Prescription medication · Monoamine Oxidase Inhibitor (MAOI)

tranylcypromine

Also sold as Parnate. Tranylcypromine is used to treat major depressive disorder (MDD) in adults.

Data updated 2026-05-15

329
FDA reportsRarely reported
42
InteractionsMany interactions
In shortage
FDA status

What the data shows

tranylcypromine (Parnate) is a prescription Monoamine Oxidase Inhibitor (MAOI), among the least-reported drugs the FDA tracks (329 FDA reports), with 42 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.

tranylcypromine (Parnate) is a prescription Monoamine Oxidase Inhibitor (MAOI). Tranylcypromine is used to treat major depressive disorder (MDD) in adults.

Tranylcypromine (Parnate) is a medicine used to treat major depression in adults. It is used when other antidepressants have not worked well enough.

Drug Shortage Alert

tranylcypromine 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

$0.70/unit

Generic Available

Yes (3 manufacturers)

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

NADAC price trail: TRANYLCYPROMINE SULF 10 MG TAB

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: -14.5% vs prior release.

Effective NADAC / unit vs prior NDCs
February 21, 2024 $0.8192/EA - 1
December 18, 2024 $0.7003/EA -14.5% 5
View Alternatives → Compare with Another Drug → Full Side Effects Report →

What it does

Tranylcypromine is used to treat major depressive disorder (MDD) in adults.

Common side effects

Dry mouth, Dizziness, Trouble sleeping

Key warnings

Tranylcypromine can increase the risk of suicidal thoughts and behaviors in young adults.

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

How It Works

Tranylcypromine belongs to a class of drugs called MAO inhibitors. It works by increasing the levels of certain chemicals in your brain. These chemicals can help improve your mood.

Side Effects (from patient reports)

Based on 329 FDA adverse event reports.

Most-reported reactions

Adverse reactions in FAERS for tranylcypromine, 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 tranylcypromine each year to the FDA Adverse Event Reporting System (FAERS).

0204060 2004201220152018202120242025 25

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

Where tranylcypromine sits

tranylcypromine has more FDA adverse-event reports than 2% 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 tranylcypromine; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 329 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

329

Reports Mentioning Death

49

14.9% of reports — not proof of cause

Hospitalization Reports

116

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 170 (63%)
Male 95 (35%)

Age Distribution

0–17 3
18–44 58
45–64 86
65–74 40
75+ 34

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
1 DRUG INTERACTION 68
2 DEPRESSION 36
4 SEROTONIN SYNDROME 27
5 HEADACHE 24
6 HYPERTENSION 24
7 SUICIDAL IDEATION 24
8 ATRIOVENTRICULAR SEPTAL DEFECT 23
9 HYPERTENSIVE CRISIS 23
10 CONTRAINDICATED PRODUCT ADMINISTERED 22
11 DYSMORPHISM 22
12 HYPERHIDROSIS 22
13 MUSCLE SPASMS 21
14 INSOMNIA 20
15 NAUSEA 20
16 FOETAL EXPOSURE DURING PREGNANCY 19

Reactions in Death Reports

COMPLETED SUICIDE 18
DYSMORPHISM 12
ATRIOVENTRICULAR SEPTAL DEFECT 11
FOETAL EXPOSURE DURING PREGNANCY 10
DRUG INTERACTION 9
FOETAL DEATH 8
HYPERTHERMIA 7
SEROTONIN SYNDROME 7
TOXICITY TO VARIOUS AGENTS 7
HYPERTELORISM OF ORBIT 6

Reactions in Hospitalization Reports

DRUG INTERACTION 20
DEPRESSION 18
SEROTONIN SYNDROME 14
HYPERTENSION 13
HYPERTENSIVE CRISIS 13
BLOOD PRESSURE FLUCTUATION 12
CONTRAINDICATED PRODUCT ADMINISTERED 11
OVERDOSE 11
COMPLETED SUICIDE 10
HEADACHE 10

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

Serious Warnings

Tranylcypromine can increase the risk of suicidal thoughts and behaviors in young adults. It can also cause a dangerous increase in blood pressure if you eat foods high in tyramine or take certain medicines. Make sure to follow all food and drug restrictions.

