Megaoflox Tablet (Ofloxacin)

Adult dosage

○ Adults generally take 300～600 mg of ofloxacin in 2～3 divided doses daily. ○ For Hansen's disease, take 400～600 mg of this medicine in 2～3 divided doses daily. In principle, use in combination with other anti-Hansen's disease drugs. Adjust the dose as appropriate according to age and symptoms.

This medication may cause serious side effects related to tendons, such as tendonitis and tendon rupture; if these symptoms occur, you should stop taking the medication immediately. Caution is needed as it may affect peripheral neuropathy or the central nervous system, resulting in abnormal sensations or neurological symptoms. Patients with myasthenia gravis should not use this medication as it may worsen symptoms. Elderly patients or those with impaired kidney function may have higher drug concentrations; therefore, dosages and administration intervals should be adjusted, and adverse reactions may manifest more easily. Women who are pregnant or may become pregnant, as well as nursing mothers, should avoid taking this medication for safety. It is not recommended for use in children or adolescents in growth, as safety has not been established. This medication may cause severe allergic reactions or anaphylactic shock; if symptoms such as rash, itching, or difficulty in breathing occur, you must stop taking it immediately and consult medical personnel. Regular monitoring is required as it may impact liver and kidney function, and if digestive symptoms such as abdominal pain or diarrhea worsen, you should discontinue use. This medication can cause phototoxic reactions, so avoid strong sunlight or artificial UV exposure; if skin rashes or phototoxic symptoms occur, you should stop taking it. It may affect blood sugar control, so diabetic patients should closely monitor their blood sugar levels, and report any occurrence of hypoglycemia symptoms to medical personnel immediately. There are many interactions with other medications, so especially when taking it with anticoagulants, blood pressure medications, antacids, iron supplements, etc., you should consult with medical personnel. While taking this medication, dizziness or drowsiness may occur, so avoid driving or operating dangerous machinery. If tendon pain, inflammation, or muscle pain develops during treatment, immediately discontinue use and consult a doctor, and it is advisable to abstain from exercise. Patients with heart or aortic issues, or family histories should use it cautiously, and if any related symptoms occur, immediate medical consultation is necessary. In case of overdose, symptoms such as drowsiness, nausea, and dizziness may appear; if suspected, visit a medical facility immediately for proper treatment. This medication must be used according to the doctor's prescription and directions; it is best to avoid taking certain antacids or vitamins within 2 hours before and after administration.

tendinitis, tendon rupture, peripheral neuropathy, central nervous system effects, exacerbation of myasthenia gravis, anaphylactic shock, anaphylactoid reactions, rash, pruritus, erythema, edema, fever, warmth, blisters, erythema, photodermatosis, hematuria, acute kidney failure, nephrolithiasis, interstitial nephritis, elevated BUN, elevated serum creatinine, jaundice, hepatic failure, elevated AST/ALT, elevated ALP, elevated γ-GTP, increased total bilirubin, cholestatic jaundice, fulminant hepatitis, pseudomembranous colitis, abdominal pain, diarrhea, nausea, vomiting, gastric and abdominal discomfort, cirrhosis, loss of appetite, abdominal discomfort, dyspepsia, chest pain, thirst, taste disturbance, stomatitis, glossitis, abdominal distension, constipation, dysphagia, gastrointestinal bleeding, oral mucosal pain, intestinal perforation, anemia, leukopenia, decreased hemoglobin, decreased hematocrit, thrombocytopenia, increased eosinophils, agranulocytosis, thrombotic thrombocytopenic purpura, petechial and purpuric hemorrhages, prolonged prothrombin time, reversible bone marrow suppression, lymphopenia, neutropenia, increased ESR, insomnia, dizziness, headache, seizures, tremors, paresthesia, sensory abnormalities, sensory impairment, diplopia, neglect, nystagmus, tinnitus, hearing loss, hallucinations, drowsiness, irritable nerves, sleep disorders, confusion, anxiety, depression, agitation, fortune, delirium, seizures, nightmares, paranoia, loss of orientation, attention deficits, memory impairment, delirium, suicidal ideation, suicide, perceptual disturbances, olfactory and vestibular sensory disorders, ataxia, aphasia, heaviness of the head, mucocutaneous syndrome, Stevens-Johnson syndrome, toxic epidermal necrolysis, Riele syndrome, arthralgia, myalgia, muscle weakness, myositis, rhabdomyolysis, pharyngitis, dyspnea, bronchospasm, allergic pneumonia, epistaxis, stridor, fever, cough, interstitial pneumonia, cerebral thrombosis, pulmonary edema, tachycardia, hypertension, hypotension, palpitations, vasodilation, circulatory collapse, QT prolongation, ventricular tachycardia, dysuria, frequent urination, urinary retention, anuria, polyuria, hematuria, storage urine, pyuria, diabetes, proteinuria, alkaline urine, vaginitis, vulvovaginal candidiasis, increased vaginal discharge, vulvar pruritus, menstrual irregularities, uterine cramps, female genital rash, pain, irritation, burning sensation, hypoglycemic symptoms, limb pain, malaise, fever

This medication should be stored in a tightly sealed container to prevent air from entering, and it is recommended to keep it at room temperature between 1 and 30 degrees Celsius. Storing it this way helps maintain the medication's effectiveness and prevents deterioration.

Appearance

White to off-white round film-coated tablets

Package unit

30 tablets/bottle, 300 tablets/bottle