Gelofoxacin Tablet 100 mg

Adult dosage

The usual adult dose is 300～600 mg of ofloxacin per day, divided into 2～3 doses. For Hansen's disease, the dose is 400～600 mg of this medicine per day, divided into 2～3 doses. In principle, it should be used in combination with other anti-Hansen's disease drugs. The dose may be adjusted appropriately according to age and symptoms.

This drug is a fluoroquinolone antibiotic used in the treatment of various bacterial infections. Caution should be exercised when taking this medication, as serious adverse effects such as tendinitis or tendon rupture, peripheral neuropathy, central nervous system effects, and exacerbation of myasthenia gravis may occur. If symptoms of tendinitis or tendon rupture appear, the use of this medication should be stopped immediately, and a physician should be consulted. Patients with severe myasthenia gravis may experience an exacerbation of symptoms when using this drug, so it is advisable to avoid administration. Moreover, this drug is recommended for use only when there are no other treatment options available for certain bacterial infections. Elderly patients, those with impaired kidney function, and patients taking corticosteroids should be cautious as the risk of tendon rupture may increase. Pregnant women or those who may become pregnant, nursing mothers, adolescents under 18 years of age, and patients allergic to this drug or similar medications should not use it. This drug may increase the risk of seizures in patients with a history of epilepsy or convulsions, so it should be used with caution. Throughout the course of treatment, various side effects may occur, including skin rash, allergic reactions, liver or kidney function abnormalities, gastrointestinal disturbances, blood abnormalities, neurological symptoms, muscle and joint pain, so if any abnormal symptoms arise, immediate consultation with a physician is necessary. This drug can increase sensitivity to sunlight, resulting in skin rashes or inflammation, so it is advisable to avoid strong sunlight or UV exposure. Diabetic patients who require blood glucose control may experience symptoms of hypoglycemia or hyperglycemia, so blood glucose should be monitored carefully. Additionally, this drug may interact with other medications, so patients should inform their physician or pharmacist of any other medications they are taking. Sufficient fluid intake is necessary during treatment, and caution should be exercised when performing tasks that require attention, such as driving or operating machinery, as neurological adverse reactions may occur. Finally, this drug should be used strictly according to a physician's prescription and instructions, and the medication should be discontinued immediately and medical advice should be sought in case of any adverse reactions.

Tendinitis, tendon rupture, peripheral neuropathy, central nervous system effects, worsening of myasthenia gravis, anaphylactic shock, anaphylaxis, rash, itching, redness, swelling, fever, warmth, vesicles, erythema, hematuria, acute renal failure, kidney stones, interstitial nephritis, increased BUN, elevated serum creatinine, jaundice, liver failure, increased AST, increased ALT, increased ALP, elevated γ-GTP, increased total bilirubin, cholestatic jaundice, membranous colitis, abdominal pain, diarrhea, nausea, vomiting, gastrointestinal discomfort, cirrhosis, loss of appetite, abdominal pain, dyspepsia, chest pain, thirst, taste disorder, stomatitis, glossitis, abdominal bloating, constipation, dysphagia, gastrointestinal hemorrhage, oral mucosa pain, intestinal perforation, anemia, leukopenia, decreased hemoglobin, reduced hematocrit, thrombocytopenia, increased eosinophils, agranulocytosis, thrombocytopenic purpura, petechiae and ecchymosis, prolonged prothrombin time, bone marrow suppression, lymphocytopenia, neutropenia, increased ESR, insomnia, dizziness, headache, seizures, tremors, numbness, sensory abnormalities, decreased sensation, diplopia, neglect, nystagmus, tinnitus, hearing loss, hallucinations, drowsiness, nervousness, sleep disorders, confusion, anxiety, depression, agitation, dysphoria, delirium, seizure, nightmares, paranoia, disorientation, attention deficit, memory impairment, delirium, suicidal thoughts, suicide, perceptual disturbances, olfactory disorders, balance disorders, ataxia, aphasia, heaviness in the head, skin mucous membrane syndrome, Stevens-Johnson syndrome, toxic epidermal necrolysis, Lye syndrome, arthralgia, myalgia, muscle weakness, myositis, malaise, increased CPK, elevated myoglobin, rhabdomyolysis, pharyngitis, dyspnea, bronchospasm, allergic pneumonia, epistaxis, stridor, fever, cough, abnormal chest X-ray, increased eosinophils, interstitial pneumonia, cerebral thrombosis, pulmonary edema, tachycardia, hypertension, hypotension, palpitations, vasodilation, circulatory collapse, prolonged QT, ventricular tachycardia, dysuria, frequency of urination, urinary retention, anuria, polyuria, pyuria, diabetes, proteinuria, alkaline urine, vaginitis, vaginal candidiasis, increased vaginal discharge, pruritus of the female external genitalia, menstrual irregularities, uterine cramps, female genital rash, pain, irritation, burning sensation, hypoglycemic symptoms, limb pain, fatigue, fever

This medication should be stored in a tightly sealed container to prevent air or moisture from entering, and it should be kept at room temperature between 1 to 30 degrees Celsius. Storing it this way will help to maintain the drug's efficacy for a long time.

Appearance

White to off-white round film-coated tablet

Package unit

30 tablets per bottle, 300 tablets per bottle