Carlina-M Tablet 2.5 mg + 1000 mg is a combination oral antidiabetic medication formulated to manage type 2 diabetes mellitus in adults. It combines Linagliptin 2.5 mg, a DPP-4 inhibitor, and Metformin Hydrochloride 1000 mg, a biguanide, offering complementary mechanisms to control blood glucose levels effectively.
Metformin primarily reduces hepatic glucose production and improves peripheral insulin sensitivity, while Linagliptin enhances incretin hormone activity, increasing insulin release in response to meals and decreasing glucagon secretion. This dual action helps lower both fasting and postprandial blood glucose levels, promoting better glycemic control.
Carlina-M is suitable for patients who require combination therapy due to insufficient glycemic control with Metformin alone, and it may be used as part of a comprehensive diabetes management plan including diet and lifestyle modifications.
রেজিস্টার্ড চিকিৎসকের পরামর্শ অনুযায়ী ঔষধ সেবন করুন
Antidiabetic Agent
Combination Therapy: DPP-4 Inhibitor + Biguanide
Carlina-M Tablet is indicated for:
Type 2 diabetes mellitus in adults
Patients not achieving adequate glycemic control with Metformin monotherapy
Patients who benefit from combination therapy to reduce both fasting and postprandial glucose levels
Adjunct therapy to diet and exercise for improved glycemic control
Metformin Hydrochloride:
Reduces hepatic glucose production (gluconeogenesis)
Increases peripheral glucose uptake and utilization
Improves insulin sensitivity
Does not stimulate insulin secretion, thus minimizing risk of hypoglycemia
Linagliptin:
Inhibits the enzyme dipeptidyl peptidase-4 (DPP-4)
Prolongs activity of incretin hormones (GLP-1 and GIP)
Enhances glucose-dependent insulin secretion
Suppresses postprandial glucagon release
The combination of Linagliptin and Metformin provides synergistic glucose-lowering effects while maintaining a low risk of hypoglycemia.
Adults: 1 tablet daily with meals, preferably with breakfast or as prescribed by a physician
Tablets should be swallowed whole with water
Dosage may be adjusted based on glycemic response and patient tolerance
Should be used in conjunction with diet and exercise to maximize therapeutic benefits
Note: Renal and hepatic function should be assessed prior to initiation and periodically during therapy.
Known hypersensitivity to Linagliptin, Metformin, or any component of the formulation
Severe renal impairment (eGFR <30 mL/min/1.73 m²)
Acute or chronic metabolic acidosis, including diabetic ketoacidosis
Hepatic impairment
Conditions predisposing to hypoxia (e.g., cardiac or respiratory failure)
Common side effects may include:
Gastrointestinal disturbances: nausea, vomiting, diarrhea, abdominal discomfort
Mild headache
Hypoglycemia is rare when used without insulin or sulfonylureas
Rare but serious adverse effects include lactic acidosis (primarily due to Metformin), pancreatitis (with Linagliptin), or severe hypersensitivity reactions.
Safety in pregnancy and lactation has not been fully established
Use only if clearly needed and under medical supervision
Monitor renal and hepatic function regularly
Adjust dosage in elderly patients or those with renal impairment
Maintain adequate hydration
Use caution when co-administered with drugs that may affect renal function or glucose metabolism
Store below 30°C in a dry place
Protect from light and moisture
Keep out of reach of children
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