Brand Name: Etrafon, Trilafon
Outside U.S., Brand Names also known as: PMS Levazine
Perphenazine (Trilafon) is an Antipsychotic medication used in the treatment of Schizophenia and Tourette's disorder. Detailed info on uses, dosage and side-effects of Perphenazine below.
Contents:
Description
Pharmacology
Indications and Usage
Contraindications
Warnings
Precautions
Drug Interactions
Adverse Reactions
Overdose
Dosage
Supplied
This medicine, perphenazine, is a phenothiazine and tricyclic antidepressant
combination used to treat anxiety and depression. Phenothiazines are used to
treat nervous, mental, and emotional disorders. Some are used also to control
anxiety or agitation in certain patients, severe nausea and vomiting, severe
hiccups, and moderate to severe pain in some hospitalized patients.
Category of Use: Anxiolytic, Antipsychotic, Antiemetic
Several days to a few weeks may pass before you feel the full effect of this
medicine. Do not stop taking this medicine without checking with your doctor.
For use in the management of the manifestations of psychotic disorders and for
the control of severe nausea and vomiting in adults.
In comatose or greatly obtunded patients and in patients receiving large doses
of CNS depressants (barbiturates, alcohol, analgesics or antihistamines); in the
presence of blood dyscrasias, bone marrow depression or liver damage; and in
patients who have shown hypersensitivity to the components of the injection or
related compounds.
It is also contraindicated in patients with suspected or established subcortical
brain damage, with or without hypothalamic damage.
Tardive dyskinesia, a syndrome consisting of potentially irreversible,
involuntary dyskinetic movements, may develop in patients treated with
neuroleptic (antipsychotic) drugs. Although the prevalence of the syndrome
appears to be highest among the elderly, especially elderly women, it is
impossible to rely upon prevalence estimates to predict, at the inception of
neuroleptic treatment, which patients are likely to develop the syndrome.
Whether neuroleptic drug products differ in their potential to cause tardive
dyskinesia is unknown.
Perphenazine can lower the convulsive threshold in susceptible individuals;
therefore, it should be used with caution in alcohol withdrawal and in patients
with convulsive disorders. If the patient is being treated with an
anticonvulsive agent, increased dosage of that agent may be required when
perphenazine is used concomitantly.
This medicine will add to the effects of alcohol and other CNS depressants
(medicines that cause drowsiness). Check with your doctor before taking any such
depressants while you are taking this medicine.
Do not stop taking this medicine without checking with your doctor.
Before having any kind of surgery or dental or emergency treatment, tell the
physician or dentist in charge that you are taking this medicine.
The drug may cause exacerbation of psychosis in schizophrenic patients.
Perphenazine should be used with caution in patients with psychic depression.
The possibility of suicide in depressed patients continues during treatment
until significant remission occurs. Potentially suicidal patients should not
have access to large quantities of perphenazine.
Since perphenazine treatment increases serum prolactin levels, caution is
suggested in the use of phenothiazine derivatives in breast cancer patients.
The possible occurrence of liver damage, corneal and lenticular deposits,
retinal changes and irreversible dyskinesia should be considered when patients
are on long-term therapy.
Do not become overheated in hot weather, during exercise, or other activities
since heat stroke may occur while you are using this medicine. This medicine may
cause increased sensitivity to the sun. Avoid exposure to the sun or sunlamps
until you know how you react to this medicine. Use a sunscreen or protective
clothing if you must be outside for a prolonged period.
Pregnancy and Withdrawal: In newborn infants of mothers treated with
phenothiazines during pregnancy, extrapyramidal reactions, including agitation,
hypertonicity, opisthotonus, tremors, hyperreflexia and bizarre motor activity
have been reported. In rare cases the movement disorders persisted for 3 to 12
months. Respiratory depression persisting for several days occurred in a newborn
whose mother had received a phenothiazine for schizophrenia. Congenital
cataracts occurred in an infant whose mother had been treated with promazine
during pregnancy.
Perphenazine should not be used in pregnant women prior to labor unless in the
judgment of the physician the potential benefits to the mother outweigh the
potential risks to the infant. Since both the usual drugs given to the woman in
labor and phenothiazine drugs cross the placental barrier, the infant may be
exposed to unwanted individual and combined effects of therapy.
Because of the potential for serious adverse effects in nursing infants from
perphenazine injection, a decision should be made whether to discontinue nursing
or to discontinue the medication, taking into account the importance of therapy
to the mother.
Usage in Children: Safety and effectiveness of perphenazine in children
less than 12 years of age have not been established.
Interference with Cognitive or Motor Performance: Perphenazine may impair
the mental and/or physical abilities. Using this medicine alone, with other
medicines, or with alcohol may lessen your ability to drive or to perform other
potentially dangerous tasks. Do not drive, operate machinery, or do anything
else that could be dangerous until you know how you react to this medicine.
Drug Interactions
Concurrent administration of phenothiazines may potentiate CNS depressant
effects of opiates, barbiturates or other sedatives, anesthetics, tranquilizers
and alcohol.
