Sitaphomin Alpha Tablet 50/850 mg

Adult dose

This medication is generally taken twice a day with food, and the dosage is gradually increased to reduce gastrointestinal side effects caused by metformin. 1. For patients who are not currently receiving metformin: This medication 50/500 mg is taken twice a day, with 1 tablet per dose, and can be increased to 50/1000 mg taken twice a day, with 1 tablet per dose. 2. For patients currently treated with metformin

This medication contains both sitagliptin and metformin and is used for blood sugar control in patients with type 2 diabetes. During the course of taking this medication, severe allergic reactions may occur, so if symptoms such as rash, hives, difficulty breathing, or swelling of the face or neck develop, you should immediately stop taking the medication and consult a doctor. There is also a risk of pancreatitis, which is inflammation of the pancreas, so if symptoms such as sudden abdominal pain, nausea, vomiting, or fever occur, immediate medical attention should be sought. Due to the metformin component, lactic acidosis, a rare but serious metabolic abnormality, may occur. If symptoms such as muscle pain, weakness, difficulty breathing, abdominal pain, or unusual drowsiness occur, you should inform your doctor immediately. This medication should not be administered to patients with significantly reduced kidney function, severe liver disease, acute heart conditions, severe infections, or dehydration. Patients scheduled to undergo tests with radiologic contrast agents should discontinue the use of this medication for a certain period before and after the examination, so it is crucial to discuss this with healthcare professionals. It is safer for women who are pregnant or may become pregnant, as well as lactating women, to avoid taking this medication. During treatment, there may be symptoms of hypoglycemia, such as extremely low blood sugar, therefore irregular eating, excessive exercise, and alcohol consumption should be avoided. If symptoms of hypoglycemia (dizziness, cold sweat, shaking, etc.) occur, immediate action should be taken. Regular tests of kidney function and blood tests should be conducted, and since vitamin B12 levels may decrease, supplementation may be necessary. If undergoing surgery, this medication should be temporarily discontinued 48 hours before the procedure, and resumed only after normal oral intake is restored and kidney function is confirmed. This medication may interact with other hypoglycemic agents, antihypertensives, diuretics, etc., so if you are taking other medications, it is essential to inform your doctor or pharmacist. In the event of an overdose, immediate medical attention should be sought, and blood dialysis may be beneficial. It is advisable to avoid alcohol consumption while taking this medication, and if sudden changes in symptoms or adverse reactions are suspected, immediately consult a physician.

Serious side effects

Hives, severe swelling (angioedema), chest tightness, difficulty breathing, anaphylaxis, severe allergic reactions, severe rash with high fever, blisters, skin peeling, pain in oral/conjunctival mucosa, Stevens-Johnson syndrome, severe skin adverse reactions, acute pancreatitis, jaundice (yellowing of the body), elevated liver enzymes, acute renal failure, severe swelling or urination abnormalities, sudden and very severe headache, seizures, or altered consciousness

Mild side effects

Diarrhea, nausea, vomiting, abdominal pain, upper respiratory infection, nasopharyngitis, headache, muscle pain, limb pain, back pain, itching, thrombocytopenia, decreased appetite, pruritus, dizziness, hypoglycemia, joint pain associated with severity and disability

This medication should be stored in a tightly sealed container to prevent air ingress, at a temperature between 1 and 30 degrees Celsius. Storing it this way will ensure the safe maintenance of the medication's effectiveness.

Appearance

Pink oval film-coated tablet

Package unit

30 tablets per box [10 tablets/PTP x 3]