Примери за използване на Treated with empagliflozin на Английски и техните преводи на Български
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Of these, 266 or264 patients were treated with empagliflozin 10 mg or 25 mg as add-on to metformin plus insulin, respectively.
The intensity(mild, moderate, severe)of urinary tract infection was similar in patients treated with empagliflozin and placebo.
Consistently, in the EMPA-REG OUTCOME study, patients treated with empagliflozin experienced an initial fall in eGFR(mean: 3 ml/min/1.73 m2).
Postmarketing cases of complicated urinary tract infections including pyelonephritis andurosepsis have been reported in patients treated with empagliflozin.
Urinary tract infection was reported more frequently in female patients treated with empagliflozin compared to placebo, but not in male patients.
In clinical trials with Glyxambi, there was no notable difference of the frequency of urinary tract infections in patients treated with Glyxambi(Glyxambi 25 mg/5 mg: 8.5%; Glyxambi 10 mg/5 mg: 7.5%)compared to the patients treated with empagliflozin and linagliptin.
Urinary tract infection was reported more frequently in females treated with empagliflozin compared to placebo; there was no difference in males.
Complicated urinary tract infections(including serious urinary tract infections, pyelonephritis or urosepsis)occurred at a similar frequency in patients treated with empagliflozin compared to placebo.
These infections were reported more frequently in females treated with empagliflozin compared to placebo, and the difference in frequency was less pronounced in males.
Complicated urinary tract infection(e.g. pyelonephritis or urosepsis)occurred at a similar frequency in patients treated with empagliflozin compared to placebo.
A greater proportion of patients treated with empagliflozin and with a baseline HbA1c≥7.0% achieved a target HbA1c of< 7% compared to placebo(Table 8).
A higher risk of volume depletion adverse reactions were reported in patients aged 75 years and older, treated with empagliflozin, especially at 25 mg/day(see section 4.8).
After 24 weeks, rescue therapy was used in 4(3.6%)patients treated with empagliflozin 25 mg and in 2(1.8%) patients treated with empagliflozin 10 mg, compared to 13(12.0%) patients treated with placebo(all patients on background metformin+ linagliptin 5 mg).
Of these, a total of 530 patients received empagliflozin as add-on to metformin plus insulin,of which 266 patients were treated with empagliflozin 10 mg and 264 with empagliflozin 25 mg.
Major hypoglycaemic events occurred in 0.5%, 0% and0.5% of patients treated with empagliflozin 10 mg,empagliflozin 25 mg and placebo when added on to metformin and insulin, respectively.
Complicated urinary tract infections(including serious urinary infections, pyelonephritis or urosepsis)occurred at a similar frequency in patients treated with empagliflozin compared to placebo.
Initial increases in creatinine andinitial decreases in estimated glomerular filtration rates in patients treated with empagliflozin were generally transient during continuous treatment or reversible after drug discontinuation of treatment.
In Glyxambi clinical trials, the incidence of urinary tract infections was overall similar between the patients treated with Glyxambi and the patients treated with empagliflozin or linagliptin.
The overall frequency of urinary tract infection reported as adverse event was similar in patients treated with empagliflozin 25 mg and placebo and higher in patients treated with empagliflozin 10 mg(see section 4.8).
A total of 7052 patients with type 2 diabetes were treated in clinical studies to evaluate the safety of empagliflozin as add-on to metformin,of which 4740 patients were treated with empagliflozin as add-on to metformin.
In empagliflozin trials, the overall frequency of urinary tract infection was similar in patients treated with empagliflozin 25 mg and placebo(7.0% and 7.2%), and higher in patients treated with empagliflozin 10 mg(8.8%).
The overall frequency of volume depletion(including the predefined terms blood pressure(ambulatory) decreased, blood pressure systolic decreased, dehydration, hypotension, hypovolaemia, orthostatic hypotension, and syncope)was similar in patients treated with empagliflozin(empagliflozin 10 mg: 0.5%, empagliflozin 25 mg: 0.3%) and placebo(0.3%).
Initial increases in creatinine andinitial decreases in estimated glomerular filtration rates in patients treated with empagliflozin as add-on to metformin therapy were generally transient during continuous treatment or reversible after drug discontinuation of treatment.
Major hypoglycaemia(events requiring assistance) The overall frequency of patients with major hypoglycaemic events was low(< 1%) and similar for empagliflozin and placebo as add-on to metformin, andfor the combination of empagliflozin with metformin in drug-naïve patients compared to those treated with empagliflozin and metformin as individual components, and as adjunct to standard care therapy.
The overall frequency of urinary tract infection reported as adverse event was higher in patients treated with empagliflozin 10 mg on a background of metformin compared to patients treated with placebo or empagliflozin 25 mg on a background of metformin(see section 4.8).
The frequency of hypoglycaemia depended on the background therapy in the respective studies and was similar for empagliflozin and placebo as add-on to metformin, as add-on to linagliptin and metformin,for the combination of empagliflozin with metformin in drug-naïve patients compared to those treated with empagliflozin and metformin as individual components, and as adjunct to standard care therapy.
A greater proportion of patients with a baseline HbA1c≥7.0% and treated with empagliflozin plus linagliptin achieved a target.
In clinical trials with empagliflozin, increased urination(including the predefined terms pollakiuria, polyuria, nocturia)was observed at higher frequencies in patients treated with empagliflozin(empagliflozin 10 mg: 3.5%, empagliflozin 25 mg: 3.3%) compared to placebo(1.4%).
The overall frequency of urinary tract infection reported as adverse event was similar in patients treated with empagliflozin 25 mg and placebo(7.0% and 7.2%) and higher in empagliflozin 10 mg(8.8%).
Placebo controlled double-blinded trials of 18 to 24 weeks of exposure included 3456 patients,of which 1271 were treated with empagliflozin 10 mg as add-on to metformin and 1259 with empagliflozin 25 mg as add-on to metformin.