Geneuone Lomefloxcin Hydrochloride Tablets

Adult dose

1. Administer 100 ～ 200 mg of lomefloxacin orally 2 ～ 3 times daily. 2. However, for acute exacerbations of chronic obstructive pulmonary disease, including chronic bronchitis, the usual adult dose is 400 mg of this medicine orally once daily, with or without food. The duration of treatment varies according to the severity of the infection, but is usually up to 14 days. Treatment should be continued for at least 2 days after the infection symptoms have resolved. 3. Patients with renal impairment 1) In patients with a creatinine clearance of less than 30 mL per minute, administer an initial dose of 400 mg of this medicine once, followed by 200 mg once daily starting the next day. 2) In patients on hemodialysis, administer an initial dose of 400 mg of this medicine, followed by 200 mg once daily starting the next day. 3) No dose adjustment is necessary in patients with hepatic impairment; adjust the dose according to renal function.

This drug can cause serious side effects such as tendonitis or tendon rupture, so use should be discontinued immediately if such symptoms occur. This drug should not be used in patients with myasthenia gravis as it may worsen symptoms. This drug is used only for the treatment of specific bacterial infections and should be administered only when no alternative treatment is available. Caution is needed in elderly patients, those with impaired kidney function, or when taken with corticosteroids, as the risk of tendon damage may increase. This drug is not recommended for use in growing adolescents under 18 years of age, pregnant women or women who may become pregnant, and patients allergic to this drug or similar medications. Patients with epilepsy or heart and aortic diseases should be cautious when using this drug. During treatment with this drug, allergic reactions, skin rash, severe gastrointestinal disorders, liver or kidney dysfunction, or neurological symptoms may occur, so consult a doctor immediately if any abnormal symptoms arise. Excessive exposure to sunlight may cause skin reactions, so it is advisable to avoid strong sunlight or UV exposure during treatment. This drug may cause dizziness or drowsiness, so caution should be exercised when driving or operating machinery. Diabetic patients taking blood sugar control medications should frequently check blood sugar levels as fluctuations may occur. This drug can interact with other medications, so inform your healthcare provider of any other medications you are taking. Pregnant or breastfeeding women should not use this drug, and breastfeeding should be discontinued during treatment. In cases of overdose, appropriate emergency measures such as inducing vomiting or gastric lavage may be required, so immediate medical attention should be sought.

• Tendinitis
• tendon rupture
• peripheral neuropathy
• central nervous system effects
• exacerbation of myasthenia gravis
• anaphylactic shock
• anaphylactoid reaction
• rash
• urticaria
• erythema

This drug should be stored in a tightly closed container that can block light and kept at room temperature between 1 °C and 30 °C. Storing it this way can maintain the drug's effectiveness.

Appearance

White oval film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle