Teriparatide is a lab-made copy of the first 34 amino acids of human parathyroid hormone, sold as Forteo, Bonsity and as generic teriparatide injection.[1] The FDA first approved it in 2002, and it is a daily bone-building shot for osteoporosis in people at high risk of breaking a bone.[2][1] In its main trial, it cut new spine fractures from 14% to 5% compared with placebo.[3]

What is teriparatide?

Most osteoporosis drugs, such as alendronate, slow the breakdown of bone. Teriparatide works the other way: once-daily doses stimulate bone-forming cells and build new bone.[1] It binds the same receptors as natural parathyroid hormone and is made in modified E. coli bacteria.[1]

Teriparatide is approved for three groups at high fracture risk, or who could not tolerate other treatment:[1]

  • Postmenopausal women with osteoporosis
  • Men with primary or low-testosterone (hypogonadal) osteoporosis
  • Men and women with osteoporosis from long-term steroid (glucocorticoid) use of 5 mg prednisone a day or more

Teriparatide sits in our healing peptides category because it builds bone, but it is a prescription drug with large trials, unlike most peptides there.

What the research shows

  • Fracture Prevention Trial (1,637 women): new spine fractures occurred in 5% on 20 mcg versus 14% on placebo; non-spine fragility fractures fell from 6% to 3%. Spine bone density rose 9 percentage points more than placebo.[3]
  • Men (437 men): spine bone density rose 5.9% on 20 mcg after a median 11 months. The trial was stopped early because of the rat osteosarcoma finding.[4]
  • Steroid users (428 patients): spine bone density rose 7.2% versus 3.4% with alendronate, and new spine fractures were 0.6% versus 6.1%.[5]
  • VERO (1,360 women with severe osteoporosis): new spine fractures were 5.4% with teriparatide versus 12.0% with weekly risedronate, and clinical fractures were roughly halved. Non-spine fractures were lower but not significantly so.[6]

International research

In Japan, a once-weekly 56.5 mcg form was tested in the TOWER trial of 578 older adults; new spine fractures were 3.1% versus 14.5% on placebo.[7] This weekly form is not sold in the US. A Russian study of 100 adults aged 60 and older with severe osteoporosis and falls reported fewer new low-energy fractures, less chronic pain and higher bone density over 24 months of daily teriparatide, though it had no control group.[15]

Teriparatide dosage

Forteo label
Dose20 mcg injected under the skin once a day[1]
WhereThigh or abdomen[1]
PenOne pen holds 28 daily doses; discard 28 days after first use[1]
StorageKeep refrigerated at 2 to 8°C at all times except when injecting[1]
First dosesTake where you can sit or lie down in case of dizziness[1]
DurationOver 2 years in a lifetime only if fracture risk stays high[1]

The label also suggests calcium and vitamin D if dietary intake is low.[1] Teriparatide comes ready to use in a prefilled pen, so no mixing is needed.

Teriparatide side effects

Events more common than placebo in the two main trials (Forteo label):[1]

Side effectTeriparatidePlacebo
Joint pain10.1%8.4%
Nausea8.5%6.7%
Dizziness8.0%5.4%
Leg cramps2.6%1.3%
Fainting (syncope)2.6%1.4%
  • High calcium: blood calcium peaks 4 to 6 hours after a dose. At least one high reading occurred in 11% of women and 6% of men, versus 2% and 0% on placebo.[1]
  • Dizziness on standing: in healthy volunteers, 5% had brief orthostatic hypotension, usually within 4 hours of early doses.[1]
  • Other warnings: allergic reactions, skin calcification (calciphylaxis), kidney stones and digoxin toxicity.[1]

The osteosarcoma warning and the 2020 label change

Rats given high doses for most of their lives developed osteosarcoma, a bone cancer, so Forteo launched with a boxed warning and a 2-year lifetime limit.[8][1] A 15-year US surveillance study interviewed 1,173 adults with osteosarcoma and found 3 prior teriparatide users, when about 4.2 were expected by chance.[9] In November 2020 the FDA removed the boxed warning and relaxed the 2-year limit.[2][8] The current label still says to avoid teriparatide in people at higher baseline risk, such as children with open growth plates, Paget’s disease or prior skeletal radiation.[1]

Teriparatide for fracture and tendon healing

Animal studies prompted interest in using teriparatide to speed fracture repair, but human results are mixed and this is off-label.

  • Wrist fractures (102 women): the 40 mcg dose did not speed healing, which was the main goal. In a later analysis, 20 mcg shortened healing time (7.4 vs 9.1 weeks), but the authors urged caution.[12]
  • 2026 meta-analysis: teriparatide did not delay healing and may shorten time to union, but the authors said more evidence is needed.[13]
  • Rotator cuff repair (50 patients): 3 months of 20 mcg daily gave no better function or retear rate than placebo at 1 year.[14]

Teriparatide vs abaloparatide

Abaloparatide (Tymlos) is the other daily PTH1 receptor drug. In the ACTIVE trial, which included an open-label teriparatide group, high blood calcium occurred in 3.4% on abaloparatide versus 6.4% on teriparatide.[16] A meta-analysis of manufacturer-sponsored trials found slightly larger hip bone density gains with abaloparatide, but not enough fracture data to compare.[17]

Who should not use teriparatide

  • People with a history of severe allergy to teriparatide.[1]
  • People with high blood calcium or a disorder that raises it, such as primary hyperparathyroidism.[1]
  • Children and young adults with open growth plates, and people with Paget’s disease, bone cancer or bone metastases, or prior radiation to the skeleton.[1]
  • People taking digoxin should be monitored, since a rise in calcium can raise the risk of digoxin toxicity.[1]

Generics and cost

Bonsity was approved in 2019 through a separate application, and generic teriparatide injection followed, including an Amphastar version approved in December 2025.[10][11] All carry the same 20 mcg daily dose and indications. Prices vary by product and insurance.

Yes, by prescription. It is FDA-approved for osteoporosis, and products sold online as research chemicals are not FDA-approved teriparatide.[1]

What users report