To characterize safety associated with the use of Kyprolis under the locally approved label.
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Number of Participants Who Experienced Treatment-emergent Adverse Events (TEAEs)
Timeframe: From the first dose date of any IP until the end of trial; median (min, max) time on trial was 8.7 (0.1, 37.2) months
Number of Participants Who Experienced Serious TEAEs
Timeframe: From the first dose date of any IP until the end of trial; median (min, max) time on trial was 8.7 (0.1, 37.2) months