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Escitalopram, the S-enantiomer of citalopram, is a selective serotonin reuptake inhibitor (SSRI) widely prescribed for the treatment of depression and anxiety disorders. It is known for its high selectivity for serotonin reuptake inhibition, improved tolerability, and efficacy. This article synthesizes information from the British National Formulary (BNF), Lippincott Textbook of Pharmacology, and Lange Basic & Clinical Pharmacology to provide a detailed overview of escitalopram, including its mechanism of action, therapeutic uses, dosing, side effects, precautions, drug interactions, and availability.
Escitalopram selectively inhibits the reuptake of serotonin (5-HT) at the presynaptic neuronal membrane, increasing serotonin availability in the synaptic cleft. This enhances serotonergic neurotransmission, which is associated with improved mood and emotional regulation (Lippincott Textbook of Pharmacology). Escitalopram is the S-enantiomer of citalopram and is twice as potent, with fewer side effects due to its higher selectivity for serotonin transporters (Lange Basic & Clinical Pharmacology).
Administration:
Escitalopram is the generic name. It is marketed under the brand name Lexapro® in some regions. Generic formulations are widely available as:
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