Tranylcypromine
Sulfate
(tran-ill-sip′roe-meen)
Parnate
Classification:
ANTIDEPRESSANT; MONOAMINE OXIDASE
INHIBITOR (MAOI)
Therapeutic: ANTIDEPRESSANT; MAOI
Prototype: Phenelzine
Pregnancy
Category: C
AVAILABILITY
Tablet
ACTION
& THERAPEUTIC EFFECT
Potent MAO
with a antidepressant activity that arises from the increased availability of
monoamines resulting from the inhibition of the enzyme MAO. This leads to increased
concentration of neurotransmitters, such as epinephrine, norepinephrine, and
dopamine in the CNS. Drug of last choice for severe
depression unresponsive to other
MAO inhibitors.
USES
Major
depression.
UNLABELED
USES
Orthostatic
hypotension, panic disorder, social anxiety disorder.
CONTRAINDICATIONS
Confirmed
or suspected cerebrovascular defect, cardiovascular disease; hepatic disease or
abnormal LFT; hypertension, pheochromocytoma, history of severe or recurrent
headaches; recent acute MI; angina; renal failure; suicidal ideation; anuria; lactation.
CAUTIOUS
USE
Bipolar
disorder; Parkinson’s disease; psychosis; schizophrenia, anxiety/agitation;
CHF; DM; seizure disorders; hyperthyroidism; history of suicidal attempts;
renal impairment; older adults;
pregnancy (category C); children and
adolescents with major depressive
disorder or other psychiatric
disorders.
ROUTE & DOSAGE
Major Depression
Adult: PO 30 mg/day in 2 divided doses, may increase by 10 mg/ day at 2–3 wk
intervals (max: 60 mg/day)
ADMINISTRATION
Oral
- Contraindicated drugs should be discontinued 1–2
weeks before starting therapy.
- Crush tablet and give with fluid or mix with
food if patient cannot swallow pill.
- Note: Doses given in the late evening may cause
insomnia.
ADVERSE EFFECTS (≥1%)
CNS: Vertigo, dizziness, tremors, muscle twitching, headache, blurred vision suicidality. CV:
Orthostatic hypotension, arrhythmias, hypertensive crisis. GI: Dry mouth, anorexia, constipation,
diarrhea, abdominal discomfort. Skin: Rash. Urogenital: Impotence. Body as a Whole: Peripheral edema, sweating.
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INTERACTIONS
Drug: TRICYCLIC ANTIDEPRESSANTS, SSRIS, AMPHETAMINES, ephedrine, reserpine, guanethidine, buspirone, methyldopa, dopamine,
levodopa, tryptophan may precipitate hypertensive crisis, and must be discontinued before tranylcypromine treatment. Alcohol and other CNS DEPRESSANTS add to CNS depressant effects; meperidine can cause fatal cardiovascular collapse; ANESTHETICS exaggerate hypotensive and CNS depressant effects; metrizamide increases risk of seizures;
DIURETICS and other ANTIHYPERTENSIVE AGENTS add to hypotensive effects. Food: Tyramine-containing foods may precipitate hypertensive
crisis (e.g., aged or matured cheese, air-dried or cured meats including sausages and salamis; fava or broad
bean pods, tap/draft beers, sauerkraut, soy sauce, and other soybean condiments). Herbal: Ginseng, ephedra, ma huang,
St. John’s wort may lead to hypertensive crisis; ginseng may lead to manic episodes.
PHARMACOKINETICS
Absorption: Completely from GI tract. Onset: 10 days. Metabolism:
Rapidly in liver to active metabolite. Elimination: Primarily in urine. Half-Life:
90–190 min.
NURSING IMPLICATIONS
Black Box Warning
Tranylcypromine
sulfate has been associated with suicidal thinking and behavior in children,
adolescents, and young adults.
Assessment & Drug Effects
- Monitor BP closely. Severe hypertensive reactions
are known to occur with MAO inhibitors.
- Report immediately to prescriber signs of
worsening mental status such as suicidal ideation, aggressiveness, agitation, anxiety,
hostility, impulsivity, insomnia, irritability, panic attacks, and worsening of
depression.
- Expect therapeutic response within 3 days, but
full antidepressant effects may not be obtained until 2–3 wk of drug therapy.
Patient & Family Education
- Do not eat tyramine-containing foods (see FOOD–DRUG INTERACTIONS).
- Be aware that excessive use of caffeine- containing
beverages (chocolate, coffee, tea, cola) can contribute to development of rapid
heartbeat, arrhythmias, and hypertension.
- Report promptly emergence of anxiety, agitation,
panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity,
mania, worsening depression, suicidal ideation, or other unusual changes in
behavior.
- Make position changes slowly, particularly from
recumbent to upright posture.
- Avoid potentially hazardous activities until
response to drug is known.
- Avoid alcohol or other CNS depressants because
of their possible additive effects.
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