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Journal Abstract Search
237 related items for PubMed ID: 21606101
1. A quantitative analysis of adverse events and "overwarning" in drug labeling. Duke J, Friedlin J, Ryan P. Arch Intern Med; 2011 May 23; 171(10):944-6. PubMed ID: 21606101 [No Abstract] [Full Text] [Related]
2. Invited commentary--prescription drug label adverse events: a call for prioritization: comment on "A quantitative analysis of adverse events and 'overwarning' in drug labeling". Cheng C, Guglielmo BJ. Arch Intern Med; 2011 May 23; 171(10):946-7. PubMed ID: 21606102 [No Abstract] [Full Text] [Related]
3. Postmarketing modifications in the safety labeling of the new antiepileptics. Buck ML, Gurka MJ, Goodkin HP. Neurology; 2007 May 01; 68(18):1536-7. PubMed ID: 17470758 [No Abstract] [Full Text] [Related]
4. Red sky in the morning: modifying prescription drug labels as a result of postmarket surveillance. Jacobson JD, Feigal D. Food Drug Law J; 2007 May 01; 62(3):529-46. PubMed ID: 17915395 [No Abstract] [Full Text] [Related]
5. Improving drug safety monitoring. Karande S, Gogtay NJ, Kshirsagar NA. Indian Pediatr; 2003 Dec 01; 40(12):1167-75. PubMed ID: 14722367 [Abstract] [Full Text] [Related]
6. Pin the tail on the other donkey: allocating and avoiding injury losses after drug or device approval. O'Reilly JT. Food Drug Law J; 2007 Dec 01; 62(3):559-72. PubMed ID: 17915397 [No Abstract] [Full Text] [Related]
7. Evaluating drugs after their approval for clinical use. Ray WA, Griffin MR, Avorn J. N Engl J Med; 1993 Dec 30; 329(27):2029-32. PubMed ID: 8018139 [No Abstract] [Full Text] [Related]
8. Flight 483 now boarding. Czap A. Altern Med Rev; 2010 Sep 30; 15(3):183-5. PubMed ID: 21155619 [No Abstract] [Full Text] [Related]
9. FDA post-marketing safety decisions. Klein DF. J Clin Psychiatry; 2006 Aug 30; 67(8):1305-6. PubMed ID: 16965212 [No Abstract] [Full Text] [Related]
10. The drug safety system conundrum. Tiedt TN. Food Drug Law J; 2007 Aug 30; 62(3):547-558. PubMed ID: 17915396 [No Abstract] [Full Text] [Related]
11. Form for reporting serious adverse events and product problems with human drug and biological products and devices; availability--FDA. Notice. Fed Regist; 1993 Jun 03; 58(105):31596-614. PubMed ID: 10171452 [Abstract] [Full Text] [Related]
12. Lessons from cisapride. CMAJ; 2001 May 01; 164(9):1269, 1271. PubMed ID: 11341130 [No Abstract] [Full Text] [Related]
14. FDA attempting to overcome major roadblocks in monitoring drug safety. Zielinski SL. J Natl Cancer Inst; 2005 Jun 15; 97(12):872-3. PubMed ID: 15956645 [No Abstract] [Full Text] [Related]
15. "Safer, but not safe enough". Crombie HD. Conn Med; 2006 Jun 15; 70(10):645. PubMed ID: 17190395 [No Abstract] [Full Text] [Related]
16. Cisapride and patient information leaflets. Sukkari SR, Sasich LD. CMAJ; 2001 May 01; 164(9):1276-8; author reply 1278-9. PubMed ID: 11341134 [No Abstract] [Full Text] [Related]
17. Reporting of serious adverse drug reactions of targeted anticancer agents in pivotal phase III clinical trials. Seruga B, Sterling L, Wang L, Tannock IF. J Clin Oncol; 2011 Jan 10; 29(2):174-85. PubMed ID: 21135271 [Abstract] [Full Text] [Related]
18. Reporting of adverse drug events: a key to postmarketing drug safety. Rheinstein PH. Am Fam Physician; 1992 Sep 10; 46(3):873-4. PubMed ID: 1514478 [No Abstract] [Full Text] [Related]
19. The black box warning. Abourjaily HM, Rosenberg M. J Mass Dent Soc; 2002 Sep 10; 51(3):54-6. PubMed ID: 12380043 [No Abstract] [Full Text] [Related]
20. Strategy for surveillance of adverse drug events. Bright RA. Food Drug Law J; 2007 Sep 10; 62(3):605-16. PubMed ID: 17915403 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]