Examples of using Pegvisomant in English and their translations into Polish
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Pegvisomant is licensed for the treatment of acromegaly in patients with inadequate response to surgery,
The active substance in SOMAVERT, pegvisomant, is very similar to human growth hormone, but it has been designed
The active substance in Somavert, pegvisomant, is very similar to human growth hormone,
demonstrate pegvisomant mean serum concentrations(± SD)
dose-titration study for at least 12 consecutive months of daily dosing with pegvisomant mean 55 weeks.
30 mg pegvisomant in a vial and 1 ml of solvent in a pre-filled syringe.
82% of subjects treated with placebo, 10 mg/day, 15 mg/day or 20 mg/day pegvisomant respectively.
Dose-dependent, statistically significant reductions in mean IGF-I(p< 0.0001), free IGF-I(p< 0.05), IGFBP-3(p< 0.05) and ALS(p< 0.05) were observed at all post-baseline visits in the pegvisomant treatment groups.
this medicine is discontinued: this decision should take into account the benefit of pegvisomant therapy to the mother and the benefit of breast-feeding to the child.
solvent for solution for injection Pegvisomant.
Inhibition of growth hormone action with pegvisomant leads to decreased serum concentrations of insulin-like growth factor-I(IGF-I), as well as
For pegvisomant no data on fertility are available.
For pegvisomant no clinical data on exposed pregnancies are available.
It contains the active substance pegvisomant 10, 15 or 20 mg/ ml.
Pegvisomant is produced in E. Coli by recombinant DNA technology.
A loading dose of 80 mg pegvisomant should be administered subcutaneously under medical supervision.
The active substance in SOMAVERT, pegvisomant is known as a growth hormone receptor antagonist.
Pegvisomant is not recommended during pregnancy see section 4.6.
Pegvisomant is a potent antagonist of growth hormone action.
Therefore, pegvisomant should not be used in breast-feeding women.