Pharmacopsychiatry 2004; 37(2): 43-45
DOI: 10.1055/s-2004-815523
Original Paper
© Georg Thieme Verlag Stuttgart · New York

Reduction Of Clozapine-Induced Hypersalivation By Pirenzepine Is Safe

B. Schneider1 , H. Weigmann2 , C. Hiemke2 , B. Weber1 , J. Fritze1 , 3
  • 1Center of Psychiatry, Department of Psychiatry and Psychotherapy I, Johann Wolfgang Goethe-University of Frankfurt/Main, Germany
  • 2Department of Psychiatry, University of Mainz, Germany
  • 3German Association of Private Health Insurers
Weitere Informationen

Publikationsverlauf

Received: 26.4.2002 Revised: 19.9.2002

Accepted: 8.1.2003

Publikationsdatum:
29. März 2004 (online)

Introduction: Hypersalivation is known as a frequent, disturbing, and socially stigmatizing side effect of therapy with the atypical antipsychotic clozapine. It has been shown that the addition of the anticholinergic pirenzepine is able to reduce clozapine-induced hypersalivation, probably by blocking M4-receptors. Nevertheless, a pharmacokinetic interaction between both compounds cannot be excluded. Methods: In this pilot study, 29 schizophrenic patients (ICD-10; 51.7 % female; age: 36.7 ± 8.7 years [mean ± SD]) were included. Serum concentrations of clozapine and its pharmacologically active metabolite N-desmethylclozapine were determined under steady-state conditions by automated HPLC with UV detection before and after addition of pirenzepine for 3 days.

Results: Significantly fewer patients reported hypersalivation after addition of pirenzepine (69 % vs. 34.5 %, P = 0.002). No significant differences of clozapine and N-desmethylclozapine serum levels before (329 ± 181 ng/ml and 218.0 ± 123.4 ng/ml, respectively) and 3 days after (336 ± 215 ng/ml and 235.9 ± 164.4 ng/ml, respectively) addition of pirenzepine were found. In three patients, however, clozapine serum levels increased; this was probably unrelated to pirenzepine. Conclusion: In conclusion, treatment of clozapine-induced hypersalivation with pirenzepine is a recommendable combination with low risk of additional side effects.

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Barbara Schneider, M.D.

Center of Psychiatry, Department of Psychiatry and Psychotherapy I

Johann Wolfgang Goethe-University of Frankfurt/Main

Heinrich-Hoffmann-Str. 10

D-60528 Frankfurt/Main

Germany

Telefon: +49-69-630 14784

Fax: +49-69-630 15920

eMail: B.Schneider@em.uni-frankfurt.de