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. 2015 Jun 4;17(3):10.4088/PCC.14m01741. doi: 10.4088/PCC.14m01741

Table 1.

Safety Population Baseline Demographics and Clinical Characteristics

Pooled Short-Term Studies
Long-Term Study(n = 874)a,b
Characteristic Desvenlafaxine 50 mg (n = 1,425) Desvenlafaxine 100 mg (n = 574) Placebo(n = 1,400)
Age, y
 Mean 43.7 42.2 43.3 45.0
 Range 18–86 18–78 18–85 18–87
Sex, n (%)
 Female 981 (68.8) 366 (63.8) 953 (68.1) 608 (69.6)
Race, n (%)
 White 1,033 (72.5) 457 (79.6) 1,001 (71.5) 729 (83.4)
 Black 217 (15.2) 70 (12.2) 192 (13.7) 55 (6.3)
 Asian 132 (9.3) 12 (2.1) 139 (9.9) 9 (1.0)
 Other 43 (3.0) 35 (6.1) 68 (4.9) 81 (9.3)
Weight, kg
 Mean (SD) 83.3 (23.3) 81.7 (21.0) 81.6 (22.5) 77.2 (19.5)
BMI category, n (%)c
 Underweight 37 (2.6) 13 (2.3) 36 (2.6) 24 (2.8)
 Normal 409 (28.7) 190 (33.1) 446 (31.8) 321 (36.7)
 Overweight 399 (28.0) 166 (28.9) 399 (28.5) 271 (31.0)
 Obese 580 (40.7) 205 (35.7) 519 (37.1) 258 (29.5)
Baseline HDRS-17 total score
 Mean (SD) 23.0 (3.1) 23.7 (2.6) 23.1 (3.1) 24.2 (2.8)
a

Twenty weeks of open-label desvenlafaxine 50 mg/d, followed by 6 months of double-blind desvenlafaxine 50 mg/d or placebo.

b

From open-label baseline.

c

BMI categories: normal = BMI ≤ 25 kg/m2, overweight = 25 kg/m2 < BMI ≤ 30 kg/m2, obese = BMI > 30 kg/m2.

Abbreviations: BMI = body mass index, HDRS-17 = 17-item Hamilton Depression Rating Scale.