Compare common side effects, interactions, warnings, and more.
Bupropion
Cymbalta
*image for illustrative purpose only
Bupropion is the active ingredient in the brand-name medication Wellbutrin SR®. The information below is about brand name Wellbutrin SR. According to the FDA, “Generic medicines use the same active ingredients as brand-name medicines and work the same way, so they have the same risks and benefits as the brand-name medicines.”
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.
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.
Aminoketone antidepressant
Serotonin and norepinephrine reuptake inhibitor (SNRI)
Wellbutrin SR (bupropion hydrochloride) is indicated:
For the treatment of major depressive disorder (MDD)
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
Typically taken orally twice daily
Comes in 100 mg, 150 mg, and 200 mg tablets
Typically taken orally once daily
Comes in 20 mg, 30 mg, and 60 mg delayed-release capsules
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
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
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
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
Neuropsychiatric adverse events during smoking cessation
Seizure risk
High blood pressure
Activation of mania/hypomania
Psychosis and other neuropsychiatric reactions
Angle-closure glaucoma
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
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 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 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.
*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.
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