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Q51912208-0EE7EB1B-3278-40A4-BD19-B17D6488F867
Q51912208-0EE7EB1B-3278-40A4-BD19-B17D6488F867
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51912208-0EE7EB1B-3278-40A4-BD19-B17D6488F867
A novel in vitro pharmacokinetic/pharmacodynamic model based on two-compartment open model used to simulate serum drug concentration-time profiles.
P2860
Q51912208-0EE7EB1B-3278-40A4-BD19-B17D6488F867
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51912208-0EE7EB1B-3278-40A4-BD19-B17D6488F867
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
7647b5a320437ddfc11f2f7707eb6b513d9501b7
P2860
Activities of trovafloxacin and ampicillin-sulbactam alone or in combination versus three strains of vancomycin- intermediate Staphylococcus aureus in an in vitro pharmacodynamic infection model.