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CN102266444A - A drug for treating allergic purpura - Google Patents

A drug for treating allergic purpura Download PDF

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Publication number
CN102266444A
CN102266444A CN2011102011280A CN201110201128A CN102266444A CN 102266444 A CN102266444 A CN 102266444A CN 2011102011280 A CN2011102011280 A CN 2011102011280A CN 201110201128 A CN201110201128 A CN 201110201128A CN 102266444 A CN102266444 A CN 102266444A
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medicine
parts
purpura
examples
patient
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杭盖巴特尔
斯琴
高钰思
旭日
宝音德力格尔
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Inner Mongolia Autonomous Region Traditional Chinese And Mongolian Medicine Hospital
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Inner Mongolia Autonomous Region Traditional Chinese And Mongolian Medicine Hospital
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Abstract

本发明涉及一种治疗过敏性紫癜的药物,其成分配伍(按重量份计)为:木鳖子25份,地锦草35g,红花50份,熊胆25份,草果25份,射干35份,紫檀香38份,扁豆花40份。该药物主治过敏性紫癜,治愈率可达95%以上,总有效率98%。The invention relates to a medicine for treating allergic purpura, and the composition (by weight) is: 25 parts of Momordica cochinchinensis, 35g of Herba Euphorbiae, 50 parts of Carthamus tinctorius, 25 parts of Bear Gallbladder, 25 parts of Amomum villosum, 35 parts of Belamcanda chinensis, 38 parts of Pterocarpus santalinus, and 40 parts of Lentinula odoratum. The medicine is mainly used to treat allergic purpura, and the cure rate can reach more than 95%, and the total effective rate is 98%.

