Statistical Methods to Analyze Adverse Events Data of Randomized Clinical Trials-Reference-Cited by-同舟云学术

Statistical Methods to Analyze Adverse Events Data of Randomized Clinical Trials

Published:2009-08-07 Issue:5 Volume:19 Page:889-899
ISSN:1054-3406
Container-title:Journal of Biopharmaceutical Statistics
language:en
Short-container-title:Journal of Biopharmaceutical Statistics

Author:

Siddiqui Ohidul¹

Affiliation:

1. a Office of Biostatistics, Office of Translational Sciences, Center for Drug Evaluation and Research, Food and Drug Administration , Silver Spring, Maryland, USA

Publisher

Informa UK Limited

Subject

Pharmacology (medical),Pharmacology,Statistics and Probability

Link

https://www.tandfonline.com/doi/pdf/10.1080/10543400903105463

Reference11 articles.

1. Accounting for Multiplicities in Assessing Drug Safety: A Three-Level Hierarchical Mixture Model

2. MARGINAL ANALYSIS OF RECURRENT EVENTS AND A TERMINATING EVENT

3. Introduction/Overview: Gender-Based Differences in Pharmacologic and Toxicologic Responses

4. Safety Analysis in Controlled Clinical Trials

5. General Accounting Office (GAO) . ( 2001 ). Drug Safety: Most Drugs Withdrawn in Recent Years Had Greater Health Risks for Women. Draft Report 01-286 . Washington , DC : GAO .

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