Medication info

Aimet Tablet 50/1000 Milligrams

Prescription medicationTablet경구
Ingredient · strength
Sitagliptin Phosphate Hydrate›64.25mg / 1 tabletMetformin Hydrochloride›1000mg / 1 tablet
Manufacturer / importer
(주)인트로바이오파마
Appearance
Dark red oval film-coated tablet
Packaging
Bottle packaging - 30 tablets per bottle, Bottle packaging - 120 tablets per bottle
Approval status
Active

MFDS item code 202201027 · Approved 2022.03.11

Summary

Main use
Improvement in blood glucose control in type 2 diabetes
Who takes it
Adults
Adult dose
This drug is generally taken twice daily with food, with dosage increased gradually to reduce gastrointestinal side effects caused by Metformin. 1. For patients not currently treated with Metformin: The starting dose is 50/500 mg, taken as 1 tablet twice daily, with potential to increase to 50/1000 mg at 1 tablet twice daily. 2. For patients currently treated with Metformin: Sitagliptin 50

Ingredients

Manufacturer
(주)인트로바이오파마

Efficacy & effects

Improvement in blood glucose control in type 2 diabetes

View approved original text

This medication is prescribed to help/control blood sugar in patients with type 2 diabetes who use Sitagliptin and Metformin together. When taken in conjunction with dietary and exercise therapy, it can effectively manage blood sugar levels. This helps maintain steady blood sugar levels and reduces the risk of complications. Consistent usage can greatly aid in blood sugar control.

How to take

Adult dose

This drug is generally taken twice daily with food, with dosage increased gradually to reduce gastrointestinal side effects caused by Metformin. 1. For patients not currently treated with Metformin: The starting dose is 50/500 mg, taken as 1 tablet twice daily, with potential to increase to 50/1000 mg at 1 tablet twice daily. 2. For patients currently treated with Metformin: Sitagliptin 50

Precautions

This medication contains Sitagliptin and Metformin and is used for diabetes treatment. During treatment with this drug, severe allergic reactions may occur; if you notice symptoms such as skin rash, difficulty breathing, or swelling of the face or neck, stop taking the medication immediately and inform healthcare professionals. Acute pancreatitis, a serious pancreatic inflammation, may occur; if symptoms like abdominal pain, vomiting, or nausea arise, consult your doctor immediately. Patients with severely impaired kidney function, acute heart failure, severe infections, or those scheduled for surgery should not take this medication. Women who are pregnant or may become pregnant and those who are breastfeeding should also refrain from taking this medication. This medication carries a risk of hypoglycemia, so it is vital to regularly check blood sugar levels when taken alongside insulin or sulfonylureas and to watch for symptoms of hypoglycemia. Due to the Metformin component, rare but potentially fatal metabolic anomalies such as lactic acidosis may occur, so symptoms such as shortness of breath, muscle pain, fatigue, or abdominal pain should be reported to medical personnel immediately. Regular monitoring of kidney function and blood vitamin B12 levels during the course of this medication is essential. Alcohol consumption may raise the risk of lactic acidosis, so it is advisable not to drink excessively while on this medication. In the event of surgery, stop taking this medication 48 hours prior to the procedure and resume only after kidney function has returned to normal post-surgery. Safety and efficacy for children and adolescents under 18 have not been established, so its use is not recommended for this population. Elderly individuals may have compromised kidney function, so kidney function should be monitored frequently when taking this medication, and dose adjustments may be necessary. This medication may interact with other drugs, so it is imperative to inform healthcare providers of all medications currently being taken. If any blisters on the skin or severe joint pain occur while taking this medication, consult a doctor immediately.

Side effects and when to seek care immediately

Serious side effects

Hives, angioedema, anaphylaxis, Stevens-Johnson syndrome, exfoliative skin conditions, acute pancreatitis, acute renal failure, difficulty breathing, acute pancreatitis, acute renal failure, hypoglycemia, severe hypoglycemia, severe lactic acidosis, lactic acidosis, acute or chronic metabolic acidosis, severe edema, acute myocardial infarction, cardiovascular collapse (shock), liver abnormalities (including jaundice) symptoms (elevation of liver enzymes), severe joint pain with disability

Mild side effects

  • Diarrhea
  • upper respiratory infection
  • headache
  • nausea
  • vomiting
  • abdominal pain
  • nasopharyngitis
  • constipation
  • muscle pain
  • limb pain
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  • back pain
  • pruritus
  • itching
  • thrombocytopenia
  • dizziness
  • loss of appetite
  • weight loss
  • vitamin B12 deficiency
  • weakness

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

Storage

This medication should be stored in an airtight container away from air and kept at room temperature between 1 to 30 degrees Celsius. This ensures that the drug's components remain stable and safe for use.

Appearance and packaging

Appearance

Dark red oval film-coated tablet

Package unit

Bottle packaging - 30 tablets per bottle, Bottle packaging - 120 tablets per bottle

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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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.