Posidi Tablet 5 mg (Dapagliflozin Monohydrate Mixture)
Dapagliflozin Anhydrous Lactose Mixture 7.635mg
Tablet · Prescription medication
International Pharmaceuticals Co., Ltd.
MFDS item code 202005318 · Approved 2020.07.23
This product's status changed to Expired on 2025.07.23. It may no longer be sold, so consult a doctor or pharmacist before taking it.
Effect of blood sugar control in type 2 diabetes and prevention of cardiovascular events
This medication is used to help control blood sugar levels in patients with type 2 diabetes. It can be administered alone or in combination therapy while combining with meal planning and exercise. It should be appropriately used under the guidance of a healthcare professional, especially in patients with cardiovascular disease or risk factors who are not sufficiently controlling their blood sugar. This medication helps improve blood sugar management and prevent complications of diabetes.
The recommended dose of this medication is 10 mg once a day for monotherapy and additional combination therapy. For initial combination therapy with metformin, it is 5 mg or 10 mg once a day. This medication can be taken orally once a day at any time, regardless of food intake, and the tablets should be swallowed whole.
The efficacy and safety of dapagliflozin in children under the age of 18 have not been established. There is no relevant data.
This medication should not be used in certain patients. Patients who are allergic to the active ingredients or excipients of this medication should not take it. This medication should not be administered to patients with type 1 diabetes or diabetic ketoacidosis. Patients with inherited conditions that prevent lactose breakdown should not take this medication. It is also not suitable for patients undergoing dialysis. Patients with reduced fluid volume or poor kidney function should use this medication cautiously. This medication can cause blood pressure reduction or changes in kidney function, so these patients should have their fluid status and kidney function carefully evaluated before taking it. During use, symptoms of hypotension or changes in kidney function should be monitored periodically. In patients with moderate to severe reductions in kidney function, blood sugar control effectiveness may decrease, and the decision to administer should be made carefully as needed. This medication contains yellow dye, so patients who are allergic to it should use caution when taking it. This medication can increase the risk of genital infections and urinary tract infections. Especially women and those with a history of infections should be cautious of infection symptoms and receive appropriate treatment if infections occur. If taken with drugs that pose a risk of hypoglycemia, hypoglycemic symptoms may appear, so dosage adjustments may be necessary when combined with insulin or sulfonylureas. Symptoms of dehydration or hypotension due to fluid volume reduction may occur, so particularly elderly patients or those taking diuretics should manage their fluid status closely. This medication can cause serious metabolic abnormalities known as diabetic ketoacidosis, so if symptoms like vomiting, abdominal pain, or difficulty breathing occur, the patient should consult a healthcare provider immediately. It is recommended that pregnant or breastfeeding women do not take this medication, and if pregnancy is confirmed, discontinuation is advised. In the case of overdose, there is no specific antidote, so it is important to receive appropriate treatment based on symptoms. This medication does not significantly affect driving or machinery operation, but caution is needed if there is a risk of hypoglycemia. Always keep out of reach of children and store in the original container to maintain quality.
Hives, severe swelling (angioedema), chest tightness, difficulty breathing, cold sweat, paleness, severe rash with fever, blisters, skin peeling, pain in oral/ocular mucosa, difficulty breathing or shortness of breath, asthma attack, respiratory issues accompanied by cough and fever, yellowing of the skin or eyes (jaundice), severe lethargy, sudden and severe headache, thunderclap headache, seizures, confused state of consciousness, visual disturbances, paralysis,
Not everyone experiences these, and they can vary from person to person.
This medication should be stored in a tightly closed container to protect it from air and moisture. It is important to maintain a storage temperature between 1 degree Celsius and 30 degrees Celsius.
Yellow, biconvex, round film-coated tablets
28 tablets/box [(14 tablets/PTP×2, 7 tablets/PTP×4)]
Even with the same ingredient, strength, dosage form and how it is taken can differ.
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.

Dapagliflozin Anhydrous Lactose Mixture 15.27mg
Tablet · Prescription medication
AlboGen 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.