Bulimia Nervosa
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Sign up freeTop drugs studied for this disease
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CLINICAL_TRIALS trial_result · 2012-05-28Clinical Trial Update: Cholecystokinin for Reducing Binge Eating in People With Bulimia Nervosa [NA]
A clinical trial evaluating cholecystokinin for reducing binge eating in bulimia nervosa was terminated.
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FDA approval · 2012-04-19FDA Approved: FLUOXETINE — Supplemental Application (TIME CAP LABORATORIES, INC.)
FDA approved a supplemental application for fluoxetine hydrochloride from Time Cap Laboratories, Inc., updating the regulatory status of thi…
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FDA approval · 2012-02-28FDA Approved: FLUOXETINE — Supplemental Application (QUALLENT PHARMACEUTICALS HEALTH LLC)
FDA approves a supplemental application for a generic fluoxetine hydrochloride product from Quallent Pharmaceuticals Health LLC.
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FDA approval · 2012-02-28FDA Approved: FLUOXETINE — Supplemental Application (Alembic Pharmaceuticals Limited)
FDA approves the supplemental application for fluoxetine from Alembic Pharmaceuticals Limited, enabling the generic fluoxetine product to be…
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CLINICAL_TRIALS trial_result · 2012-01-25Clinical Trial Update: Developing Identity: An Eating Disorder Randomized Clinical Trial [NA]
A randomized clinical trial examining identity development in individuals with eating disorders has completed, sponsored by the University o…
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FDA approval · 2011-11-22FDA Approved: FLUOXETINE — Supplemental Application (TIME CAP LABORATORIES, INC.)
FDA approved a supplemental application for fluoxetine hydrochloride from Time Cap Laboratories, Inc., enabling the generic product Fluoxeti…
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CLINICAL_TRIALS trial_result · 2011-11-07Clinical Trial Update: Guided Self-Help Treatment for Binge Eating Disorder [NA]
Clinical trial update noting completion of a study evaluating guided self-help treatment for binge eating disorder.
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FDA label_change · 2010-09-20FDA Approved: FLUOXETINE — Supplemental Application (PAI Holdings, LLC dba PAI Pharma)
FDA approved a supplemental application for fluoxetine hydrochloride by PAI Holdings to modify the product labeling.
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FDA approval · 2010-06-25FDA Approved: FLUOXETINE — Supplemental Application (QUALLENT PHARMACEUTICALS HEALTH LLC)
FDA approved a supplemental application for fluoxetine hydrochloride (fluoxetine) from QUALLENT PHARMACEUTICALS HEALTH LLC, updating the app…
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FDA approval · 2010-05-19FDA Approved: FLUOXETINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for fluoxetine submitted by Teva Pharmaceuticals USA, Inc. (the snippet does not specify the exact c…
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FDA approval · 2010-03-22FDA Approved: FLUOXETINE HYDROCHLORIDE — Original Application (Dr.Reddy's Laboratories Limited)
FDA approved a generic version of fluoxetine hydrochloride (an SSRI) from Dr. Reddy's Laboratories Limited under an Original Application (AN…
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CLINICAL_TRIALS trial_result · 2010-02-15Clinical Trial Update: Cognitive Behavioral Therapy to Treat Bulimia Nervosa in Adolescents [Phase 1, Phase 2]
This update reports on a Phase 1/Phase 2 clinical trial evaluating cognitive behavioral therapy for bulimia nervosa in adolescents, conducte…
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CLINICAL_TRIALS trial_result · 2010-01-14Clinical Trial Update: Treatment of Bulimia Nervosa in a Primary Care Setting [NA]
The document notes the completion of a clinical trial evaluating treatment strategies for bulimia nervosa in a primary care setting.
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CLINICAL_TRIALS trial_result · 2010-01-13Clinical Trial Update: Treatment of Binge Eating Disorder [NA]
This document reports a completed clinical trial update for the treatment of binge eating disorder, with bulimia nervosa and obesity listed …
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FDA approval · 2009-09-28FDA Approved: FLUOXETINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for fluoxetine from Teva Pharmaceuticals USA, Inc., updating the approval status of the drug. Th…
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FDA approval · 2009-09-28FDA Approved: FLUOXETINE — Supplemental Application (Chartwell Governmental & Specialty RX, LLC)
FDA approved a supplemental application for fluoxetine (generic) filed by Chartwell Governmental & Specialty RX, LLC. The approval confirms …
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FDA approval · 2009-08-21FDA Approved: FLUOXETINE — Supplemental Application (Dr.Reddy's Laboratories Limited)
FDA approved a supplemental application for generic fluoxetine from Dr. Reddy's Laboratories Limited.
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FDA label_change · 2009-03-30FDA Approved: FLUOXETINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
FDA approved a supplemental application for Fluoxetine from Teva Pharmaceuticals USA, Inc., updating the labeling of the approved product.
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FDA approval · 2009-03-19FDA Approved: FLUOXETINE — Original Application (Alembic Pharmaceuticals Limited)
FDA approved the original ANDA for fluoxetine from Alembic Pharmaceuticals Limited, enabling a generic version of fluoxetine to be marketed.
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FDA approval · 2009-03-19FDA Approved: FLUOXETINE — Original Application (Aurobindo Pharma Limited)
FDA approved the original application for Fluoxetine by Aurobindo Pharma Limited, enabling a generic Fluoxetine product. The approved indica…
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CLINICAL_TRIALS trial_result · 2009-03-03Clinical Trial Update: Studies of Neuroendocrine and Energy Metabolism in Patients With Eating Disorders
This clinical trial update describes studies investigating neuroendocrine function and energy metabolism in patients with eating disorders, …
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FDA approval · 2009-01-30FDA Approved: PROZAC — Supplemental Application (Dista Products Company)
FDA approves a supplemental application for Prozac (fluoxetine hydrochloride) submitted by Dista Products Company.
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FDA approval · 2008-10-22FDA Approved: FLUOXETINE — Supplemental Application (Teva Pharmaceuticals USA, Inc.)
The FDA approved a supplemental application for fluoxetine from Teva Pharmaceuticals USA, Inc., indicating a modification to the product's a…
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CLINICAL_TRIALS trial_result · 2008-10-08Clinical Trial Update: Topiramate for Binge Eating Disorder Among Adolescents [NA]
A completed clinical trial investigated topiramate for binge eating disorder in adolescents (including bulimia nervosa) with the study statu…
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FDA approval · 2008-09-25FDA Approved: FLUOXETINE — Supplemental Application (QUALLENT PHARMACEUTICALS HEALTH LLC)
FDA approved a supplemental application for Fluoxetine hydrochloride from Quallent Pharmaceuticals Health LLC.