It can relieve heat and stagnation, eliminate toxins and detoxify; speed up intestinal peristalsis, relieve liver fire, gallbladder fire, heart fire, and stomach fire; defecation without diarrhea, pain, easy and long-lasting; relieve pain for patients with anal fissures and hemorrhoids; expel old stool in the body, remove toxins, boost spirits, harmonize Qi, and enhance appetite; regulate the stomach and intestines to restore natural defecation function.

Nourishes blood and moistens dryness, warms yang and strengthens the body; removes residual toxins from the body, promotes intestinal peristalsis, and restores bowel movement.

Warming Yang and strengthening the body; removing residual toxins from the body, promoting intestinal peristalsis, and restoring bowel movement.

It is a potent and highly selective competitive antagonist of 5-hydroxytryptamine 3 (5-HT3) receptors in peripheral neurons and the central nervous system. It inhibits the vomiting reflex by selectively blocking the presynaptic 5-HT3 receptors of peripheral neurons. Its antiemetic effect may also be related to its inhibition of the stimulation of the vagus nerve in the rearmost area by directly blocking the central 5-HT3 receptors.

This product is a H2 receptor blocker of the guanyl thiazole class, which has the characteristics of high affinity for H2 receptors, and has a significant inhibitory effect on gastric acid secretion, and has an inhibitory effect on basal secretion and the increase of gastric acid and pepsin caused by various stimuli. This product does not change the gastric emptying rate, does not interfere with pancreatic function, and has no adverse effects on the cardiovascular system and kidney function. This product is different from cimetidine, but it is similar to ranitidine, that is, long-term high-dose treatment does not cause adverse reactions of androgen antagonism such as male breast development, impotence, lack of sexual desire, and female breast pain, galactorrhea, etc. It has no teratogenic, carcinogenic, drug enzyme inhibitory and androgen inhibitory effects.

It has a significant effect on increasing the number of peripheral blood leukocytes in normal rabbits. The peak value of leukocyte count occurs on the 4th day after the first administration, which is 72% higher than that before administration, which is better than the leukocyte-raising drug shark liver alcohol. It has a significant effect on increasing leukocytes in rabbits caused by cobalt 60-gamma ray and deep X-ray irradiation. It also has a preventive effect on leukocyte decrease when administered two days before irradiation. It can prevent leukopenia in mice caused by mitomycin C. It has a synergistic inhibitory effect on the solid type of Ehrlich carcinoma when used in combination with cyclophosphamide, and the toxicity of leukocyte decrease caused by cyclophosphamide is significantly reduced.

It has a significant effect of increasing the number of peripheral blood leukocytes in normal rabbits. The peak of the leukocyte count occurs on the 4th day after the first administration, which is 72% higher than before the administration, which is better than the leukocyte-raising drug shark liver alcohol. It has a significant effect of increasing leukocytes in rabbits with leukopenia caused by cobalt 60-gamma ray and deep X-ray irradiation. It also has a preventive effect on leukopenia when administered two days before irradiation. It can also prevent leukopenia in mice caused by mitomycin C. It has a synergistic inhibitory effect on the solid type of Ehrlich carcinoma when used in combination with cyclophosphamide, and the toxicity of leukopenia caused by cyclophosphamide is significantly reduced.