Viewing nowLevofloxacin Tablet 250 mg (Levofloxacin Hemihydrate)
Levofloxacin Hydrate 256.15mg
Tablet · Prescription medication
Ildong Pharmaceutical Co., Ltd.

MFDS item code 200710882 · Notified 2007.09.28 · Insurance code 642900260
Treatment of complicated skin and soft tissue infections, community-acquired pneumonia, etc.
This drug is effective against various types of bacteria and is used for complicated skin and soft tissue infections, community-acquired pneumonia, acute bacterial exacerbation of chronic bronchitis, acute sinusitis, chronic bacterial prostatitis, complicated and uncomplicated urinary tract infections, acute pyelonephritis, etc. As it belongs to the fluoroquinolone class of drugs, there is a risk of serious adverse reactions, so it is recommended to use it only when there are no other treatment options for these infections. Therefore, this medication is utilized as an appropriate treatment option when other treatment options are limited.
The usual adult dose is 250 to 750 mg of levofloxacin administered orally once daily. For patients with normal kidney function, the dosage and duration of treatment vary depending on the type of infection. Complicated skin and soft tissue infections should be treated with 750 mg at 24-hour intervals for 10 to 14 days. Community-acquired pneumonia should be treated with 500 mg at 24-hour intervals for 7 days. Acute bacterial exacerbation of chronic bronchitis should be treated for 7 days. Acute sinusitis treatment should last for 10 to 14 days.
This medication may cause problems with tendons, such as tendonitis or tendon rupture; therefore, it should be discontinued immediately if there is pain or inflammation in the tendons. Peripheral neuropathy, such as tingling or sensory abnormalities in the hands and feet, may occur, so if these symptoms arise, stop taking the medication and consult a doctor. It may affect the central nervous system, leading to symptoms like dizziness, anxiety, depression, or seizures, so caution is needed if such symptoms occur. Patients with myasthenia gravis should not use this medication as it may worsen their symptoms. This medication should not be administered to pregnant women, women of childbearing potential, nursing mothers, or children and adolescents in growth. Elderly patients or those with impaired kidney function may have prolonged drug presence in their bodies, increasing the risk of side effects, so dose adjustment and caution are necessary. During treatment with this medication, it is important to avoid strong sunlight or artificial ultraviolet exposure, and if a skin rash or blistering occurs, treatment should be immediately stopped. Diabetes patients who require blood sugar control should frequently check their blood sugar levels as this medication may cause changes in blood sugar levels. Drug interactions may occur when taken with other medications, so it is especially important to consult a doctor or pharmacist if taking antacids, iron supplements, calcium supplements, anticoagulants, theophylline, etc. Caution is needed while driving or operating machinery, as dizziness or drowsiness may occur. Overdose of this medication could lead to central nervous system symptoms and cardiac arrhythmias, so immediate medical attention is necessary in cases of overdose. If any abnormal symptoms occur during treatment, it is crucial to immediately stop taking the medication and consult healthcare professionals.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in oral/ocular mucosa, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough and fever, jaundice (yellowing of skin or eyes), extreme lethargy, sudden and severe headaches, thunderclap headache, seizures, confusion of consciousness, visual disturbances, paralysis, etc.
Nausea, diarrhea, vulvovaginitis, insomnia, abdominal pain, bloating, itching, dizziness, rash, dyspepsia, stomatitis, glossitis, dry mouth, constipation, taste distortion, vomiting, fungal infections, genital itching, headache, neuropathy, erythema rash, drowsiness, agitation, thirst, tremors, allergic reactions, palpitations, elevated BUN and serum creatinine, elevated liver enzyme levels (AST/ALT), blood system abnormalities (leukopenia, anemia, etc.)
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to protect it from air and moisture, and it is safely stored at room temperature between 1 and 30 degrees Celsius. Storing it this way will help maintain the drug's effectiveness and prevent degradation.
Oblong film-coated tablet with a reddish-pink color
30 tablets/bottle, 100 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Viewing nowLevofloxacin Hydrate 256.15mg
Tablet · Prescription medication
Ildong Pharmaceutical Co., Ltd.

Levofloxacin Hydrate 100mg
Tablet · Prescription medication
Ildong Pharmaceutical Co., Ltd.

Levofloxacin 100mg
Tablet · Prescription medication
Jeil Pharmaceutical Co., Ltd.

Levofloxacin Hydrate 100mg
Tablet · Prescription medication
International Pharmaceuticals Co., Ltd.
Levofloxacin 5.1246mg
Prescription medication
Jeil Pharmaceutical Co., Ltd.

Levofloxacin Hydrate 100mg
Tablet · Prescription medication
SS Pharm Co., Ltd.

Levofloxacin Hydrate 102.49mg
Tablet · Prescription medication
Samchundang Pharmaceutical Co., Ltd.

Levofloxacin Hydrate 100mg
Tablet · Prescription medication
Medica Korea 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.