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Betamethasone

From Wikipedia, the free encyclopedia
Steroid medication

Pharmaceutical compound
Betamethasone
Clinical data
Trade namesCelestone, Eleuphrat, others
AHFS/Drugs.comMonograph
MedlinePlusa682799
License data
Pregnancy
category
Routes of
administration
By mouth,topical,intramuscular
ATC code
Legal status
Legal status
Pharmacokinetic data
MetabolismLiverCYP3A4
Eliminationhalf-life36-54 hours
ExcretionKidney (in urine)
Identifiers
  • (8S,9R,10S,11S,13S,14S,16S,17R)-9-Fluoro- 11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl- 6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro- 3H-cyclopenta[a]phenanthren-3-one
CAS Number
PubChemCID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.006.206Edit this at Wikidata
Chemical and physical data
FormulaC22H29FO5
Molar mass392.467 g·mol−1
3D model (JSmol)
  • O=C(CO)[C@]3(O)[C@]2(C[C@H](O)[C@]4(F)[C@@]/1(\C(=C/C(=O)\C=C\1)CC[C@H]4[C@@H]2C[C@@H]3C)C)C
  • InChI=1S/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15-,16-,17-,19-,20-,21-,22-/m0/s1 checkY
  • Key:UREBDLICKHMUKA-DVTGEIKXSA-N checkY
  (verify)

Betamethasone is asteroid medication.[3] It is used for a number of diseases includingrheumatic disorders such asrheumatoid arthritis andsystemic lupus erythematosus, skin diseases such asdermatitis andpsoriasis, allergic conditions such asasthma andangioedema,preterm labor to speed the development of the baby's lungs,Crohn's disease, cancers such asleukemia, and along withfludrocortisone foradrenocortical insufficiency, among others.[3] It can be taken by mouth,injected into a muscle, or applied to the skin, typically in cream, lotion, or liquid forms.[3][4]

Serious side effects include an increased risk of infection, muscle weakness,severe allergic reactions, andpsychosis.[3] Long-term use may cause adrenal insufficiency.[3] Stopping the medication suddenly following long-term use may be dangerous.[3] The cream commonly results inincreased hair growth and skin irritation.[4] Betamethasone belongs to theglucocorticoid class of medication.[3] It is astereoisomer ofdexamethasone, the two compounds differing only in the spatial configuration of themethyl group at position 16 (seesteroid nomenclature).[5]

Betamethasone was patented in 1958, and approved for medical use in the United States in 1961.[3][6] It is on theWorld Health Organization's List of Essential Medicines.[7] It is available as ageneric medication.[3] In 2023, it was the 280th most commonly prescribed medication in the United States, with more than 700,000 prescriptions.[8][9]

Medical uses

[edit]
Betnovate ointment

Betamethasone is acorticosteroid that is available as a pill, by injection, and as an ointment, cream, lotion, gel, or aerosol (spray) for the skin, and a foam for the scalp.[10] When given by injection,anti-inflammatory effects begin in around two hours and last for seven days.[3]

It is used as a topical cream to relieve skin irritation, such as itching and flaking fromeczema. It is used as a treatment for localpsoriasis, asbetamethasone dipropionate andsalicylic acid, or as the combinationcalcipotriol/betamethasone dipropionate.[citation needed]Betamethasone sodium phosphate is used orally and viainjection with the same indications as othersteroids. Many betamethasone-basedpharmaceuticals include the steroid as thevalerate ester.[citation needed]

In a randomized controlled trial betamethasone was shown to reduce some of theataxia (poor coordination) symptoms associated withataxia telangiectasia (A-T) by 28-31%.[11]

Betamethasone is also used to stimulate fetal maturation of the lungs and cerebral blood vessels.[3]

A cream with 0.05% betamethasone appears effective in treatingphimosis in boys,[12] and often averts the need forcircumcision.[13][14][15] Longer-term research is needed on this treatment method.[12] This approach has replaced circumcision as the preferred treatment method for some physicians in theBritishNational Health Service.[16][17]

Side effects

[edit]

Betamethasone crosses the placenta.[3]

When injected into theepidural space or the spine, it may cause serious side effects like loss of vision, stroke, and paralysis.[19]

Pharmacology

[edit]
Main article:Glucocorticoid § Pharmacology

Forms

[edit]
This sectionrelies largely or entirely on asingle source. Relevant discussion may be found on thetalk page. Please helpimprove this article byintroducing citations to additional sources.
Find sources: "Betamethasone" – news ·newspapers ·books ·scholar ·JSTOR
(November 2023)

Betamethasone is available in a number of compound forms:betamethasone dipropionate (branded as Diprosone, Diprolene, Celestamine, Procort (in Pakistan), and others), betamethasone sodium phosphate (branded as Bentelan in Italy) andbetamethasone valerate (branded as Audavate, Betnovate, Celestone,Fucibet, and others).[citation needed] In the United States and Canada, betamethasone is mixed withclotrimazole and sold as Lotrisone and Lotriderm. It is also available in combination withsalicylic acid (branded as Diprosalic) for using in psoriatic skin conditions. In some countries, it is also sold mixed with bothclotrimazole andgentamicin to add an antibacterial agent to the mix.[citation needed]

