{"description":"Same event may appear as both an AE and SAE. However, what is presented are distinct events. An event may be categorized as serious in one participant and as non-serious in another, or a participant may have experienced both a serious and non-serious event. Data reported in this section was collected and analyzed only for participants who were treated with at least 1 dose of study drug.","eventGroups":[{"deathsNumAffected":285,"deathsNumAtRisk":930,"description":"Participants received 4 capsules of Enzalutamide 40 mg each (total dose 160 mg per day) orally, once daily in double-blind and open-label phase (up to a maximum of 68.8 months) until radiographic progression. Participants after last dose of study drug, were followed up for safety up to 30 days, and were long term followed up (for survival status and new prostate cancer therapies) from last dose to the death date or last known survival date.","id":"EG000","otherNumAffected":762,"otherNumAtRisk":930,"seriousNumAffected":372,"seriousNumAtRisk":930,"title":"Enzalutamide 160 mg"},{"deathsNumAffected":173,"deathsNumAtRisk":465,"description":"Participants received 4 capsules of placebo (matched to Enzalutamide) orally, once daily in double blind phase (up to a maximum of 51.3 months) until radiographic progression. Participants were given an opportunity to switch to open-label enzalutamide after completion of double blind phase. Participants after last dose of study drug, were followed up for safety up to 30 days and were long term followed up (for survival status and new prostate cancer therapies) to the death date or last known survival date.","id":"EG001","otherNumAffected":299,"otherNumAtRisk":465,"seriousNumAffected":100,"seriousNumAtRisk":465,"title":"Placebo"},{"deathsNumAffected":4,"deathsNumAtRisk":87,"description":"Participants who received placebo in double-blind phase and who agreed to proceed to open-label phase, received 4 capsules of Enzalutamide 40 mg each (total dose of 160 mg per day), orally once daily (up to a maximum of 18.8 months) until radiographic progression. Participants after last dose of study drug, were followed up for safety up to 30 days and were long term followed up (for survival status and new prostate cancer therapies) to the death date or last known survival date.","id":"EG002","otherNumAffected":45,"otherNumAtRisk":87,"seriousNumAffected":12,"seriousNumAtRisk":87,"title":"Placebo Patients Crossover to Enzalutamide 160 mg"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA 16.1","stats":[{"groupId":"EG000","numAffected":94,"numAtRisk":930},{"groupId":"EG001","numAffected":32,"numAtRisk":465},{"groupId":"EG002","numAffected":10,"numAtRisk":87}],"term":"Asthenia"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA 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