Compare common side effects, interactions, warnings, and more.
Lexapro
*image for illustrative purpose only
Pristiq
*image for illustrative purpose only
Lexapro® (escitalopram) is a selective serotonin reuptake inhibitor (SSRI) used to treat anxiety and depression by increasing available serotonin levels in the brain, which helps improve mood and reduce anxiety. Its FDA-approved indications include the treatment of major depressive disorder (MDD) and generalized anxiety disorder (GAD) in adults and adolescents. Off-label uses may include treating panic disorder, obsessive-compulsive disorder (OCD), and social anxiety disorder. Lexapro is available in tablet and oral solution forms, taken once daily. Common side effects include nausea, insomnia, and sexual dysfunction, and it carries a boxed warning for an increased risk of suicidal thoughts and behaviors in children, adolescents, and young adults, particularly during the initial stages of treatment.
Pristiq® (desvenlafaxine) is a serotonin-norepinephrine reuptake inhibitor (SNRI) used to treat major depressive disorder (MDD) by increasing the available levels of serotonin and norepinephrine in the brain, which helps improve mood and emotional balance. Its FDA-approved indication is for the treatment of major depressive disorder in adults. Off-label uses may include managing anxiety disorders, hot flashes related to menopause, and other mood disorders. Pristiq comes in extended-release tablet form, taken once daily. Common side effects include nausea, dizziness, dry mouth, male sexual dysfunction, and insomnia. It carries a boxed warning for an increased risk of suicidal thoughts and behaviors in children, adolescents, and young adults, particularly during the initial stages of treatment.
Selective serotonin reuptake inhibitor (SSRI)
Serotonin and norepinephrine reuptake inhibitor (SNRI)
Lexapro (escitalopram) is indicated for the:
Treatment of major depressive disorder (MDD) in adults and pediatric patients 12 years of age and older
Treatment of generalized anxiety disorder (GAD) in adults and pediatric patients 7 years and older
Pristiq (desvenlafaxine succinate) is indicated:
For the treatment of adults with major depressive disorder (MDD)
Typically taken orally once daily
Comes in 5 mg, 10 mg (scored), and 20 mg (scored) tablets
Typically taken orally once daily
Comes in 25 mg, 50 mg, and 100 mg extended-release tablets
Most commonly observed adverse reactions (incidence ≥ 5% and at least twice the incidence of placebo patients) are:
Insomnia
Ejaculation disorder (primarily ejaculatory delay),
Nausea
Sweating increased
Fatigue and sleepiness
Decreased libido
Inability to orgasm
Most common adverse reactions (incidence ≥5% and twice the rate of placebo in the 50 or 100 mg dose groups) were:
Nausea
Dizziness
Insomnia
Excessive sweating
Constipation
Sleepiness
Decreased appetite
Anxiety
Specific male sexual function disorders
Do not use MAOIs intended to treat psychiatric disorders with Lexapro or within 14 days of stopping treatment with Lexapro. Do not use Lexapro within 14 days of stopping an MAOI intended to treat psychiatric disorders. In addition, do not start Lexapro in a patient who is being treated with linezolid or intravenous methylene blue
Concomitant use of pimozide
Known hypersensitivity to escitalopram or citalopram or any of the inactive ingredients
Drug interactions: SSRIs, SNRIs, tryptophan, drugs that affect hemostasis (NSAIDs, aspirin, warfarin)
Hypersensitivity to desvenlafaxine succinate, venlafaxine hydrochloride, or any excipients in the Pristiq formulation
Serotonin syndrome and MAOIs
Serotonin syndrome
Discontinuation syndrome
Seizures
Activation of mania/hypomania
Low blood sodium: Can occur in association with syndrome of inappropriate antidiuretic hormone secretion
Increased risk of bleeding
Interference with cognitive and motor performance
Angle closure glaucoma
Use in patients with concomitant illness
Sexual dysfunction
Pregnancy: SSRI use, particularly later in pregnancy, may increase the risk for persistent pulmonary hypertension and symptoms of poor adaptation (respiratory distress, temperature instability, feeding difficulties, hypotonia, tremor, irritability) in the neonate
Serotonin syndrome
Elevated blood pressure
Increased risk of bleeding
Angle closure glaucoma
Activation of mania/hypomania
Discontinuation syndrome
Seizure
Low blood sodium: Can occur in association with SIADH.
Interstitial lung disease and eosinophilic pneumonia
Sexual dysfunction
WARNING: SUICIDAL THOUGHTS AND BEHAVIORS
Increased risk of suicidal thoughts and behavior in pediatric and young adult patients taking antidepressants. Closely monitor all antidepressant-treated patients for clinical worsening and emergence of suicidal thoughts and behaviors. Lexapro is not approved for use in pediatric patients less than 7 years of age.
WARNING: SUICIDAL THOUGHTS AND BEHAVIORS
Increased the risk of suicidal thoughts and behaviors in children, adolescents and young adults taking antidepressants.
Closely monitor for clinical worsening and emergence of suicidal thoughts and behaviors.
Pristiq is not approved for use in pediatric patients.
*This information is from the label for brand name Lexapro®. See the Full Prescribing Information for more complete information. Escitalopram, the active ingredient in Lexapro, may also be the active ingredient in other medications, and this information may not be accurate for all medications that include the active ingredient escitalopram.
*This information is from the label for brand name Pristiq®. See the Full Prescribing Information for more complete information. Desvenlafaxine, the active ingredient in Pristiq, may also be the active ingredient in other medications, and this information may not be accurate for all medications that include the active ingredient desvenlafaxine.
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.