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1 Medical uses  





2 Side effects  





3 Pharmacology  





4 Chemistry  





5 History  





6 Society and culture  



6.1  Brand names  







7 References  














Terbinafine






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This article needs additional citations for verification. Please help improve this articlebyadding citations to reliable sources. Unsourced material may be challenged and removed.
Find sources: "Terbinafine" – news · newspapers · books · scholar · JSTOR
(January 2023) (Learn how and when to remove this message)

Terbinafine

Clinical data

Trade names

Lamisil, Terbin, others

AHFS/Drugs.com

Monograph

MedlinePlus

a699061

License data

Routes of
administration

By mouth, topical

ATC code

Legal status

Legal status

  • AU: S4 (Prescription only)
  • CA: ℞-only
  • UK: POM (Prescription only) / GSL
  • US: ℞-only / OTC
  • Pharmacokinetic data

    Bioavailability

    Readily absorbed: 70–90%

    Protein binding

    >99%

    Metabolism

    Liver

    Elimination half-life

    Highly variable

    Identifiers

    • [(2E)-6,6-dimethylhept-2-en-4-yn-1-yl](methyl)(naphthalen-1-ylmethyl)amine

    CAS Number

    PubChem CID

    DrugBank

    ChemSpider

    UNII

    KEGG

    ChEBI

    ChEMBL

    CompTox Dashboard (EPA)

    ECHA InfoCard

    100.119.605 Edit this at Wikidata

    Chemical and physical data

    Formula

    C21H25N

    Molar mass

    291.438 g·mol−1

    3D model (JSmol)

    • C(#C\C=C\CN(C)Cc2cccc1ccccc12)C(C)(C)C

    • InChI=1S/C21H25N/c1-21(2,3)15-8-5-9-16-22(4)17-19-13-10-12-18-11-6-7-14-20(18)19/h5-7,9-14H,16-17H2,1-4H3/b9-5+ checkY

  • Key:DOMXUEMWDBAQBQ-WEVVVXLNSA-N checkY

  •  ☒NcheckY (what is this?)  (verify)

    Terbinafine is an antifungal medication used to treat pityriasis versicolor, fungal nail infections, and ringworm including jock itch and athlete's foot.[1][2][3] It is either taken by mouth or applied to the skin as a cream or ointment.[1][4] The cream and ointment should not be used for fungal nail infections.[5]

    Common side effects when taken by mouth include nausea, diarrhea, headache, cough, rash, and elevated liver enzymes.[1] Severe side effects include liver problems and allergic reactions.[1] Liver injury is, however, unusual.[6] Oral use during pregnancy is not typically recommended.[1] The cream and ointment may result in itchiness but are generally well tolerated.[2] Terbinafine is in the allylamines family of medications.[1] It works by decreasing the ability of fungi to synthesize ergosterol.[1] It appears to result in fungal cell death.[7]

    Terbinafine was discovered in 1991.[8] It is on the World Health Organization's List of Essential Medicines.[4] In 2021, it was the 245th most commonly prescribed medication in the United States, with more than 1 million prescriptions.[9][10]

    Medical uses[edit]

    Terbinafine is mainly effective on molds of the order Onygenales and some yeasts in the genus Candida.[citation needed]

    As a cream or powder, it is used topically for superficial skin infections such as jock itch (tinea cruris), athlete's foot (tinea pedis), and other types of ringworm (tinea corporis).[11]

    Tablets by mouth are often prescribed for the treatment of onychomycosis, a fungal nail infection, typically by a dermatophyte or Candida species. Fungal nail infections are located deep under the nail in the cuticle to which topically applied treatments are unable to penetrate in sufficient amounts. The tablets may, rarely, cause hepatotoxicity, so patients are warned of this and may be monitored with liver function tests. Alternatives to oral administration have been studied.[citation needed]

    Terbinafine may induce or exacerbate subacute cutaneous lupus erythematosus. Persons with lupus erythematosus should first discuss possible risks with their doctor before initiation of therapy.[12]

    Side effects[edit]

    Many side effects and adverse drug reactions have been reported with oral terbinafine hydrochloride,[13][14] possibly due to its extensive biodistribution and the often extended durations involved in antifungal treatment (longer than two months). A comprehensive list of adverse events associated with terbinafine use includes:

    In 2015 physicians reported[16] that a patient with an MTHFR enzyme mutation (specifically the C677T variant) had developed an adverse reaction to Lamisil (headache, fatigue, and dizziness). Genetic testing revealed the MTHFR C677T mutation. It was noted that Lamisil interferes with the methylation cycle and that this can cause side effects in individuals with the MTHFR C677T mutation.

