Switching from Vyvanse and Adderall to Strattera While Continuing Intuniv and Zoloft
Yes, you can safely switch from Vyvanse (lisdexamfetamine) and Adderall (amphetamine/dextroamphetamine) to Strattera (atomoxetine) while continuing Intuniv (guanfacine) and Zoloft (sertraline), using a cross-taper approach over 1-2 weeks. 1
Switching Strategy
Initiation and Cross-Tapering Approach
- Start atomoxetine at 40 mg daily while gradually reducing the stimulant dose over 7-14 days 2
- Atomoxetine can be co-administered with stimulants during the switching period without undue concern for cardiovascular effects, though blood pressure and heart rate monitoring is necessary 1
- Use a slow titration schedule with divided doses to minimize adverse events during the first several weeks of treatment 1
- Titrate atomoxetine every 7-14 days to 60 mg, then 80 mg daily, with a maximum dose of 1.4 mg/kg/day or 100 mg/day (whichever is less) 2
Timeline for Evaluation
- Allow at least 6-8 weeks, possibly longer, before evaluating the overall tolerability and efficacy of atomoxetine 1
- This extended timeline is critical because atomoxetine has a different mechanism of action (selective norepinephrine reuptake inhibition) compared to the dopaminergic effects of stimulants 1
Expected Response Rates
- Approximately 50% of methylphenidate non-responders will respond to atomoxetine therapy 1
- Approximately 75% of stimulant responders will also respond to atomoxetine 1
- Nearly 90% of ADHD patients respond to either stimulants or atomoxetine if both are tried sequentially 3
Drug Interaction Considerations
Continuation of Intuniv (Guanfacine)
- Guanfacine can be safely continued during and after the switch 2
- There are no significant pharmacokinetic interactions between atomoxetine and guanfacine
- Both medications can provide complementary benefits for ADHD symptoms and executive function
Continuation of Zoloft (Sertraline)
- Sertraline can be safely continued, but requires monitoring 2
- Sertraline is a moderate CYP2D6 inhibitor, which can increase atomoxetine plasma concentrations
- This interaction may necessitate slower atomoxetine titration or lower maintenance doses
- Monitor for increased atomoxetine side effects (nausea, decreased appetite, dizziness)
Clinical Reasons for Switching
Valid Indications for Switching to Atomoxetine
- Incomplete response or non-response to stimulant treatment 1
- Poor tolerability of stimulants (41% of medication-naive adults require switching from their initial stimulant family due to poor tolerability) 4
- Co-morbid conditions such as tics, anxiety, or depression 1
- Sleep disturbances or eating problems that are exacerbated by stimulants 1
- Concerns about potential for drug abuse or diversion 1
- Need for consistent symptom coverage extending into late evening 1
Safety Profile
Atomoxetine Safety
- Atomoxetine does not appear to be associated with major congenital malformations or significant adverse obstetrical outcomes 2
- Common side effects include decreased appetite, nausea, dizziness, and fatigue, which are typically mild to moderate and transient 1
- Cardiovascular monitoring (blood pressure and heart rate) is recommended during initiation and dose adjustments 1
Discontinuation Characteristics
- Atomoxetine can be discontinued abruptly without rebound effects or discontinuation syndrome 1
- Patients may miss occasional doses without significant clinical consequences 1
- This contrasts with stimulants, which can cause rebound symptoms when discontinued abruptly
Common Pitfalls to Avoid
- Do not evaluate treatment failure too early: Allow the full 6-8 week trial period before concluding atomoxetine is ineffective 1
- Do not abruptly discontinue stimulants: Use gradual cross-tapering to minimize withdrawal symptoms and maintain symptom control during the transition 1
- Do not ignore the sertraline-atomoxetine interaction: Adjust atomoxetine dosing expectations when CYP2D6 inhibitors are present
- Do not assume equivalent immediate efficacy: Atomoxetine's therapeutic effects build gradually, unlike the immediate effects of stimulants 1