In postmenopausal women with osteoporosis, fewer patients reported adverse events with teriparatide than strontium ranelate.
In plain wordsIn postmenopausal women with osteoporosis, fewer patients reported adverse events with teriparatide than strontium ranelate.
- Peptide
- Teriparatide (PTH 1-34)
- Outcome
- DecreasePatients with adverse events
- Study
n = 79
- Comparator
- Strontium ranelate
- Outcome group
- Adverse events · Whole body
- Studied dose
- 20 microg/d · subcutaneous · 6 monthsAs given in this study (human).
Measurements
- Patients with adverse events
- 41%
- teriparatide
- Patients with adverse events
- 70%
- strontium ranelate
Source sentences
There were more patients with adverse events after SrR (70%) than teriparatide (41%) treatment (p = 0.013).
2 context sentences(design, population, supporting numbers)
We assessed the effects on bone remodeling and histomorphometry after daily subcutaneous injections of teriparatide (n = 39, 20 microg/d) or oral strontium ranelate (SrR, n = 40, 2 g/d) in postmenopausal women with osteoporosis.
Evaluable biopsies were obtained from 29 patients in the teriparatide group and 22 in the SrR group after 6 mo of treatment.