
Metformin (500mg) + Sitagliptin (100mg)
Active composition
+1 more active ingredient
Metformin reduces hepatic glucose production and enhances peripheral insulin sensitivity, lowering blood glucose levels.
Sitagliptin inhibits DPP-4, increasing incretin levels, which stimulate insulin release and reduce glucagon secretion.
Medical applications
Kaisita-M 100/500 Tablet ER is a combination oral antidiabetic medication containing Sitagliptin 100 mg and Metformin 500 mg in an extended-release formulation. It is indicated for the management of type 2 diabetes mellitus in adults, particularly in patients inadequately controlled on diet and exercise alone or on monotherapy. Sitagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor, enhances the incretin system by increasing levels of active incretin hormones, which stimulate insulin release and decrease glucagon secretion in a glucose-dependent manner. Metformin, a biguanide, primarily reduces hepatic glucose production and improves insulin sensitivity, thereby enhancing peripheral glucose uptake and utilization. The extended-release formulation allows for once-daily dosing, improving patient compliance and minimizing gastrointestinal side effects commonly associated with immediate-release metformin. Kaisita-M 100/500 Tablet ER should be used as part of a comprehensive diabetes management plan including diet, exercise, and regular blood glucose monitoring. It is contraindicated in patients with renal impairment, metabolic acidosis, or hypersensitivity to its components. Common adverse effects may include gastrointestinal disturbances, headache, and nasopharyngitis. Dose adjustments and monitoring of renal function are recommended to ensure safety and efficacy during therapy.
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 Kaisita-M 100/500 Tablet ER during pregnancy is not available. Please consult your doctor.
High Risk
Kaisita-M 100/500 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
Kaisita-M 100/500 Tablet ER should be used with caution in patients with kidney disease. Dose adjustment of Kaisita-M 100/500 Tablet ER may be needed. Please consult your doctor. Use of Kaisita-M 100/500 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
Kaisita-M 100/500 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 Kaisita-M 100/500 Tablet ER

Sitagliptin (100mg) + Metformin (500mg)
Cheaper alternative availability
This medicine doesn't have a cheaper alternative with the same composition. Our health advisors can help you find other savings options based on your prescription.
Active composition
+1 more active ingredient
Metformin reduces hepatic glucose production and enhances peripheral insulin sensitivity, lowering blood glucose levels.
Sitagliptin inhibits DPP-4, increasing incretin levels, which stimulate insulin release and reduce glucagon secretion.
Medical applications
Kaisita-M 100/500 Tablet ER is a combination oral antidiabetic medication containing Sitagliptin 100 mg and Metformin 500 mg in an extended-release formulation. It is indicated for the management of type 2 diabetes mellitus in adults, particularly in patients inadequately controlled on diet and exercise alone or on monotherapy. Sitagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor, enhances the incretin system by increasing levels of active incretin hormones, which stimulate insulin release and decrease glucagon secretion in a glucose-dependent manner. Metformin, a biguanide, primarily reduces hepatic glucose production and improves insulin sensitivity, thereby enhancing peripheral glucose uptake and utilization. The extended-release formulation allows for once-daily dosing, improving patient compliance and minimizing gastrointestinal side effects commonly associated with immediate-release metformin. Kaisita-M 100/500 Tablet ER should be used as part of a comprehensive diabetes management plan including diet, exercise, and regular blood glucose monitoring. It is contraindicated in patients with renal impairment, metabolic acidosis, or hypersensitivity to its components. Common adverse effects may include gastrointestinal disturbances, headache, and nasopharyngitis. Dose adjustments and monitoring of renal function are recommended to ensure safety and efficacy during therapy.
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 Kaisita-M 100/500 Tablet ER during pregnancy is not available. Please consult your doctor.
High Risk
Kaisita-M 100/500 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
Kaisita-M 100/500 Tablet ER should be used with caution in patients with kidney disease. Dose adjustment of Kaisita-M 100/500 Tablet ER may be needed. Please consult your doctor. Use of Kaisita-M 100/500 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
Kaisita-M 100/500 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 Kaisita-M 100/500 Tablet ER













