Abstract
Background:The WHO Programme for International Drug Monitoring, maintained by the Uppsala Monitoring Centre (UMC), has more than 90 member countries contributing individual case safety reports (ICSRs) from their existing national pharmacovigilance systems; these reports are stored in the WHO global ICSR database, VigiBase. A continuous increase of ICSRs of alopecia in suspected connection to lamotrigine use has been observed in VigiBase; however, only limited information has been published on this topic.
Objective:To examine in greater detail the association between lamotrigine and alopecia by outlining the characteristics of the accumulated reports in VigiBase.
Method:An analysis of all reports in VigiBase, up to 1 April 2009, where lamotrigine was suspected of having caused alopecia.
Results:Lamotrigine was suspected of being involved in the development of alopecia in 337 patients, reported from 19 countries. The age of the patients ranged between 5 months and 84 years (mean 36 years), with a predominance (58%) of patients <40 years of age. 272 patients were female. In 291 reports, lamotrigine was the only drug suspected by the reporter, and in 112 reports, lamotrigine was the sole reported drug. Commonly co-reported drugs were other antiepileptic drugs. For 217 patients, alopecia was reported as the single event. In 11 patients, the reaction abated on cessation of lamotrigine. One patient was reported to have had a recurrence of alopecia on re-administration of lamotrigine.
Conclusions:The UMC continues to receive reports of alopecia associated with the use of lamotrigine. Although alopecia may not be regarded as serious from a regulatory perspective, this adverse reaction has the potential to affect compliance, resulting in decreased efficacy of the treatment regimen and detrimental effects on patient health outcomes.
References
Hillemacher T, Bleich S, Kornhuber J, et al. Hair loss as a side effect of lamotrigine treatment [letter]. Am J Psychiatry 2006 Aug; 163(8): 1451
Patrizi A, Savoia F, Negosanti F, et al. Telogen effluvium caused by magnesium valproate and lamotrigine. Acta Derm Venereol 2005; 85(1): 77–8
Sullivan JR, Watson A. Lamotrigine-induced toxic epidermal necrolysis treated with intravenous cyclosporin: a discussion of pathogenesis and immunosuppressive management. Australas J Dermatol 1996 Nov; 37(4): 208–12
Netherlands Pharmagovigilance Centre, Lareb. Lamotrigine and alopecia. ’s-Hertogenbosch: Netherlands Pharmacovigilance Centre, Nov 2007 [online]. Available from URL: http://www.lareb.nl/documents/kwb_2007_2_lamotr.pdf [Accessed 2009 Apr 24]
Lindquist M. Vigibase, the WHO global ICSR database system: basic facts. Drug Inf J 2008; 42(5): 409–19
Martindale, Thomson Micromedex database [online]. Available from URL: http://www.thomsonhc.com [Accessed 2009 Apr 24]
Summary of product characteristics for Lamictal combined tablets. Electronic medicine compendium, Datapharm Communications Ltd [online]. Available from URL: http://www.medicines.org.uk/EMC/medicine/4228/SPC/Lamictal+Combined+Tablets/ [Accessed 2009 Apr 24]
Fauci A, Braunwald E, Kasper D, et al. Harrison’s principles of internal medicine. 17th ed. New York: The McGraw-Hill Companies Inc., 2008
Uppsala Monitoring Centre. Lamotrigine and alopecia. In: WHO SIGNAL [restricted document] 2004 Jun: 5–8
Summary of product characteristics for Lamictal tablet. FASS [online]. Available from URL: http://www.fass.se/LIF/produktfakta/artikel_produkt.jsp?NplID=20010518000014&DocTypeID=6 [Accessed 2009 Apr 24]
Drugdex, Thomson Micromedex database [online]. Available from URL: http://www.thomsonhc.com [Accessed 2009 Apr 24]
Physician’s desk reference, Thomson Micromedex database. Lamictal tablets [online]. Available from URL: http://www.thomsonhc.com [Accessed 2009 Apr 24]
Bate A, Lindquist M, Edwards IR, et al. A Bayesian neural network method for adverse drug reaction signal generation. Eur J Clin Pharmacol 1998 Jun; 54(4): 315–21
Norén GN, Bate A, Orre R, et al. Extending the methods used to screen the WHO drug safety database towards analysis of complex associations and improved accuracy for rare events. Stat Med 2006 Nov 15; 25(21): 3740–57
Norén GN, Orre R, Bate A, et al. Duplicate detection in adverse drug reaction surveillance. Data Min Knowl Discov 2007; 14: 305–28
Summary of product characteristics. Electronic medicine compendium, Datapharm Communications Ltd [online]. Available from URL: http://www.medicines.org.uk/[Accessed 2009 Apr 24]
Pillans PI, Woods DJ. Drug-associated alopecia. Int J Dermatol 1995 Mar; 34(3): 149–58
Mercke Y, Sheng H, Khan T, et al. Hair loss in psychopharmacology. Ann Clin Psychiatry 2000 Mar; 12(1): 35–42
Tosti A, Misciali C, Piraccini BM, et al. Drug-induced hair loss and hair growth: incidence, management and avoidance. Drug Saf 1994 Apr; 10(4): 310–7
Acknowledgements
The authors are indebted to the national centres contributing data to the WHO Programme for International Drug Monitoring. The opinions and conclusions, however, are not necessarily those of either the various centres or the WHO. The authors would also like to acknowledge Professor Ralph Edwards for editing assistance, and Mr Anders Viklund for assistance in data collection, both of whom work at the UMC.
No sources of funding were used to assist in the preparation of this study. The authors have no conflicts of interest that are directly relevant to the content of this study.
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Tengstrand, M., Star, K., van Puijenbroek, E.P. et al. Alopecia in Association with Lamotrigine Use. Drug-Safety 33, 653–658 (2010). https://doi.org/10.2165/11536190-000000000-00000
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DOI: https://doi.org/10.2165/11536190-000000000-00000