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. 2008 Jan 25;10(1):42–46. doi: 10.1208/s12248-007-9000-9

Table 1.

Pharmacokinetic Parameters Obtained after Ivermectin Oral Administration

Reference Dose Absorption Elimination
C max (ng·ml−1) t max (h) t 1/2(abs) (h) t 1/2 (h) Cl (1 kg−1·day−1)
Healthy subjects
9a 12 mg (tablet) 12
8a 6 mg (tablet) 23.1 4.3 0.5 12.6 4.28
8a 12 mg (tablet) 30.4 10.3 2.5 13.4 4.03
9a 6 mg (tablet) 20.2 4.7 1.4 11.1 7.57
9a 12 mg (tablet) 23.5 5.3 1.4 21.1 6.53
9a 18 mg (tablet) 31.2 5.1 1.7 16.7 10.6
11 12 mg (solution) 81 3.6
11 12 mg (tablet) 50 3.4
11 12 mg (capsule) 46 3.6
12 150 μg/kg 54.4 4.9 36.6
13 150 μg/kg 37.9
14 150 μg/kg 33.8   4.70 (♂) 8.40 (♀)
Onchocerciasis patients
12 150 μg/kg 52.2 5.2 35.0
15 150 μg/kg 39 5.6 16
16 6 mg (tablet) 38.2 4.7 54.5 3.1
17 150 μg/kg       19.9

– Unknown data; C max maximum plasma concentration; t max time to reach C max; t 1/2abs absorption half-life; t 1/2 elimination half-life; Cl total body clearance

aOne-compartment model