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26.1","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":30,"numEvents":1},{"groupId":"EG001","numAffected":0,"numAtRisk":40,"numEvents":0}],"term":"Hypogammaglobulinaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Reproductive system and breast disorders","sourceVocabulary":"MedDRA 26.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":30,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":40,"numEvents":1}],"term":"Benign prostatic hyperplasia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Surgical and medical procedures","sourceVocabulary":"MedDRA 26.1","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":30,"numEvents":0},{"groupId":"EG001","numAffected":1,"numAtRisk":40,"numEvents":1}],"term":"Vitrectomy"}],"timeFrame":"All cause mortality, non-serious adverse events (Non-SAEs) and serious adverse events (SAEs) were collected up to approximately 32 months. The results presented are until the primary completion date. Additional results will be provided within a year of study completion."}