Примери за използване на Semaglutide на Английски и техните преводи на Български
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The active substance is semaglutide.
Semaglutide is not a substitute for insulin.
Ozempic contains the active substance semaglutide.
Semaglutide improves beta-cell function.
In lactating rats, semaglutide was excreted in milk.
Semaglutide 0.25 mg is not a maintenance dose.
The starting dose is 0.25 mg semaglutide once weekly.
Semaglutide did not affect male fertility in rats.
There is no specific antidote for overdose with semaglutide.
Semaglutide lowered fasting glucose after the first dose.
One ml solution for injection contains 1.34 mg semaglutide.
Semaglutide reduces fasting and postprandial glucose concentrations.
Body weight has an effect on the exposure of semaglutide.
The active substance in Ozempic, semaglutide, is a‘GLP-1 receptor agonist'.
Semaglutide lowers the fasting and postprandial glucagon concentrations.
No episodes of severe hypoglycaemia were observed when semaglutide was used as monotherapy.
In addition, semaglutide reduces the preference for high fat foods.
For diastolic blood pressure, there were no significant differences between semaglutide and comparators.
Paediatric population Semaglutide has not been studied in paediatric patients.
Injection site reactions(e.g. injection site rash, erythema) have been reported by 0.6% and0.5% of patients receiving semaglutide 0.5 mg and 1 mg, respectively.
Furthermore, semaglutide is stabilised against degradation by the DPP-4 enzyme.
Caution should be exercised when using semaglutide in patients with diabetic retinopathy treated with insulin.
Semaglutide exposure increased in a dose proportional manner for doses of 0.5 mg and 1 mg.
If pancreatitis is suspected, semaglutide should be discontinued; if confirmed, semaglutide should not be restarted.
Semaglutide should be discontinued at least 2 months before a planned pregnancy due to the long half-life(see section 5.2).
In addition, semaglutide treatment increased fasting insulin concentrations compared to placebo.
Semaglutide compared to placebo lowered fasting triglyceride and very low density lipoproteins(VLDL) cholesterol concentrations by 12% and 21%, respectively.
However, upon initiation of semaglutide treatment in patients on warfarin or other coumarin derivatives, frequent monitoring of INR is recommended.
SUSTAIN(Semaglutide Unabated Sustainability in Treatment of Type 2 Diabetes)is a clinical trial programme for semaglutide, administered once weekly, that comprises seven phase 3a global clinical trials and a cardiovascular outcomes trial, involving more than 8,000 adults with type 2 diabetes.
In this post-hoc analysis, semaglutide was well tolerated, with a safety profile similar to that of other glucagon-like peptide-1 receptor agonists.