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nortriptyline

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Brand names: Pamelor

Tricyclic Antidepressant (TCA) Rx

Nortriptyline (Pamelor) is a medicine used to treat depression. It can help improve your mood.

Drug Shortage Alert

nortriptyline is currently listed as to be discontinued by the FDA. Affected manufacturer: Teva Pharmaceuticals USA, Inc..

View all drug shortages →

Drug Pricing (NADAC)

Generic Price

$0.30/unit

Generic Available

Yes (6 manufacturers)

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

What it does

Nortriptyline is used to relieve the symptoms of depression.

Common side effects

Dry mouth, Blurred vision, Constipation

Key warnings

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

How It Works

Nortriptyline is a tricyclic antidepressant (TCA). It works by increasing the levels of certain natural chemicals in the brain. These chemicals help regulate mood.

How to Take It

Take nortriptyline capsules by mouth. Adults usually take 25 mg three or four times daily. Your doctor may adjust your dose as needed. You can also take your total daily dose once a day if your doctor approves.

Pregnancy & Breastfeeding

Tell your doctor if you are pregnant, plan to become pregnant, or are breastfeeding. Nortriptyline may not be safe for your baby. Talk to your doctor about the risks and benefits.

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 continue with your regular schedule.

Storage

Store nortriptyline capsules at room temperature (68° to 77°F) in a tight, child-resistant container.

Side Effects (from patient reports)

Based on 5,736 FDA adverse event reports.

The medicine is not working
777
Using the medicine for something it's not approved for
705
Pain
695
Headache
679
Tiredness
594
Feeling sick to your stomach
514
Increased sweating
485
Allergic reaction
460
Allergic reaction to the medicine
430
High blood pressure
397

FDA Adverse Event Report Analysis

Detailed analysis of 5,503 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

5,503

Death-Related Reports

674

Hospitalization Reports

1,439

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 3,671 (75%)
Male 1,179 (24%)

Age Distribution

0–17 53
18–44 852
45–64 1,575
65–74 500
75+ 292

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 DRUG INEFFECTIVE 777
2 OFF LABEL USE 705
3 PAIN 695
4 HEADACHE 679
5 FATIGUE 593
6 NAUSEA 513
7 HYPERHIDROSIS 485
8 HYPERSENSITIVITY 460
9 DRUG HYPERSENSITIVITY 430
10 HYPERTENSION 396
11 CONSTIPATION 395
12 RHEUMATOID ARTHRITIS 388
13 HEPATIC ENZYME INCREASED 383
14 OVERDOSE 374
15 BACK PAIN 365

Reactions in Death Reports

COMPLETED SUICIDE 203
OVERDOSE 131
PAIN 110
TOXICITY TO VARIOUS AGENTS 110
OFF LABEL USE 109
HYPERTENSION 105
PYREXIA 104
THROMBOCYTOPENIA 104
DRUG INEFFECTIVE 103
FATIGUE 103

Reactions in Hospitalization Reports

SOMNOLENCE 226
GASTROOESOPHAGEAL REFLUX DISEASE 214
COMA 199
PNEUMONIA ASPIRATION 195
DRUG INEFFECTIVE 176
PAIN 175
NAUSEA 170
FATIGUE 148
DIARRHOEA 146
FALL 133

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, teenagers, and young adults. Your doctor will monitor you closely for worsening depression or unusual changes in behavior. Families and caregivers should also watch for these changes.

Known Drug Interactions

( 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 the enzyme that clears nortriptyline from your body, which can cause nortriptyline levels to rise.

What to do: Your doctor may need to lower your dose of nortriptyline and monitor you more closely for side effects.

In addition, carbamazepine causes, or would be expected to cause, decreased levels of the following drugs, for which monitoring of concentrations or dosage adjustment may be necessary: acetaminophen, albendazole, alprazolam, aprepitant, buprenorphone, bupropion, citalopram, clonazepam, clozapine, corticosteroids (e.g., prednisolone, dexamethasone), cyclosporine, dicumarol, dihydropyridine calcium channel blockers (e.g., felodipine), doxycycline, ethosuximide, everolimus, haloperidol, imatinib, itraconazole, lamotrigine, levothyroxine, methadone, methsuximide, mianserin, midazolam, olanzapin...

