| DICOM PS3.16 2019b - Content Mapping Resource |
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This template provides information on adverse events occurring to a patient as a result of administration of an Imaging Agent.
Table TID 11021. Imaging Agent Administration Adverse Events
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Indicates whether the administration is discontinued due to the adverse event. There is no indication of which adverse event if any contributed to the decision to discontinue the administration. |
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Note that presence of this row means the injector was informed about the adverse event by the operating clinician. |
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Date and time when the adverse event was noted by the observer. |
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UID of the performed step (as recorded in Row 3 of TID 11007) in which the adverse event occurred. |
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UID of the performed phase (as recorded in Row 3 of TID 11008) in which the adverse event occurred. |
| DICOM PS3.16 2019b - Content Mapping Resource |
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