References
Kelly WN, Arellano FM, Barnes J, et al. Guidelines for submitting adverse event reports for publication. Drug Saf 2007; 30(5): 367–73
Aronson JK. Anecdotes as evidence. BMJ 2003 Jun 21; 326(7403): 1346
Auriche M, Bertrand P, Blay N, et al. Good practices of publication of clinical cases of pharmacovigilance: comments, Groupe de Travail sur les Bonnes Pratiques de Publication de Cliniques en Pharmacovigilance: commentary in French]. Therapie 1997 Mar–Apr; 52(2): 123–7
Moore N, Montero D, Coulson R, et al. The single case format: proposal for a structured message for the telematic transmission of information on individual case reports in pharmacovigilance. Pharmacoepidemiol Drug Saf 1994; 3: 157–62
Venulet J. Informativity of adverse drug reactions data in medical publications. Drug Inf J 1985; 19: 357–65
Venulet J, Blattner R, von Bulow J, et al. How good are articles on adverse drug reactions? Br Med J (Clin Res Ed) 1982 Jan 23; 284(6311): 252–4
Haramburu F, Begaud B, Pere JC, et al. Role of medical journals in adverse drug reaction alerts. Lancet 1985 Sep 7; 2(8454): 550–1
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Kelly, W., Moore, N., Goldsmith, D.I. et al. The Authors’ Reply. Drug-Safety 31, 356–357 (2008). https://doi.org/10.2165/00002018-200831040-00010
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DOI: https://doi.org/10.2165/00002018-200831040-00010