670
[Pharmacovigilance in the hospital. First results]Q68545715
[Pharmacovigilance in the framework of recording and control of drugs in the United Kingdom]Q68901101
QT prolongation and torsade de pointes ventricular tachycardia produced by KetanserinQ68981738
[Information centers on undesirable effects of drugs: also on alerting function]Q69174376
Adverse-drug-reaction monitoringQ69522196
Adverse drug reaction monitoring: doing it the French wayQ69872137
Comparing the toxicity of two drugs in the framework of spontaneous reporting: a confidence interval approachQ70994189
Cough and ACE inhibitorsQ72207759
Quantitative estimation of rare adverse events which follow a biological progression: a new model applied to chronic NSAID useQ73487778
Comment on 'Quantitative estimation of rare adverse events which follow a biological progression: a new model applied to chronic NSAID use' Tramer et al., Pain 2000;85:169-182Q73949595
Incidence of serious adverse drug reactions in general practice: a prospective studyQ74020853
Under-reporting of adverse drug reactions. Estimate based on a spontaneous reporting scheme and a sentinel systemQ77425506
Rates of spontaneous reporting of adverse drug reactions in FranceQ78288415
Educating European (junior) doctors for safe prescribingQ81419718
The history of disproportionality measures (reporting odds ratio, proportional reporting rates) in spontaneous reporting of adverse drug reactionsQ81554845
Clinical pharmacology in research, teaching and health care: Considerations by IUPHAR, the International Union of Basic and Clinical PharmacologyQ84507174
Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patientsQ28169189
Benfluorex and valvular heart disease: a cohort study of a million people with diabetes mellitusQ28295644
A method for estimating the probability of adverse drug reactionsQ29616247
A data mining approach for signal detection and analysisQ30699387
Disproportionality analysis using empirical Bayes data mining: a tool for the evaluation of drug interactions in the post‐marketing settingQ30881243
Atypical antipsychotics: from potassium channels to torsade de pointes and sudden deathQ33152239
Effect of date of drug marketing on disproportionality measures in pharmacovigilance: the example of suicide with SSRIs using data from the UK MHRA.Q33439923
Hospitalizations for gastrointestinal and cardiovascular events in the CADEUS cohort of traditional or Coxib NSAID users.Q33692833
Patterns and correlates of benzodiazepine use in the French general populationQ33980983
Use of proportional reporting ratios (PRRs) for signal generation from spontaneous adverse drug reaction reportsQ34112790
Active safety monitoring of new medical products using electronic healthcare data: selecting alerting rulesQ34135347
Admission international normalized ratio levels, early treatment strategies, and major bleeding risk among non-ST-segment-elevation myocardial infarction patients on home warfarin therapy: insights from the National Cardiovascular Data RegistryQ34154285
Spontaneous reporting: how many cases are required to trigger a warning?Q34358944
Impact of a focussed teaching programme on practical prescribing skills among final year medical studentsQ34476064
Case-population studies in pharmacoepidemiology.Q34512879
Agranulocytosis associated with calcium dobesilate clinical course and risk estimation with the case-control and the case-population approachesQ34513698
A comparison of measures of disproportionality for signal detection in spontaneous reporting systems for adverse drug reactions.Q34629802
Drug hypersensitivity: pharmacogenetics and clinical syndromesQ34701492
Antipsychotic-related QTc prolongation, torsade de pointes and sudden deathQ34730759
Causality assessment of adverse drug reactions: comparison of the results obtained from published decisional algorithms and from the evaluations of an expert panel, according to different levels of imputability.Q35114141
Clinical Pharmacology Education in Europe: Undergraduate through Postgraduate to Continuing Professional DevelopmentQ35587377
Insulin glargine and risk of cancer: a cohort study in the French National Healthcare Insurance DatabaseQ35714366
Frequency and cost of serious adverse drug reactions in a department of general medicineQ35802171
The reporting odds ratio and its advantages over the proportional reporting ratioQ35865910
Applying propensity scores estimated in a full cohort to adjust for confounding in subgroup analysesQ36060576
Under-reporting of adverse drug reactions in general practiceQ36093893
