NCT00248547 · ADVERSE EVENTS
Adverse events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.
- Collection time frame
- Not reported
- Other-event reporting threshold
- 5%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Aprepitant | 2 / 20 | 0 / 20 | Not reported / Not reported |
| Placebo | 0 / 20 | 0 / 20 | Not reported / Not reported |
Serious adverse events
- organ System
- Gastrointestinal disorders
- stats
- group Id
- EG000
- num Affected
- 2
- num At Risk
- 20
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 20
- term
- Subileus
Other reported adverse events
Complete source fields
- event Groups
- description
- Loading dose of 125 mg capsule once a day for one day, then maintenance dose of 80 mg capsule daily through Day +4 of Bone Marrow Transplant
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 20
- serious Num Affected
- 2
- serious Num At Risk
- 20
- title
- Aprepitant
- description
- Loading dose of 125 mg capsule once a day for one day, then maintenance dose of 80 mg capsule daily through Day +4 of Bone Marrow Transplant
- id
- EG001
- other Num Affected
- 0
- other Num At Risk
- 20
- serious Num Affected
- 0
- serious Num At Risk
- 20
- title
- Placebo
- frequency Threshold
- 5
- serious Events
- organ System
- Gastrointestinal disorders
- stats
- group Id
- EG000
- num Affected
- 2
- num At Risk
- 20
- group Id
- EG001
- num Affected
- 0
- num At Risk
- 20
- term
- Subileus
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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