Megatrue 633

Adult dose

For individuals aged 12 years and older: Take 1 tablet at a time, 1 to 2 times a day

This medicine should not be taken by patients with hypercalcemia or sarcoidosis, which is an unknown systemic inflammatory disease, and those with kidney diseases. Additionally, individuals with allergies to this drug or its components, infants under 12 months, patients with kidney stones, and severe renal failure should avoid taking it. It is important not to take this medication with phosphate, calcium salts, oral tetracycline agents, antacids, and medications such as levodopa. If you are currently receiving treatment from a physician, are pregnant or breastfeeding, or are an infant or a premature baby, be sure to consult a doctor or pharmacist before taking it. In particular, caution is needed as Vitamin D can affect newborns through breast milk. Those with gastrointestinal diseases such as peptic ulcer, chronic ulcerative colitis, focal colitis, cardiac and circulatory dysfunction, kidney disorders, hypoproteinemia, and a history of kidney stones should also consult before use. If symptoms such as nausea, vomiting, diarrhea, loss of appetite, abdominal bloating, skin rash, irregular heartbeat, central nervous system function impairment, or hair loss occur while taking this medicine, stop taking it immediately and consult a specialist. Especially long-term use of high doses of pyridoxine may cause neurological disorders, so caution is required. High doses of Vitamin B12 can cause blood anomaly reactions, so caution is also necessary. High-dose use may lead to worsened peptic ulcers, impaired glucose tolerance, hyperuricemia, and liver damage. Overdosing may show symptoms such as gastrointestinal symptoms, edema, and congestive heart failure, so caution is essential. In particular, co-administration with aldosterone antagonists or triamterene may increase the risk of hyperkalemia. If doses exceed the prescribed amount or if symptoms do not improve after more than one month of use, consult a specialist immediately. This medicine must be taken according to prescribed dosage and administration, and it may turn urine yellow, affecting clinical test results. Avoid beverages containing tannins, such as green tea and black tea, during treatment. When stored, keep it out of reach of children, keep away from direct sunlight, and store in a cool, dry place. It is also safe not to transfer it to other containers to maintain quality.

Serious side effects

Heart contraction failure (cardiac arrest), pulmonary edema (swelling)

Mild side effects

Nausea, vomiting, diarrhea, loose stools, loss of appetite, abdominal bloating, red spots, central nervous system function impairment, dermatitis, foul odor from sweat/breath, hair loss, irritability, gastrointestinal discomfort, digestive disorders, upper abdominal pain, hypotension, pulmonary edema, sensory neuropathy or neurological symptoms, hematological abnormal reactions, promotion of peptic ulcers, impaired glucose tolerance, hyperuricemia, liver damage, hypernatremia, congestive heart failure, edema, caution for hyperkalemia, yellowing of urine

Drug interactions

This medicine should not be taken with phosphates, calcium salts, oral tetracycline agents, antacids, and levodopa. Additionally, if being used with aldosterone antagonists or triamterene, consult a physician or pharmacist.

Food interactions

Avoid taking this medicine with tannin-containing teas such as green tea or black tea during or before and after dosing.

This medicine must be stored in a tightly sealed container to protect it from air and humidity. To maintain the medicine's efficacy, it should be kept at room temperature, specifically between 1°C and 30°C.

Appearance

Brown oval film-coated tablets

Package unit

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