Generalized anxiety disorder, major depressive disorder
藥理
Escitalopram oxalate, a selective serotonin reuptake inhibitor (SSRI) and S-enantiomer of racemic citalopram, enhances serotonergic activity in the central nervous system (CNS) as a result of its inhibition of serotonin (5-HT) reuptake in CNS neurons.
藥動學
Absorption: Escitalopram oxalate, Oral: time to peak concentration, about 5 h.
Distribution: Protein binding: approximately 56%.
Metabolism: Escitalopram oxalate-Hepatic; P450 CYP3A4 and CYP2C19; N-demethylation.
Excretion: Renal: 10% as S-DCT, 8% unchanged.
Elimination Half Life: Escitalopram oxalate: 27 h to 32 h (mean).
禁忌症
Increased risk of serotonin syndrome with concomitant use with an MAOI, including linezolid or IV methylene blue, or use of escitalopram within 14 days of discontinuing an MAOI used to treat psychiatric disorders, or use of an MAOI used to treat psychiatric disorders within 14 days of discontinuing escitalopram.
Hypersensitivity to citalopram, escitalopram, or any other component of the product.
Generalized anxiety disorder:
Initial, 10 mg/day orally as a single dose in the morning or evening; may increase to 20 mg/day after a minimum of 1 week.
Major depressive disorder:
Initial, 10 mg/day orally as a single dose in the morning or evening; may increase to 20 mg/day after a minimum of 1 week.
小兒調整劑量
Major depressive disorder (12 years or older) Initial, 10 mg/day orally as a single dose in the morning or evening; may increase to 20 mg/day after a minimum of 3 weeks.
腎功能調整劑量
Renal impairment, mild to moderate: No adjustment necessary.