Mega B-Ten Premium Tablet

Adult dose

For ages 8 and above and adults: 1 tablet per dose, taken once a day

This medicine should not be taken by individuals with hypercalcemia, sarcoidosis, or kidney disease. Additionally, those allergic to this medication or its components, babies under 12 months, individuals with kidney stones, and those with severe renal failure should not take it. People with lactose intolerance or certain genetic conditions should also not take this medicine. During the course of taking this medicine, it is essential not to combine it with phosphates, calcium salts, oral tetracycline antibiotics, antacids, or levodopa. Infants under 1 year, individuals under medical treatment, children exposed to sunlight frequently, and those with hyperoxaluria should consult a professional before taking. Women who are pregnant or may become pregnant, nursing mothers, premature infants, and infants are also advised to consult a doctor before use. Caution is necessary for individuals with a history of peptic ulcers, chronic ulcerative colitis, heart and kidney disorders, hypoproteinemia, gout, or kidney stones. If nausea, vomiting, diarrhea, skin rashes, abnormal heart rhythms, or central nervous system symptoms occur during administration, discontinue use immediately and consult a professional. Women taking contraceptive pills containing estrogen, or individuals at risk of thrombosis may have an increased risk of thrombosis. Prolonged high-dose use may lead to tolerance, neurological damage, blood disorders, exacerbation of peptic ulcers, and liver damage, so caution is required. In cases of overdose, consulting a professional immediately is necessary. If symptoms do not improve after one month of use, stop and seek advice. Dosage and administration must be strictly followed, and administration to children should be supervised by a guardian. This medicine can affect urinalysis results and may change urine color to yellow, so it is advisable to inform before tests. It is recommended to avoid drinks containing tannins, such as green tea and black tea, before and after taking this medication. Patients with lipid metabolism issues should monitor plasma lipid levels and adjust dosages accordingly. This medicine should be stored out of reach of children and in a cool place protected from direct sunlight and humidity. It should not be transferred to another container, and to prevent misuse and maintain quality, it should be stored in its original container.

Serious side effects

• Failure contraction (cardiac arrest)
• central nervous system dysfunction
• pulmonary edema

Mild side effects

Nausea, vomiting, diarrhea, loose stools, constipation, feeling of discomfort in the stomach, gastrointestinal disturbances, digestive disorders, abdominal pain, rash, redness, red spots, dermatitis, sweating, foul odor during breathing, hair loss, agitation, low blood pressure, menstruation occurring earlier than expected or in greater volume, prolonged bleeding, sensory neuropathy, neurological symptoms, hematological adverse reactions, glucose tolerance impairment due to high-dose administration, hyperuricemia, liver damage, hypernatremia, and others.

Drug interactions

This medicine should not be taken with phosphates, calcium salts, oral tetracycline preparations, antacids, levodopa, or oral contraceptives containing estrogen. If taken with aldosterone antagonists and triamterene, consult a physician or pharmacist.

Food interactions

This medicine should not be taken with tea containing tannins, such as green tea or black tea, during use or immediately before and after.

This medicine must be stored in a tightly sealed container to prevent exposure to air and moisture. Additionally, it is safest to store it at room temperature between 1 to 30 degrees Celsius. This storage condition helps maintain the efficacy of the medication.

Appearance

Brownish rectangular film-coated tablet

Package unit

60 tablets/bottle, 120 tablets/box [60 tablets/bottle X 2]