Exemplos de uso de Mild or moderate hepatic impairment em Inglês e suas traduções para o Português
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Dose adjustment is not necessary in patients with mild or moderate hepatic impairment.
For patients with mild or moderate hepatic impairment, dosing can be initiated at 2 mg 4 ml.
This medicinal product can be used in patients with mild or moderate hepatic impairment.
In patients with mild or moderate hepatic impairment the recommended dose of cabozantinib is 60 mg once daily.
Thus, no dose adjustment is necessary in patients with mild or moderate hepatic impairment.
Administration of pazopanib to patients with mild or moderate hepatic impairment should be undertaken with caution and close monitoring of tolerability.
No adjustment to the starting dose is required for patients with mild or moderate hepatic impairment.
Patients with mild or moderate hepatic impairment exhibited comparable pharmacokinetics and pharmacodynamics to their matched healthy control group.
Naltrexone/ bupropion is not recommended in patients with mild or moderate hepatic impairment.
Following a single doseof 10 mg vortioxetine, no impact of mild or moderate hepatic impairment(Child-Pugh Criteria Aor B; n=8 per group) was observed on the pharmacokinetics of vortioxetine changes in AUC were less than 10.
Adjustments to the starting dose are not necessary in patients with mild or moderate hepatic impairment.
In a study of a combination dose of dextromethorphan 23 mg/ quinidine 26 mg twice daily in 12 subjects with mild or moderate hepatic impairment(as indicated by the Child-Pugh method; 6 each) compared to 9 healthy subjects(matched in gender, age, and weight range to impaired subjects), subjects with moderate hepatic impairment showed similar dextromethorphan AUC and Cmax and clearance compared to healthy subjects.
No dose adjustment is deemed necessary in patients with mild or moderate hepatic impairment.
No dose adjustment is necessary in patients with mild or moderate hepatic impairment(Child-Pugh classes A and B) see section 5.2.
The pharmacokinetics of fingolimod-phosphate were not evaluated in patients with mild or moderate hepatic impairment.
The average Cmax of deferasirox in subjects with mild or moderate hepatic impairment was increased by 22.
Naltrexone/ bupropion is contraindicated in patients with severe hepatic impairment andis not recommended in patients with mild or moderate hepatic impairment.
No dose adjustment is recommended for patients with mild or moderate hepatic impairment see sections 4.4 and 5.2.
Although Xeplion was not studied on patients with hepatic impairment, no dose adjustment is required in patients with mild or moderate hepatic impairment.
No particular studies on the pharmacokinetics of carbidopa and levodopa in patients with hepatic impairment are reported, however,it is advised that Stalevo should be administered cautiously to patients with mild or moderate hepatic impairment.
Lixiana should be used with caution in patients with mild or moderate hepatic impairment see section 4.2.
No dose adjustment is required when initiating treatment with Zydelig in patients with mild or moderate hepatic impairment, but an intensified monitoring of adverse reactions is recommended see sections 4.4 and 5.2.
The pharmacokinetics of ranolazine have been evaluated in patients with mild or moderate hepatic impairment.
No dose adjustment is necessary for SIRTURO in patients with mild or moderate hepatic impairment see section 5.2.
Clinical data suggest that no dose adjustments are required in patients with mild or moderate hepatic impairment.
Close monitoring of the overall safety is recommended in patients with mild or moderate hepatic impairment see also sections 4.2 and 5.2.
Patients with hepatic impairment No dose adjustment is required in patients with mild or moderate hepatic impairment.
It is unlikely that a dose adjustment would be required for Eviplera in patients with mild or moderate hepatic impairment see sections 4.2 and 5.2.