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bupropion

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Brand names: Wellbutrin, Zyban

Norepinephrine-Dopamine Reuptake Inhibitor (NDRI) Rx

Bupropion is a medicine used to treat depression and prevent seasonal affective disorder (SAD). It can help improve your mood and energy levels.

Drug Pricing (NADAC)

Generic Price

$0.11/unit

Generic Available

Yes (41 manufacturers)

Pricing data from NADAC (CMS), effective December 18, 2024. Compare all drug costs →

What it does

Bupropion is used to treat major depressive disorder (MDD), which can cause you to feel sad, lose interest in activities, and have trouble sleeping or eating.

Common side effects

Dry mouth, Nausea, Trouble sleeping

Key warnings

Antidepressants may increase the risk of suicidal thoughts and behaviors in children, teenagers, and young adults.

How It Works

Bupropion works by affecting certain chemicals in the brain called norepinephrine and dopamine. It helps to increase the levels of these chemicals, which can improve mood and reduce symptoms of depression.

How to Take It

Take bupropion once a day in the morning. You can take it with or without food. Swallow the tablet whole; do not crush, divide, or chew it. Your doctor may start you on a low dose and increase it gradually.

Pregnancy & Breastfeeding

Talk to your doctor if you are pregnant or plan to become pregnant. It is important to consider the risks of untreated depression during pregnancy. There is a pregnancy registry to monitor outcomes in women exposed to antidepressants during pregnancy. You can register by calling 1-844-405-6185.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is almost time for your next dose, skip the missed dose and take your next dose at the regular time.

Storage

Store bupropion at room temperature (between 59°F and 86°F) and protect it from light.

Side Effects (from patient reports)

Based on 26,482 FDA adverse event reports.

Suicide
4,408
Medicine not working
3,504
Poisoning
3,113
Tiredness
2,665
Feeling sick to your stomach
2,309
Using the medicine for something it's not approved for
2,280
Headache
2,218
Depression
2,175
Pain
1,955
Taking too much medicine
1,855

FDA Adverse Event Report Analysis

Detailed analysis of 41,778 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

41,778

Death-Related Reports

8,506

Hospitalization Reports

13,230

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 24,398 (66%)
Male 12,560 (34%)

Age Distribution

0–17 1,174
18–44 9,568
45–64 12,586
65–74 4,423
75+ 1,705

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 COMPLETED SUICIDE 4,408
2 DRUG INEFFECTIVE 3,504
3 TOXICITY TO VARIOUS AGENTS 3,113
4 FATIGUE 2,665
5 NAUSEA 2,309
6 OFF LABEL USE 2,280
7 HEADACHE 2,218
8 DEPRESSION 2,175
9 PAIN 1,955
10 OVERDOSE 1,855
11 DRUG INTERACTION 1,690
12 ANXIETY 1,678
13 DIZZINESS 1,579
14 DIARRHOEA 1,522
15 INTENTIONAL OVERDOSE 1,352

Reactions in Death Reports

COMPLETED SUICIDE 4,401
TOXICITY TO VARIOUS AGENTS 2,185
DEATH 1,036
CARDIO-RESPIRATORY ARREST 813
CARDIAC ARREST 689
DRUG ABUSE 586
SUSPECTED SUICIDE 583
OVERDOSE 491
RESPIRATORY ARREST 436
INTENTIONAL OVERDOSE 258

Reactions in Hospitalization Reports

COMPLETED SUICIDE 1,580
TOXICITY TO VARIOUS AGENTS 1,475
OVERDOSE 1,251
INTENTIONAL OVERDOSE 1,095
SEIZURE 895
DRUG INTERACTION 789
DRUG INEFFECTIVE 766
NAUSEA 713
OFF LABEL USE 707
HYPOTENSION 675

Source: FDA FAERS (Adverse Event Reporting System) FDA FAERS (Adverse Event Reporting System) Reports are voluntary and do not establish causation

Serious Warnings

Antidepressants may increase the risk of suicidal thoughts and behaviors in children, teenagers, and young adults. Watch closely for worsening depression or suicidal thoughts. Tell your doctor right away if you notice any changes in mood or behavior.

