Classes
DEA Class; Rx
Common Brand Names; Marplan
- Antidepressants, MAO Inhibitors
Description
Non-selective monoamine oxidase A and B inhibitor (MAOI) antidepressant
FDA-approved for the treatment of major depressive disorder (MDD); used off-label as a second- or third-line agent for anxiety disorders such as panic disorder and social anxiety disorder
Primarily used for treatment-resistant cases of depression and anxiety disorders, due to dietary restrictions, adverse effect profile, and the potential for serious drug-drug interactions and drug-food interactions
Indications
Indicated for use in treatment-resistant depression.
Contraindications
Hypersensitivity
Pheochromocytoma, CHF, CVD, severe renal impairment
Confirmed or suspected cerebrovascular defect or any patient with cardiovascular disease, hypertension, or history of headache
Schizophrenia
History of liver disease or abnormal liver function tests
Adverse Effects
Common
Orthostatic hypotension
Dizziness
Drowsiness
Fatigue
Headache
Hyperreflexia
Sleep disturbance
Weakness
Tremor
Constipation
Dry mouth
Less Common
Confusion
Decreased memory
Paresthesia
Anorexia
Nausea
Vomiting
Impotence
Urinary frequency or retention
Nystagmus
Uncommon
Edema
Anxiety
Hypomania
Irritation
Hypermetabolic syndrome (hyperpyrexia, tachycardia, tachypnea, incr CPK, acidosis)
SIADH
Arthralgia
Rare
Risk of hypertensive crisis (usually due to drug interaction)
Ataxia
Seizure
Jaundice
Visual disturbancea
Warnings
Use caution with doses >40 mg/day
Clinical worsening & suicide ideation may occur despite medication in adolescents & young adults (18-24 years)
Caution in patients with diabetes mellitus (monitor glucose closely), glaucoma, hepatic/renal impairment, thyroid dysfunction
Therapy can cause serious side effects; not recommended as initial therapy; should be reserved for patients who have not responded satisfactorily to other antidepressants
Hypotension may occur; seen most commonly in patients with preexistent hypertension; blood pressure usually returns rapidly to pretreatment levels upon discontinuation of drug; dosage increases should be made more gradually in patients showing a tendency toward hypotension at beginning of therapy; postural hypotension may be relieved by having the patient lie down until blood pressure returns to normal
Therapy lowers convulsive threshold in some animal experiments, use caution if epileptic patients treated; therapy appears to have varying effects in epileptic patients; while some have a decrease in frequency of seizures, others have more seizures; discontinue at least 48 hours before myelography; should not resume therapy for at least 24 hours postprocedure
There is low incidence of altered liver function or jaundice in patients receiving therapy; periodic liver chemistry tests should be performed during therapy; discontinue use at first sign of hepatic dysfunction or jaundice
MAO inhibitors can suppress anginal pain that would otherwise serve as a warning of myocardial ischemia
Pregnancy and Lactation
There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to antidepressants, during pregnancy
Levels of excretion in human milk have not been determined, and effects on nursing infant are unknown; therapy should be used in women who are nursing only if clearly needed
Maximum Dosage
60 mg/day PO.
60 mg/day PO.
>= 16 years: 60 mg/day PO.
< 16 years: Safety and efficacy have not been established.
Safety and efficacy have not been established.
How supplied
Isocarboxazid
tablet
- 10 mg