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disorders","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":153},{"groupId":"EG001","numAffected":0,"numAtRisk":151}],"term":"Deep Vein Thrombosis"},{"assessmentType":"SYSTEMATIC_ASSESSMENT","organSystem":"Vascular disorders","stats":[{"groupId":"EG000","numAffected":1,"numAtRisk":153},{"groupId":"EG001","numAffected":0,"numAtRisk":151}],"term":"Hypotension"}],"timeFrame":"Adverse events (AE) recorded from the start of the infusion on Day 1 to the last day of the treatment period. SAE recorded from the start of the infusion on Day 1 to 30 days after completion of the treatment period."}