Chinese medicinal composition for treating endometritis of cow
A technology of endometritis and composition, which is applied in the direction of drug combination, medical formula, plant raw materials, etc., can solve the problems of large dosage, excessive drug residue, food safety hazards, etc., and achieve simple preparation method and good anti-inflammatory effect , the effect of convenient operation
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Embodiment 1
[0009] Take the medicine according to the following formula:
[0010] Dandelion 40g Ground Ding 40g
[0011] Astragalus 20g Kuncao 20g
[0012] Green peel 30g Anemarrhena 30g
[0013] Ophiopogon 30g White Poria 10g
[0014] Scutellariae 20g Honeysuckle 20g
[0015] The preparation method is that the above-mentioned traditional Chinese medicine is dried in the sun, cleaned out impurities, crushed, passed through an 80-mesh sieve, divided into 3 equal parts, and sealed with double-layer plastic bags respectively.
Embodiment 2
[0017] Take the medicine according to the following formula:
[0018] Dandelion 45g Ground Ding 35g
[0019] Astragalus 25g Kuncao 25g
[0020] Green peel 25g Anemarrhena 25g
[0021] Ophiopogon japonicus 30g White Poria cocos 8g
[0022] Scutellaria 20g Honeysuckle 25g
Embodiment 3
[0024] Take the medicine according to the following formula:
[0025] Dandelion 40g Ground Ding 35g
[0026] Astragalus 25g Kuncao 25g
[0027] Green peel 30g Anemarrhena 30g
[0028] Ophiopogon 40g White Poria 15g
[0029] Scutellaria 25g Honeysuckle 15g
[0030] Rinse this prescription with boiling water, leave it at room temperature, and then administer it. Take it once a day in three divided doses. Generally, it can be cured after 3 to 5 days. The cure and manifestation rate can reach more than 90%.
[0031] The preparation method provided by the present invention is a powder. In actual production, the decoction can be made into a decoction by adding additives such as preservatives according to the usual methods of decoction, concentration, and pH adjustment. It can also be made into tablets, powders, pills, granules, etc.
[0032] The following describes the animal safety test and clinical efficacy test of the drug of the present invention.
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