Medication info
Rinadiem Met Extended-Release Tablet 2.5/1000 mg (Linagliptin, Metformin)

Rinadiem Met Extended-Release Tablet 2.5/1000 mg (Linagliptin, Metformin)

Prescription medicationTablet경구
Ingredient · strength
Metformin Hydrochloride›1000mg / 1 tabletLinagliptin Micronized›2.5mg / 1 tablet
Manufacturer / importer
동화약품(주)
Appearance
Yellow, double convex, oval extended-release film-coated tablet
Packaging
30 tablets/bottle
Approval status
Active

MFDS item code 202400388 · Approved 2024.02.22 · Insurance code 642707560

Summary

Main use
Improvement of blood glucose control in type 2 diabetes
Who takes it
Adults
Adult dose
This medication should be taken once daily with dinner. 5/1000 mg extended-release tablets are to be taken as 1 tablet once daily. Patients taking 2.5/1000 mg extended-release tablets should take 2 tablets at once once daily. The maximum recommended daily dose should not exceed Linagliptin 5 mg and extended-release Metformin Hydrochloride 2000 mg.

Ingredients

Manufacturer
동화약품(주)

Efficacy & effects

Improvement of blood glucose control in type 2 diabetes

View approved original text

This medication is used to assist blood glucose control in patients with type 2 diabetes who are also following dietary and exercise regimens. By administering Linagliptin and Metformin together, it helps manage blood glucose more effectively.

How to take

Adult dose

This medication should be taken once daily with dinner. 5/1000 mg extended-release tablets are to be taken as 1 tablet once daily. Patients taking 2.5/1000 mg extended-release tablets should take 2 tablets at once once daily. The maximum recommended daily dose should not exceed Linagliptin 5 mg and extended-release Metformin Hydrochloride 2000 mg.

Precautions

This medication may cause severe lactic acidosis or hypoglycemia, therefore caution is required. Individuals with an allergy to any of the ingredients or other components should not use this medication. It is not indicated for patients with type 1 diabetes, lactic acidosis, or diabetic ketoacidosis. Patients with severely impaired kidney function or in a state where acute kidney damage is anticipated should not use this medication. Administration should be avoided during acute illnesses affecting kidney function, such as dehydration, severe infections, severe injuries, or acute myocardial infarction. Patients with very poor cardiac function or severe pulmonary dysfunction should exercise caution when using this medication. Patients with liver dysfunction or severe gastrointestinal disorders should preferably avoid this medication. It should not be used in cases of acute or chronic alcohol intoxication. Administration should be avoided in patients with very poor nutritional status or states of starvation or frailty. Patients with acute and unstable heart failure, pregnant women at risk of placental insufficiency or pre-eclampsia, or those with a history of myocardial infarction should not use this medication. Due to the risk of hypoglycemia, careful dose adjustment is necessary, especially when used in combination with sulfonylureas or insulin. Although lactic acidosis is very rare, it is a serious complication that requires immediate consultation with a doctor in cases of worsening kidney function, cardiopulmonary disease, or sepsis. Regular monitoring of kidney function is recommended, especially for elderly patients or those with deteriorated kidney function. If iodinated contrast agents are used for imaging studies, it is necessary to discontinue this medication before and after the exam and check the kidney function status. It is advised to temporarily stop taking this medication for a certain period before and after surgery. If symptoms of acute pancreatitis or bullous skin disease occur, promptly inform a physician and discontinue this medication. Long-term use may lead to vitamin B12 deficiency; therefore, regular blood tests are recommended. This medication should be swallowed whole without chewing or crushing, and some tablet coatings may be excreted in the stool, which is normal. There may be interactions when taken with other medications, especially those affecting kidney function, so caution is necessary when used in combination. Use during pregnancy or breastfeeding is not recommended, and those planning to become pregnant should consult healthcare professionals. Safety for pediatric use has not been established, hence it should not be used in children. For the elderly, the possibility of kidney function decline is higher, thus starting at the lowest dosage and regularly checking kidney function is advised. In case of overdose, there is a risk of lactic acidosis, and immediate hospital treatment is required; hem dialysis may be necessary. Keep this medication out of the reach of children, and store it away from moisture.

Side effects and when to seek care immediately

Serious side effects

  • Urticaria
  • angioedema
  • lactic acidosis
  • liver function abnormalities
  • hepatitis
  • sudden and severe headache
  • acute pancreatitis
  • bullous dermatitis herpetiformis
  • angioedema
  • severe edema
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  • respiratory distress
  • asthma
  • acute myocardial infarction
  • shock
  • heart failure
  • congestive heart failure
  • angina
  • unstable angina
  • cardiac arrest
  • severe allergic reaction
  • severe skin reactions
  • respiratory issues
  • liver abnormalities (jaundice)
  • severe neurological symptoms
  • severe edema or urination issues.

Mild side effects

  • Hypoglycemia
  • taste disturbance
  • cough
  • decreased appetite
  • diarrhea
  • constipation
  • nausea
  • vomiting
  • abdominal pain
  • oral ulcers
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  • liver function abnormalities
  • hepatitis
  • itching
  • erythema
  • rash
  • severe and disabling joint pain
  • rhabdomyolysis
  • increased lipase
  • increased amylase
  • nasopharyngitis
  • hypersensitivity reactions
  • angioedema
  • abnormal vitamin B12 absorption tests
  • angioedema
  • dermatitis herpetiformis
  • urticaria
  • angioedema
  • chest pain
  • fever
  • fatigue
  • facial edema

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

Storage

This medication should be stored in a tightly closed container to prevent exposure to air or moisture. It is important to maintain a storage temperature between 1 to 30 degrees Celsius.

Appearance and packaging

Appearance

Yellow, double convex, oval extended-release film-coated tablet

Package unit

30 tablets/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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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.