Nuclera Capsule (Cefaclor Hydrate)

Adult dose

As cefaclor hydrate, 250mg (potency) should be administered orally every 8 hours. In the case of severe infections (such as pneumonia) and low susceptibility infections, it may be increased to double the dose. For acute gonococcal urethritis, administer this drug 3g with probenecid 1g in a single dose.

Child dose

Administer 20mg (potency) per kg of body weight divided every 8 hours. In cases of severe infections, otitis media, and low susceptibility infections, a dose of 40mg (potency) per kg of body weight may be administered, with a maximum dose of

This drug is an antibiotic that kills specific bacteria by interfering with cell wall synthesis to treat infections. Before using this drug, it is essential to inform if there has been a history of severe allergic reactions or shock from this medicine or similar classes of antibiotics. Patients with atopy or those who frequently experience symptoms such as bronchial asthma, rashes, or hives should use this medication with caution. Patients with severely impaired renal function need dosage adjustments and regular checks while using this drug, and should report to healthcare providers if symptoms worsen. Patients with gastrointestinal diseases should be carefully monitored as symptoms like colitis may particularly occur. This medication can rarely exhibit severe allergic reactions, skin diseases, blood abnormalities, liver or kidney dysfunction, digestive issues, or central nervous system disorders, so it should be discontinued immediately if symptoms occur and medical assistance must be sought. It is important to administer only for the minimum necessary period after confirming the bacterial sensitivity to prevent antibiotic resistance. Discuss with healthcare providers if taking other medications that may interact, especially those affecting the kidneys, anticoagulants, or oral contraceptives. Pregnant or breastfeeding women should only take this medication with caution if necessary, and monitor the effects on the baby while breastfeeding. It should be avoided in neonates under one month of age as safety has not been established. Elderly patients may experience side effects more easily due to decreased bodily functions, hence careful monitoring of dosage and intervals is advised. It is essential to inform healthcare providers during testing as this medication may influence certain test results.

Serious side effects

Hives, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, paleness, severe allergic reactions, high fever with severe rash, blisters, skin desquamation, pain in mucous membranes of mouth/eyes, severe skin reactions, shortness of breath or difficulty breathing, asthma attacks, respiratory problems accompanied by cough and fever, jaundice (yellowing of skin or eyes), profound lethargy, liver dysfunction (jaundice), sudden and very severe

Mild side effects

• Generalized flushing
• edema
• vascular edema
• sensory disturbances
• syncope
• hypertension
• vasodilation
• rash
• itching
• fever

This medication is sensitive to light, so it should be stored in a dark place, and the temperature should be maintained between 1 and 30 degrees Celsius at room temperature for safe storage. Storage in this manner can help maintain the drug's efficacy.

Appearance

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

Package unit

30 capsules/bottle, 100 capsules/bottle