Using clinical trial data and linked administrative health data to reduce the risk of adverse events associated with the uptake of newly released drugs by older Australians: a model process-Reference-Cited by-同舟云学术

Using clinical trial data and linked administrative health data to reduce the risk of adverse events associated with the uptake of newly released drugs by older Australians: a model process

Published:2011-05-21 Issue:1 Volume:11 Page:
ISSN:1471-2458
Container-title:BMC Public Health
language:en
Short-container-title:BMC Public Health

Author:

Whitstock Margaret T,Pearce Christopher M,Ridout Stephen C,Eckermann Elizabeth J

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health

Link

http://link.springer.com/content/pdf/10.1186/1471-2458-11-361.pdf

Reference37 articles.

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2. Roughead ER, Lexchin J: Adverse drug events: counting is not enough, action is needed. MJA. 2006, 184 (7): 315-316.

3. Burgess CL, Holman CD, Satti AG: Adverse drug reactions. MJA. 2005, 182 (6): 267-270.

4. Zhang M, Holman CDJ, Preen DB, Brameld K: Repeat adverse drug reactions causing hospitalization in older Australians: a population-based longitudinal study 1980-2003. Br J Clin Pharmacol. 2007, 63 (2): 163-170. 10.1111/j.1365-2125.2006.02839.x.

5. Kerr SJ, Mant A, Horn FE, McGeechan K, Sayer GP: Lessons from early large-scale adoption of celecoxib and rofecoxib by Australian general practitioners. MJA. 2003, 179: 403-407.

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