ArticleDrug safety2009
Data mining in pharmacovigilance--detecting the unexpected: the role of index of suspicion of the reporter.
Article in Drug safety, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
5 citing papers in PubMed, 15 citations in OpenAlex.
- A disproportionality analysis of adverse events associated to pertuzumab in the FDA Adverse Event Reporting System (FAERS).BMC pharmacology & toxicology · 2023Article
- A Qualitative Assessment of Current Pharmacovigilance Education in Lebanese Pharmacy Schools.Medical science educator · 2020Article
- Article
- A signal for an abuse liability for pregabalin--results from the Swedish spontaneous adverse drug reaction reporting system.European journal of clinical pharmacology · 2010Article
- Information technology in pharmacovigilance: Benefits, challenges, and future directions from industry perspectives.Drug, healthcare and patient safety · 2009Article
Corrections and comments
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Authors and funding
2 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundOne of the most important aims of pharmacovigilance is to detect signals of adverse drug reactions (ADRs) as early as possible. However, some ADRs are difficult to detect, one example being so called 'type C' reactions. These are effects that present as seemingly 'spontaneous' diseases occurring during treatment with a drug, such as the occurrence of a cardiovascular event while the patient is taking rofecoxib. As this type of ADR is often mistaken for a spontaneous disease, the causative agent may appear as an innocent bystander.
objectiveThe primary aim of this study was to investigate the possibility of using data mining approaches to detect signals of 'type C' reactions. We hypothesized that by including concomitant, and not only suspected medications in the calculations of disproportionality analyses, we would be able to identify such reactions. STUDY
designWe used data from the Swedish Drug Information System, SWEDIS, which contains spontaneous reports submitted by Swedish physicians to the Swedish Medical Products Agency, and applied Bayesian confidence propagation neural network (BCPNN) methodology to calculate the information component (IC) value for drug-event combinations for drugs belonging to the Anatomic Therapeutic Chemical (ATC) classes cardiovascular system, musculoskeletal system and nervous system (number of reports = 51 270) where only the suspected drug was considered, and also where both concomitant and suspected drugs were considered. We then classified drug-event combinations that were signalled by a statistically significantly raised IC value as labelled or unlabelled based on the approved summary of product characteristics (SPC) in Sweden as of November 2007, and further classified them as 'type C' reactions or not 'type C'.
main outcome measureThe proportion of 'type C' reactions signalled when considering both concomitant and suspected drugs compared with suspected drugs only.
resultsThe proportion of labelled drug-event combinations when considering suspected drugs was 78.6%. Drug-event combinations classified as 'type C' reactions were more likely to be found when considering both concomitant and suspected drugs compared with suspected drugs only; 18/449 versus 0/248 when considering drug-event combinations that were signalled exclusively by one of the approaches. Such drug-event combinations included, for example, sudden death and celecoxib, myocardial infarction and diclofenac, suicide-related events and several antidepressants.
conclusionIncluding both concomitant and suspected drugs in data mining practices may be a way of detecting 'type C' reactions earlier. This could constitute an advance in data mining for pharmacovigilance practices.
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