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1 oice response system to receive subcutaneous romosozumab (210 mg once monthly) or subcutaneous teripa
2 a 1:1 ratio to receive monthly subcutaneous romosozumab (210 mg) or weekly oral alendronate (70 mg)
3 y nonrecurring injection-site reactions with romosozumab, adverse events were similar among groups.
5 events were reported in 17 (8%) patients on romosozumab and in 23 (11%) on teriparatide; none were j
7 real BMD was 2.6% (95% CI 2.2 to 3.0) in the romosozumab group and -0.6% (-1.0 to -0.2) in the teripa
10 were nasopharyngitis (28 [13%] of 218 in the romosozumab group vs 22 [10%] of 214 in the teriparatide
13 re randomly assigned to receive subcutaneous romosozumab monthly (at a dose of 70 mg, 140 mg, or 210
16 udy, we evaluated the efficacy and safety of romosozumab over a 12-month period in 419 postmenopausal
18 adverse events were observed more often with romosozumab than with alendronate (50 of 2040 patients [
19 steonecrosis of the jaw (1 event each in the romosozumab-to-alendronate and alendronate-to-alendronat
20 new vertebral fractures was observed in the romosozumab-to-alendronate group (6.2% [127 of 2046 pati
21 nvertebral fractures was lower by 19% in the romosozumab-to-alendronate group than in the alendronate
22 curred in 198 of 2046 patients (9.7%) in the romosozumab-to-alendronate group versus 266 of 2047 pati
23 oporosis who were at high risk for fracture, romosozumab treatment for 12 months followed by alendron
25 In postmenopausal women with low bone mass, romosozumab was associated with increased bone mineral d
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