Potential increased systemic exposure by inhibitors of hepatic uptake transporter OATP1B1 (eg, rifampin, cyclosporine) or hepatic efflux transporter MRP2 (eg, ritonavir). Increased serum K or creatinine (in heart failure patients) w/ K-sparing diuretics (eg, spironolactone, triamterene, amiloride), K supplements or salt substitutes containing K.