{"description":"The table of Other Adverse Events summarizes the most frequent non-serious occurrences of adverse events. One adult patient and one pediatric patient did not receive the investigational product and were not included in the adverse event table.","eventGroups":[{"description":"Romiplostim administered to adult participants subcutaneously weekly at doses up to 30 µg/kg based on platelet counts. After Amendment 1 the maximum weekly dose was reduced to 15 µg/kg, and after Amendment 2 the maximum weekly dose was reduced to 10 µg/kg. However, participants enrolled prior to Amendment 2 who were receiving \\>10 µg/kg were permitted to remain on that higher dose, but could not increase their dose. In addition, if the participant's dose was decreased, it could not be increased to \\>10 µg/kg.","id":"EG000","otherNumAffected":270,"otherNumAtRisk":291,"seriousNumAffected":117,"seriousNumAtRisk":291,"title":"Romiplostim in Adults"},{"description":"Romiplostim administered to pediatric participants subcutaneously weekly at doses up to 10 µg/kg based on platelet counts.","id":"EG001","otherNumAffected":18,"otherNumAtRisk":20,"seriousNumAffected":2,"seriousNumAtRisk":20,"title":"Romiplostim in Pediatric Population"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 12.0","stats":[{"groupId":"EG000","numAffected":17,"numAtRisk":291},{"groupId":"EG001","numAffected":1,"numAtRisk":20}],"term":"Anaemia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Blood and lymphatic system disorders","sourceVocabulary":"MedDRA 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