Table 3.
Duration of TEAEs of interest among participants taking SXB.
TEAE | SXB-15 | SXB-22 | ||
---|---|---|---|---|
With TEAE, n | Median (Range) Duration, Days | With TEAE, n | Median (Range) Duration, Days | |
Dizziness | 36 | 9.0 (1.0–69.0) | 20 | 17.5 (1.0–53.0) |
Nausea | 38 | 4.5 (1.0–57.0) | 29 | 3.0 (1.0–60.0) |
Headache | 55 | 2.0 (1.0–58.0) | — | — |
TEAEs that occurred more frequently in participants treated with SXB than placebo and at an incidence ≥5% in any SXB treatment group during week 1 are shown for the all treated population. Data are not shown for headache in SXB-22 because this TEAE did not meet these criteria. SXB = sodium oxybate; TEAE = treatment-emergent adverse event.