Fluconazole is an antifungal medication used for a number of fungal infections.[4] This includes candidiasis, blastomycosis, coccidioidomycosis, cryptococcosis, histoplasmosis, dermatophytosis, and tinea versicolor.[4] It is also used to prevent candidiasis in those who are at high risk such as following organ transplantation, low birth weight babies, and those with low blood neutrophil counts.[4] It is given either by mouth or by injection into a vein.[4]

Fluconazole
Clinical data
Trade namesDiflucan, others
AHFS/Drugs.comMonograph
MedlinePlusa690002
License data
Pregnancy
category
  • AU: D
Routes of
administration
By mouth, intravenous, topical
ATC code
Legal status
Legal status
Pharmacokinetic data
Bioavailability>90% (oral)
Protein binding11–12%
MetabolismLiver 11%
Elimination half-life30 hours (range 20–50 hours)
ExcretionKidney 61–88%
Identifiers
  • 2-(2,4-Difluorophenyl)-1,3-bis(1H-1,2,4-triazol-1-yl)propan-2-ol
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.156.133 Edit this at Wikidata
Chemical and physical data
FormulaC13H12F2N6O
Molar mass306.277 g·mol−1
3D model (JSmol)
Melting point139[3] °C (282 °F)
  • OC(Cn1cncn1)(Cn1cncn1)c1ccc(F)cc1F
  • InChI=1S/C13H12F2N6O/c14-10-1-2-11(12(15)3-10)13(22,4-20-8-16-6-18-20)5-21-9-17-7-19-21/h1-3,6-9,22H,4-5H2 checkY
  • Key:RFHAOTPXVQNOHP-UHFFFAOYSA-N checkY
  (verify)

Common side effects include vomiting, diarrhea, rash, and increased liver enzymes.[4] Serious side effects may include liver problems, QT prolongation, and seizures.[4] During pregnancy it may increase the risk of miscarriage while large doses may cause birth defects.[5][4] Fluconazole is in the azole antifungal family of medication.[4] It is believed to work by affecting the fungal cellular membrane.[4]

Fluconazole was patented in 1981 and came into commercial use in 1988.[6] It is on the World Health Organization's List of Essential Medicines.[7] Fluconazole is available as a generic medication.[4] In 2021, it was the 165th most commonly prescribed medication in the United States, with more than 3 million prescriptions.[8][9]

Medical uses edit

Fluconazole is a first-generation triazole antifungal medication. It differs from earlier azole antifungals (such as ketoconazole) in that its structure contains a triazole ring instead of an imidazole ring. While the imidazole antifungals are mainly used topically, fluconazole and certain other triazole antifungals are preferred when systemic treatment is required because of their improved safety and predictable absorption when administered orally.[10]

Fluconazole's spectrum of activity includes most Candida species (but not Candida krusei or Candida glabrata), Cryptococcus neoformans, some dimorphic fungi, and dermatophytes, among others.[medical citation needed] Common uses include:[1][10][11][12][13]

  • The treatment of non-systemic Candida infections of the vagina ("yeast infections"), throat, and mouth.
  • Certain systemic Candida infections in people with healthy immune systems, including infections of the bloodstream, kidney, or joints. Other antifungals are usually preferred when the infection is in the heart or central nervous system, and for the treatment of active infections in people with weak immune systems.
  • The prevention of Candida infections in people with weak immune systems, such as those neutropenic due to cancer chemotherapy, those with advanced HIV infections, transplant patients, and premature infants.
  • As a second-line agent for the treatment of cryptococcal meningoencephalitis, a fungal infection of the central nervous system.

