Pemoline: Difference between revisions
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Latest revision as of 16:54, 20 August 2015
Clinical data | |
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Routes of administration | Oral |
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Pharmacokinetic data | |
Bioavailability | 50% bound to plasma proteins |
Metabolism | Hepatic |
Elimination half-life | 12 hours |
Excretion | ? |
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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 | C9H8N2O2 |
Molar mass | 176.172 g/mol |
WikiDoc Resources for Pemoline |
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Most recent articles on Pemoline |
Media |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on Pemoline at Clinical Trials.gov Clinical Trials on Pemoline at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on Pemoline
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Directions to Hospitals Treating Pemoline Risk calculators and risk factors for Pemoline
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Healthcare Provider Resources |
Causes & Risk Factors for Pemoline |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Pemoline (sold as Cylert) is a medication used to treat attention-deficit hyperactivity disorder (ADHD) and narcolepsy. Under the Convention on Psychotropic Substances, it is a Schedule IV drug.[1]
Pemoline has some advantages over other stimulants in that it does not reduce the appetite or cause dry mouth.
Hepatotoxicity and discontinuation
In some patients Pemoline is suspected of causing hepatotoxicity, so regular liver tests are performed on those treated with it. Since receiving FDA approval in 1975, it has been linked with 21 cases of liver failure, of which 13 resulted in liver replacement or death. In 2005, the Food and Drug Administration (FDA) withdrew approval for pemoline due to pressure from certain public advocacy groups, including Public Citizen. The patient support group "Narcolepsy Network"[2] tried to persuade the FDA not to ban it, on the grounds that some patients find all other treatments ineffective or to have debilitating side effects. The medication was used by an estimated 10,000 Americans afflicted with narcolepsy. A more potent analogue of pemoline, 4-methylaminorex has appeared as a black market drug with abuse potential similar to methamphetamine.
In March 2005, Abbott Laboratories (Cylert marketer) had discontinued the production of Cylert arguing economic reasons.
References
See also
External links
- Pemoline monograph at HealthyPlace.com
- AScribe Newswire press release about the withdrawal.
- Pemoline (patient information)
- Cylert Discontinued Press Release
Template:Stimulants Template:Psychostimulants, agents used for ADHD and nootropics
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