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PUBMED FOR HANDHELDS

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]

  • 13. Xyrem (sodium oxybate) postmarketing adverse event reporting system.
    Wang YG.
    Sleep Med; 2010 Jun 01; 11(6):595; author reply 595-6. PubMed ID: 20362501
    [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]


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