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Exact(11)
The bleeding events were recorded throughout the observation period.
Bleeding events were recorded and graded from 0 to 4 according to the World Health Organization (WHO) classification [6, 9].
Bleeding events were recorded for 28 days.
Ischemic and bleeding events were recorded during the trial.
Living donors.- After surgery, donors' liver function recovered well and no bleeding events were recorded.
For this subset, all serious bleeding events were recorded for 7 days following the start of infusion and study drug-related serious bleeding events were recorded for up to 28 days.
Similar(49)
There were three occurrences of grade-4 thrombocytopenia requiring platelet transfusion in three patients; no bleeding event was recorded.
Because there was no significant difference between major bleeding events in both the intervention and the control groups in the RECORD trials [ 15], the costs of major bleeding events were not considered in our analysis.
When bleeding events were analysed as ordinal data (no bleed, minor bleed, major bleed)[19], significantly increased rates were seen in the triple therapy group (p<0.01).
Adverse bleeding events were also examined.
Five major bleeding events were noted.
More suggestions(18)
bleeding episodes were recorded
bleeding events were considered
bleeding events were included
bleeding rates were recorded
bleeding events were observed
bleeding events were related
bleeding events were categorized
bleeding events were analyzed
bleeding patterns were recorded
bleeding events were defined
bleeding events were documented
bleeding events were associated
bleeding events were reported
bleeding symptoms were recorded
bleeding events was recorded
bleeding events were analysed
bleeding volumes were recorded
bleeding events were adjudicated
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