Acticom Soft Capsule

Adult dosage

1 capsule once daily for adults and children aged 8 years and older

Children's dosage

1 capsule once daily for children aged 8 years and older

Care should be taken with this medication as administering over 5,000 IU of vitamin A daily to women in the first 3 months of pregnancy or those who may become pregnant can pose a risk of congenital malformations. Those allergic to ingredients in this medication, infants under 12 months of age, or individuals with hypersensitivity to soybean oil, soy, or peanuts should not take this medication. It is advisable not to take this medication concurrently with phosphates, calcium salts, oral tetracyclines, or antacids. Those receiving medical treatment, those with certain diseases (hyperoxaluria, peptic ulcers, chronic ulcerative colitis, heart and kidney disorders, hypoproteinemia, gout, hyperlipoproteinemia, etc.), pregnant or breastfeeding women, premature infants, and infants should consult a specialist before taking this medication. This medication contains color additive Yellow No. 5, so those allergic to this component should take it with caution. If any unusual symptoms such as nausea, vomiting, skin itching, joint swelling, gastrointestinal discomfort, diarrhea, rash, hair loss, hypotension, or pulmonary edema occur while taking this medication, stop taking it immediately and consult a professional. Women may experience menstrual changes while taking this medication, and caution is advised when taken with certain contraceptives due to the increased risk of thrombosis. Long-term high-dose use can lead to tolerance, gastrointestinal symptoms, swelling, and an increased risk of osteoporosis, so adhere to the specified dosage. This medication should be taken with caution if used concurrently with aldosterone antagonists or triamterene due to the risk of hyperkalemia. When administered to children, parental supervision is required, and the supplemental dosage of vitamin A should not exceed 5,000 IU daily. It is advisable to avoid intake of tannin-containing teas such as green tea or black tea before and after taking this medication, and those with lipid metabolism disorders should monitor plasma lipid levels while taking it. This medication should be stored in a cool, dry place away from direct sunlight and out of reach of children.

Mild side effects

• Nausea
• vomiting
• itching
• dry and rough skin
• painful joint swelling
• gastrointestinal discomfort
• diarrhea
• constipation
• rash
• redness

Drug interactions

This medication should not be taken concurrently with phosphates, calcium salts, oral tetracyclines, or antacids. Consult with a physician or pharmacist when using with oral contraceptives containing estrogen, aldosterone antagonists, triamterene, or injectable lipid formulations.

Food interactions

This medication should be avoided when taking tannin-containing teas such as green tea or black tea, both during and before and after the intake.

This medication should be stored in a tightly sealed container to prevent air exposure and is best stored at room temperature between 1 and 30 degrees Celsius. Storing this way helps maintain drug efficacy and prevent degradation.

Appearance

Dark brown oblong soft capsule containing reddish-brown contents

Package unit

60 capsules/box (10 capsules/PTP X 6), 120 capsules/box [(60 capsules/box (10 capsules/PTP X 6) X 2]