Conmax Tablet

Adult dose

Adults aged 19 years and older: 1 tablet per dose, taken once daily

This medicine should not be taken by patients with hypercalcemia or sarcoidosis, a systemic inflammatory disease of unknown cause, and those with kidney disorders. Also, patients who have had allergic reactions to this medicine or any of its ingredients should avoid taking it. Infants under 12 months of age and individuals with kidney stones should also refrain from using this medicine. While taking this medicine, it is advisable not to take phosphates, calcium salts, oral tetracycline antibiotics, antacids, and drugs such as levodopa concurrently. Individuals receiving medical treatment, pregnant or potentially pregnant women, breastfeeding individuals, premature infants, and young babies should consult with their physician or pharmacist before using this medicine. This is because vitamin D can be transmitted to the newborn through breast milk, potentially causing hypercalcemia. Individuals with heart or circulatory issues, kidney disorders, hypoalbuminemia, or a history of kidney stones should also seek advice from a specialist. If symptoms such as nausea, vomiting, diarrhea, loss of appetite, abdominal distention, gastrointestinal discomfort, skin rash, itching, or swelling occur while taking this medicine, stop usage immediately and consult with healthcare providers. Additionally, prolonged high-dose use of pyridoxine may lead to neurological disorders, and in cases of folate deficiency, high-dose administration of vitamin B12 may result in hematological abnormalities. High-dose usage may lead to side effects such as peptic ulcers, blood sugar control issues, liver damage, and hyperuricemia, requiring caution. Excessive intake may cause gastrointestinal symptoms, hypernatremia, symptoms of heart failure, and can elevate potassium levels when taken with certain diuretics. If overdose occurs or if symptoms do not improve after a month of taking this medicine, consult healthcare providers promptly. This medicine must be taken strictly according to prescribed dosages and administration methods, and it may cause urine discoloration, which can affect clinical test results. It is also recommended to avoid beverages containing tannins, such as green tea or black tea, during or before and after taking this medicine. Store this medicine out of reach of children and keep it in a cool, dry place away from direct sunlight. Take care not to transfer it to other containers to maintain quality.

Serious side effects

Hives, swelling, edema or fluid retention (in patients with kidney or heart failure), hypotension, pulmonary edema

Mild side effects

Nausea, vomiting, diarrhea, loose stools, loss of appetite, abdominal distention, gastrointestinal disorders, digestive discomfort, upper abdominal pain, hypotension, constipation, erythema, eczema, rash, papular rash, itching, swelling, edema or fluid retention (in patients with kidney or heart failure), sensory neuropathy or neurological symptoms, hematological abnormalities, exacerbation of peptic ulcers, impaired glucose tolerance, hyperuricemia, liver damage, hypernatremia, congestive heart failure, edema (swelling), hypercalcemia

Drug interactions

This medicine should not be taken with phosphates, calcium salts, oral tetracycline preparations, antacids, or levodopa. If concomitantly administered with aldosterone antagonists or triampterene, consult with a physician or pharmacist.

Food interactions

This medicine should be avoided with tannin-containing teas such as green tea or black tea during or before and after taking.

This medicine must be stored in an airtight container and kept at room temperature between 1 to 30 degrees Celsius. Proper storage will maintain the effectiveness of the medicine and prevent deterioration.

Appearance

Reddish-brown oblong film-coated tablet

Package unit

30 tablets/bottle, 60 tablets/box [(30 tablets/bottle x 2)]