In patients with glucocorticoid-induced osteoporosis, the number reporting at least one adverse event did not differ significantly between teriparatide and alendronate in either the Hispanic or the non-Hispanic cohort.
In plain wordsIn patients with glucocorticoid-induced osteoporosis, the number reporting at least one adverse event did not differ significantly between teriparatide and alendronate in either cohort.
- Peptide
- Teriparatide (PTH 1-34)
- Outcome
- No significant changeAt least one adverse event, both cohorts
- Study
n = 428
- Comparator
- Alendronate
- Outcome group
- Adverse events · Whole body
- Studied dose
- 20 microg/d · 18 monthsAs given in this study (human).
Source sentences
The number of patients reporting >or=1 adverse event was not significantly different between treatments in either cohort, with more patients reporting nausea in the teriparatide group.
2 context sentences(design, population, supporting numbers)
This post hoc analysis compared teriparatide vs alendronate on bone mineral density (BMD) in Hispanic and non-Hispanic patients with glucocorticoid-induced osteoporosis.
The present study analyzed results from the Hispanic (n=61) and non-Hispanic (n=367) cohorts.