http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2530625-C2

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P17-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-196
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-573
filingDate 2012-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_175f64d45b89d2c83c03545548deeff9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e840fd19a7ecf7418b9dd92f0641fbf8
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publicationDate 2014-10-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2530625-C2
titleOfInvention Method of treating pemphigus vulgaris
abstract FIELD: medicine. n SUBSTANCE: invention refers to medicine, specifically dermatology, and can be used for treating patients with pemphigus vulgaris. That is ensured by prescribing prednisolone in a dose of 1 mg/kg/day for 7 days. On the 7 th day, Metoject is administered subcutaneously in a dose of 7.5 mg once a day for 3-4 weeks. On the following day of the above administration, the dose of prednisolone is reduced by 1/3, after the following injections, the dose of prednisolone is reduced by 5-10 mg after each following injection. n EFFECT: invention enables providing higher clinical effectiveness in the patients with pemphigus vulgaris with a lower risk of complications. n 2 ex, 2 tbl
priorityDate 2012-12-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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