Itraconazole interactions
Full monograph for ItraconazoleCheck it against another medicine
Medicines
606 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Abemaciclib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of abemaciclib and its pharmacologically active… | 4 sources — open the full entry |
| Acalabrutinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of acalabrutinib, which is primarily metabolized by… | 4 sources — open the full entry |
| Alfuzosin Hydrochloride | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of alfuzosin, which is primarily metabolized by the… | 8 sources — open the full entry |
| Alprazolam | Major | Metabolism | Coadministration with itraconazole or ketoconazole may significantly increase the plasma concentrations and pharmacologic effects of benzodiazepines that are… | 28 sources — open the full entry |
| Amiodarone Hydrochloride | Major | Metabolism | Coadministration with azole antifungal agents may significantly increase the plasma concentrations of amiodarone. The proposed mechanism is azole inhibition of… | 8 sources — open the full entry |
| Amisulpride | Major | Synergy | Amisulpride can cause dose- and concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the… | 3 sources — open the full entry |
| Amlodipine Besilate | Major | Metabolism · Synergy | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically… | 36 sources — open the full entry |
| Amlodipine Besilate + Atenolol | Major | Metabolism · Synergy · Unknown | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms | 36 sources — open the full entry |
| Amlodipine Besilate + Atorvastatin | Major | Metabolism · Synergy | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms | 61 sources — open the full entry |
| Amlodipine Besilate + Benazepril Hydrochloride | Major | Metabolism · Synergy | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically… | 36 sources — open the full entry |
| Amlodipine Besilate + Olmesartan Medoxomil | Major | Metabolism · Synergy | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically… | 36 sources — open the full entry |
| Amlodipine Besilate + Telmisartan | Major | Metabolism · Synergy · Unknown | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms | 36 sources — open the full entry |
| Amlodipine Besilate + Valsartan | Major | Metabolism · Synergy · Unknown | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically…2 documented mechanisms | 36 sources — open the full entry |
| Apixaban | Major | Absorption · Metabolism | Coadministration with potent inhibitors of CYP450 3A4 that can also inhibit P-glycoprotein (P-gp) may significantly increase the plasma concentrations of… | 6 sources — open the full entry |
| Artemether + Lumefantrine | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of artemether and lumefantrine, both of which are primarily metabolized…2 documented mechanisms | 9 sources — open the full entry |
| Asciminib | Major | Others | Coadministration with itraconazole oral solution containing hydroxypropyl-beta-cyclodextrin may decrease the plasma concentrations of asciminib and reduce its… | 2 sources — open the full entry |
| Atorvastatin + Ezetimibe | Major | Metabolism · Unknown | Coadministration with itraconazole may significantly increase the plasma concentrations of atorvastatin and potentiate the risk of statin-induced myopathy. The…2 documented mechanisms | 25 sources — open the full entry |
| Atorvastatin Calcium | Major | Metabolism | Coadministration with itraconazole may significantly increase the plasma concentrations of atorvastatin and potentiate the risk of statin-induced myopathy. The… | 25 sources — open the full entry |
| Avanafil | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Axitinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of axitinib, which is primarily metabolized by the… | 7 sources — open the full entry |
| Azelastine Hydrochloride + Fluticasone Propionate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may increase the systemic exposure to fluticasone following intranasal administration or oral inhalation… | 40 sources — open the full entry |
| Betrixaban | Major | Others | Coadministration with inhibitors of P-glycoprotein (P-gp) may significantly increase the plasma concentrations of betrixaban, which is a substrate of the… | 11 sources — open the full entry |
| Bisoprolol Fumarate + Amlodipine Besilate | Major | Metabolism · Synergy | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically… | 36 sources — open the full entry |
| Brexpiprazole | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 and/or 2D6 may significantly increase the plasma concentrations of brexpiprazole, which is metabolized by these… | 5 sources — open the full entry |
| Brigatinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of brigatinib, which is partially metabolized by the… | 4 sources — open the full entry |
| BudesonideInhalerNebuliser SuspensionTablet | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive… | 19 sources — open the full entry |
| Budesonide + Formoterol Fumarate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive… | 19 sources — open the full entry |
