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Nizoral is an extra-class medicine which is taken in treatment of infections such as throat yeast infections, vaginal yeast infections, fungal infections, esophagus. Nizoral is a helpful for patients with Cushing's syndrome, hair growth, prostate cancer, eumycetoma, tinea versicolor, leishmaniasis, high blood levels of calcium. Nizoral acts as an anti-fungal drug.

Other names for this medication:
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Similar Products:
Grifulvin, Lamisil, Sporanox, Grifulvin V, Diflucan, Fluconazole, Sporanox PulsePak, Onmel, Amphocin, Voriconazole, Abelcet, Fungizone, Vfend, Onmel, Abelcet


Also known as:  Ketoconazole.


Nizoral is developed with a help of medical professionals to fight with infections (throat yeast infections, vaginal yeast infections, fungal infections, esophagus), Cushing's syndrome, women hair growth, prostate cancer, eumycetoma, tinea versicolor, leishmaniasis, high blood levels of calcium. Target of Nizoral is to control, ward off, reduce and terminate fungi growth.

Nizoral acts as an anti-fungal drug. Nizoral operates by reducing fungi growth spreads by infection.

Nizoral is also known as Ketoconazole, Fung.

Nizoral is imidazole.


You should take it by mouth with full glass of water.

Take Nizoral once a day at the same time.

If you want to achieve most effective results do not stop taking Nizoral suddenly.


If you overdose Nizoral and you don't feel good you should visit your doctor or health care provider immediately. Symptoms of Generic Nizoral overdosage: feeling lightheaded, diarrhea, migraine, abnormal pain, ears ringing, nausea, rething.


Store at room temperature between 15 and 25 degrees C (59 and 77 degrees F) away from moisture and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

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Side effects

Antimycotics suppress the Malassezia extract-induced production of CXC chemokine ligand 10 in human keratinocytes. Identification of CYP isozymes involved in benzbromarone metabolism in human liver microsomes. Effects of antimycotics on hepatic steroid metabolism. Metabolites and metabolic pathways of mesaconitine in rat liver microsomal investigated by using UPLC-MS/MS method in vitro. Pharmacokinetics of all-trans-retinoic acid: clinical implications in acute promyelocytic leukemia. Buy nizoral. Ketoconazole suppresses interleukin-4 plus anti-CD40-induced IgE class switching in surface IgE negative B cells from patients with atopic dermatitis.


Do not take Nizoral if you are allergic to Nizoral components.

Do not take Nizoral if you are pregnant, planning to become pregnant, or are breast-feeding.

Do not use Nizoral if you take astemizole (Hismanal), cisapride (Propulsid), midazolam (Versed), triazolam (Halcion).

Be careful if you are taking oral diabetes medicine as glipizide (Glucotrol), chlorpropamide (Diabinese), glyburide (Glynase, Diabeta, Micronase), tolazamide (Tolinase), tolbutamide (Orinase); tacrolimus (Prograf); rifampin (Rimactane, Rifadin); warfarin (Coumadin); cyclosporine (Neoral, Sandimmune); antacids; famotidine (Pepcid, AC Pepcid), cimetidine (Tagamet HB, Tagamet), ranitidine (Zantac 75, Zantac), nizatidine (Axid AR, Axid); digoxin (Lanoxicaps, Lanoxin); methylprednisolone (Medrol); phenytoin (Dilantin); rabeprazole (Aciphex), omeprazole (Prilosec), lansoprazole (Prevacid).

Be careful if you have liver disease, achlorhydria.

Avoid consuming alcohol.

Try to avoid machine driving.

It can be dangerous to stop Nizoral taking suddenly.

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Enhanced effect in combination of curcumin- and ketoconazole-loaded methoxy poly (ethylene glycol)-poly (ε-caprolactone) micelles. Hydroxylation of pregnenolone at the 7 alpha- and 7 beta- positions by mouse liver microsomes. Effects of cytochrome p450 inhibitors and structure-specific inhibition by steroid hormones. Toxicity of thienopyridines on human neutrophil granulocytes and lymphocytes. Development and evaluation of new microemulsion-based hydrogel formulations for topical delivery of fluconazole.

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Cocaine-reinforced responding in rhesus monkeys: pharmacological attenuation of the hypothalamic-pituitary-adrenal axis response. Disseminated paracoccidioidomycosis: correlation between clinical and in vitro resistance to ketoconazole and trimethoprim sulphamethoxazole. Description of a 96-well plate assay to measure cytochrome P4503A inhibition in human liver microsomes using a selective fluorescent probe. Evaluation of herb-drug interaction of a polyherbal Ayurvedic formulation through high throughput cytochrome P450 enzyme inhibition assay.

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High-dose itraconazole in the treatment of severe mycoses. Outbreak of histoplasmosis in Pedro Leopoldo, Minas Gerais, Brazil. Effects of ketoconazole on ovulatory changes in the rat: implications on the role of a meiosis-activating sterol. Outcomes after repeat transsphenoidal surgery for recurrent Cushing's disease.

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Biofilm formation in Malassezia pachydermatis strains isolated from dogs decreases susceptibility to ketoconazole and itraconazole. Retention of ketoconazole in the skin following oral treatment. Pharmacokinetic study of the interaction between rifampicin and ketoconazole. Stress-restress evokes sustained iNOS activity and altered GABA levels and NMDA receptors in rat hippocampus.

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Activity of orally, topically, and parenterally administered itraconazole in the treatment of superficial and deep mycoses: animal models. Basidiobolomycosis: a case report. Cutaneous cryptococcosis successfully treated with itraconazole. In vivo pharmacokinetics and in vitro antifungal activity of iodiconazole, a new triazole, determined by microdialysis sampling.

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Diagnosis and treatment of oral candidosis. Activity of antibiotics and azole antimycotics against Helicobacter pylori. Molecular docking to understand the metabolic behavior of GNF-351 by CYP3A4 and its potential drug-drug interaction with ketoconazole. Activity of terbinafine in experimental fungal infections of laboratory animals.

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In vitro activities of antifungal agents against clinical isolates of dermatophytes from animals. Renal aspergilloma--a case illustrating the problems of medical therapy. Comparison of efficacy criteria across onychomycosis trials: need for standardization. Effect of cytochrome P450 inhibitors (diethyl dithiocarbamate, ketoconazole and grapefruit juice) on the pharmacokinetics of all-trans-retinoic acid.

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Identification of the human liver cytochrome P450 enzymes involved in the metabolism of zileuton (ABT-077) and its N-dehydroxylated metabolite, Abbott-66193. Genotype analysis of the rRNA gene of Malassezia colonizing the skin surface of patients with atopic dermatitis. Cutaneous infection due to acremonium. New azole compounds: vibunazole (Bay n7133) and Bay L9139, compared with ketoconazole in the therapy of systemic candidosis and in pharmacokinetic studies, in mice.

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