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desipramine

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Brand names: Norpramin

Tricyclic Antidepressant (TCA) Rx

Desipramine is a medicine used to treat depression. It belongs to a class of drugs called tricyclic antidepressants.

Drug Shortage Alert

desipramine is currently listed as to be discontinued by the FDA. Affected manufacturer: Avet Pharmaceuticals, Inc..

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Drug Pricing (NADAC)

Generic Price

$0.11/unit

Generic Available

Yes (9 manufacturers)

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

What it does

Desipramine is used to treat depression.

Common side effects

Drowsiness, Dizziness, Dry mouth

Key warnings

Antidepressants may increase the risk of suicidal thoughts or actions in children, teens, and young adults.

How It Works

Desipramine works by affecting certain chemicals in the brain. It helps to increase the levels of norepinephrine. This can improve mood and reduce symptoms of depression.

How to Take It

Take desipramine exactly as your doctor tells you. The usual adult dose is 100 to 200 mg per day. Your doctor may start you on a lower dose and increase it slowly. You can take it as a single dose or divided doses.

Pregnancy & Breastfeeding

Tell your doctor if you are pregnant or plan to become pregnant. Desipramine may affect your baby. Talk to your doctor about the risks and benefits of taking this medicine while pregnant or breastfeeding.

Missed Dose

If you miss a dose, take it as soon as you remember. If it is close to your next dose, skip the missed dose and continue with your regular schedule.

Storage

Store desipramine at room temperature (68°-77°F) away from heat and moisture.

Side Effects (from patient reports)

Based on 818 FDA adverse event reports.

Medicine not working
125
Tiredness
119
Death by suicide
116
Feeling sick to your stomach
77
Head pain
70
Gaining weight
68
Feeling lightheaded
63
Using the medicine for something it's not approved for
61
Harm from different substances
60
Aches
59

FDA Adverse Event Report Analysis

Detailed analysis of 1,275 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

1,275

Death-Related Reports

217

Hospitalization Reports

341

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 816 (71%)
Male 338 (29%)

Age Distribution

0–17 14
18–44 202
45–64 385
65–74 139
75+ 113

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 DRUG INEFFECTIVE 125
2 FATIGUE 119
3 COMPLETED SUICIDE 116
4 NAUSEA 77
5 HEADACHE 70
6 WEIGHT INCREASED 68
7 DIZZINESS 63
8 OFF LABEL USE 61
9 TOXICITY TO VARIOUS AGENTS 60
10 PAIN 59
11 ARTHRALGIA 58
12 DRUG INTOLERANCE 57
13 DYSPNOEA 53
14 DYSPNOEA EXERTIONAL 46
15 ANXIETY 43

Reactions in Death Reports

COMPLETED SUICIDE 116
TOXICITY TO VARIOUS AGENTS 58
DEATH 36
CARDIO-RESPIRATORY ARREST 18
DYSPNOEA 17
OVERDOSE 17
LOSS OF CONSCIOUSNESS 16
CONFUSIONAL STATE 13
CARDIAC ARREST 12
ANTIDEPRESSANT DRUG LEVEL ABOVE THERAPEUTIC 11

Reactions in Hospitalization Reports

DRUG INEFFECTIVE 29
ACUTE KIDNEY INJURY 28
FATIGUE 23
HEADACHE 23
DYSPNOEA 22
DIZZINESS 21
FALL 21
NAUSEA 21
PAIN 21
COMPLETED SUICIDE 20

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 or actions in children, teens, and young adults. Watch for worsening depression, unusual behavior, or thoughts of suicide. Desipramine is not approved for use in children.

Known Drug Interactions

CYP2D6 Substrate (e.g., Desipramine) — Coadministration of atomoxetine (40 or 60 mg BID for 13 days) with desipramine, a model compound for CYP2D6 metabolized drugs (single dose of 50 mg), did not alter the pharmacokinetics of desipramine.

Mechanism: Atomoxetine does not change how the body processes desipramine, even though both drugs use the same liver enzyme.

What to do: No dosage changes are usually needed when taking these two medications together.

( 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 interferes with the way your body breaks down desipramine, causing the drug to stay in your system longer.

What to do: Your doctor may need to reduce your dose of desipramine to prevent side effects from high drug levels.

Tricyclic Antidepressants (TCAs): amitriptyline, desipramine, imipramine, nortriptyline ↑ amitriptyline ↑ desipramine ↑ imipramine ↑ nortriptyline Use a lower dose of the tricyclic antidepressants and trazodone due to potential increased adverse events such as nausea, dizziness, hypotension and syncope.

