Medication info
Posidabe Tablet 10/100 mg

Posidabe Tablet 10/100 mg

Prescription medicationTablet
Ingredient · strength
Dapagliflozin Propanediol Hydrate›12.3mg / 1 tabletSitagliptin Phosphate Hydrate›128.5mg / 1 tablet
Manufacturer / importer
(주)라이트팜텍
Appearance
Bright yellow rectangular film-coated tablet
Packaging
Box - 30 tablets/box [(10 tablets/Alu-Alu x 3)], Box - 28 tablets/box [(7 tablets/Alu-Alu x 4)]
Approval status
Active

MFDS item code 202200052 · Approved 2022.01.04 · Insurance code 690303480

Summary

Main use
Improvement in blood sugar control in type 2 diabetes
Who uses it
Adults
Adult dosage
For patients receiving 100 mg of sitagliptin and 10 mg of dapagliflozin, one tablet may be taken once daily, regardless of meals. The tablet should be swallowed whole.

Ingredients

Manufacturer
(주)라이트팜텍

Efficacy & effects

Improvement in blood sugar control in type 2 diabetes

View approved original text

This medication helps patients with type 2 diabetes achieve better blood sugar control while following dietary and exercise therapies. The two active ingredients, sitagliptin and dapagliflozin, work together to help stabilize blood sugar levels. It is especially suitable for those who struggle with blood sugar control with monotherapy. Continuous use can improve blood sugar management and help prevent complications. This medication is used for blood sugar control in type 2 diabetes.

Dosage and Administration

Adult dosage

For patients receiving 100 mg of sitagliptin and 10 mg of dapagliflozin, one tablet may be taken once daily, regardless of meals. The tablet should be swallowed whole.

Precautions

This medication can cause severe allergic reactions within the first 3 months of use; therefore, if symptoms such as skin rash, difficulty breathing, or swelling of the face or neck occur, you must stop using the medication immediately and consult a physician. This medication carries the risk of pancreatitis, which is inflammation of the pancreas; therefore, if severe abdominal pain or vomiting occurs, you should inform medical personnel immediately. This medication should not be used in individuals with allergies to specific ingredients, in patients with type 1 diabetes, or in patients undergoing dialysis. Patients with impaired kidney function or decreased fluid volume should have their kidney function and blood pressure periodically monitored while using this medication, and caution is advised if symptoms of hypotension occur. This medication can increase the risk of genital infections and urinary tract infections, so if infection symptoms appear, immediate treatment is necessary. There is a risk of serious metabolic conditions such as diabetic ketoacidosis; contact medical personnel immediately if symptoms like vomiting, abdominal pain, difficulty breathing, or lethargy occur. When administering to older adults, regularly assess kidney function and pay special attention to fluid volume depletion or symptoms of hypoglycemia. Pregnant or breastfeeding women should refrain from using this medication, and if pregnancy is confirmed, use should be discontinued immediately. Caution is necessary while driving or operating machinery, as there is a risk of hypoglycemia during use. In the case of overdose, there are no specific antidotes, so appropriate treatment based on symptoms should be provided, and in severe cases, dialysis may be needed. This medication should be stored in its original container, out of reach of children.

Side effects and when to seek care immediately

Serious side effects

Hives, severe swelling (angioedema), anaphylaxis, severe skin adverse reactions (Stevens-Johnson syndrome, exfoliative dermatitis, pemphigus-like blistering), acute pancreatitis, hemorrhagic or necrotizing pancreatitis, difficulty breathing, asthma attacks, jaundice, liver abnormalities, sudden and severe headache, seizures, confusion, visual disturbances, paralysis, acute renal failure, elevated blood pressure, and severe swelling, marked decrease in urine output, perineum

Mild side effects

  • Headache
  • dizziness
  • constipation
  • dry mouth
  • hypoglycemia
  • vulvovaginitis
  • balanitis
  • fungal infections
  • urinary tract infections
  • weight loss
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  • weakness
  • pain
  • itching
  • sweating
  • nausea
  • diarrhea
  • vomiting
  • abdominal pain
  • indigestion
  • fever
  • facial swelling
  • eye pain
  • dry eyes
  • insomnia
  • palpitations
  • hunger
  • vaginal discharge
  • menstrual irregularities
  • blepharitis
  • cataract
  • conjunctivitis
  • diplopia
  • eyelid swelling
  • tinnitus
  • bronchitis
  • asthma
  • voice disorders
  • cough
  • chest discomfort

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

Storage

This medication may be sensitive to air or moisture; therefore, it should be stored in a sealed container. It is recommended to maintain a storage temperature between 1 and 30 degrees Celsius to preserve the efficacy and safety of the medication for an extended period.

Appearance and packaging

Appearance

Bright yellow rectangular film-coated tablet

Package unit

Box - 30 tablets/box [(10 tablets/Alu-Alu x 3)], Box - 28 tablets/box [(7 tablets/Alu-Alu x 4)]

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.