Description

A kind of medicine for the treatment of anaphylactoid purpura
Technical field
The present invention relates to a kind of medicine for the treatment of anaphylactoid purpura, especially, relate to a kind of Mongolian medicine for the treatment of anaphylactoid purpura.
Background technology
Anaphylactoid purpura be by anaphylactogen cause disease whole body skin that the little blood vessel wall generation of person immune inflammation causes go out purpura, purpura can cause arthralgia swelling, stomachache have blood in stool and urinate in anaphylactic diseases such as albumen, blood appear.Also claim Allergic purpura (being called for short AP).This disease is along with various air, water source, food pollution and inappropriate medication etc. have increase trend at present.This is sick owing to add up a plurality of organs and organize protracted course of disease to have caused the multiple burden of health, psychology and economic dispatch for vast patient, has a strong impact on patient's physical and mental health.This sick child child, juvenile prevalence height see that from present clinical development trend the trend that becomes frequently-occurring disease should draw attention.
Modern medicine is treated this sick first-selected desensitizer, antihistaminic medicine, glucocorticoid medicine and immunosuppressant treatment at present.For example, Claritin: hismanal, chlorphenamine, calcium gluconate; Reduce the vascular permeability medicine: carbazochrome salicylate, rutin, vitamin C; Anticoagulant medicine: persantin; Adrenocortical hormone: hydrocortisone, prednisone (prednisone), dexamethasone; For kidney type or prednisone treatment gastrointestinal disease patient, also adopt immunosuppressant (as chemotherapeutics such as cyclophosphamide, azathioprines).But these methods treatment times is long, toxic and side effects is big, therapeutic effect is undesirable.
Also have the hemostasis of use Flos Carthami eight-medicine powder to treat in existing Mongolian medicine's treatment, but Herba indigoferae Pseudotinctoriae is a Vermilion in this powder, this medicine is a heavy metal, and its main component is cinnabar (HgS).Can certain infringement be arranged to gastrointestinal tract and hepatic and renal function as taking this medicine for a long time.From the disease characteristics of anaphylactoid purpura, this sickly complexion is easily involved internal organs such as gastrointestinal tract Liver and kidney, so the Vermilion among the former side is unfavorable to this disease, so this prescription exists bigger side effect and treatment risk.
Summary of the invention
Anaphylactoid purpura Mongolian medicine is called " purpura mass formed by blood stasis ".Be to make intravital three disorders of people because exopathogen is invaded human body.That is: its duty is not taken charge of in the mutual disorder of " conspicuous complying with " " association's day " " Ba Dagan "." association day " heat drop is in blood vessels, CUN KOU is opened and caused that purpura appears in whole skin." association day " heat is attacked gastrointestinal mucosa and is caused that then stomachache has blood in stool; Invade kidney then hematuria and albuminuria, lumbago and edema; The invasion and attack joint causes arthralgia, limitation of activity; Also can accumulate a plurality of internal organs such as skin, gastrointestinal, kidney, joint simultaneously and form the mixed type purpura.
The Mongolian medicine mainly carries out symptomatic treatment to regulate three lock arteries and veins " association day " heat that purifies the blood.The inventor improves original prescription, and deleterious medicinal ingredient Vermilion is replaced with other medicinal ingredients, can promote digestive functions after the replacement, and this cooler side heat of balance has avoided Vermilion to the side effect that GI irritation causes, is that prescription is more reasonable; Simultaneously the compatibility dose is readjusted, use amount is more reasonable.Can obtain more effectively therapeutic effect after the improvement.
Therefore, an object of the present invention is to provide a kind of medicine for the treatment of anaphylactoid purpura, its components compatibility (by weight) is: 25 parts of Semen Momordicaes, Herba Euphorbiae Humifusae 35g, 50 parts on Flos Carthami, 25 parts of Fel Ursis, 25 parts of Fructus Tsaokos, 35 parts of Rhizoma Belamcandae, 38 parts of Lignum pterocarpi indici, 40 parts of Flos dolichoris.Compatibility of drugs dosage need not to float.
This medicine property of medicine is cold, and function heat clearing away, removing heat from blood, lock arteries and veins, hemostasis, adjusting voxel cure mainly various hemorrhages.This Drug therapy is the main treatment anaphylactoid purpura, and cure rate can reach more than 95%, total effective rate 98%.
Another object of the present invention has provided a kind of preparation method of described medicine, it is characterized in that the single medicine of above eight flavors is ground into fine powder in proportion behind the compatibility to break into the watered pill and get final product.Described watered pill makes instructions of taking more convenient with respect to traditional powder.
The clinical practice proof is evident in efficacy with Drug therapy anaphylactoid purpura of the present invention, and toxic and side effects is little, is difficult for recurrence, no drug dependence after the drug withdrawal.This medicine is a pure natural medical, dosage 3g-6g/ days, can cooperate to take with other mongolian medicine to form serial medication.、
Medicine of the present invention clinical practice had ten surplus year.We treat 20,000 many cases patients with anaphylactoid purpura every year in the outpatient service ward at present.Its total effective rate has reached more than 98%, and cure rate reaches more than 95%.And toxic and side effects is little, and relapse rate is low, and is economical convenient.Compare with former side: its former side is a powder, and it is bad that the patient takes mouthfeel.Especially the patient in anaphylactoid purpura patient 6-10 year is in the majority.The children taking mouthfeel of getting up is bad, relatively difficulty.Medicine of the present invention breaks into pill with powder, taking convenience, and mouthfeel is good.Efficiently solve the bad shortcoming of child patient oral powder mouthfeel.Its two, contain heavy metal medicine Vermilion (composition HgS) in the former dosage form and take for a long time gastrointestinal tract is had stimulation, and the purpura renal patient more should not take for a long time.Replace Vermilion with Fructus Tsaoko, solved the problem of above side effect.Can also regulate the effect of taste, promote interior absorption of body of whole dosage form.Make medicine of the present invention be fit to take for a long time.Its three, medicine of the present invention has reduced half with former side's invasion by pathogenic cold medicine of a cold nature Fel Ursi, croceous consumption.Having reduced cold and cool medicine stimulates gastrointestinal.Also significantly reduced the expense of prescription finished product.And do not subtract the therapeutical effect of medicine.Effectively reduced patient's financial burden.Every dose of 3g of present former side, 102 yuan every dose.40 yuan of the every 12g of medicine of the present invention.Average 10 yuan every dose.Be former side's 1/10th.Though medicine of the present invention has reduced price, do not reduce therapeutical effect.The advantage place of Here it is medicine of the present invention.
