Medication info
Posia Tablets 10/100 Milligrams (Dapagliflozin, Sitagliptin)

Posia Tablets 10/100 Milligrams (Dapagliflozin, Sitagliptin)

Prescription medicationTablet
Ingredient · strength
Dapagliflozin Propanediol Hydrate›12.3mg / 1 tabletSitagliptin Phosphate Hydrate›128.5mg / 1 tablet
Manufacturer / importer
(주)중헌제약
Appearance
Beige oval film-coated tablet
Packaging
30 tablets/PTP [10 tablets/PTP (Alu-Alu) x 3]
Approval status
Active

MFDS item code 202300389 · Approved 2023.01.30 · Insurance code 053301140

Summary

Main use
Improvement of blood sugar control in type 2 diabetes
Who uses it
Adults
Adult dosage
This medication is administered once daily at a dose of 1 tablet containing sitagliptin 100 mg and dapagliflozin 10 mg, regardless of meals. The tablet should be swallowed whole.

Ingredients

Manufacturer
(주)중헌제약

Efficacy & effects

Improvement of blood sugar control in type 2 diabetes

View approved original text

This medication is used to assist in blood sugar control in patients with type 2 diabetes by using sitagliptin and dapagliflozin together. It enhances blood sugar control effectiveness through conjunction with meal and exercise therapy, which is helpful to patients who have difficulty managing their blood sugar levels. As a result, it effectively improves blood sugar levels and supports diabetes treatment.

Dosage and Administration

Adult dosage

This medication is administered once daily at a dose of 1 tablet containing sitagliptin 100 mg and dapagliflozin 10 mg, regardless of meals. The tablet should be swallowed whole.

Precautions

This medication may cause severe allergic reactions due to the sitagliptin component; therefore, if symptoms such as skin rash, difficulty breathing, or swelling of the face or neck occur after taking it, immediately discontinue use and consult a physician. Additionally, this medication may cause serious pancreatic inflammation known as pancreatitis during use, so if symptoms such as abdominal pain, vomiting, or nausea arise, promptly inform medical personnel. This medication should not be administered to patients with type 1 diabetes, diabetic ketoacidosis, or those undergoing dialysis. Use with caution in patients with reduced fluid volume or renal dysfunction, particularly in elderly patients or those on diuretics, who should be closely monitored for hypotension or dehydration symptoms. Dose adjustment may be required for patients with reduced kidney function, and regular kidney function tests should be conducted before and during treatment. There may be an increased risk of genital infections and urinary tract infections during use; thus, rapid treatment should be sought if infection symptoms arise. Moreover, caution is warranted for hypoglycemia risk when taken with other hypoglycemic agents such as insulin or sulfonylureas, and dosage adjustment of those medications may be necessary as needed. Pregnant or breastfeeding women are advised not to take this medication, and if pregnancy is confirmed, use should be immediately discontinued. This medication should not be used in patients under 18 years of age as safety and efficacy have not been established. In cases of overdose, as there are no specific antidotes, appropriate treatment according to symptoms should be sought, and hospital observation and treatment may be required if necessary. Lastly, caution is advised during driving or operating machinery as there may be risks of hypoglycemia during use of this medication.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling, chest tightness, difficulty breathing, cold sweat, pallor, severe hypersensitivity reactions, anaphylaxis, angioedema, Stevens-Johnson syndrome, exfoliative dermatitis, acute pancreatitis, life-threatening hemorrhagic or necrotizing pancreatitis, severe allergic reactions, acute kidney injury, hypotension, renal impairment, diabetic ketoacidosis, ketosis, urosepticemia, pyelonephritis, rash, severe skin adverse reactions, headache

Mild side effects

  • Headache
  • dizziness
  • thirst
  • constipation
  • dry mouth
  • back pain
  • dysuria
  • polyuria
  • nocturia
  • fainting
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  • palpitations
  • insomnia
  • itching
  • cold sweat
  • hunger
  • chest pain
  • fatigue
  • pain
  • facial pain
  • hives
  • dyspepsia
  • nausea
  • diarrhea
  • vomiting
  • abdominal discomfort
  • abdominal pain
  • vaginal discharge
  • menstrual irregularities
  • increased blood lactate levels
  • lymphopenia
  • weight gain
  • increased blood triglycerides
  • elevated blood urea
  • dyslipidemia
  • myopathy

Not everyone experiences these, and they can vary from person to person.

Storage

This medication may be sensitive to air and moisture and should be stored in a tightly closed container. It is important to maintain a storage temperature between 1 and 30 degrees Celsius (room temperature) to ensure the medication's effectiveness.

Appearance and packaging

Appearance

Beige oval film-coated tablet

Package unit

30 tablets/PTP [10 tablets/PTP (Alu-Alu) x 3]

Same-ingredient medicines

Even with the same ingredient, strength, dosage form and how it is taken can differ.

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.

Questions about this medicine

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For anything that needs medical judgment, consult a doctor or pharmacist.

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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.