Parathyroid hormone (rhPTH 1-84)
Brand names: Natpar
Recombinant human parathyroid hormone (rhPTH 1-84) is a hormone replacement used as an adjunct to calcium and active vitamin D in adults with chronic hypoparathyroidism that is inadequately controlled on standard therapy alone.
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.
Clinical monograph
How it works
It replaces endogenous parathyroid hormone, raising serum calcium by increasing renal tubular calcium reabsorption, promoting renal activation of vitamin D and enhancing calcium release from bone.
Prescribing in practice
- Because of a theoretical osteosarcoma risk seen with parathyroid hormone analogues in animal studies, use is generally avoided in patients at increased risk of osteosarcoma, such as those with prior skeletal radiotherapy or unexplained raised alkaline phosphatase.
- It is an adjunct to, not a replacement for, calcium and active vitamin D, and these should be titrated together to avoid hyper- or hypocalcaemia.
- Abrupt discontinuation can precipitate severe hypocalcaemia, so stopping requires reinstatement or up-titration of conventional therapy.
Monitoring
Monitor serum and urinary calcium, renal function and vitamin D status, particularly during initiation and any dose adjustment of background therapy.
Counselling the patient
- Report symptoms of low calcium such as tingling around the mouth, muscle cramps or spasms.
- Do not stop the injection suddenly without medical advice, as calcium levels can fall dangerously.
- Keep all scheduled blood test appointments so calcium can be tracked.
Evidence & guidelines
Its use in chronic hypoparathyroidism is supported by the SPC and regulatory approval as adjunctive therapy when conventional treatment is insufficient.
Reference: NICE HST3; SmPC; 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