Examples of using Normal hepatic function in English and their translations into German
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clinical laboratory profiles as previous studies of HIV-1 infected subjects with normal hepatic function.
The mean AUC was unchanged in subjects with mild hepatic  impairment compared to subjects with normal hepatic function; however,
hypocalcaemia compared with patients with normal hepatic function.
Compared to healthy subjects with normal hepatic function, the mean steady-state AUC of simeprevir was 2.4-fold higher in non-HCV infected subjects with moderate hepatic  impairment(Child-Pugh class B) and 5.2-fold higher in non-HCV infected subjects with severe hepatic  impairment Child-Pugh class C.
severe hepatic  impairment compared to those with normal hepatic function.
The pharmacokinetics of trastuzumab emtansine and DM1-containing catabolites were evaluated after the administration of 3.6 mg/kg of trastuzumab emtansine to metastatic HER2+ breast cancer patients with normal hepatic function(n=10), mild(Child-Pugh A;
compared to individuals with normal hepatic function.
compared to subjects with normal hepatic function.
38% higher ritonavir C12 than achieved in subjects with normal hepatic function receiving the standard fosamprenavir with ritonavir 700 mg/ 100 mg twice daily regimen.
severe groups, respectively compared to 22.1 hours in subjects with normal hepatic function.
after administration of 800 mg once daily are similar to the median in patients with normal hepatic function see Table 7.
1.5-3.0 times ULN, n 1) hepatic  impairment compared to patients with normal hepatic function total bilirubin and AST≤ ULN, n 126.
the pharmacokinetic profile of vismodegib was comparable to that of subjects with normal hepatic function(n=9) see section 4.2.
similar unbound plasma amprenavir C12 values than achieved in subjects with normal hepatic function receiving the standard fosamprenavir with ritonavir 700 mg/ 100 mg twice daily regimen.
approximately 117% higher plasma unbound amprenavir C12 values compared to subjects with normal hepatic function receiving the standard fosamprenavir/ ritonavir 700 mg/ 100 mg twice daily regimen.
approximately 88% higher plasma unbound amprenavir C12 values than achieved in subjects with normal hepatic function receiving the standard fosamprenavir with ritonavir 700 mg/ 100 mg twice daily regimen.
serum half-life may be twofold longer than in patients with normal hepatic function.
Compared to subjects with normal hepatic function, systemic exposure following a single dose of axitinib was similar in subjects with mild hepatic  impairment(Child-Pugh class A)
The usually recommended dose in patients with normal hepatic function is 30 mg q. d.