{"description":"Adverse Event investigations were done for the 733 participants which were in the predialysis (N=96) or dialysis subgroups (N=637).","eventGroups":[{"description":"Participants with chronic kidney disease and a diagnosis of secondary hyperparathyroidism, and who were not yet on dialysis received paricalcitol injection or capsules, on an on-label basis in an everyday setting. Participants were observed for 12 months.","id":"EG000","otherNumAffected":0,"otherNumAtRisk":96,"seriousNumAffected":16,"seriousNumAtRisk":96,"title":"Paricalcitol Pre-dialysis Group"},{"description":"Participants with chronic kidney disease and a diagnosis of secondary hyperparathyroidism, and on dialysis received paricalcitol injection or capsules, on an on-label basis in an everyday setting. 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