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Trifaron Brand names, Trifaron Analogs

Trifaron Brand Names Mixture

  • Apo Peram Tab 2-25 (Amitriptyline Hydrochloride + Perphenazine)
  • Apo Peram Tab 3-15 (Amitriptyline Hydrochloride + Perphenazine)
  • Elavil Plus Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Etrafon 2 10 (Amitriptyline Hydrochloride + Perphenazine)
  • Etrafon a Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Etrafon D Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Etrafon F Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Pms-Levazine 2/25 Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Pms-Levazine 3/15 Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Pms-Levazine 4/25 Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Proavil Tab (Amitriptyline Hydrochloride + Perphenazine)
  • Triavil Tab (Amitriptyline Hydrochloride + Perphenazine)

Trifaron Chemical_Formula

C21H26ClN3OS

Trifaron RX_link

http://www.rxlist.com/cgi/generic3/perphenazine.htm

Trifaron fda sheet

Trifaron FDA

Trifaron msds (material safety sheet)

Trifaron MSDS

Trifaron Synthesis Reference

Cusic, U.S. pat. 2860138

Trifaron Molecular Weight

403.969 g/mol

Trifaron Melting Point

97 oC

Trifaron H2O Solubility

28.3 mg/L

Trifaron State

Solid

Trifaron LogP

4.176

Trifaron Dosage Forms

Liquid; Solution; Syrup; Tablet (2, 4, 8, or 16 mg)

Trifaron Indication

For use in the management of the manifestations of psychotic disorders and for the control of severe nausea and vomiting in adults.

Trifaron Pharmacology

Perphenazine is a piperazinyl phenothiazine, acts on the central nervous system, and has a greater behavioral potency than other phenothiazine derivatives whose side chains do not contain a piperazine moiety. It is a member of a class of drugs called phenothiazines, which are dopamine D1/D2 receptor antagonists. Perphenazine is 10 to 15 times as potent as chlorpromazine; that means perphenazine is a highly potent antipsychotic. In equivalent doses it has approximately the same frequency and severity of early and late extrapypramidal side-effects compared to Haloperidol.

Trifaron Absorption

Absolute bioavailability is 40% following oral administration.

Trifaron side effects and Toxicity

Symptoms of overdose include stupor or coma, and children may have convulsive seizures. Signs of arousal may not occur for 48 hours. Oral LD50=318 mg/kg (rat); IPR LD50=64 mg/kg (mouse)

Trifaron Patient Information

This information is intended to aid in the safe and effective use of this medication. It is not a disclosure of all possible adverse or intended effects.

Given the likelihood that a substantial proportion of patients exposed chronically to neuroleptics will develop tardive dyskinesia, it is advised that all patients in whom chronic use is contemplated be given, if possible, full information about this risk. The decision to inform patients and/or their guardians must obviously take into account the clinical circumstances and the competency of the patient to understand the information provided.

Trifaron Organisms Affected

Humans and other mammals