http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SU-1611340-A1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_06d12299559f675d6f05985a26a236f7
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K35-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-08
filingDate 1987-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e0ef254f38dc402b86ff5e6bd5915bf7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_22ab848e6bd65b28028cd48f47ecdf32
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f34c44ac6849f2ac87638ff578293f24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_25074465ace62fb3bd134c655af08aa2
publicationDate 1990-12-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SU-1611340-A1
titleOfInvention Method of infusion therapy of premature infants
abstract The invention relates to medicine, namely to pediatrics, and can be used in clinical neonatology. The aim of the invention is to reduce the incidence of complications. This goal is achieved through the internal administration of antihypoxic drug mixtures from the following calculation: on the first day of life no more than 4.84-5.56 ml per 1 kg of body weight of the newborn, on the second day not more than 5.84-6.36 ml per 1 kg of body weight; on the third day, no more than 7.12-7.68 ml per 1 kg of body weight; for 4-6 days, no more than 7.97-9.03 ml per 1 kg of body weight are administered. The method allows to reduce the frequency of adverse reactions after infusion therapy.
priorityDate 1987-06-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454411861
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9068

Total number of triples: 17.