Примери за използване на Incidence of severe на Английски и техните преводи на Български
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There was no difference in the incidence of severe hypoglycaemia.
The incidence of severe cases was similar for clopidogrel and ASA.
Haemorrhagic events were reported in 29% of patients with EBC and the incidence of severe haemorrhagic events(Grade≥3) was 0.4%, including one Grade 5 event.
The incidence of severe cases was similar for clopidogrel and ASA.
In the study in RCC following prior VEGF-targeted therapy(METEOR), the incidence of severe haemorrhagic events(Grade≥ 3) was 2.1%(7/331) in cabozantinib-treated RCC patients.
The incidence of severe cases was 1.4% for clopidogrel and 1.6% for ASA.
It is absolutely unacceptable to engage in self-treatment of newborns(from birth to one year), since the incidence of severe complications in this group of children is quite high!
The incidence of severe bleeding events was higher in patients with AP-CML, BP-CML and Ph+ ALL.
In patients initially not reperfused, the incidence of severe haemorrhage was 1.2% for fondaparinux vs 1.5% for controls.
The incidence of severe(Grade 3 or 4) nausea, vomiting, diarrhoea and mucositis was 4, 3, 2 and 1%, respectively.
Haemorrhage Haemorrhagic events were reported in 34.8% of patients in MBC clinical trials with trastuzumab emtansine and the incidence of severe haemorrhagic events(Grade≥3) occurred in 2.2%.
In this population, the incidence of severe hypoglycaemia was 0.4% in each group.
The incidence of severe haemorrhagic events(Grade≥ 3) was 2.1% in cabozantinib-treated RCC patients(7/331).
Among patients who were using sulfonylurea at baseline, the incidence of severe hypoglycaemia was 2.0% in linagliptin-treated patients and 1.7% in placebo treated patients.
The incidence of severe infections was low and opportunistic infections associated with immunocompromise were not seen.
For patients receiving primary PCI, the incidence of severe haemorrhage was 1.0% for fondaparinux and 0.4% for controls.
The incidence of severe RV gastro-enteritis associated with the individual genotypes was too small to allow calculation of efficacy.
Among patients who were using insulin at baseline, the incidence of severe hypoglycaemia was 4.4% in linagliptin-treated patients and 4.9% in placebo treated patients.
The incidence of severe reactions was greater following the second infusion(2.1% vs. 0.8% following the first infusion), and decreased to 1.3% following the third infusion.
The blood glucose levels,hypoglycemic awareness and incidence of severe hypoglycemic events among participants were assessed 1 and 2 years after transplantation.
The incidence of severe hypoglycaemia and rates of documented hypoglycaemia(overall and nocturnal) were lower on sotagliflozin compared to insulin alone in the 52-week studies, as shown in Table 7.
In the treatment-naïve RCC study(CABOSUN), the incidence of severe haemorrhagic events(Grade≥ 3) was 5.1%(4/78) in cabozantinib-treated RCC patients.
The incidence of severe local skin responses that occurred at an incidence> 1% in both the‘face/scalp' and the‘trunk/extremities', respectively are: application site erythema(24% and 15%), application site exfoliation(9% and 8%), application site scab(6% and 4%), application site swelling(5% and 3%) and application site pustules(5% and 1%).
Among patients who were not using insulin and/or a sulfonylurea at baseline, the incidence of severe hypoglycaemia was 1.0% in sitagliptin-treated patients and 0.7% in placebo-treated patients.
Although the incidence of severe marrow suppression with clinical consequences is relatively low, patients have been treated with Pixuvri were closely monitored by frequent blood counts, particularly for neutropenia.
In the intention-to-treat population,among patients who were using insulin and/or a sulfonylurea at baseline, the incidence of severe hypoglycaemia was 2.7% in sitagliptin-treated patients and 2.5% in placebo-treated patients;
Since the incidence of severe renal-related adverse events was increased with the monotherapy as compared to the combination therapy with a xanthine oxidase inhibitor, Zurampic should not be used as monotherapy(see sections 4.2 and 5.1).
While liver function monitoring continues to be an important measure to detect liver injury, andlikely reduce the incidence of severe cases, it is unclear at this stage whether any alternative monitoring regimen would necessarily prevent further severe cases.
A retrospective review suggests that the incidence of severe anaphylactic reactions to aprotinin may further increase when patients are re-exposed more than twice within 6 months.
In the HCC study(CELESTIAL), the incidence of severe haemorrhagic events(Grade≥ 3) was 7.3% in cabozantinib-treated patients(34/467).