Nebenwirkungen · Fintepla
Fintepla 2.2 mg/ml oral solution · Abschnitt 4.8 · PDF-Seite 12
HOS-132993 · Präparat HOS-097342
In the LGS controlled trial through the open-label trial, diarrhoea and constipation were observed more frequently in the higher dose groups. The mean time to onset of diarrhoea was 215.7 days, 95.2 days, and 79.6 days in the >0 - <0.4 mg/kg/day, 0.4 - <0.6 mg/kg/day, and ≥0.6 mg/kg/day mean daily dose groups respectively while the mean time to onset of constipation was 113.0 days, 173.7 days, and 140.1 days in the >0 - <0.4 mg/kg/day, 0.4 - <0.6 mg/kg/day, and ≥0.6 mg/kg/day mean daily dose groups respectively.
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Version 2026-04-09T15:00:00Z · SHA-256 e175f94af1e49d4a11fbbc3e861df1256bc1a0a5d612baaf0706babc5f1fc781 · Passage 1bcfad33a90297f2ff99dcb0e82a8e41f352bb151dcaf49e408b3bd9c989c5af · Zeichen 8193–8710 im Abschnitt