http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1311202-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61B17-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-02
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P7-02
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filingDate 2001-08-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fff3134413cd42c386b934c4a96fe617
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6124b92073c9fa74a85538c8865d7064
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d0948ed755a90e6f87103d05afa51cc
publicationDate 2003-05-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1311202-A1
titleOfInvention Method and system for anticoagulant dose revision
abstract A method and system for use in treating a patient receiving an anticoagulant or a substance containing warfarin to optimize therapy and prevent an adverse drug response. The system performs the steps shown in blocks (10, 12) of the flow chart. The system employs surrogate markers or indicators including blood levels of the anticoagulant to determine the next required dose for a patient. Because the surrogate markers are employed as a percent change in status, virtually any indicator can be used. Surrogate markers could include any measure of effectiveness of the anticoagulant's action. Given the effectiveness of the anticoagulant's action relative to the surrogate markers, a change in anticoagulant dose is calculated by the system. Conversely, by employing this system, one could determine the expected result of the anticoagulant dose change on the surrogate markers.
priorityDate 2000-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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