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,...

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.

If in the absence of therapeutic alternatives and emergency treatment with a contraindicated drug (e.g., linezolid, intravenous methylene blue, direct-acting sympathomimetic drugs such as epinephrine) becomes necessary and cannot be delayed, discontinue tranylcypromine tablets as soon as possible before initiating treatment with the other agent, and monitor closely for adverse reactions. 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...

Mechanism: Both drugs act as MAO inhibitors, and using them together can cause a toxic buildup of chemicals in the brain. This can lead to a medical emergency with very high blood pressure.

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,...

Mechanism: Both drugs increase serotonin levels in the brain, which can lead to a dangerous and life-threatening condition called serotonin syndrome.

If in the absence of therapeutic alternatives and emergency treatment with a contraindicated drug (e.g., linezolid, intravenous methylene blue, direct-acting sympathomimetic drugs such as epinephrine) becomes necessary and cannot be delayed, discontinue tranylcypromine tablets as soon as possible before initiating treatment with the other agent, and monitor closely for adverse reactions. 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...

Mechanism: Tranylcypromine prevents the body from breaking down epinephrine, which can cause a sudden and dangerously high spike in blood pressure.

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,...

Mechanism: This combination stops the body from clearing norepinephrine, which can cause blood pressure to rise to levels that may cause a stroke or heart attack.

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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 start tranylcypromine right after stopping another antidepressant?
No, you need to wait a certain amount of time. This could be from 1 week to 5 weeks, depending on the other antidepressant. Talk to your doctor.
What foods should I avoid while taking tranylcypromine?
You should avoid foods high in tyramine, such as aged cheeses, cured meats, and fermented foods.
Can I take over-the-counter medicines with tranylcypromine?
You should talk to your doctor or pharmacist before taking any over-the-counter medicines or supplements.
What should I do if I experience a severe headache while taking tranylcypromine?
A severe headache could be a sign of a hypertensive crisis. Seek immediate medical attention.
Can tranylcypromine cause problems if I need surgery?
Yes, it can affect your blood pressure during surgery. If possible, stop taking tranylcypromine before elective surgery.
Will this medicine make me gain weight?
Weight gain is a possible side effect, but significant anorexia (loss of appetite) is also possible.
Can I drink alcohol while taking tranylcypromine?
You should avoid alcohol, as it can interact with tranylcypromine and cause dangerous side effects.
What are the signs of a hypertensive crisis?
Signs include severe headache, stiff neck, nausea, vomiting, sweating, and very high blood pressure.
Is tranylcypromine safe for children and teenagers?
No, tranylcypromine is not approved for use in children and teenagers.
What should I do if I feel my depression is getting worse?
Tell your doctor right away if you feel your depression is getting worse or if you have thoughts of harming yourself.
What are the common side effects of tranylcypromine?
The registry lists Dry mouth, Dizziness, Trouble sleeping, Feeling sleepy, Headache among the most-reported FAERS reaction terms for tranylcypromine. The compiled record contains 329 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does tranylcypromine interact with other medications?
The registry has 42 documented interaction rows for tranylcypromine. Notable source-record pairings include bupropion, linezolid, vilazodone. These rows are not a complete medication review.
What drug class is tranylcypromine?
tranylcypromine belongs to the Monoamine Oxidase Inhibitor (MAOI) drug class. It requires a prescription (Rx). Tranylcypromine is used to treat major depressive disorder (MDD) in adults.
What pregnancy or breastfeeding source fields are listed for tranylcypromine?
The FDA label for tranylcypromine contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.
Is tranylcypromine currently in shortage?
Yes, tranylcypromine 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.

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

Compare tranylcypromine vs acamprosate side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for tranylcypromine: 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 tranylcypromine

The FDA label for tranylcypromine (sold under brand names such as Parnate) classifies it as a prescription-only medication in the Monoamine Oxidase Inhibitor (MAOI) class. Tranylcypromine is used to treat major depressive disorder (MDD) in adults. Official labeling lists 9 commonly reported side effects, including Dry mouth, Dizziness, Trouble sleeping.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 329 voluntary reports. The database also lists 42 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 $0.70.

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 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 20, 2024

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