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Participants who achieved platelet counts \\&gt;=100 Gi/L during the OL Phase (maximum of up to 9 weeks) were eligible to enter the Double-blind (DB) Antiviral Treatment Phase, whereas those who failed to reach platelet counts \\&gt;=100 Gi/L were discontinued from eltrombopag and had to attend the post-treatment follow-up visits.","id":"EG000","otherNumAffected":0,"otherNumAtRisk":805,"seriousNumAffected":9,"seriousNumAtRisk":805,"title":"Eltrombopag: OL Phase"},{"description":"Participants completing the OL Phase were administered matching placebo tablets QD in combination with antiviral therapy (peginterferon alfa-2b and ribavirin) for a duration of either 24 or 48 weeks (for participants with Genotype 2/3) or 48 weeks (for participants with Non-Genotype 2/3).","id":"EG001","otherNumAffected":226,"otherNumAtRisk":252,"seriousNumAffected":49,"seriousNumAtRisk":252,"title":"Placebo+Antiviral Therapy: DB Phase"},{"description":"Participants completing the OL Phase continued on the same dose of eltrombopag received in the OL Phase (dose that effectively raised platelets to \\>=100 Gi/L) in combination with antiviral therapy (peginterferon alfa-2b and ribavirin) for a duration of either 24 or 48 weeks (for participants with Genotype 2/3) or 48 weeks (for participants with Non-Genotype 2/3).","id":"EG002","otherNumAffected":459,"otherNumAtRisk":506,"seriousNumAffected":119,"seriousNumAtRisk":506,"title":"Eltrombopag+Antiviral Therapy: DB Phase"}],"frequencyThreshold":"5","otherEvents":[{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"General disorders","sourceVocabulary":"MedDRA","stats":[{"groupId":"EG000","numAffected":0,"numAtRisk":805},{"groupId":"EG001","numAffected":60,"numAtRisk":252},{"groupId":"EG002","numAffected":141,"numAtRisk":506}],"term":"Pyrexia"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"General 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