Viewing nowJinse tyl tablet (Cefuroxime axetil)
Cefuroxime Axetil 300.72mg
Tablet · Prescription medication
Medica Korea Co., Ltd.

MFDS item code 201603127 · Approved 2016.05.31 · Insurance code 646004230
Treatment of respiratory and genitourinary infections (e.g., gonorrhea), skin and soft tissue infections, and early Lyme disease
Cefuroxime is a broad-spectrum antibiotic effective against various bacteria, used to treat upper respiratory infections such as otitis media, sinusitis, tonsillitis, and pharyngitis. It is also effective for lower respiratory infections such as acute and chronic bronchitis and pneumonia. It treats urinary tract infections like pyelonephritis, cystitis, and urethritis, and is used for skin and soft tissue infections such as furunculosis, pyoderma, and impetigo. It is effective in the treatment of gonorrhea and uncomplicated acute gonococcal urethritis and cervicitis, and is beneficial in the initial treatment of Lyme disease. This medicine is stable against beta-lactamase resistant strains, effectively treating infections. Therefore, cefuroxime is a very useful drug for the treatment of various bacterial infections.
For optimal absorption, take after meals. Adults and children 12 years of age or older Most infections: 250mg per dose, 2 times daily. Severe lower respiratory tract infections, pneumonia, severe infections, or suspected infections caused by less susceptible organisms: 500mg per dose, 2 times daily. Urinary tract infections: 250mg per dose, 2 times daily. Uncomplicated gonorrhea: 1g as a single dose. Lyme disease: 500mg per dose, 2 times daily for 14 days (10~21 days). For the treatment of infections caused by Streptococcus pyogenes (Group A beta-hemolytic), this medicine should be administered for 7~10 days. Patients with renal impairment Cefuroxime is primarily excreted by the kidneys. To compensate for delayed excretion in patients with significantly impaired renal function, reducing the dose of cefuroxime as follows is recommended. Creatinine clearance ≥ 30 mL/min/1.73m2, T1/2 (hours) 1.4 - 2.4: No dose adjustment necessary (standard dose: 125mg-500mg per dose, 2 times daily) Creatinine clearance 10 - 29 mL/min/1.73m2, T1/2 (hours) 4.6: Administer the standard single dose every 24 hours Creatinine clearance < 10 mL/min/1.73m2, T1/2 (hours) 16.8: Administer the standard single dose every 48 hours Patients on hemodialysis, T1/2 (hours) 2 - 4: Administer an additional standard single dose at the end of each dialysis session
Infants and children under 12 years of age, most infections: 125mg per dose, 2 times daily. Otitis media in children 2 years of age or older, and severe infections: 250mg per dose, 2 times daily. Infants and children under 12 years of age, Lyme disease: 250mg per dose, 2 times daily for 14 days (10~21 days). There is insufficient experience with use in infants under 3 months of age. This medicine should not be divided and is therefore not appropriate for treating patients who cannot swallow tablets, such as young infants and children.
This medicine is a cephalosporin antibiotic and should never be administered to patients with known allergies to this class. Caution should be exercised in patients with a history of hypersensitivity reactions to penicillins or other beta-lactam antibiotics, those with allergic tendencies, patients with severely impaired renal function, and those who may have difficulty taking oral medications or are elderly. Mild side effects such as headache, dizziness, diarrhea, nausea, and skin rash may occur during the course of treatment, and serious allergic reactions, hepatitis, renal function abnormalities, and severe skin disorders may occur infrequently, thus careful monitoring is necessary. When using antibiotics, it is important to check the susceptibility of the infectious bacteria to prevent the development of resistant strains, and to use the medication for the necessary duration only. This medication may cause dizziness, so caution is advised when driving or operating machinery. Additionally, co-administration with other diuretics or certain antibiotics may impact renal function, so prudence is required in such cases. The use of this medicine in pregnant or breastfeeding women should be carefully determined, and caution is necessary as the drug may be passed to the baby during breastfeeding. Safety has not been established for infants under 3 months; for young children, it is recommended to use a dry syrup formulation due to the bitter taste. In the elderly, side effects may occur more readily due to decreased bodily functions, so dose adjustments and monitoring of conditions are necessary. This medicine may affect the results of certain clinical tests, so inform healthcare providers during testing. In cases of overdose, neurological anomalies such as seizures may occur, and immediate contact with a medical institution is required. Lastly, this medicine should be stored out of reach of children and sealed well in its original container.
Not everyone experiences these, and they can vary from person to person.
This medicine should be stored in a sealed container to prevent air exposure, and it is advisable to keep the temperature below 25 degrees Celsius. Storing in this manner helps to maintain the medicine's effectiveness and prevent deterioration.
This medicine is a white to off-white rectangular film-coated tablet.
100 tablets/box [(10 tablets/PTP) × 10]
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.