Vitacoplus Soft Capsule

Adult dose

Adults: take 1 capsule twice a day

This medication should be used with caution in women in the first three months of pregnancy or those who may become pregnant, as administering more than 5,000 IU of vitamin A daily may induce the risk of congenital disabilities. Patients with hypercalcemia, sarcoidosis, renal diseases, or allergies to any of the ingredients in this medication should not take it. Infants under 3 months old, patients with kidney stones, and those allergic to soybean oil or peanuts should also avoid this medication. Individuals undergoing treatment from a physician, or those with specific kidney diseases, pregnant or breastfeeding women, premature infants, infants, gout patients, or those with hyperlipidemia or diabetic dyslipidemia should consult a specialist before use. If symptoms such as nausea, vomiting, skin itching, dryness, joint swelling, diarrhea, loss of appetite, or abdominal bloating occur during use, consumption should be stopped immediately and a specialist consulted. Long-term high-dose administration may lead to tolerance or complications such as peptic ulcers, blood glucose regulation disorders, hyperuricemia, and liver damage, thus caution is necessary. Women after menopause may be at increased risk of osteoporosis from prolonged high-dose vitamin A intake. Dosages must adhere strictly to prescribed methods and dosages, and the daily intake of vitamin A should not exceed 5,000 IU. This medication may affect blood sugar test results during urinalysis and can change urine color to yellow, affecting clinical tests. Patients with abnormalities in lipid metabolism should take this medication while monitoring plasma lipid levels, and dosage adjustment may be needed when taken with other lipid medications. Store this medication out of the reach of children, away from direct sunlight, in a cool, dry place in a tightly sealed container. Additionally, to preserve quality and prevent misuse, do not transfer to other containers.

Serious side effects

Painful joint swelling may indicate severe edema, which requires caution. Patients with underlying conditions such as hypercalcemia or renal diseases should not take it, and if severe allergic reactions such as difficulty breathing, severe swelling, or hives occur during use, consumption should be stopped immediately and a doctor consulted.

Mild side effects

• Nausea
• vomiting
• itching
• dry and rough skin
• painful joint swelling (edema)
• diarrhea
• loose stools
• loss of appetite
• abdominal bloating

Drug interactions

This medication should be used in conjunction with intravenous lipid drugs under the guidance of a physician or pharmacist.

This medication must be stored in a tightly sealed container to protect it from air and moisture. It is best to maintain a storage temperature between 1 and 30 degrees Celsius at room temperature, as this helps to retain the medication's efficacy for a longer period.

Appearance

A reddish-brown oblong soft capsule containing yellow contents

Package unit

1 capsule/strip, 500 capsules/strip