Compare common side effects, interactions, warnings, and more.
Lexapro
*image for illustrative purpose only
Wellbutrin SR
*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.
Wellbutrin SR® (bupropion sustained-release) is an antidepressant that works by inhibiting the reuptake of norepinephrine and dopamine in the brain, which helps improve mood and reduce symptoms of depression. Its FDA-approved indication includes the treatment of major depressive disorder (MDD). Off-label uses may include smoking cessation, anxiety, and attention-deficit hyperactivity disorder (ADHD). Wellbutrin SR is available in sustained-release tablet form, typically taken once or twice daily. Common side effects include insomnia, dry mouth, constipation, and headache, and it has a boxed warning for an increased risk of suicidal thoughts and behaviors in children, adolescents, and young adults during the initial stages of treatment.
Selective serotonin reuptake inhibitor (SSRI)
Aminoketone antidepressant
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
Wellbutrin SR (bupropion hydrochloride) is indicated:
For the treatment of major depressive disorder (MDD)
Typically taken orally once daily
Comes in 5 mg, 10 mg (scored), and 20 mg (scored) tablets
Typically taken orally twice daily
Comes in 100 mg, 150 mg, and 200 mg 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 ≥2% more than placebo rate) are:
Headache
Dry mouth
Nausea
Insomnia
Dizziness
Inflammation of the throat
Constipation
Agitation
Anxiety
Abdominal pain
Ringing in the ears
Tremor
Fluttering heartbeat
Muscle pain
Sweating
Rash
Anorexia
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)
Seizure disorder
Current or prior diagnosis of bulimia or anorexia nervosa
Abrupt discontinuation of alcohol, benzodiazepines, barbiturates, antiepileptic drugs
Monoamine oxidase inhibitors (MAOIs)
Known hypersensitivity to bupropion or other ingredients of Wellbutrin SR.
Drug interactions: CYP2B6 inducers, drugs metabolized by CYP2D6, digoxin, drugs that lower seizure threshold, dopaminergic drugs (levodopa and amantadine), MAOIs
Drug-laboratory test interactions: Wellbutrin SR can cause false-positive urine test results for amphetamines
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
Neuropsychiatric adverse events during smoking cessation
Seizure risk
High blood pressure
Activation of mania/hypomania
Psychosis and other neuropsychiatric reactions
Angle-closure glaucoma
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 risk of suicidal thinking and behavior in children, adolescents and young adults taking antidepressants.
Monitor for worsening and emergence of suicidal thoughts and behaviors.
*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 Wellbutrin SR®. See the Full Prescribing Information for more complete information. Bupropion, the active ingredient in Wellbutrin XL, may also be the active ingredient in other medications, and this information may not be accurate for all medications that include the active ingredient bupropion.
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.