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Participants also received a stable dose of 10-25 mg/week of MTX and ≥ 5 mg/week folic acid for the duration of their participation in the study.\n\nAll participants entered a 48-week safety follow-up (SFU) period following the treatment period.","id":"EG000","otherNumAffected":112,"otherNumAtRisk":172,"seriousNumAffected":16,"seriousNumAtRisk":172,"title":"Placebo + MTX"},{"description":"Participants received 0.5 g rituximab administered by intravenous infusion on Days 1 and 15. After Week 24, participants received further courses of rituximab every 24 weeks for up to 5 years if they were not in clinical remission and safety criteria were met. Rituximab infusions were preceded with 100 mg intravenous methylprednisolone. Participants also received a stable dose of 10-25 mg/week of methotrexate and ≥ 5 mg/week folic acid for the duration of their participation in the study.\n\nAll participants entered a 48-week safety follow-up (SFU) period following the treatment period.","id":"EG001","otherNumAffected":149,"otherNumAtRisk":167,"seriousNumAffected":52,"seriousNumAtRisk":167,"title":"Rituximab 2 x 0.5 g + MTX"},{"description":"Participants received 1.0 g rituximab administered by intravenous infusion on Days 1 and 15. After Week 24, participants received further courses of rituximab every 24 weeks for up to 5 years if they were not in clinical remission and safety criteria were met. Rituximab infusions were preceded with 100 mg intravenous methylprednisolone. Participants also received a stable dose of 10-25 mg/week of methotrexate and ≥ 5 mg/week folic acid for the duration of their participation in the study.\n\nAll participants entered a 48-week safety follow-up (SFU) period following the treatment period.","id":"EG002","otherNumAffected":151,"otherNumAtRisk":170,"seriousNumAffected":46,"seriousNumAtRisk":170,"title":"Rituximab 1.0 g + MTX"},{"description":"Includes all data up to the point of switch for participants in the Placebo + Methotrexate treatment group who switched to treatment with rituximab after Week 24.","id":"EG003","otherNumAffected":99,"otherNumAtRisk":155,"seriousNumAffected":12,"seriousNumAtRisk":155,"title":"Switch Population: Placebo + MTX"},{"description":"Includes all data from the point of switch for participants who switched from Placebo + Methotrexate to treatment with rituximab.","id":"EG004","otherNumAffected":131,"otherNumAtRisk":155,"seriousNumAffected":45,"seriousNumAtRisk":155,"title":"Switch Population: 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infestations","sourceVocabulary":"MedDRA 16.0","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":172},{"groupId":"EG001","numAffected":17,"numAtRisk":167},{"groupId":"EG002","numAffected":20,"numAtRisk":170},{"groupId":"EG003","numAffected":1,"numAtRisk":155},{"groupId":"EG004","numAffected":13,"numAtRisk":155},{"groupId":"EG005","numAffected":0,"numAtRisk":82},{"groupId":"EG006","numAffected":0,"numAtRisk":44}],"term":"Influenza"},{"assessmentType":"NON_SYSTEMATIC_ASSESSMENT","organSystem":"Infections and infestations","sourceVocabulary":"MedDRA 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