Drug safety assessment in clinical trials / edited by Gene Sogliero-Gilbert.
Material type:
TextLanguage: English Series: Statistics, textbooks and monographsPublication details: New York : Marcel dekker, Inc., c1993. Description: x, 437 p. : ill. ; 24 cmISBN: 0824788931; 9780824788933Subject(s): Drugs -- Testing | Drugs -- Testing -- Statistical methods | Drugs -- ToxicologyDDC classification: 615.1901 LOC classification: RM301.27 | .D79 1993NLM classification: QV 771 D7948 1993Online resources: WorldCat details | Item type | Current library | Collection | Call number | Copy number | Status | Date due | Barcode | Item holds |
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EWU Library Reserve Section | Non-fiction | 615.1901 DRU 1993 (Browse shelf(Opens below)) | C-1 | Not For Loan | 14574 |
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| 615.1901 COT 2002 A textbook of pharmaceutical analysis / | 615.1901 COT 2002 A textbook of pharmaceutical analysis / | 615.1901 COT 2002 A textbook of pharmaceutical analysis / | 615.1901 DRU 1993 Drug safety assessment in clinical trials / | 615.1901 HAN Handbook of modern pharmaceutical analysis / | 615.1901 HAN Handbook of modern pharmaceutical analysis / | 615.1901 HAN Handbook of pharmaceutical analysis / |
Includes bibliographical references and index.
TOC Preclinical drug safety evaluation / James T. Mayne --
Adverse drug events in clinical trials / Deborah S. Kirby --
Laboratory testing in clinical trials / Deborah S. Kirby --
Drug Research in the elderly / Piet M. Hooymans and Robert Janknegt --
Drug assessment in critical illness / M.I. Bowden and J.F. Bion --
Laboratory data in multicenter trials: monitoring, adjustment, and summarization / Lawrence K. Oliver and Christy Chuang-Stein --
Genie score: a multivariate assessment of laboratory abnormalities / Gene Sogliero-Gilbert, Lonni Zubkoff-Schulz and Naitee Ting --
Laboratory parameters and drug safety / Norman E. Pitts --
Unified approach to the analysis of safety data in clinical trials / Christy Chuang-Stein and Noel R. Mohberg --
Use of hazard functions in safety analysis / David S. Salsburg --
Meta-analysis of drug safety data / Gary G. Koch ... [et al.] --
Design and analysis considerations for safety data, particularly adverse events / Karl E. Peace --
Clinical trial adverse drug experience reporting requirements in the major countries: one manufacturer's approach / Max W. Talbott and Ellen D. Kelso. (cont.) Safety surveillance / Norman E. Pitts --
Postmarketing surveillance: applications and limitations with special reference to the fluoroquinolones / Robert Janknegt and Yechiel A. Hekskter
Pharmacy
Saifun Momota
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