Viewing nowTriconazole Tablet (Itraconazole Solid Dispersion)
Itraconazole Solid Dispersions 253mg
Tablet · Prescription medication
TDS Pharm Co., Ltd.

MFDS item code 201404542 · Approved 2014.09.30 · Insurance code 679801380
Treatment of fungal infections of the skin and nails, mucosal and corneal fungal infections, and systemic fungal infections
This medication is used to treat fungal infections such as candidal vulvovaginitis, tinea, and various forms of tinea corporis caused by dermatophytes. It is also effective against oral candidiasis, fungal keratitis, and onychomycosis (fungal infections of the nails). Furthermore, it is applicable for systemic fungal infections like aspergillosis, candidiasis, cryptococcosis (including meningitis), and Paracoccidioidomycosis. It is used to improve various types of fungal infections.
To increase absorption, this medicine should preferably be administered immediately after a meal. 1. Short-term treatment 1) Candidal vaginitis: Administer itraconazole 200 mg twice daily (morning and evening) for 1 day, or 200 mg once daily for 3 days. 2) Tinea versicolor: Administer 200 mg once daily for 7 days. 3) Tinea corporis and tinea cruris (jock itch): Administer 100 mg once daily for 15 days. 4) Tinea manuum (interdigital) and tinea pedis (interdigital): Administer 100 mg once daily for 15 days. 5) Tinea manuum (palmar) and tinea pedis (plantar): Administer 100 mg once daily for 30 days or 200 mg twice daily for 7 days. 6) Oral candidiasis: Administer 100 mg once daily for 15 days. 7) Fungal keratitis: Administer 200 mg once daily for 21 days. 2. Onychomycosis 1) Pulse therapy Administer 200 mg twice daily for 1 week, followed by 3 weeks without treatment; this constitutes 1 cycle. Administer up to 2 cycles if only the fingernails are infected, and up to 3 cycles if the toenails are infected. 2) Continuous therapy Administer 200 mg once daily for 3 months. 3. Systemic fungal infections In patients with impaired immune function, such as those with neutropenia or AIDS or those who have undergone organ transplantation, the oral bioavailability of this medicine may be reduced; if necessary, double the dose. Aspergillosis: 200mg once daily, with an average treatment duration of 2~5 months. For invasive or disseminated disease, increase to 200mg twice daily. Candidiasis: 100~200mg once daily, with an average treatment duration of 3 weeks~7 months. Cryptococcal meningitis: 200mg twice daily, with an average treatment duration of 2 months~1 year. Maintenance therapy: 200mg once daily. Paracoccidioidomycosis: 100mg once daily, with an average treatment duration of 6 months.
This medication should not be used in patients with impaired heart function. Caution is particularly needed if there is a history of heart failure or ventricular dysfunction, as this medication can cause serious heart issues. Patients who have had allergic reactions to this medication or are sensitive to its components should absolutely not use it. Furthermore, there are various medications that may pose risks when taken concurrently, so consultation with a doctor or pharmacist is essential. It is advisable not to use this medication in pregnant women or those who may become pregnant, as it could affect the fetus or baby. Patients with impaired liver or kidney function should exercise caution when using this medication and should regularly undergo liver function tests, adjusting the dosage according to the physician's instructions. This medication can interact with various drugs, so if other medications are being taken, consultation with a professional is necessary. Co-administration with certain drugs may exacerbate side effects, making it necessary to avoid such combinations or adjust dosages. When using this medication, gastrointestinal symptoms such as headaches, nausea, abdominal pain, diarrhea, or allergic reactions such as skin rashes and itching may occur; if any unusual symptoms arise, medical personnel should be notified immediately. Caution is required when driving or operating machinery, as dizziness, visual disturbances, or hearing loss may occur. In case of overdose, there is no specific antidote available. It is imperative to adhere to the prescribed doses, and if any unusual symptoms are noticed, visit a medical facility immediately. This medication should be stored out of reach of children and kept in its original container to prevent misuse or degradation of quality.
Headache, nausea, abdominal pain, rhinitis, sinusitis, upper respiratory tract infection, leukopenia, hypersensitivity, taste disorder, sensory impairment, sensory anomaly, tinnitus, constipation, diarrhea, indigestion, bloating, vomiting, impaired liver function, hyperbilirubinemia, itching, rash, urticaria, polyuria, erectile dysfunction, menstrual disorders, edema, leukopenia, thrombocytopenia, anaphylactoid reaction, hyperglycemia, hyperkalemia, hypokalemia, hypomagnesemia, confusion, peripheral neuropathy, dizziness, drowsiness, tremor, heart failure, left ventricular failure, tachycardia, hypertension, hypotension, pulmonary edema, dysphonia, cough, liver failure, hepatitis, jaundice, erythematous rash, sweating, myalgia, arthralgia, renal impairment, urinary incontinence, systemic edema, facial edema, chest pain, fever, pain, fatigue, chills, leukocytosis, eosinophilia, anemia, vascular edema, serum sickness, angioedema, anaphylaxis, anaphylactic shock, allergic reaction, diplopia, visual impairment, temporary hearing loss, permanent hearing loss, ventricular ectopic beats, atrioventricular block, palpitations, increased bowel motility, belching, glossitis, stomatitis, abdominal lumbar pain, pancreatitis, elevated serum total protein, elevated total bilirubin, elevated LAP, decreased appetite, malaise, brown urine, increased liver enzyme levels, mucous membrane syndrome, Stevens-Johnson syndrome, toxic epidermal necrolysis, Riel syndrome, erythema multiforme, hair loss, photosensitivity reaction, exfoliative dermatitis, leukotoxic vasculitis, acute generalized exanthematous pustulosis, elevated BUN, positive urine protein reaction, positive urine glucose reaction, decreased libido, drowsiness, shoulder stiffness, insomnia, chest pain, elevated serum triglyceride levels, burning sensation, elevated serum uric acid levels, elevated serum potassium levels, serum sickness, angioedema, anaphylactic reaction, hypertriglyceridemia, tremor, visual impairment, congestive heart failure, dyspnea, severe hepatotoxicity, toxic epidermal necrolysis, acute generalized exanthematous pustulosis, increased serum creatine phosphokinase levels
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to prevent air and moisture exposure. It is best kept at room temperature between 1 to 30 degrees Celsius.
This medication is a round film-coated tablet that is white or off-white in color.
30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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TDS Pharm Co., Ltd.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.