Levofuracin Tablet 250 Milligrams (Levofloxacin Hemihydrate)

Adult dose

Generally, for adults, Levofloxacin is administered orally once daily at a dose of 250–750 mg. For patients with normal kidney function (creatinine clearance above 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 bacterial prostatitis: 28 days - Complex urinary tract infections, including mild to moderate acute pyelonephritis: 250 mg every 24 hours for 10 days - Uncomplicated urinary tract infections: 3 days

This medication is a fluoroquinolone antibiotic used for treating specific bacterial infections. Serious side effects such as tendonitis or tendon rupture, peripheral neuropathy, central nervous system effects, and worsening of myasthenia gravis may occur, so caution is required. If these side effects are suspected, discontinue use immediately and consult a healthcare professional. It is not safe to use this medication in patients with myasthenia gravis. Additionally, this medication is only recommended for use when there are no other treatment options available for certain infections. Elderly patients, those with poor kidney function, solid organ transplant recipients, and those using concurrently with corticosteroids are at increased risk for tendon rupture and should be particularly cautious. It is advisable to avoid concurrent use with corticosteroids, and if symptoms of tendonitis or tendon rupture occur, rest and avoid vigorous exercise. This medication may increase the risk of seizures, so it should be used with caution in patients with a history of seizures or central nervous system disorders. Patients with a history of hypersensitivity to this medication or similar medications, pregnant women, breastfeeding mothers, growing children, and adolescents should not be given this medication. During treatment, severe allergic reactions, skin rashes, photosensitivity reactions, gastrointestinal disturbances, liver or kidney dysfunction, and blood abnormalities may occur; if any unusual symptoms occur, inform a healthcare professional immediately. This medication can interact with certain drugs, so taking it with antacids, iron supplements, or calcium supplements can reduce its effectiveness, necessitating a time gap between doses. Furthermore, when used with hypoglycemic agents or anticoagulants, there is a risk of blood sugar changes or bleeding, so caution is advised. Dizziness or drowsiness may occur when driving or operating machinery, requiring caution. In the case of overdose, central nervous system symptoms and cardiac abnormalities may occur, requiring immediate treatment. This medication is not removed by dialysis. It is important to adhere strictly to the prescribed dosage and administration as instructed by a physician during treatment, and to consult a healthcare professional promptly in case of side effects.

Serious side effects

• Hives
• severe swelling (edema)
• tightness in chest
• difficulty breathing
• cold sweat
• paleness
• shock
• severe allergic reactions
• cardiovascular collapse
• hypotensive shock

Mild side effects

• Nausea
• diarrhea
• vaginitis
• insomnia
• abdominal pain
• bloating
• itching
• dizziness
• rash
• dyspepsia

This medication should be stored in a well-sealed container to protect it from air and moisture. The ideal storage temperature is between 1 to 30 degrees Celsius. Proper storage will help maintain the drug's effectiveness for a longer period.

Appearance

Pinkish rectangular film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle