Megapixim Capsule 100 Milligrams (Cefixime Hydrate)

Adult dose

Adults: Administer cefixime 50～100mg (potency) per dose orally twice daily. For severe infections or when the effect is inadequate, administer 200mg (potency) per dose twice daily. Adjust the dose as appropriate according to age and symptoms.

Child dose

Children weighing 30 Kg or more: Cefixime 50～100mg (potency) per dose, taken orally twice daily. For severe cases or when the effect is insufficient, administer 200mg (potency) per dose twice daily.

This medication should not be used in patients who have previously experienced shock due to this drug. Furthermore, individuals with allergies to cephalosporins should not take this medication. Since this medication contains lactose, it should be avoided in patients with genetic conditions such as galactose intolerance or lactase deficiency, or glucose-galactose malabsorption. Patients with a history of allergic reactions to this drug or other cephalosporin antibiotics should use it with caution, and it is recommended to avoid use if possible. Caution is also needed for patients allergic to penicillin antibiotics when using this drug. Individuals with a constitution that is prone to allergy symptoms such as bronchial asthma, skin rashes, and hives should take this medication with care. Patients with severely impaired kidney function may have elevated drug concentrations in the body, so dosage and administration intervals should be carefully adjusted. Patients who have difficulty swallowing, those receiving parenteral nutrition, the elderly, and those in poor general condition should be closely monitored for symptoms of vitamin K deficiency. This drug contains the dye Yellow No. 5, so patients with allergy or hypersensitivity to this ingredient should use it cautiously. Rarely, during the administration of this drug, adverse effects such as shock, anaphylaxis (rapid allergic reactions), skin rashes, severe diarrhea or pseudomembranous colitis, interstitial pneumonia, blood disorders, renal dysfunction, and liver dysfunction may occur. If any of these symptoms appear, discontinue use immediately and consult a physician. Additionally, this drug may affect the generation of vitamin K, increasing the risk of bleeding when taken with anticoagulants like warfarin. Women who are pregnant or may become pregnant should discuss this medication with their physician before use, and breastfeeding should be avoided during the medication period. It is not recommended for infants, newborns, and premature infants under 6 months of age due to insufficient safety data. Elderly patients may experience increased side effects due to decreased bodily function, thus dosage and intervals should be adjusted, and their condition should be closely monitored. During the administration of this medication, some clinical test results may be affected, so patients should inform healthcare professionals about taking this medication. Finally, this medication should only be used for the necessary duration to prevent the development of resistant bacteria, and if prepared in suspension form, it should not be stored for more than two weeks.

shock

This medication should be stored in a tightly closed container to prevent air from entering, preferably at room temperature between 1 and 30 degrees Celsius. This way, the effectiveness of the drug can be maintained for a longer period.

Appearance

Light orange opaque capsule containing a crystalline powder that is white to light yellow.

Package unit

30 capsules/bottle, 100 capsules/bottle