| Budesonide + Glycopyrronium Bromide + Formoterol Fumarate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive… | 19 sources — open the full entry |
| Cabozantinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may increase the plasma concentrations of cabozantinib, which is a substrate of the isoenzyme. High… | 7 sources — open the full entry |
| Capmatinib Hydrochloride | Major | Metabolism | Coadministration of capmatinib with strong CYP450 3A4 inhibitors may increase the risk and severity of capmatinib adverse effects, such as interstitial lung… | 3 sources — open the full entry |
| Cariprazine | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of cariprazine and its major active metabolite… | 5 sources — open the full entry |
| Ceritinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of ceritinib, which is a substrate of the isoenzyme… | 6 sources — open the full entry |
| Cilostazol | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 and/or 2C19 may increase the plasma concentrations of cilostazol and or its pharmacologically active… | 12 sources — open the full entry |
| Clindamycin + Tretinoin | Major | Metabolism | Coadministration with azole antifungal agents may increase the plasma concentrations and toxicities of tretinoin. The proposed mechanism is inhibition of…2 documented mechanisms | 15 sources — open the full entry |
| Colchicine | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 may significantly increase the serum concentrations of colchicine, which is primarily metabolized by the… | 44 sources — open the full entry |
| Crizotinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of crizotinib, which is primarily metabolized by the… | 6 sources — open the full entry |
| Cyclosporine (Oral) | Major | Metabolism | Certain azole antifungal agents such as ketoconazole and itraconazole that are potent inhibitors of CYP450 3A4 may significantly increase the blood levels of… | 26 sources — open the full entry |
| Dabigatran Etexilate Mesylate | Major | Absorption | Coadministration with potent inhibitors of P-glycoprotein (P-gp) may increase the bioavailability of dabigatran following oral administration of dabigatran… | 5 sources — open the full entry |
| Daclatasvir | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of daclatasvir, which is primarily metabolized by… | 4 sources — open the full entry |
| Daclatasvir + Sofosbuvir | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of daclatasvir, which is primarily metabolized by… | 4 sources — open the full entry |
| Darifenacin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of darifenacin, which is partially metabolized by… | 7 sources — open the full entry |
| Dasatinib | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations and pharmacologic effects of dasatinib, which is primarily metabolized by… | 8 sources — open the full entry |
| Deflazacort | Major | Metabolism | Coadministration with potent or moderate inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of 21-desdeflazacort, the active… | 3 sources — open the full entry |
| Digoxin | Major | Absorption · Excretion | Coadministration with itraconazole may significantly increase the serum concentrations of digoxin. The proposed mechanism is inhibition of the… | 24 sources — open the full entry |
| Diltiazem Hydrochloride | Major | Metabolism · Synergy | Itraconazole exhibits a dose-related negative inotropic effect which may be additive to those of calcium channel blockers (CCBs). Theoretically… | 36 sources — open the full entry |
| Docetaxel Trihydrate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma… | 21 sources — open the full entry |
| Drospirenone | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by… | 9 sources — open the full entry |
| Drospirenone + Estetrol | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by… | 9 sources — open the full entry |
| Drospirenone + Estradiol | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…2 documented mechanisms | 17 sources — open the full entry |
| Drospirenone + Ethinyl Estradiol0.02 mg0.03 mg | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…2 documented mechanisms | 17 sources — open the full entry |
Food & lifestyle
cola
ModerateAbsorption
Food increases the absorption of itraconazole capsules but decreases the absorption of itraconazole oral solution. Cola beverages may increase the bioavailability of itraconazole capsules. Itraconazole capsules require an acidic gastric pH for adequate dissolution and subsequent absorption. Cola beverages help lower gastric pH and improve absorption.
What to do: The manufacturer recommends that the capsules be taken immediately after a full meal and the solution be taken on an empty stomach to ensure maximal absorption. Cola beverages may help increase the bioavailability of itraconazole capsules, particularly in patients with hypochlorhydria or those treated concomitantly with gastric acid suppressants. Until more information is available, it may be advisable to avoid the consumption of grapefruits and grapefruit juice during itraconazole therapy.
