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Bulletin of Clinical Psychopharmacology, Vol: 21, Supplement: 2, 2011 - www.psikofarmakoloji.org<br />

Poster Presentations<br />

intervention (p = 0.144), severity of combined physical-mental symptoms before intervention (p = 0.242) in the first group. There was a<br />

significant difference among the severity of physical (p= 0.000), mental (p= 0.000), combined physical-mental symptoms (p= 0.000) before<br />

and after intervention. The reduction in severity of physical, mental, and combined physical-mental symptoms after intervention was<br />

significant between the two groups (p= 0.000).<br />

Conclusion: Based on our results 1000mg/day fish oil may reduce the severity of physical, mental, and combined physical-mental<br />

symptoms of PMS.<br />

Key words: Premenstrual syndrome, fish oil, placebo, physical symptom, mental symptom<br />

Bulletin of Clinical Psychopharmacology 2011;21(Suppl. 2):S134-5<br />

[PP-024] Ref. No: 145<br />

Improvement of risperidone-induced hyperprolactinemia with the addition<br />

of aripiprazole: Case report<br />

Medine Gıynaş Ayhan, Faruk Uguz, Nazmiye Kaya<br />

Department of Psychiatry, Selcuk University,Meram School of Medicine, Konya, Turkey.<br />

E-mail: drmedineayhan@gmail.com<br />

Objective: Hyperprolactinemia is an important side effect of antipsychotic treatment. All typical antipsychotics and some atypical<br />

antipsychotics such as risperidone and amisulpiride have been shown to cause marked elevation in serum prolactin levels, whereas most<br />

other atypical antipsychotics such as quetiapine, olanzapine, clozapine, ziprasidone, and aripiprazole appear to have little or no effect on<br />

serum prolactin levels. Hyperprolactinemia can lead to gynecomastia, galactorrhea, sexual dysfunction, infertility, oligomenorrhea, and<br />

amenorrhea. It also reduces the bone mineral density and contributes to osteoporosis in the long term. These important side effects cause<br />

patients in remission not to continue treatment.<br />

Case: We report two clinical cases of risperidone-induced hyperprolactinemia and amenorrhea, who with treatment by the partial<br />

dopamine agonist aripiprazole, showed prolactin normalization.<br />

Conclusion: Addition of aripiprazole to treatment may be considered as a first option in hyperprolactinemia cases with significant<br />

improvement in psychotic symptoms.<br />

Key words: Hyperprolactinemia, amenorrhea, antipsychotic, risperidone, aripiprazole<br />

Bulletin of Clinical Psychopharmacology 2011;21(Suppl. 2):S135<br />

[PP-025] Ref. No: 146<br />

Atomoxetine for the treatment of ADHD in young adults with an assessment<br />

of associated functional outcomes<br />

Murat Altın 1 , Levent Alev 1 , Todd M. Durell 2 , Leonard A. Adler 3 , Dave W. Williams 2 , Ahmed Deldar 2 , James J. Mcgough 4 ,<br />

Paul E. Glaser 5 , Richard L. Rubin 6 , Elias S. Sarkis 7 , Teresa A. Pigott 8 , Bethany K. Boardman 2<br />

1 Eli Lilly and Company, Istanbul,Turkey<br />

2 Eli Lilly and Company and/or one of its subsidiaries, Indianapolis, IN, USA<br />

3 Department of Psychiatry, NYU School of Medicine; and Psychiatry Service, New York VA Harbor Healthcare System, New York, NY, USA<br />

4 UCLA Semel Institute for Neuroscience and Human Behavior, Los Angeles, CA, USA<br />

5 University of Kentucky, Department of Psychiatry, Lexington, KY, USA,<br />

6 Vermont Clinical Study Center, Burlington, VT, USA<br />

7 Division of Child and Adolescent Psychiatry, University of Florida, Gainesville, FL, USA<br />

8 Department of Psychiatry, University of Florida, Gainesville, FL, USA<br />

E-mail: altin_murat@lilly.com<br />

Objectives: ADHD in young adults is associated with significant impairment in multiple functional domains. This trial examined the<br />

efficacy of atomoxetine (ATX) in young adults and evaluated improvements in core ADHD symptoms and associated functional outcomes.<br />

Method: Patients aged 18-30 years were randomized to 12 weeks of double-blind treatment with ATX (n=220) or placebo (PBO, n=225).<br />

Patients in the atomoxetine treatment arm began treatment with 40 mg/day (dosed 20 mg BID) for a minimum of 7 days followed by<br />

S135

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