Betamethasone sodium phosphate mixed withbetamethasone acetate is available in the United States as Celestone Soluspan.[20]

See also

[edit]

References

[edit]
  1. ^"Betamethasone Use During Pregnancy".Drugs.com. 30 December 2019. Retrieved29 March 2020.
  2. ^"Betamethasone 500 microgram Soluble Tablets - Summary of Product Characteristics (SmPC)".(emc). 5 April 2018. Retrieved29 March 2020.
  3. ^abcdefghijkl"Betamethasone". The American Society of Health-System Pharmacists.Archived from the original on 8 December 2015. Retrieved2 December 2015.
  4. ^ab"Betamethasone topical". The American Society of Health-System Pharmacists.Archived from the original on 8 December 2015. Retrieved2 December 2015.
  5. ^Antignac JP, Le Bizec B, Monteau F, Andre F (January 2002). "Differentiation of betamethasone and dexamethasone using liquid chromatography/positive electrospray tandem mass spectrometry and multivariate statistical analysis".Journal of Mass Spectrometry.37 (1):69–75.Bibcode:2002JMSp...37...69A.doi:10.1002/jms.260.PMID 11813313.
  6. ^Fischer J, Ganellin CR (2006).Analogue-based Drug Discovery. John Wiley & Sons. p. 485.ISBN 978-3-527-60749-5.
  7. ^World Health Organization (2023).The selection and use of essential medicines 2023: web annex A: World Health Organization model list of essential medicines: 23rd list (2023). Geneva: World Health Organization.hdl:10665/371090. WHO/MHP/HPS/EML/2023.02.
  8. ^"The Top 300 of 2023".ClinCalc.Archived from the original on 17 August 2025. Retrieved17 August 2025.
  9. ^"Betamethasone Drug Usage Statistics, United States, 2014 - 2023".ClinCalc. Retrieved17 August 2025.
  10. ^"Betamethasone Topical".MedlinePlus. 19 March 2020. Retrieved29 March 2020.
  11. ^Zannolli R, Buoni S, Betti G, Salvucci S, Plebani A, Soresina A, et al. (September 2012). "A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia".Movement Disorders.27 (10):1312–1316.doi:10.1002/mds.25126.PMID 22927201.S2CID 23696748.
  12. ^abMoreno G, Ramirez C, Corbalán J, Peñaloza B, Morel Marambio M, Pantoja T (January 2024)."Topical corticosteroids for treating phimosis in boys".The Cochrane Database of Systematic Reviews.1 (1) CD008973.doi:10.1002/14651858.CD008973.pub3.PMC 10809033.PMID 38269441.
  13. ^Van Howe RS (October 1998)."Cost-effective treatment of phimosis".Pediatrics.102 (4) E43.doi:10.1542/peds.102.4.e43.PMID 9755280. A review of estimated costs and complications of 3 phimosis treatments.
  14. ^Esposito C, Centonze A, Alicchio F, Savanelli A, Settimi A (April 2008). "Topical steroid application versus circumcision in pediatric patients with phimosis: a prospective randomized placebo controlled clinical trial".World Journal of Urology.26 (2). Springer Science and Business Media LLC:187–190.doi:10.1007/s00345-007-0231-2.PMID 18157674.S2CID 8922151.
  15. ^Zampieri N, Corroppolo M, Zuin V, Bianchi S, Camoglio FS (April 2007). "Phimosis and topical steroids: new clinical findings".Pediatric Surgery International.23 (4):331–335.doi:10.1007/s00383-007-1878-x.PMID 17308904.S2CID 22849471.
  16. ^Berdeu D, Sauze L, Ha-Vinh P, Blum-Boisgard C (February 2001)."Cost-effectiveness analysis of treatments for phimosis: a comparison of surgical and medicinal approaches and their economic effect".BJU International.87 (3):239–244.doi:10.1046/j.1464-410x.2001.02033.x.PMID 11167650.S2CID 2161551.
  17. ^Chu CC, Chen KC, Diau GY (September 1999). "Topical steroid treatment of phimosis in boys".The Journal of Urology.162 (3 Pt 1):861–863.doi:10.1097/00005392-199909010-00078.PMID 10458396.
  18. ^abcdefg"betamethasone"(PDF). F.A. Davis. 2017.Archived(PDF) from the original on 8 September 2017. Retrieved7 March 2017.
  19. ^"FDA Drug Safety Communication: FDA requires label changes to warn of rare but serious neurologic problems after epidural corticosteroid injections for pain".FDA. 23 April 2014.Archived from the original on 11 August 2016. Retrieved15 August 2016.
  20. ^"Celestone Soluspan- betamethasone acetate and betamethasone sodium phosphate injection, suspension".DailyMed. 18 November 2019. Retrieved29 March 2020.
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