Viewing nowDapaglime Tablet 10mg (Dapagliflozin Propanediol Hydrate)
Dapagliflozin Propanediol Hydrate 12.3mg
Tablet · Prescription medication
Mothers Pharmaceuticals Co., Ltd.

MFDS item code 202300411 · Approved 2023.01.31 · Insurance code 622805000
Treatment for type 2 diabetes blood sugar control and chronic heart failure (reduction of cardiovascular disease risk), chronic kidney disease (suppression of kidney function deterioration)
This medicine is used as an adjunct to diet and exercise to help control blood sugar in patients with type 2 diabetes. It also lowers the risk of death or hospitalization due to cardiovascular disease in patients with chronic heart failure, and helps slow the decline in kidney function and reduce the associated mortality risk in patients with chronic kidney disease. This medication is used in conjunction with standard treatments for each condition, considering the risk of cardiovascular events. It effectively improves blood sugar, heart, and kidney function tailored to the patient's health status.
The recommended dose of this medication is 10 mg once daily. It can be taken orally at any time of day, regardless of meals. The tablet should be swallowed whole.
The efficacy and safety of dapagliflozin in pediatric patients under 18 years of age have not been established.
This medication should not be used in certain patients. Patients who are allergic to the active ingredient or any additives, patients with type 1 diabetes or diabetic ketoacidosis, those with lactose intolerance or related genetic disorders, and patients on dialysis should not take this medication. Patients with reduced fluid volume or decreased kidney function should use this medication with caution. This drug may lower blood pressure or affect kidney function, so fluid status and kidney function should be carefully evaluated before administration, and blood pressure symptoms and changes in kidney function should be closely monitored during treatment. Especially in patients with significantly decreased kidney function, the blood sugar control effect of this medication may be reduced, and administration is not recommended. This medication can cause side effects such as genital infections, urinary tract infections, hypoglycemia, decreased fluid volume, and ketoacidosis. Genital infections may occur more frequently in women and those with a past history of infections, so caution is needed. Hypoglycemia may occur more commonly when this medication is used with insulin or sulfonylureas, so blood sugar should be carefully managed in such cases. Due to decreased fluid volume, dehydration or hypotension may occur, so elderly patients or those taking diuretics should monitor their fluid status closely. Ketoacidosis can occur even when blood sugar is within the normal range, so immediate medical attention should be sought if symptoms such as nausea, vomiting, abdominal pain, or difficulty breathing arise. This drug is not recommended for patients with severely impaired liver function, and should be avoided in women who are pregnant or breastfeeding. Additionally, glucose may be detected in urine tests during the use of this medication. When this medication is taken with insulin or sulfonylureas, dosage adjustments of these medications may be necessary to reduce hypoglycemia risk. In case of overdose, there is no specific antidote, and appropriate treatment should be provided according to symptoms; it has not been confirmed whether dialysis can remove this medication. Lastly, the safety and efficacy of this medication have not been established in children, so it should not be used in pediatric patients. During the use of this drug, caution should be exercised for symptoms of hypoglycemia when driving or operating machinery, and medication should be kept out of the reach of children.
Urticaria, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, skin peeling, pain in the mouth/eyes mucosa, shortness of breath or difficulty breathing, asthma attacks, respiratory signs with cough and fever, yellowing of skin or eyes (jaundice), extreme fatigue, sudden severe headache, lightning headache, seizures, confusion of consciousness, visual disturbances, paralysis, urination issues
Vulvovaginitis, balanitis and related genital infections, urinary tract infections, fungal infections, hypoglycemia, thirst, dizziness, constipation, dry mouth, back pain, dysuria, polyuria, nocturia, interstitial nephritis, increased hematocrit, decreased renal creatinine clearance at the beginning of treatment, dyslipidemia, increased serum creatinine at the beginning of treatment, elevated blood urea, weight loss, urticaria, cold sweat, dermatitis, dry skin, hyperkeratosis, skin lesions
Not everyone experiences these, and they can vary from person to person.
This medication may be sensitive to air or moisture, so it must be stored in a tightly sealed container. Additionally, it is safe to store the medication at room temperature, which is between 1°C and 30°C, avoiding extremely hot or cold places.
Yellow, biconvex, diamond-shaped film-coated tablet
28 tablets/box [(14 tablets/PTP×2)]
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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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.