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Desvenlafaxine

Published: July 26, 2026Updated: July 26, 2026

Desvenlafaxine is an antidepressant medication classified as a serotonin-norepinephrine reuptake inhibitor (SNRI). It is primarily used to treat major depressive disorder (MDD) in adults by increasing the levels of serotonin and norepinephrine in the brain. This medication is the active metabolite of venlafaxine and is available in extended-release form for once-daily dosing.

Quick summary

Desvenlafaxine is an SNRI antidepressant used to treat major depressive disorder by increasing serotonin and norepinephrine levels in the brain.

Medically reviewed by WellAlly Editorial TeamLast reviewed July 26, 2026Editorial policy
BOXED WARNING

This medication carries a boxed (black box) warning — the strongest type of FDA warning. Review the full prescribing information before use.

Key facts at a glance

ATC
N06AX23
RxNorm
734064
Generic
Desvenlafaxine
Class
atc-n06
Brands
Khedezla, Pristiq
Availability
rx
Lactation
unknown
Routes
oral
Forms
tablet
Regions
US, EU, CN, JP
Monitoring
—

This page is for informational purposes only.

Do not use this information to diagnose yourself or to replace a physician's advice. Always consult a qualified healthcare provider before starting, stopping, or changing any medication. If you believe you are experiencing a medical emergency, call your local emergency number immediately.

Dosage and administration

adult (standard)tablet
Usual dose
50mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
pediatric (not approved)tablet
Usual dose
not FDA approved for patients under 18 years
Maximum
consult physician
Frequency
not applicable
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard
geriatric (standard)tablet
Usual dose
50mg once daily
Maximum
consult physician
Frequency
once daily
Instructions
Follow physician instructions
Duration limits
as prescribed
Monitoring
standard

Overdose information

Important overdose information
Toxic dose: Single dose that may cause serious toxicity
Chronic overdose: cumulative daily doses exceeding 600mg may lead to toxicity
Immediate actions
gastric lavage within 1-2 hours, activated charcoal, symptomatic and supportive care, cardiac monitoring
Antidote
no specific antidote(treatment is supportive and symptomatic)
Poison Control: 1-800-222-1222

Special Populations

11 groups
✗

pregnancy

first trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

Use of this medication in this population requires careful consideration of risks and benefits.

✗

pregnancy

second trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

avoid use during pregnancy unless benefits outweigh risks

Monitor

regular fetal monitoring

Use of this medication in this population requires careful consideration of risks and benefits.

✗

pregnancy

third trimester
unsafe
FDA Category
C
Dose Adjustment

avoid if possible

Key Recommendations

discontinue gradually before delivery if possible

Monitor

fetal monitoring and assessment of newborn for withdrawal symptoms

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

lactation

breastfeeding
caution
FDA Category
N
Dose Adjustment

use lowest effective dose

Key Recommendations

monitor infant for signs of sedation, poor feeding, or irritability

Monitor

observe infant for adverse effects

Use with caution and monitor for adverse effects.

✗

pediatric_age

adolescents 12 17
unsafe
FDA Category
N
Dose Adjustment

not recommended

Key Recommendations

not approved for use in pediatric patients; increased risk of suicidal ideation

Monitor

close monitoring for behavioral changes

Use of this medication in this population requires careful consideration of risks and benefits.

⚠

geriatric

elderly 65 years and older
caution
FDA Category
C
Dose Adjustment

start with lower dose, consider renal function

Key Recommendations

use with caution due to increased sensitivity and comorbidities

Monitor

monitor blood pressure, renal function, and for adverse effects

Use with caution and monitor for adverse effects.

⚠

renal_impairment

mild
caution
FDA Category
C
Dose Adjustment

no adjustment needed

Key Recommendations

use with caution, monitor renal function

Monitor

periodic renal function monitoring

Use with caution and monitor for adverse effects.

⚠

renal_impairment

moderate
caution
FDA Category
C
Dose Adjustment

reduce dose by 50%

Key Recommendations

reduce dose to 50mg daily if starting treatment

Monitor

regular monitoring of renal function

Use with caution and monitor for adverse effects.

⚠

renal_impairment

severe
caution
FDA Category
C
Dose Adjustment

reduce dose to 50mg every other day

Key Recommendations

use with extreme caution, consider alternative therapy

Monitor

close monitoring of renal function and drug levels

Use with caution and monitor for adverse effects.

⚠

hepatic_impairment

mild to moderate
caution
FDA Category
C
Dose Adjustment

no specific adjustment recommended

Key Recommendations

use with caution, monitor for adverse effects

Monitor

monitor liver function tests

Use with caution and monitor for adverse effects.

✗

alcohol_users

concurrent alcohol use
unsafe
FDA Category
C
Dose Adjustment

avoid concomitant use

Key Recommendations

do not consume alcohol while taking this medication

Monitor

monitor for increased sedation and CNS depression

Use of this medication in this population requires careful consideration of risks and benefits.

Statistics and clinical data

prescribingFDA
2023

FDA approval year

Value:2008

FDA approval date for Desvenlafaxine

drug_classFDA
2023

Drug class

Value:SNRI (Serotonin-Norepinephrine Reuptake Inhibitor)

Pharmacological classification

usageFDA
2023

Primary indication

Value:Major Depressive Disorder (MDD)

Primary therapeutic use

mechanismFDA
2023

Mechanism of action

Value:Inhibits reuptake of serotonin and norepinephrine

Pharmacodynamic properties

Desvenlafaxine is FDA-approved for the treatment of major depressive disorder (MDD) in adults. It may also be used off-label for conditions such as anxiety disorders, vasomotor symptoms associated with menopause, and chronic pain conditions.

Desvenlafaxine works by inhibiting the reuptake of both serotonin and norepinephrine in the central nervous system, thereby increasing the availability of these neurotransmitters. While the exact antidepressant mechanism is not fully understood, this dual reuptake inhibition is believed to be responsible for its therapeutic effects.

Desvenlafaxine should not be stopped abruptly, as withdrawal symptoms may occur; dosing should be tapered gradually. It carries a boxed warning for increased suicidal thoughts and behaviors in young adults under 25, particularly during initial treatment. Common side effects include nausea, headache, dry mouth, dizziness, and insomnia. Patients should avoid alcohol and inform their doctor of any bipolar history, as antidepressants may trigger manic episodes.

Contraindications

Conditions and patient states where this medication should be avoided or used with caution.

Do not use (1)

ABSOLUTEhypersensitivity

Known allergy to this medication or its components

Use caution (1)

RELATIVEpregnancy

Consult healthcare provider for benefits vs risks assessment

Official drug label

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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed July 26, 2026. · Read our editorial policy