Viewing nowLamon Tablets (Terbinafine Hydrochloride)
Terbinafine Hydrochloride 140.625mg
Tablet · Prescription medication
Dongku Bio Pharmaceutical Co., Ltd.

MFDS item code 200301101 · Notified 2003.08.19 · Insurance code 657301200
Treatment of dermatophytosis (tinea pedis, tinea corporis, etc.) and onychomycosis
This medication is used to treat dermatophytosis caused by dermatophytes in adults, such as tinea pedis, tinea corporis, and tinea cruris, as well as onychomycosis. It is also effective for the treatment of tinea capitis in children. Therefore, it helps alleviate fungal infections in the skin and nails.
As terbinafine, administer 125 mg once or twice daily, or 250 mg once daily. For dermatophytosis, tinea pedis treatment is usually for 2 to 6 weeks, and tinea corporis and tinea cruris for 2 to 4 weeks. Onychomycosis is generally treated for 6 weeks to 3 months; however, in cases of infections involving the fingernails or small toes, or in younger patients, it may be shortened to less than 3 months. Treatment duration for nail infections is typically 3 months, though some patients may require treatment for 6 months or more.
Administer to children aged 2 years and older; it is not recommended for children under 2 years of age. Tinea capitis is treated for 4 weeks. For children weighing less than 20 kg (under 5 years), administer 62.5 mg once daily.
This medication should preferably not be used in patients with chronic liver disease or active liver disease. Before taking this medication, it is imperative to confirm liver health status, and regular liver function tests should be conducted. If symptoms of liver dysfunction, persistent nausea, fatigue, jaundice, etc., occur, notify a doctor immediately and discontinue this medication. This medication can have serious effects on liver function; therefore, if liver failure is suspected, use should be stopped immediately and professional examination should be sought. It should not be used in individuals who have had an allergic reaction to this medication or those with blood disorders, severe renal impairment, children under 2 years of age, or nursing women. In cautious cases, it should be administered carefully to individuals with impaired renal function, elderly patients, or young children with low body weight. If skin rashes or serious skin reactions occur, use should be stopped immediately. This medication can cause various side effects, including gastrointestinal disturbances, headaches, dizziness, and depression, so any symptoms should be discussed with healthcare professionals. Precautions should be taken when driving or operating machinery, as side effects such as dizziness may occur. There may be drug interactions when taken with other medications, so it is necessary to inform your doctor of all medications you are currently taking, and dose adjustments may be needed as appropriate. Women who are pregnant or may become pregnant should carefully weigh the benefits and risks of using this medication, and nursing mothers should discontinue breastfeeding while on this medication. In case of overdose, symptoms such as headaches, nausea, and dizziness may occur. If suspected, seek immediate medical attention for appropriate treatment. This medication should be stored out of the reach of children and kept in a tightly sealed container away from direct sunlight at room temperature.
Urticaria, facial swelling, lymphadenopathy, hepatobiliary failure, hepatitis, cholestasis, jaundice, neutropenia, pancytopenia, agranulocytosis, thrombocytopenia, mucocutaneous syndrome (Stevens-Johnson syndrome), toxic epidermal necrolysis (Lyell syndrome), acute generalized exanthematous pustulosis, erythema multiforme, toxic skin rash, exfoliative dermatitis, blistering dermatitis, rhabdomyolysis, hypotension, respiratory distress, chest tightness, anaphylactic reactions (angioedema,
Rash, itching, fever, nausea, vomiting, loss of appetite, malaise, musculoskeletal reactions (arthralgia, myalgia), muscle pain, weakness, gastrointestinal symptoms (abdominal distension, dyspepsia, diarrhea), abdominal discomfort, dry mouth, glossitis, depression, anxiety, headaches, taste disturbances, dizziness, drowsiness, sensory anomalies, decreased sensation, decreased attention, insomnia, increased BUN, frequent urination, visual disturbances, tinnitus, increased total cholesterol in the blood, increased triglycerides
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to prevent air exposure, and it is recommended to keep it at a temperature between 1°C and 30°C. Storing it in this manner helps maintain the medication's effectiveness and prevent deterioration.
White round tablet
30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Viewing nowTerbinafine Hydrochloride 140.625mg
Tablet · Prescription medication
Dongku Bio Pharmaceutical Co., Ltd.
Terbinafine Hydrochloride 10mg
Cream · OTC medication
GP Therapeutics Korea Co., Ltd.
Terbinafine Hydrochloride 10mg
Cream · OTC medication
Korea Hutex Pharmaceutical Co., Ltd.
Terbinafine Hydrochloride 10mg
Cream · OTC medication
Anguk Pharmaceutical Co., Ltd.
Terbinafine Hydrochloride 10mg
Cream · OTC medication
Medica Korea Co., Ltd.
Terbinafine Hydrochloride 10mg
Cream · OTC medication
Gyeongnam Pharmaceutical Co., Ltd.
Terbinafine Hydrochloride 10mg
Cream · OTC medication
Daehwa Pharmaceutical Co., Ltd.
Terbinafine Hydrochloride 10mg
Cream · OTC medication
Korea Pharmaceutical Co., Ltd.
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.
No questions yet.
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.