Voorbeelden van het gebruik van Vortioxetine in het Engels en hun vertalingen in het Nederlands
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Therefore, caution should be exercised when treating patients≥ 65 years of age with doses higher than 10 mg vortioxetine once daily see sections 4.8 and 5.2.
was observed on the multiple-dose pharmacokinetics of vortioxetine in healthy subjects.
However, caution should be exercised when prescribing to elderly patients at doses higher than 10 mg vortioxetine once daily see section 4.4.
memory observed with vortioxetine in animal studies.
In one study, vortioxetine was superior to placebo on subjective measures, evaluated using the Perceived Deficits Questionnaire with results of -14.6 for vortioxetine and -10.5 for placebo p=0.002.
Furthermore, vortioxetine, in the dose range of 5-20 mg/day,
a 72% decrease in AUC of vortioxetine was observed.
However, by recommended patient usage vortioxetine is considered to pose negligible risk to the aquatic and terrestrial environment for
The exposure to vortioxetine increased 2.3-fold for area under the curve(AUC) when vortioxetine 10 mg/day was co-administered with bupropion(a strong CYP2D6 inhibitor 150 mg twice daily) for 14 days in healthy subjects.
Following a single dose of 10 mg vortioxetine, no impact of mild or moderate hepatic impairment(Child-Pugh Criteria A or B; n=8 per group) was observed on the pharmacokinetics of vortioxetine changes in AUC were less than 10.
Vortioxetine did not separate from placebo on subjective measures when evaluated using the Cognitive and Physical Functioning Questionnaire with results of -8.1 for vortioxetine versus -6.9 for placebo p=0.086.
the dose may be increased to a maximum of 20 mg vortioxetine once daily or decreased to a minimum of 5 mg vortioxetine once daily.
The dose may be increased by your doctor to a maximum of 20 mg vortioxetine per day or lowered to a minimun of 5 mg vortioxetine per day depending on your response to treatment.
The efficacy of vortioxetine is supported by the pooled responder analysis, in which the proportion of responders ranged from 46% to 49% for vortioxetine versus 34% for placebo p< 0.01; NRI analysis.
For doses of 20 mg vortioxetine once daily,
in cognitive function were observed when vortioxetine in a single dose of 20 mg
In severely depressed patients(baseline MADRS total score≥30) and in depressed patients with a high level of anxiety symptoms(baseline HAM-A total score≥20) vortioxetine also demonstrated efficacy in the short-term studies in adults the overall mean difference to placebo in MADRS total score at Week 6/8 ranged from 2.8 to 7.3 points
Administration of vortioxetine in the general toxicity studies in mice,
One study assessed the effect of vortioxetine on functional capacity using the University of California San Diego Performance-Based Skills Assessment UPSA.
The starting and recommended dose of Brintellix is 10 mg vortioxetine once daily in adults less than 65 years of age.