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Administration of octreotide was performed every 28 days (± 4 days) starting on Cycle 1, Day 1.","id":"EG000","otherNumAffected":214,"otherNumAtRisk":215,"seriousNumAffected":126,"seriousNumAtRisk":215,"title":"Everolimus + Octreotide"},{"description":"Matching placebo was administered in accordance with a 10-mg daily dosing regimen (two 5-mg tablets) in conjunction with octreotide 30 mg intramuscularly (i.m.) every 28 days. Patients were treated until progression or unacceptable toxicity; Each treatment cycle lasted 28 days. Patients received their first dose of matching placebo at Cycle 1, Day 1. Administration of octreotide was performed every 28 days (± 4 days) starting on Cycle 1 Day 1.","id":"EG001","otherNumAffected":194,"otherNumAtRisk":211,"seriousNumAffected":74,"seriousNumAtRisk":211,"title":"Placebo + Octreotide"},{"description":"Open Label - Patients who had progressive disease in this arm, can move to the open label Everolimus + depot octreotide by choice.","id":"EG002","otherNumAffected":162,"otherNumAtRisk":170,"seriousNumAffected":93,"seriousNumAtRisk":170,"title":"Everolimus Open Label"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA","stats":[{"groupId":"EG000","numAffected":58,"numAtRisk":215},{"groupId":"EG001","numAffected":21,"numAtRisk":211},{"groupId":"EG002","numAffected":34,"numAtRisk":170}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system 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