Leflufloxacin 500mg Tablets (Lefloxacin Hydrate)

Adult dose

Typically, levofloxacin for adults is administered orally once daily at 250-750 mg. 1. For patients with normal renal function (creatinine clearance greater than 80 mL/min) - Complicated skin and soft tissue infections: 750 mg every 24 hours for 10-14 days. - Community-acquired pneumonia: 500 mg every 24 hours for 7 days. - Acute bacterial exacerbation of chronic bronchitis: 7 days. - Acute sinusitis: 10-14 days. - Chronic

This medication, as a fluoroquinolone antibiotic, may cause tendon-related issues, such as tendonitis or tendon rupture. It may also cause peripheral neuropathy, central nervous system symptoms, and worsen symptoms in patients with myasthenia gravis, so caution is necessary. Patients should immediately discontinue use and consult a doctor if pain, inflammation, or symptoms of tendon rupture occur while taking this medication. Patients with myasthenia gravis or those who have had hypersensitivity reactions to this medication or similar drugs should not use this medication. Administration is also prohibited in children, pregnant women, nursing mothers, patients with epilepsy, and those with certain genetic conditions. Patients with severely impaired kidney function, those with central nervous system diseases or a history of seizures, and elderly patients should be more cautious when using this medication. This drug may increase the risk of seizures, so patients with a history of seizures should be especially careful. Additionally, this medication can affect blood sugar control, so diabetic patients should check their blood sugar regularly. Severe allergic reactions or skin reactions, liver function abnormalities, blood disorders, gastrointestinal disturbances, musculoskeletal problems, etc. may occur; if any unusual symptoms arise, patients should consult a doctor immediately. It is recommended to avoid strong sunlight or exposure to artificial ultraviolet light while taking this medication. Caution is advised when driving or operating machinery as symptoms such as dizziness or drowsiness may occur. The efficacy of this medication can be reduced when taken together with certain antacids or medications containing iron or calcium, so dosing intervals should be adjusted. Also, there may be interactions with some NSAIDs, anticoagulants, and diabetes medications, so patients should inform their doctor or pharmacist of all medications they are currently taking. In the case of overdose, symptoms of central nervous system disturbances and the risk of cardiac arrhythmia may arise, so immediate medical attention should be sought. This medication may increase the risk of hepatotoxicity and aortic aneurysm or dissection in elderly patients, and thus should be used with greater caution.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe allergic reactions, severe rash with high fever, blistering, peeling skin, pain in mucous membranes of the mouth/eyes, severe skin reactions, respiratory problems, yellowing of the skin or eyes (jaundice), extreme malaise, liver dysfunction (jaundice), sudden and severe headaches, thunderclap headaches, seizures, confusion, visual disturbances, paralysis,

Mild side effects

• Dizziness
• headache
• insomnia
• tremors
• anxiety
• depression
• hallucinations
• paranoia
• neurosis
• delirium

This medication should be stored in a tightly sealed container to prevent exposure to air or moisture. It is safe to store at room temperature between 1 and 30 degrees Celsius. Storing it this way will help maintain the medication's efficacy and prevent deterioration.

Appearance

Pink oblong film-coated tablet

Package unit

28 tablets/bottle, 100 tablets/bottle