    Pharmacology[edit]

    This section needs additional citations for verification. Please help improve this articlebyadding citations to reliable sources in this section. Unsourced material may be challenged and removed. (March 2024) (Learn how and when to remove this message)
    Generic terbinafine hydrochloride pills

    Like other allylamines, terbinafine inhibits ergosterol synthesis by inhibiting squalene epoxidase, an enzyme that catalyzes the conversion of squalenetolanosterol. In fungi, lanosterol is then converted to ergosterol; in humans, lanosterol becomes cholesterol. However, as fungi and animals diverged around 1.1 billion years ago - there is enough difference in this enzyme that terbinafine preferentially binds fungal squalene epoxidase, making it selective for inhibiting ergosterol production in fungi without significantly affecting cholesterol production in mammals. This is thought to fatally disrupt the fungal cell membrane.[citation needed]

    Terbinafine is highly lipophilic and tends to accumulate in hair, skin, nails, and fat cells.

    This accumulation results in therapeutic levels of terbinafine even after 80 days following one week treatment of 250 mg/day. Different dosing schedules have been proposed such as 500 mg/day for one week or 250 mg/day for two weeks each followed by a drug-free period of three or two weeks, totaling 3 months of treatment including the drug-free periods. Such intermittent dosing schedules appear to be as effective as continuous regimens.[17]

    Chemistry[edit]

    Terbinafine hydrochloride is a white crystalline powder that is freely soluble in methanol and dichloromethane, soluble in ethanol, and slightly soluble in water. [citation needed]

    Terbinafine is produced from olefin metathesisof1,3-dichloropropene and neohexene followed by reaction with N-methyl-1-naphthalenemethanamine.[citation needed]

    Despite its name it does not contain terbium.

    History[edit]

    Terbinafine first became available in Europe in 1991 and in the United States in 1996. The U.S. Food and Drug Administration has approved the first generic versions of prescription Lamisil (terbinafine hydrochloride) tablets. The remaining patent or exclusivity for Lamisil expired on June 30, 2007.

    On September 28, 2007, the FDA stated that terbinafine is now approved for use by children age four and up. The antifungal granules can be sprinkled on a child's food to treat scalp fungus.[18]

    In the United States the price in 1999 was $547 for a 12-week course; this fell to $10 by 2015, after the patent had expired.[19]

    Society and culture[edit]

    Brand names[edit]

    References[edit]

