Padoxime (Cefpodoxime Proxetil)

Adult dose

○ Adults: Administer cefpodoxime 100mg (potency) orally twice daily after meals. If the infection is severe or the response is considered inadequate, administer 200mg (potency) orally twice daily after meals. Adjust the dose appropriately according to age, symptoms, etc.

This drug should not be used in patients who have experienced severe allergic reactions or shock due to this medication. This medication contains lactose monohydrate, therefore it should not be administered to patients with galactose intolerance or specific genetic metabolic disorders. Patients who have previously shown allergic reactions to this medication or similar antibiotics should avoid use except in special circumstances, and if necessary, it should be administered with great caution. Patients allergic to penicillin antibiotics or those with a family history of asthma or allergic symptoms must consult a physician before use. Patients with severely impaired kidney function may require dosage adjustments and caution as the excretion of this medication may be delayed. Patients who are unable to take orally, elderly individuals, or those in poor general condition should be closely monitored for the risk of bleeding due to vitamin K deficiency during treatment. This medication may rarely cause severe allergic reactions, skin rashes, gastrointestinal disturbances, respiratory problems, hematological abnormalities, neurological issues, or liver and kidney dysfunction. If symptoms occur, discontinue use immediately and consult healthcare personnel. During treatment, susceptibility testing should be conducted to prevent the emergence of resistant strains, and it should be used for the minimum necessary duration only. Caution is required as dizziness may occur when driving or operating machinery. If taken for more than 10 days, it is advisable to perform blood tests to check white blood cell counts. In cases of poor kidney function, dosage adjustments are required, and if seizures occur, administration should be stopped immediately. As severe skin adverse reactions have been reported, skin condition should be closely monitored, and discontinuation is necessary if any abnormal symptoms arise. This drug may put a strain on the kidneys when used with certain diuretics or other antibiotics, so caution is advised during concomitant administration. Additionally, the blood concentration of this medication may change when taken with specific drugs, so consult a physician or pharmacist. Safety during pregnancy has not been established; cautious use is advised only when necessary, and it is recommended to discontinue breastfeeding if nursing. Safety in children, particularly neonates or premature infants, has not been sufficiently confirmed, so caution is required for use. Elderly patients may have an increased risk of side effects due to decreased bodily function, so dosage and intervals must be adjusted while closely monitoring their condition. Finally, this medication may affect the results of some clinical tests; it is important to inform the testing personnel when undergoing examinations.

shock

Store this medication in a tightly closed container to avoid exposure to air or moisture, and it is best to keep it at a temperature between 1 to 30 degrees Celsius. Proper temperature and environment for storage will help maintain the effectiveness of the medication.

Appearance

White round film-coated tablet

Package unit

30 tablets/bottle, 200 tablets/bottle