If you wish to report an adverse event or product complaint, please call 1-800-LILLYRX (1-800-545-5979)
Forteo ® (teriparatide [rDNA origin] injection)
20-mcg daily dose in a 2.4-mL prefilled delivery deviceThis information is provided in response to your request. Resources may contain information about doses, uses, formulations and populations different from product labeling. See Prescribing Information above, if applicable.
Teriparatide reduced the risk of vertebral and nonvertebral fractures in postmenopausal women with osteoporosis.1
Teriparatide was effective in reducing the risk for vertebral fractures regardless of age, baseline rate of bone turnover, or baseline BMD.1
Compared to placebo, teriparatide treatment significantly reduced the risk of incident vertebral fractures and nonvertebral fractures (Table 1).1
Table 1. Effect of Teriparatide on Risk of Vertebral and Nonvertebral Fractures in Postmenopausal Women With Osteoporosis1
|
Placebo n=544 % |
Teriparatide n=541 % |
Absolute Risk Reduction % |
Relative Risk Reduction % (95% CI) |
Incident vertebral fracture (≥1) |
14.3 |
5.0a |
9.3 |
65 (45-78) |
Incident nonvertebral fracture (≥1) |
5.5 |
2.6b |
2.9 |
53 (12-75) |
a p<.001 compared to placebo.
Enclosed Prescribing Information
FORTEO® (teriparatide [rDNA origin] injection), Lilly
1. Forteo [package insert]. Indianapolis IN: Eli Lilly and Company; 2019.
Glossary
BMD = bone mineral density
Date of Last Review: February 18, 2020
If you need information about a Lilly product or want to report an Adverse Event or Product Complaint, you may call us.
Available Mon - Fri, 9am - 7pm EST