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The transport of critically ill patients is often logistically difficult and exposes the patient to increased likelihood for adverse events and risk to safety [ 43- 46].
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However, most analyses performed involved comparisons between different CD treatment regimens, and there is no evidence indicating that SAE reporting would be inconsistent between treatment groups, outside of the fact that maintenance infliximab therapy requires regular office visits and thus a stronger likelihood for adverse event reporting.
No difference were found for adverse events.
Common Terminology Criteria for Adverse Events.
Throughout the study, subjects were monitored for adverse events (AEs).
The adverse event was considered as grade 3 in the common terminology criteria for adverse events version 4.0.
Adverse events were graded using Common Terminology Criteria for Adverse Events v3.0 (CTCAE v3.0).
‡‡ for adverse events only.
Patients were monitored for adverse events (AEs).
Threshold for adverse events was routinely investigated.
All patients were monitored for adverse events.
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