COVID- 19 Drug interactions
COVID- 19 Drug interactions provides evidence-based assessments of drug–drug interactions for experimental COVID-19 therapies to inform clinical management by evaluating pharmacokinetic interactions, overlapping toxicities, and QT-prolongation risk.
Key Features:
- Comprehensive Database: Contains a curated set of 2,378 ClinicalTrials.gov records identified using search terms 'COVID-19', '2019-nCoV', '2019 novel coronavirus', and 'SARS-CoV-2', yielding 249 drugs that met inclusion criteria.
- Interaction Grading System: Categorizes interactions into four grades—GREEN (no clinically significant interaction), YELLOW (caution advised), AMBER (requires caution due to potential risks), and RED (serious risk)—to indicate severity.
- Focus on Pharmacokinetics and Toxicity: Evaluates interactions based on known pharmacokinetic profiles, overlapping toxicities, and QT interval prolongation risk.
- Highlighting High-Risk Therapies: Identifies lopinavir/ritonavir, chloroquine, and hydroxychloroquine as therapies with notable pharmacokinetic interactions and QT-prolongation risks.
Scientific Applications:
- Clinical management: Supports clinicians managing critically ill COVID-19 patients receiving experimental therapies by informing medication selection and monitoring to minimize adverse interactions.
Methodology:
Systematic search of experimental drugs on ClinicalTrials.gov using 'COVID-19', '2019-nCoV', '2019 novel coronavirus', and 'SARS-CoV-2'; evaluation of potential drug–drug interactions using pharmacokinetic data, toxicity profiles, and QT risk assessments; comorbidities identified through PubMed searches using relevant MeSH terms.
Topics
Collections
Details
- Cost:
- Free of charge
- Tool Type:
- web application
- Added:
- 1/18/2021
- Last Updated:
- 3/3/2021
Operations
Publications
Hodge D, Marra F, Marzolini C, Boyle A, Gibbons S, Siccardi M, Burger D, Back D, Khoo S. Drug interactions: a review of the unseen danger of experimental COVID-19 therapies. Journal of Antimicrobial Chemotherapy. 2020;75(12):3417-3424. doi:10.1093/jac/dkaa340. PMID:32750131. PMCID:PMC7454591.