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Table 3 Bioequivalence comparison of three drugs described by their name (overt) or as placebo (covert)

From: Does the placebo effect modulate drug bioavailability? Randomized cross-over studies of three drugs

Drug name

Cephalexin

Ibuprofen

Paracetamol

AUCT

 PE (CI)

98.47% (95.04–102.02)

96.66% (91.79–101.79)

100.62% (98.77–102.50)

 MSR

0.011

0.014

0.003

 CV

10.5%

11.9%

5.5%

AUCI

 PE (CI)

98.54% (95.34–101.83)

99.96% (96.30–103.76)

100.56% (98.71–102.45)

 MSR

0.009

0.007

0.003

 CV

9.5%

8.4%

5.5%

Cmax

 PE (CI)

97.87% (89.81–106.65)

87.11% (76.66–98.99)

106.79% (98.84–115.37)

 MSR

0.063

0.085

0.052

 CV

25.5%

29.8%

23.1%

AUCOverttmax

 PE (CI)

96.64% (82.17–113.66)

64.44% (45.32–91.62)

71.36% (51.45–98.96)

 MSR

0.224

0.642

0.931

 CV

50.1%

94.9%

124.0%

Cmax/AUCI

 PE (CI)

99.32% (93.00–106.08)

87.15% (77.19–98.39)

106.19% (99.15–113.73)

 MSR

0.037

0.076

0.041

 CV

19.4%

28.1%

20.5%

  1. AUCT is area-under-the-plasma-concentration-time curve from time 0 to last measured concentration. AUCI is area-under-the-plasma-concentration-time curve extrapolated to infinity. Cmax is first measured maximum plasma level. AUCOverttmax is area-under-the-plasma-concentration-time curve to Tmax under overt drug administration. PE is point estimate (antilog of the difference between means of log-transformed data). CI is parametric 90% confidence interval on PE. MSR is mean square residual from analysis of variance. CV is intra-subject coefficient of variation, calculated as 100× (exp(MSR)-1)0.5. The number of subjects that were analyzed was 48 for cephalexin, 30 for ibuprofen, and 48 for paracetamol.