DuoMet XR Tablet 1000/10 mg

Adult dose

This medication is to be taken by adults once daily with the evening meal.

This medication can rarely cause a serious condition called lactic acidosis, which may lead to death, so caution is needed. When used with other blood glucose lowering medications, severe hypoglycemic symptoms may occur, requiring careful monitoring. Individuals allergic to the ingredients of this medication or similar drugs should not use it. Patients with severe liver dysfunction or those with liver disease should not take this medication. Individuals who have muscle disorders or are prone to muscle problems should avoid using this medication, especially at higher doses where the risk is greater. Patients with severely impaired kidney function, dehydration, serious infections, acute heart problems, etc., should not use this medication. This medication must be discontinued in cases of acute heart failure or before certain radiation tests, and it can be resumed once normal kidney function is confirmed post-examination. This medication is not appropriate for type 1 diabetes patients or those with diabetic ketoacidosis. Patients with severe infections, trauma, or those undergoing surgery should temporarily stop using this medication and can resume once their condition stabilizes. Extra caution is required for patients with very poor nutritional status or certain endocrine disorders when using this medication. This medication contains lactose, and individuals with lactose intolerance should not take it. Discontinuities in meal timing or insufficient food intake, as well as rigorous exercise, should be considered when using this medication. If symptoms of muscle pain or weakness occur, you should immediately inform your doctor and get evaluated, and discontinue use if necessary. Regular liver and kidney function tests should be performed while taking this medication, and it is particularly important for elderly patients or those with compromised kidney function to exercise further caution. Alcohol consumption during treatment should be avoided, as it may increase the risk of lactic acidosis. Women who are pregnant or may become pregnant should not take this medication and should use adequate contraception. Breastfeeding women are also advised not to take this medication. The safety and efficacy of this medication have not been established in children or adolescents under 19 years of age, and it should not be used in this population. In case of overdose, immediate medical attention should be sought, and blood dialysis or other treatment may be required. Care should be taken when driving or operating machinery, as dizziness may occur with this medication. This medication should be kept out of reach of children and stored in its original container to maintain quality.

Serious side effects

Hives, hypersensitivity reactions including angioedema, lactic acidosis, severe hypoglycemia, jaundice, severe edema, Stevens-Johnson syndrome, drug reaction with eosinophilia and systemic symptoms (DRESS), acute renal failure, oliguria, thrombocytopenia, increased serum creatinine, rhabdomyolysis, severe muscle weakness and ocular muscle weakness, severe allergic reactions, severe skin reactions, respiratory problems, liver abnormalities (jaundice), severe

Mild side effects

• Diarrhea
• upper abdominal pain
• constipation
• abdominal pain
• belching
• gastroesophageal reflux disease
• upper abdominal discomfort
• dyspepsia
• cellulitis
• paresthesia

This medication should be stored in a tightly closed container to prevent exposure to air or moisture. It is important to maintain a storage temperature between 1 and 30 degrees Celsius to preserve the drug's effectiveness and safety for an extended period.

Appearance

Pink oval film-coated tablet

Package unit

PTP - 30 tablets/PTP [(10 tablets/PTP x 3)], Bottle - 30 tablets/bottle