Beijing Shunxin Xiangyun Pharmaceutical Co., Ltd.

It has the effect of promoting hematopoietic function; it can to a certain extent counteract the atrophy of the thymus, spleen, and adrenal glands of mice with "qi deficiency" caused by dietary restriction, and prolong the loaded swimming time

It has the effect of promoting hematopoietic function; it can to a certain extent counteract the atrophy of the thymus, spleen, and adrenal glands of mice with "qi deficiency" caused by dietary restriction, and prolong the loaded swimming time

It has the effect of promoting hematopoietic function; it can to a certain extent counteract the atrophy of the thymus, spleen, and adrenal glands of mice with "qi deficiency" caused by dietary restriction, and prolong the loaded swimming time

It promotes hematopoietic function

It promotes hematopoietic function

It promotes hematopoietic function

It promotes hematopoietic function

It promotes hematopoietic function

It has a certain synergistic effect on the hypnotic effect of sodium pentobarbital, which can shorten the sleep latency of mice and prolong the sleep time of mice.

It promotes hematopoietic function

It promotes hematopoietic function

Potassium is the main cation in cells, with a concentration of 150-160 mmol/L; while the main cation outside cells is sodium ion, with a potassium concentration of only 3.5-5 mmol/L. The body mainly relies on Na+-Kplusmn;ATPase on the cell membrane to maintain the concentration difference between K+ and Na+ in cells. The acid-base balance in the body has an impact on potassium metabolism. For example, when acidosis occurs, H+ enters the cell. In order to maintain the potential difference of the cell, K+ is released outside the cell, causing or aggravating hyperkalemia. Metabolic disorders can also affect acid-base balance. The normal intracellular and extracellular potassium ion concentration and concentration difference are closely related to some important functions of cells, including maintaining carbohydrate metabolism, glycogen storage, protein metabolism, intracellular osmotic pressure and acid-base balance, myocardial excitability and conductivity; maintaining normal skeletal muscle tension and nerve impulse conduction, and increasing the tension of intestinal, uterine and bronchial smooth muscles.

Before use, dissolve one bag of this product in 500 ml of warm water and take it orally at any time.

Before use, dissolve one bag of this product in 500 ml of warm water and take it orally at any time.

Before use, dissolve one bag of this product in 500 ml of warm water and take it orally at any time.

Before use, dissolve one bag of this product in 500 ml of warm water and take it orally at any time.

This product belongs to Class III antiarrhythmic drugs. The main electrophysiological effect is to prolong the action potential and effective refractory period of various myocardial tissues, which is conducive to eliminating reentrant excitation. At the same time, it has mild non-competitive α and β adrenergic receptor blocking and mild Class I and IV antiarrhythmic properties. Reduce the automaticity of the sinus node. It has no effect on the resting membrane potential and action potential height. The inhibition of forward conduction of the atrioventricular bypass pathway is greater than the reverse. Due to excessive prolongation of repolarization, the electrocardiogram has QT interval prolongation and T wave changes after oral administration, which can slow down the heart rate by 15~20% and prolong the PR and Q-T intervals by about 10%. It has a direct dilation effect on the coronary arteries and peripheral blood vessels. It can affect thyroid hormone metabolism. The characteristics of this product are long half-life, so the number of medications is small, the therapeutic index is large, and the antiarrhythmic spectrum is wide.