CRED Practical Document Writing and Management

Narrative listing of data

During the clinical studies, adverse events with an incidence greater than 1.0 % were headache (7.3 %), fatigue (4.5 %), nausea (2.9 %), abdominal pain (1.6 %), somnolence (1.4 %) for the active (n=1730), and for the placebo (n=1250) they were headache (7.8 %), fatigue (2.8 %), nausea (1.9 %), abdominal pain (0.3 %), somnolence (0.6 %)