Dexfenfluramine: Difference between revisions
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Latest revision as of 19:46, 18 August 2015
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Pharmacokinetic data | |
Protein binding | 36% |
Elimination half-life | 17-20 hours |
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DrugBank | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C12H16F3N |
Molar mass | 231.257 g/mol |
WikiDoc Resources for Dexfenfluramine |
Articles |
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Most recent articles on Dexfenfluramine Most cited articles on Dexfenfluramine |
Media |
Powerpoint slides on Dexfenfluramine |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Dexfenfluramine at Clinical Trials.gov Trial results on Dexfenfluramine Clinical Trials on Dexfenfluramine at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Dexfenfluramine NICE Guidance on Dexfenfluramine
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Patient resources on Dexfenfluramine Discussion groups on Dexfenfluramine Patient Handouts on Dexfenfluramine Directions to Hospitals Treating Dexfenfluramine Risk calculators and risk factors for Dexfenfluramine
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Healthcare Provider Resources |
Causes & Risk Factors for Dexfenfluramine |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Dexfenfluramine, also marketed under the name Redux, is a serotoninergic anorectic drug. It was for some years in the mid-1990s approved by the United States Food and Drug Administration for the purposes of weight loss. However, following multiple concerns about the cardiovascular side-effects of the drug, such approval was withdrawn. After it was removed in the US, dexfenfluramine was also pulled out in other global markets. It was later superseded by sibutramine, which is a safer alternative to both dexfenfluramine and fenfluramine.
The drug was manufactured by Interneuron Pharmaceuticals and marketed by Wyeth-Ayerst Laboratories. It is the enantiomer of levofenfluramine.
See also
References
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