Cinacalcet 90mg tablets
Requires a prescription from a doctor or prescriber
Cinacalcet is a calcimimetic sold by Amgen under the trade name Sensipar® in North America and Australia and as Mimpara® in Europe.
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Safety monitoring data
Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Cinacalcet
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Submit a Yellow Card report to the MHRA
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.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Cinacalcet
About EudraVigilance
Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
16 branded products available
MHRA licensed products
View all licensed products for Cinacalcet on the MHRA register
Cinacalcet 90mg tablets
Cinacalcet 90mg tablets
Cinacalcet 90mg tablets
Cinacalcet 90mg tablets
Cinacalcet 90mg tablets
Cinacalcet 90mg tablets
Cinacalcet 90mg tablets
Cinacalcet 90mg tablets
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
WHO defined daily dose (DDD)
60 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary BNF/ATC mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
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(5)
Cinacalcet for the treatment of secondary hyperparathyroidism in patients with end-stage renal disease on maintenance dialysis therapy (TA117)
Hyperparathyroidism (primary): diagnosis, assessment and initial management (NG132)
Etelcalcetide for treating secondary hyperparathyroidism (TA448)
Thoracoscopic excision of mediastinal parathyroid tumours (HTG159)
Chronic kidney disease: assessment and management (NG203)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
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
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. 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: 21 · Randomised trials: 4 · 2003–2026
Showing the 50 most relevant studies, sorted by most relevant.
Suetonia C. Palmer, Ionuţ Nistor, Jonathan C. Craig, et al.
PLoS Medicine, 2013
- Cinacalcet
- Calcium Metabolism Disorders
- Cardiovascular Diseases
Willemijn Y van der Plas, R. R. Dulfer, Anton F. Engelsman, et al.
Nephrology Dialysis Transplantation, 2017
- Cinacalcet
- Combined Modality Therapy
- Hyperparathyroidism, Secondary
Xiaosong Li, W. Ding, Hong Zhang
Frontiers in Endocrinology, 2023
Lei He, Yuzhe Li, Jingjing Jin, et al.
BMC Nephrology, 2024
Landsberg A, Brockman NK, Sevinc E, et al.
2025
BackgroundPeople with advanced chronic kidney disease (CKD) and secondary hyperparathyroidism (sHPT) refractory to medical therapy often require surgical parathyroidectomy. Severe and prolonged hypocalcemia immediately following parathyroidectomy for sHPT is often termed "hungry bone syndrome" (HBS).ObjectiveTo systematically review the effect of pre-operative interventions on post-operative hypocalcemia, HBS, and other related outcomes in patients with CKD and sHPT undergoing parathyroidectomy.DesignThis is a systematic review study.SettingDiverse study designs conducted in any country.PatientsAdult patients with CKD complicated by sHPT undergoing parathyroidectomy.MeasurementsPost-operative hypocalcemia, HBS, symptomatic hypocalcemia, and other related outcomes.MethodsWe searched Ovid MEDLINE, Embase, and Cochrane Controlled Trials Registry from inception until June 2024 for trials and observational studies of adults with CKD and sHPT that evaluated pre-operative interventions aimed at reducing the risk of hypocalcemia following parathyroidectomy. After 2 phases of study screening conducted in duplicate, we extracted data on study design, patient characteristics, interventions, and outcomes. Hypocalcemia was defined as serum calcium ResultsWe identified 3616 studies; 35 underwent full-text review, and 9 met final eligibility criteria. Interventions included pre-operative calcitriol (n = 2), pre-operative cinacalcet (n = 3), pre-operative alkaline phosphatase (ALP) measurement to guide intravenous (IV) calcium administration (n = 3), and pre-operative pamidronate (n = 1). All studies reported on at least one of: median/mean post-operative calcium (n = 7), incidence of post-operative hypocalcemia (n = 3), HBS (n = 1), and symptomatic hypocalcemia (n = 4). Interventions that reported on the risk of post-operative hypocalcemia included pre-operative pamidronate (n = 1, 37 participants, odds ratio [OR] = 0.003, 95% confidence interval [CI] = 0.000-0.072) and IV calcium guided by pre-operative ALP (n = 1, 271 participants, OR = 0.292, 95% CI = 0.175-0.488). There were insufficient data to meta-analyze study-specific effects for any intervention or outcome.LimitationsOur study was limited by significant heterogeneity in outcome reporting, which resulted in substantial outcome reporting bias and prevented pooled analyses. Furthermore, no randomized control trials met our inclusion criteria, which limited assessment of publication bias.ConclusionsPre-operative risk factors for HBS have been established in patients with CKD undergoing parathyroidectomy. However, limited research has evaluated pre-operative interventions to reduce the risk of HBS, and due to heterogeneity in outcome reporting across studies, there is still uncertainty about the effectiveness of such interventions. These findings support the need for future clinical trials.
