
Release date: 2024-12-31 14:09:08 Article From: Lucius Laos Recommended: 196
Encidipine is a commonly used calcium channel blocker, which is widely used in clinical applications for the treatment of hypertension and angina, and its efficacy is highly recognized.
In clinical use, encidipine may interact with other drugs, affecting the efficacy of the drug or increasing the risk of adverse reactions.
Encidipine is metabolized mainly by the CYP3A4 enzyme in the liver. When combined with CYP3A4 inhibitors (e.g., erythromycin, ketoconazole, itraconazole, etc.), these inhibitors slow down the metabolism of encidipine, resulting in an increase in its blood concentration, which may enhance the antihypertensive effect, but also increase the risk of adverse effects such as hypotension.
When encidipine is used in combination with β blockers (such as metoprolol, atenolol, etc.), it can produce a synergistic antihypertensive effect. This combination may also cause adverse effects such as heart rate slowing and heart block, and should be used with caution, especially in patients with cardiac insufficiency.
Encidipine is used in combination with diuretics (e.g., hydrochlorothiazide, furosemide, etc.) to further enhance the antihypertensive effect. However, it should be noted that excessive blood pressure lowering may lead to adverse consequences such as orthostatic hypotension and renal impairment. When combined, the patient's blood pressure and renal function should be closely monitored.
The use of encidipine in different special populations requires special attention to its efficacy and safety.
Older patients tend to have a weak ability to metabolize and excrete drugs, and encidipine should be started with a small dose and titrated to an effective dose. Patients should be closely monitored for changes in blood pressure to avoid adverse effects such as hypotension.
Encidipine is mainly metabolized by the liver and excreted by the kidneys. In patients with liver and kidney insufficiency, the rate of metabolism and excretion of the drug may be slowed, resulting in an increase in blood concentrations. The use of encidipine in such patients should be appropriately lowered and the adverse effects of the drug should be closely monitored.
There are limited data on the safety of ensidipine in pregnant and lactating women. Encidipine should be used with caution in these special populations, under the guidance of a physician if necessary, and with close monitoring of fetal or infant safety.
The rational use of encidipine requires an understanding of some key precautions in the process of its use.
The dose of ensidipine should be individualized according to the patient's specific situation. Initial treatment should be given in a small dose and gradually increased according to the patient's blood pressure control. The patient's blood pressure and heart rate should be monitored regularly to ensure the effectiveness and safety of the drug.
Patients who have been taking ensidipine for a long time should gradually taper the dose when stopping the drug to avoid adverse reactions such as rebound hypertension that may result from sudden discontinuation. Discontinuation should be performed under the guidance of a physician, and the patient's blood pressure should be closely monitored.
Encidipine may cause some adverse reactions during use, such as headache, flushing, palpitations, etc. Patients should pay close attention to their physical condition during use, seek medical attention in time if they have uncomfortable symptoms, and adjust the medication regimen under the guidance of a doctor.
Encidipine is an effective antihypertensive drug with a wide range of application prospects in clinical applications. In the process of use, it is necessary to fully consider factors such as drug interactions, effects on special populations, and medication precautions. Patients should use ensidipine rationally under the guidance of a doctor and closely monitor the adverse effects of the drug to achieve the best treatment effect.
Lung cancer is the most rapidly increasing malignant tumor with the fastest increasing morbidity and···【more】
Recommended:3282024-09-07
On December 12, 2025, the U.S. Food and Drug Administration (FDA) approved niraparib in combination ···【more】
Recommended:22025-15-12
The U.S. Food and Drug Administration (FDA) announced today that it has approved Omisirge (omidubice···【more】
Recommended:212025-10-12
On December 4, 2025, the U.S. Food and Drug Administration (FDA) approved lisocabtagene maraleucel (···【more】
Recommended:212025-08-12
On December 3, 2025, the U.S. Food and Drug Administration (FDA) granted full approval to pirtobruti···【more】
Recommended:242025-04-12
Primary analysis data from the randomized, double-blind, placebo-controlled phase III HER2CLIMB-02 s···【more】
Recommended:352025-01-12
The Cure SMA Foundation, a global leading non-profit organization dedicated to spinal muscular atrop···【more】
Recommended:362025-27-11
On November 14, 2024, the Committee for Medicinal Products for Human Use (CHMP) of the European Medi···【more】
Recommended:3152025-13-01

Lucius Pharmaceutical Co., Ltd., was established in 2020 in Vientiane, the capital of Laos. It aims to offer safe, effective, and affordable medicines globally. With a factory spanning 25,000 square meters, the company manufactures 200+ generic drugs in diverse therapeutic fields.
Address:No.26 Thongmang village, Xaythany district, Vientiane Capital, Laos
E-mail:laoslucius@gmail.com
Whatsapp: