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If a child vomited within 30 minutes of receiving the drug, the full dose was repeated.
The full dose was repeated if vomiting occurred within 30 minutes, and half-dose given if vomiting occurred within 30 60 minutes.
If vomiting occurred during the first 30 minutes, a full dose was re-administered and only half dose, if vomiting occurred 30 minutes after drug intake.
After each treatment dose, patients were observed for one hour, if the drug was vomited during the first half hour a full dose was repeated, if vomiting occurred after one hour half a dose was repeated.
In case of vomiting, a full dose was repeated if this occurred within the first half an hour, or half a dose if it occurred between 30 minutes and 1 h.
Patients were observed for 1 hour: if vomiting occurred within 30 min of dosing, a full dose was re-administered; if vomiting occurred between 30 min and 1 hour only half dose was re-administered.
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Meta-regression in a recent meta-analysis suggested that the duration of treatment at full dose is a strong predictor of survival benefit from corticosteroids with the "neutrality line" being crossed by the regression line for time equal to 120 hours arguing for maintaining treatment at full dose for at least 5 days [26, 36].
A technique known as tube-current modulation has been developed to adjust the current to the x-ray tube such that the full dose is delivered during the quiescent phase of the cardiac cycle for high-resolution imaging, while a much reduced dose is delivered in other phases of the cycle to allow reconstruction of lower resolution functional images.
The 1/10th dose is 0.3 mg, and full dose is 3 mg.
Haematological recovery after 1 week resulted in the full dose being given at the next treatment cycle.
In the 2005, 2007 and 2009 tender processes UNICEF signalled to industry its preference for devices with early activation (disabling mechanism activated before full dose is administered).
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