Medication info
Lidipom Extended Release Tablet 5/1000 mg (Linagliptin, Metformin Hydrochloride)

Lidipom Extended Release Tablet 5/1000 mg (Linagliptin, Metformin Hydrochloride)

Prescription medicationTablet경구
Ingredient · strength
Metformin Hydrochloride›1000mg / 1 tabletLinagliptin Micronized›5mg / 1 tablet
Manufacturer / importer
동광제약(주)
Appearance
Oval extended release tablet, white to almost white, engraved with L5M on one side
Packaging
28 tablets/box [7 tablets/PTP x 4], 30 tablets/bottle
Approval status
Active

MFDS item code 202400623 · Approved 2024.03.22 · Insurance code 645907540

Summary

Main use
Improvement in blood glucose control in type 2 diabetes
Who takes it
Adults
Adult dose
The 5/1000 mg extended release tablet is taken once daily, with one tablet per dose. For patients taking the 2.5/1000 mg extended release tablet, two tablets should be taken simultaneously once daily. 1. If not currently being treated with Metformin: The initial dose of this medication is a total daily amount of 5 mg linagliptin and 1000 mg metformin hydrochloride, and the metformin hydrochloride may be gradually increased to the maximum recommended daily dose of 2000.

Ingredients

Manufacturer
동광제약(주)

Efficacy & effects

Improvement in blood glucose control in type 2 diabetes

View approved original text

This medication helps control blood glucose in patients with type 2 diabetes through the combined use of linagliptin and metformin. Patients can effectively manage their blood glucose levels by taking this medication alongside dietary and exercise therapy. This combination treatment improves blood glucose management and helps prevent complications from diabetes. Therefore, it is appropriately used for blood glucose control in patients with type 2 diabetes.

How to take

Adult dose

The 5/1000 mg extended release tablet is taken once daily, with one tablet per dose. For patients taking the 2.5/1000 mg extended release tablet, two tablets should be taken simultaneously once daily. 1. If not currently being treated with Metformin: The initial dose of this medication is a total daily amount of 5 mg linagliptin and 1000 mg metformin hydrochloride, and the metformin hydrochloride may be gradually increased to the maximum recommended daily dose of 2000.

Precautions

This medication may cause a rare side effect called lactic acidosis, therefore caution is required. It should not be administered to patients with severely impaired renal function or those in a state of severe infection or dehydration. Patients with allergies to this medication or those with type 1 diabetes or diabetic ketoacidosis should also avoid use. Patients with severely impaired cardiac function or liver dysfunction should also refrain from using this medication. It should not be used during pregnancy or in cases of acute alcohol intoxication. This medication carries a risk of hypoglycemia; thus, when used with insulin or sulfonylureas, blood glucose must be closely monitored. Symptoms of lactic acidosis include difficulty breathing, weakness, and abdominal pain, and if such symptoms occur, the doctor must be notified immediately. Renal function is crucial, and regular kidney function tests should be performed before and during treatment, and the medication should be discontinued if renal function declines. If iodinated contrast is used for radiological tests, this medication should be suspended for a certain period before and after the tests, and renal function should also be re-evaluated. Patients scheduled for surgery should discontinue this medication 48 hours prior to surgery and resume it once renal function is normal after the surgery. While taking this medication, rare side effects such as acute pancreatitis or skin vesicles resembling bullous pemphigoid may occur, so any symptoms should be reported immediately. This medication should be swallowed whole without crushing or chewing, and it is normal for the tablet coating to pass out in stool. Long-term use may lead to vitamin B12 deficiency, so regular blood tests may be required. This medication may interact with several other medications; therefore, if other medications are being taken, one must consult a physician or pharmacist. Elderly patients are commonly prone to impaired renal function, therefore dosing adjustments and monitoring of kidney function are particularly important. It is not recommended for use during pregnancy or breastfeeding without consulting healthcare professionals. Overdose may result in serious side effects such as lactic acidosis, necessitating immediate hospital treatment. This medication should be stored out of reach of children and kept away from moisture, avoiding transfer to other containers.

Side effects and when to seek care immediately

Serious side effects

Hives, angioedema, lactic acidosis, severe allergic reactions, angioedema, severe swelling (edema), difficulty breathing, severe skin adverse reactions (fever with severe rash, blisters, skin peeling, mucosal pain in mouth/eyes), severe swelling or urination abnormalities (significant reduction in urine output, severe systemic edema, accompanied by increased blood pressure), acute pancreatitis, sudden and severe headaches, seizures, confusion, vision abnormalities, paralysis

Mild side effects

Nasopharyngitis, immune system abnormalities (excluding hypersensitivity), taste disorders, cough, decreased appetite, diarrhea, constipation, nausea, vomiting, abdominal pain, oral ulcers, abnormal liver function tests, hepatitis, itching, erythema, rashes, severe and non-disabling arthralgia, increased serum lipase, increased amylase, abnormal vitamin B12 absorption test, hypoglycemia (when combined with sulfonylureas), increased serum creatinine, dizziness, headache, drowsiness

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

Storage

This medication may be sensitive to air or moisture, and should therefore be stored in a sealed container. Additionally, for safe use of the medication, it is best to store it at room temperature between 1°C and 30°C.

Appearance and packaging

Appearance

Oval extended release tablet, white to almost white, engraved with L5M on one side

Package unit

28 tablets/box [7 tablets/PTP x 4], 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.

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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.