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Participants also received oral lenalidomide (including generics) 20 mg once daily (QD), administered at approximately the same time every day on Days 1 to 21 of Cycles 1 to 12, and rituximab (including biosimilars) 375 mg/meters squared (m\\^2) IV, administered on Days 1, 8, 15, and 22 of Cycle 1 and on Day 1 of Cycles 2 to 5. A treatment cycle was defined as 28 calendar days.","id":"EG000","otherNumAffected":318,"otherNumAtRisk":327,"seriousNumAffected":125,"seriousNumAtRisk":327,"title":"Tafasitamab + Rituximab + Lenalidomide"},{"deathsNumAffected":24,"deathsNumAtRisk":325,"description":"Participants with FL or MZL were randomized to receive placebo 0.9% saline solution IV, administered on Days 1, 8, 15, and 22 of Cycles 1 to 3 and on Days 1 and 15 of Cycles 4 to 12. Participants also received oral lenalidomide (including generics) 20 mg QD, administered at approximately the same time every day on Days 1 to 21 of Cycles 1 to 12, and rituximab (including biosimilars) 375 mg/m\\^2 IV, administered on Days 1, 8, 15, and 22 of Cycle 1 and on Day 1 of Cycles 2 to 5. A treatment cycle was defined as 28 calendar days.","id":"EG001","otherNumAffected":315,"otherNumAtRisk":325,"seriousNumAffected":110,"seriousNumAtRisk":325,"title":"Placebo + Rituximab + Lenalidomide"},{"deathsNumAffected":46,"deathsNumAtRisk":652,"description":"Total","id":"EG002","otherNumAffected":633,"otherNumAtRisk":652,"seriousNumAffected":235,"seriousNumAtRisk":652,"title":"Total"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 26","stats":[{"groupId":"EG000","numAffected":25,"numAtRisk":327,"numEvents":33},{"groupId":"EG001","numAffected":28,"numAtRisk":325,"numEvents":30},{"groupId":"EG002","numAffected":53,"numAtRisk":652,"numEvents":63}],"term":"Abdominal pain"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Investigations","sourceVocabulary":"MedDRA 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