What the studies show
In a direct comparison against a standard bisphosphonate in women with severe osteoporosis, teriparatide produced fewer new vertebral fractures. The result that moved it from second-line to first-line for the highest-risk patients in many guidelines.
Several well-run randomised trials in people, pointing the same way. You can plan around this. It still says nothing about whether the effect is worth the side effects for you.
- 1
In context
Teriparatide is the first 34 amino acids of human parathyroid hormone, given as a daily injection for severe osteoporosis. Continuous parathyroid hormone strips bone; a brief daily pulse builds it — which is why the drug works and the hormone's excess does not. In the 1,637-woman trial behind its approval, new spinal fractures fell from 14% to 5% over about 21 months and non-spinal fragility fractures roughly halved. It is a prescription medicine, approved everywhere, with a long safety record; the original two-year lifetime limit was lifted by the FDA in 2020.
Teriparatide is approved (rx). Legal status differs by country — see the regulation section or the jurisdiction pages.
Questions
Is Teriparatide proven to help with versus risedronate?
What studies are behind the grade?
Is Teriparatide approved for this?
Other outcomes for Teriparatide
- AVertebral fracture risk (postmenopausal osteoporosis)1 large RCT (n=1,637, median 21 mo)
- ANon-vertebral fracture riskSame RCT
- ABone mineral densitySame RCT + many
- AAdverse effectsadverseApproval trial + 20 years of surveillance
Written and maintained by LYO Research — how pages are written and checked. Reviewed 10 September 2026. Grades count human evidence only; see how LYO grades. Not medical advice. Correct this page →