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Candistat

Candistat is an antifungal medicine. It is used to treat infections in different parts of the body caused by fungi. It works by killing and stopping the growth of fungi. This provides relief from various symptoms caused by the infection and speeds up the healing process.

Other names for this medication:
Biospore, Candiloss, Candistat, Canditral, Caritra, Citroz, Fulcover, Fungixit, Intracan, Itaspor, Itcona, Itraconazole, Itracross, Itral, Itrasig, Itrole

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Also known as: Itraconazole

Description

{name} (itraconazole) is an antifungal medication that fights infections caused by fungus.

{name} is used to treat infections in adults caused by fungus, which can invade any part of the body including the lungs, mouth or throat, toenails, or fingernails.

It is not known if {name} is safe and effective in children.

Dosage

Generic Candistat should be taken by mouth after food and oral solution which should be taken on empty stomach. If you want to achieve most effective results do not stop taking Generic Candistat.

Overdose

If you overdose Generic Candistat and you don't feel good you should visit your doctor or health care provider immediately.

Storage

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

Side effects

The most common side effects associated with Candistat are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.

Contraindications

You should not take this medicine if you are allergic to Candistat PulsePak or similar medicines such as fluconazole or ketoconazole, or if you have ever had congestive heart failure.

Life-threatening side effects may occur if you take Candistat PulsePak with certain other drugs. Your doctor may change your treatment plan if you have used other medicines in the past 2 weeks, especially:

avanafil; cisapride; eliglustat; irinotecan; isavuconazonium; methadone; naloxegol; ranolazine; ticagrelor; lurasidone or pimozide (anti-psychotic medications); lomitapide, lovastatin, simvastatin (cholesterol-lowering medicines); dihydroergotamine, ergonovine, ergotamine, or methylergonovine (ergot medicines); eplerenone, felodipine, ivabradine, or nisoldipine (heart or blood pressure medicines); disopyramide, dofetilide, dronedarone, or quinidine (medicines for heart rhythm disorders); or oral midazolam, or triazolam (Valium-like sedatives).

If you have liver or kidney disease, you should not take Candistat PulsePak with colchicine, fesoterodine, solifenacin, or telithromycin.

Candistat PulsePak may harm an unborn baby. Use effective birth control to prevent pregnancy while you are using this medicine and for at least 2 months after your last dose. Tell your doctor if you become pregnant.

Tell your doctor if you have ever had:

heart problems; cystic fibrosis or other lung problems; liver or kidney disease; or a weak immune system.

It may not be safe to breastfeed while using this medicine. Ask your doctor about any risk.

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Emerging therapeutic options for managing diabetic kidney disease. Sensory, spectrometric (PTR-ToF-MS) and chemometric analyses to distinguish extra virgin from virgin olive oils. Thoracoscopic enucleation of a submucosal bronchogenic cyst of the esophagus: report of two cases. The consequences of government regulation in the post-acute care sector are not well understood. Many people are not aware that the federal government and some state governments have specific moral and legal rights and responsibilities toward Native Americans, unlike other groups in the United States.

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The clinical use of all-trans-retinoic acid (ATRA) in the treatment of cancer is significantly hampered by the prompt emergence of resistance, believed to be caused by increased ATRA catabolism. Clinical presentation was a progressive respiratory failure, and radiographic findings showed a consolidation of the left lung, associated with a pneumothorax in one and an ascites in the other. Immunohistochemistry was evaluated by experienced pathologists and quantified by use of an automated image analysis system. Bosutinib also increased survival in vitro of ALS iPSC-derived motor neurons from patients with sporadic ALS or other forms of familial ALS caused by mutations in TAR DNA binding protein (TDP-43) or repeat expansions in C9orf72 Furthermore, bosutinib treatment modestly extended survival of a mouse model of ALS with an SOD1 mutation, suggesting that Src/c-Abl may be a potentially useful target for developing new drugs to treat ALS. Pedigree analysis of a subject with abnormally slow renal elimination of 6-hydroxychlorzoxazone. The primary outcomes for efficacy and acceptability were the response rate and all-cause discontinuation. The pharmacological inhibition of TLR4 or shRNA-mediated TLR4 knockdown improved wound healing and transwell migration in high-glucose-treated RPTC. The effect of moderate total body hypothermia on experimental irreversible renal failure. Histologically embryonal rhabdomyosarcoma is the most common variant. The rate of patients who were prescribed the recommended antiemetic drugs was calculated.

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