Known Drug Interactions

Excessive reduction of blood glucose (additive effect) [See Warnings and Precautions (5.14)] ; CNS depressant agents (including opioids, alcohol, sedatives, hypnotics) Use with caution Increased CNS depression Dietary supplements containing sympathomimetics Contraindicated Antidepressants including but not limited to: • Other MAOIs (e.g., linezolid, intravenous methylene blue, selective MAOIs) • Selective serotonin reuptake inhibitors (SSRIs) and serotonin and norepinephrine reuptake inhibitors (SNRIs) • Tricyclic antidepressants • Amoxapine, bupropion, maprotiline, nefazodone, trazodone, v...

Mechanism: These two antidepressants can cause a severe reaction when used at the same time. They both change brain chemicals in a way that can lead to dangerously high blood pressure.

What to do: Do not take these medications together. You must wait a specific amount of time when switching between these drugs to avoid serious side effects.

7.3 Drugs That Lower Seizure Threshold Use extreme caution when coadministering bupropion hydrochloride extended-release tablets (XL) with other drugs that lower the seizure threshold (e.g., other bupropion products, antipsychotics, antidepressants, theophylline, or systemic corticosteroids).

Mechanism: Both of these medicines can increase the risk of having a seizure. Taking them at the same time makes this risk even higher.

What to do: Use extreme caution when taking these two drugs together. Your doctor will need to carefully check if this combination is safe for you.

Bupropion Use with Caution Concomitant administration of CRESEMBA and bupropion results in decrease in bupropion exposure. Dose increase of bupropion may be necessary when coadministered with CRESEMBA, but should not exceed the maximum recommended dose [see Clinical Pharmacology ( 12.3 )] .

Mechanism: Taking isavuconazonium can lower the amount of bupropion in your system, making the medication less effective. This happens because the body clears the drug faster than normal.

What to do: Your doctor may need to increase your dose of bupropion to ensure it still works correctly.

( 7.1 ) Drugs metabolized by CYP2D6: Bupropion inhibits CYP2D6 and can increase concentrations of: antidepressants (e.g., venlafaxine, nortriptyline, imipramine, desipramine, paroxetine, fluoxetine, sertraline), antipsychotics (e.g., haloperidol, risperidone, thioridazine), beta-blockers (e.g., metoprolol), and Type 1C antiarrhythmics (e.g., propafenone, flecainide). Such drugs include certain antidepressants (e.g., venlafaxine, nortriptyline, imipramine, desipramine, paroxetine, fluoxetine, and sertraline), antipsychotics (e.g., haloperidol, risperidone, and thioridazine), beta-blockers (e...

Mechanism: Bupropion blocks a liver enzyme that normally breaks down metoprolol. This causes the amount of metoprolol in your blood to rise to higher levels than expected.

What to do: Your doctor may need to lower your dose of metoprolol. They should also check your heart rate and blood pressure more frequently.

( 7.1 ) Drugs metabolized by CYP2D6: Bupropion inhibits CYP2D6 and can increase concentrations of: antidepressants (e.g., venlafaxine, nortriptyline, imipramine, desipramine, paroxetine, fluoxetine, sertraline), antipsychotics (e.g., haloperidol, risperidone, thioridazine), beta-blockers (e.g., metoprolol), and Type 1C antiarrhythmics (e.g., propafenone, flecainide). Such drugs include certain antidepressants (e.g., venlafaxine, nortriptyline, imipramine, desipramine, paroxetine, fluoxetine, and sertraline), antipsychotics (e.g., haloperidol, risperidone, and thioridazine), beta-blockers (e...

Mechanism: Bupropion slows down the process your liver uses to clear sertraline from your body. This can cause sertraline to build up in your system, increasing the risk of side effects.

