Compare common side effects, interactions, warnings, and more.
Cymbalta
*image for illustrative purpose only
Strattera
*image for illustrative purpose only
Cymbalta® (duloxetine) is a serotonin-norepinephrine reuptake inhibitor (SNRI) used to treat depression and anxiety by increasing the available levels of serotonin and norepinephrine in the brain, which helps improve mood and relieve pain. Its FDA-approved indications include major depressive disorder (MDD), generalized anxiety disorder (GAD), fibromyalgia, and chronic pain conditions such as diabetic peripheral neuropathy and musculoskeletal pain. Off-label uses may include treatment for stress urinary incontinence and as migraine prevention. Cymbalta is available in capsule form, taken orally. Common side effects include nausea, dry mouth, drowsiness, and dizziness, and it carries a boxed warning for an increased risk of suicidal thoughts and behaviors in children, adolescents, and young adults, especially during the initial stages of treatment.
Strattera® (atomoxetine) is a non-stimulant medication used to treat attention-deficit hyperactivity disorder (ADHD) by selectively inhibiting the reuptake of norepinephrine, which helps improve focus and reduce impulsivity. Its FDA-approved indication is for the treatment of ADHD in both children and adults. Strattera is available in capsule form, taken once or twice daily. Common side effects include dry mouth, insomnia, decreased appetite, and nausea, while more serious risks include increased heart rate and blood pressure. Strattera carries a boxed warning for an increased risk of suicidal thoughts in children and adolescents, especially during the initial treatment period.
Serotonin and norepinephrine reuptake inhibitor (SNRI)
Selective norepinephrine reuptake inhibitor (SNRI)
Cymbalta (duloxetine hydrochloride) is indicated for the treatment of the following conditions:
Major depressive disorder (MDD) in adults
Generalized anxiety disorder (GAD) in adults and pediatric patients 7 years of age and older
Diabetic peripheral neuropathic pain (DPNP) in adults
Fibromyalgia (FM) in adults and pediatric patients 13 years of age and older
Chronic musculoskeletal pain in adults
Strattera (atomoxetine hydrochloride) is indicated:
For the treatment of attention-deficit/hyperactivity disorder (ADHD)
Typically taken orally once daily
Comes in 20 mg, 30 mg, and 60 mg delayed-release capsules
Typically taken orally once or twice daily
Comes in 10 mg, 18 mg, 25 mg, 40 mg, 60 mg, 80 mg, and 100 mg capsules
Most common adverse reactions (≥5% and at least twice the incidence of placebo-treated patients):
Adults:
Nausea
Dry mouth
Sleepiness
Constipation
Decreased appetite
Excessive sweating
Pediatric patients:
Decreased weight
Decreased appetite
Nausea
Vomiting
Fatigue
Diarrhea
Most common adverse reactions (≥5% and at least twice the incidence of placebo patients):
Child and adolescent clinical trials:
Nausea
Vomiting
Fatigue
Decreased appetite
Abdominal pain
Sleepiness
Adult clinical trials:
Constipation
Dry mouth
Nausea
Decreased appetite
Dizziness
Erectile dysfunction
Urinary hesitation
Concomitant use of an MAOI antidepressant with Cymbalta is contraindicated
Use of Cymbalta within 14 days of stopping an MAOI antidepressant is contraindicated
In linezolid- or intravenous methylene blue-treated patients, initiation of Cymbalta is contraindicated
Drug interactions: potent inhibitors of CYP1A2, potent inhibitors of CYP2D6
Hypersensitivity to atomoxetine or other constituents of product
Strattera use within 2 weeks after discontinuing MAOI or other drugs that affect brain monoamine concentrations
Narrow angle glaucoma
Pheochromocytoma or history of pheochromocytoma
Severe cardiovascular disorders that might deteriorate with clinically important increases in HR and BP
Drug interactions: monoamine oxidase inhibitors (MAOIs), CYP2D6 inhibitors, antihypertensive drugs and pressor agents, albuterol (or other beta agonists)
Liver toxicity
Postural low blood pressure, falls, and fainting
Serotonin syndrome
Increased risk of bleeding
Severe skin reactions
Activation of mania or hypomania
Angle-closure glaucoma
Seizures
Blood pressure increases
Inhibitors of CYP1A2 or thioridazine: Avoid co-administration with Cymbalta
Low blood sodium: Can occur in association with SIADH
Glucose control in diabetes
Conditions that slow gastric emptying
Sexual dysfunction
Pregnancy: Third trimester use may increase risk for symptoms of poor adaptation (respiratory distress, temperature instability, feeding difficulty, hypotonia, tremor, irritability) in the neonate
Suicidal ideation
Severe liver injury
Serious cardiovascular events
Emergent cardiovascular symptoms
Effects on blood pressure and heart rate
Emergent psychotic or manic symptoms
Bipolar disorder
Aggressive behavior or hostility should be monitored
Possible allergic reactions, including anaphylactic reactions, angioneurotic edema, urticaria, and rash
Effects on urine outflow
Prolonged erection
Growth
Concomitant use of potent CYP2D6 inhibitors or use in patients known to be CYP2D6 PMs
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.
WARNING: SUICIDAL IDEATION IN CHILDREN AND ADOLESCENTS
Increased risk of suicidal ideation in children or adolescents.
No suicides occurred in clinical trials.
Patients started on therapy should be monitored closely.
*This information is from the label for brand name Cymbalta®. See the Full Prescribing Information for more complete information. Duloxetine, the active ingredient in Cymbalta, may also be the active ingredient in other medications, and this information may not be accurate for all medications that include the active ingredient duloxetine.
*This information is from the label for brand name Strattera®. See the Full Prescribing Information for more complete information. Atomoxetine, the active ingredient in Strattera, is also the active ingredient in other medications, and this information may not be accurate for all medications that include the active ingredient atomoxetine.
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.