Abstract
Because CsA is subject to extensive hepatic metabolism (1), the possibility of pharmacokinetic drug interaction can be anticipated if drugs which enhance or inhibit its metabolism are co-administered (2–4). In addition to this, there is the possibility of interaction if other drugs given with CsA are nephrotoxic, since they may enhance the toxicity of CsA (5).
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© 1989 Kluwer Academic Publishers
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Castelao, A.M. et al. (1989). Cyclosporin A (CSA) Drug Interactions. In: Andreucci, V.E., Dal Canton, A. (eds) Current Therapy in Nephrology. Developments in Nephrology, vol 24. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-0865-2_139
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DOI: https://doi.org/10.1007/978-1-4613-0865-2_139
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