The specific embodiment
Embodiment 1
Prepare raw material by following weight proportion: 25 parts of Semen Momordicaes, Herba Euphorbiae Humifusae 35g, 50 parts on Flos Carthami, 25 parts of Fel Ursis, 25 parts of Fructus Tsaokos, 35 parts of Rhizoma Belamcandae, 38 parts of Lignum pterocarpi indici, 40 parts of Flos dolichoris, the conventional method by this area is ground into fine powder with raw material then, breaks into the watered pill afterwards promptly.
Embodiment 2 (test of pesticide effectiveness data)
Medicine of the present invention is to the influence (capillary glass-tube method) of normal clotting time of mice
[purpose]
Desire is understood the influence of medicine of the present invention to normal clotting time of mice, thereby further studies the mechanism of action of this medicine treatment anaphylactoid purpura.
[material]
Animal: Kunming white mouse, secondary cleaning, ♂, body weight 20 ± 2g is purchased by University of the Inner Mongol Animal Experimental Study center, the quality certification number: 8806M35.Equipment: glass capillary (internal diameter 1mm, long 10cm, Huhehaote City's scientific and technological development institute product, the metering quality certification number: 92 amount machine words the 003rd), stopwatch (Shanghai) etc.Reagent: by reagent-medicine of the present invention, normal saline, purified water (heavily steaming self-control).
[method]
1. by the preparation of reagent: accurately take by weighing medicine of the present invention (giving coarse pulverization earlier) 5.0g, be made into 3% suspension by 30 times of clinical consumption (3g/50kg body weight people consumption per day), bottled standby.
2. get 20 of white mice, by two groups of body weight random stratified compatibilities, i.e. processed group and matched group, 10 every group, the labelling of weighing.Adapt to 24h post processing group and press the administration volume gastric infusion of 0.2ml/10g body weight, 1 time/day, at 9 o'clock in the morning is to administration between 9 thirty, totally 5 days.Matched group is given and is waited the capacity normal saline.The two treated animals water inlet of taking food naturally during the administration, all the other are identical.Insert mice eyes ball rear vein beard with capillary glass tube behind the last administration 1h and get blood.Pick up counting in the autoblood inflow pipe, blood is filled with the back and is taken out glass capillary, lie on the desk, the about 0.5cm in capillary tube two ends that fractureed every 15~20 seconds also slowly draws back to the left and right, whether the observation place of fractureing has the blood clotting silk, till the appearance of blood clotting silk, between lasting, institute is clotting time, and the meansigma methods of glass capillary two end datas is the blood clotting time of this white mice.
[result]
Medicine of the present invention can obviously shorten the clotting time of its normal white mice, and Blood clotting is promptly arranged.This hemostatic mechanism remains further to be studied.
[discussion]
This result of the test has verified that medicine of the present invention has hemostasia effect.This medicine Blood clotting and treatment anaphylactoid purpura have internal relation, need further research to illustrate.
Table 1: experimental animal body weight table (g)
Table 2: to the influence (test data (second)) of normal clotting time of mice
Figure BSA00000539920800061
Embodiment 3
Clinical trial
Materials and methods
1.1 material
1.1.1 case is selected
The anaphylactoid purpura infant of selecting in JIUYUE, the 2005-2006 year Decembers Mongolian medicine of Mongolian medicine hospital Hematology hospitalization in Inner Mongolia Autonomous Region is totally 191 examples, be divided into observation group and matched group at random, wherein male 93 examples, women 98 examples, be first attack or recurrence for the first time, and meet diagnostic criteria person.
1.1.2 diagnostic criteria
Meet " practical paidonosology " the 7th edition diagnostic criteria in 2002 (being the new diagnostic criteria of anaphylactoid purpura of nineteen ninety American Rheumatism Association's formulation) of Zhu Futang chief editor, national institution of higher education's state-compiled textbook sixth version " internal medicine " diagnostic criteria that various diagnosis is edited with reference to Ye Rengao, Lu Zaiying simultaneously.
1.1.3 clinical material
Observation group: male 45 examples, women 50 examples, totally 95 examples, age 3-14 year, average (9.81 ± 2.75) year, the preceding course of disease of being admitted to hospital (6.39 ± 4.43) day, 68 examples of falling ill first, 27 examples of falling ill for the second time; 84 examples have the skin purpura in the 95 routine infants, and digestive tract is impaired 45 examples, accounts for 47.37%; Just positive 23 examples of occulting blood account for 24.21%; Joint injury 31 examples are arranged, account for 32.63%; Kidney is impaired 34 examples, accounts for 35.79%, and wherein gross hematuria has 10 examples, microscopic hematuria 24 examples, albuminuria 33 examples.Clinical classification situation: skin-type 16 examples, joint type 13 examples, abdomen type 20 examples, kidney type 34 examples, mixed type 26 examples.
