The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles

Second generation triazoles are widely used as first-line drugs for the treatment of invasive fungal infections, including aspergillosis and candidiasis. This class, along with itraconazole, voriconazole, posaconazole, and isavuconazole, is characterized by a broad range of activity, however, indivi...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Andrzej Czyrski, Matylda Resztak, Paweł Świderski, Jan Brylak, Franciszek K. Główka
Formato: article
Lenguaje:EN
Publicado: MDPI AG 2021
Materias:
Acceso en línea:https://doaj.org/article/8c6f41a950264a1995cf13296a6765fa
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:8c6f41a950264a1995cf13296a6765fa
record_format dspace
spelling oai:doaj.org-article:8c6f41a950264a1995cf13296a6765fa2021-11-25T18:42:23ZThe Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles10.3390/pharmaceutics131119611999-4923https://doaj.org/article/8c6f41a950264a1995cf13296a6765fa2021-11-01T00:00:00Zhttps://www.mdpi.com/1999-4923/13/11/1961https://doaj.org/toc/1999-4923Second generation triazoles are widely used as first-line drugs for the treatment of invasive fungal infections, including aspergillosis and candidiasis. This class, along with itraconazole, voriconazole, posaconazole, and isavuconazole, is characterized by a broad range of activity, however, individual drugs vary considerably in safety, tolerability, pharmacokinetics profiles, and interactions with concomitant medications. The interaction may be encountered on the absorption, distribution, metabolism, and elimination (ADME) step. All triazoles as inhibitors or substrates of CYP isoenzymes can often interact with many drugs, which may result in the change of the activity of the drug and cause serious side effects. Drugs of this class should be used with caution with other agents, and an understanding of their pharmacokinetic profile, safety, and drug-drug interaction profiles is important to provide effective antifungal therapy. The manuscript reviews significant drug interactions of azoles with other medications, as well as with food. The PubMed and Google Scholar bases were searched to collect the literature data. The interactions with anticonvulsants, antibiotics, statins, kinase inhibitors, proton pump inhibitors, non-nucleoside reverse transcriptase inhibitors, opioid analgesics, benzodiazepines, cardiac glycosides, nonsteroidal anti-inflammatory drugs, immunosuppressants, antipsychotics, corticosteroids, biguanides, and anticoagulants are presented. We also paid attention to possible interactions with drugs during experimental therapies for the treatment of COVID-19.Andrzej CzyrskiMatylda ResztakPaweł ŚwiderskiJan BrylakFranciszek K. GłówkaMDPI AGarticledrug-drug interactiondrug-food interactionitraconazolevoriconazoleketoconazoleisavuconazolePharmacy and materia medicaRS1-441ENPharmaceutics, Vol 13, Iss 1961, p 1961 (2021)
institution DOAJ
collection DOAJ
language EN
topic drug-drug interaction
drug-food interaction
itraconazole
voriconazole
ketoconazole
isavuconazole
Pharmacy and materia medica
RS1-441
spellingShingle drug-drug interaction
drug-food interaction
itraconazole
voriconazole
ketoconazole
isavuconazole
Pharmacy and materia medica
RS1-441
Andrzej Czyrski
Matylda Resztak
Paweł Świderski
Jan Brylak
Franciszek K. Główka
The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles
description Second generation triazoles are widely used as first-line drugs for the treatment of invasive fungal infections, including aspergillosis and candidiasis. This class, along with itraconazole, voriconazole, posaconazole, and isavuconazole, is characterized by a broad range of activity, however, individual drugs vary considerably in safety, tolerability, pharmacokinetics profiles, and interactions with concomitant medications. The interaction may be encountered on the absorption, distribution, metabolism, and elimination (ADME) step. All triazoles as inhibitors or substrates of CYP isoenzymes can often interact with many drugs, which may result in the change of the activity of the drug and cause serious side effects. Drugs of this class should be used with caution with other agents, and an understanding of their pharmacokinetic profile, safety, and drug-drug interaction profiles is important to provide effective antifungal therapy. The manuscript reviews significant drug interactions of azoles with other medications, as well as with food. The PubMed and Google Scholar bases were searched to collect the literature data. The interactions with anticonvulsants, antibiotics, statins, kinase inhibitors, proton pump inhibitors, non-nucleoside reverse transcriptase inhibitors, opioid analgesics, benzodiazepines, cardiac glycosides, nonsteroidal anti-inflammatory drugs, immunosuppressants, antipsychotics, corticosteroids, biguanides, and anticoagulants are presented. We also paid attention to possible interactions with drugs during experimental therapies for the treatment of COVID-19.
format article
author Andrzej Czyrski
Matylda Resztak
Paweł Świderski
Jan Brylak
Franciszek K. Główka
author_facet Andrzej Czyrski
Matylda Resztak
Paweł Świderski
Jan Brylak
Franciszek K. Główka
author_sort Andrzej Czyrski
title The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles
title_short The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles
title_full The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles
title_fullStr The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles
title_full_unstemmed The Overview on the Pharmacokinetic and Pharmacodynamic Interactions of Triazoles
title_sort overview on the pharmacokinetic and pharmacodynamic interactions of triazoles
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/8c6f41a950264a1995cf13296a6765fa
work_keys_str_mv AT andrzejczyrski theoverviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT matyldaresztak theoverviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT pawełswiderski theoverviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT janbrylak theoverviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT franciszekkgłowka theoverviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT andrzejczyrski overviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT matyldaresztak overviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT pawełswiderski overviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT janbrylak overviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
AT franciszekkgłowka overviewonthepharmacokineticandpharmacodynamicinteractionsoftriazoles
_version_ 1718410786294988800