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. Author manuscript; available in PMC: 2014 Sep 1.
Published in final edited form as: Vet Clin North Am Small Anim Pract. 2013 Sep;43(5):10.1016/j.cvsm.2013.05.002. doi: 10.1016/j.cvsm.2013.05.002

Table 1.

Pharmacokinetic parameters determined for drugs that have longer (or shorter) elimination half-life values in cats versus dogs and humans. Results are the averages of published studies as referenced. Data from Obach et al, 2008 1 represent a compilation of all available human data up to 2008. Intravenous administration data were used if available to exclude bioavailability differences.

Drug Species Half-life (h) CL (mL/min/kg) Vd (L/kg)
Acetylsalicylic acid* Cat 22 0.088 0.17
Dog 4.5 0.68 0.29
Human 2.3 0.66 0.19
Acetaminophen Cat** 5.0 2.9 1.3
Dog** 1.1 13 1.3
Human** 2.6 5 1.0
Propofol Cat 8.8 17 6.8
Dog 2.4 51 5.1
Human 1.9 30 4.7
Carprofen Cat 18 0.10 0.15
Dog 12 0.28 0.17
Human** 12 0.48 0.48
Piroxicam Cat 11 0.52 0.48
Dog 40 0.044 0.29
Human** 47 0.050 0.16

Data from Refs 1-15.

*

Data for disposition of the active metabolite, salicylic acid.

**

Oral dosing data provided since IV or other parental administration data not available. CL is therefore CL/F and Vd is Vd/F. However for these drugs bioavailability is considered to be high.