HIGHLIGHTS
- who: Gang Wang and colleagues from the A, week, prospective, multi-center, open-label, postmarketing surveillance was conductedPatients with schizophrenia were recruited from September , to May , from , clinical sites across China. All patients taking blonanserin during the period were included and then followed up. Enrolled patients should orally receive, mg/day of blonanserin according to its approved dose and administration. The dose could be adjusted according to the treatment response and tolerability. The maximum daily dose is , mg. Female patients aged, years were included in this analysis. Efficacy and safety analyses were performed based on the full . . .
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