Forteo ® (teriparatide [rDNA origin] injection)

20-mcg daily dose in a 2.4-mL prefilled delivery device

This 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.

FORTEO® (teriparatide [rDNA origin] injection): Approval and Indications

FORTEO® (teriparatide) is indicated for osteoporosis treatment in postmenopausal women, increased bone mass in men with primary or hypogonadal osteoporosis, and glucocorticoid induced osteoporosis.

US_cFAQ_TER053_INDICATIONS

What Are Teriparatide's Indications?

Teriparatide was approved by the FDA on November 26, 2002.

Teriparatide is indicated for

  • the treatment of postmenopausal women with osteoporosis at high risk for fracture

  • increase of bone mass in men with primary or hypogonadal osteoporosis at high risk for fracture, and

  • treatment of men and women with osteoporosis associated with sustained systemic glucocorticoid therapy at high risk for fracture.

Regarding teriparatide’s indication for treatment of postmenopausal women with osteoporosis at high risk for fracture, high risk for fracture is defined as

  • a history of osteoporotic fracture

  • multiple risk factors for fracture, or

  • patients who have failed or are intolerant to other available osteoporosis therapy.

In postmenopausal women with osteoporosis, teriparatide reduces the risk of vertebral and nonvertebral fractures.

Enclosed Prescribing Information

FORTEO® (teriparatide [rDNA origin] injection), Lilly

Date of Last Review: August 13, 2020


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