Prescription medication · Tricyclic Antidepressant (TCA)

desipramine

Also sold as Norpramin. Desipramine is used to treat depression.

Data updated 2026-05-15

1,275
FDA reportsRarely reported
18
InteractionsSeveral interactions
In shortage
FDA status

What the data shows

desipramine (Norpramin) is a prescription Tricyclic Antidepressant (TCA), among the least-reported drugs the FDA tracks (1,275 FDA reports), with 18 documented drug interactions.

Reporting volume reflects how widely a drug is used and studied, not how dangerous it is, a FAERS report documents a temporal association, never proof of cause.

desipramine (Norpramin) is a prescription Tricyclic Antidepressant (TCA). Desipramine is used to treat depression.

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..

View all drug shortages →

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 →

NADAC price trail: DESIPRAMINE 10 MG TABLET

Same CMS presentation as the headline generic unit price above (2 effective dates). Adjacent % compares consecutive NADAC releases for this description only, not a patient out-of-pocket quote. Latest step: -10.1% vs prior release.

Effective NADAC / unit vs prior NDCs
February 21, 2024 $0.1171/EA - 1
December 18, 2024 $0.1053/EA -10.1% 6
View Alternatives → Compare with Another Drug → Full Side Effects Report →

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.

The sections below are summarized in plain English from desipramine's FDA-approved prescribing information. They describe what the official label says, and are not personal medical advice.

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.

Side Effects (from patient reports)

Based on 1,275 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for desipramine, by number of reports

reports

What this shows Bars show how often each reaction was reported, not how likely it is to happen, a report records a temporal association, never proof that the drug caused it.

Source FDA Adverse Event Reporting System (FAERS) As of 2025

Reports over time

Adverse-event reports filed for desipramine each year to the FDA Adverse Event Reporting System (FAERS).

050100150 20042007201120142017202020232025 48

Year-to-year volume tracks usage, prescribing, and scrutiny, not a change in per-patient risk. Source: FDA FAERS.

Where desipramine sits

desipramine has more FDA adverse-event reports than 8% of the drugs FAERS tracks. A high position reflects how widely a drug is used and watched, not how dangerous it is.

fewest reports most reports

Percentile across all drugs PlainMeds tracks by FAERS report volume. The dot is desipramine; the line is the median (50th percentile).

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

Reports Mentioning Death

217

17.0% of reports — not proof of cause

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
2 FATIGUE 119
3 COMPLETED SUICIDE 116
4 NAUSEA 77
5 HEADACHE 70
6 WEIGHT INCREASED 68
7 DIZZINESS 63
9 TOXICITY TO VARIOUS AGENTS 60
10 PAIN 59
11 ARTHRALGIA 58
13 DYSPNOEA 53
14 DYSPNOEA EXERTIONAL 46
15 ANXIETY 43
16 DEPRESSION 43
17 DIARRHOEA 43
18 ACUTE KIDNEY INJURY 42

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

ACUTE KIDNEY INJURY 28
FATIGUE 23
HEADACHE 23
DYSPNOEA 22
DIZZINESS 21
FALL 21
NAUSEA 21
PAIN 21
COMPLETED SUICIDE 20
INTESTINAL OBSTRUCTION 20

Source: 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.

( 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...

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

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.

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.

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.

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This is a plain-language summary of FDA-label interaction records and does not provide individual medication-combination directions.

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 registry lists Drowsiness, Dizziness, Dry mouth, Constipation, Blurred vision among the most-reported FAERS reaction terms for desipramine. The compiled record contains 1,275 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does desipramine interact with other medications?
The registry has 18 documented interaction rows for desipramine. Notable source-record pairings include atomoxetine, bupropion, darunavir. These rows are not a complete medication review.
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.
What pregnancy or breastfeeding source fields are listed for desipramine?
The FDA label for desipramine contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.
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

Other drugs grouped near desipramine - same-class peers and common alternatives.

Compare desipramine vs acamprosate side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for desipramine: nearest FDA FAERS report volume and nearest death-report share among drugs with at least 1,000 logged reports, excluding same-class neighbors listed above. Counts reflect reporting volume, not proven individual harm.

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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 1,275 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 are separate source-record fields. This page is a public FDA/CMS registry and does not provide medical, treatment, substitution, or medication-change directions.

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. This registry does not provide medication decisions.

Last updated: December 9, 2025

PlainMeds is rendered directly from FDA openFDA/FAERS extracts, DailyMed labels, and CMS drug-pricing files, no number is typed in by an editor. FAERS counts, recalls, shortages, and price figures on this page are queried live from those federal extracts. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of 2026-05-15. Primary sources: openFDA / FAERS, DailyMed and CMS Part B ASP.

Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled from the source snapshot dated . See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a data issue.

All federal data sources used on this page