Improving how we evaluate the toxicity of approved drugs
- PMID: 16815311
- DOI: 10.1016/j.clpt.2006.03.006
Improving how we evaluate the toxicity of approved drugs
Similar articles
-
A proposal for radical changes in the drug-approval process.N Engl J Med. 2006 Aug 10;355(6):618-23. doi: 10.1056/NEJMsb055203. N Engl J Med. 2006. PMID: 16899784 No abstract available.
-
Importance and challenges of studying marketed drugs: what is a phase IV study? Common clinical research designs, registries, and self-reporting systems.J Clin Pharmacol. 2007 Sep;47(9):1074-86. doi: 10.1177/0091270007304776. J Clin Pharmacol. 2007. PMID: 17766697
-
Clinical trials and public trust.Science. 2004 Dec 3;306(5702):1649. doi: 10.1126/science.1107657. Science. 2004. PMID: 15576574 No abstract available.
-
The safety of niacin in the US Food and Drug Administration adverse event reporting database.Am J Cardiol. 2008 Apr 17;101(8A):9B-13B. doi: 10.1016/j.amjcard.2008.02.027. Am J Cardiol. 2008. PMID: 18375244 Review.
-
Criteria supporting the study of drugs in the newborn.Clin Ther. 2006 Sep;28(9):1385-98. doi: 10.1016/j.clinthera.2006.09.007. Clin Ther. 2006. PMID: 17062311 Review.
Cited by
-
Gap in publication of comparative information on new medicines.Br J Clin Pharmacol. 2008 May;65(5):716-22. doi: 10.1111/j.1365-2125.2007.03092.x. Epub 2008 Feb 21. Br J Clin Pharmacol. 2008. PMID: 18294324 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical