Примери за използване на Glucose excretion на Английски и техните преводи на Български
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Empagliflozin increased urine glucose excretion leading to an increase in urine volume.
Dapagliflozin improves both fasting andpost-prandial plasma glucose levels by reducing renal glucose reabsorption leading to urinary glucose excretion.
Urinary glucose excretion may be associated with an increased risk of urinary tract infections.
The steady-state inhibition of renal glucose reabsorption and the amount of urinary glucose excretion over a 24-hour period was the same for both dosing regimens.
The 24-hour urinary glucose excretion declined with increasing severity of renal impairment(see section 4.4).
Dapagliflozin improves both fasting andpost-prandial plasma glucose levels by reducing renal glucose reabsorption leading to urinary glucose excretion.
Increased urinary glucose excretion was maintained at the end of the 4-week treatment period, averaging approximately 78 g/day.
By inhibiting SGLT2, ertugliflozin reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, andthereby increases urinary glucose excretion.
The effect of empagliflozin on urinary glucose excretion is associated with osmotic diuresis, which could affect the hydration status.
By inhibiting SGLT2, sotagliflozin reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, andthereby increases urinary glucose excretion.
Increased urinary glucose excretion resulted in an immediate reduction in plasma glucose levels in patients with type 2 diabetes.
Dose-response modelling indicates that ertugliflozin 5 mg and15 mg result in near maximal urinary glucose excretion(UGE) in patients with type 2 diabetes mellitus, providing 87% and 96% of maximal inhibition, respectively.
Increased urinary glucose excretion was maintained at the end of the 4-week treatment period, averaging approximately 78 g/day with empagliflozin 25 mg.
Use in patients at risk for adverse reactions related to volume depletion Due to its mechanism of action, canagliflozin, by increasing urinary glucose excretion(UGE), induces an osmotic diuresis, which may reduce intravascular volume and decrease blood pressure(see section 5.1).
In addition, urinary glucose excretion triggers calorie loss, associated with body fat loss and body weight reduction.
Following coadministration of dapagliflozin with mefenamic acid(an inhibitor of UGT1A9), a 55% increase in dapagliflozin systemic exposure was seen, butwith no clinically meaningful effect on 24-hour urinary glucose excretion.
The increased urinary glucose excretion with SGLT2 inhibition produces an osmotic diuresis, and can result in a reduction in systolic BP.
Following coadministration of dapagliflozin with mefenamic acid(an inhibitor of UGT1A9), a 55% increase in dapagliflozin systemic exposure was seen, butwith no clinically meaningful effect on 24-hour urinary glucose excretion.
The increased urinary glucose excretion with SGLT2 inhibition produces an osmotic diuresis, and can result in a reduction in systolic BP.
Following coadministration of dapagliflozin with rifampicin(an inducer of various active transporters and drug-metabolising enzymes) a 22% decrease in dapagliflozin systemic exposure(AUC) was observed, butwith no clinically meaningful effect on 24-hour urinary glucose excretion.
The effect of empagliflozin on urinary glucose excretion is associated with osmotic diuresis, which could affect hydration status of patients age 75 years and older.
Following coadministration of dapagliflozin with rifampicin(an inducer of uridine 5'-diphosphoglucuronosyl transferase[UGT] and CYP3A4/5), a 22% decrease in dapagliflozin systemic exposure(AUC) was observed, butwith no clinically meaningful effect on 24-hour urinary glucose excretion.
Urinary glucose excretion may be associated with an increased risk of urinary tract infection; therefore, temporary interruption of treatment should be considered when treating pyelonephritis or urosepsis.
Based on the mode of action of sodium glucose co-transporter 2(SGLT-2) inhibitors,by increasing urinary glucose excretion(UGE), sotagliflozin induces an osmotic diuresis which may reduce intravascular volume and decrease blood pressure(see sections 4.8 and 5.1).
Urinary glucose excretion may be associated with an increased risk of urinary tract infection; therefore, temporary interruption of dapagliflozin should be considered when treating pyelonephritis or urosepsis.
Due to its mechanism of action, canagliflozin, by increasing urinary glucose excretion(UGE) induces an osmotic diuresis, which may reduce intravascular volume and decrease blood pressure(see section 5.1).
The steady-state 24-hour urinary glucose excretion was highly dependent on renal function and 85, 52, 18 and 11 g of glucose/day was excreted by subjects with type 2 diabetes mellitus and normal renal function or mild, moderate or severe renal impairment, respectively.
The steady-state 24-hour urinary glucose excretion was highly dependent on renal function and 85, 52, 18 and 11 g of glucose/day was excreted by subjects with type 2 diabetes mellitus and normal renal function or mild, moderate or severe renal impairment, respectively.