Примери за използване на Used in patients with severe hepatic на Английски и техните преводи на Български
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Prasugrel must not be used in patients with severe hepatic impairment see section 4.
Esbriet has not been studied in individuals with severe hepatic impairment andEsbriet must not be used in patients with severe hepatic impairment(see section 4.3).
Sertraline should not be used in patients with severe hepatic impairment(see section 4.2).
Symtuza has not been studied in patients with severe hepatic impairment(Child-Pugh Class C),therefore, Symtuza must not be used in patients with severe hepatic impairment(see sections 4.3, 4.4 and 5.2).
ZYTIGA should not be used in patients with severe hepatic impairment(see sections 4.3, 4.4 and 5.2).
Unboosted Atazanavir Krka must not be used in patients with severe hepatic impairment.
Atripla must not be used in patients with severe hepatic impairment(see section 4.3) and is not recommended for patients with moderate hepatic impairment.
Crizotinib should not be used in patients with severe hepatic impairment(including patients with total bilirubin>3× ULN regardless of ALT/AST)(see sections 4.2, 4.3 and 4.8).
Crizotinib should not be used in patients with severe hepatic impairment(see sections 4.3, 4.4 and 4.8).
VIRAMUNE must not be used in patients with severe hepatic impairment(Child-Pugh C) or pre- treatment ASAT or ALAT> 5 ULN until baseline ASAT/ ALAT are stabilised< 5 ULN.
Tivozanib should not be used in patients with severe hepatic impairment(see section 4.2 and section 4.4).
Atripla must not be used in patients with severe hepatic impairment(CPT Grade C)(see section 5.2).
Abiraterone acetate should not be used in patients with severe hepatic impairment(see sections 4.2, 4.3 and 4.4).
Efavirenz must not be used in patients with severe hepatic impairment(Child Pugh Grade C)(see section 5.2).
Signifor should not be used in patients with severe hepatic impairment(Child Pugh C)(see sections 4.3 and 4.4).
The combination should be used in patients with severe hepatic impairment only if the anticipated benefit exceeds the risk.
Vyxeos liposomal should only be used in patients with severe hepatic impairment if the benefits outweigh the risks(see section 4.4).
Therefore, darunavir must not be used in patients with severe hepatic impairment(Child-Pugh Class C)(see sections 4.3, 4.4 and 5.2).
Vyxeos liposomal should only be used in patients with severe hepatic and/or renal impairment if the benefits outweigh the risks(see section 4.2).
Esbriet therapy should not be used in patients with severe hepatic impairment or end stage liver disease(see section 4.3, 4.4 and 5.2).
Lynparza is not recommended for use in patients with severe hepatic impairment(Child-Pugh classification C), as safety and pharmacokinetics have not been studied in these patients. .
Victoza is not recommended for use in patients with severe hepatic impairment(see section 5.2).
Due to the liraglutide component, Xultophy is not recommended for use in patients with severe hepatic impairment(see section 5.2).
Therefore, Odefsey is not recommended for use in patients with severe hepatic impairment(see sections 4.4 and 5.2).
The dose of zaleplon should be reduced in patients with mild to moderate hepatic impairment, andzaleplon is not recommended for use in patients with severe hepatic impairment.
Stivarga is not recommended for use in patients with severe hepatic impairment(Child-Pugh C) as Stivarga has not been studied in this population and exposure might be increased in these patients. .
Cabometyx is not recommended for use in patients with severe hepatic impairment(Child-Pugh C) as cabozantinib has not been studied in this population and exposure might be increased in these patients. .
Ivabradine is contra-indicated for use in patients with severe hepatic insufficiency, since it has not been studied in this population and a large increase in systemic exposure is anticipated(see sections 4.3 and 5.2).
Ivabradine is contraindicated for use in patients with severe hepatic insufficiency, since it has not been studied in this population and a large increase in systemic exposure is anticipated(see sections 4.3 and 5.2).