Matched group: male 48 examples, women 48 examples, totally 96 examples, age 3-14 year, average (9.08 ± 2.55) year, the preceding course of disease of being admitted to hospital (7.03 ± 4.38) day, 70 examples of falling ill first, 26 examples of falling ill for the second time; 89 examples have the skin purpura in the 96 routine infants, and digestive tract is impaired 47 examples, accounts for 48.96%; Just positive 22 examples of occulting blood account for 22.92%; Joint injury 33 examples are arranged, account for 34.38%; Kidney is impaired 32 examples, accounts for 33.33%, and wherein gross hematuria has 9 examples, microscopic hematuria 23 examples, albuminuria 30 examples.Clinical classification situation: skin-type 20 examples, joint type 12 examples, abdomen type 16 examples, kidney type 32 examples, mixed type 32 examples.
1.1.4 two groups of basic conditions
Basic condition when table 3 a liang group infant is admitted to hospital
Figure BSA00000539920800081
Two groups of patient's sexes, age, the course of disease, Clinical typing etc. all do not have significant difference P>0.05, have comparability.
Method
1.2.1 the side's of treatment medicine and method
Matched group gives conventional western medicines such as vitamin C, calcium preparation, cimetidine, chlorphenamine, hydrocortisone by the routine clinical Therapeutic Method of doctor trained in Western medicine.Observation group uses medicine of the present invention when giving conventional Western medicine, every day 1-2 time, and each 5-15 grain (being equivalent to 1.0-3g), 14 days is a course of treatment; Observing the treatment time limit is 2 courses of treatment of renal purpura, and other are various to be a course of treatment.Follow Mongolian medicine's Coryza Treated by Syndrome Differentiation principle simultaneously, according to different situations abdomen type compatibility Bart day-7 of pathological changes symptom, joint type compatibility Gu Gule-11, treatments such as kidney type compatibility Sa Ri loud, high-pitched sound day enlightening, Ulan-3 soup, Su Gemu happy-10.
1.2.2 observational technique:
Do all cases the next day once just conventional in the therapeutic process, do routine urinalysis in 3 days one time, examine the record skin purpura situation of taking off that disappears when doing a routine blood test week, symptom of digestive tract disappearance situation, joint transference cure situation, hematuria, albuminuria disappearance situation; Produce effects after 1-2 course of treatment, effective, invalid total routine number and various purpura produce effects, effective, invalid routine number; The routine number of kidney damage and skin purpura routine number repeatedly etc. appear in the therapeutic process.
1.2.3 statistical method
Measurement data is added up with X2 check or definite probabilistic method with the T method of inspection or the approximate T method of inspection, enumeration data.
1.2.4 efficacy assessment standard
All evaluation is all unified with reference to Zhang Zhinan chief editor " hematopathy diagnosis and criterion of therapeutical effect " in case treatment back.Produce effects: resolution of symptoms such as skin purpura, arthralgia, stomachache, routine urinalysis is normal.Effectively: symptoms such as skin purpura major part disappears, arthralgia, stomachache disappear substantially, and routine urinalysis is the result obviously improve.Invalid: the skin purpura occurs repeatedly, and symptoms such as arthralgia, stomachache are for disappearing, and routine urinalysis does not have improvement.
2 results
2.1 observation group and matched group total effective rate (seeing Table 4)
Table 4 liang group patient total effective rate
Annotate: ※ is for comparing (P<0.05) with matched group
There were significant differences (P<0.05) for two groups of total effective rates, and observation group's curative effect is better than matched group.
Two groups of various purpura effective percentage (seeing Table 5)
The table 5 liang various purpura effective percentage of group
Figure BSA00000539920800102
Annotate: ※ is for comparing no significant difference (P>0.05) with matched group, there were significant differences (P<0.05) in order to compare with matched group for ※ ※.
The effective percentage of two groups of skin-types, joint type, abdomen type, mixed type does not have significant difference (P>0.05); There were significant differences for the effective percentage of kidney type and total effective rate (P<0.05), and observation group is better than matched group.
2.3 two groups of patient's cardinal symptoms and fecal occult blood extinction time (seeing Table 6)
The comparison of table 6 liang group patient's cardinal symptom and fecal occult blood extinction time
Figure BSA00000539920800111
Annotate: there were significant differences (P<0.05) in order to compare with matched group for ※, and ※ ※ is for comparing no significant difference with matched group
(P>0.05)。
Two groups of patient skin purpura regression times, stomachache extinction time, there were significant differences for the fecal occult blood extinction time (P<0.05), and observation group is shorter than matched group the time.Two groups of patient joint transference cure times do not have significant difference (P>0.05).This has illustrated that this Therapeutic Method is evident in efficacy to skin-type, purpura abdominalis.
2.4 a situation arises (seeing Table 7) for two groups of patient's renal damages
Table 7 liang group patient renal damage incidence rate relatively
Figure BSA00000539920800112
Annotate: ※ is for comparing no significant difference (P>0.05) with matched group.
Two groups of patient's renal damage incidence rates do not have significant difference (P>0.05), and this may have relation with weak point observing time, awaits further research.
2.5 two groups of patient's ERY disappearance situations (seeing Table 8)
Table 8 liang group patient ERY disappearance rate relatively
Annotate: there were significant differences (P<0.05) in order to compare with matched group for ※
There were significant differences (P<0.05) for two groups of patient's ERY disappearance rate, and observation group is better than matched group.
2.6 two groups of patient's urine protein disappearance situations (seeing Table 9)
Table 9 liang group patient urine protein disappearance rate relatively
Figure BSA00000539920800122
Annotate: ※ is for comparing no significant difference (P>0.05) with matched group
Two groups of patient's urine protein disappearance rate do not have significant difference (P>0.05), and this may have relation with weak point observing time, awaits further research.
2.7 two groups of patient skin purpuras are situation (seeing Table 10) repeatedly
Table 10 liang group patient skin purpura rate is repeatedly compared
Figure BSA00000539920800123
Figure BSA00000539920800131
Annotate: there were significant differences (P<0.05) in order to compare with matched group for ※, and observation group is starkly lower than matched group.

