Viewing nowSuga Tablet 10 mg (Dapagliflozin Monohydrate Mixed Powder)
Dapagliflozin Anhydrous Lactose Mixture
Tablet · Prescription medication
Unimed Pharmaceuticals Co., Ltd.

MFDS item code 202103301 · Approved 2021.04.22 · Insurance code 649508140
Blood sugar control in type 2 diabetes and reduced risk of chronic heart failure (cardiovascular disease), inhibition of chronic kidney disease progression
This medication is used alongside diet and exercise to help control blood sugar in patients with type 2 diabetes and is also applicable to patients at risk of cardiovascular diseases. It helps reduce cardiovascular mortality and hospitalization risks in patients with chronic heart failure and is administered in conjunction with standard heart failure treatments. For patients with chronic kidney disease, it is used alongside other renal disease treatments to lower the risk of renal function decline and related mortality. In summary, this medication is effectively used for treating type 2 diabetes, chronic heart failure, and chronic kidney disease.
The recommended dosage of this medication for both monotherapy and additional combination therapy with other hypoglycemic agents such as insulin is 10 mg once daily. When this medication is used in combination with insulin or insulin secretagogues such as sulfonylureas, a lower dose of insulin or insulin secretagogues may be considered to reduce the risk of hypoglycemia. For initial combination therapy, if there is no previous experience of diabetes medication treatment,
The efficacy and safety of this medication in children under 18 years of age have not been established.
This medication should not be used in certain patients. Patients who are allergic to this medication's active ingredient or additives, patients with type 1 diabetes, patients with diabetic ketoacidosis, and patients with lactose intolerance should not take this medication. Also, patients undergoing dialysis should not use this medication. Patients with reduced fluid volume or renal dysfunction should use this medication cautiously. This medication may lower blood pressure or cause temporary changes in renal function; therefore, fluid status and renal function must be checked prior to administration, and caution should be taken to observe for symptoms of hypotension and renal function during use. Especially in patients with moderate to severe renal impairment, blood sugar control efficacy may be diminished. This medication contains colorants Yellow No. 4 and Yellow No. 5, so patients with allergies to these components should use it carefully. Various side effects may occur during treatment with this medication. The most common side effect is genital infections, which may occur more frequently in females. Other reported side effects include hypoglycemia, fluid volume reduction, dizziness, constipation, dry mouth, and urinary tract infections. This medication can affect renal function and may temporarily increase serum creatinine levels in some patients. Such changes may occur more frequently in patients with chronic kidney disease or in older adults, so caution is necessary. Rarely, serious infections like necrotizing fasciitis may occur, so if pain, swelling, or redness around the genital area appears, immediate consultation with healthcare professionals is necessary. This medication is not recommended for pregnant women, and administration should be discontinued immediately upon confirmation of pregnancy. Additionally, breastfeeding women should not use this medication. When used in conjunction with hypoglycemic agents such as insulin or sulfonylureas, there may be an increased risk of hypoglycemia; therefore, dose adjustment may be necessary when using these drugs together. There is no specific antidote for overdose; therefore, it is crucial to receive symptomatic treatment. Finally, this medication has not been established for safety and efficacy in children, so its use should be avoided. Close observation of hypoglycemia symptoms and fluid volume changes is important during treatment with this medication, and immediate consultation with a physician is necessary if any abnormal symptoms occur.
Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with fever, blisters, peeling skin, mucosal pain in the mouth/eyes, difficulty breathing or dyspnea, asthma attacks, respiratory anomalies accompanied by cough and fever, jaundice (yellowing of the skin or eyes), extreme lethargy, sudden and severe headache, thunderclap headache, seizures, altered consciousness, visual disturbances, paralysis, urination
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air and moisture; therefore, it must be stored in a tightly closed container. The recommended storage temperature is room temperature between 1 and 30 degrees Celsius. This will help maintain the effectiveness of the medication safely.
Yellow, biconvex, diamond-shaped film-coated tablet
28 tablets/box (14 tablets/PTP × 2, 7 tablets/PTP × 4), 30 tablets/bottle
Even with the same ingredient, strength, dosage form and how it is taken can differ.
Viewing nowDapagliflozin Anhydrous Lactose Mixture
Tablet · Prescription medication
Unimed Pharmaceuticals Co., Ltd.
Dapagliflozin Anhydrous Lactose Mixture 7.635mg
Tablet · Prescription medication
International Pharmaceuticals Co., Ltd.

Dapagliflozin Anhydrous Lactose Mixture 15.27mg
Tablet · Prescription medication
International Pharmaceutical Co., Ltd.
Dapagliflozin Anhydrous Lactose Mixture 7.635mg
Tablet · Prescription medication
Shinil Pharmaceutical Co., Ltd.

Dapagliflozin Anhydrous Lactose Mixture 15.27mg
Tablet · Prescription medication
Sinil Pharmaceutical Co., Ltd.
Dapagliflozin Anhydrous Lactose Mixture 7.635mg
Tablet · Prescription medication
Dongwha Pharmaceutical Co., Ltd.

Dapagliflozin Anhydrous Lactose Mixture 15.27mg
Tablet · Prescription medication
Donghwa Pharmaceutical Co., Ltd.
Dapagliflozin Anhydrous Lactose Mixture 7.635mg
Tablet · Prescription medication
Albozen Korea Co., Ltd.
Even with the same ingredient, the dose and directions can differ by strength and dosage form. Talk to a doctor or pharmacist before switching from a medication you are already taking.
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For anything that needs medical judgment, consult a doctor or pharmacist.
This drug information is based on data provided by the Korea Ministry of Food and Drug Safety.
Consult a doctor or pharmacist for accurate dosage, administration, and usage instructions.