S. Ozeren et al., FLUOXETINE IN THE TREATMENT OF PREMENSTRUAL-SYNDROME, European journal of obstetrics, gynecology, and reproductive biology, 73(2), 1997, pp. 167-170
Background: Premenstrual syndrome (PMS) is defined as the disabling an
d cyclic occurrence of emotional and behavioral symptom complex during
the latter half of the menstrual cycle. Although its etiology is unkn
own, it has been speculated that premenstrual syndrome is linked to a
deficiency of central serotoninergic activity. Method: The study consi
sted of a double-blind, placebo controlled trial of fluoxetine at a do
se of 20 mg/day or placebo for three menstrual cycles. The 440 women w
ho appeared to meet the eligibility criteria were instructed to record
the 'Calendar of Premenstrual Experiences' (CPE) scale for two comple
te menstrual cycles. Of 410 women who successfully completed two cycle
s of recording their symptoms daily only 35 met the criteria for PMS.
These criteria included psychiatric interviews which were made before
treatment. Thirty-five PMS patients were randomized into placebo or fl
uoxetine treatment groups. Results: Our study suggests that fluoxetine
at a dose of 20 mg per day was significantly superior to placebo in a
lleviating the symptoms of PMS. The most common side effects were gast
rointestinal irritability (15%), insomnia (11%) and sexual dysfunction
(8.5%). Conclusion: Fluoxetine is an effective and well-tolerated dru
g and appears to have considerable promise in treating a range of symp
toms in women with PMS. (C) 1997 Elsevier Science Ireland Ltd.