10 sources
- Van Peer A, Woestenborghs R, Heykants J, et al. "The effects of food and dose on the oral systemic availability of itraconazole in healthy subjects." Eur J Clin Pharmacol 36 (1989): 423-6
- Wishart JM "The influence of food on the pharmacokinetics of itraconazole in patients with superficial fungal infection." J Am Acad Dermatol 17 (1987): 220-3
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- Barone JA, Koh JG, Bierman RH, Colaizzi JL, Swanson KA, Gaffar MC, Moskovitz BL, Mechlinski W, Van de Velde V "Food interaction and steady-state pharmacokinetics of itraconazole capsules in healthy male volunteers." Antimicrob Agents Chemother 37 (1993): 778-84
- Zimmermann T, Yeates RA, Albrecht M, Laufen H, Wildfeuer A "Influence of concomitant food intake on the gastrointestinal absorption of fluconazole and itraconazole in japanese subjects." Int J Clin Pharmacol Res 14 (1994): 87-93
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
- Kawakami M, Suzuki K, Ishizuka T, Hidaka T, Matsuki Y, Nakamura H "Effect of grapefruit juice on pharmacokinetics of itraconazole in healthy subjects." Int J Clin Pharmacol Ther 36 (1998): 306-8
- Barone JA, Moskotitz BL, Guarnieri J, Hassell AE, Colaizzi JL, Bierman RH, Jessen L "Food interaction and steady-state pharmacokinetics of itraconazole oral solution in healthy volunteers." Pharmacotherapy 18 (1998): 295-301
Show all 10 sourcesShow fewer sources
- Penzak SR, Gubbins PO, Gurley BJ, Wang PL, Saccente M "Grapefruit juice decreases the systemic availability of itraconazole capsules in healthy volunteers." Ther Drug Monit 21 (1999): 304-9
- Katz HI "Drug interactions of the newer oral antifungal agents." Br J Dermatol 141 (1999): 26-32
grapefruit juice
ModerateMetabolism
Food increases the absorption of itraconazole capsules but decreases the absorption of itraconazole oral solution. Cola beverages may increase the bioavailability of itraconazole capsules. Itraconazole capsules require an acidic gastric pH for adequate dissolution and subsequent absorption. Cola beverages help lower gastric pH and improve absorption.
What to do: The manufacturer recommends that the capsules be taken immediately after a full meal and the solution be taken on an empty stomach to ensure maximal absorption. Cola beverages may help increase the bioavailability of itraconazole capsules, particularly in patients with hypochlorhydria or those treated concomitantly with gastric acid suppressants. Until more information is available, it may be advisable to avoid the consumption of grapefruits and grapefruit juice during itraconazole therapy.
10 sources
- Van Peer A, Woestenborghs R, Heykants J, et al. "The effects of food and dose on the oral systemic availability of itraconazole in healthy subjects." Eur J Clin Pharmacol 36 (1989): 423-6
- Wishart JM "The influence of food on the pharmacokinetics of itraconazole in patients with superficial fungal infection." J Am Acad Dermatol 17 (1987): 220-3
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- Barone JA, Koh JG, Bierman RH, Colaizzi JL, Swanson KA, Gaffar MC, Moskovitz BL, Mechlinski W, Van de Velde V "Food interaction and steady-state pharmacokinetics of itraconazole capsules in healthy male volunteers." Antimicrob Agents Chemother 37 (1993): 778-84
- Zimmermann T, Yeates RA, Albrecht M, Laufen H, Wildfeuer A "Influence of concomitant food intake on the gastrointestinal absorption of fluconazole and itraconazole in japanese subjects." Int J Clin Pharmacol Res 14 (1994): 87-93
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
- Kawakami M, Suzuki K, Ishizuka T, Hidaka T, Matsuki Y, Nakamura H "Effect of grapefruit juice on pharmacokinetics of itraconazole in healthy subjects." Int J Clin Pharmacol Ther 36 (1998): 306-8
- Barone JA, Moskotitz BL, Guarnieri J, Hassell AE, Colaizzi JL, Bierman RH, Jessen L "Food interaction and steady-state pharmacokinetics of itraconazole oral solution in healthy volunteers." Pharmacotherapy 18 (1998): 295-301
Show all 10 sourcesShow fewer sources
- Penzak SR, Gubbins PO, Gurley BJ, Wang PL, Saccente M "Grapefruit juice decreases the systemic availability of itraconazole capsules in healthy volunteers." Ther Drug Monit 21 (1999): 304-9
- Katz HI "Drug interactions of the newer oral antifungal agents." Br J Dermatol 141 (1999): 26-32
Conditions
Conditions in which Itraconazole needs care, as documented in this source.
