Compare common side effects, interactions, warnings, and more.
Effexor XR
*image for illustrative purpose only
Trazodone
*image for illustrative purpose only
The information below is about Effexor XR®, an extended-release formulation of venlafaxine. This information may not be accurate for the immediate-release formulation, Effexor®.
Effexor XR (venlafaxine extended-release) is a serotonin-norepinephrine reuptake inhibitor (SNRI) used to treat mood disorders by increasing the available levels of serotonin and norepinephrine in the brain, which helps regulate mood and anxiety. Its FDA-approved indications include major depressive disorder (MDD), generalized anxiety disorder (GAD), social anxiety disorder, and panic disorder. Off-label uses may include treatment for migraine prevention as well as treatment for premenstrual dysphoric disorder (PMDD) and neuropathic pain. Effexor XR comes in extended-release capsules, taken once daily. Common side effects include nausea, dizziness, insomnia, and sweating. It has a boxed warning for an increased risk of suicidal thoughts and behaviors in children, adolescents, and young adults, particularly during the early stages of treatment.
Trazodone is an antidepressant that works by inhibiting serotonin reuptake and blocking certain serotonin receptors, helping to improve mood and alleviate symptoms of depression. Its FDA-approved indication is for the treatment of major depressive disorder (MDD) in adults. Off-label uses include treating insomnia, anxiety, and chronic pain. Trazodone is available in tablet form, typically taken once or twice daily, often at bedtime due to its sedating effects. Common side effects include swelling, drowsiness, nasal congestion, dizziness, and dry mouth. There is a risk of increased suicidal thoughts and behaviors in children, adolescents, and young adults, similar to other antidepressants.
Serotonin and norepinephrine reuptake inhibitor (SNRI)
Selective serotonin reuptake inhibitor (SSRI)
Effexor XR (venlafaxine hydrochloride) is indicated for the treatment of adults with:
Major depressive disorder (MDD)
Generalized anxiety disorder (GAD)
Social anxiety disorder (SAD)
Panic disorder (PD)
Trazodone is indicated:
For the treatment of major depressive disorder (MDD)
Typically taken orally once daily
Comes in 37.5 mg, 75 mg, and 150 mg extended-release capsules
Typically taken orally in divided doses per day
Comes in 50 mg, 100 mg, 150 mg, and 300 mg tablets
Most common adverse reactions (incidence ≥5% and at least twice the rate of placebo):
Nausea
Sleepiness
Dry mouth
Sweating
Abnormal ejaculation
Anorexia
Constipation
Impotence (men)
Libido decreased
Most common adverse reactions (incidence ≥ 5% and twice that of placebo) are:
Swelling
Blurred vision
Fainting
Drowsiness
Fatigue
Diarrhea
Nasal congestion
Weight loss
Hypersensitivity to venlafaxine hydrochloride, desvenlafaxine succinate, or any excipients in the Effexor XR formulation
Concomitant use of monoaminoxidase inhibitors (MAOIs) or within 14 days of discontinuing an MAOI
Concomitant use of monoamine oxidase inhibitors (MAOIs), or use within 14 days of stopping MAOIs
Drug interactions: CNS depressants, CYP3A4 inhibitors, CYP3A4 inducers, digoxin, phenytoin, warfarin
Serotonin syndrome
Elevated blood pressure
Increased risk of bleeding
Angle‑closure glaucoma
Activation of mania or hypomania
Discontinuation syndrome
Seizures
Low blood sodium
Interstitial lung disease and eosinophilic pneumonia
Sexual dysfunction
Pregnancy: Third trimester use may increase risk for symptoms of poor neonatal adaptation (respiratory distress, temperature instability, feeding difficulty, hypotonia, tremor, irritability) in the neonate
Serotonin syndrome
Cardiac arrhythmias
Positional low blood pressure and fainting
Increased risk of bleeding
Prolonged erection
Activation of mania or hypomania
Potential for cognitive and motor impairment
Angle-closure glaucoma
WARNING: SUICIDAL THOUGHTS AND BEHAVIORS
Increased risk of suicidal thoughts and behavior in pediatric patients and young adults taking antidepressants. Closely monitor all antidepressant-treated patients for clinical worsening and emergence of suicidal thoughts and behaviors.
Effexor XR is not approved for use in pediatric patients.
WARNING: SUICIDAL THOUGHTS and BEHAVIORS
Antidepresants increased the risk of suicidal thoughts and behaviors in pediatric and young adult patients.
Closely monitor for clinical worsening and emergence of suicidal thoughts and behaviors.
Trazodone hydrochloride tablet is not approved for use in pediatric patients.
*This information is from the label for brand name Effexor XR®. See the Full Prescribing Information for more complete information. Venlafaxine, the active ingredient in Effexor XR, is also the active ingredient in other medications, and this information may not be accurate for all medications that include the active ingredient venlafaxine.
*This information is from the trazodone hydrochloride label used by Accord Healthcare, Inc. See the Full Prescribing Information for more complete information. This information may not be accurate for all medications that include the active ingredient trazodone.
The information provided here is NOT MEDICAL ADVICE and is for informational and educational purposes only. The drug comparison tool does not determine eligibility for medications or treatments provided via the Hims/Hers platform. Consultation with a healthcare provider is required to assess suitability for any medical treatment based on individual health and medical history. All product names and associated trademarks are the property of their respective owners.