For research use only. Not for human consumption. Not medical advice — consult a licensed clinician.

Healing & Recovery

Teriparatide

Also known as: PTH 1-34, Parathyroid Hormone (1-34), rhPTH(1-34), Forteo, Bonsity

FDA approved

Recombinant human parathyroid hormone fragment consisting of the biologically active N-terminal 34 amino acids of endogenous PTH (PTH 1-34). It is a PTH1 receptor (PTH1R) agonist; when administered as a once-daily intermittent injection it preferentially stimulates osteoblast-mediated bone formation, increasing bone mineral density and reducing fracture risk. Teriparatide is FDA-approved (originally as Forteo, approved 2002) for osteoporosis at high fracture risk in postmenopausal women, men, and glucocorticoid-induced osteoporosis, and was the first anabolic (bone-building) osteoporosis therapy. It is one of the few peptides in this directory with full FDA marketing approval.

Where to buy · live market data

Who's worth your money for Teriparatide

Every current seller, ranked by independent evidence — Merit Score, latest COA purity, and live $/mg (size-normalized). Prices refresh daily. Rankings are never paid.

Average price

—/mg

Sellers

3

45-day trend

building…

0 of 3 sellers have a current price

Prices observed from public storefronts (last 24h), normalized to $/mg. "Evidence" is Merit's 0–100 Merit Score, derived only from observable verification evidence (methodology on /about); "Purity" is the latest independent COA. Some buy links are affiliate links — Merit may earn a commission at no extra cost to you, and where a vendor offers one, the code shown gets you a discount at their checkout. Affiliate status never affects price data, ranking, or the Merit Score (full policy on /disclosure). Research use only.

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Compound reference

About Teriparatide

CAS

52232-67-4

Molecular formula

C181H291N55O51S2

Sequence

SVSEIQLMHNLGKHLNSMERVEWLRKKLQDVHNF

Typical dose range

20 mcg once daily subcutaneous (approved labeling); maximum cumulative use historically limited to ~2 years

Half-life

~1 hour after subcutaneous injection (serum), though the systemic exposure window is short; longer than after intravenous administration (~5 minutes)

Common research uses

treatment of osteoporosis at high fracture risk (FDA-approved)glucocorticoid-induced osteoporosis (FDA-approved)off-label investigational use in fracture healing and bone defects

Safety notes

FDA-approved. Labeling carried a boxed warning for osteosarcoma based on rat studies (the 2-year cumulative-use limit and boxed warning were removed by the FDA in 2020 after long-term human data did not show increased osteosarcoma risk). Contraindicated/cautioned in patients at increased baseline osteosarcoma risk (e.g., Paget disease, prior skeletal radiation, unexplained elevated alkaline phosphatase). Common effects include orthostatic hypotension and transient hypercalcemia. Not a WADA-prohibited substance.

Reconstitution

Supplied as a prefilled multi-dose pen; refrigerate (2-8 C), do not freeze, and use within the labeled in-use period after first injection.

Research depth

20 citations indexed for Teriparatide

All research on Teriparatide →

review · 2026

Bone Anabolic Treatment in Patients With Chronic Kidney Disease: A Systematic Review

Background Chronic kidney disease (CKD) associated osteoporosis leads to an increased risk of bone fracture in patients with CKD. Evidence on the efficacy and safety of anti-osteoporotic medications is limited for this group.

Study · 2026

Teriparatide treatment of osteoporosis in solid organ transplant recipients-a single-center experience

Solid organ transplant recipients face high fracture risk with limited evidence guiding anabolic therapy. In this real-world cohort, teriparatide was associated with significant improvements in bone mineral density and acceptable safety without adverse graft effects.

Study · 2026

Is teriparatide linked to osteosarcoma? A disproportionality analysis of the FAERS database

Background Teriparatide is approved for the treatment of osteoporosis and is generally well-tolerated. However, concerns remain about a possible association with osteosarcoma, a rare but aggressive bone malignancy.

Study · 2026

Differential efficacy of initial versus sequential combination of denosumab and teriparatide in osteoporosis at high fracture risk

For patients already on denosumab, adding teriparatide is a suboptimal last resort: it offers limited spinal benefit but carries a significant risk of hip bone loss, mandating a site-specific risk-benefit assessment.

Study · 2026

Response to "Interpreting bone turnover responses and treatment persistence with once-weekly teriparatide"

case-report · 2026

Conservative Treatment with Adjunctive Use of Teriparatide for Periprosthetic Humeral Fractures after Reverse Total Shoulder Arthroplasty: A Report of 6 Cases

Background Periprosthetic humeral fractures (PPHFs) after reverse total shoulder arthroplasty (RTSA) are challenging complications, particularly in elderly patients with osteoporotic bone and multiple comorbidities.