Primjeri korištenja Macitentan na Engleski i njihovi prijevodi na Hrvatskom
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Warfarin: Macitentan given as multiple doses of 10 mg once daily had no effect on exposure to S-warfarin(CYP2C9 substrate)
At clinically relevant concentrations, macitentan and its active metabolite do not interact with proteins involved in hepatic bile salt transport,
Treatment with macitentan 10 mg at Month 6 led to a 74% higher chance of WHO FC improvement relative to placebo risk ratio 1.74;
If you are allergic to macitentan or any of the other ingredients of this medicine(listed in section 6). if you are pregnant,
29.4% of patients on macitentan 10 mg(Absolute Risk Reduction 15.2%)
the incidences of peripheral oedema AEs ranged from 13.4% to 16.1% in the macitentan 10 mg groups and from 6.2% to
In a double-blind study in patients with PAH, macitentan 10 mg was associated with a decrease in mean leucocyte count from baseline of 0.7× 109/L versus no change in placebo-treated patients.
with idiopathic pulmonary fibrosis, the incidence of peripheral oedema AEs in the macitentan and placebo treatment groups was 11.8% and 6.8%, respectively.
In a double-blind study in patients with PAH, macitentan 10 mg was associated with a decrease in mean platelet count of 17× 109/L, versus a mean decrease of 11× 109/L in placebo-treated patients.
Macitentan and its active metabolite are not inhibitors of hepatic
The incidence of aminotransferase elevations(ALT/AST)> 3× ULN was 3.4% on macitentan 10 mg and 4.5% on placebo in a double-blind study in patients with PAH.
capability of the offspring, which was exposed to macitentan during late intrauterine life
Macitentan and its active metabolite.
The active substance is macitentan.
Macitentan has four primary metabolic pathways.
Macitentan is only excreted after extensive metabolism.
Macitentan is not a substrate for P- gp/MDR-1.
Opsumit is a medicine that contains the active substance macitentan.
Macitentan inhibits the breast cancer resistance protein(BCRP)
Macitentan and its active metabolite do not have clinically relevant inhibitory or inducing effects on cytochrome P450 enzymes.