Mechanism: Carbamazepine speeds up how your body breaks down nortriptyline, which can lower the amount of medicine in your blood.

What to do: Your doctor may need to adjust your dose or check your blood levels to make sure the medicine is still working.

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 body's ability to get rid of this antidepressant, leading to higher levels in your blood. This can cause side effects like nausea, dizziness, and fainting.

What to do: Your doctor should use a lower dose of nortriptyline and watch you for signs of low blood pressure or dizziness.

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

Mechanism: Nortriptyline makes the body more reactive to dopamine's effects. This can result in a much stronger effect on your blood pressure than intended.

What to do: Your doctor should monitor your heart and blood pressure frequently. They might need to adjust your dopamine dose.

Amitriptyline, nortriptyline : Fluconazole increases the effect of amitriptyline and nortriptyline. 5-Nortriptyline and/or S-amitriptyline may be measured at initiation of the combination therapy and after 1 week. Dosage of amitriptyline/nortriptyline should be adjusted, if necessary.

Mechanism: Fluconazole slows down how the body breaks down nortriptyline, which causes the drug to stay in the system longer.

What to do: Your doctor may need to check your blood levels and adjust your dose when starting this combination.

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Common Questions

Can children take nortriptyline?
Nortriptyline is not recommended for children.
What should I do if I experience side effects?
If you experience minor side effects, your doctor may lower your dose. If you experience serious side effects, stop taking the medicine and contact your doctor immediately.
Can I take nortriptyline with other medications?
Tell your doctor about all the medications you take, including over-the-counter drugs and supplements. Do not take nortriptyline with MAOIs.
How long does it take for nortriptyline to work?
It may take several weeks for nortriptyline to start working. Continue taking the medicine as prescribed, even if you do not feel better right away.
Can I stop taking nortriptyline suddenly?
Do not stop taking nortriptyline suddenly. This can cause withdrawal symptoms. Talk to your doctor about how to gradually stop taking the medicine.
What is serotonin syndrome?
Serotonin syndrome is a serious condition that can occur if you take nortriptyline with certain other medications. Symptoms include agitation, hallucinations, rapid heartbeat, and fever.
Can nortriptyline cause weight changes?
Nortriptyline can cause weight gain or weight loss in some people.
Can nortriptyline affect my heart?
Nortriptyline can cause heart problems, such as changes in heart rate or blood pressure. Tell your doctor if you have a history of heart problems.
Can nortriptyline cause confusion?
Nortriptyline can cause confusion, especially in elderly people.
Is it safe to drive while taking nortriptyline?
Nortriptyline can cause drowsiness or dizziness. Be careful driving or operating machinery until you know how the medicine affects you.
What are the common side effects of nortriptyline?
The most commonly reported side effects of nortriptyline include Dry mouth, Blurred vision, Constipation, Drowsiness, Dizziness. Based on 5,736 FDA adverse event reports. Always consult your healthcare provider about potential side effects.
Does nortriptyline interact with other medications?
Yes, nortriptyline has 8 known drug interactions. Notable interactions include bupropion, carbamazepine, darunavir. Always inform your doctor about all medications you are taking.
What drug class is nortriptyline?
nortriptyline belongs to the Tricyclic Antidepressant (TCA) drug class. It requires a prescription (Rx). Nortriptyline is used to relieve the symptoms of depression.
Is nortriptyline safe during pregnancy?
Tell your doctor if you are pregnant, plan to become pregnant, or are breastfeeding. Nortriptyline may not be safe for your baby. Always consult your healthcare provider before using any medication during pregnancy or breastfeeding.
Is nortriptyline currently in shortage?
Yes, nortriptyline is currently listed as to be discontinued by the FDA. Affected manufacturer: Teva Pharmaceuticals USA, Inc.. Visit the FDA Drug Shortages database for the latest updates.

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What the FDA Data Shows for nortriptyline

The FDA label for nortriptyline (sold under brand names such as Pamelor) classifies it as a prescription-only medication in the Tricyclic Antidepressant (TCA) class. Nortriptyline is used to relieve the symptoms of depression. Official labeling lists 10 commonly reported side effects, including Dry mouth, Blurred vision, Constipation.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 5,736 voluntary reports. The database also lists 8 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 $0.30.

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, 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: January 13, 2026

All federal data sources used on this page