
Metoprolol Succinate (47.5mg) + 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 50 Tablet ER is a combination antihypertensive medication containing Telmisartan 40 mg and Metoprolol Succinate 47.5 mg in an extended-release formulation. Telmisartan, an angiotensin II receptor blocker (ARB), functions by selectively inhibiting the binding of angiotensin II to the AT1 receptor, leading to vasodilation and reduced aldosterone secretion, thereby lowering blood pressure. Metoprolol Succinate, a cardioselective beta-1 adrenergic receptor blocker, decreases heart rate, myocardial contractility, and cardiac output, contributing to antihypertensive effects and reducing myocardial oxygen demand. The extended-release formulation ensures sustained plasma concentrations, promoting once-daily dosing and improved patient compliance. Gudtel-M 50 is indicated for the management of hypertension, either as monotherapy or in patients inadequately controlled on monotherapy. 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 50 Tablet ER should be prescribed and used under medical supervision to optimize therapeutic outcomes and minimize risks.
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 50 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 50 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 50 Tablet ER is safe to use in patients with kidney disease. No dose adjustment of Gudtel-M 50 Tablet ER is recommended.
Exercise Caution
Gudtel-M 50 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 50 Tablet ER should be used with caution in patients with liver disease. Dose adjustment of Gudtel-M 50 Tablet ER may be needed. Please consult your doctor.
Regular Checkup
0 reviews for Gudtel-M 50 Tablet ER

Telmisartan (40mg) + Metoprolol Succinate (47.5mg)
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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 50 Tablet ER is a combination antihypertensive medication containing Telmisartan 40 mg and Metoprolol Succinate 47.5 mg in an extended-release formulation. Telmisartan, an angiotensin II receptor blocker (ARB), functions by selectively inhibiting the binding of angiotensin II to the AT1 receptor, leading to vasodilation and reduced aldosterone secretion, thereby lowering blood pressure. Metoprolol Succinate, a cardioselective beta-1 adrenergic receptor blocker, decreases heart rate, myocardial contractility, and cardiac output, contributing to antihypertensive effects and reducing myocardial oxygen demand. The extended-release formulation ensures sustained plasma concentrations, promoting once-daily dosing and improved patient compliance. Gudtel-M 50 is indicated for the management of hypertension, either as monotherapy or in patients inadequately controlled on monotherapy. 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 50 Tablet ER should be prescribed and used under medical supervision to optimize therapeutic outcomes and minimize risks.
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 50 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 50 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 50 Tablet ER is safe to use in patients with kidney disease. No dose adjustment of Gudtel-M 50 Tablet ER is recommended.
Exercise Caution
Gudtel-M 50 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 50 Tablet ER should be used with caution in patients with liver disease. Dose adjustment of Gudtel-M 50 Tablet ER may be needed. Please consult your doctor.
Regular Checkup
0 reviews for Gudtel-M 50 Tablet ER















