Incoramin Special Tablets

Adult dose

Ages 12 and older: 1 tablet once a day

This medication should not be used in patients with hypercalcemia or sarcoidosis, a systemic inflammatory disease of unknown cause, or in patients with kidney diseases. Additionally, those with allergic reactions to any component of this medication, infants under 12 months, patients with kidney stones, and those with severe renal failure should not take this medication. This medication contains lactose, so individuals with lactose intolerance, lactose enzyme deficiency, or genetic disorders affecting glucose-galactose absorption should avoid taking it. It is advisable not to take this medication simultaneously with phosphates, calcium salts, oral tetracyclines, antacids, and levodopa. Patients receiving treatment from a physician or with a history of oxalate nephropathy, gastrointestinal diseases, heart or circulatory system dysfunction, renal impairment, hypoalbuminemia, gout, kidney stones, pregnant women or those who may become pregnant, nursing mothers, premature infants, and young children should consult with a specialist before taking this medication. If symptoms such as nausea, vomiting, diarrhea, loss of appetite, abdominal bloating, skin rashes, irregular heartbeats, or central nervous system depression occur during treatment, discontinue use immediately and consult a specialist. Long-term high-dose use can lead to tolerance, and excessive pyridoxine may result in neurological symptoms. Moreover, taking high doses of Vitamin B12 can trigger hematological reactions and may lead to side effects such as exacerbation of peptic ulcers, blood sugar control issues, liver damage, and hyperuricemia. If overdose occurs or if symptoms do not improve after one month of use, consult a specialist immediately. During treatment, be sure to adhere to the specified dosage and wording, and note that it may affect blood sugar detection in urine tests, and urine color may change. It is advisable to avoid consuming tannin-containing teas like green tea or black tea before and after taking this medication. Finally, this medication should be stored out of reach of children, away from direct sunlight, in a cool and dry, tightly sealed place. Additionally, to prevent medication misuse, do not transfer it to other containers.

Mild side effects

Nausea, vomiting, diarrhea, loose stools, loss of appetite, abdominal bloating, constipation, low blood pressure, facial flushing, irregular heartbeat, skin rash, red spots, contraction, central nervous system depression, dermatitis, bad smell during sweating or breathing, hair loss, agitation, gastrointestinal disturbances, digestive disorders, epigastric pain, pulmonary edema, sensory neuropathy or neurological symptoms, hematological adverse reactions, exacerbation of peptic ulcers, impaired glucose tolerance, hyperuricemia, liver damage, high sodium

Drug interactions

This medication should not be taken with phosphates, calcium salts, oral tetracycline preparations, antacids, or levodopa. Additionally, if taking cardiac glycosides, anti-aldosterone agents, or triamterene, consult with a physician or pharmacist.

Food interactions

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

This medication should be kept in a tightly sealed container to avoid exposure to air or moisture and should ideally be stored at room temperature between 1 to 30 degrees Celsius. Proper storage will maintain the medication's effectiveness and prevent deterioration.

Appearance

Pale yellow oblong film-coated tablet

Package unit

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