{"description":"In the event a single participant has experienced both a serious and a non-serious form of the same adverse event term, the individual has been included in the numerator (\"number of affected participants\") of both adverse event tables. Each AE table includes events, regardless of reported relationship to study treatment or grade.","eventGroups":[{"description":"Participants with NHL who followed the Plerixafor PM treatment arm regimen. Participants received chemotherapy and G-CSF mobilization for 7 days according to standard procedures at the study center. When participants achieved a target CD34+ count of ≥20 cells/µL, apheresis began. G-CSF was given daily in the morning on the days of apheresis. After the first apheresis, plerixafor (240 µg/kg) was administered each evening (approximately 10pm) followed by apheresis 10 to 11 hours later for up to 4 consecutive days.","id":"EG000","otherNumAffected":7,"otherNumAtRisk":7,"seriousNumAffected":1,"seriousNumAtRisk":7,"title":"Non-Hodgkin's Lymphoma (NHL): Plerixafor PM"},{"description":"Participants with NHL who followed the Plerixafor AM treatment arm regimen. Participants received chemotherapy and G-CSF mobilization for 7 days according to standard procedures at the study center. When participants achieved a target CD34+ count of ≥20 cells/µL, apheresis began. G-CSF was given daily in the morning on the days of apheresis. The morning of the second day after the first apheresis, plerixafor (240 µg/kg) was administered followed by apheresis 6 hours later. Plerixafor (240 µg/kg) was administered in the morning followed by apheresis 6 hours later for up to 4 consecutive days.","id":"EG001","otherNumAffected":6,"otherNumAtRisk":6,"seriousNumAffected":0,"seriousNumAtRisk":6,"title":"Non-Hodgkin's Lymphoma (NHL): Plerixafor AM"},{"description":"Participants with NHL who followed the Plerixafor After Chemo treatment arm regimen.\n\nParticipants received mobilizing chemotherapy, followed by 5 consecutive days of G-CSF (10 µg/kg). Starting on the sixth day, participants received G-CSF (10 µg/kg) plus plerixafor (240 µg/kg) daily for up to 3 consecutive days. If CD34+ counts reached \\>= 20 cells/µL 6 hours after any of the 3 plerixafor doses, apheresis began. If not, G-CSF administration continued until the participant qualified for one of the other treatment arms.","id":"EG002","otherNumAffected":1,"otherNumAtRisk":1,"seriousNumAffected":0,"seriousNumAtRisk":1,"title":"Non-Hodgkin's Lymphoma (NHL): Plerixafor After Chemo"},{"description":"Participants with MM who followed the Plerixafor PM treatment arm regimen. Participants received chemotherapy and G-CSF mobilization for 7 days according to standard procedures at the study center. When participants achieved a target CD34+ count of ≥20 cells/µL, apheresis began. G-CSF was given daily in the morning on the days of apheresis. After the first apheresis, plerixafor (240 µg/kg) was administered each evening (approximately 10pm) followed by apheresis 10 to 11 hours later for up to 4 consecutive days.","id":"EG003","otherNumAffected":12,"otherNumAtRisk":12,"seriousNumAffected":2,"seriousNumAtRisk":12,"title":"Multiple Myeloma (MM): Plerixafor PM"},{"description":"Participants with MM who followed the Plerixafor AM treatment arm regimen. Participants received chemotherapy and G-CSF mobilization for 7 days according to standard procedures at the study center. When participants achieved a target CD34+ count of ≥20 cells/µL, apheresis began. G-CSF was given daily in the morning on the days of apheresis. The morning of the second day after the first apheresis, plerixafor (240 µg/kg) was administered followed by apheresis 6 hours later. Plerixafor (240 µg/kg) was administered in the morning followed by apheresis 6 hours later for up to 4 consecutive days.","id":"EG004","otherNumAffected":9,"otherNumAtRisk":9,"seriousNumAffected":2,"seriousNumAtRisk":9,"title":"Multiple Myeloma (MM): Plerixafor AM"},{"description":"Participants with MM who followed the Low CD34+ Count/Plerixafor PM treatment arm regimen.\n\nParticipants received chemotherapy and G-CSF mobilization for 7 days according to standard procedures at the study center. If participants had a CD34+ count of \\>=10 cells/µL but \\<20 cells/µL on 2 consecutive days, plerixafor (240 µg/kg) was given in the evening. G-CSF was adminstered and apheresis performed in the morning. Plerixafor (240 µg/kg) administered in the evening followed by G-CSF and apheresis 10 to 11 hours later was repeated for up to 4 consecutive days.","id":"EG005","otherNumAffected":1,"otherNumAtRisk":1,"seriousNumAffected":0,"seriousNumAtRisk":1,"title":"Multiple Myeloma (MM): Low CD34+ Count/Plerixafor PM"},{"description":"Participants with MM who followed the Plerixafor After Chemo treatment arm regimen.\n\nParticipants received mobilizing chemotherapy, followed by 5 consecutive days of G-CSF (10 µg/kg). Starting on the sixth day, participants received G-CSF (10 µg/kg) plus plerixafor (240 µg/kg) daily for up to 3 consecutive days. If CD34+ counts reached \\>= 20 cells/µL 6 hours after any of the 3 plerixafor doses, apheresis began. If not, G-CSF administration continued until the participant qualified for one of the other treatment arms.","id":"EG006","otherNumAffected":2,"otherNumAtRisk":4,"seriousNumAffected":1,"seriousNumAtRisk":4,"title":"Multiple Myeloma (MM): Plerixafor After Chemo"}],"frequencyThreshold":"0","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":7},{"groupId":"EG001","numAffected":1,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":3,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Thrombocytopenia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Cardiac disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":1,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Tachycardia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Ear and labyrinth disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Tinnitus"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Eye disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":1,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Eyelid oedema"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Eye disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":1,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Vision blurred"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Abdominal distension"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":1,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Abdominal pain"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Abdominal pain lower"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Abdominal pain upper"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":1,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Anal fistula"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":7},{"groupId":"EG001","numAffected":1,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":6,"numAtRisk":12},{"groupId":"EG004","numAffected":3,"numAtRisk":9},{"groupId":"EG005","numAffected":1,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Diarrhoea"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":1,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Dyspepsia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":2,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":1,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Flatulence"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Gastrointestinal toxicity"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":1,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":0,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Haemorrhoids"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":1,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":1,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Hypoaesthesia oral"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":4,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":6,"numAtRisk":12},{"groupId":"EG004","numAffected":7,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":1,"numAtRisk":4}],"term":"Nausea"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":1,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Paraesthesia oral"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal 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discomfort"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 10.0","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":7},{"groupId":"EG001","numAffected":0,"numAtRisk":6},{"groupId":"EG002","numAffected":0,"numAtRisk":1},{"groupId":"EG003","numAffected":0,"numAtRisk":12},{"groupId":"EG004","numAffected":1,"numAtRisk":9},{"groupId":"EG005","numAffected":0,"numAtRisk":1},{"groupId":"EG006","numAffected":0,"numAtRisk":4}],"term":"Swollen tongue"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Gastrointestinal disorders","sourceVocabulary":"MedDRA 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