Примери за използване на Subgroup of patients на Английски и техните преводи на Български
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There are no diagnostic tests orrecommended treatments for this subgroup of patients.
Only one subgroup of patients, those with“early Lyme disease,” has been clinically characterized.
No death reduction was observed in the subgroup of patients with lower disease severity.
In a subgroup of patients not receiving an ACE inhibitor(n=366), the morbidity benefits were greatest.
Additional secondary outcome measures in the subgroup of patients treated with concomitant clobazam.
In this subgroup of patients, the safety profile of ivabradine is in line with the one of the overall population.
Survival estimates were lower in the subgroup of patients with PAH secondary to systemic sclerosis.
As for the overall population, a statistically significant improvement in CFS in favour of IKERVIS was observed in this subgroup of patients.
These figures were 23% and 15% in the subgroup of patients on hemodialysis and peritoneal dialysis, respectively.
All cause mortality was 10.9%(77/708) for atorvastatin versus 9.1%(64/701)for placebo in the subgroup of patients with prior lacunar infarct.
For efficacy results in the subgroup of patients corresponding to the approved indication, see text above.
Moreover, the safety profile of clopidogrel in this subgroup of patients did not raise any particular concern.
The subgroup of patients with predominantly classic CNV lesions(N=243; Visudyne 159, placebo 84) were more likely to exhibit a larger treatment benefit.
Moreover, the safety profile of clopidogrel in this subgroup of patients did not raise any particular concern.
In the subgroup of patients with hormone receptor-negative disease(n=426), the hazard ratios for PFS and OS were 0.56(95% CI: 0.44, 0.72) and 0.75(95% CI: 0.54, 1.03), respectively.
Moreover, the safety profile of clopidogrel in this subgroup of patients did not raise any particular concern.
In the subgroup of patients undergoing PCI, major bleeding was observed commonly, in 9.7% of eptifibatide-treated patients vs 4.6% of placebo-treated patients. .
Limited evidence of PFS benefit was reported in the subgroup of patients with ileum as primary tumour origin(see section 5.1).
In the subgroup of patients with recent symptom onset(< 3 years) the clinical benefit of ChondroCelect over microfracture was significantly larger, confirming the results at 36 months after treatment.
The limited sample size andshorter duration of TYSABRI exposure for this subgroup of patients should be considered when interpreting these data.
There is no experience in the subgroup of patients with both high body weight(> 100 kg) and moderate renal impairment(creatinine clearance 30-50 ml/min).
CHMP concluded that the magnitude of benefit was clinically important in a subgroup of patients, and that response can be adequately assessed after three months of treatment.
An a-posteriori analysis was performed on a subgroup of patients from the TROPOS study of particular medical interest and at high-risk of fracture defined by a femoral neck BMD T-score≤- 3 SD(manufacturer' s range corresponding to -2.4 SD using NHANES III) and an age≥ 74 years n=1,977, i. e.
The majority of patients had relapsing-remitting multiple sclerosis(97.5%), but a subgroup of patients had secondary progressive(0.8%) or progressive relapsing multiple sclerosis(1.7%).
An a-posteriori analysis was performed on a subgroup of patients from the TROPOS study of particular medical interest and at high-risk of fracture[defined by a femoral neck BMD T-score≤- 3 SD(manufacturer's range corresponding to -2.4 SD using NHANES III) and an age≥ 74 years(n=1,977, i.e. 40% of the TROPOS study population)].
E(see sections 4.2, 4.3 and 5.2). ng There is no experience in the subgroup of patients with both high body weight(> 100 kg) and moderate renal impairment(creatinine clearance 30-50 ml/ min).
The PFS benefit was less in the subgroup of patients with CR than in the subgroup of patients who had not achieved a CR.
The PFS benefit was observed both in the subgroup of patients with CR and in the subgroup of patients who had not achieved a CR.
There is accumulating evidence that a subgroup of patients is at an increased risk of developing hypersensitivity reactions.
These survival estimates were similar in the subgroup of patients with PAH associated with CTD for the Thelin treated group(98%, 78% and 67% respectively).