Sera Capsule (Cefaclor Hydrate)

Adult dose

For cefaclor hydrate, administer 250mg (potency) orally every 8 hours. In cases of severe infections (such as pneumonia) and infections with low susceptibility, the dosage may be doubled. In acute gonococcal urethritis, a single dose of this medication 3g together with probenecid 1g should be administered.

Child dose

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

This drug is an antibiotic that kills specific bacteria. Individuals who have experienced severe allergic reactions or shock from this drug should not use it. Also, it should not be administered to those allergic to this drug or similar classes of medication. Special caution is necessary for individuals allergic to penicillin antibiotics, those with a history of allergies, and those with severely impaired kidney function. Elderly individuals who have difficulty swallowing orally or have poor nutritional status also require caution, as there is a risk of bleeding due to vitamin K deficiency. People with a past history of gastrointestinal diseases, especially colitis, should be administered this drug carefully. While taking this medication, rare instances of shock, severe allergic reactions, skin rashes, blood abnormalities, liver or kidney function abnormalities, gastrointestinal issues, respiratory problems, and neurological changes may occur, thus symptoms necessitating immediate discontinuation and consultation with a physician should be observed. To prevent the development of resistant bacteria, it is recommended to verify the sensitivity of the causative bacteria and use it only for the necessary minimum duration. Furthermore, when taking this medication alongside others, potential interactions should be discussed with a physician or pharmacist. Women who are pregnant or may become pregnant should use this medication only when the benefits of treatment outweigh the risks, and breastfeeding women should use it with caution. It is not advisable to use this medication in neonates under one month of age as its safety has not been established. Elderly patients may exhibit more pronounced adverse reactions due to decreased bodily functions, so adjustments in dosage and administration intervals should be made with care. This medication may affect urine or blood test results, so this should be communicated during tests.

Serious side effects

• Shock
• urticaria
• severe swelling (edema)
• dyspnea
• angioedema
• symptoms of anaphylaxis
• Stevens-Johnson syndrome
• toxic epidermal necrolysis
• agranulocytosis
• neutropenia

Mild side effects

General flushing, rash, itching, fever, lymphadenopathy, arthralgia, serum sickness-like reaction, erythema multiforme, arthritis, nausea, vomiting, diarrhea, abdominal pain, discomfort in the upper abdomen, heartburn, loss of appetite, agitation, anxiety, excessive muscle tension, nervousness, insomnia, confusion, dizziness, hallucinations, drowsiness, stomatitis, candidiasis, symptoms of vitamin K deficiency (hypoprothrombinemia, bleeding tendency, etc.), symptoms of vitamin B group deficiency (stomatitis, glossitis, loss of appetite,

This medication should be stored in a tightly sealed container to protect it from air and moisture and kept at room temperature between 1 degree and 30 degrees Celsius. Maintaining proper temperature and container conditions ensures the safe efficacy of the medication.

Appearance

Hard capsule containing a pale yellow powder with a purple upper part and a white lower part

Package unit

Capsule/bottle - 30 capsules/bottle, Capsule/bottle - 300 capsules/bottle