Cutaneous adverse drug reactions to psychotropic drugs and their risk factors - a case-control study.


Journal

European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology
ISSN: 1873-7862
Titre abrégé: Eur Neuropsychopharmacol
Pays: Netherlands
ID NLM: 9111390

Informations de publication

Date de publication:
01 2019
Historique:
received: 22 06 2018
revised: 11 09 2018
accepted: 23 10 2018
pubmed: 15 11 2018
medline: 6 8 2019
entrez: 15 11 2018
Statut: ppublish

Résumé

Cutaneous adverse drug reactions (CADRs) in patients with psychotropic drugs are common. Large studies on the relevant drugs and other risk factors are still scarce. 594 cases of severe CADRs ("cases") were compared with 8085 cases of other adverse drug reactions ("non-cases") documented in a pharmacovigilance program in psychiatry (AMSP) from 1993 to 2014. Logistic regression was carried out to determine risk factors and between-drug differences. CADRs were relatively more prevalent in patients treated with clomipramine, maprotiline, carbamazepine, lamotrigine, acamprosate, clomethiazole and disulfiram as well as with antidepressants and anticonvulsants as drug classes (p < 0.01). For these drugs, significantly more women were found in patients using maprotiline, lamotrigine (not carbamazepine) and in the groups of antidepressants, tricyclics and anticonvulsants (p < 0.01). Women were more vulnerable to CADRs (67% in cases and 56% in non-cases, p < 0.01). The significantly higher rate of CADRs in women was mainly observed under age of 50 years, i.e. during female reproductive years. In a multivariate logistic regression, female sex, the diagnostic group ICD F1 (substance abuse), maprotiline, carbamazepine, lamotrigine and clomethiazole were identified as risk factors of CADRs. The case/non-case approach allowed to identify risk factors based on empirical data rather than experts' evaluations. The new findings of substance abuse and clomethiazole as risk factors for CADRs have to be confirmed in further studies. Since CADRs can be life-threatening, it is important to be aware of risk factors, especially women during their reproductive period and with lamotrigine treatment.

Identifiants

pubmed: 30424913
pii: S0924-977X(18)30845-9
doi: 10.1016/j.euroneuro.2018.10.010
pii:
doi:

Substances chimiques

Psychotropic Drugs 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Pagination

111-121

Informations de copyright

Copyright © 2018. Published by Elsevier B.V.

Auteurs

Waldemar Greil (W)

Department of Psychiatry, Ludwig-Maximilian University, Nussbaumstr. 7, Munich D-80331, Germany; Psychiatric Hospital, Kilchberg, Zurich, Switzerland. Electronic address: waldemar.greil@med.uni-muenchen.de.

Xueqiong Zhang (X)

Department of Psychiatry, Ludwig-Maximilian University, Nussbaumstr. 7, Munich D-80331, Germany; Psychiatric Hospital, Kilchberg, Zurich, Switzerland.

Hans Stassen (H)

Psychiatric Hospital, Kilchberg, Zurich, Switzerland; Institute for Response-Genetics, Psychiatric University Hospital (KPPP), Zurich, Switzerland.

Renate Grohmann (R)

Department of Psychiatry, Ludwig-Maximilian University, Nussbaumstr. 7, Munich D-80331, Germany.

René Bridler (R)

Psychiatric Hospital, Kilchberg, Zurich, Switzerland.

Gregor Hasler (G)

Division of Molecular Psychiatry, University Psychiatry Department (UPD), University of Bern, Bern, Switzerland.

Sermin Toto (S)

Department of Psychiatry, Socialpsychiatry & Psychotherapy, Hannover Medical School, Hannover, Germany.

Stefan Bleich (S)

Department of Psychiatry, Socialpsychiatry & Psychotherapy, Hannover Medical School, Hannover, Germany.

Siegfried Kasper (S)

Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.

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