BEFORE USING THIS MEDICINE: INFORM YOUR DOCTOR OR
PHARMACIST of all prescription and over-the-counter medicine that you are
taking. This includes anticoagulants, guanethidine, clonidine, and guanfacine.
Inform your doctor of any other medical conditions, allergies, pregnancy, or
breast-feeding.
Some people who take this medicine may become more sensitive to sunlight. Stay
out of direct sunlight. Wear a hat, protective clothing, and sunglasses. Use a
full-protection sunscreen lotion. Do not use a sunlamp.
This medicine may make you sweat less, causing your body temperature to rise. Do
not become overheated during exercise or hot weather while you are taking this
medicine, since overheating may result in heat stroke.
Side effects, that may go away during treatment, include drowsiness, dizziness,
dry mouth, nausea, diarrhea or constipation. If they continue or are bothersome,
check with your doctor. CHECK WITH YOUR DOCTOR AS SOON AS
POSSIBLE if you experience itching or hives; uncontrollable movements of
the tongue, mouth, or face; restlessness; weakness or rigidity of the arms or
legs; or muscle rigidity. If you notice other effects not listed above, contact
your doctor, nurse, or pharmacist.
Less common or rare side effects: Abdominal or stomach pain; aching
muscles or joints; back or leg pain; confusion; constipation; difficult
urination; eye pain; fever and chills; hair loss; hallucinations; hot, dry skin
or lack of sweating; increased skin sensitivity to sun; irritability; loss of
appetite; muscle weakness or twitching; nausea, vomiting, or diarrhea;
nosebleeds; prolonged, painful penile erection; ringing or other noises in ears;
skin rash and itching; slow pulse or irregular heartbeat; sore throat and fever;
swelling of testicles; unusual bleeding or bruising; yellow eyes or skin
Physical/Psychological Dependence:
In general, phenothiazines do not produce psychic dependence. However, following
abrupt cessation of high-dose therapy, gastritis, nausea, vomiting, dizziness,
tremulousness and motor hyperactivity have been reported. These symptoms may be
reduced by continuing concomitant antiparkinsonian agents for several weeks
after phenothiazine withdrawal.
Signs and Symptoms
Emergency treatment should be started immediately. Patients should be
hospitalized as soon as possible. Concurrent ingestion of alcohol or other drugs
or some medical explanation for the patient's condition should be considered.
Symptoms of overdose may include drowsiness; rapid pulse; dilated pupils;
convulsions; lightheadedness; vomiting; muscle rigidity; and uncontrollable
movements of the tongue, mouth, or face.
Treatment
If you or someone you know may have used more than the recommended dose of this
medicine, contact your local poison control center or emergency room
immediately.
Treatment is symptomatic and supportive. There is no specific antidote. The
patient should be induced to vomit even if emesis has occurred spontaneously.
Pharmacologic vomiting by the administration of ipecac syrup is a preferred
method. It should be noted that ipecac has central mode of action in addition to
its local gastric irritant properties, and the central mode of action may be
blocked by the antiemetic effect of perphenazine products. Vomiting should not
be induced in patients with impaired consciousness.
Maintain airway and other supportive measures.
Do not exceed the recommended dosage or take this medicine for longer than
prescribed.
- Follow the directions for using this medicine provided by your doctor.
- Store this medicine at room temperature, in a tightly-closed container,
away from heat and light.
- If you miss a dose of this medicine, take it as soon as possible. If you
are taking 1 dose at bedtime and do not remember until the next morning,
skip the missed dose and go back to your regular dosing schedule.
Additional Information: Do not share this medicine with others for
whom it was not prescribed. Do not use this medicine for other health
conditions. Keep this medicine out of the reach of children.
IF USING THIS MEDICINE FOR AN EXTENDED PERIOD OF TIME, obtain refills before
your supply runs out.
The dose of perphenazine will be different for different patients.
Tablets:: For nervous, mental, or emotional disorders:
Adults & Teenagers: 4 to 16 mg two to four times a day.
For Nausea and Vomiting:
Adults and teenagers: 8 to 16 mg a day, taken in smaller doses during
the day. Your doctor will lower your dose as soon as possible.
Children Under 13: Not recommended for use in children.
For oral solution form:
For Nervous, Mental, or Emotional Disorders:
Adults and teenagers: 8 to 16 milligrams (mg) two to four times a day.
For oral syrup dosage form:
For Nervous, Mental, or Emotional Disorders:
Adults and teenagers: 2 to 16 mg two to four times a day.
For Nausea and Vomiting:
Adults and teenagers: Adults and teenagers—2 to 4 mg two to four times
a day.
Available by oral solution, syrup and injection.
Tablets: Each tablet contains: Perphenazine 2 mg, 4 mg or 8 mg
(stamped black). All tablets tartrazine-free.
The information in this monograph is not intended to cover all possible uses,
directions, precautions, drug interactions or adverse effects. This information
is generalized and is not intended as specific medical advice. If you have
questions about the medicines you are taking or would like more information,
check with your doctor, pharmacist, or nurse.
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Reviewed: 01/2006
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