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Journal Abstract Search

107 related items for PubMed ID: 8598505

  • 1. Comparing the toxicity of two drugs in the framework of spontaneous reporting: a confidence interval approach.
    Tubert-Bitter P, Begaud B, Moride Y, Chaslerie A, Haramburu F.
    J Clin Epidemiol; 1996 Jan; 49(1):121-3. PubMed ID: 8598505
    [Abstract] [Full Text] [Related]

  • 2. Adverse drug reactions related to the use of NSAIDs with a focus on nimesulide: results of spontaneous reporting from a Northern Italian area.
    Conforti A, Leone R, Moretti U, Mozzo F, Velo G.
    Drug Saf; 2001 Jan; 24(14):1081-90. PubMed ID: 11735663
    [Abstract] [Full Text] [Related]

  • 3. On the assessment of adverse drug reactions from spontaneous reporting systems: the influence of under-reporting on odds ratios.
    van der Heijden PG, van Puijenbroek EP, van Buuren S, van der Hofstede JW.
    Stat Med; 2002 Jul 30; 21(14):2027-44. PubMed ID: 12111885
    [Abstract] [Full Text] [Related]

  • 4. Replication of the Weber effect using postmarketing adverse event reports voluntarily submitted to the United States Food and Drug Administration.
    Hartnell NR, Wilson JP.
    Pharmacotherapy; 2004 Jun 30; 24(6):743-9. PubMed ID: 15222664
    [Abstract] [Full Text] [Related]

  • 5. Spontaneous reporting of adverse drug reactions to non-steroidal anti-inflammatory drugs. A report from the Spanish System of Pharmacovigilance, including an early analysis of topical and enteric-coated formulations.
    Figueras A, Capellà D, Castel JM, Laorte JR.
    Eur J Clin Pharmacol; 1994 Jun 30; 47(4):297-303. PubMed ID: 7875178
    [Abstract] [Full Text] [Related]

  • 6. Drug-induced anaphylaxis : case/non-case study based on an italian pharmacovigilance database.
    Leone R, Conforti A, Venegoni M, Motola D, Moretti U, Meneghelli I, Cocci A, Sangiorgi Cellini G, Scotto S, Montanaro N, Velo G.
    Drug Saf; 2005 Jun 30; 28(6):547-56. PubMed ID: 15924506
    [Abstract] [Full Text] [Related]

  • 7. Comparing reporting rates of adverse events between drugs with adjustment for year of marketing and secular trends in total reporting.
    Tsong Y.
    J Biopharm Stat; 1995 Mar 30; 5(1):95-114. PubMed ID: 7613562
    [Abstract] [Full Text] [Related]

  • 8. Adverse drug reactions associated with the use of NSAIDs: a case/noncase analysis of spontaneous reports from the French pharmacovigilance database 2002-2006.
    Lapeyre-Mestre M, Grolleau S, Montastruc JL, Association Française des Centres Régionaux de Pharmacovigilance (CRPV).
    Fundam Clin Pharmacol; 2013 Apr 30; 27(2):223-30. PubMed ID: 21929527
    [Abstract] [Full Text] [Related]

  • 9. [Organization and results of drug vigilance in France].
    Bégaud B, Chaslerie A, Haramburu F.
    Rev Epidemiol Sante Publique; 1994 Apr 30; 42(5):416-23. PubMed ID: 7973001
    [Abstract] [Full Text] [Related]

  • 10. Bias in spontaneous reporting of adverse drug reactions in Japan.
    Matsuda S, Aoki K, Kawamata T, Kimotsuki T, Kobayashi T, Kuriki H, Nakayama T, Okugawa S, Sugimura Y, Tomita M, Takahashi Y.
    PLoS One; 2015 Apr 30; 10(5):e0126413. PubMed ID: 25933226
    [Abstract] [Full Text] [Related]

  • 11. A statistical methodology for drug-drug interaction surveillance.
    Norén GN, Sundberg R, Bate A, Edwards IR.
    Stat Med; 2008 Jul 20; 27(16):3057-70. PubMed ID: 18344185
    [Abstract] [Full Text] [Related]

  • 12. Ulcerogenicity of piroxicam: an analysis of spontaneously reported data.
    Rossi AC, Hsu JP, Faich GA.
    Br Med J (Clin Res Ed); 1987 Jan 17; 294(6565):147-50. PubMed ID: 3109543
    [Abstract] [Full Text] [Related]

  • 13. An evaluation of spontaneous adverse drug reaction monitoring systems.
    Sachs RM, Bortnichak EA.
    Am J Med; 1986 Nov 28; 81(5B):49-55. PubMed ID: 3789003
    [Abstract] [Full Text] [Related]

  • 14. A distributed, collaborative intelligent agent system approach for proactive postmarketing drug safety surveillance.
    Ji Y, Ying H, Farber MS, Yen J, Dews P, Miller RE, Massanari RM.
    IEEE Trans Inf Technol Biomed; 2010 May 28; 14(3):826-37. PubMed ID: 20007038
    [Abstract] [Full Text] [Related]

  • 15. Adverse drug reactions related to the use of non-steroidal anti-inflammatory drugs: results of spontaneous reporting from central India.
    Shrivastava MP, Chaudhari HV, Dakhale GN, Hiware SK, Solanke BP, Shinde A.
    J Indian Med Assoc; 2013 Feb 28; 111(2):99-102, 106. PubMed ID: 24003566
    [Abstract] [Full Text] [Related]

  • 16. Impact of preexisting health conditions on the outcome of an adverse drug reaction alerting program: gastrointestinal disorders before piroxicam and sulindac therapy.
    Rawson NS.
    Ann Pharmacother; 1995 Feb 28; 29(7-8):676-80. PubMed ID: 8520079
    [Abstract] [Full Text] [Related]

  • 17. Adverse drug reactions in an elderly hospitalised population: inappropriate prescription is a leading cause.
    Passarelli MC, Jacob-Filho W, Figueras A.
    Drugs Aging; 2005 Feb 28; 22(9):767-77. PubMed ID: 16156680
    [Abstract] [Full Text] [Related]

  • 18. False-positives in spontaneous reporting: should we worry about them?
    Begaud B, Moride Y, Tubert-Bitter P, Chaslerie A, Haramburu F.
    Br J Clin Pharmacol; 1994 Nov 28; 38(5):401-4. PubMed ID: 7893579
    [Abstract] [Full Text] [Related]

  • 19. Adverse drug reactions: a review of relevant factors.
    Ajayi FO, Sun H, Perry J.
    J Clin Pharmacol; 2000 Oct 28; 40(10):1093-101. PubMed ID: 11028248
    [Abstract] [Full Text] [Related]

  • 20. Is reporting rate a good predictor of risks associated with drugs?
    Pierfitte C, Bégaud B, Lagnaoui R, Moore ND.
    Br J Clin Pharmacol; 1999 Mar 28; 47(3):329-31. PubMed ID: 10215758
    [Abstract] [Full Text] [Related]

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