Studies 437 and 438 Integrated 0-48 WeeksGrade 1-4 Treatment-Related Adverse Eventsa
PLB ADV 10
(n=228) (n=294)
Asthenia 14% 13%
Abdominal pain 11% 9%
Headache 10% 9%
Nausea 8% 5%
Flatulence 4% 4%
Diarrhea 4% 3%
Dyspepsia 2% 3%
aObserved in ? 3% of ADV treated patients
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