Viewing nowLevo Tablet 500 mg (Levofloxacin Hydrate)
Levofloxacin Hydrate 512.3mg
Tablet · Prescription medication
Cosmax Pharma Co., Ltd.

MFDS item code 201901896 · Approved 2019.03.28 · Insurance code 055101030
Effective in treating bacterial infections such as complicated skin and soft tissue infections, and community-acquired pneumonia.
This medication is used effectively to treat infections caused by various bacteria. The main indications include complicated skin and soft tissue infections, community-acquired pneumonia, acute bacterial exacerbation of chronic bronchitis, acute sinusitis, chronic bacterial prostatitis, and various urinary tract infections. However, this medication is a fluoroquinolone, and due to the risk of serious adverse reactions, it is recommended to be used only when there are no alternative treatment options. Such treatment helps improve the patient's infection symptoms and aids in recovery.
Generally, in adults, levofloxacin is administered orally once daily at a dose of 250 to 750 mg. The dosage and duration of administration vary depending on the infection type for patients with normal renal function.\n- Complicated skin and soft tissue infections: 750 mg every 24 hours for 10 to 14 days\n- Community-acquired pneumonia: 500 mg every 24 hours for 7 days\n- Acute bacterial exacerbation of chronic bronchitis: 7 days\n- Acute sinusitis: 10 to 14 days\n-
This medication may cause serious side effects such as tendonitis or tendon rupture, peripheral neuropathy, central nervous system disturbances, and exacerbation of myasthenia gravis, so caution is needed. In particular, patients with myasthenia gravis should not use this medication as their symptoms may worsen. This medication is used only when there are no alternative treatment options for specific infections such as acute bacterial rhinosinusitis, acute exacerbation of chronic bronchitis, simple urinary tract infections, and acute otitis media. While taking this medication, there is a risk of tendon rupture in areas such as the shoulder, hand, and Achilles tendon, so if pain or inflammation develops, one should stop taking it immediately and avoid physical activity. Furthermore, when taken with corticosteroids, there is an increased risk of tendon rupture, so they should not be taken together. Patients with epilepsy or central nervous system diseases may have a higher risk of seizures, so they should use with caution. Patients with a history of allergic reactions to this medication or who have previously experienced tendonitis or tendon rupture should not take it. Pediatric patients and adolescents under 18 years of age, pregnant or potentially pregnant women, and breastfeeding mothers should not use this medication. Elderly patients may have reduced kidney function, so the dosage and administration intervals should be adjusted and used with caution. This medication can affect the liver and kidneys, so if any unusual symptoms occur, one should consult a healthcare professional immediately. If dizziness, drowsiness, or visual disturbances occur while taking this medication, it is advisable to avoid driving or operating machinery. One should avoid exposure to strong sunlight or artificial UV light while taking this medication, and if skin rashes or blisters develop, one should stop taking it immediately. Diabetic patients requiring blood sugar control should regularly check their blood sugar levels, and if abnormalities occur, they should inform their healthcare provider immediately. This medication can interact with other drugs, so one must inform the healthcare provider of any medications being taken, especially antacids, iron preparations, and calcium supplements, and maintain a gap of at least 2 hours between doses. Overdose may cause central nervous system symptoms and cardiac rhythm disturbances, so appropriate treatment should be sought immediately.
Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, paleness, severe allergic reactions, high fever with severe rash, blisters, skin peeling, pain in oral/eye mucosa, severe skin adverse reactions, difficulty breathing, asthma attacks, respiratory distress accompanied by coughing and fever, jaundice, liver disorders (jaundice), sudden and very severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, severe kidney issues.
Insomnia, dizziness, headache, tremors, anxiety, depression, psychotic reactions (hallucinations, paranoia, hyperactivity, confusion, disorientation, attention deficit, nightmares, sleep disorders, suicidal thoughts, etc.), agitation, confusion, visual and auditory disturbances, taste and smell disturbances, auditory hallucinations, mania, sensory disturbances, sensory loss, weakness, palpitations, QT interval prolongation, arrhythmia, elevated BUN and serum creatinine, nausea, vomiting, abdominal discomfort.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to protect it from air and humidity, and it is best to keep it at room temperature between 1 and 30 degrees Celsius. By doing so, the efficacy and safety of the drug can be maintained.
Pink oval film-coated tablet
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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Cosmax Pharma Co., Ltd.

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Tablet · Prescription medication
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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.