Viewing nowZepogajeong 10 mg (Dapagliflozin Propanediol Hydrate)
Dapagliflozin Propanediol Hydrate 12.3mg
Tablet · Prescription medication
Jeil Pharmaceutical Co., Ltd.

MFDS item code 202201082 · Approved 2022.03.16 · Insurance code 645406280
Treatment for blood sugar control in type 2 diabetes and reduction of cardiovascular risks associated with chronic heart failure and kidney disease
This medication is used in conjunction with dietary and exercise regimens to help control blood sugar in patients with type 2 diabetes. It also helps reduce the occurrence of cardiovascular events in patients at risk for cardiovascular disease. In patients with chronic heart failure, it is administered along with other heart failure therapies to reduce the risk of death and hospitalization due to cardiovascular disease. Additionally, it contributes to mitigating the decline in kidney function and the risk of cardiovascular disease and kidney-related mortality in patients with chronic kidney disease. This medication is effectively used not only for blood sugar control but also for preventing complications of heart failure and kidney disease.
The recommended dosage of this medication is 10 mg once daily for monotherapy and as an adjunct in combination with other hypoglycemic agents, including insulin. When this medication is used in conjunction with insulin or secretagogues such as sulfonylureas, lower doses of insulin or secretagogues may be considered to reduce the risk of hypoglycemia. In cases where there has been no prior treatment with diabetes medications, metformin may be used.
The efficacy and safety of dapagliflozin in children under 18 years of age have not been established. There is no related data.
This medication should not be administered to certain patients. It should not be used in patients who are allergic to the active ingredients or excipients, patients with type 1 diabetes or diabetic ketoacidosis, those with genetic lactose intolerance issues, and patients who are undergoing dialysis. It should be used cautiously in patients with reduced fluid volume or kidney dysfunction, and fluid status and kidney function should be assessed before administration. After administration, symptoms of hypotension and kidney function should be monitored periodically. This medication is not recommended for patients with severely reduced kidney function. In clinical trials and post-marketing studies, the most common side effect has been genital infections, which may occur more frequently in women or patients with a history of infections. Hypoglycemia may occur primarily when used in combination with insulin or sulfonylureas; thus, dosage adjustment of insulin or secretagogues may be necessary to reduce the risk of hypoglycemia. Symptoms of dehydration or hypotension due to reduced fluid volume may occur; immediate consultation with healthcare personnel is required if such symptoms arise. Diabetic ketoacidosis can occur even when blood sugar levels are not high; symptoms such as nausea, vomiting, abdominal pain, and difficulty breathing require immediate investigation and treatment. There is an increased risk of urinary tract infections and pyelonephritis; rapid treatment is necessary if signs of infection occur. There is limited experience using this medication in patients with severely impaired liver function, so caution is required. It is recommended that women who are pregnant or breastfeeding do not use this medication, and administration should be discontinued if pregnancy is confirmed. Elderly patients should have careful monitoring of kidney function and fluid status. During the course of this medication, glucose may be detected in urine tests, which should be taken into account when evaluating blood sugar control. There is no specific antidote for overdose; appropriate treatment should be administered according to symptoms. Finally, while this medication does not significantly impact the ability to drive or operate machinery, caution is needed due to the risk of hypoglycemia when used in combination with insulin and others.
Rash, severe swelling (edema), chest tightness, difficulty breathing, cold sweat, pallor, severe rash with high fever, blisters, peeling skin, pain in mucous membranes of mouth/eyes, shortness of breath or difficulty breathing, asthma attacks, respiratory abnormalities accompanied by cough + fever, yellowing of skin or eyes (jaundice), profound lethargy, sudden and severe headache, lightning headache, seizures, confusion, visual disturbances, paralysis, urination
Vulvitis, glansitis, and related genital infections, urinary tract infections, fungal infections, hypoglycemia, dry mouth, dizziness, constipation, dry mouth, back pain, dysuria, polyuria, nocturia, increased hematocrit, reduced creatinine clearance at the start of treatment, dyslipidemia, elevated blood creatinine, elevated blood urea, weight loss, dyspepsia, nausea, diarrhea, vomiting, itching, rash, sweating, headache, fatigue, hunger, vaginal discharge
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly sealed container to avoid exposure to air or moisture. It is important to maintain storage temperatures between 1 degree and 30 degrees Celsius. Proper storage will ensure that the medication's effectiveness and safety are maintained for an extended period.
Yellow, biconvex, diamond-shaped film-coated tablets
28 tablets (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.