Parathyroid hormone 50micrograms/71.4microlitre dose powder and solvent for solution for injection cartridges
Requires a prescription from a doctor or prescriber
Parathyroid hormone (PTH) is a single-chain polypeptide composed of 84 amino acids.
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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Natpar 50micrograms/dose powder and solvent for solution for injection cartridges
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(11)
Recombinant human parathyroid hormone for treating hypoparathyroidism (terminated appraisal) (TA625)
Etelcalcetide for treating secondary hyperparathyroidism (TA448)
Hyperparathyroidism (primary): diagnosis, assessment and initial management (NG132)
Thoracoscopic excision of mediastinal parathyroid tumours (HTG159)
Cinacalcet for the treatment of secondary hyperparathyroidism in patients with end-stage renal disease on maintenance dialysis therapy (TA117)
Minimally invasive video‑assisted parathyroidectomy (HTG350)
Chronic kidney disease: assessment and management (NG203)
Thyroid cancer: assessment and management (NG230)
Raloxifene and teriparatide for the secondary prevention of osteoporotic fragility fractures in postmenopausal women (TA161)
The NxStage System One NX1000‑1 home haemodialysis device for renal replacement therapy in chronic kidney disease (MIB12)
Difelikefalin for treating pruritus in people having haemodialysis (TA890)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 41 · Randomised trials: 4 · 1925–2026
Showing the 50 most relevant studies, sorted by most relevant.
A. Sai, R. Walters, X. Fang, et al.
The Journal of clinical endocrinology and metabolism, 2011
R. Lindsay, J. Nieves, C. Formica, et al.
Lancet, 1997
N. Lane, S. Sanchez, G. Modin, et al.
The Journal of clinical investigation, 1998
Marc N. Wein, H. Kronenberg
Cold Spring Harbor perspectives in medicine, 2018
Roy R, Swaminathan N, Kasmirski J, et al.
2026
- Hypocalcemia
- Postoperative Complications
- Parathyroid Hormone
Lai J, Yu X, Prabahar K, et al.
2026
- Calcium
- Phosphorus
- Ergocalciferols
ContextThere is a clear link between ergocalciferol, parathyroid hormone (PTH), phosphorus, and calcium. Various randomized trials have examined the effectiveness of ergocalciferol on vitamins and minerals. However, conflicting results have been reported, and the optimal dose and duration of ergocalciferol remain unclear.ObjectiveThis systematic review and meta-analysis of RCTs aim to evaluate the effect of vitamin D2 on PTH, calcium, and phosphorus in humans.Data sourcesA comprehensive literature search was conducted with the assistance of a librarian. Independent reviewers performed searches across multiple databases, including Web of Science, Scopus, PubMed/Medline, and Embase, from their inception until September 20, 2024.Data extractionThe random-effects model, based on the DerSimonian and Laird method, was applied to compute pooled estimates of the intervention's impact on the outcomes.Data analysesA total of 26 articles were included in the meta-analysis. The pooled analysis, using a random-effects model, demonstrated a significant reduction in serum PTH concentrations (WMD, -12.77 pg/mL, 95% CI, -20.03 to -5.51, P = .001, I2 = 96%, P ConclusionVitamin D2 supplementation appears to improve serum calcium levels while decreasing PTH levels. Given the low cost and wide availability of ergocalciferol, it can be recommended, especially for older adults, to help maintain bone strength.
Abstract licence: CC BY-NC-ND
Chew BMH, Lim SSA, Gan TRX, et al.
2026
- Parathyroid Hormone
- Parathyroidectomy
- Hyperparathyroidism, Primary
Kindaro D, Chiu J, Hariharan M, et al.
2026
- Osteoporosis
- Parathyroid Hormone
- Dental Implants
BackgroundDental implant osseointegration remains a significant clinical challenge in patients with compromised bone health, particularly in those affected by osteoporosis. Parathyroid hormone (PTH; teriparatide, PTH 1-34) is an established osteoanabolic agent with recognized impacts on bone remodelling. Its use has been proposed as an adjunctive strategy to enhance peri-implant bone regeneration under osteoporotic conditions. This updated systematic review provides evidence from preclinical evaluations of the effects of PTH supplementation on dental implant osseointegration in osteoporotic animal models. We conducted an indexed database search for studies published between January 2015 and August 2025. Outcomes were assessed using histomorphometry, microcomputed tomography, and biomechanical parameters. Methodological quality was assessed using SYRCLE's risk-of-bias tool.Highlights• Intermittent PTH administration consistently enhanced peri-implant outcomes in osteoporotic animal models. • Combination regimens outperform PTH monotherapy in osteoporotic models. • Methodological heterogeneity limits clinical translation of preclinical findings.ConclusionPreclinical evidence supports PTH supplementation as a promising adjunct to enhance peri-implant bone quality and mechanical stability in osteoporotic settings. To date, substantial heterogeneity in experimental design, outcome assessment, and study quality limits meta-analysis and translational interpretation. Standardized outcome measures and robust human trials are required before clinical applications can be considered.
Abstract licence: CC BY
Li Z, Li Y, Jin Q, et al.
2026
- Parathyroid Hormone
- Exercise
- Exercise Therapy
Crooks SA, Kuršumović K, Lewis TL, et al.
2026
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
1.5 hours
Mechanism
The biological actions of rhPTH are mediated through binding to at least two dis…
Food interactions
None known
Human targets
2 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
55%
Half-life
1.5 hours
Volume of distribution
40%
Metabolism
30%
Elimination
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Preotact is used in the treatment of osteoporosis in postmenopausal women at high risk of osteoporotic fractures and is marketed in Europe by Nycomed. Preos is a registered trade mark owned by NPS Pharmaceuticals, Inc. The name Preos and the New Drug Application is pending approval by the U.S. Food and Drug Administration (FDA).
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 215 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
It may play a significant role in pancreatic function. PTH2R presence in neurons indicates that it may function as a neurotransmitter receptor (By similarity)
PMID:10913300 PMID:18375760 PMID:19674967 PMID:27160269 PMID:30975883 PMID:35932760 PMID:8397094
Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G proteins) and modulates the activity of downstream effectors, such as adenylate cyclase (cAMP) .
PMID:30975883 PMID:35932760
PTH1R is coupled to G(s) G alpha proteins and mediates activation of adenylate cyclase activity .
PMID:20172855 PMID:30975883 PMID:35932760
PTHLH dissociates from PTH1R more rapidly than PTH; as consequence, the cAMP response induced by PTHLH decays faster than the response induced by PTH PMID:35932760
ATC H05AA03
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Parathyroid hormone
Additional database identifiers
Drugs Product Database (DPD)
5252
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9609
GeneCards
PTH2R
Guide to Pharmacology
332
UniProt Accession
PTH2R_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:9608
GenAtlas
PTHR1
GeneCards
PTH1R
GenBank Gene Database
BC112247
Guide to Pharmacology
331
UniProt Accession
PTH1R_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72