http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102861198-B

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dc112a498fb8006ce5c7d17b4886743f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K36-89
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K35-583
filingDate 2012-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0941519f73116ee44a78924544cbc51e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f60fd348b97a7ff031fbf4b42ca3a2d4
publicationDate 2014-07-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102861198-B
titleOfInvention Pure traditional Chinese medicine preparation for treating cirrhosis with ascites
abstract The invention belongs to the field of medicinal preparation, in particular to a pure traditional Chinese medicine preparation for treating cirrhosis with ascites, which is characterized by comprising the following raw materials by weight: 40 to 50 parts of scirpus tabernaemontani, 15 to 21 parts of radix astragali, 20 to 26 parts of herba elsholtziae, 12 to 18 parts of fructus lycii, 16 to 24 parts of houttuynia cordata, 70 to 80 parts of zaocys dhumnade and 5 to 11 parts of liquorice. The pure traditional Chinese medicine preparation inherits the tradition of treating both symptoms and root causes in the traditional Chinese medical science, is the safe and high efficient pure traditional Chinese medicine preparation with the characteristics of being convenient to take, short in course of treatment, high in cure rate and taking effect quickly and the like. The effect can be produced after the general patients take the pure traditional Chinese medicine preparation for three to five days, ascites can be drained out for about 20 days, and the clinical healing level can be reached after the general patients are subjected to consolidated therapy for one to two months.
priorityDate 2012-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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