Примери за използване на Observed more frequently на Английски и техните преводи на Български
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Observed more frequently with fresh, not cured malaria.
Such bubbles are observed more frequently in the lung.
When doses higher than 9.5 mg/ 24 h were used in the above-mentioned study, dizziness, insomnia, agitation, decreased appetite,atrial fibrillation and cardiac failure were observed more frequently than.
These reactions have been observed more frequently within 24 hours of infusion.
In a clinical trial of children and adolescents receiving rosuvastatin for 52 weeks, CK elevations> 10xULN and muscle symptoms following exercise orincreased physical activity were observed more frequently compared to observations in clinical trials in adults(see Section 4.8).
Viral shedding was observed more frequently in children and adolescents(28/39) compared to adults.
It seems to occur in populations throughout the world, although it is observed more frequently in certain ethnic groups, such as Asians.
The serious adverse reactions observed more frequently(≥5%) with lenalidomide in combination with low dose dexamethasone(Rd and Rd18) than with melphalan, prednisone and thalidomide(MPT) were.
Neutropenia, thrombocytopenia andpalmar-plantar erythrodysaethesia syndrome were observed more frequently in patients of East Asian descent.
Some adverse reactions were observed more frequently in studies of combination use of sitagliptin with other anti-diabetic medicinal products than in studies of sitagliptin monotherapy.
In patients where Zevalin is usedfollowing remission induction therapy, infections were observed more frequently than described above(very common).
The serious adverse reactions observed more frequently(≥5%) with lenalidomide maintenance than placebo were.
Shadows, which have been mistaken for gallstones,have been detected on sonograms of the gallbladder and have been observed more frequently at ceftriaxone doses of 1 g per day and above.
Transaminase elevations have been observed more frequently in paediatric patients than in adult patients(see section 4.8).
When doses higher than 9.5 mg/ 24 h were used in the above-mentioned study, dizziness, insomnia, agitation, decreased appetite, atrial fibrillation andcardiac failure were observed more frequently than with 9.5 mg/ 24 h or placebo, suggesting a dose effect relationship.
Transaminase elevations have been observed more frequently in paediatric patients than in adult patients.
In the 96 week analysis, the safety profile of PREZISTA/ritonavir 800/100 mg once daily in treatment-naïve subjects was similar to that seen with PREZISTA/ritonavir 600/100 mg twice daily in treatment-experienced subjects except fornausea which was observed more frequently in treatment-naïve subjects.
Severe cardiovascular events were observed more frequently in patients with NSCLC than breast or ovarian carcinoma.
Based on the clinical trial database of 196 adolescents exposed to perampanel from double-blind studies for partial-onset seizures and primary generalised tonic-clonic seizures,the overall safety profile in adolescents was similar to that of adults, except for aggression, which was observed more frequently in adolescents than in adults.
In the paediatric population somnolence andfatigue were observed more frequently in patients with bipolar disorder compared to patients with schizophrenia.
Some adverse reactions were observed more frequently in studies of combination use of sitagliptin and metformin with other anti-diabetic medicinal products than in studies of sitagliptin and metformin alone.
In patients followed for up to 16 weeks after discontinuation of treatment at one year,post-treatment ALT elevations were observed more frequently in patients who had received lamivudine than in patients who had received placebo.
Injection site reactions were observed more frequently in prolonged-release exenatide treated patients versus comparator-treated patients(16% versus range of 2-7%) during the 6-month controlled phase of studies.
In patients followed for up to 16 weeks after discontinuation of treatment at one year,post-treatment ALT elevations were observed more frequently in patients who had received lamivudine than in patients who had received placebo.
The serious adverse reactions observed more frequently(≥5%) with melphalan, prednisone and lenalidomide followed by lenalidomide maintenance(MPR+R) or melphalan, prednisone and lenalidomide followed by placebo(MPR+p) than melphalan, prednisone and placebo followed by placebo(MPp+p) were.
When doses higher than 13.3 mg/24 h were used in the above-mentioned placebo-controlled study, insomnia andcardiac failure were observed more frequently than with 13.3 mg/24 h or placebo, suggesting a dose effect relationship.
Weight loss of at least 5% baseline body weight was observed more frequently for subjects treated with naltrexone/ bupropion(31%) compared to placebo(12%)(Table 4).
In addition to the adverse reactions reported in adults(see section 4.8, Tabulated summary of adverse reactions),the following adverse reactions were observed more frequently in paediatric patients: anaemia was common(9.5%) and skin discolouration(increased pigmentation) was very common(31.8%) in paediatric patients.
In clinical studies,events of malignancies were observed more frequently in cladribine-treated patients compared to patients who received placebo(see section 4.8).
During the controlled period of the clinical studies, injection site reactions were observed more frequently in patients treated with Bydureon BCise versus comparator-treated patients(24% versus 4% with immediate-release exenatide).