Viewing nowAnticler Capsule (Cefaclor Hydrate)
Cefaclor Hydrate 250mg
Hard capsule · Prescription medication
Medix Pharmaceutical Co., Ltd.

MFDS item code 201400342 · Approved 2014.01.24 · Insurance code 625800030
Treatment of otitis media, respiratory infections (such as pneumonia, pharyngitis) and urinary tract infections (such as pyelonephritis, cystitis).
This medication is effective against various bacterial infections including Streptococcus pneumoniae, Haemophilus influenzae, and Staphylococcus. It is mainly used for respiratory infections such as otitis media, pneumonia, pharyngitis, tonsillitis, and bronchitis. It is also effective against urinary tract infections such as pyelonephritis, cystitis, and gonococcal urethritis. It is utilized in the treatment of skin infections including furuncles, carbuncles, folliculitis, soft tissue infections, infectious granulomas, subcutaneous abscesses, infected wounds. This medication is used for improving various types of bacterial infections.
For cefaclor hydrate, administer 250mg (potency) every 8 hours orally. In cases of severe infections (such as pneumonia) or infections with low susceptibility, the dosage may be doubled. For acute gonococcal urethritis, administer 3g of this medication with 1g of probenecid in a single dose.
Administer 20mg/kg (potency) every 8 hours. In cases of severe infections, otitis media, or infections with low susceptibility, a dose of up to 40mg/kg (potency) can be administered per day, with a maximum dosage of
This medication is an antibiotic that works by disrupting the synthesis of the bacterial cell wall to kill bacteria. This medication should not be administered to patients who have previously experienced severe allergic reactions or shock due to this drug or cephalosporin antibiotics. Those allergic to penicillin drugs or with a history of asthma, rash, or urticaria should use this medication with caution. Patients with very poor kidney function, those unable to take medication orally, elderly patients, and those in poor overall condition should be carefully monitored for signs of vitamin K deficiency. Patients with a history of gastrointestinal disease, especially colitis, should also be cautious when using this medication. This medication can rarely cause severe shock or hypersensitivity reactions such as anaphylaxis; if symptoms occur during use, the medication should be stopped immediately and appropriate treatment should be obtained. Severe rashes on the skin or serious skin reactions such as Stevens-Johnson syndrome may appear, so the condition of the skin should be carefully monitored. Check regularly for blood-related abnormalities such as leukopenia, anemia, and thrombocytopenia through blood tests. Liver dysfunction or decreased kidney function can occur, therefore, liver and kidney conditions should be checked periodically, and if abnormalities are found, the use of the drug should be stopped. In the gastrointestinal system, symptoms such as diarrhea, vomiting, and abdominal pain may appear, and especially if severe colitis develops, the medication should be stopped immediately. Respiratory effects can occur, so if fever, cough, or difficulty breathing is present, the medication should be discontinued and treated. Central nervous system symptoms such as anxiety, agitation, dizziness, drowsiness, and hallucinations can rarely occur, and any such symptoms should be reported. Using this medication can lead to phenomena such as oral inflammation or candidiasis due to bacterial overgrowth. Rarely, bleeding tendencies due to vitamin K deficiency or deficiency symptoms of vitamin B group may occur, so caution is required. This medication may interact with other drugs, so particularly when used with probenecid, drugs affecting the kidneys, anticoagulants, or oral contraceptives, consult a specialist and monitor carefully. Pregnant women or those who could become pregnant should carefully weigh the benefits and risks before using this medication, and nursing mothers should be cautious as the drug can be transferred to breast milk in small amounts. Safety and efficacy in newborns less than 1 month old have not been established, so usage is not recommended. Elderly patients may experience adverse reactions more easily due to decreased physiological functions, so dosage adjustments and monitoring are necessary. When using this medication, administer only for the minimum duration necessary to prevent the development of bacterial resistance, and it is advisable to conduct susceptibility testing before treatment. Also, while using this medication, some test results in clinical examinations may show false positives, so caution is needed in interpreting the results.
Not everyone experiences these, and they can vary from person to person.
This medication is sensitive to light and should be stored in a container that blocks light. Additionally, it is important to maintain a room temperature, specifically between 1 degree and 30 degrees, when storing this medication. Proper storage helps ensure the medication's efficacy is maintained safely.
A hard capsule with upper blue opaque and lower white opaque, filled with a light yellow powder.
30 capsules/bottle, 100 capsules/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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Medix Pharmaceutical Co., Ltd.

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Hard capsule · Prescription medication
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Syrup · Prescription medication
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Syrup · Prescription medication
Shinpoong Pharmaceutical Co., Ltd.
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.