Noroxin (generic name: Norfloxacin; brand names include: Norfloxacine / Apo-Norflox / Norflohexal / Roxin / Utinor) belongs to a group of medicines called fluoroquinolone antibiotics.
Noroxin is used to treat various bacterial infections, including urinary tract infections, cystitis, and some STDs such as urethral and cervical gonorrhea.
Ask your health care provider any questions you may have about how to use Noroxin. confusion, hallucinations, tremors, feeling restless or anxious, unusual thoughts or behavior, feeling light-headed; The following additional adverse reactions have been reported since the drug was marketed: This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA. sudden pain, snapping or popping sound, bruising,... Do not take any products containing magnesium, aluminum, calcium, iron, or zinc (eg, antacids, quinapril, vitamins/minerals); didanosine; sucralfate; or bismuth subsalicylate within 2 hours before or 2 hours after taking Noroxin. Hypersensitivity reactions have been reported including anaphylactoid reactions, angioedema, dyspnea, vasculitis, urticaria, arthritis, arthralgia and myalgia (see WARNINGS). Noroxin is used for: clomid jumeaux pourcentage
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Lab tests, including complete blood cell counts and liver and kidney function, may be performed while you use Noroxin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments. Hepatic failure, including fatal cases. Other adverse events reported with quinolones include: agranulocytosis, albuminuria, candiduria, crystalluria, cylindruria, dysphagia, elevation of blood glucose, elevation of serum cholesterol, elevation of serum potassium, elevation of serum triglycerides, hematuria, hepatic necrosis, symptomatic hypoglycemia, nystagmus, postural hypotension, prolongation of prothrombin time, and vaginal candidiasis. Store Noroxin at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Do not freeze. Keep Noroxin out of the reach of children and away from pets. Seek medical attention right away if any of these SEVERE side effects occur:
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Diminished urinary excretion of norfloxacin has been reported during the concomitant administration of probenecid and norfloxacin. PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of taking Noroxin while you are pregnant. It is not known if Noroxin is found in breast milk. Do not breast-feed while taking Noroxin. Special Senses Toxic epidermal necrolysis, Stevens-Johnson syndrome and erythema multiforme, exfoliative dermatitis, photosensitivity/phototoxicity reactions (see PRECAUTIONS), leukocytoclastic vasculitis. If OVERDOSE is suspected: Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen) because the risk of side effects, such as seizures, may be increased Drinking extra fluids while you are taking Noroxin is recommended. Check with your doctor for instructions.
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Use Noroxin with caution in the ELDERLY; they may be more sensitive to its effects (eg, tendon problems), especially if they take corticosteroids (eg, prednisone). They may also be more sensitive to other effects (eg, irregular heartbeat). Store Noroxin at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Do not freeze. Keep Noroxin out of the reach of children and away from pets. Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficult breathing; swelling of your face, lips, tongue, or throat.
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Hypersensitivity reactions have been reported including anaphylactoid reactions, angioedema, dyspnea, vasculitis, urticaria, arthritis, arthralgia and myalgia (see WARNINGS). DOSAGE AND ADMINISTRATION Renal Impairment Renal Hepatic failure, including fatal cases. Neutropenia; leukopenia; agranulocytosis; hemolytic anemia, sometimes associated with glucose-6phosphate dehydrogenase deficiency; thrombocytopenia. The following additional adverse reactions have been reported since the drug was marketed:
July 24 2025 01:46:13
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