New Pacler Capsule (Cefaclor Hydrate)

Adult dose

As cefaclor hydrate, take 250mg (potency) orally every 8 hours. In cases of severe infections (such as pneumonia) and infections with low sensibility, dosages can be increased to twice the normal. In acute gonococcal urethritis, this drug 3g should be administered in a one-time combination with probenecid 1g.

Child dose

Administer 20mg (potency) per kg of body weight once daily, divided every 8 hours. In cases of severe infections, otitis media, and infections with low sensibility, doses of up to 40mg (potency) per kg of body weight can be administered, with a maximum dose of.

This drug is an antibiotic that kills bacteria by binding to certain proteins and disrupting the synthesis of bacterial cell walls. Patients who have experienced severe allergic reactions or shock from this drug in the past should not use it. It is also safe to avoid administering this drug to patients who have an allergy to this drug or to similar classes of antibiotics. Patients with a history of allergy to penicillin antibiotics, those with allergic tendencies, patients with severely impaired kidney function, patients who have difficulty swallowing, elderly patients, and those with a history of gastrointestinal disease should use this drug with special caution. This drug can rarely cause shock or severe allergic reactions, so symptoms should be closely monitored during administration, and if abnormal symptoms appear, treatment should be discontinued immediately and appropriate care should be sought. There can be severe skin reactions, blood abnormalities, liver or kidney dysfunctions, and gastrointestinal problems, so it is important to regularly check the condition. This drug may interact with other medications; patients taking medications that affect the kidneys, anticoagulants, or oral contraceptives should inform healthcare providers. Women who are pregnant or breastfeeding should use this drug cautiously, as its safety has not been fully established, and careful attention is also necessary while breastfeeding. It is recommended to avoid using this drug in infants less than one month old, as its safety has not been confirmed. Elderly patients may experience adverse reactions more easily due to weakened body functions, so monitoring should be done carefully with adjustments in dosage and administration intervals. This drug can affect the results of some tests, so it is necessary to inform healthcare providers during examinations. It is recommended to administer this drug only for the appropriate duration to prevent the emergence of bacterial resistance. Before taking this drug, it is essential to consult with healthcare providers regarding past medical history and currently used medications to ensure safe usage.

Serious side effects

Urticaria, severe swelling (edema), difficulty breathing, rash, blistering, skin peeling, mucosal pain in the mouth/eyes, Stevens-Johnson syndrome, toxic epidermal necrolysis, liver dysfunction (jaundice), sudden and severe headache, seizures, confusion, visual disturbances, paralysis, markedly reduced urine output, severe generalized edema with accompanying hypertension, shock, anaphylactic symptoms, interstitial pneumonia, eosinophilic pulmonary infiltration, acute renal failure, severe.

Mild side effects

• Rash
• urticaria
• erythema
• itching
• fever
• lymphadenopathy
• arthralgia
• serum sickness-like reactions
• nausea
• vomiting

This drug may be sensitive to air or moisture, so it should be stored in a sealed container. It is best to maintain a storage temperature between 1 degree and 30 degrees Celsius at room temperature. This will help maintain the drug's effectiveness and prevent deterioration.

Appearance

A capsule with a light yellow powder, with a purple upper part and a white lower part.

Package unit

30 capsules, 300 capsules