Trade Names:Eldepryl- Capsules 5 mg
Trade Names:Selegiline- Tablets 5 mg
Trade Names:Zelapar- Tablets, orally disintegrating 1.25 mgApo-Selegiline (Canada)
Selective type B MAOI thought to increase dopaminergic activity. MAO enzyme breaks down catecholamines and serotonin. Selegiline may also interfere with dopamine reuptake at synapse.
C max of metabolites following a single oral dose of 10 mg are from 4 to almost 20 times more than the C max of selegiline (1 ng/mL). Bioavailability is increased 3- to 4-fold when taken with food.
Compared with the swallowed tablet, absorption is more rapid with the orally disintegrating tablet. After single doses of 1.25 and 2.5 mg orally disintegrating tablets, the mean C max is 3.34 and 4.47 ng/mL, respectively, compared with 1.12 ng/mL with the swallowed tablet.
Bioavailability is increased 3- to 4-fold when selegiline capsules are taken with food. When the orally disintegrating tablet is taken with food, the C max and AUC are about 60% of those values measured when selegiline is taken in the fasted state.
Protein binding is up to 85%.
Selegiline undergoes extensive metabolism. Major metabolites are N-desmethylselegiline, L-amphetamine, and L-methamphetamine. Only N-desmethylselegiline has MAO-B–inhibiting activity. Metabolism is via CYP2B6 and CYP3A4 isozymes, and, to a minor extent, CYP2A6.
Excretion is primarily in the urine. Following a single oral dose, the mean half-life is 2 h. The half-life increases to 10 h under steady-state conditions.
No information is available in patients with renal function impairment.Hepatic Function Impairment
No information is available in patients with hepatic function impairment.Elderly
Systemic exposure is about twice as high in elderly patients compared with a younger population given a single 10 mg oral dose.GenderOrally disintegrating tablets
There are no differences between men and women in overall AUC, T max , or elimination half-life. The C max is approximately 25% lower in men than women; this difference is not likely to be clinically important.Race
Pharmacokinetic studies have not been conducted.
Adjunct to levodopa/carbidopa in Parkinson disease.
Meperidine, other opioid analgesics, certain other analgesics (dextromethorphan, methadone, propoxyphene, and tramadol); do not administer MAOIs with selegiline (at least 14 days should elapse between discontinuation of selegiline and administration of an MAOI, including other selegiline products); hypersensitivity to any component of the product.
PO 10 mg/day as divided dose of 5 mg each taken at breakfast and lunch. Do not exceed 10 mg/day. After 2 to 3 days of treatment, try reducing levodopa/carbidopa dose by 10% to 30%. Further reductions may be possible during continued selegiline therapy.Orally disintegrating tabletAdults
PO Start with 1.25 mg once a day for at least 6 wk. After 6 wk, the dosage may be increased to 2.5 mg once a day if desired benefit has not been achieved and the medication is tolerated.
Store tablets and capsules at 68° to 77°F. Dispense tablets in a tight, light-resistant container. Store orally disintegrating tablet at 59° to 86°F. Use within 3 mo of opening pouch and immediately upon opening individual blister.
