Why the study?
Comorbidity and polypharmacy can cause relevant drug-drug interactions by affecting the exposure or pharmacological activities of DOACs, compromising their safety profile in multimorbid patients.
What are the potential drug-drug interactions of DOACs and how should they be managed in clinical practice?
Design
Review
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Supports preferring DOACs to reduce DDI burden; leaves open precise interaction risks and management protocols.
What are the potential drug-drug interactions of DOACs and how should they be managed in clinical practice?
While DOACs have fewer drug-drug interactions than warfarin, their co-administration with P-glycoprotein or CYP modulators requires careful evaluation to avoid adverse bleeding or thrombotic events.
Ferri et al. (2022) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: