Itex Hydrochloride Lomefloxacin Tablets

Adult dosage

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 of this medicine is 400 mg orally once daily, with or without food. The duration of administration depends on the severity of infection, but is usually up to 14 days; treatment should continue for at least 2 days after the signs and symptoms of infection have resolved. 3. Patients with renal impairment 1) In patients with a creatinine clearance of less than 30 mL/min, administer 400 mg of this medicine as a single initial dose, followed by 200 mg once daily starting the next day. 2) In patients undergoing hemodialysis, administer 400 mg of this medicine as a single initial dose, 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 medication is used as a fluoroquinolone antibiotic to treat bacterial infections. However, it can cause serious side effects such as tendinitis, tendon rupture, peripheral neuropathy, central nervous system disorders, and exacerbation of myasthenia gravis. If these symptoms occur, discontinue the medication immediately and consult a healthcare professional. It is not used in patients with a history of myasthenia gravis. Furthermore, it is used only restrictively in certain infections such as acute bacterial sinusitis, acute exacerbation of chronic bronchitis, uncomplicated urinary tract infections, and acute otitis media. Caution is required in elderly patients, those with impaired kidney function, and those co-administered with corticosteroids as the risk of tendon rupture may increase. This medication should not be administered to adolescents under 18, pregnant women or women who may become pregnant, nursing mothers, and patients with a history of hypersensitivity. It should also be used cautiously in patients with a history of seizure disorders, severe renal impairment, elderly patients, and those with a history of aneurysms or heart valve disease. Various side effects such as hypersensitivity reactions, skin rashes, gastrointestinal disorders, psychiatric symptoms, respiratory issues, blood disorders, central nervous system disorders, and cardiovascular abnormalities may occur, so any unusual symptoms should be reported to a healthcare professional immediately. During the administration of this medicine, exposure to strong sunlight or ultraviolet light should be avoided, and caution should be taken in driving or operating machinery as dizziness or visual disturbances may occur. Also, interactions may occur when co-administered with certain medications, so it is important to inform healthcare professionals of all medications being taken. Pregnant or nursing women should not take this medication, and breastfeeding should be discontinued during treatment. In case of overdose, emergency treatments such as inducing vomiting and gastric lavage may be necessary. This medication has side effects and risks; therefore, it must be taken exactly as directed by healthcare professionals, and immediate consultation should be sought if any unusual symptoms occur.

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

This medication should be stored in a tightly closed container that blocks light and prevents air from entering. It is important to maintain a storage temperature in the range of 1 to 30 degrees Celsius.

Appearance

White oblong film-coated tablets

Package unit

30 tablets/bottle, 100 tablets/bottle