Примери за използване на Immediate-release exenatide на Английски и техните преводи на Български
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Immediate-release exenatide 10 mcg BID.
Mean difference in change from baseline versus immediate-release exenatide 95%.
Immediate-release exenatide should not be administered after a meal.
There were no episodes of major hypoglycaemia in the immediate-release exenatide arm.
Immediate-release exenatide has shown no adverse effects on lipid parameters.
These reactions have usually been mild and usually did not result in discontinuation of immediate-release exenatide.
Immediate-release exenatide must not be administered by intravenous or intramuscular injection.
Most adverse reactions associated with immediate-release exenatide were mild to moderate in intensity.
A delay in tmax of about 2 h was observed when warfarin was administered 35 min after immediate-release exenatide.
Patients may experience hypoglycaemia when immediate-release exenatide is used with a sulphonylurea.
Studies of immediate-release exenatide with metformin, a thiazolidinedione or both as background therapy.
Paracetamol AUC, Cmax and tmax were not significantly changed when paracetamol was given 1 hour before immediate-release exenatide injection.
Immediate-release exenatide use can be continued when a basal insulin is added to existing therapy.
In patients treated with 5 mcg or 10 mcg immediate-release exenatide, 36% reported at least one episode of nausea.
Immediate-release exenatide is available as either a 5 mcg or a 10 mcg exenatide per dose pre-filled pen.
Prolonged-release exenatide resulted in a statistically significant reduction in HbA1c compared to patients receiving immediate-release exenatide(Table 4).
When immediate-release exenatide is used in combination with basal insulin, the dose of basal insulin should be evaluated.
During the controlled period of the clinical study comparing Bydureon BCise with immediate-release exenatide, nausea was reported in 9.6% and 20.5% of patients in each group.
The dose of immediate-release exenatide does not need to be adjusted on a day-by-day basis depending on self-monitored glycaemia.
In patients with end-stage renal disease receiving dialysis,single doses of immediate-release exenatide 5 mcg increased frequency and severity of gastrointestinal adverse reactions.
Immediate-release exenatide is not expected to have any clinically relevant effects on the pharmacokinetics of metformin or sulphonylureas.
INR should be closely monitored during initiation and dose increase of immediate-release exenatide therapy in patients on warfarin and/or cumarol derivatives(see section 4.8).
Rate based on immediate-release exenatide completed long-term efficacy and safety studies n=5763 total(patients on sulphonylurea n=2971).
There were no clinically significant differences in the incidence of hypoglycaemic episodes in the immediate-release exenatide compared to the placebo group(25% and 29% respectively).
At the end of the study, immediate-release exenatide(n=137) demonstrated a statistically significant reduction in the HbA1c and weight compared to placebo(n=122).
Immediate-release exenatide is recommended for use in patients with type 2 diabetes mellitus who are already receiving metformin, a sulphonylurea, pioglitazone and/or a basal insulin.
A clinically relevant effect of prolonged-release exenatide and immediate-release exenatide treated subjects was observed on HbA1c, regardless of the background anti-diabetic therapy in both studies.
Immediate-release exenatide can be administered at any time within the 60-minute period before the morning and evening meal(or two main meals of the day, approximately 6 hours or more apart).
Effects of overdoses with exenatide(based on immediate-release exenatide clinical studies) included severe nausea, severe vomiting and rapidly declining blood glucose concentrations.
When immediate-release exenatide was used in combination with a thiazolidinedione, the incidence of hypoglycaemia was similar to that of placebo in combination with a thiazolidinedione.