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Atomoxetine

Generic Name: Atomoxetine

Brand Names: Strattera

Atomoxetine is used to treat attention deficit hyperactivity disorder (ADHD). It is available as Strattera and is commonly prescribed in the mental health category.

Mental HealthADHDNon-Stimulants

Drug Class

Selective Norepinephrine Reuptake Inhibitor (Non-Stimulant)

Pregnancy

Category C — Animal studies showed decreased fetal weight at maternally toxic doses. Human data are limited. Use during pregnancy only if the potential benefit justifies the potential fetal risk; many clinicians defer or pause atomoxetine when pregnancy is planned or confirmed.

Available Forms

Oral capsule (10 mg, 18 mg, 25 mg, 40 mg, 60 mg, 80 mg, 100 mg)

What It's Used For

Dosage Quick Reference

These are general dosage guidelines. Your doctor will determine the appropriate dose for your specific situation.

ConditionStarting DoseMaintenance Dose
ADHD (adults and children >= 70 kg)40 mg once daily for 3 daysIncrease to 80 mg/day; max 100 mg/day after 2–4 weeks if needed
ADHD (children and adolescents < 70 kg)0.5 mg/kg/day for 3 daysTarget 1.2 mg/kg/day; max 1.4 mg/kg/day or 100 mg/day, whichever is less
ADHD with concurrent strong CYP2D6 inhibitor or known poor metabolizer40 mg once daily (adults)Titrate slowly; consider not exceeding 80 mg/day
Hepatic impairment (Child-Pugh B)Reduce starting and target dose by 50%50% of usual maintenance dose

Side Effects

Common side effects may include:

Nausea or stomach upset • Headache • Dizziness or lightheadedness • Fatigue or tiredness • Mild rash or itching

Serious side effects (seek immediate medical attention):

• Severe allergic reactions (rash, hives, swelling, difficulty breathing) • Unusual bleeding or bruising • Severe stomach pain • Signs of liver problems (yellowing of skin/eyes, dark urine) • Chest pain or irregular heartbeat • Severe dizziness or fainting • Signs of serious adverse effects

Drug Interactions

Atomoxetine is primarily metabolized by CYP2D6, and its norepinephrine activity creates several pharmacodynamic interactions. About 7% of Caucasians and 2% of African Americans are CYP2D6 poor metabolizers and experience higher exposure.

  • Strong CYP2D6 inhibitors (e.g., paroxetine, fluoxetine, bupropion, quinidine): Increase atomoxetine plasma levels several-fold. Initiate at the standard starting dose but do not titrate up for at least 4 weeks; cap maintenance dosing at lower levels.
  • MAO inhibitors (e.g., phenelzine, tranylcypromine, linezolid): Concurrent use can produce hypertensive crisis or serotonin-syndrome-like reactions. Do not use within 14 days of an MAO inhibitor.
  • Other sympathomimetics or pressor agents (e.g., pseudoephedrine, albuterol systemic, stimulant ADHD medications): Additive increases in heart rate and blood pressure. Monitor vital signs and avoid combinations when possible.
  • QT-prolonging drugs (e.g., methadone, ondansetron, certain antipsychotics): Atomoxetine can modestly prolong QT. Combine cautiously and review baseline ECG in patients with cardiac risk factors.
  • Antihypertensives: Atomoxetine can blunt the effect of some antihypertensives by raising sympathetic tone. Monitor blood pressure when starting therapy.

Additional Information

What is Atomoxetine?

Atomoxetine (generic name: Atomoxetine) is a medication primarily used to treat attention deficit hyperactivity disorder (ADHD). It is marketed under the brand name(s) Strattera and belongs to the Mental Health category of medications.

How Does Atomoxetine Work?

Atomoxetine works through several mechanisms to provide therapeutic benefits:

  • Acts on specific receptors or pathways in the body
  • Modulates biological processes related to the treated condition
  • Provides symptom relief and improves quality of life
  • Helps manage the underlying condition effectively
  • Works best when combined with appropriate lifestyle modifications

The medication is designed to target the specific pathways involved in attention deficit hyperactivity disorder (ADHD), making it an effective treatment option.

Common Uses

Primary Indications

Atomoxetine is commonly prescribed for:

  • Attention deficit hyperactivity disorder (adhd): The main indication for this medication
  • Related Conditions: Associated symptoms and complications
  • Prevention: May help prevent progression of certain conditions
  • Symptom Management: Reduces discomfort and improves daily function

Additional Uses

In some cases, Atomoxetine may also be prescribed for:

  • Off-label uses as determined by your healthcare provider
  • Combination therapy with other medications
  • Long-term management of chronic conditions
  • Short-term treatment of acute symptoms

Dosage and Administration

Atomoxetine dosing varies based on the specific condition being treated and individual patient factors.

Typical Dosing:

  • Starting dose is typically determined by your healthcare provider
  • May be adjusted based on response and tolerability
  • Can be taken with or without food (follow specific instructions)
  • Usually taken once or twice daily

Administration Tips:

  • Take at the same time(s) each day for best results
  • Swallow tablets/capsules whole unless instructed otherwise
  • Don't skip doses
  • Complete full course of treatment as prescribed
  • Follow your doctor's specific instructions carefully

Important Safety Information

Who Should Not Take Atomoxetine?

Do not take Atomoxetine if you:

  • Are allergic to Atomoxetine or any ingredients
  • Have certain medical conditions (discuss with your doctor)
  • Are taking medications that interact with Atomoxetine
  • Have severe liver or kidney disease (without dose adjustment)

Drug Interactions

Inform your doctor about all medications you take, including:

  • Prescription medications
  • Over-the-counter drugs
  • Vitamins and supplements
  • Herbal products

Some medications may interact with Atomoxetine, affecting its efficacy or increasing side effect risk.

