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Selegiline

MAO Inhibitor · Antiparkinsonian

Also known as selegiline hydrochloride

MAO InhibitorAntiparkinsonian
CDSCO approvedSchedule H
EXCRETION
not curated
INTERACTIONS
12 major
incl. contraindicated
PREGNANCY
not curated
Top interactionssee all 12
  • SympathomimeticsContraindicatedTextbookG&G 14e
  • Tyramine Containing FoodsContraindicatedTextbookG&G 14e
  • TramadolContraindicatedDatabaseDDInter
  • 5ht Reuptake Inhibiting AntidepressantsSevereTextbookG&G 14e

Mechanism

As a monoamine-oxidase-B inhibitor, selegiline selectively inhibits the enzyme monoamine oxidase B, which is responsible for the breakdown of dopamine in the brain. This action leads to increased dopamine levels in the brain, thereby improving motor symptoms in Parkinson's disease.

Indications

Early Parkinson's disease (when motor symptoms do not affect quality of life)Adjunct to levodopa for dyskinesia or motor fluctuations in Parkinson's diseaseParkinson's diseasedepressionSymptomatic treatment of early or mild PDAdjunctive therapy in patients with deteriorating response to levodopaParkinson's disease (mild antiparkinsonian action in early cases, adjuvant to levodopa to prolong action and attenuate motor fluctuations)

Dosing

Adult
weight of the child to enable the dose prescribed to be checked. Consideration should also be given to including the dose per unit mass e.g. mg/kg or the dose per m2 bodysurface area e.g. mg /m2 where this would reduce error. The following should be noted: . The strength or quantity to be contained in capsules, lozenges, tablets etc. should be stated by the prescriber.…

Pharmacokinetics

Bioavailability
Negligible
Protein binding
94%
Metabolism
Metabolised
Excretion
Negligible

Contraindications

  • convulsive disorders

Side effects

Common
anxietyinsomniaaccentuate adverse motor and cognitive effects of levodopa therapypostural hypotensionnauseaconfusionagitation
Serious
  • Acute akinesia (upon abrupt withdrawal)
  • Neuroleptic malignant syndrome (upon abrupt withdrawal)
  • hypertensive crisis (reduced risk with transdermal patch, or at low doses where MAOA is spared)
  • serotonin syndrome (with 5HT reuptake inhibitors, tryptophan, substituted amphetamines)
  • hypertensive interactions (with higher doses or indirectly acting sympathomimetic amines)
  • accentuation of levodopa induced involuntary movements
  • psychosis

Drug interactions

Sympathomimetics
Contraindicated
Textbook

Potentially life-threatening elevation of blood pressure (hypertensive crisis).

Avoid concurrent use of MAOIs and medications containing sympathomimetic compounds.

Source: G&G 14e

Tyramine Containing Foods
Contraindicated
Textbook

Marked increases in blood pressure (hypertensive crisis).

Patients on MAOIs must avoid foods containing high levels of tyramine, such as soy products, dried meats and sausages, dried fruits, home-brewed and tap beers, red wine, pickled or fermented foods, and aged cheeses.

Source: G&G 14e

Tramadol
Contraindicated
Database

Serious drug interaction.

Avoid coadministration.

Source: DDInter

5ht Reuptake Inhibiting Antidepressants
Severe
Textbook

Serotonin syndrome, characterized by hyperthermia, muscle rigidity, myoclonus, tremors, autonomic instability, confusion, irritability, and agitation, which can progress to coma and death.

SSRIs should not be started until at least 14 days following discontinuation of treatment with an irreversible MAOI. For all SSRIs except fluoxetine, at least 14 days should pass prior to beginning treatment with an MAOI following the end of SSRI treatment. For fluoxetine, at least 5 weeks should pass. For venlafaxine, a 7-day interval is considered safe between ending MAOI therapy and starting venlafaxine. For duloxetine, a 5-day waiting period is needed before beginning MAOI treatment after ending duloxetine.

Source: G&G 14e

Albuterol
Severe
Textbook

Increased risk of adverse cardiovascular effects.

At least 2 weeks should elapse between the use of MAO inhibitors and administration of β2 agonists or other sympathomimetics.

Source: G&G 14e · p264

Altretamine
Severe
Textbook

Severe, life-threatening orthostatic hypotension.

Not specified, but implies avoidance due to severe, life-threatening effect.

Source: G&G 14e · p1349

Anticholinergic Antiparkinsonian Drugs
Severe
Textbook

Delirium may occur.

Source: KDT 7e · p121

Bitolterol
Severe
Textbook

Increased risk of adverse cardiovascular effects.

At least 2 weeks should elapse between the use of MAO inhibitors and administration of β2 agonists or other sympathomimetics.

Source: G&G 14e · p264

Fenoterol
Severe
Textbook

Increased risk of adverse cardiovascular effects.

At least 2 weeks should elapse between the use of MAO inhibitors and administration of β2 agonists or other sympathomimetics.

Source: G&G 14e · p264

Furazolidone
Severe
Textbook

Risk of hypertensive crisis.

Source: Harrison 22e · p1743

Levalbuterol
Severe
Textbook

Increased risk of adverse cardiovascular effects.

At least 2 weeks should elapse between the use of MAO inhibitors and administration of β2 agonists or other sympathomimetics.

Source: G&G 14e · p264

Meperidine
Severe
Textbook

Serious drug interaction.

Avoid coadministration.

Source: G&G 14e

Related guidelines

Other MAO Inhibitor drugs

Ask House about Selegiline

Continue into a citation-backed clinical answer with the drug context already attached.

Sources: KD Tripathi 7e, Goodman & Gilman 14e, BNF·Verified: 2026-05-13 · House clinical team