What happens when lynopril hydrochlorothiazide tablets are discontinued?

Lenopril hydrochlorothiazide tablets may cause an increase in blood pressure after discontinuation. Clinically, lynopril hydrochlorothiazide tablets are diuretics, which can enhance plasma renin activity and aldosterone secretion. Secondly, it can also inhibit angiotensin-converting enzyme, leading to a decrease in aldosterone secretion. This leads to a decrease in blood pressure, and is therefore mainly used in the treatment of hypertension. If Lenopril Hydrochlorothiazide Tablets are suddenly discontinued, the blood pressure may rise for a short period of time, thus returning to the level before the treatment, or in severe cases, continuing to rise above the original level, thus discontinuation of the drug is not conducive to the control of blood pressure. Dizziness, headache, cough, diarrhea, nausea, vomiting and other discomforts may usually occur after taking the drug. It is also forbidden to take the drug if you are allergic to the components of the drug, have hereditary or congenital angioedema, are pregnant, or have bilateral renal artery stenosis. Secondly, it should be used with caution for athletes, pregnant and lactating women. If you need to take Lenopril hydrochlorothiazide tablets for treatment of your condition, it is recommended to consult a cardiovascular physician in time to decide on the dose of the drug and learn the precautions after the doctor evaluates your condition.