BOXED WARNING Suicidal thoughts and behaviors in children, adolescents, and young adults
FDA dosing
Population
Start
Target
Max
Major depressive disorder
Adults
150 mg QAM
150 mg BID (300 mg/day)
200 mg BID (400 mg/day)
Titration After 3 days may increase to 300 mg/day; wait several weeks before 400 mg/day; ≥8 h between doses
Renal Reduce dose and/or frequency (GFR <90 mL/min)
Hepatic Moderate–severe (Child-Pugh 7–15): max 100 mg/day or 150 mg every other day; mild: reduce dose/frequency
Do not exceed 400 mg/day (seizure risk)
Instructions
Swallow whole; do not crush, divide, or chew
Take with or without food
Do not exceed 200 mg in any single dose
Increase dose gradually to reduce seizure risk
Contraindications
Seizure disorder
Current or prior diagnosis of bulimia or anorexia nervosa
Patients undergoing abrupt discontinuation of alcohol, benzodiazepines, barbiturates, and antiepileptic drugs
Use of MAOIs (intended to treat psychiatric disorders) concomitantly with WELLBUTRIN SR or within 14 days of discontinuing treatment; starting WELLBUTRIN SR in a patient treated with reversible MAOIs such as linezolid or intravenous methylene blue is contraindicated
Cautions
Seizure (dose-related)
Hypertension/elevated blood pressure
Activation of mania/hypomania
Psychosis and other neuropsychiatric reactions
Angle-closure glaucoma
Neuropsychiatric adverse events in smoking-cessation use
Hypersensitivity reactions
Adverse reactions
Headache
Dry mouth
Nausea
Insomnia
Dizziness
Pharyngitis
Constipation
Agitation
Anxiety
Tremor
Sweating
Weight loss
Pregnancy First-trimester epidemiologic data show no increased risk of congenital malformations overall
Lactation Bupropion and metabolites present in human milk; seizures reported in breastfed infants
⚠ BOXED WARNING
Suicidal thoughts and behaviors in patients under 25