Ciprofloxacin Tablet 250 mg (Ciprofloxacin Hydrochloride Hydrate)

Adult dose

Typically, for adults, Ciprofloxacin is administered orally at a dose of 250 - 500 mg twice daily between meals. In cases of severe complicated infections, the dose may be increased to 750 mg twice daily. In the case of acute infections, treatment is usually given for 5 - 10 days, and even after symptoms have resolved, treatment should continue for at least 3 more days. In patients with renal impairment, the dose should be adjusted according to creatinine clearance. - Creatinine clearance > 50 mL/min

This medication may cause severe side effects, such as tendinitis, tendon rupture, peripheral neuropathy, and central nervous system adverse reactions, so usage should be immediately discontinued if any of these symptoms occur. Patients with myasthenia gravis may experience exacerbation of symptoms when using this drug, thus it should not be administered. This medication is intended for the treatment of certain bacterial infections and should be used only when there are no alternative treatment options. In elderly patients, those with impaired renal function, transplant recipients, and those using corticosteroids, the risk of tendon rupture is increased, so co-administration should be avoided. Individuals with a history of allergy to this medication or similar drugs, pregnant or lactating women, adolescents under 18 years, and patients with epilepsy should not use this medication. There may be an increased risk of side effects when co-administered with certain drugs, so patients should discuss any current medications with healthcare professionals. This medication can cause various side effects, including liver function abnormalities, gastrointestinal disturbances, skin rash, and neurological symptoms, so patients should consult a doctor immediately if any abnormal symptoms occur. Photosensitivity reactions may occur, so exposure to strong sunlight or artificial UV light should be avoided, and use should be discontinued if symptoms arise. Diabetic patients should carefully monitor their blood sugar levels as this medication may affect blood sugar control. Caution is advised when driving or operating machinery, especially when taken with alcohol as it can be dangerous. Overdosage may result in renal damage; thus, the dosage should be followed as prescribed by a physician. This medication has not been established as safe for use in children and growing adolescents.

Serious side effects

Hives, severe swelling, chest tightness, difficulty breathing, cold sweats, paleness, severe rash with fever, blisters, skin peeling, pain in the mucous membranes of the mouth/eyes, shortness of breath or difficulty breathing, asthmatic attacks, respiratory distress accompanied by cough and fever, yellowing of the skin or eyes (jaundice), extreme lethargy, sudden and severe headaches, thunderclap headaches, seizures, altered consciousness, vision abnormalities, paralysis, decreased urination.

Mild side effects

Fungal superinfection, thrombocytosis, thrombocytopenia, anemia, leukopenia, leukocytosis, eosinophilia, neutropenia, thrombotic venous inflammation, syndrome of inappropriate antidiuretic hormone secretion, decreased appetite and reduced food intake, increased serum alkaline phosphatase, hyperglycemia, hypoglycemia, increased lipase, abnormal prothrombin levels, increased amylase, psychomotor agitation/nervousness, confusion, disorientation, emotional instability, abnormal.

Store this medication in a tightly closed container to prevent air exposure, preferably at room temperature between 1°C and 30°C. This will help maintain the effectiveness of the medicine for an extended period.

Appearance

White round film-coated tablets

Package unit

30 tablets/bottle, 100 tablets/bottle