Примери за използване на Major bleeding на Английски и техните преводи на Български
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Major Bleeding n(%) n.
Stop any major bleeding.
Major bleeding from any part of the body.
If you have any major bleeding.
Major bleeding occurred in 0.97 per 100 patient-years.
However, the actual risk of major bleeding is low.
Major bleeding occurred in 2.1 per 100 patient years.
Type or Location of Major Bleeding.
Major bleeding event/clinical relevant bleeds. .
The primary safety endpoint was major bleeding.
Major bleeding rates with this dose were comparable to warfarin.
Lesion or condition,if considered a significant risk factor for major bleeding.
The incidence of major bleeding was similar between groups.
Lesion or condition,if considered to be a significant risk for major bleeding.
Ra adjudicated major bleeding was 2.1%(fondaparinux) vs.
A further ongoing study involved patients taking a factor Xa inhibitor anticoagulant who had major bleeding.
Major bleeding occurred most frequently at the sheath puncture site.
For the primary safety endpoint of major bleeding there was an interaction of treatment effect and age.
Major bleeding during treatment occurred in 1(0.1%) fondaparinux patient and in 1(0.1%) placebo patient.
After the birth of CONTEFINO GRANDE, Grenada has received major bleeding and the next day 14 hours after birth she left us….
The rate of major bleeding was 3.40% per year in the group receiving 150 mg of dabigatran(P=0.41).
There is less information about other types of surgery butthe overall evidence does not suggest an excessive risk of major bleeding.
At Day 9 the incidence of major bleeding on fondaparinux and enoxaparin was 2.1% and 4.1%, na.
The uncontrolled use of vegetable infusion leads to problems such as incomplete miscarriage, cardiac arrest,the development of major bleeding, life-threatening.
Rates of major bleeding were similar in patients treated with 5 mg prasugrel and those treated with 75 mg clopidogrel.
The prespecified net clinical benefit(primary efficacy outcome plus major bleeding events) was reported with a HR of 0.849(95% CI: 0.633- 1.139).
Major bleeding was observed in 3.4% of the patients in the fondaparinux group and in 2.4% of the dalteparin group.
The prespecified net clinical benefit(primary efficacy outcome plus major bleeding events) of the pooled analysis was reported with a HR of 0.771(95% CI: 0.614- 0.967).
Major bleeding was defined as either an intracranial haemorrhage or a decrease in haemoglobin concentrations of more than 5 g/ dl(see table 1).
Use of either anticoagulants or medicinal products that inhibit platelet function(antiplatelet agents)concomitantly with IMBRUVICA increases the risk of major bleeding.