Classes
DEA Class; Rx
Common Brand Names; Trilafon
- Antipsychotics, 1st Generation;
- Antipsychotics, Phenothiazine
Description
Used primarily as an antipsychotic agent
Boxed warning regarding increased risk of death in elderly patients with dementia
Indications
Indicated for the treatment of schizophrenia
Contraindications
Documented hypersensitivity to phenothiazines
Coma, severe hypotension, severe CNS depression, concurrency with large amounts of CNS depressants, poorly controlled seizure disorder, subcortical brain damage with or without hypothalamic damage, myelosuppression, liver damage, blood dyscrasias
Severe cardiovascular disease
Adverse Effects
Akathisia (60%)
Confusion
Decreased gag reflex
EPS
Akathisia (60%)
Dystonia
Muscle stiffness
Neuroleptic malignant syndrome (infrequent but serious)
Parkinsonism
Tardive dyskinesia
Common
Anticholinergic effects
Sedation
Weight gain
Oligomenorrhea/amenorrhea
Erectile dysfunction
Less Common
Orthostatic hypotension (post-IM inj), tachycardia
Anxiety, agitation, cerebral edema, depression, dizziness, euphoria, headache, insomnia, restless, weakness
Anorexia, dyspepsia, constipation, ileus
Lens opacities (prolonged use)
Uncommon
ECG changes
Photosensitivity
Pruritis
Galactorrhea
Ejaculatory disorder
Diarrhea
Blood dyscrasia
Rare
Seizure
Priapism
Cholestatic jaundice
Warnings
Avoid using in children with suspected Reye’s syndrome
Use caution in prostatic hypertrophy, stenosing PUD, tardive dyskinesia, hypocalcemia, renal/hepatic impairment, patients who have exhibited a severe reaction to insulin or ECT, history of seizures, asthma, respiratory tract infections, cardiovascular disease
Perphenazine products can lower convulsive threshold in susceptible individuals; they should be used with caution in alcohol withdrawal and in patients with convulsive disorders; if patient is being treated with an anticonvulsant agent, increased dosage of that agent may be required when perphenazine products are used concomitantly
Should be used with caution in patients with psychiatric depression; possibility of suicide in depressed patients remains during treatment and until significant remission occurs; this type of patient should not have access to large quantities of this drug
Caution should be observed in giving it to patients who have previously exhibited severe adverse reactions to other phenothiazines some of the untoward actions of perphenazine tend to appear more frequently when high doses are used; patients should be kept under close supervision
A significant, not otherwise explained, rise in body temperature may suggest individual intolerance to perphenazine, in which case it should be discontinued
Patients on large doses who are undergoing surgery should be watched carefully for possible hypotensive phenomena; reduced amounts of anesthetics or central nervous system depressants may be necessary
If abnormalities in hepatic tests occur, phenothiazine treatment should be discontinued
Pregnancy and Lactation
Pregnancy Category: C
Lactation: avoid
Maximum Dosage
24 mg/day PO; dosage may be increased to 64 mg/day PO for short periods.
24 mg/day PO; dosage may be increased to 64 mg/day PO for short periods.
24 mg/day PO; dosage may be increased to 64 mg/day PO for short periods.
12 years: 24 mg/day PO; dosage may be increased to 64 mg/day PO for short periods.
Less than 12 years: Safety and efficacy have not been established.
Not indicated.
How supplied
Perphenazine
tablet
- 2mg
- 4mg
- 8mg
- 16mg