
Telmisartan (40mg) + Hydrochlorothiazide (12.5mg)
Active composition
+1 more active ingredient
Telmisartan selectively blocks angiotensin II receptors, leading to vasodilation and decreased blood pressure.
Hydrochlorothiazide inhibits sodium reabsorption in the distal convoluted tubule, leading to increased urine output and decreased blood volume.
Medical applications
Keitel-H Tablet contains a combination of Telmisartan 40mg and Hydrochlorothiazide 12.5mg, formulated for the treatment of hypertension. Telmisartan is an angiotensin II receptor antagonist that selectively blocks the binding of angiotensin II to the AT1 receptor, thereby inhibiting vasoconstriction and aldosterone secretion, which results in vasodilation and reduced blood pressure. Hydrochlorothiazide is a thiazide diuretic that promotes diuresis by inhibiting sodium reabsorption in the distal convoluted tubules of the kidneys, leading to decreased plasma volume and reduced peripheral vascular resistance. The synergistic effect of these two agents provides effective blood pressure control, reducing the risk of cardiovascular events such as stroke and myocardial infarction. Keitel-H is indicated for patients whose blood pressure is not adequately controlled by monotherapy. It is contraindicated in patients with hypersensitivity to either component, anuria, or severe renal impairment. Caution is advised in patients with electrolyte imbalances, diabetes, or gout. Regular monitoring of renal function, electrolytes, and blood pressure is recommended during therapy. Keitel-H should be used under medical supervision, with dosage adjustments based on clinical response and tolerability.
Dosage information not available. Please consult your doctor or pharmacist.
Important precautions
Based on clinical trials and patient reports.
Overall Tolerance
Common Side Effects
Keitel-H Tablet 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
Keitel-H Tablet 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
Keitel-H Tablet should be used with caution in patients with severe kidney disease. Dose adjustment of Keitel-H Tablet may be needed. Please consult your doctor. Use of Keitel-H Tablet is not recommended in patients with severe kidney disease.
Exercise Caution
Keitel-H Tablet may decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.
Consult Doctor
Keitel-H Tablet should be used with caution in patients with liver disease. Dose adjustment of Keitel-H Tablet may be needed. Please consult your doctor.
Regular Checkup
0 reviews for Keitel-H Tablet

Telmisartan (40mg) + Hydrochlorothiazide (12.5mg)
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Active composition
+1 more active ingredient
Telmisartan selectively blocks angiotensin II receptors, leading to vasodilation and decreased blood pressure.
Hydrochlorothiazide inhibits sodium reabsorption in the distal convoluted tubule, leading to increased urine output and decreased blood volume.
Medical applications
Keitel-H Tablet contains a combination of Telmisartan 40mg and Hydrochlorothiazide 12.5mg, formulated for the treatment of hypertension. Telmisartan is an angiotensin II receptor antagonist that selectively blocks the binding of angiotensin II to the AT1 receptor, thereby inhibiting vasoconstriction and aldosterone secretion, which results in vasodilation and reduced blood pressure. Hydrochlorothiazide is a thiazide diuretic that promotes diuresis by inhibiting sodium reabsorption in the distal convoluted tubules of the kidneys, leading to decreased plasma volume and reduced peripheral vascular resistance. The synergistic effect of these two agents provides effective blood pressure control, reducing the risk of cardiovascular events such as stroke and myocardial infarction. Keitel-H is indicated for patients whose blood pressure is not adequately controlled by monotherapy. It is contraindicated in patients with hypersensitivity to either component, anuria, or severe renal impairment. Caution is advised in patients with electrolyte imbalances, diabetes, or gout. Regular monitoring of renal function, electrolytes, and blood pressure is recommended during therapy. Keitel-H should be used under medical supervision, with dosage adjustments based on clinical response and tolerability.
Dosage information not available. Please consult your doctor or pharmacist.
Important precautions
Based on clinical trials and patient reports.
Overall Tolerance
Common Side Effects
Keitel-H Tablet 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
Keitel-H Tablet 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
Keitel-H Tablet should be used with caution in patients with severe kidney disease. Dose adjustment of Keitel-H Tablet may be needed. Please consult your doctor. Use of Keitel-H Tablet is not recommended in patients with severe kidney disease.
Exercise Caution
Keitel-H Tablet may decrease alertness, affect your vision or make you feel sleepy and dizzy. Do not drive if these symptoms occur.
Consult Doctor
Keitel-H Tablet should be used with caution in patients with liver disease. Dose adjustment of Keitel-H Tablet may be needed. Please consult your doctor.
Regular Checkup
0 reviews for Keitel-H Tablet