Increased risk of serious reactions; coadministration with selegiline is contraindicated.Bupropion
Coadministration of bupropion and selegiline is contraindicated. Allow at least 14 days to elapse between discontinuing selegiline and starting bupropion.CYP3A4 inducers (eg, carbamazepine, phenytoin, rifampin)
May reduce selegiline concentrations; use with caution.Dextromethorphan
Brief episodes of psychosis or bizarre behavior may occur.Hormonal contraceptives
Selegiline plasma concentrations may be elevated, causing a loss of selective inhibition of MAO-B and increasing the risk of selegiline adverse reactions.Levodopa
The dopaminergic adverse reactions of levodopa may be potentiated and preexisting dyskinesia may be exacerbated.MAOIs
Increased risk of nonselective MAO inhibition, leading to hypertensive crisis. Allow at least 14 days between discontinuation of selegiline and administration of other MAOIs, including other selegiline products. Hyperpyrexia and death have been reported with coadministration of other MAOIs (eg, phenelzine).Meperidine
Serious, life-threatening reactions (eg, agitation, diaphoresis, fever, seizures), which may progress to apnea, coma, and death, may occur. Coadministration is contraindicated.SSRIs (eg, fluoxetine, fluvoxamine, paroxetine, sertraline)
Severe, life-threatening toxicity, including serotonin syndrome (eg, agitation, altered consciousness, ataxia, myoclonus, overactive reflexes, shivering), may occur. At least 14 days should elapse between discontinuation of selegiline and initiation of treatment with an SSRI; at least 5 weeks should elapse between discontinuation of fluoxetine and initiation of selegiline.Sympathomimetics (eg, ephedrine)
Hypertensive crisis has been reported.Tricyclic antidepressants (eg, amitriptyline)
Severe toxicity, including hyperpyrexia and death, may occur. At least 14 days should elapse between discontinuation of selegiline and starting treatment with a tricyclic antidepressant.Tyramine-containing food
Rare, hypertensive reactions may occur even at the recommended dosage of 10 mg/day.
None well documented.
Dizziness/light-headedness/fainting (14%); headache, insomnia (7%); confusion, dyskinesia (6%); hallucinations, vivid dreams (4%); ataxia, confusion, somnolence, tremor (3%); depression (2%); impulse control symptoms, increased libido, including hypersexuality; pathological gambling; seizures (postmarketing).
Skin disorders (6%); rash (4%).
Rhinitis (7%); pharyngitis (4%).
Nausea (11%); abdominal pain (8%); dyspepsia, stomatitis (5%); constipation, dry mouth (4%); vomiting (3%); diarrhea, dysphagia, flatulence, tooth disorder (2%).
Back pain (5%); leg cramps, myalgia (3%).
Pain (8%); chest pain (2%).
Category C .
Safety and efficacy not established.Orally disintegrating tablets
Safety and efficacy not established in children younger than 16 yr of age.
In patients 65 yr of age and older compared with younger patients, the relative risk for treatment-related adverse reactions was at least 2-fold higher for abnormal dreams, anxiety, cheilitis, diarrhea, dizziness, dyspepsia, ECG abnormality, flu syndrome, hyperkalemia, hypertension, infection, nausea, orthostatic hypotension, pharyngitis, and somnolence.
Serum BUN and creatinine may be increased. Use with caution in patients with history of, or known or suspected, renal function impairment.
Use with caution in patients with a history of, or known or suspected, hepatic function impairment.
In patients who were healthy prior to therapy, the frequency of mild oropharyngeal abnormality (eg, mouth pain, swallowing pain, ulceration) was higher at the end of selegiline therapy compared with placebo.
When used as an adjunct to levodopa, hallucinations have been reported.
Rapid dose reduction of, withdrawal of, or changes in antiparkinsonian therapy have been associated with a symptom complex resembling NMS.
Intense urges to gamble, increased sexual urges, or other intense urges, and the inability to control these urges have been reported in patients taking selegiline.
Do not exceed recommended daily dosage of 10 mg/day (2.5 mg/day for orally disintegrating tablets) because of risks associated with nonselective inhibition of MAO (potentially serious food or drug interactions may occur at higher doses).
Risk of melanoma is higher in patients with Parkinson disease compared with the general population; however, it has not been determined if this is caused by the disease or the treatment.
There may be an increased risk for orthostatic hypotension in the period after increasing the daily dose of selegiline.
Selegiline orally disintegrating tablets contain phenylalanine.
Selegiline selectivity may not be absolute even at the recommended daily dose of 10 mg for the capsule or 2.5 mg for the orally disintegrating tablet. Rare cases of hypertensive reactions associated with tyramine-containing food have been reported in patients taking selegiline 10 mg/day.
Agitation; coma; convulsions; cool, clammy skin; death; diaphoresis; dizziness; drowsiness; faintness; hallucinations; hyperactivity; hyperpyrexia; hypertension; hypotension; irritability; opisthotonos; precordial pain; rapid and irregular pulse; respiratory depression and failure; severe headache; trismus; vascular collapse.
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