Pharmaceutical preparation for treating insomnia and dreaminess
A technology for pharmaceutical preparations and insomnia and dreaminess, which is applied to drug combinations, medical preparations containing active ingredients, medical raw materials derived from gymnosperm subphylum, etc. repeated problems
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Embodiment 1
[0036] The pharmaceutical preparation for insomnia and dreaminess is characterized in that it is prepared from the following raw materials in weight ratio,
[0037] 35 parts of angelica, 35 parts of schisandra, 30 parts of lily, 30 parts of clove, 30 parts of big belly skin,
[0038] 28 parts of amaranth, 28 parts of grass fruit, 25 parts of dandelion, 25 parts of Polygonatum odoratum, 25 parts of astragalus,
[0039] 20 parts of Rhodiola rosea, 20 parts of cinnamon, 20 parts of medlar, 20 parts of Caulis Spatholobus, 20 parts of Poria cocos,
[0040] 15 parts Cyperus Cyperi, 15 parts Cocklebur, 15 parts Radix Ophiopogonis, 15 parts Epimedium, 10 parts Cypress Kernel,
[0041] 10 parts of polygala, 10 parts of Shichangpu, 10 parts of jujube, 8 parts of acacia bark, 8 parts of licorice,
[0042] Rehmannia glutinosa 5 parts, ginseng 3 parts.
[0043] The preparation method is as follows:
[0044] (1) Weigh the raw material medicine according to the parts by weight for later ...
Embodiment 2
[0050] Acute Toxicity Study
[0051]Healthy rats and mice were given the pharmaceutical preparation for treating insomnia and dreaminess of the present invention by oral gavage respectively, and the gavage dose was 50 times of the intended clinical dosage. After the administration, the mice showed a slight decrease in activity and returned to normal in about 1 hour. After the administration was observed continuously for 7 days, no animal died. Their general conditions, diet, water intake, urination and weight growth were normal, and no obvious acute symptoms appeared. Toxic reactions did not cause animal death. Mice did not show obvious acute toxicity, but rats showed loose stools and decreased activity, and the target organs of acute toxicity were liver and spleen. It is suggested that the drug has low acute toxicity and is safe for clinical use.
[0052] Drug efficacy experiment: effect on sleep time of pentobarbital sodium
[0053] Animals: Kunming mice, half male and ha...
Embodiment 3
[0078] typical embodiment
[0079] Liu, female, 17 years old, high school student, due to the pressure of the college entrance examination, nervousness caused insomnia, poor spirits, headache and dizziness. Feeling difficult to study, not concentrating in class, memory loss, upset and headache when reading books, emotional irritability, poor sleep at night with frequent dreams, listlessness during the day, unclear mind, general fatigue and weakness, I have gone to the hospital for many examinations and found nothing Found organic lesions, took drugs such as diazepam for more than half a year, no obvious improvement, insomnia is also more serious, give the drug prepared in Example 1 a course of treatment combined with psychotherapy, feel good after two courses of treatment, continue to consolidate the treatment for one After the course of treatment, I can now sleep until dawn. I wake up in the morning in good spirits, and my memory has improved significantly.
[0080] Wang, fe...
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