Examples of using Bazedoxifene in English and their translations into German
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Colloquial
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Official
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Ecclesiastic
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Medicine
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Financial
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Ecclesiastic
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Political
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Computer
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Programming
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Official/political
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Political
When single doses of CE 0.625 mg/bazedoxifene 20 mg were administered with a high-fat meal,
Bazedoxifene is highly bound(98%- 99%)
CE/bazedoxifene has not been studied in patients with impaired liver function(see sections 4.2 and 5.2) or history of cholestatic jaundice.
Following multiple doses of CE 0.45 mg/bazedoxifene 20 mg,
Duavive therefore also contains the active substance bazedoxifene, which blocks the effects of oestrogens on the womb
Bazedoxifene does not induce or inhibit the activities of major CYP isoenzymes,
In a 1 year study, CE 0.45 mg/bazedoxifene 20 mg showed a significant difference from baseline in lumbar spine BMD(+1.52%) at Month 12 compared to placebo.
The metabolic disposition of CE and bazedoxifene, after administration of CE/bazedoxifene, has not been studied.
venous thromboembolism which is similar to the risk with conjugated oestrogens and bazedoxifene when used alone.
In studies conducted in rabbits, bazedoxifene alone has shown reproductive toxicity see section 5.3.
Studies in rats with bazedoxifene have shown adverse effects on fertility see section 5.3.
Bazedoxifene caused corticomedullar nephrocalcinosis and enhanced spontaneous chronic progressive nephropathy(CPN) in male rats.
Bazedoxifene undergoes little or no cytochrome P450(CYP)-mediated metabolism.
Bazedoxifene is eliminated with a half-life of approximately 30 hours.
The active substances are conjugated oestrogens and bazedoxifene.
The following data are based on the findings in studies with bazedoxifene.
The absolute bioavailability of bazedoxifene is approximately 6.
A single 20 mg dose of bazedoxifene was administered to these subjects.
Adverse reactions that have been observed with bazedoxifene monotherapy.
conjugated oestrogens and bazedoxifene.