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Venlafaxine IR and Venlafaxine XR

North Dakota State University · FDA-approved active Small molecule

Venlafaxine inhibits the reuptake of serotonin and norepinephrine in the central nervous system, increasing their availability at synaptic sites.

Venlafaxine inhibits the reuptake of serotonin and norepinephrine in the central nervous system, increasing their availability at synaptic sites. Used for Major depressive disorder, Generalized anxiety disorder, Social anxiety disorder.

At a glance

Generic nameVenlafaxine IR and Venlafaxine XR
Also known asEffexor and Effexor XR
SponsorNorth Dakota State University
Drug classSerotonin-norepinephrine reuptake inhibitor (SNRI)
TargetSerotonin transporter (SERT) and norepinephrine transporter (NET)
ModalitySmall molecule
Therapeutic areaPsychiatry / Mental Health
PhaseFDA-approved

Mechanism of action

Venlafaxine is a serotonin-norepinephrine reuptake inhibitor (SNRI) that blocks the reuptake transporters for both serotonin and norepinephrine, leading to increased concentrations of these neurotransmitters in the synaptic cleft. The IR (immediate-release) formulation provides rapid onset of action, while the XR (extended-release) formulation delivers the drug over an extended period for once-daily dosing. This mechanism is thought to restore normal mood regulation and reduce symptoms of depression and anxiety.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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