Nebenwirkungen · Brintellix
Brintellix 20 mg/ml oral drops, solution · Abschnitt 4.8 · PDF-Seite 30
HOS-128802 · Präparat HOS-096615
Paediatric population A total of 304 children aged 7 to 11 years and 308 adolescents aged 12 to 17 years with MDD were treated with vortioxetine in two double-blind, placebo-controlled studies, respectivily. In general, the adverse reaction profile of vortioxetine in children and adolescents was similar to that observed in adults except for a higher incidence of abdominal pain-related events and a higher incidence of suicidal ideation in adolescents specially, compared to adults (see section 5.1).
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Version 2026-01-19T08:59:00Z · SHA-256 39c9a9149ac76ca0fbe73df123a7c9f5de7dcd96ddbd144fa863659dff9cbf06 · Passage c94b73f4c88b7cd408124f7fb319cf72af0c912909b4e48baede32cd19f0d352 · Zeichen 5117–5619 im Abschnitt