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Resting ECG was normal with no prolongation of the QT interval.
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As with this approach, there is no prolongation of clinically overt hyperthyroidism and the associated risks are non-existent.
There is no association with QT prolongation, seizure activity, serotonin toxicity, delirium or any need for intervention.
The median QRS was 80 ms (Range: 80 120 ms) and there were no cases with QT prolongation.
DHA-P was associated with borderline prolongation of QTc interval but no difference was seen in prolonged QTc (low quality evidence) and no cardiac arrhythmias were reported.
Treatment with GSK961081 was associated with prolongation of various QTc intervals ranging from 3 to 5 ms more compared to placebo or salmeterol.
We are proceeding with the full study with prolongation of the duration of recruitment and consideration for inclusion of other centres to meet study targets.
Most adverse events related to the nervous system, ear, and labyrinth disorders were transient and reversible, and there were no adverse events associated with QTc prolongation.
However, with prolongation of reperfusion, NO synthase activity decreases and NO is also consumed by reaction with superoxide and hydroxyl radicals.
In some studies of human SIDS, no correlation has been made with QT prolongation.
The maximum QTc interval observed in the current study was 518 ms, and no ventricular tachyarrhythmias were associated with QTc prolongation in any patient.
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