Linatab M 2.5/850 Tablet
by Incepta Pharmaceuticals Ltd
৳14.00
SK+F
Linagliptin + Metformin Hydrochloride
When treatment with both Linagliptin and Metformin Hydrochloride is appropriate, this is advised as an addition to diet and exercise to enhance glycemic control in persons with type 2 diabetes mellitus.
Linagliptin is used to improve blood sugar control in patients with type 2 diabetes. Linagliptin is an inhibitor of DPP4 (dipeptidyl peptidase 4), which is an enzyme that degrades the incretin hormones GLP1 (glucagon-like peptide 1) and GIP (insulin-stimulating polypeptide-dependent glucose). Therefore, Linagliptin increases the concentration of active incretin hormone, stimulates pancreatic β (β) cells to release insulin in a glucose-dependent manner, and reduces the secretion of glucagon from pancreatic α (α) cells in the circulation.
Metformin hydrochloride is an oral biguanide hypoglycemic agent, used to treat type 2 diabetes, which can reduce basal and postprandial blood sugar. Its mechanism of action is different from that of sulfonylureas and does not produce hypoglycemia. Metformin hydrochloride reduces the production of liver glucose, reduces the absorption of intestinal glucose, and improves insulin sensitivity by increasing the absorption and utilization of peripheral glucose.
Linagliptin & Metformin immediate release tablet: The dosage of Linagliptin & Metformin should be individualized on the basis of both effectiveness and tolerability. Maximum recommended dose of 2.5 mg Linagliptin and 1000 mg Metformin Hydrochloride twice daily with meals. Dose escalation should be gradual to reduce the gastrointestinal (GI) side effects associated with Metformin Hydrochloride use.
Recommended starting dose: In patients currently not treated with Metformin Hydrochloride, initiate treatment with 2.5 mg Linagliptin and 500 mg Metformin Hydrochloride twice daily.
In patients already treated with Metformin Hydrochloride, start with 2.5 mg Linagliptin and the current dose of Metformin Hydrochloride twice daily.
Patients already treated with Linagliptin and Metformin Hydrochloride, individual components may be switched to this combination containing the same doses of each component.
Linagliptin & Metformin extend release tablet: The dosage of this combination should be individualized on the basis of both effectiveness and tolerability, while not exceeding the maximum recommended total daily dose of Linagliptin 5 mg and Metformin Hydrochloride 2000 mg. this combination should be given once daily with a meal.
Recommended starting dose: In patients currently not treated with metformin, initiate this combination treatment with 5 mg Linagliptin/1000 mg Metformin Hydrochloride extended-release once daily with a meal.
In patients already treated with Metformin, start this combination with 5 mg of Linagliptin total daily dose and a similar total daily dose of Metformin once daily with a meal.
In patients already treated with Linagliptin & Metformin immediate release tablet, switch to extend release tablet containing 5 mg of Linagliptin total daily dose and a similar total daily dose of Metformin once daily with a meal.
5 mg Linagliptin & 1000 mg Metformin Hydrochloride extended-release tablet should be taken as a single tablet once daily. Patients using 2.5 mg Linagliptin & 1000 mg Metformin extended release tablets should take two tablets together once daily.
Amiloride, digoxin, morphine, ranitidine, trimethoprim, and other cationic medicines may impair metformin elimination.
P-glycoprotein/CYP3A4 inducer (i.e. rifampin): When used together, the efficacy of this medicine may be diminished.
Metformin Hydrochloride is known to be considerably eliminated by the kidney, notwithstanding Linagliptin's limited renal excretion. With the severity of renal impairment, the risk of Metformin Hydrochloride buildup and lactic acidosis increases. As a result, people with renal impairment should avoid this combination. Acute or chronic metabolic acidosis (diabetic ketoacidosis) and hypersensitivity to Linagliptin or Metformin Hydrochloride are other contraindications.
Most common side effects are nasopharyngitis and diarrhea. Hypoglycemia is more common in patients treated with this combination and sulfonylureas.
There are no adequate and well-controlled studies in pregnant women with this combination or its individual component; so it should be used during pregnancy only if clearly needed. Caution should also be excercised when it is administered to a lactating mother.
Metformin should be stopped immediately in patients with lactic acidosis who are taking it, and supportive care should be started very once. Acute pancreatitis has been reported after the drug's release. If pancreatitis is detected, stop taking Linagliptin and Metformin very away. In patients having radiologic investigations with intravascular infusion of iodinated contrast materials or any surgical procedures requiring restricted food and fluid intake, temporarily stop taking Linagliptin and Metformin. Because metformin can lower Vitamin B12 levels, hematologic markers should be checked at least once a year.
Combination Oral hypoglycemic preparations
Store in a cool, dry place (below 30° C), away from light & moisture. Keep out of the reach of children.
Eskayef Pharmaceuticals Ltd.