    1. ^ a b c d e f g "Terbinafine Hydrochloride". The American Society of Health-System Pharmacists. Archived from the original on 21 December 2016. Retrieved 8 December 2016.
  • ^ a b "Lamisil 1% w/w Cream – Summary of Product Characteristics (SPC) – (eMC)". electronic Medicines Compendium (eMC). 17 March 2016. Archived from the original on 20 December 2016. Retrieved 17 December 2016.
  • ^ Crawford F (July 2009). "Athlete's foot". BMJ Clinical Evidence. 2009. PMC 2907807. PMID 21696646.
  • ^ a b World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
  • ^ Rang & Dale's Pharmacology (9th ed.). Elsevier. 2018. p. 694. ISBN 9780702074479.
  • ^ Yan J, Wang X, Chen S (August 2014). "Systematic review of severe acute liver injury caused by terbinafine". International Journal of Clinical Pharmacy. 36 (4): 679–683. doi:10.1007/s11096-014-9969-y. PMID 24986266. S2CID 12867807.
  • ^ "Terbinafine". www.drugbank.ca. Retrieved 2017-11-14.
  • ^ Ravina E (2011). The Evolution of Drug Discovery: From Traditional Medicines to Modern Drugs. John Wiley & Sons. p. 90. ISBN 978-3-527-32669-3. Archived from the original on 2016-12-20.
  • ^ "The Top 300 of 2021". ClinCalc. Archived from the original on 15 January 2024. Retrieved 14 January 2024.
  • ^ "Terbinafine - Drug Usage Statistics". ClinCalc. Retrieved 14 January 2024.
  • ^ Markova T (January 2002). "Clinical inquiries. What is the most effective treatment for tinea pedis (athlete's foot)?". The Journal of Family Practice. 51 (1). Frontline Medical Communications: 21. PMID 11927056. Archived from the original on 2012-04-06.
  • ^ Callen JP, Hughes AP, Kulp-Shorten C (September 2001). "Subacute cutaneous lupus erythematosus induced or exacerbated by terbinafine: a report of 5 cases". Archives of Dermatology. 137 (9): 1196–1198. doi:10.1001/archderm.137.9.1196. PMID 11559217.
  • ^ "Lamisil (terbinafine): Side Effects". Doublecheckmd.com. 2010-06-16. Archived from the original on 2013-09-21. Retrieved 2013-11-09.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  • ^ McGuire S (2008-02-05). "Australian regulators issue warning on Novartis' Lamisil". Medical Marketing and Media. Mmm-online.com. Archived from the original on 2013-11-09. Retrieved 2013-11-09.
  • ^ Duxbury AJ, Oliver RJ, Pemberton MN (March 2000). "Persistent impairment of taste associated with terbinafine". British Dental Journal. 188 (6): 295–296. doi:10.1038/sj.bdj.4800461. PMID 10800234. Persistent loss of taste associated with terbinafine would however appear to be extremely rare.
  • ^ Trachtman JN, Pagano V (December 2015). "Antifolates and MTHFR". Therapeutic Drug Monitoring. 37 (6): 697–698. doi:10.1097/FTD.0000000000000215. PMID 25929315. S2CID 205604356.
  • ^ Gupta AK, Stec N, Bamimore MA, Foley KA, Shear NH, Piguet V (March 2020). "The efficacy and safety of pulse vs. continuous therapy for dermatophyte toenail onychomycosis" (PDF). Journal of the European Academy of Dermatology and Venereology. 34 (3): 580–588. doi:10.1111/jdv.16101. PMID 31746067. S2CID 208185915.
  • ^ "US FDA approves oral granules for scalp ringworm". Reuters. 2007-09-28. Archived from the original on 2009-03-23.
  • ^ Mikailov A, Cohen J, Joyce C, Mostaghimi A (March 2016). "Cost-effectiveness of Confirmatory Testing Before Treatment of Onychomycosis". JAMA Dermatology. 152 (3): 276–281. doi:10.1001/jamadermatol.2015.4190. PMID 26716567.
  • ^ "Terbinafine brands in India". Brand index. DrugsUpdate India. Archived from the original on 2015-09-23.
  • ^ "Lamisil". Medex.com.bd. Archived from the original on 2019-01-19. Retrieved January 17, 2019.
  • ^ "Mercury Drug – The Leading Drugstore in the Philippines". www.mercurydrug.com. Archived from the original on 2016-11-18. Retrieved 2016-11-18.
  • ^ "Terbinafine". Pharmaceutical Benefits Scheme: A-Z list. Australian Government. Archived from the original on 2014-02-12.
  • ^ "PI and CMI Trade Names and Active Ingredients containing Terbinafine". Therapeutic Goods Administration. Australian Government. Archived from the original on 2017-09-10.
  • Wall/
    membrane

    Ergosterol
    inhibitors

  • clotrimazole#
  • croconazole
  • eberconazole
  • econazole
  • fenticonazole
  • flutrimazole
  • isoconazole
  • ketoconazole
  • luliconazole
  • miconazole#
  • neticonazole
  • omoconazole
  • oxiconazole
  • sertaconazole
  • sulconazole
  • tioconazole
  • Triazoles

  • fluconazole#
  • terconazole
  • Thiazoles

    Polyene antimycotics
    (ergosterol binding)

  • natamycin
  • nystatin#
    Systemic: amphotericin B#, hamycin
  • Squalene monooxygenase
    inhibitors

    Allylamines

  • terbinafine
    Systemic: terbinafine
  • Benzylamines

    Others

    β-glucan synthase
    inhibitors

  • caspofungin
  • cilofungin
  • micafungin
  • rezafungin)
  • ibrexafungerp
  • Intracellular

    Pyrimidine analogues/
    thymidylate synthase inhibitors

    Mitotic inhibitors

    Aminoacyl tRNA synthetase inhibitors

    Others

  • chlorophetanol
  • chlorphenesin
  • ciclopirox
  • crystal violet
  • dimazole
  • ethylparaben
  • haloprogin
  • polynoxylin
  • potassium iodide#
  • salicylic acid
  • selenium disulfide#
  • sodium thiosulfate#
  • sulbentine
  • taurolidine
  • ticlatone
  • tolciclate
  • tolnaftate
  • tribromometacresol
  • undecylenic acid
  • Whitfield's ointment#
  • Withdrawn from market
  • Clinical trials:
  • §Never to phase III

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Terbinafine&oldid=1235091472"

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