Abstract
Adverse drug reactions (ADRs) represent one of the major clinical challenges to patient’s health and are a key reason for attrition in drug development. An understanding of how drug–drug interactions (DDIs) can influence and cause ADRs is critical in managing patients using several prescriptions at the same time. Whilst it may be possible to control on-target ADRs that occur from DDIs, due to predictable pharmacokinetic and pharmacodynamic interactions, the impact of DDIs in triggering off-target ADRs still remains difficult to understand. This chapter will examine clinical, in vivo and in vitro examples to look at how DDIs can potentially lead to both on- and off-target ADRs.
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Walsh, R.J., Srivastava, A., Antoine, D.J., Williams, D.P., Park, B.K. (2010). Toxicological Consequences of Drug–Drug Interactions. In: Pang , K., Rodrigues, A., Peter, R. (eds) Enzyme- and Transporter-Based Drug-Drug Interactions. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-0840-7_25
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