Literature DB >> 8011181

A risk-benefit appraisal of drugs used in the management of premenstrual syndrome.

J F Mortola1.   

Abstract

Recent advances in the understanding of the pathogenesis of premenstrual syndrome (PMS) have allowed the development of appropriate pharmacological interventions. Although at the present time there are no approved medications for this indication in the US, several well-designed studies have been conducted that guide the clinician's treatment of PMS. As a result, less-proven nonpharmacological modalities, such as dietary modification, exercise regimens and psychotherapy, are more quickly supplanted by the use of medication. Three classes of agents have been proven efficacious and are widely used to treat the disorder. These include benzodiazepines (especially alprazolam), selective serotonin reuptake inhibitors (especially fluoxetine), and gonadotropin-releasing hormone (GnRH) [luteinising hormone-releasing hormone (LHRH)] agonists. In addition to these medications which are used to treat the generalised syndrome of PMS, a variety of other drugs are used in the treatment of specific aspects of this disorder. Despite the success of these treatments, each has a substantial adverse effect profile which modulates their use in some patients. Knowledge of these potential adverse effects and their management should help optimise therapy. In addition, a variety of less well-proven pharmacological remedies are commonly in use. The adverse effects of these medications may well outweigh their benefits.

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Year:  1994        PMID: 8011181     DOI: 10.2165/00002018-199410020-00005

Source DB:  PubMed          Journal:  Drug Saf        ISSN: 0114-5916            Impact factor:   5.606


  40 in total

1.  The premenstrual syndrome.

Authors:  R GREENE; K DALTON
Journal:  Br Med J       Date:  1953-05-09

Review 2.  Endocrine properties and clinical application of danazol.

Authors:  W P Dmowski
Journal:  Fertil Steril       Date:  1979-03       Impact factor: 7.329

3.  Alteration of platelet serotonergic mechanisms and monoamine oxidase activity in premenstrual syndrome.

Authors:  C R Ashby; L A Carr; C L Cook; M M Steptoe; D D Franks
Journal:  Biol Psychiatry       Date:  1988-06       Impact factor: 13.382

4.  Progesterone and the premenstrual syndrome: a double blind crossover trial.

Authors:  L Dennerstein; C Spencer-Gardner; G Gotts; J B Brown; M A Smith; G D Burrows
Journal:  Br Med J (Clin Res Ed)       Date:  1985-06-01

5.  Further analyses of mortality in oral contraceptive users. Royal College of General Practitioners' Oral Contraception Study.

Authors: 
Journal:  Lancet       Date:  1981-03-07       Impact factor: 79.321

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Authors:  K N Muse; N S Cetel; L A Futterman; S C Yen
Journal:  N Engl J Med       Date:  1984-11-22       Impact factor: 91.245

7.  Fluoxetine in the treatment of premenstrual syndrome.

Authors:  A B Stone; T B Pearlstein; W A Brown
Journal:  Psychopharmacol Bull       Date:  1990

8.  A prospective study of postmenopausal estrogen therapy and coronary heart disease.

Authors:  M J Stampfer; W C Willett; G A Colditz; B Rosner; F E Speizer; C H Hennekens
Journal:  N Engl J Med       Date:  1985-10-24       Impact factor: 91.245

9.  Treatment of premenstrual syndrome with alprazolam: results of a double-blind, placebo-controlled, randomized crossover clinical trial.

Authors:  S Smith; J S Rinehart; V E Ruddock; I Schiff
Journal:  Obstet Gynecol       Date:  1987-07       Impact factor: 7.661

10.  Lasting response to ovariectomy in severe intractable premenstrual syndrome.

Authors:  P Casson; P M Hahn; D A Van Vugt; R L Reid
Journal:  Am J Obstet Gynecol       Date:  1990-01       Impact factor: 8.661

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  2 in total

1.  Ovarian steroid action on tryptophan hydroxylase protein and serotonin compared to localization of ovarian steroid receptors in midbrain of guinea pigs.

Authors:  N Z Lu; T A Shlaes; C Gundlah; S E Dziennis; R E Lyle; C L Bethea
Journal:  Endocrine       Date:  1999-12       Impact factor: 3.633

Review 2.  Ovarian steroids and serotonin neural function.

Authors:  C L Bethea; M Pecins-Thompson; W E Schutzer; C Gundlah; Z N Lu
Journal:  Mol Neurobiol       Date:  1998-10       Impact factor: 5.590

  2 in total

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