Claims (2)

1.一种治疗过敏性紫癜的药物,其成分配伍(按重量份计)为:木鳖子25份,地锦草35g,红花50份,熊胆25份,草果25份,射干35份,紫檀香38份,扁豆花40份。1. A medicine for treating anaphylactoid purpura, its composition compatibility (by weight) is: 25 parts of Scutellaria japonicus, 35g of Dijincao, 50 parts of safflower, 25 parts of bear bile, 25 parts of Tsaoguo, 35 parts of Shegan 38 parts of red sandalwood, 40 parts of lentil flower. 2.根据权利要求1的一种治疗过敏性紫癜的药物,其中所述药物是一种水丸。2. A kind of medicine for treating allergic purpura according to claim 1, wherein said medicine is a kind of water pill.
CN2011102011280A 2011-07-19 2011-07-19 A drug for treating allergic purpura Pending CN102266444A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108261479A (en) * 2018-01-16 2018-07-10 内蒙古医科大学 A kind of Mongolian medicine prescription for treating immunologic thrombocytopenic purpura

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101785810A (en) * 2010-01-26 2010-07-28 张云平 Traditional Chinese medicine preparation for anaphylactoid purpura treatment

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101785810A (en) * 2010-01-26 2010-07-28 张云平 Traditional Chinese medicine preparation for anaphylactoid purpura treatment

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
《中国民族医药杂志》 20100430 韩咏梅等 新古日古木-8胶囊剂挥发油提取和包合工艺研究 第54-55页 1-2 , 第4期 *
《北方药学》 20100430 董志强等 新古日古木-8胶囊剂成型工艺的研究 第21-23页 1-2 第7卷, 第2期 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108261479A (en) * 2018-01-16 2018-07-10 内蒙古医科大学 A kind of Mongolian medicine prescription for treating immunologic thrombocytopenic purpura

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Application publication date: 20111207