Safety assessment of drotrecogin alfa (activated) in the treatment of adult patients with severe sepsis
Abstract Introduction Drotrecogin alfa (activated; recombinant activated protein C) was shown to reduce 28-day all-cause mortality in patients with severe sepsis and to have an acceptable safety profile in 1690 patients studied in the F1K-MC-EVAD (PROWESS) trial. We analyzed all available data on th...
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Hlavní autoři: | , , , , , |
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Médium: | Revisão |
Jazyk: | angličtina |
Vydáno: |
2003
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On-line přístup: | https://doi.org/10.1186/cc2167 https://ccforum.biomedcentral.com/counter/pdf/10.1186/cc2167 |
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