Resistance edit

Antifungal resistance to drugs in the azole class tends to occur gradually over the course of prolonged drug therapy, resulting in clinical failure in immunocompromised patients (e.g., patients with advanced HIV receiving treatment for thrush or esophageal Candida infection).[14]

In C. albicans, resistance occurs by way of mutations in the ERG11 gene, which codes for 14α-demethylase. These mutations prevent the azole drug from binding, while still allowing binding of the enzyme's natural substrate, lanosterol. Development of resistance to one azole in this way will confer resistance to all drugs in the class. Another resistance mechanism employed by both C. albicans and C. glabrata is increasing the rate of efflux of the azole drug from the cell, by both ATP-binding cassette and major facilitator superfamily transporters. Other gene mutations are also known to contribute to development of resistance.[14] C. glabrata develops resistance by up regulating CDR genes, and resistance in C. krusei is mediated by reduced sensitivity of the target enzyme to inhibition by the agent.[1]

The full spectrum of fungal susceptibility and resistance to fluconazole can be found in the product data sheet.[15] According to the US Centers for Disease Control and Prevention, fluconazole resistance among Candida strains in the US is about 7%.[16]

Contraindications edit

Fluconazole is contraindicated in patients who:[13]

Side effects edit

Adverse drug reactions associated with fluconazole therapy include:[13]

If taken during pregnancy it may result in harm.[18][19] These cases of harm, however, were only in women who took large doses for most of the first trimester.[18]

Fluconazole is secreted in human milk at concentrations similar to plasma.[1]

Fluconazole therapy has been associated with QT interval prolongation, which may lead to serious cardiac arrhythmias. Thus, it is used with caution in patients with risk factors for prolonged QT interval, such as electrolyte imbalance or use of other drugs that may prolong the QT interval (particularly cisapride and pimozide).[20]

Some people are allergic to azoles, so those allergic to other azole drugs might be allergic to fluconazole.[21] That is, some azole drugs have adverse side-effects. Some azole drugs may disrupt estrogen production in pregnancy, affecting pregnancy outcome. [22]

Oral fluconazole is not associated with a significantly increased risk of birth defects overall, although it does increase the odds ratio of tetralogy of Fallot, but the absolute risk is still low.[23] Women using fluconazole during pregnancy have a 50% higher risk of spontaneous abortion.[24]

Fluconazole should not be taken with cisapride (Propulsid) due to the possibility of serious, even fatal, heart problems.[20] In rare cases, severe allergic reactions including anaphylaxis may occur.[25]

Powder for oral suspension contains sucrose and should not be used in patients with hereditary fructose, glucose/galactose malabsorption or sucrase-isomaltase deficiency. Capsules contain lactose and should not be given to patients with rare hereditary problems of galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption [26]

Interactions edit

Fluconazole is an inhibitor of the human cytochrome P450 system, particularly the isozyme CYP2C19 (CYP3A4 and CYP2C9 to lesser extent) [27] In theory, therefore, fluconazole decreases the metabolism and increases the concentration of any drug metabolised by these enzymes. In addition, its potential effect on QT interval increases the risk of cardiac arrhythmia if used concurrently with other drugs that prolong the QT interval. Berberine has been shown to exert synergistic effects with fluconazole even in drug-resistant Candida albicans infections.[28] Fluconazole may increase the serum concentration of Erythromycin (Risk X: avoid combination).[27]

Pharmacology edit

Pharmacodynamics edit

Like other imidazole- and triazole-class antifungals, fluconazole inhibits the fungal cytochrome P450 enzyme 14α-demethylase. Mammalian demethylase activity is much less sensitive to fluconazole than fungal demethylase. This inhibition prevents the conversion of lanosterol to ergosterol, an essential component of the fungal cytoplasmic membrane, and subsequent accumulation of 14α-methyl sterols.[29] Fluconazole is primarily fungistatic; however, it may be fungicidal against certain organisms in a dose-dependent manner, specifically Cryptococcus.[30]

Pharmacokinetics edit

Following oral dosing, fluconazole is almost completely absorbed within two hours.[31] Bioavailability is not significantly affected by the absence of stomach acid. Concentrations measured in the urine, tears, and skin are approximately 10 times the plasma concentration, whereas saliva, sputum, and vaginal fluid concentrations are approximately equal to the plasma concentration, following a standard dose range of between 100 mg and 400 mg per day.[32] The elimination half-life of fluconazole follows zero order, and only 10% of elimination is due to metabolism, the remainder being excreted in urine and sweat. Patients with impaired renal function will be at risk of overdose.[20]

