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Specimen Atlas of Research Peptides81 plates · MIT
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71Plate 71FDA approved · 2002Reviewed 2026-04-27

Teriparatide

PTH Fragment

also known as Forteo, PTH (1-34), rhPTH(1-34), parathyroid hormone (1-34)

Recombinant 1-34 fragment of human parathyroid hormone, FDA-approved (Forteo, 2002) for severe osteoporosis, glucocorticoid-induced osteoporosis, and hypoparathyroidism. Daily subcutaneous administration stimulates osteoblast-mediated bone formation, increasing bone mineral density at spine and hip. Anabolic effect wanes after 12-18 months due to receptor desensitization, depletion of bone-forming surfaces, and upregulation of endogenous Wnt antagonists.

§ I

At a glance

Daily dose
20 mcg
Anabolic window
12-18 mo
Route
SQ
Route

SQ · Thigh/Abdomen · Once Daily

§ II

Mechanism

Edit ↗

Primary target — Parathyroid hormone 1 receptor (PTH1R) on osteoblasts [xue-2026].

Pathway — PTH1R activation → cAMP/PKA signaling → osteoblast differentiation and activity.

Downstream effect — Stimulates osteoblast formation and bone matrix deposition; increases bone mineral density at trabecular and cortical sites.

Origin — Recombinant 34-amino-acid N-terminal fragment of 84-amino-acid human PTH.

Feedback intact — Yes — intermittent dosing preserves anabolic effect; continuous exposure causes catabolic bone resorption.

§ III

Dosage

Protocols described in the cited literature; not medical advice.

Edit ↗
ParameterValue
Standard dose (osteoporosis)20 mcg / dayFDA-approved regimen for severe osteoporosis.
FrequencyOnce dailyIntermittent administration preserves anabolic effect.
Maximum duration24 months lifetimeAnabolic effect wanes after 12-18 months; FDA recommends max 2-year cumulative exposure.
Hypoparathyroidism dose20 mcg / dayUsed off-label for chronic hypoparathyroidism.
Evidence basisRCT / FDA-approved
Pelvic fragility fractures20 mcg / day × 8-12 weeksAccelerates fracture healing; reduces time to union. [crooks-2026]
RouteSubcutaneous (thigh or abdomen)
TimingMorning or evening (flexible)
StorageRefrigerate 2-8 °C; pen device stable at room temp for 28 days after first use
PharmacogeneticsALDH2 polymorphisms may influence BMD response [obara-2026]ALDH2*2 variant carriers show altered PTH receptor expression. [obara-2026]
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
mg
mL
mcg
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to Teriparatide's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose
§ IV

Evidence

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Strength
0/100
theoretical

Not indicated for fat loss; anabolic bone agent only.

OutcomeFinding
Fat loss applicationNone — teriparatide is a bone anabolic agent without direct lipolytic activity
§ V

Adverse events

Severities follow the FDA / CTCAE convention.

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Hypercalcemiamild
Transient serum calcium elevation 4-6 hours post-injection
Orthostatic hypotensionmild
Dizziness, lightheadedness within hours of injection
Nauseamild
Common, usually mild and transient
Leg cramps / Arthralgiamild
Musculoskeletal pain reported in clinical trials
Hypercalciuriamoderate
Increased urinary calcium excretion; monitor for nephrolithiasis risk
Osteosarcoma (black box warning)severe
Rat studies showed dose-dependent osteosarcoma; not observed in humans to date; contraindicated in Paget's disease, skeletal malignancy, prior radiation
Injection site reactionmild
Erythema, bruising, pain (uncommon)
Absolute contraindications
  • Paget's disease of bone (increased baseline osteosarcoma risk)
  • Unexplained elevated alkaline phosphatase
  • Prior skeletal radiation therapy
  • Skeletal malignancies or bone metastases
  • Hypercalcemic disorders (primary hyperparathyroidism)
  • Pregnancy / lactation
Relative contraindications
  • Active or recent nephrolithiasis
  • Severe renal impairment (CKD G4-G5)
  • Hypercalciuria without adequate monitoring
§ VI

Administration

Edit ↗
  1. 01
    Device preparation

    Teriparatide is supplied in pre-filled pen injectors (Forteo pen). Store refrigerated at 2-8 °C until first use. After first injection, pen may be kept at room temperature for up to 28 days. Do not freeze.

  2. 02
    Injection site

    Subcutaneous injection into thigh or lower abdomen. Rotate sites daily to avoid lipodystrophy. Avoid areas with scars, bruises, or active skin conditions.

  3. 03
    Timing

    Once daily, at approximately the same time each day. Morning or evening administration is acceptable. Take while sitting or lying down to minimize orthostatic hypotension risk.

  4. 04
    Injection technique

    Clean injection site with alcohol swab. Pinch skin, insert needle at 90° angle, and inject full dose (20 mcg). Hold for 5 seconds before withdrawing needle. Do not rub injection site.

  5. 05
    Monitoring

    Baseline and periodic monitoring of serum calcium, urinary calcium, serum PTH (if hypoparathyroidism), and bone mineral density (DXA scan). Monitor for hypercalcemia 4-6 hours post-dose if symptomatic.

  6. 06
    Calcium and vitamin D supplementation

    Ensure adequate calcium (1000-1200 mg/day) and vitamin D (800-1000 IU/day) intake unless contraindicated by hypercalcemia or hypercalciuria.

Appendix

Sources

16%

of 62 rendered claims carry a resolvable citation.

  1. [crooks-2026]
    Crooks 2026Parathyroid Hormone in the Management of Pelvic Fragility Fractures: A Systematic Review and Meta-Analysis.
    journal, 2026
  2. [ferrari-2026]
    Ferrari 2026Mechanisms Underlying the Waning of Osteoanabolic Therapy Effects in Osteoporosis.
    journal, 2026
  3. [morrison-2026]
    Morrison 2026Anabolic effect of parathyroid hormone (1-34) to prevent ovariectomy induced bone loss is attenuated in Col1A1-cre floxed monocyte chemotactic protein 1 (MCP1, CCL2) mice.
    journal, 2026
  4. [obara-2026]
    Obara 2026Effect of genetic polymorphisms of aldehyde dehydrogenase 2 on the efficacy of intermittent parathyroid hormone treatment and bone mineral density: A retrospective multicenter study.
    journal, 2026
  5. [tournis-2026]
    Tournis 2026Approach to the Patient: Management of bone fragility in patients with chronic hypoparathyroidism.
    journal, 2026
  6. [xue-2026]
    Xue 2026Nutritional activation of the Nrf2-Pth1r axis by pyrroloquinoline quinone enhances peak bone mass and potentiates teriparatide in osteoporosis.
    journal, 2026
Plate composed 2026-04-27 · maturity human-reviewed · schema v1 · Contributors: peptidesdb-ai · 52 fields uncited — open contributions