This study is to assess the safety and effectiveness of Elranatamab in the real-world clinical settings for the treatment of patients with multiple myeloma in Korea.
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Incidence of an adverse event (AE)/ adverse drug reaction (ADR)
Timeframe: At least 28 days from the last dose of Elranatamab
Incidence of a serious AE (SAE)/ serious ADR (SADR)
Timeframe: At least 28 days from the last dose of Elranatamab
Incidence of an unexpected AE (UAE)/ unexpected ADR (UADR)
Timeframe: At least 28 days from the last dose of Elranatamab
Incidence of a serious unexpected AE (SUAE)/ serious unexpected ADR (SUADR)
Timeframe: At least 28 days from the last dose of Elranatamab
Incidence of an adverse event special interest (AESI)
Timeframe: At least 28 days from the last dose of Elranatamab