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Low severity group: Escitalopram
Escitalopram selectively inhibits the reuptake of serotonin at the neuronal synapse, increasing serotonin availability in the brain.
Escitalopram selectively inhibits the reuptake of serotonin at the neuronal synapse, increasing serotonin availability in the brain. Used for Major depressive disorder, Generalized anxiety disorder.
At a glance
| Generic name | Low severity group: Escitalopram |
|---|---|
| Also known as | Lexapro, Selective serotonin reuptake inhibitor (SSRI) |
| Sponsor | University of Texas Southwestern Medical Center |
| Drug class | Selective serotonin reuptake inhibitor (SSRI) |
| Target | Serotonin transporter (SERT) |
| Modality | Small molecule |
| Therapeutic area | Psychiatry / Neurology |
| Phase | FDA-approved |
Mechanism of action
Escitalopram is the active S-enantiomer of citalopram and works as a selective serotonin reuptake inhibitor (SSRI). By blocking the serotonin transporter protein, it prevents the reabsorption of serotonin from the synaptic cleft back into the presynaptic neuron, thereby prolonging serotonin's effects on postsynaptic receptors. This increased serotonergic neurotransmission is thought to improve mood and reduce anxiety symptoms.
Approved indications
- Major depressive disorder
- Generalized anxiety disorder
Common side effects
- Nausea
- Headache
- Insomnia
- Somnolence
- Sexual dysfunction
- Diarrhea
- Dry mouth
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
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