
Sitagliptin (50mg) + Metformin (500mg)
Active composition
+1 more active ingredient
Sitagliptin inhibits DPP-4, increasing incretin levels, which stimulate insulin release and reduce glucagon secretion.
Metformin reduces hepatic glucose production and enhances peripheral insulin sensitivity, lowering blood glucose levels.
Medical applications
Ignalis-M 50/500 Tablet ER is a combination oral antidiabetic medication containing Sitagliptin 50 mg and Metformin 500 mg in an extended-release formulation. It is indicated for the management of type 2 diabetes mellitus, particularly in patients whose hyperglycemia is inadequately controlled by diet and exercise alone. Sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that enhances the incretin system, thereby increasing insulin secretion and decreasing glucagon levels in a glucose-dependent manner. Metformin, a biguanide, primarily acts by reducing hepatic glucose production and improving peripheral insulin sensitivity. The extended-release formulation allows for once-daily dosing, improving patient compliance and minimizing gastrointestinal side effects commonly associated with immediate-release metformin. Ignalis-M 50/500 Tablet ER should be used as part of a comprehensive diabetes management plan including diet, exercise, and regular blood glucose monitoring. Caution is advised in patients with renal impairment, hepatic dysfunction, or conditions predisposing to lactic acidosis. Common adverse effects may include gastrointestinal disturbances such as nausea, diarrhea, and abdominal discomfort. Regular monitoring of renal function and glycemic control is recommended during therapy. This combination therapy offers a synergistic approach to glycemic control by targeting multiple pathophysiological defects in type 2 diabetes.
Dosage information not available. Please consult your doctor or pharmacist.
Important precautions
Based on clinical trials and patient reports.
Overall Tolerance
Common Side Effects
Information regarding the use of Ignalis-M 50/500 Tablet ER during pregnancy is not available. Please consult your doctor.
High Risk
Ignalis-M 50/500 Tablet ER is probably unsafe to use during breastfeeding. Limited human data suggests that the drug may pass into the breastmilk and harm the baby.
Medical Advice
Ignalis-M 50/500 Tablet ER should be used with caution in patients with kidney disease. Dose adjustment of Ignalis-M 50/500 Tablet ER may be needed. Please consult your doctor. Use of Ignalis-M 50/500 Tablet ER is, however, not recommended in patients with severe kidney disease. Regular monitoring of kidney function test is advisable while you are taking this medicine.
Exercise Caution
Your ability to drive may be affected if your blood sugar is too low or too high. Do not drive if these symptoms occur.
Consult Doctor
Ignalis-M 50/500 Tablet ER is probably unsafe to use in patients with liver disease and should be avoided. Please consult your doctor.
Regular Checkup
0 reviews for Ignalis-M 50/500 Tablet ER

Sitagliptin (50mg) + Metformin (500mg)
Cheaper alternative availability
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Active composition
+1 more active ingredient
Sitagliptin inhibits DPP-4, increasing incretin levels, which stimulate insulin release and reduce glucagon secretion.
Metformin reduces hepatic glucose production and enhances peripheral insulin sensitivity, lowering blood glucose levels.
Medical applications
Ignalis-M 50/500 Tablet ER is a combination oral antidiabetic medication containing Sitagliptin 50 mg and Metformin 500 mg in an extended-release formulation. It is indicated for the management of type 2 diabetes mellitus, particularly in patients whose hyperglycemia is inadequately controlled by diet and exercise alone. Sitagliptin is a dipeptidyl peptidase-4 (DPP-4) inhibitor that enhances the incretin system, thereby increasing insulin secretion and decreasing glucagon levels in a glucose-dependent manner. Metformin, a biguanide, primarily acts by reducing hepatic glucose production and improving peripheral insulin sensitivity. The extended-release formulation allows for once-daily dosing, improving patient compliance and minimizing gastrointestinal side effects commonly associated with immediate-release metformin. Ignalis-M 50/500 Tablet ER should be used as part of a comprehensive diabetes management plan including diet, exercise, and regular blood glucose monitoring. Caution is advised in patients with renal impairment, hepatic dysfunction, or conditions predisposing to lactic acidosis. Common adverse effects may include gastrointestinal disturbances such as nausea, diarrhea, and abdominal discomfort. Regular monitoring of renal function and glycemic control is recommended during therapy. This combination therapy offers a synergistic approach to glycemic control by targeting multiple pathophysiological defects in type 2 diabetes.
Dosage information not available. Please consult your doctor or pharmacist.
Important precautions
Based on clinical trials and patient reports.
Overall Tolerance
Common Side Effects
Information regarding the use of Ignalis-M 50/500 Tablet ER during pregnancy is not available. Please consult your doctor.
High Risk
Ignalis-M 50/500 Tablet ER is probably unsafe to use during breastfeeding. Limited human data suggests that the drug may pass into the breastmilk and harm the baby.
Medical Advice
Ignalis-M 50/500 Tablet ER should be used with caution in patients with kidney disease. Dose adjustment of Ignalis-M 50/500 Tablet ER may be needed. Please consult your doctor. Use of Ignalis-M 50/500 Tablet ER is, however, not recommended in patients with severe kidney disease. Regular monitoring of kidney function test is advisable while you are taking this medicine.
Exercise Caution
Your ability to drive may be affected if your blood sugar is too low or too high. Do not drive if these symptoms occur.
Consult Doctor
Ignalis-M 50/500 Tablet ER is probably unsafe to use in patients with liver disease and should be avoided. Please consult your doctor.
Regular Checkup
0 reviews for Ignalis-M 50/500 Tablet ER













