NCT02958969 · 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
- 1 year
- Other-event reporting threshold
- 5%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Apixaban | 0 / 50 | 3 / 50 | 0 / 50 |
Serious adverse events
Other reported adverse events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Blood and lymphatic system disorders
- stats
- group Id
- EG000
- num Affected
- 3
- num At Risk
- 50
- num Events
- 3
- term
- non-major bleeding
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 50
- description
- apixaban 2.5 mg orally twice daily for primary prevention of VTE for a duration of 6 months Apixaban: apixaban 2.5 mg orally twice daily for primary prevention of VTE for a duration of 6 months
- id
- EG000
- other Num Affected
- 3
- other Num At Risk
- 50
- serious Num Affected
- 0
- serious Num At Risk
- 50
- title
- Apixaban
- frequency Threshold
- 5
- other Events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Blood and lymphatic system disorders
- stats
- group Id
- EG000
- num Affected
- 3
- num At Risk
- 50
- num Events
- 3
- term
- non-major bleeding
- time Frame
- 1 year
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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