Teriparatide
Brand names: Forsteo, Terrosa, Movymia
Teriparatide is a recombinant parathyroid hormone analogue used for severe osteoporosis. Unlike bisphosphonates it is anabolic (bone-building) and is given by daily subcutaneous injection for a limited lifetime treatment duration.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
US labelling (FDA)
Reference — US labelling, may differ from UKRecommended dosage is 20 mcg subcutaneously once a day ( 2.1 ) Consider supplemental calcium and Vitamin D based on individual patient needs ( 2.1 ) Administer as a subcutaneous injection into the thigh or abdominal region ( 2.2 ) Administer initially under circumstances in which the patient can sit or lie down if symptoms of orthostatic hypotension occur ( 2.2 ) Use of teriparatide for more than 2 years during a patient's lifetime should only be considered if a patient remains at or has returned to having a high risk for fracture ( 2.3 ) 2.1 Recommended Dosage The recommended dosage is 20 mcg given subcutaneously once a day. Instruct patients to take supplemental calcium and vitamin D if …
Source: US FDA prescribing information (openFDA / DailyMed), label dated 2025-05-27. Accessed 2026-06-12. US dosing and indications can differ from UK practice — use UK sources for prescribing decisions.
Clinical monograph
How it works
It is a recombinant fragment of parathyroid hormone; intermittent administration preferentially stimulates osteoblast activity, increasing bone formation.
Prescribing in practice
- It is contraindicated where there is increased osteosarcoma risk, including Paget's disease of bone, prior skeletal radiotherapy and unexplained raised alkaline phosphatase.
- Transient hypercalcaemia can occur after dosing.
- Lifetime treatment duration is limited and it is given as a once-daily subcutaneous injection.
Monitoring
Monitor calcium status and clinical response; review against the maximum lifetime treatment duration.
Counselling the patient
- Inject under the skin once daily as shown, and rotate injection sites.
- Dizziness can occur after the first few doses; give the injection where you can sit or lie down.
- This is a time-limited course; follow-on treatment is usually needed to maintain the benefit.
Evidence & guidelines
Specialist-initiated anabolic option for severe osteoporosis (NICE).
Reference: NICE TA161; NICE TA160; Forteo SPC; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Diabetic Ketoacidosis (DKA) · JBDS 2013 / Joint British Diabetes Societies; NICE NG17
- Adult Hypoglycaemia (Treated Diabetes) · JBDS-IP (2023): Hospital Management of Hypoglycaemia
- Adrenal Crisis · Society for Endocrinology Emergency Guidance (2024)
- Type 2 Diabetes Management · NICE NG28 2022
- Hyperthyroidism Management · BTA / ETA 2018
- Adrenal Insufficiency · Society of Endocrinology / ESE 2016