Boryung Ceftriaxone Injection 0.5 grams (Ceftriaxone Sodium Hydrate)
Ceftriaxone Sodium Hydrate 0.5g
Prescription medication
(Boryung)
MFDS item code 199201089 · Notified 1992.10.16 · Insurance code 641901351
Treatment of infections in the respiratory system (pneumonia, bronchitis) and the reproductive system (gonorrhea)
This medication is effective against a variety of bacteria and is used to treat respiratory infections such as pneumonia and bronchitis. It is also effective for ENT infections such as otitis media, kidney and urinary tract infections, and genital infections such as gonorrhea. It helps prevent sepsis and infections before and after surgery, and is applicable for bone or joint infections, as well as skin and wound infections. Additionally, it is employed in the treatment of gastrointestinal infections like peritonitis, cholecystitis, and cholangitis, as well as infections in immunocompromised patients and meningitis. It is a drug that supports the recovery of patients from extensive bacterial infections.
For adults and children over 12 years, administer 1-2g (potency) of ceftriaxone once daily via intravenous or intramuscular injection. For infections caused by pathogens showing severe or moderate susceptibility, the dose may be increased up to 4g (potency) once daily. Elderly patients follow the adult dosing regimen without the need for changes. In the treatment of gonorrhea, a single intramuscular injection of 250mg (potency) is recommended. Pre- and post-operative infections...
For newborns (within 14 days of birth), administer 20-50mg/kg (potency) once daily, not exceeding 50mg (potency). For infants and children (15 days to 12 years), administer 20mg/kg.
This medication should not be mixed with solutions or drugs containing calcium, and co-administration can be risky. In particular, it must not be used in newborns under 28 days of age when given with calcium, as precipitation may occur leading to potentially fatal problems. It should not be administered to patients with a history of allergies to this drug or to cephalosporins or penicillins, and it may pose risks to premature infants or newborns with jaundice, hypoalbuminemia, or acidosis. Patients with a history of allergic reactions, those with asthma or a tendency to develop skin rashes, and those with severe kidney dysfunction should exercise special caution when using this medication. Furthermore, elderly patients or those in poor health who have difficulty taking by mouth may show signs of vitamin K deficiency, so blood tests should be conducted to monitor their condition, and vitamin K should be given if necessary. This drug may cause a variety of side effects, including eosinophilia, leukopenia, thrombocytopenia, diarrhea, rash, and liver function abnormalities, so the patient's condition should be closely monitored during administration. If severe allergic reactions or shock symptoms occur, administration should be stopped immediately and emergency treatment sought. Additionally, long-term use or high-dose administration may lead to precipitation in the gallbladder, and kidney damage could occur in patients with compromised kidney function, necessitating regular check-ups. This drug may impact kidney function when used with other cephalosporin antibiotics, certain diuretics, or aminoglycoside antibiotics, so caution is needed when combining treatments. Calcium should especially not be co-administered due to serious interactions. Women who are pregnant or breastfeeding should carefully consider the risks and benefits of using this drug, and it is safer not to administer it to newborns or premature infants to mitigate the risk of bilirubin encephalopathy. Elderly patients may experience side effects more readily due to decreased bodily function and should be closely monitored with adjustments to dosage and administration intervals. During administration, pain, inflammation, or thrombophlebitis at the injection site may occur, requiring careful management of injection methods and speeds, and the prepared solution should be used as soon as possible while adhering to proper storage conditions. Finally, if diarrhea or abdominal pain worsens while using this medication, consider the possibility of a Clostridium difficile infection and notify medical personnel immediately.
Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweats, pallor, severe rash with high fever, blisters, skin sloughing, pain in mucous membranes of mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, cough with fever and respiratory abnormalities, jaundice (yellowing of the skin or eyes), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, confusion, vision abnormalities, paralysis, urinary retention.
Not everyone experiences these, and they can vary from person to person.
This medication should be stored at room temperature in a sealed container to prevent air from entering. This will help maintain the drug's effectiveness for a longer period.
A colorless vial filled with a white to pale yellow 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.