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Fluphenazine

IUPAC chemical name
CAS number
69-23-8 (Base)
ATC code
N05AB02
Chemical formula C22H26F3N3OS
Molecular weight 437.52
Bioavailability 40% - 50%
Metabolism Hepatic
Elimination half-life 15 to 30 hours
Excretion bile/feces
Pregnancy category USA:C
Legal status Rx-only, not a narcotic drug
Routes of administration oral, rectal, intramuscular

Fluphenazine is a typical antipsychotic drug used for the treatment of psychoses such as schizophrenia and acute manic phases of bipolar depression. It belongs to the piperazine class of phenothiazines and is extremely potent; more potent than haloperidol and around fifty to seventy times the potency of chlorpromazine.

Brand names

Fluphenazine decanoate Modecate®, Prolixin Decanoate®, Dapotum D®, Anatensol®, Fludecate®, Sinqualone Deconoate®
Fluphenazine enanthate Dapotum Injektion®, Flunanthate®, Moditen Enanthate Injection®, Sinqualone Enanthate®
Fluphenazine hydrochloride Prolixin®, Permitil®, Dapotum®, Lyogen®, Moditen®, Omca®, Sediten®, Selecten®, Sevinol®, Sinqualone®, Trancin®

Pharmacokinetics

Fluphenazine has an incomplete oral bioavailability of 40% to 50% (due to extensive first pass metabolization in the liver). Its half life is 15 to 30 hours.

Side effects

Most common are extrapyramidal side effects, including tardive dyskinesia. The frequency and severity of extrapyramidal side effects are direct proportional to the dose given and the duration of treatment.

Other side effects (sedation, hypotension, anticholinergic effects like dry mouth, blurred vision etc.) also vary with the dose given.

As a member of the phenothiazine class of drugs, fluphenazine shares in general all side-effects of chlorpromazine. Sedative, allergic-toxic and anticholinergic/sympatholytic side effects are less likely to occur compared with chlorpromazine. The direct deposition of fluphenazine in the cornea and retina has so far not been reported.

References


ru:Флуфеназин sv:Flufenazin

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