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. Author manuscript; available in PMC: 2014 Mar 1.
Published in final edited form as: Clin Pharmacol Ther. 2013 May 9;94(3):394–399. doi: 10.1038/clpt.2013.96

Table 2. Pooled analysis of R- and S-metoprolol pharmacokinetics stratified by CYP2D6 phenotype.

n Cmax/dose (ng/mL/mg) AUC/dose (ug*h/L/mg) t 1/2 (h) CL/F (L/h)

R S R S R S R S
UM 12 0.32
[0.24–0.40]
0.47
[0.33-0.61]
1.27
[0.86-1.68]
1.90
[1.34-2.46]
ND ND 547
[393-701]
380
[272-488]
EM 90 0.66
[0.50-0.81]
0.89
[0.69-1.09]
2.94
[2.31-3.58]
4.27
[3.53-5.01]
3.1
[2.7-3.6]
3.3
[2.7-3.8]
170
[131-208]
104
[91-117]
IM 12 1.09
[0.89-1.29]
1.24
[1.04-1.44]
7.61
[5.54-9.68]
9.59
[7.31-11.87]
4.6
[3.9-5.3]
5.2
[4.5-5.9]
61
[46-75]
48
[36-60]
PM 14 1.69
[122-216]
1.77
[129-225]
18.39
[16.55-20.24]
18.03
[16.23-19.84]
7.8
[7.3-8.3]
6.8
[6.3-7.3]
18
[9-27]
17
[4-31]

Data presented as mean [95% confidence interval]. UM- ultra-rapid metabolizer, EM- extensive metabolizer, IM- intermediate metabolizer, PM- poor metabolizer, Cmax/dose- peak metoprolol concentration divided by the dose of metoprolol given, AUC/dose- area under the curve divided by the dose of metoprolol given, t½ - half-life, CL/F- oral clearance, ND- not done