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Endotoxin-Like Reactions With Intravenous Gentamicin Results From Pharmacovigilance Tools Under Investigation

Published online by Cambridge University Press:  21 June 2016

Manfred Hauben
Affiliation:
Risk Management Strategy, Pfizer, Inc., New York, New York Division of Clinical Pharmacology, New York University School of Medicine, New York Departments of Community and Preventive Medicine and Pharmacology, New York Medical College, Valhalla, New York
Lester Reich*
Affiliation:
Risk Management Strategy, Pfizer, Inc., New York, New York Departments of Community and Preventive Medicine and Pharmacology, New York Medical College, Valhalla, New York
*
Risk Management Strategy, Pfizer, Inc., 235 E. 42nd Street, New York, NY 10017[email protected]

Abstract

Objective:

To apply two data mining algorithms (DMAs) to Food and Drug Administration (FDA) Adverse Event Reporting System (AERS) reports that involved endotoxin-like reactions with intravenous gentamicin to determine whether a signal of disproportionate reporting of these events would have been generated concurrently with surveillance based on clinical observation.

Design:

Multi-item gamma-Poisson shrinker (MGPS) and proportional reporting ratios (PRRs) were used. Data used for data mining consisted of an extract of the FDA AERS database. Previously published details of clusters of endotoxin-like reactions to intravenous gentamicin were used to select adverse events for data mining.

Results:

The first signal of disproportionate reporting with any relevant event occurred in 1998, the year in which the outbreak was identified and evaluated by the Centers for Disease Control and Prevention and the FDA. In 1997, there were only 6 reports of rigors in the AERS; this jumped to 68 in 1998. In 1998, a signal was generated for endotoxic shock with PRRs but not with MGPS, based on one case.

Conclusions:

The two DMAs generated signals concurrently with the influx of reports. It would have been difficult for safety reviewers to ignore an increase in rigors by traditional methods of safety surveillance; therefore, DMAs might not have had a great deal to offer in this instance. If data mining were considered as a second-line defense to diligent clinical observations under similar circumstances, simple disproportionality methods such as PRRs might be more useful than DMAs such as MGPS when commonly cited thresholds are used.

Type
Orginal Articles
Copyright
Copyright © The Society for Healthcare Epidemiology of America 2005

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References

1.Hauben, M. Trimethoprim-induced hyperkalemia: lessons in data mining. Br J Clin Pharmacol 2004;58:338339.Google Scholar
2.Hauben, M, Reich, L. Drug-induced pancreatitis: more lessons in data mining. Br J Clin Pharmacol 2004;58:560562.Google Scholar
3.Evans, S, Waller, P, Davis, S. Use of proportional reporting ratios (PRRs) for signal generation from spontaneous adverse drug reaction reports. Pharmacoepidemiol Drug 2001;10:483486.Google Scholar
4.van Puijenbroek, E, Diemont, W, van Grootheest, K. Application of quantitative signal detection in the Dutch spontaneous reporting system for adverse reactions. Drug 2003;26:293301.Google Scholar
5.Bate, ALindquist, M, Edwards, I, et al.A Bayesian neural network method for adverse drug reaction signal detection. Eur J Clin Pharmacol 1998;54:315321.Google Scholar
6.Szarfman, A, Machado, SG, O'Neill, R. Use of screening algorithms and computer systems to efficiently signal higher than expected combinations of drugs and events in the US FDA's spontaneous reports database. Drug Sage 2002;25:381382.Google Scholar
7.Centers for Disease Control and Prevention. Endotoxin-like reactions associated with intravenous gentamicin: California, 1998. MMWR 1998;47:877880.Google Scholar
8.Fanning, M, Wassel, R, Piazza-Hepp, T. Pyrogenic reactions to gentamicin therapy. N Engl J Med 2000;343:16581659.Google Scholar
9.Buchholz, U, Chesley, R, Murphy, R, et al.Pyrogenic reactions associated with single daily dosing of intravenous gentamicin. Infect Control Hosp Epidemiol 2000;21:771774.Google Scholar
10.Krieger, JA, Duncan, L. Gentamicin contaminated with endotoxin. N Engl J Med 1999;340:1122.Google Scholar
11.DuMouchel, W. Bayesian data mining in large frequency tables, with an application to the FDA spontaneous reporting system. The American Statistician 1999;53:170190.Google Scholar
12.Krieger, JA, Duncan, L. Gentamicin contaminated with endotoxin. N Engl J Med 1999;340:1122.Google Scholar
13.Jaber, BL. Pyrogenic reactions following gentamicin therapy: an alternative explanation. Med Hypotheses 2001;57:727728.Google Scholar
14.Safety reporting requirements for human drug and biological products: proposed rule. 68 Federal Register 1240512497 (2003).Google Scholar