Mechanism: Darunavir slows down the process your body uses to get rid of desipramine, leading to higher levels of the drug in your blood.

What to do: Your doctor should use a lower dose of desipramine and watch for side effects like dizziness or fainting.

Examples desipramine, atomoxetine, dextromethorphan, metoprolol, nebivolol, perphenazine, tolterodine 7.2 Drugs Having No Clinically Important Interactions with PRISTIQ Based on pharmacokinetic studies, no dosage adjustment is required for drugs that are mainly metabolized by CYP3A4 (e.g., midazolam), or for drugs that are metabolized by both CYP2D6 and CYP3A4 (e.g., tamoxifen, aripiprazole), when administered concomitantly with PRISTIQ [see Clinical Pharmacology (12.3) ].

Mechanism: Desvenlafaxine may interfere with the way your body breaks down desipramine, potentially leading to higher levels of the medication in your blood.

What to do: Your doctor likely does not need to adjust your dose, but they may want to monitor your response to the treatment more closely.

Examples: amitriptyline, desipramine, doxepin, imipramine, nortriptyline.

Mechanism: This drug makes your body more sensitive to dopamine's effects on the heart and blood pressure. It prevents the body from soaking up chemicals that dopamine works with, making the effect stronger.

What to do: Your healthcare provider should watch your vital signs carefully. The dose of dopamine might need to be lowered.

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Common Questions

Can I stop taking desipramine suddenly?
Do not stop taking desipramine suddenly. This can cause withdrawal symptoms like nausea and headache.
How long does it take for desipramine to work?
It may take several weeks for desipramine to start working. Talk to your doctor if you do not feel better after a few weeks.
Can I drink alcohol while taking desipramine?
Avoid drinking alcohol while taking desipramine. Alcohol can worsen the side effects of this medicine.
What should I do if I overdose on desipramine?
Seek emergency medical attention immediately if you overdose on desipramine.
Can desipramine cause weight gain?
Desipramine can cause weight gain or weight loss in some people.
Is desipramine addictive?
Desipramine is not addictive, but stopping it suddenly can cause withdrawal symptoms.
Can I take desipramine with other medications?
Tell your doctor about all the medications you take, including over-the-counter drugs and supplements.
What if I have side effects?
Tell your doctor if you have any side effects while taking desipramine.
Can older adults take desipramine?
Older adults may be more sensitive to the effects of desipramine. Your doctor may prescribe a lower dose.
Can I drive while taking desipramine?
Desipramine can cause drowsiness or dizziness. Be careful driving or operating machinery until you know how this medicine affects you.
What are the common side effects of desipramine?
The most commonly reported side effects of desipramine include Drowsiness, Dizziness, Dry mouth, Constipation, Blurred vision. Based on 818 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does desipramine interact with other medications?
Yes, desipramine has 18 known drug interactions. Notable interactions include atomoxetine, bupropion, darunavir. Always inform your doctor about all medications you are taking.
What drug class is desipramine?
desipramine belongs to the Tricyclic Antidepressant (TCA) drug class. It requires a prescription (Rx). Desipramine is used to treat depression.
Is desipramine safe during pregnancy?
Tell your doctor if you are pregnant or plan to become pregnant. Desipramine may affect your baby. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.
Has desipramine been recalled?
There are 2 recalls associated with desipramine products. CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level. Check the recalls section below for full details and affected products.
Is desipramine currently in shortage?
Yes, desipramine is currently listed as to be discontinued by the FDA. Affected manufacturer: Avet Pharmaceuticals, Inc.. Visit the FDA Drug Shortages database for the latest updates.

Active Recalls

Class II October 6, 2025

CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.

Heritage Pharmaceuticals Inc

Class II October 6, 2025

CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.

Heritage Pharmaceuticals Inc

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Medication Guides

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What the FDA Data Shows for desipramine

The FDA label for desipramine (sold under brand names such as Norpramin) classifies it as a prescription-only medication in the Tricyclic Antidepressant (TCA) class. Desipramine is used to treat depression. Official labeling lists 9 commonly reported side effects, including Drowsiness, Dizziness, Dry mouth.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 818 voluntary reports. The database also lists 18 documented drug interactions derived from FDA labeling, with the top-flagged interaction rated minor 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). Shortage status: FDA Drug Shortages Database.

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: December 9, 2025

All federal data sources used on this page