The Effects of Daily Fluoxetine in Treatment of Premenstrual Dysphoric Disorder

Document Type : Original Article

Authors

Abstract

Introduction: Premenstrual Syndrome (PMS) which is accompanied by
Psychological and Physical Symptoms regularly occurs during the second half of the
menstrual cycle and is estimated to affect up to 95% of women to some degree. Only
3-8% of these women have Premenstrual Symptoms that meet the criteria for
premenstrual dysphoric disorder (PMDD), which significantly interferes with social
activities or relationships with others. In this case there are medications one of which
is serotonin reuptake inhibitors, including Fluoxetine.
The aim of this study is To evaluate premenstrual daily dosing of fluoxetine for
treatment of Premenstrual dysphoric disorder.
Materials and Methods: This was a double-blind clinical trial study. After a two
cycle Screening 260 women were randomly prescribed fluoxetine 10mg capsules,
fluoxetine 20mg capsules and placebo capsules (dosed daily from the 14th day before
next expected menses through the first fall day of bleeding) for three cycles, and they
had a follow-up visit without taking drugs. After this time data was gathered with
questionnaire and analyzed by descriptive statistics.
Results: Baseline demographics and severity of illness and length of menstrual cycle
measures showed that the treatment groups were balanced. Premenstrual daily
fluoxetine 20mg demonstrated significant improvement in symptoms compared with
placebo (P = 0.005) and Premenstrual daily fluoxetine 10mg groups. Both active
treatment groups significantly improved by the first treatment cycle. Both fluoxetine
groups showed significant improvement.
All 20 symptoms such as fatigue, sleep disorder, irritability, depression, appetite
changes, and physical symptoms such as body dimorphic, breast tenderness, acnea,
headache, arthralgia, low back pain, and weight increase had significant reduction or
completely disappeared with Fluoxetine 20mg capsules.
Discontinuation due to adverse side effects did not differ among the three groups.
Conclusion: Premenstrual daily dosing with Fluoxetine effectively treats mood, physical
and social function and symptoms associated with premenstrual dysphonic disorder.
Fluoxetine 20mg appears to have comparably better efficacy than floxetine 10mg. 

Keywords


1. Rivera Tovar AD, Frank Lue. Luteal phase dysphoric disorder in young woman. Is J
Psych. 1990; 117:1634-6.
2. Ramcharan Sm, Love EJ, Fick GH, Goldfien A. The epidemiology of premenstrual
symptoms in a population based sample of 2650 urban woman: attibutable risk and risk
factor. J Clin Epidemiol. 1992; 15:377-92. 
 
3. American sychiatric Association Diagnostic and statisica1 manual of mental disorders.
4th ed. Washington DC: American Psychiatric Association; 1994.
4. Yonkers KA, Halbreich U, Freeman E, Brown C, Endicott J, Frank E, et al.
Symptomatic improvement of premenstrual dysphoric disorder with sertraline treatment.
A randomized controlled trial. Sertraline Premenstrual Dysphoric Collaborative Study
Group. JAMA. 1997 Sep 24; 278(12):983-8.
5. Endicott J, Amsterdam J, Eriksson E, Frank E, Freeman E, et a1. Is premenstrual
dysphoric disorder a distinct clinical entity? J Womens Health Gend Based Med 1999
Jun;8(5):663-79.
6. Steiner M, Steninberg S, Stewart D, Carter D, Berger C, Reid R, et al. Fluoxetin in the
treatment of premenstrual dysphoria . Canadian Fluoxetine/premenstrual Dyshoria
Collaborative Study Group. N Engl Med. 1995 Jun 8; 332(23):1529-34.
7. Su TP, Schmidt PJ, Danaceau MA, Tobin MB, Rosenstein DL, Murphy DL, et al.
Fluoxetin in the treatment of premenstrual dysphoria. Neuropsychopharacology. 1997
May;16(5):346-56.
8. Pearlstein TB, Stone AB. Long-term fluoxetin treatment of late luteal phase dysphoric
disorder. J Clin Psychiatry. 1994 Aug;55(8):332-5.
9. Freeman EW, Rickels K, Arredondo F, Kao LC, Pollack SE, Sondheimer SJ. Full- or
half-cycle treatment of severe premenstrual syndrome with a serotonregic
antidepressant. J Clin Psychopharmacol. 1999 Feb;19(1):3-8.
10. Steiner M, Korzekwa M, Lamont J, Wlkins A. Intermittent fluoxetine dosing in the
treatment of women with premenstrual dysphoria. Psychopharmacol Bull.
1997;33(4):771-4.
11. Sundblad C, Wikander I, Andersch B, Eriksson E. A naturalistic study of paroxetine in
premenstrual syndrome: efficacy and side-effects during ten cycles of treatment. Eur
Neuropsychopharmacol. 1997 Aug;7(3):201-6.
12. Carpenter SE, Rock JK. Premenstrual syndrome. In: Keye WR Jr . Pediatric and
adolescent gynecology. 2nd ed, Philadelphia:Lippincott Williams & Wilkins;2000: 247.
13. Kaplan HZ, Sadocek BJ. Synopsis of psychiatry. 8th ed, Philadelphia:Williams &
Wilkins;1998:530-582.
14. Wikander I, Sundblad C, Andersch B, Dagnell I, Zylber stein D, Bengtsson F, et al.
Citalopram in premenstrual dysphoria: is intermittent during luteal phases more
effective than continuous medication throughout the menstrual cycle?. J Clin
Psychopharmacol. 1998 Oct;18(5):390-8.
15. Schmidt PJ, Nieman LK, Danaceau MA, Adams LF, Ruinow DR. Differential
behavioral effects of gonadal steroids in women with and in those without premenstrual
syndrome. N Engl J Med. 1998 Jan;388(4):209-16.
16. Rubinow DR, Schmidt PJ. The treatmemt of premenstrual syndrome-forward into the
past. N Engl J Med. 1995 Jun 8;332(23):1529-34.
17. Stahl SM. Essential psychopharmacology. Cambridge: Cambridge University Press;
2000.
18. Hylant TR, Sundell K, Judge R. The impact of premenstrual symptomatology on
functioning and treatment-seeking behavior: experience from the United Staes, United
Kingdom, and France. J Womens Health Gend Based Med. 1999 Oct;8(8):1043-52.