Drugs, Supplies and Delivery
Citalopram is a selective serotonin reuptake inhibitor (SSRI) widely prescribed for the treatment of depression and certain anxiety disorders. Known for its efficacy and tolerability, citalopram is a first-line agent in managing major depressive disorder (MDD). 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 citalopram, including its mechanism of action, therapeutic uses, dosing, side effects, precautions, drug interactions, and availability.
Citalopram 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). Unlike older antidepressants, citalopram has minimal affinity for histamine, acetylcholine, or adrenergic receptors, reducing the risk of anticholinergic or sedative side effects (Lange Basic & Clinical Pharmacology).
Administration:
Citalopram is the generic name. It is marketed under the brand name Celexa® in some regions. Generic formulations are widely available as:
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