Shanxi Lifeng Huarui Pharmaceutical Co., Ltd.

After entering the body, this product can combine with poisons containing hydroxyl or carboxyl groups to form low-toxic or non-toxic combinations that are excreted in the urine, protecting the liver and detoxifying. In addition, glucuronic acid can increase the content of liver glycogen and reduce fat reserves.

This product is an analogue of diphenhydramine, which mainly suppresses cough center and relieves cough. It also has a weak antihistamine effect and has no dependence or tolerance. It takes effect 20-30 minutes after taking it and the effect lasts for 3-4 hours.

Adrenergic neurosuppressants can block the storage of mediators in adrenergic nerve endings and deplete the mediators with pressor effects in the vesicles.

Vasodilators relax arteriolar smooth muscle and reduce peripheral resistance

Diuretic antihypertensive drugs can increase the antihypertensive effect of reserpine and hydralazine sulfate, and can also reduce their side effects of water and sodium retention

Reserpine is an adrenergic nerve inhibitor that can prevent the storage of mediators in adrenergic nerve endings and deplete the mediators with pressor effects in the vesicles. Hydralazine sulfate is a vasodilator that can relax arteriolar smooth muscle and reduce peripheral resistance. Hydrochlorothiazide is a diuretic and antihypertensive drug. The combined use of the three drugs has a significant synergistic effect. It promotes blood pressure and improves the efficacy, thereby reducing the dosage and adverse reactions of each drug. At the same time, hydrochlorothiazide can increase the antihypertensive effect of reserpine and hydralazine sulfate; it can also reduce their side effects of water and sodium retention.

Reserpine is an adrenergic nerve inhibitor that can prevent the storage of mediators in adrenergic nerve endings and deplete the mediators with pressor effects in the vesicles. Hydralazine sulfate is a vasodilator that can relax arteriolar smooth muscle and reduce peripheral resistance. Hydrochlorothiazide is a diuretic and antihypertensive drug. The combined use of the three drugs has a significant synergistic effect. It promotes blood pressure and improves the efficacy, thereby reducing the dosage and adverse reactions of each drug. At the same time, hydrochlorothiazide can increase the antihypertensive effect of reserpine and hydralazine sulfate; it can also reduce their side effects of water and sodium retention.

Reserpine is an adrenergic nerve inhibitor that can prevent the storage of mediators in adrenergic nerve endings and deplete the mediators with pressor effects in the vesicles. Hydralazine sulfate is a vasodilator that can relax arteriolar smooth muscle and reduce peripheral resistance. Hydrochlorothiazide is a diuretic and antihypertensive drug. The combined use of the three drugs has a significant synergistic effect. It promotes blood pressure and improves the efficacy, thereby reducing the dosage and adverse reactions of each drug. At the same time, hydrochlorothiazide can increase the antihypertensive effect of reserpine and hydralazine sulfate; it can also reduce their side effects of water and sodium retention.

Reserpine is an adrenergic nerve inhibitor that can prevent the storage of mediators in adrenergic nerve endings and deplete the mediators with pressor effects in the vesicles. Hydralazine sulfate is a vasodilator that can relax arteriolar smooth muscle and reduce peripheral resistance. Hydrochlorothiazide is a diuretic and antihypertensive drug. The combined use of the three drugs has a significant synergistic effect. It promotes blood pressure and improves the efficacy, thereby reducing the dosage and adverse reactions of each drug. At the same time, hydrochlorothiazide can increase the antihypertensive effect of reserpine and hydralazine sulfate; it can also reduce their side effects of water and sodium retention.

Reserpine is an adrenergic nerve inhibitor that can prevent the storage of mediators in adrenergic nerve endings and deplete the mediators with pressor effects in the vesicles. Hydralazine sulfate is a vasodilator that can relax arteriolar smooth muscle and reduce peripheral resistance. Hydrochlorothiazide is a diuretic and antihypertensive drug. The combined use of the three drugs has a significant synergistic effect. It promotes blood pressure and improves the efficacy, thereby reducing the dosage and adverse reactions of each drug. At the same time, hydrochlorothiazide can increase the antihypertensive effect of reserpine and hydralazine sulfate; it can also reduce their side effects of water and sodium retention.

Reserpine is an adrenergic nerve inhibitor that can prevent the storage of mediators in adrenergic nerve endings and deplete the mediators with pressor effects in the vesicles. Hydralazine sulfate is a vasodilator that can relax arteriolar smooth muscle and reduce peripheral resistance. Hydrochlorothiazide is a diuretic and antihypertensive drug. The combined use of the three drugs has a significant synergistic effect. It promotes blood pressure and improves the efficacy, thereby reducing the dosage and adverse reactions of each drug. At the same time, hydrochlorothiazide can increase the antihypertensive effect of reserpine and hydralazine sulfate; it can also reduce their side effects of water and sodium retention.

As a histamine H1 receptor antagonist, this product can counteract the capillary dilation caused by allergic reactions, reduce the permeability of capillaries, and relieve wheezing caused by bronchial smooth muscle contraction. This product has a long-lasting antihistamine effect and also has a significant central inhibitory effect, which can increase the effects of anesthetics, analgesics, hypnotics and local anesthetics. This product is mainly metabolized in the liver.

Antiepileptic drugs and antiarrhythmic drugs increase the outflow of sodium ions from cells, reduce the inflow of sodium ions, stabilize the nerve cell membrane, increase the excitation threshold, and reduce the spread of high-frequency discharges in the lesions; shorten the action potential interval and the effective refractory period, inhibit the influx of calcium ions, reduce myocardial automaticity, inhibit the sympathetic center, have an inhibitory effect on ectopic rhythm points in the atria and ventricles, and increase the thresholds for atrial fibrillation and ventricular fibrillation.