Do observational studies using propensity score methods agree with randomized trials? A systematic comparison of studies on acute coronary syndromes.Q36131480
Drug-induced QT interval prolongation--regulatory guidance and perspectives on hERG channel studies.Q36210671
Learning curves, taking instructions, and patient safety: using a theoretical domains framework in an interview study to investigate prescribing errors among trainee doctorsQ36539116
Effect of increased warfarin use on warfarin-related cerebral hemorrhage: a longitudinal population-based study.Q51167842
Communication in drug safety: a report from an interactive debate held at the 10th annual meeting of the international society of pharmacovigilance (ISoP), 2010.Q51169048
Methodology for a multinational case-population study on liver toxicity risks with NSAIDs: the Study of Acute Liver Transplant (SALT).Q51190369
Healthcare professionals' self-reported experiences and preferences related to direct healthcare professional communications: a survey conducted in the Netherlands.Q51310674
Using high-dimensional propensity scores to automate confounding control in a distributed medical product safety surveillance system.Q51440489
Comparison of three methods (consensual expert judgement, algorithmic and probabilistic approaches) of causality assessment of adverse drug reactions: an assessment using reports made to a French pharmacovigilance centre.Q51650731
Comparative performance of two quantitative safety signalling methods: implications for use in a pharmacovigilance department.Q51933528
A new method for assessing drug causation provided agreement with experts' judgment.Q51949776
A Bayesian approach to causality assessment.Q52076627
A Bayesian neural network method for adverse drug reaction signal generation.Q52238255
Effect of competition bias in safety signal generation: analysis of a research database of spontaneous reports in France.Q53105748
Serum sickness-like reactions to cefaclor.Q53393338
The proportion of patient reports of suspected ADRs to signal detection in the Netherlands: case-control study.Q53897535
European network for the case-population surveillance of rare diseases (Euronet). A prospective feasibility study.Q55067432
Post-marketing surveillance of adverse reactions to new medicinesQ55342932
THALIDOMIDE AND CONGENITAL ABNORMALITIESQ56486313
Genetics and the Potential for Predictive Tests in Adverse Drug ReactionsQ57302670
A potential competition bias in the detection of safety signals from spontaneous reporting databasesQ57521230
The New Sentinel Network — Improving the Evidence of Medical-Product SafetyQ61836841
The reporting odds ratio versus the proportional reporting ratio:‘deuce’Q63865876
Transplantation for acute liver failure in patients exposed to NSAIDs or paracetamol (acetaminophen): the multinational case-population SALT studyQ36597715
The influence of primary care prescribing rates for new drugs on spontaneous reporting of adverse drug reactionsQ36780091
Undergraduate preparation for prescribing: the views of 2413 UK medical students and recent graduatesQ36792783
Novel statistical tools for monitoring the safety of marketed drugsQ36835511
Warfarin dose prediction in children using pharmacometric bridging--comparison with published pharmacogenetic dosing algorithmsQ36836979
Bayesian confidence propagation neural networkQ36866517
Admissions to hospital caused by adverse drug reactions: cross sectional incidence study. French Pharmacovigilance CentresQ37324712
Case series in drug safety: a review to determine characteristics and qualityQ37809529
Proarrhythmic actions of antiarrhythmic drugs: a reviewQ37942028
Impact of safety-related regulatory action on clinical practice: a systematic review.Q38000336
A decade of safety-related regulatory action in the Netherlands: a retrospective analysis of direct healthcare professional communications from 1999 to 2009.Q39871580
Teaching basic and clinical pharmacology to medical students: a 2006 survey in French schools of medicineQ40249491
False-positives in spontaneous reporting: should we worry about them?Q40614212
Harmonisation in pharmacovigilanceQ40661017
Is reporting rate a good predictor of risks associated with drugs?Q40816305
Drug-related hospital admissionsQ40842331
A signal of increased risk of hypoglycaemia with angiotensin receptor blockers caused by confoundingQ40944247
Random models for margins of a 2 x 2 contingency table and application to pharmacovigilanceQ41158958
Drug-induced cardiac arrhythmias: incidence, prevention and managementQ41628830
