Table 6.
Dose adjustment for renal impairment | Dose adjustment for hepatic impairment | |
---|---|---|
Exenatide twice daily [17] | Not appropriate for patients with severe renal impairment (CrCL <30 mL/min) or end-stage renal disease. Caution should be applied when initiating or escalating doses from 5 to 10 µg in patients with moderate renal impairment (CrCL 30–50 mL/min). | Exenatide undergoes renal elimination, thus hepatic impairment is not expected to affect blood concentrations. Dose adjustment is not indicated. |
Liraglutide [22] | Few post-marketing reports of acute renal failure with liraglutide exist in patients with pre-existing kidney disease. Utilize with caution in patients with chronic kidney disease. Dose adjustment is not recommended. | Dose adjustment is not necessary. |
Exenatide once weekly [26] | Not recommended for use in patients with end-stage renal disease or severe renal impairment (CrCL <30 mL/min). Exercise caution in patients with moderate renal impairment (CrCL 30–50 mL/min). Dose adjustment is not necessary. | Exenatide undergoes renal elimination, thus hepatic impairment is not expected to affect blood concentrations. Dose adjustment is not indicated. |
Dulaglutide [35] | Dose adjustment is not necessary. Exercise caution when initiating or escalating doses in patients with renal impairment. | Dose adjustment is not necessary. |
Abliglutide [30] | Dose adjustment is not necessary. Exercise caution when initiating or escalating doses in patients with renal impairment. | Dose adjustment is not necessary. |
CrCL, creatinine clearance.