Abstract licence: CC BY-NC
Paladino NC, Scerrino A, Raglione D, et al.
2026
Background and objectiveSecondary hyperparathyroidism (SHPT) in patients with chronic kidney disease (CKD) is a major challenge in the context of patients awaiting renal transplantation. Optimal timing of parathyroidectomy (PTX) for these patients remains controversial, particularly to prevent tertiary hyperparathyroidism (THPT) and minimize postoperative complications such as hungry bone syndrome (HBS). The aim of this study is to evaluate current evidence on optimal timing of PTX in renal transplant candidates.MethodsTo review the current evidence regarding the optimal timing of PTX in patients with SHPT undergoing renal transplantation, a systematic search of PubMed/MEDLINE, Scopus, and Web of Science was performed using the following keywords: hyperparathyroidism; renal transplant; parathyroidectomy timing; secondary hyperparathyroidism; tertiary hyperparathyroidism; hungry bone syndrome; CKD-MBD; graft survival; cinacalcet; cost-effectiveness. Biochemical outcomes, graft survival, and risk of THPT were assessed. Studies in English language from 2017-2025 were included. Study selection followed PRISMA criteria. Outcomes analyzed included biochemical control, graft function, recurrence rates, and postoperative complications.Key content and findingsFifteen studies met inclusion criteria, including one systematic review, two narrative reviews, three cost-effectiveness analyses, eight retrospective studies and one randomized controlled trial. Early PTX (pre-transplant or within 12-18 months post-transplant) was associated with lower rates of persistent hyperparathyroidism (HPT), better biochemical control, reduced vascular calcifications, and decreased hospitalization rates. Delayed PTX (>18-24 months post-transplant) was linked to higher rates of THPT, bone loss, nephrocalcinosis, and reduced graft function. HBS occurred more frequently in pre-transplant PTX but was manageable with structured calcium/vitamin D replacement.ConclusionsPTX remains the most effective treatment for persistent HPT in renal transplant candidates. Current evidence supports pre-transplant PTX in severe SHPT or within 12-18 months after transplant if HPT persists. A multidisciplinary approach and early biochemical surveillance are essential for optimal outcomes.
Abstract licence: CC BY-NC-ND
Karen Gabriela Sulca-Espín, John Sebastián Carvajal-Gavilanes, Miguel Alejandro Alvarado-Salán, et al.
Sanitas. Revista arbitrada de ciencias de la salud, 2024
Objetivo: analizar el uso de Cinacalcet para el tratamiento de hiperparatiroidismo secundario. Método: Revisión sistemática. Resultados y conclusión: El cinacalcet constituye una intervención terapéutica eficaz y segura para el manejo del hiperparatiroidismo secundario en pacientes con enfermedad renal crónica en hemodiálisis, al modular los niveles de hormona paratiroidea, disminuir las complicaciones óseas y cardiovasculares, y ofrecer una alternativa no invasiva frente a la paratiroidectomía. Los avances en su síntesis mediante procesos más sostenibles y la aplicación de herramientas como el aprendizaje automático han optimizado su evaluación clínica y disponibilidad.
