2015
DOI: 10.1586/17512433.2015.1049598
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Toward standardized reporting of drug interactions: the READI checklist for anecdotal reports

Abstract: Anecdotal reports contribute 30% of the literature on adverse drug reactions and interactions. However, the quality of such reports has not been uniformly high. Standardized reporting of clinical studies is of increasing interest, including the CARE guidelines on reporting anecdotal cases in general. Although there are guidelines on evaluating and managing drug-drug interactions, there are none recommending methods for reporting suspected drug interactions. Here, based on published guidelines for reporting sus… Show more

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Cited by 3 publications
(3 citation statements)
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“…As the latter is the most important risk factor for DDIs, it is likely that the populational exposure to the risk conveyed by these deleterious drug associations will rise in the future, except if dedicated interventions succeed to constrain it (Guthrie et al, 2015; Stoll and Kopittke, 2015). If the overall impact and health burden represented by DDIs is difficult to assess given the wide heterogeneity of the adverse events they can induce (Lopez-Gonzalez et al, 2009; Aronson, 2015), the populational exposure to the risk of DDIs can conversely be estimated and characterized by identifying codispensings of drug pairs that are contraindicated or discommended, and by describing which of such drug pairs are frequently codispensed despite their concomitant use is advised against.…”
Section: Introductionmentioning
confidence: 99%
“…As the latter is the most important risk factor for DDIs, it is likely that the populational exposure to the risk conveyed by these deleterious drug associations will rise in the future, except if dedicated interventions succeed to constrain it (Guthrie et al, 2015; Stoll and Kopittke, 2015). If the overall impact and health burden represented by DDIs is difficult to assess given the wide heterogeneity of the adverse events they can induce (Lopez-Gonzalez et al, 2009; Aronson, 2015), the populational exposure to the risk of DDIs can conversely be estimated and characterized by identifying codispensings of drug pairs that are contraindicated or discommended, and by describing which of such drug pairs are frequently codispensed despite their concomitant use is advised against.…”
Section: Introductionmentioning
confidence: 99%
“…39 A specific checklist for reporting suspected drug interactions, the REporting Anecdotal Drug Interactions checklist (READI), based on the PHARMA and ISoP/ISPE guidelines has also been proposed. 40…”
Section: Report Suspected Drug-herb Interactionsmentioning
confidence: 99%
“…Results from in vitro studies may offer mechanistic insight but may not translate well into clinical practice [ 10 , 20 , 21 , 22 ]. Animal models may offer insight into the role of metabolites in interaction, but these metabolites may not always be applicable to humans and require further clinical confirmation [ 23 ]. Clinical trials are often performed in healthy homogenous adult populations, and sometimes test inappropriate plant parts or inappropriately prepared products [ 10 , 19 ].…”
Section: Introductionmentioning
confidence: 99%