Hepacoen Active Tablet

Adult dose

Adults aged 19 and over should take 1 tablet once a day.

This medication should not be taken by individuals with hypercalcemia, sarcoidosis, or kidney diseases. Additionally, those allergic to this medication or any of its components, infants under 12 months old, patients with kidney stones, patients with severe renal failure, and individuals allergic to soy oil, beans, or peanuts should also avoid taking it. During the course of this medication, it is advised not to take phosphate, calcium salts, oral tetracycline preparations, antacids, or levodopa. Individuals receiving treatment from a physician, those with oxalosis, pregnant or potentially pregnant women, nursing mothers, those with gastrointestinal diseases, cardiovascular disorders, renal disorders, hypoproteinemia, gout, or a history of kidney stones should consult a specialist before taking this medication. If symptoms such as nausea, vomiting, diarrhea, rash, dermatitis, hair loss, gastrointestinal disorders, hypotension, or pulmonary edema occur during administration, usage should be discontinued immediately and a specialist consulted. There is a risk of menstrual changes, increased risk of thrombosis, tolerance development, neurological symptoms, hematological adverse reactions, aggravation of peptic ulcers, liver damage, and edema as potential side effects, so caution is advised. It is important to adhere to the prescribed dosage, as it may affect urinalysis or clinical tests, thus consulting a specialist before and after tests is recommended. It’s advisable to avoid teas containing tannins like green tea and black tea before and after taking this medication, and patients at risk of fat overload should monitor plasma lipid levels while adjusting the dosage accordingly. This medication should be kept out of reach of children, stored in a cool, dry place away from direct sunlight, and kept sealed. To maintain quality, it is also important not to transfer it to another container.

Serious side effects

• Defibrillation (cardiac arrest)
• central nervous system dysfunction
• pulmonary edema (swelling)

Mild side effects

Nausea, vomiting, diarrhea, abdominal discomfort, constipation, rash, erythema, loose stools, red spots, dermatitis, unpleasant odor during sweating or breathing, hair loss, restlessness, gastrointestinal disturbances, digestive disorders, upper abdominal pain, hypotension, menstruation occurring earlier or increasing in amount, prolonged bleeding, sensory neuropathy or neurological symptoms, hematological adverse reactions, glucose intolerance impairment, hyperuricemia, liver damage, hypernatremia, congestive heart failure, edema, high

Drug interactions

This medication should not be taken with phosphates, calcium salts, oral tetracycline preparations, antacids, or levodopa. Women taking oral contraceptives containing estrogen should consult their doctor or pharmacist. Consultation with a doctor or pharmacist is also advised when taking in combination with aldosterone antagonists or triamterene.

Food interactions

This medication should avoid consumption with teas that contain tannins, such as green tea and black tea, during or before and after taking.

This medication should be stored in a tightly sealed container to prevent air or moisture ingress, preferably at room temperature between 1 to 30 degrees Celsius. Proper storage will help maintain the efficacy of the medication for a longer time.

Appearance

Brown oblong film-coated tablet

Package unit

Bottle - 90 tablets/bottle