Incidence, Patterns, and Severity of Potential Drug Interactions Among Cancer Patients on Chemotherapy in a Tertiary Care Hospital
Anuradha H.V.1, Vinayak V. Maka2, Prakash Patil3, Anupama C.4★★ Corresponding author
- 1Department of Pharmacology, MS Ramaiah Medical College, Bangalore, Karnataka,, India.
- 2Department of Medical Oncology, MS Ramaiah Medical College, Bangalore, Karnataka,, India.
- 3Central Research Laboratory, KS Hegde Medical Academy, NITTE (Deemed to be University), Mangaluru, Karnataka, India 4Department of Pharmacology, KS Hegde Medical Academy, NITTE (Deemed to be University), Mangaluru, Karnataka, India. *Correspondence: Anupama C., Department of Pharmacology, KS Hegde Medical Academy, NITTE (Deemed to be University), Mangaluru, Karnataka 575018, India. Email: anupamac87@gmail.com 2023 14 1 35 40 9 9 2022 5 1 2023 13 1 2023 2023 Author(s) 2023 Author(s) This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. Objective: To study the incidence of potential drug−drug interactions (DDIs) and evaluate their pattern and severity in cancer inpatients. Materials and Methods: A detailed clinical data and prescriptions of 150 inpatients with different malignancies were subjected to DDI screening using Micromedex software. The frequency of potential DDIs and their types, patterns, and severity were investigated. Results: A total of 360 potential DDIs were present in 111 (74%) of 150 inpatients, dominated by female (67.33%) and breast cancer (30%) patients. The incidence of severe interactions was 63.88%, moderate interactions 35.83%, and mild interactions 0.27%. The potential mechanisms of DDIs were 38.33% pharmacodynamic, 48.33% pharmacokinetic, and 13.33% unspecified. The drug interactions were found to be positively correlated (p < 0.01) with the 6–10 number of prescribed medicines. Conclusion: According to this study, the number of medicines prescribed to cancer inpatients increased the chance of DDIs. As a result, the drug surveillance program could save a sizable number of patients from the potentially hazardous clinical effects of DDIs. Anti-cancer drugs chemotherapy drug−drug interactions micromedex pharmacodynamics pharmacokinetics
CORRESPONDENCE
Anupama C.
Department of Pharmacology, KS Hegde Medical Academy, NITTE (Deemed to be University), Mangaluru, Karnataka 575018, India.
Received: 09-09-2022; Revised: 05-01-2023; Accepted: 13-01-2023.
Volume 14, Issue 1 · pp. 35–40 · PUBLISHED 2023 · DOI: 10.1177/0976500X231162712
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ABSTRACT
Objective: To study the incidence of potential drug−drug interactions (DDIs) and evaluate their pattern and severity in cancer inpatients. Materials and Methods: A detailed clinical data and prescriptions of 150 inpatients with different malignancies were subjected to DDI screening using Micromedex software. The frequency of potential DDIs and their types, patterns, and severity were investigated. Results: A total of 360 potential DDIs were present in 111 (74%) of 150 inpatients, dominated by female (67.33%) and breast cancer (30%) patients. The incidence of severe interactions was 63.88%, moderate interactions 35.83%, and mild interactions 0.27%. The potential mechanisms of DDIs were 38.33% pharmacodynamic, 48.33% pharmacokinetic, and 13.33% unspecified. The drug interactions were found to be positively correlated (p < 0.01) with the 6–10 number of prescribed medicines. Conclusion: According to this study, the number of medicines prescribed to cancer inpatients increased the chance of DDIs. As a result, the drug surveillance program could save a sizable number of patients from the potentially hazardous clinical effects of DDIs.
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H.V., A., Maka, V. V., Patil, P., & C., A. (2023). Incidence, Patterns, and Severity of Potential Drug Interactions Among Cancer Patients on Chemotherapy in a Tertiary Care Hospital. Journal of Pharmacology and Pharmacotherapeutics, 14(1), 35–40. https://doi.org/10.1177/0976500X231162712
