Cephunig Dry Syrup (Cefpodoxime Proxetil)

Adult dose

For cases deemed severe or where effects are insufficient, the dose is 4.5 mg (potency) per kg of body weight per dose, administered orally 3 times daily. Adjust appropriately according to age and symptoms.

Child dose

○ Infants and children: Suspend before use and administer orally as cefpodoxime at a dose of 3mg (potency) per kg of body weight 2~3 times daily. For severe cases or cases considered to have an insufficient response, administer orally at a dose of 4.5mg (potency) per kg of body weight 3 times daily. Adjust the dose as appropriate according to age, symptoms, etc.

This medication contains the artificial sweetener aspartame, which is broken down in the body into phenylalanine. Therefore, patients with phenylketonuria, a hereditary condition that requires restricting phenylalanine intake, should not take this medication. Before using this medication, be sure to inform whether you have ever experienced severe allergic reactions or shock due to this medication. Additionally, this medication contains lactose, so patients with genetic conditions such as galactose intolerance, lactose deficiency, or glucose-galactose malabsorption should not be given this medication. Patients with a history of allergic reactions to this medication or other cephalosporin antibiotics should generally avoid using this medication, but if necessary, it should be administered with extreme caution. If you have an allergy to penicillin antibiotics or if there is a family history of easy allergic symptoms such as asthma, skin rashes, or hives, you must inform before administration. Patients with severe kidney impairment may experience delayed excretion of this medication, thus requiring careful monitoring and dosage adjustments. Patients who cannot take medication orally, patients receiving non-oral nutrition, elderly patients, and those with poor general health should be closely monitored as they may exhibit symptoms of vitamin K deficiency. This medication can rarely cause serious allergic reactions such as shock or anaphylaxis; therefore, if symptoms such as discomfort, oral abnormalities, shortness of breath, dizziness, or sweating occur, discontinue use immediately and consult a healthcare professional. If allergic symptoms such as rash, hives, itching, fever, or joint pain occur, discontinue use and seek appropriate treatment. If symptoms of abdominal pain, diarrhea, or bloody stools appear, discontinue use immediately and consult a doctor. If symptoms such as shortness of breath, cough, or fever occur, it may indicate pulmonary side effects, so notify a healthcare professional promptly. Blood tests may indicate abnormalities in white blood cell and platelet counts, thus regular tests are necessary during long-term use. Neurological symptoms such as impaired perception or seizures may occur; hence dosage adjustment is critical, especially for those with reduced kidney function. If severe rashes or blisters appear on the skin, discontinue use immediately. Liver function anomalies may occur, so it is advisable to conduct regular liver function tests. Kidney function anomalies may occur, and regular kidney function tests are necessary; discontinue use if abnormalities are detected. Be cautious as infections such as oral inflammation or candidiasis may occur. Symptoms related to bleeding tendencies from vitamin K deficiency or symptoms of vitamin B complex deficiency should be monitored closely. Rare symptoms such as headaches, swelling, and weakness may occur. To prevent resistance, this medication should ideally only be administered for the minimally required duration based on susceptibility tests. It is desirable to conduct sufficient inquiries and skin reaction tests to prevent shock reactions. Dizziness may occur during use, so caution is advised while driving or operating machinery. If prolonged use lasts more than 10 days, blood tests to check white blood cell counts are important. Caution is needed in patients with reduced kidney function where failure to adjust dosages can lead to seizures. This medication increases the risk of kidney dysfunction when used alongside certain diuretics or aminoglycoside antibiotics, therefore it should be administered cautiously. Concurrent use with probenecid may elevate the serum concentration of this medication, thus caution is advised. When taken with drugs affecting gastric acidity, the efficacy of this medication may vary; ensure to inform about concomitant medications. Safety during pregnancy has not been established, hence pregnant women or women of childbearing potential should only use this medication cautiously when necessary. This medication may pass into breast milk, therefore breastfeeding women are advised to suspend breastfeeding. Safety for use in neonates, premature infants, and infants under 2 months has not been established, so caution is advised. Elderly patients may experience increased adverse reactions due to reduced physiological functions, therefore careful adjustment of dosages and intervals is necessary. This medication may affect the results of certain clinical tests, so caution is required when interpreting test results.

shock

This medication should be stored in a tightly sealed container to protect it from air and moisture. The recommended storage temperature is preferably at room temperature between 1 and 30 degrees Celsius. Proper storage will help maintain its efficacy and safety.

Appearance

Pale pink to pale purple granules

Package unit

200 milliliters per bottle