Study completion rates were comparable (fluoxetine 20 … If you do not receive an email within 10 minutes, your email address may not be registered, Fluoxetine at 60 mg also improved depression, carbohydrate binges, and eating attitudes, as demonstrated by reduced scores on most subscales of the Eating Attitudes Test (EAT) and the Eating Disorder Inventory (EDI). et al. 1), combined with strict supervision and a 900 kcal American Diabetes Association (ADA) diet caused minimal weight loss and no change in picking behavior. Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN, Dept, of Pediatrics, Methodist Hospital, Indianapolis, IN, and Dept, of Pharmacology and Toxicology and Dept, of Psychiatry, Indiana University School of Medicine, Indianapolis, IN.Use the link below to share a full-text version of this article with your friends and colleagues.

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Plodkowski R, Patients that gained ⩾3% of their baseline weight in the initial 8 weeks of olanzapine treatment (n=31) were randomized to double-blind treatment with placebo or fluoxetine (60 mg/day). A randomized, phase 3 trial of naltrexone SR/bupropion SR on weight and obesity-related risk factors (COR-II). By continuing to browse this site, you agree to its use of cookies as described in our I have read and accept the Wiley Online Library Terms and Conditions of UseA Focus on Evaluating Major Study Limitations in Order to Apply Clinical Trials to Patient Care: Implications for the Healthcare Team, Fluoxetine for adults who are overweight or obese, SSRI or CRF antagonism partially ameliorate depressive-like behavior after adolescent social defeat, Long‐Term Drug Treatment of Obesity in a Private Practice Setting, The Addition of Dexfenfluramine to Fluoxetine in the Treatment of Obesity: A Randomized Clinical Trial, Sertraline and Relapse Prevention Training Following Treatment by Very‐Low‐Calorie Diet: A Controlled Clinical Trial, No Specific Effect of Fluoxetine Treatment on Fasting Glucose, Insulin, Lipid Levels, and Blood Pressure in Healthy Men with Abdominal Obesity, ; 8/90-mg extended-release tablet. The average excess weight loss over 6-12 months was about 6 lbs, and the maximum recommended dose was used– 400 mg QD.

Qualification phase clinic visits were biweekly; maintenance phase visits were monthly for 4 months, then bimonthly for 6 months. The same options for weight loss exist as for those who have gained weight for other reasons, including: Implementing a healthy diet; Engaging in regular exercise, which has the added benefit of naturally boosting your mood; Weight loss drugs; Other Options . All rights Reserved. COR-I Study Group.

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