Pregnancy and Breastfeeding

Pregnancy:

  • Discuss risks and benefits with your doctor if pregnant or planning pregnancy
  • May require special monitoring or dose adjustments
  • Some medications should be avoided during pregnancy

Breastfeeding:

  • Consult your doctor about safety while breastfeeding
  • May pass into breast milk
  • Benefits and risks should be carefully considered

Monitoring and Follow-Up

While taking Atomoxetine, your doctor may monitor:

  • Effectiveness of treatment (symptom improvement)
  • Side effects or adverse reactions
  • Laboratory values if applicable
  • Blood pressure, heart rate, or other vital signs as appropriate
  • Overall response to therapy

Regular follow-up appointments are important to ensure the medication is working properly and to make any necessary adjustments.

Managing Side Effects

Most side effects are mild and improve with time. Here are strategies for common side effects:

Gastrointestinal Upset

  • Take with food if allowed
  • Stay well hydrated
  • Eat smaller, more frequent meals
  • Report persistent nausea or vomiting

Dizziness

  • Rise slowly from sitting or lying positions
  • Avoid sudden movements
  • Stay hydrated
  • Avoid alcohol
  • Report severe or persistent dizziness

Fatigue

  • Get adequate rest
  • Maintain regular sleep schedule
  • Exercise as tolerated
  • Report excessive tiredness that interferes with daily activities

Lifestyle Considerations

To maximize the benefits of Atomoxetine:

  • Follow a healthy, balanced diet
  • Exercise regularly as recommended by your doctor
  • Maintain a healthy weight
  • Avoid alcohol or limit consumption
  • Don't smoke
  • Manage stress through relaxation techniques
  • Get adequate sleep
  • Stay well hydrated
  • Keep all follow-up appointments
  • Take medication consistently as prescribed

When to Contact Your Doctor

Seek immediate medical attention if you experience:

  • Signs of severe allergic reaction (difficulty breathing, severe rash, swelling)
  • Chest pain or rapid heartbeat
  • Severe dizziness or fainting
  • Unusual bleeding or bruising
  • Signs of liver problems (yellowing of skin/eyes, dark urine, severe fatigue)
  • Severe stomach pain
  • Any symptoms that concern you

Contact your doctor for non-emergency issues:

  • Mild to moderate side effects that persist
  • Questions about your medication
  • Concerns about effectiveness
  • New medications prescribed by another doctor
  • Scheduled surgery or dental procedures
  • Planning pregnancy

Storage

Store Atomoxetine at room temperature (68-77°F or 20-25°C) away from light, heat, and moisture. Keep in original container. Keep out of reach of children and pets. Do not use past expiration date.

Important Reminders

  • Take exactly as prescribed by your doctor
  • Don't stop suddenly without medical advice
  • Keep all follow-up appointments
  • Report any unusual symptoms
  • Don't share medication with others
  • Store safely away from children
  • Check expiration dates
  • Ask your pharmacist if you have questions

Clinical Benefits

When used appropriately, Atomoxetine provides several benefits:

  • Effective management of attention deficit hyperactivity disorder (ADHD)
  • Improvement in quality of life
  • Reduction in symptoms
  • Prevention of complications
  • Generally well-tolerated when used as directed
  • Backed by clinical research and extensive use

Disclaimer: This information is for educational purposes only and is not intended to replace professional medical advice, diagnosis, or treatment. Always consult your physician or other qualified healthcare provider with any questions about a medical condition or medication.

Frequently Asked Questions

Unlike stimulant ADHD medications, atomoxetine does not produce an immediate effect on the day it is taken. Most patients begin to notice symptom improvement after 2 to 4 weeks of consistent dosing, and full benefit is typically assessed at 6 to 12 weeks. Patience and steady daily use are essential.
Atomoxetine can be given as a single morning dose or split into morning and late afternoon. Twice-daily dosing may help patients who experience GI upset or sleep disturbance. Taking it with food can reduce nausea, especially when starting therapy.
No. Atomoxetine is not a controlled substance and is not classified as a stimulant. It does not produce euphoria and is not associated with abuse or dependence. This makes it a useful option for patients with a history of substance use disorder or those who prefer to avoid stimulants.
Atomoxetine can modestly raise heart rate (typically by 5–10 beats per minute) and blood pressure. Most patients tolerate these changes without difficulty, but baseline and periodic monitoring is recommended, particularly for patients with a history of hypertension, arrhythmia, or structural heart disease.
Rare but important risks include severe liver injury (report fatigue, dark urine, yellowing of skin), suicidal thoughts in children and adolescents (especially in the first months of treatment), and significant cardiovascular events in those with underlying heart disease. Report any new mood changes, jaundice, or chest symptoms promptly.

Questions to Ask Your Doctor

Consider discussing these topics at your next appointment:

  • How will we measure whether atomoxetine is helping my ADHD symptoms?
  • Should I have a baseline ECG or cardiology evaluation before starting?
  • How often should my blood pressure, heart rate, and weight be checked while on this medication?
  • What signs of liver problems or mood changes should prompt me to call you between visits?
  • Would a stimulant be a more effective option for my situation, and what are the trade-offs?

Medical Disclaimer: This information is for educational purposes only and should not be considered medical advice. Always consult with your healthcare provider before starting, stopping, or changing any medication. Your doctor can provide personalized recommendations based on your specific health condition and medical history.