View source for 10 CFR 35.3045(a)(1)

(a) A licensee shall report any event, except for an event that results from patient intervention, in which the administration of byproduct material or radiation from byproduct material results in-
:(1) A dose that differs from the prescribed dose or dose that would have resulted from the prescribed dosage by more than 0.05 Sv (5 rem) effective dose equivalent, 0.5 Sv (50 rem) to an organ or tissue, or 0.5 Sv (50 rem) shallow dose equivalent to the skin; and
::(i) The total dose delivered differs from the prescribed dose by 20 percent or more;
::(ii) The total dosage delivered differs from the prescribed dosage by 20 percent or more or falls outside the prescribed dosage range; or
::(iii) The fractionated dose delivered differs from the prescribed dose, for a single fraction, by 50 percent or more.


{{Reporting criterion-Nav}}