In a bulk powder form, it appears as a white crystalline powder, and it is very slightly soluble in water and soluble in alcohol.[33]

History edit

Fluconazole was patented by Pfizer in 1981 in the United Kingdom and came into commercial use in 1988.[6] Patent expirations occurred in 2004 and 2005.[34]

References edit

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  2. ^ "Active substance: Fluconazole" (PDF). List of nationally authorised medicinal products. European Medicines Agency. 12 November 2020. Archived (PDF) from the original on 24 February 2024. Retrieved 22 December 2020.
  3. ^ Surov AO, Voronin AP, Vasilev NA, Churakov AV, Perlovich GL (20 December 2019). "Cocrystals of Fluconazole with Aromatic Carboxylic Acids: Competition between Anhydrous and Hydrated Solid Forms". Crystal Growth & Design. 20 (2): 1218–1228. doi:10.1021/acs.cgd.9b01490. S2CID 213008181.
  4. ^ a b c d e f g h i j "Fluconazole". The American Society of Health-System Pharmacists. Archived from the original on 20 December 2016. Retrieved 8 December 2016.
  5. ^ "Fluconazole (Diflucan): Drug Safety Communication - FDA Evaluating Study Examining Use of Oral Fluconazole (Diflucan) in Pregnancy". U.S. Food and Drug Administration (FDA). 26 April 2016. Archived from the original on 29 April 2016. Retrieved 29 April 2016.
  6. ^ a b Fischer J, Ganellin CR (2006). Analogue-based Drug Discovery. John Wiley & Sons. p. 503. ISBN 978-3-527-60749-5. Archived from the original on 10 September 2017.
  7. ^ 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.
  8. ^ "The Top 300 of 2021". ClinCalc. Archived from the original on 15 January 2024. Retrieved 14 January 2024.
  9. ^ "Fluconazole - Drug Usage Statistics". ClinCalc. Archived from the original on 8 July 2020. Retrieved 14 January 2024.
  10. ^ a b "US Pharmacist". Archived from the original on 10 February 2015. Retrieved 28 January 2015.
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  18. ^ a b "Fluconazole". Monograph. The American Society of Health-System Pharmacists. Archived from the original on 27 September 2014. Retrieved 27 September 2014.
  19. ^ "Prescribing medicines in pregnancy database". Australian Government. 3 March 2014. Archived from the original on 8 April 2014. Retrieved 22 April 2014.
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  21. ^ Pinto A, Chan RC (April 2009). "Lack of allergic cross-reactivity between fluconazole and voriconazole" (PDF). Antimicrobial Agents and Chemotherapy. 53 (4): 1715–1716. doi:10.1128/AAC.01500-08. PMC 2663085. PMID 19164151. Archived (PDF) from the original on 11 June 2011. Retrieved 20 October 2009.
  22. ^ Kragie L, Turner SD, Patten CJ, Crespi CL, Stresser DM (August 2002). "Assessing pregnancy risks of azole antifungals using a high throughput aromatase inhibition assay". Endocrine Research. 28 (3): 129–140. doi:10.1081/ERC-120015045. PMID 12489563. S2CID 8282678.
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  27. ^ a b "Login". Archived from the original on 21 December 2016. Retrieved 21 December 2016.
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  29. ^ Pfizer Australia Pty Ltd. Diflucan (Australian Approved Product Information). West Ryde (NSW): Pfizer Australia; 2004.
  30. ^ Longley N, Muzoora C, Taseera K, Mwesigye J, Rwebembera J, Chakera A, et al. (December 2008). "Dose response effect of high-dose fluconazole for HIV-associated cryptococcal meningitis in southwestern Uganda". Clinical Infectious Diseases. 47 (12): 1556–1561. doi:10.1086/593194. PMID 18990067.
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  33. ^ "Fluconazole". MP Biomedicals. Archived from the original on 16 January 2009.
  34. ^ "Pfizer to Expand Fluconazole Donation Program to More than 50 Developing Nations". Kaiser Health News. 7 June 2001. Archived from the original on 30 October 2020. Retrieved 18 June 2019.

Further reading edit