{"classes":[{"categories":[{"measurements":[{"groupId":"OG000","value":"357"}]}],"title":"Bone pain"},{"categories":[{"measurements":[{"groupId":"OG000","value":"230"}]}],"title":"Thrombocytopenia"},{"categories":[{"measurements":[{"groupId":"OG000","value":"222"}]}],"title":"Serum LDH increase"},{"categories":[{"measurements":[{"groupId":"OG000","value":"210"}]}],"title":"Muscle pain"},{"categories":[{"measurements":[{"groupId":"OG000","value":"200"}]}],"title":"Joint pain"},{"categories":[{"measurements":[{"groupId":"OG000","value":"178"}]}],"title":"Serum GGT increase"},{"categories":[{"measurements":[{"groupId":"OG000","value":"168"}]}],"title":"Serum ALP increase"},{"categories":[{"measurements":[{"groupId":"OG000","value":"102"}]}],"title":"Other neurological symptoms"},{"categories":[{"measurements":[{"groupId":"OG000","value":"100"}]}],"title":"Headache"},{"categories":[{"measurements":[{"groupId":"OG000","value":"88"}]}],"title":"Blood uric acid increase"}],"denoms":[{"counts":[{"groupId":"OG000","value":"1447"}],"units":"Participants"}],"description":"Objective 1: To describe the cancer patients requiring chemotherapy who, in their treating physician's best clinical judgment, are receiving EP2006 for the primary or secondary prophylaxis of FN in terms of demographics, clinical status, medical history, concomitant comorbid conditions and current status of disease, and prior and concomitant medications.\n\nANC=Absolute Neutrophil Count; CIN=Chemotherapy-Induced Neutropenia; FN=Febrile Neutropenia","groups":[{"description":"Cancer patients treated with chemotherapy and who are prescribed commercially available filgrastim biosimilar for primary or secondary prophylaxis for FN.","id":"OG000","title":"EP2006"}],"paramType":"NUMBER","populationDescription":"The evaluable sample includes all patients in the safety sample (all patients who received at least one dose of the study medication) who had no major protocol violation and have a minimum of enrollment cycle and either one follow-up cycle or study end data with valid outcome data (i.e., ANC or completed CIN/FN data)","reportingStatus":"POSTED","timeFrame":"All cycles. Patients were evaluated at the enrollment cycle and then re-evaluated at each cycle for a maximum total of 6 cycles; however, the scheduling of these evaluations was left to the discretion of the physician, mean duration of study for 105 days","title":"Clinical Events Ever During Study (Frequency Threshold: 5%)","type":"PRIMARY","unitOfMeasure":"participants"}