Sepicap (Cefixime Trihydrate)

Adult dose

(Capsules) Adults: Administer 50～100mg (potency) of cefixime orally twice daily. For severe cases or an inadequate response, administer 200mg (potency) per dose twice daily. Adjust the dose appropriately according to age and symptoms.

Child dose

(Capsules) Children weighing 30 Kg or more: Administer 50～100mg (potency) of cefixime orally twice daily. For severe cases or an inadequate response, administer 200mg (potency) per dose twice daily. (Powder) Children: Administer 1.5～3mg (potency) of cefixime per Kg of body weight per dose orally twice daily. For severe cases or an inadequate response, administer 6mg (potency) per Kg of body weight per dose twice daily. Adjust the dose appropriately according to age and symptoms.

This medication should not be administered to certain patients under any circumstances. For example, patients who have previously experienced severe allergic reactions or shock due to this medication, patients allergic to cephalosporin antibiotics, and patients with genetic lactose intolerance should not use this medication. Additionally, there are patients for whom caution is required when administering this medication. Patients who have previously shown allergic reactions to this medication or similar types, patients allergic to penicillin antibiotics, individuals with allergic constitutions, patients with severely impaired kidney function, or patients who have difficulty with oral intake, as well as the elderly, should use this medication carefully. This medication contains a dye called Yellow No. 5, so caution is also needed for those who are allergic to this ingredient. During treatment, there is a rare possibility of severe allergic reactions or dangerous symptoms such as shock; if symptoms such as discomfort, dizziness, breathing difficulties, or rash occur, discontinue the medication immediately and seek medical help. Furthermore, gastrointestinal symptoms such as diarrhea, abdominal pain, or vomiting may occur, and if severe diarrhea or blood in stool is observed, immediate treatment is required. Additionally, liver or kidney function may be affected, necessitating regular examinations, and if a severe rash or blisters occur on the skin, use should be stopped immediately. This medication may increase the risk of bleeding when taken with anticoagulants like warfarin, so caution is necessary. Also, when used with other nephrotoxic medications, kidney function should be monitored closely. Pregnant women or those who might become pregnant should consult a doctor because the safety of this medication is not assured; it should only be taken when the benefit outweighs the risk. During breastfeeding, it is advisable to avoid breastfeeding while taking this medication. It is preferable not to use this medication in neonates or infants under 6 months as safety has not been established. The elderly may experience more side effects due to decreased bodily functions, so dosages and intervals should be adjusted and monitored carefully. When taking this medication, some urine tests may yield false results; therefore, inform healthcare providers that you are taking this medication. Finally, when using this medication in suspension form, do not store it for more than 2 weeks after preparation, and avoid keeping it mixed in milk or juice for extended periods.

Shock

This medication should be stored in a tightly sealed container to prevent air or moisture from entering. It is also advised to store it at room temperature, between 1 to 30 degrees Celsius, which is not too hot or too cold.

Appearance

A hard capsule with light orange upper and lower parts containing a crystalline powder that is white to light yellow.

Package unit

30 capsules/bottle, 100 capsules/bottle