Figure 4.

Influence of sex and treatment duration over patient-reported improvement of primary symptom. Responses from participants were clustered into four groups by increasing degree of improvement, residual (0–10), slight (20–40), moderate (50–70), and robust (80–100), and are presented by sex and chemotype: (A) Female participants prescribed with FM-002 (n = 586); (B) Female participants prescribed with FM-003 (n = 1,011); (C) Male participants prescribed with FM-002 (n = 270); (D) Male participants prescribed with FM-003 (n = 230).