Bainex Cefaclor Capsule (Cefaclor Hydrate)

Adult dose

As cefaclor hydrate, administer 250 mg (potency) orally every 8 hours. For severe infections (such as pneumonia) and infections with low susceptibility, the dose can be doubled. In cases of acute gonococcal urethritis, this drug can be co-administered with 3 g of probenecid in a single dose.

Child dose

Administer 20 mg/kg (potency) every 8 hours by dividing the dose. For severe infections, otitis media, and infections with low susceptibility, the dosage can be increased to 40 mg/kg (potency) daily, with a maximum dose of

This drug works by binding to specific proteins and disrupting bacterial cell wall synthesis, killing the bacteria. Patients who have experienced severe allergic reactions or shock due to this drug should not use it. Patients allergic to this drug or similar classes of antibiotics should also refrain from administration. Patients with allergies to penicillin antibiotics or those with allergic constitutions, severely impaired kidney function, those who have difficulty with oral intake, the elderly, or those with a history of gastrointestinal disorders should take special care when using this drug. This drug can rarely cause severe allergic reactions, skin rashes, blood abnormalities, liver or kidney function problems, gastrointestinal issues, respiratory problems, neurological symptoms, and if any symptoms arise, patients should consult medical personnel immediately. Particularly, if there are severe rashes on the skin or mucosal damage, administration should be stopped immediately and appropriate treatment should be sought. During the use of this drug, it is advisable to carry out sensitivity testing to prevent the occurrence of resistant bacteria and only administer it for the minimum necessary duration. There may be interactions when used with other medications, so patients taking medications that affect the kidneys, anticoagulants, or oral contraceptives should inform their healthcare provider. Pregnant women or those who may become pregnant should use this drug only if its benefits outweigh the risks, as its safety during pregnancy has not been established. Lactating women should also use this drug carefully, as a small amount can be transmitted through breast milk, and the effects on the infant should be monitored. The safety and efficacy of this medication have not been established in infants under one month old. Elderly patients may experience adverse reactions more easily due to decreased bodily functions, and there is a risk of bleeding associated with vitamin K deficiency, so careful monitoring of dosage and intervals is essential. This drug may cause false positive results in urine tests, so caution is needed when interpreting test results.

Serious side effects

• Hives
• shock
• anaphylactic symptoms
• Stevens-Johnson syndrome
• toxic epidermal necrolysis
• agranulocytosis
• granulocytopenia
• pancytopenia
• anemia
• thrombocytopenia

Mild side effects

Rash, erythema, itching, fever, lymphadenopathy, arthralgia, serum sickness-like reactions, anaphylactic symptoms (generalized flushing, swelling, angioedema, sensory disturbances, fainting, hypertension, vasodilation), nausea, vomiting, diarrhea, abdominal pain, gastrointestinal discomfort, heartburn, loss of appetite, headache, genital itching, vaginitis, vulvovaginal candidiasis, accidental injuries, anxiety, arthralgia, asthma, bronchitis, chest pain, chills, congestive heart failure, conjunctivitis

This drug should be stored in a tightly closed container to prevent air and moisture from entering. It is important to maintain storage temperatures between 1 and 30 degrees Celsius to preserve the effectiveness of the medication.

Appearance

A hard capsule with purple upper and white lower parts containing a light yellow powder

Package unit

30 capsules/bottle, 300 capsules/bottle