Abstract licence: CC BY-NC-SA 4.0
Cheng Han Ng, Yip Han Chin, Hon Qin Marcus Tan, et al.
Endocrine Connections, 2020
M. Chandran, J. Bilezikian, J. Lau, et al.
Reviews in Endocrine and Metabolic Disorders, 2022
Primploy Greeviroj, T. Kitrungphaiboon, P. Katavetin, et al.
Nephron, 2018
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
30 to 40 hours
Mechanism
Cinacalcet directly lowers parathyroid hormone levels by increasing the sensitiv…
Food interactions
1 warning
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
30 to 40 hours
Protein binding
93 to 97%
Volume of distribution
1000 L
Metabolism
75 mg
Elimination
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 562 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
PMID:17555508 PMID:19789209 PMID:21566075 PMID:22114145 PMID:22789683 PMID:23966241 PMID:25104082 PMID:25292184 PMID:25766501 PMID:26386835 PMID:32817431 PMID:33603117 PMID:34194040 PMID:34467854 PMID:7759551 PMID:8636323 PMID:8702647 PMID:8878438
Senses fluctuations in the circulating calcium concentration: activated by elevated circulating calcium, leading to decreased parathyroid hormone (PTH) secretion in parathyroid glands (By similarity). In kidneys, acts as a key regulator of renal tubular calcium resorption (By similarity). Ligand binding causes a conformation change that triggers signaling via guanine nucleotide-binding proteins (G-proteins) and modulates the activity of downstream effectors .
PMID:38632411
CASR is coupled with different G(q)/G(11), G(i)/G(o)- or G(s)-classes of G-proteins depending on the context .
PMID:38632411
In the parathyroid and kidney, CASR signals through G(q)/G(11) and G(i)/G(o) G-proteins: G(q)/G(11) coupling activates phospholipase C-beta, releasing diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3) second messengers, while G(i)/G(o) coupling mediates inhibition of adenylate cyclase activity .
PMID:38632411 PMID:7759551
The G-protein-coupled receptor activity is activated by a co-agonist mechanism: aromatic amino acids, such as Trp or Phe, act concertedly with divalent cations, such as calcium or magnesium, to achieve full receptor activation .
PMID:27386547 PMID:27434672 PMID:32817431 PMID:33603117 PMID:34194040
Acts as an activator of the NLRP3 inflammasome via G(i)/G(o)-mediated signaling: down-regulation of cyclic AMP (cAMP) relieving NLRP3 inhibition by cAMP .
PMID:32843625
Acts as a regulator of proton-sensing receptor GPR68 in a seesaw manner: CASR-mediated signaling inhibits GPR68 signaling in response to extracellular calcium, while GPR68 inhibits CASR in presence of extracellular protons (By similarity)
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC H05BX01
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)
Cinacalcet
Additional database identifiers
Drugs Product Database (DPD)
13352
ChemSpider
137743
BindingDB
50416875
PDB
YP4
Guide to Pharmacology
3308
ZINC
ZINC000001550499
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1514
GenAtlas
CASR
GeneCards
CASR
GenBank Gene Database
X81086
GenBank Protein Database
599820
Guide to Pharmacology
54
UniProt Accession
CASR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2637
GenAtlas
CYP3A4
GeneCards
CYP3A4
GenBank Gene Database
M18907
Guide to Pharmacology
1337
UniProt Accession
CP3A4_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2625
GenAtlas
CYP2D6
GeneCards
CYP2D6
GenBank Gene Database
M20403
GenBank Protein Database
181350
Guide to Pharmacology
1329
UniProt Accession
CP2D6_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2596
GenAtlas
CYP1A2
GeneCards
CYP1A2
GenBank Gene Database
Z00036
Guide to Pharmacology
1319
UniProt Accession
CP1A2_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q193978), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.