Channelling of COX-2 inhibitors to patients at higher gastrointestinal risk but not at lower cardiovascular risk: the Cox2 inhibitors and tNSAIDs description of users (CADEUS) study.Q42162410
Reports of hypoglycaemia associated with the use of ACE inhibitors and other drugs: a case/non-case study in the French pharmacovigilance system databaseQ42281184
Assessing drug safetyQ42939005
A pharmacometric model describing the relationship between warfarin dose and INR response with respect to variations in CYP2C9, VKORC1, and age.Q43089518
Poor prescribing is continualQ43249018
The organizational structure and governing principles of the Food and Drug Administration's Mini-Sentinel pilot programQ43433884
High-dimensional versus conventional propensity scores in a comparative effectiveness study of coxibs and reduced upper gastrointestinal complications.Q43701143
Prescribing of rosiglitazone and pioglitazone following safety signals: analysis of trends in dispensing patterns in the Netherlands from 1998 to 2008.Q43703608
Computerized comparison of six adverse drug reaction assessment proceduresQ43755137
Impact of safety alerts on measures of disproportionality in spontaneous reporting databases: the notoriety biasQ43761720
Relevance of a "Dear Doctor letter" to alert healthcare providers to new recommendations for vitamin D administrationQ43799079
An updated method improved the assessment of adverse drug reaction in routine pharmacovigilanceQ43932720
Imputation of the unexpected or toxic effects of drugs. Actualization of the method used in FranceQ43965677
Developing the Sentinel System--a national resource for evidence developmentQ44120843
Factors associated with serious traffic crashes: a prospective study in southwest FranceQ44203170
Minor head injury in warfarinized patients: indicators of risk for intracranial hemorrhageQ44235538
Food and Drug Administration's adverse drug reaction monitoring programQ44270918
Biases affecting the proportional reporting ratio (PPR) in spontaneous reports pharmacovigilance databases: the example of sertindoleQ44481511
Design considerations in an active medical product safety monitoring system.Q44659710
EU-ADR healthcare database network vs. spontaneous reporting system database: preliminary comparison of signal detectionQ44668093
Perceived causes of prescribing errors by junior doctors in hospital inpatients: a study from the PROTECT programmeQ44730861
Choice of the denominator in case population studies: event rates for registration for liver transplantation after exposure to NSAIDs in the SALT study in France.Q44771754
The EU-ADR project: preliminary results and perspective.Q44943759
Adverse drug reaction reporting in the UK: a retrospective observational comparison of yellow card reports submitted by patients and healthcare professionalsQ45371649
Combining electronic healthcare databases in Europe to allow for large-scale drug safety monitoring: the EU-ADR Project.Q45915951
The case-population study design: an analysis of its application in pharmacovigilanceQ46061087
Gastrointestinal complications of prescription and over-the-counter nonsteroidal anti-inflammatory drugs: a view from the ARAMIS database. Arthritis, Rheumatism, and Aging Medical Information System.Q46108574
The U.S. Food and Drug Administration's Mini-Sentinel program: status and directionQ46362415
Benzodiazepines and injurious falls in community dwelling eldersQ46816323
Impact of safety-related regulatory action on drug use in ambulatory care in the Netherlands.Q47947189
P304page(s)33-41
P577publication date2013-05-03
P1433published inEuropean Journal of Clinical PharmacologyQ1376707
P1476titleThe past, present and perhaps future of pharmacovigilance: homage to Folke Sjoqvist
P478volume69 Suppl 1

Reverse relations

cites work (P2860)
Q40160191A Method for the Minimization of Competition Bias in Signal Detection from Spontaneous Reporting Databases
Q47779429Can drugs induce or aggravate sleep apneas? A case-noncase study in VigiBase® , the WHO pharmacovigilance database
Q57488986Comparative evaluation of pharmacovigilance regulation of the United States, United Kingdom, Canada, India and the need for global harmonized practices
Q38793916Methods for safety signal detection in healthcare databases: a literature review
Q43897779Pharmacological prioritisation of signals of disproportionate reporting: proposal of an algorithm and pilot evaluation.
Q47732295Pharmacovigilance: empowering healthcare professionals and patients

Search more.