BOXED WARNING Suicidal thoughts and behaviors: antidepressants increased risk in pediatric and young adult patients; monitor closely. Not approved for pediatric use.
FDA dosing
Population
Start
Target
Max
Major depressive disorder (MDD)
Adults
45 mg/105 mg QD (morning)
45 mg/105 mg BID (≥8 h apart) from day 4
45 mg/105 mg BID (2 doses/day)
Agitation associated with dementia due to Alzheimer's disease
Adults
30 mg/105 mg QD (morning)
30 mg/105 mg BID on day 8; then 45 mg/105 mg BID on day 15 (≥8 h apart)
45 mg/105 mg BID (2 doses/day)
Titration MDD: increase to BID on day 4. Alzheimer's agitation: increase on day 8, then day 15 based on tolerability
Renal Moderate impairment (eGFR 30-59): max 45 mg/105 mg QD; not recommended in severe (eGFR 15-29)
Hepatic No adjustment for mild/moderate (Child-Pugh A/B); not recommended in severe (Child-Pugh C)
Not indicated as an as-needed (prn) treatment for agitation associated with Alzheimer's dementia; separate BID doses by at least 8 hours
Instructions
Administer with or without food
Swallow tablets whole; do not crush, divide, or chew
Do not exceed two doses within the same day
At least 14 days between an MAOI and AUVELITY in either direction
CYP2D6 poor metabolizers or with strong CYP2D6 inhibitors: max 45 mg/105 mg QD
Available strengths
ER tab 30/105, 45/105 mg
Contraindications
Seizure disorder
Current or prior diagnosis of bulimia or anorexia nervosa
Abrupt discontinuation of alcohol, benzodiazepines, barbiturates, or antiepileptic drugs
Use with an MAOI, or within 14 days of stopping an MAOI (risk of hypertensive crisis and serotonin syndrome); includes linezolid and IV methylene blue
Cautions
Seizure (dose-related; from bupropion)
Increased blood pressure and hypertension
Activation of mania or hypomania; screen for bipolar
MDD: dizziness, headache, diarrhea, somnolence, dry mouth, sexual dysfunction, hyperhidrosis
Alzheimer's agitation: dizziness, dyspepsia
Pregnancy May cause fetal harm based on animal studies; not recommended in pregnancy; discontinue if pregnant
Lactation Bupropion and metabolites present in human milk; breastfeeding not recommended during treatment and for 5 days after final dose (neurotoxicity concern)
Cost
Auvelity
What pharmacies pay · NADAC 9/30/26
Strength
#/mo
generic $/mo
brand $/mo
CostPlus
30/105 mg
ER tab
30 qd
—
not offered
45/105 mg
ER tab
30 qd
—
$596.93
not offered
Clinical profile
Therapeutic safety burden2 / 4
Overdose danger3 / 4
Weight-gain liability0 / 4
Sedation liability1 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk2 / 4
Defining liabilitySeizure risk, dizziness and CYP2D6/serotonergic interactions
Part D rank #418.
Self-check
What dementia-related indication is listed for dextromethorphan–bupropion? Agitation in Alzheimer dementia.
What boxed psychiatric warning applies? Suicidal thoughts and behaviors.