NCT03506386 · 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
- From diagnosis up to the end of this study (up to 11.7 years)
- Other-event reporting threshold
- 0%
Only deaths were collected, and data of adverse events or adverse drug reactions were not collected as part of the study database.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Multiple Myeloma Participants | 0 / 0 | 0 / 0 | 436 / 943 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- Only deaths were collected, and data of adverse events or adverse drug reactions were not collected as part of the study database.
- event Groups
- deaths Num Affected
- 436
- deaths Num At Risk
- 943
- description
- Participants with MM were observed retrospectively since the diagnosis up to death or lost to follow-up within the eligibility window of time (between January 1, 2008 and December 31, 2016), in this study.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 0
- serious Num Affected
- 0
- serious Num At Risk
- 0
- title
- Multiple Myeloma Participants
- frequency Threshold
- 0
- time Frame
- From diagnosis up to the end of this study (up to 11.7 years)
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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