Journal of Oncology Practice · 2017 · 77 citations · 17 references
MedicineOncologyPharmacologyCancer PharmacologyDrug InteractionsOncology Medication SafetyAntineoplastic Drug InteractionsDrug Interactions In ChemotherapyDrug-drug Interaction RiskDrug-herb InteractionsHerbal Supplement InteractionsInteraction Risk AssessmentAnticancer Drug InteractionsAntineoplastic Drug TherapyDrug-herbal InteractionsHerb-drug Interaction DatabasesHerb-drug Interaction RiskHerbal Drug InteractionsHerbal SupplementsOver-the-counter Drug Use
PURPOSE: Patients with cancer frequently use herbal supplements and concomitant medications along with antineoplastic agents. These patients are at high risk of herb-drug interactions (HDIs) and drug-drug interactions (DDIs). We aimed to determine clinically relevant DDIs and HDIs leading to pharmaceutical intervention. METHODS: Patients starting a new anticancer therapy were asked to complete a questionnaire to identify concomitant use of any over-the-counter drug or herbal supplement. Potential DDIs and HDIs were identified using two different databases. If a potentially clinically relevant DDI was recognized by the clinical pharmacist, a notification was sent to the prescribing oncologist, who decided whether to carry out a suggested intervention. Regression analyses were performed to identify variables associated with clinically relevant DDIs. RESULTS: A total of 149 patients were included in this study, with 36 potentially clinically relevant DDIs identified in 26 patients (17.4%; 95% CI, 11.3% to 23.5%), all of them leading to therapy modifications. In total, four patients (2.7%; 95% CI, 0.1% to 5.3%) had experienced clinical consequences from DDIs at the time of pharmacist notification. Additionally, 84 patients (56.4%; 95% CI, 48.4% to 64.4%) reported using concurrent herbal supplements, and 122 possible HDIs were detected. Concomitant use of two or more drugs was independently associated with high risk of a clinically significant DDI (odds ratio, 2.53; 95% CI, 1.08 to 5.91; P = .03). CONCLUSION: Potentially clinically relevant DDIs and possible HDIs were frequently detected in this prospective study. A multidisciplinary approach is required to identify and avoid potentially harmful combinations with anticancer therapy.
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A method for estimating the probability of adverse drug reactions
C. A. Naranjo, U. Busto, Edward M. Sellers et al. · Clinical Pharmacology & Therapeutics · 1981 · 11.6K citations
Fatal adverse drug events: the paradox of drug treatment
Ingebjørg Buajordet, Just Ebbesen, Jan Erikssen et al. · Journal of Internal Medicine · 2001 · 205 citations
Pharmacy, Pharmacology, Toxicology +13