
Metoprolol Succinate (23.75mg) + Telmisartan (40mg)
Active composition
+1 more active ingredient
Metoprolol Succinate blocks beta-1 adrenergic receptors, leading to decreased heart rate and contractility, thereby lowering blood pressure.
Telmisartan selectively blocks angiotensin II receptors, leading to vasodilation and decreased blood pressure.
Medical applications
Gudtel-M 25 Tablet ER is a combination antihypertensive medication containing Telmisartan 40 mg and Metoprolol Succinate 23.75 mg in an extended-release formulation. Telmisartan, an angiotensin II receptor blocker (ARB), selectively inhibits the binding of angiotensin II to the AT1 receptor, thereby reducing vasoconstriction and aldosterone secretion, which leads to decreased blood pressure and improved cardiovascular outcomes. Metoprolol Succinate, a beta-1 selective adrenergic blocker, reduces heart rate, myocardial contractility, and cardiac output, contributing to blood pressure reduction and decreased myocardial oxygen demand. The extended-release formulation ensures sustained plasma concentrations, promoting once-daily dosing and improved patient compliance. Gudtel-M 25 is indicated for the management of essential hypertension, particularly in patients requiring combination therapy to achieve optimal blood pressure control. It may also be beneficial in patients with concomitant cardiovascular conditions such as ischemic heart disease or heart failure where beta-blockade is advantageous. Caution is advised in patients with bradycardia, heart block, or severe hepatic impairment. Common adverse effects include dizziness, fatigue, and hypotension. Regular monitoring of blood pressure, renal function, and electrolytes is recommended during therapy. Gudtel-M 25 should be used under medical supervision to ensure safety and efficacy.
Dosage information not available. Please consult your doctor or pharmacist.
Important precautions
Based on clinical trials and patient reports.
Overall Tolerance
Common Side Effects
Gudtel-M 25 Tablet ER is unsafe to use during pregnancy as there is definite evidence of risk to the developing baby. However, the doctor may rarely prescribe it in some life-threatening situations if the benefits are more than the potential risks. Please consult your doctor.
High Risk
Gudtel-M 25 Tablet ER is probably safe to use during breastfeeding. Limited human data suggests that the drug does not represent any significant risk to the baby.
Medical Advice
Gudtel-M 25 Tablet ER is safe to use in patients with kidney disease. No dose adjustment of Gudtel-M 25 Tablet ER is recommended.
Exercise Caution
Gudtel-M 25 Tablet ER may decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.
Consult Doctor
Gudtel-M 25 Tablet ER should be used with caution in patients with liver disease. Dose adjustment of Gudtel-M 25 Tablet ER may be needed. Please consult your doctor.
Regular Checkup
0 reviews for Gudtel-M 25 Tablet ER

Telmisartan (40mg) + Metoprolol Succinate (23.75mg)
Cheaper alternative availability
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Active composition
+1 more active ingredient
Metoprolol Succinate blocks beta-1 adrenergic receptors, leading to decreased heart rate and contractility, thereby lowering blood pressure.
Telmisartan selectively blocks angiotensin II receptors, leading to vasodilation and decreased blood pressure.
Medical applications
Gudtel-M 25 Tablet ER is a combination antihypertensive medication containing Telmisartan 40 mg and Metoprolol Succinate 23.75 mg in an extended-release formulation. Telmisartan, an angiotensin II receptor blocker (ARB), selectively inhibits the binding of angiotensin II to the AT1 receptor, thereby reducing vasoconstriction and aldosterone secretion, which leads to decreased blood pressure and improved cardiovascular outcomes. Metoprolol Succinate, a beta-1 selective adrenergic blocker, reduces heart rate, myocardial contractility, and cardiac output, contributing to blood pressure reduction and decreased myocardial oxygen demand. The extended-release formulation ensures sustained plasma concentrations, promoting once-daily dosing and improved patient compliance. Gudtel-M 25 is indicated for the management of essential hypertension, particularly in patients requiring combination therapy to achieve optimal blood pressure control. It may also be beneficial in patients with concomitant cardiovascular conditions such as ischemic heart disease or heart failure where beta-blockade is advantageous. Caution is advised in patients with bradycardia, heart block, or severe hepatic impairment. Common adverse effects include dizziness, fatigue, and hypotension. Regular monitoring of blood pressure, renal function, and electrolytes is recommended during therapy. Gudtel-M 25 should be used under medical supervision to ensure safety and efficacy.
Dosage information not available. Please consult your doctor or pharmacist.
Important precautions
Based on clinical trials and patient reports.
Overall Tolerance
Common Side Effects
Gudtel-M 25 Tablet ER is unsafe to use during pregnancy as there is definite evidence of risk to the developing baby. However, the doctor may rarely prescribe it in some life-threatening situations if the benefits are more than the potential risks. Please consult your doctor.
High Risk
Gudtel-M 25 Tablet ER is probably safe to use during breastfeeding. Limited human data suggests that the drug does not represent any significant risk to the baby.
Medical Advice
Gudtel-M 25 Tablet ER is safe to use in patients with kidney disease. No dose adjustment of Gudtel-M 25 Tablet ER is recommended.
Exercise Caution
Gudtel-M 25 Tablet ER may decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.
Consult Doctor
Gudtel-M 25 Tablet ER should be used with caution in patients with liver disease. Dose adjustment of Gudtel-M 25 Tablet ER may be needed. Please consult your doctor.
Regular Checkup
0 reviews for Gudtel-M 25 Tablet ER















