In clinical trials, the most frequently reported adverse events occurring in >1% of the study population regardless of drug relationship were: Diarrhea 10.4%, headache 10.3%, vaginitis 7.6%, nausea 5.2%, rhinitis 4.5%, back pain 3%, dysmenorrhea 2.6%, pharyngitis 2.5%, dizziness 2.3%, abdominal pain 2.2%, dyspepsia 1.8%, asthenia 1.7% and rash 1.4%.
The following adverse events occurred in clinical trials at a rate of <1% regardless of drug relationship: Abnormal stools, anorexia, constipation, dry mouth, dysuria, ear disorder, fever, flatulence, flu syndrome, hematuria, infection, insomnia, lymphadenopathy, menstrual disorder, migraine, myalgia, nervousness, paresthesia, pruritus, increased SGPT, skin disorder, somnolence and vomiting.