Repocin Tablet 100 mg (Levofloxacin)

Adult dose

Typically, the usual adult dosage of levofloxacin is 100 mg administered orally 2–3 times a day. In severe cases or when the effect is insufficient, 200 mg should be given 3 times a day. Adjustments may be made according to age and symptoms.

This medication can cause issues such as tendonitis or tendon rupture, leading to pain or swelling. Additionally, symptoms of peripheral neuropathy or central nervous system abnormalities may manifest as dizziness, headache, confusion, and seizures. It should not be used in patients with myasthenia gravis as symptoms may worsen. This medication is only used for specific infections and should be administered only when there are no other treatment methods available to ensure safety. Caution is required with elderly patients, those with impaired renal function, and patients taking corticosteroids, as the risk of tendon rupture may increase. Severe allergic reactions such as rash, itching, difficulty breathing, and in severe cases, shock may occur, and use should be discontinued immediately if these symptoms appear. Neuropsychiatric side effects such as insomnia, anxiety, depression, hallucinations, and suicidal thoughts may present, and patients should consult a doctor if abnormal symptoms occur. Cardiovascular side effects such as palpitations or arrhythmias and QT interval prolongation have been reported, requiring cautious use in patients with heart diseases. This medication can affect liver and kidney function, and it is important to monitor related symptoms or test results. Blood disorders may occur, so treatment should be discontinued and a doctor's advice sought if symptoms include anemia or thrombocytopenia. Gastrointestinal side effects such as nausea, vomiting, and diarrhea may occur, and immediate treatment should be sought for severe diarrhea or abdominal pain. Muscle pain, joint pain, tendonitis, and muscle weakness may appear, particularly with severe myasthenia gravis patients who are at risk for worsening symptoms. Rarely, severe skin reactions such as Stevens-Johnson syndrome or toxic epidermal necrolysis may occur; these require immediate discontinuation if skin abnormalities appear. Photosensitivity reactions may occur, so strong sunlight or artificial UV exposure should be avoided. Patients should be cautious about symptoms such as dizziness or drowsiness when driving or operating machinery. This medication should not be administered to women who are pregnant or may become pregnant, breastfeeding mothers, or children and adolescents in their growth stages. This medication may interact with other drugs, particularly anticoagulants, diabetes medications, and antacids, requiring caution during concurrent use. Overdose may result in central nervous system symptoms and cardiac abnormalities, so immediate medical attention should be sought for appropriate treatment. It is crucial to consult a doctor or pharmacist immediately if any abnormal symptoms occur while taking this medication.

Serious side effects

Hives, severe swelling, tightness in the chest, difficulty breathing, cold sweat, paleness, shock, hypotensive shock, seizures, confusion, tingling sensations, angioedema, airway obstruction, respiratory distress, serious skin reactions, severe allergic reactions, Stevens-Johnson syndrome, toxic epidermal necrolysis, eosinophilia with multisystem reactions to drugs, photosensitivity reactions, liver abnormalities (jaundice), elevated liver enzymes, acute liver necrosis, acute liver failure, severe liver injury.

Mild side effects

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

This medication should be stored in a tightly sealed container to prevent air or moisture from entering. It is best to maintain storage temperatures between 1°C and 30°C at room temperature.

Appearance

White to off-white round film-coated tablet

Package unit

30 tablets/bottle, 100 tablets/bottle