What to do: Your doctor may need to adjust your dose of sertraline. Be sure to report any new or worsening side effects from your antidepressant to your healthcare provider.

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Common Questions

Can I cut the tablet in half?
No, swallow the tablet whole. Do not crush, divide, or chew it.
Can I take this at night?
Take bupropion in the morning.
What if I feel worse after starting this medicine?
Tell your doctor right away if you feel worse or have any new or worsening symptoms.
Can I drink alcohol while taking this?
Talk to your doctor about drinking alcohol while taking this medicine.
How long does it take for this medicine to work?
It may take several weeks for you to feel the full effects of this medicine.
Will this medicine make me gain weight?
Weight changes can occur with this medicine. Talk to your doctor if you are concerned.
Can I stop taking this medicine suddenly?
Do not stop taking this medicine without talking to your doctor. They may need to lower your dose slowly.
What should I do if I have side effects?
Tell your doctor about any side effects you have.
Does this medicine interact with other medicines?
Yes, bupropion can interact with other medicines. Tell your doctor about all the medicines you take.
Can this medicine cause seizures?
Bupropion can increase the risk of seizures. Your doctor will consider this risk when prescribing this medicine.
What are the common side effects of bupropion?
The most commonly reported side effects of bupropion include Dry mouth, Nausea, Trouble sleeping, Dizziness, Sore throat. Based on 26,482 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does bupropion interact with other medications?
Yes, bupropion has 35 known drug interactions. Notable interactions include tranylcypromine, theophylline, isavuconazonium. Always inform your doctor about all medications you are taking.
What drug class is bupropion?
bupropion belongs to the Norepinephrine-Dopamine Reuptake Inhibitor (NDRI) drug class. It requires a prescription (Rx). Bupropion is used to treat major depressive disorder (MDD), which can cause you to feel sad, lose interest in activities, and have trouble sleeping or eating.
Is bupropion safe during pregnancy?
Talk to your doctor if you are pregnant or plan to become pregnant. It is important to consider the risks of untreated depression during pregnancy. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.
Has bupropion been recalled?
There are 2 recalls associated with bupropion products. Failed Tablet/Capsule Specifications. Check the recalls section below for full details and affected products.

Active Recalls

Class II September 15, 2025

Failed Tablet/Capsule Specifications

Graviti Pharmaceuticals Private Limited

Class II June 24, 2024

Failed Dissolution Specifications; the product is dissolving faster than the specified limits.

Amerisource Health Services LLC

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Related Health & Safety Data

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What the FDA Data Shows for bupropion

The FDA label for bupropion (sold under brand names such as Wellbutrin, Zyban) classifies it as a prescription-only medication in the Norepinephrine-Dopamine Reuptake Inhibitor (NDRI) class. Bupropion is used to treat major depressive disorder (MDD), which can cause you to feel sad, lose interest in activities, and have trouble sleeping or eating. Official labeling lists 16 commonly reported side effects, including Dry mouth, Nausea, Trouble sleeping.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 26,482 voluntary reports. The database also lists 35 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated major severity. NADAC pricing from CMS shows a generic unit cost of $0.11.

Report counts do not establish causation — a FAERS entry documents a temporal association, not proof that the drug produced the outcome. Widely prescribed medications naturally accumulate more reports than niche therapies, so raw totals must be interpreted alongside total exposure. Shortage status, recall history (currently 2 recall records on file), and patent information further shape supply and switching decisions. This page summarizes public FDA data for educational purposes only and is not a substitute for professional medical advice — always consult a licensed healthcare provider before starting, stopping, or changing any medication.

Data Sources

Drug labeling: FDA Drug Labels (SPL/DailyMed). Adverse events: FDA Adverse Event Reporting System (FAERS). Pricing: CMS National Average Drug Acquisition Cost (NADAC).

FAERS reports are voluntary and do not establish causation. Drug interactions are derived from FDA labeling and clinical references. Always consult a healthcare professional before making medication decisions.

Last updated: November 25, 2025

All federal data sources used on this page