Cefsepa 1 Gram (Ceftriaxone Sodium Hydrate)
Ceftriaxone Sodium Hydrate 1g
Prescription medication
Dasan Pharmaceutical Co., Ltd.
MFDS item code 201901822 · Notified 2019.03.26 · Insurance code 678601241
Treatment of infections in the respiratory system (pneumonia, bronchitis) and reproductive system (gonorrhea)
This medication is used to treat infections caused by various bacteria. It is particularly effective for respiratory infections such as pneumonia and bronchitis, as well as ENT infections. Additionally, it is used for infections of the kidneys and urinary tract, as well as gonorrhea, and is helpful in treating sepsis. It is also used to prevent infections before and after surgery, in bone and joint infections, and in skin and soft tissue infections. The drug is useful for treating gastrointestinal infections such as peritonitis, cholecystitis, and cholangitis, and is also used for infections and meningitis in patients with impaired immune function. Overall, it is effective in treating a wide range of bacterial infections, aiding in the recovery of patients' health.
Ceftriaxone at a dose of 1 to 2 g administered intravenously or intramuscularly once daily. For severe infections or infections with moderately susceptible pathogens, the dose can be increased up to 4 g once daily. For the treatment of gonorrhea, a single intramuscular injection of 250 mg is recommended. To prevent infections before and after surgery, it is advisable to administer 1 to 2 g once, 30 to 90 minutes prior to the surgery. In patients with kidney and liver dysfunction
For neonates (up to 14 days old), administer 20 to 50 mg per kg of body weight as a single daily dose, without exceeding 50 mg per kg. For infants and children (from 15 days old to 12 years), administer 20 to
This medication should not be mixed or administered simultaneously with solutions or drugs containing calcium. Especially in neonates, if this medication comes into contact with calcium, it may form a precipitate and cause serious side effects, thus it must not be administered. Patients with allergies to this medication or a history of hypersensitivity to cephalosporins or penicillin antibiotics should not use it. Moreover, neonates with issues related to bilirubin binding, such as those with jaundice, hypoalbuminemia, or acidosis, may be at risk if this medication is given. Those with a past history of drug allergies or individuals prone to allergic symptoms such as asthma, rashes, and urticaria should use this drug cautiously. Patients with severely impaired kidney function may have prolonged blood concentration of this medication, necessitating dosage adjustments. Common side effects upon administration may include eosinophilia, leukopenia, thrombocytopenia, diarrhea, rashes, increased liver enzyme levels, and so on. Rarely, severe allergic reactions, pseudomembranous colitis, interstitial pneumonia, severe skin reactions, and acute renal failure may occur, and symptoms should be reported to healthcare professionals immediately. This medication should be used for the prescribed duration only, determined by susceptibility testing to prevent antibiotic-resistant bacteria, and hypersensitivity should be assessed before administration. During treatment, regular monitoring of liver function, kidney function, and blood tests is essential. There is no specific antidote for overdose, so symptomatic treatment is needed, and if dizziness or similar symptoms occur during the course of treatment, driving or operating machinery should be avoided. Pregnant or nursing individuals should use this medication with caution due to uncertainty regarding its safety, and it should not be administered to neonates or premature infants due to the risk of bilirubin encephalopathy. This medication may interact with other drugs; therefore, special caution is warranted, especially when used with diuretics, aminoglycoside antibiotics, or vitamin K antagonists. It should always be administered separately from calcium-containing solutions and must not share the same injection port.
Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in oral/ocular mucosa, breathlessness or difficulty breathing, asthma attacks, respiratory abnormalities with cough and fever, jaundice (yellowing of skin or eyes), extreme lethargy, sudden and severe headaches, thunderclap headaches, seizures, confusion, visual disturbances, paralysis, urination abnormalities
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a sealed container to prevent air or moisture exposure, and it is preferably kept at room temperature between 1 to 30 degrees Celsius. Proper storage helps maintain the efficacy of the medication for a longer period.
A colorless and transparent vial filled with a white to light yellow crystalline powder.
10 vials
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.