Heart Failure
MajorItraconazole may possess a dose-related negative inotropic effect. Transient, asymptomatic decreases in left ventricular ejection fraction were observed with IV administration in healthy volunteers; these resolved before the next infusion. Additionally, cases of congestive heart failure (CHF), peripheral edema, and pulmonary edema have been reported during postmarketing experience in patients treated for onychomycosis and/or systemic fungal infections. Itraconazole should not be used to treat onychomycosis in patients with evidence of ventricular dysfunction such as CHF or history of CHF; itraconazole should not be used for other indications in such patients unless the benefit clearly outweighs the risk. The risks and benefits of itraconazole therapy should be reviewed carefully in patients with risk factors for CHF (including cardiac disease [e.g., ischemic and valvular disease], significant pulmonary disease [e.g., chronic obstructive pulmonary disease], renal failure and other edematous disorders). Patients with risk factors for CHF should be advised of the signs/symptoms of CHF, treated with caution, and monitored for signs/symptoms of CHF during therapy.
3 sources
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
- "Product Information. Tolsura (itraconazole)." Mayne Pharma Inc (2021):
Liver Diseases
MajorLimited data are available on the use of oral itraconazole in patients with liver dysfunction. Itraconazole has been associated with rare cases of serious hepatotoxicity (including liver failure and death). Caution is recommended when this drug is used in patients with liver dysfunction; such patients should be carefully monitored during therapy. Treatment with itraconazole is strongly discouraged in patients with elevated or abnormal liver enzymes, with active liver disease, or who had liver toxicity with other drugs unless the situation is serious or life-threatening and the expected benefit exceeds the risk. Liver function monitoring is recommended for patients with preexisting hepatic function abnormalities or those who had liver toxicity with other drugs.
3 sources
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
- "Product Information. Tolsura (itraconazole)." Mayne Pharma Inc (2021):
Achlorhydria
ModerateItraconazole 100-mg capsules should be administered after a full meal. Under fasted conditions, absorption of itraconazole from the 100-mg capsule formulation was diminished with decreased gastric acidity. Studies conducted under fasted conditions showed that taking the 100-mg capsule formulation with 8 ounces of a non-diet cola beverage enhanced absorption of itraconazole in AIDS patients with relative or absolute achlorhydria; this increase relative to the effects of a full meal is unknown.
1 source
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
Cystic Fibrosis
ModerateIn a study using itraconazole oral solution in cystic fibrosis patients, therapeutic drug levels varied and were not reached in some patients. Alternative therapy should be considered for patients who do not respond to itraconazole oral solution or itraconazole 100-mg capsules.
2 sources
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
Immune Deficiency Disease
ModerateThe oral bioavailability of itraconazole 100-mg capsules may be decreased in some immunocompromised patients (e.g., neutropenic patients, AIDS patients, organ transplant recipients); in addition, since hypochlorhydria has been reported in HIV-infected patients, the absorption of itraconazole may be reduced in these patients. The dose of itraconazole 100-mg capsules should be adjusted based on the clinical response of such patients.Itraconazole oral solution is not recommended for initial treatment in severely neutropenic patients at immediate risk of systemic candidiasis.
2 sources
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
Kidney Diseases
ModerateLimited data are available on the use of oral itraconazole in patients with renal dysfunction; itraconazole exposure may be lower in some of these patients. Caution is advised when using itraconazole in patients with renal dysfunction and dose adjustment may be needed. Patients with renal dysfunction should be carefully monitored when using the 65-mg capsule formulation.
3 sources
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
- "Product Information. Tolsura (itraconazole)." Mayne Pharma Inc (2021):
Long QT Syndrome
ModerateSome azole antifungals have been associated with prolongation of the QT interval on the ECG. Rare cases of QT prolongation and torsade de pointes have been reported during postmarketing experience; such reports usually involved seriously ill patients with multiple confounding risk factors, such as structural heart disease, electrolyte abnormalities, and concomitant medications. These drugs should be administered with caution to patients with potentially proarrhythmic conditions. Concomitant use with other medications that have potential to increase the risk of cardiotoxicity should be avoided.
7 sources
- "Product Information. Nizoral (ketoconazole)." Janssen Pharmaceuticals (2001):
- "Product Information. Diflucan (fluconazole)." Roerig Division (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
- "Product Information. VFEND (voriconazole)." Pfizer U.S. Pharmaceuticals (2002):
- "Product Information. Noxafil (posaconazole)." Schering-Plough Corporation (2006):
- "Product Information. Tolsura (itraconazole)." Mayne Pharma Inc (2021):