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.
Verify with FDA → · CMS NADAC pricing →
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 →
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.
How to Take It
Take tranylcypromine by mouth. The usual starting dose is 30 mg per day, divided into smaller doses. If needed, your doctor may increase the dose by 10 mg every 1 to 3 weeks. The maximum dose is 60 mg per day, divided into two doses.
This is a plain-language summary of tranylcypromine's FDA labeling, not individualized dosing advice. Ask a pharmacist or prescriber before changing how you take this medication.
Pregnancy & Breastfeeding
There is limited information about the safety of tranylcypromine during pregnancy. Talk to your doctor if you are pregnant or plan to become pregnant. It is not recommended to breastfeed while taking this medicine because it can harm the baby.
This is a plain-language summary of tranylcypromine's FDA labeling, not individualized advice. Ask a pharmacist or prescriber about pregnancy or breastfeeding on this medication.
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.
This is a plain-language summary of tranylcypromine's FDA labeling, not individualized advice. Ask a pharmacist or prescriber what to do about your specific missed dose.
Storage
Store tranylcypromine at room temperature, between 59° and 86°F (15° and 30°C), in a tightly closed, light-resistant container.
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
- Interaction between medicines
Interaction between medicines
68 reports
- Feeling sad or hopeless
Feeling sad or hopeless
36 reports
- Too much serotonin in the body 27
Too much serotonin in the body
27 reports
- Head pain 24
Head pain
24 reports
- High blood pressure 24
High blood pressure
24 reports
- Thoughts of suicide 24
Thoughts of suicide
24 reports
- Heart defect 23
Heart defect
23 reports
- Dangerous increase in blood pressure 23
Dangerous increase in blood pressure
23 reports
- Taking a medicine you shouldn't 22
Taking a medicine you shouldn't
22 reports
- Abnormal body shape 22
Abnormal body shape
22 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.
Reports over time
Adverse-event reports filed for tranylcypromine each year to the FDA Adverse Event Reporting System (FAERS).
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.
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
Age Distribution
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
Reactions in Hospitalization Reports
Source: FDA FAERS (Adverse Event Reporting System) 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.
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.
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.
What to do: Avoid this combination unless it is an emergency and no other options exist. If used together, you must stop tranylcypromine and be monitored very closely by medical staff.
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.
What to do: Do not take these medications together. Your doctor will typically require a waiting period of at least 14 days when switching between them.
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.
What to do: Avoid this combination unless it is a medical emergency. If used in an emergency, a doctor must monitor your blood pressure and heart rate very closely.
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.
What to do: Avoid using these drugs at the same time. If they must be used in a hospital setting, your vital signs must be monitored constantly by medical staff.
This is a plain-language summary of interactions documented in FDA labeling, not individualized advice. Ask a pharmacist or prescriber before combining medications.
Common Questions
Can I start tranylcypromine right after stopping another antidepressant?
What foods should I avoid while taking tranylcypromine?
Can I take over-the-counter medicines with tranylcypromine?
What should I do if I experience a severe headache while taking tranylcypromine?
Can tranylcypromine cause problems if I need surgery?
Will this medicine make me gain weight?
Can I drink alcohol while taking tranylcypromine?
What are the signs of a hypertensive crisis?
Is tranylcypromine safe for children and teenagers?
What should I do if I feel my depression is getting worse?
What are the common side effects of tranylcypromine?
Does tranylcypromine interact with other medications?
What drug class is tranylcypromine?
Is tranylcypromine safe during pregnancy?
Is tranylcypromine currently in shortage?
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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 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 20, 2024
Read our methodology - how this data is sourced, computed, and verified.
Data currency: FDA FAERS adverse-event reports through 2025, CMS NADAC acquisition-cost pricing effective December 2024, compiled and last refreshed May 2026. See our methodology for per-source dates and refresh cadence. Spot a figure that looks wrong? Report a correction.
All federal data sources used on this page
- FDA Orange Book - approved drug products with therapeutic equivalence. accessdata.fda.gov/cder/ob
- FDA DailyMed - NIH-hosted drug labeling for FDA-approved meds. dailymed.nlm.nih.gov
- FDA Adverse Event Reporting System (FAERS) - post-marketing safety surveillance. fda.gov/drugs/faers
- NLM RxNorm - standardized clinical drug nomenclature. nlm.nih.gov/research/umls/rxnorm
- CMS Medicare Part B Drug Average Sales Price Files - federal drug pricing data. cms.gov/medicare/part-b-drugs/asp
- FDA Drug Shortages Database - current and resolved drug shortage tracking. accessdata.fda.gov/drugshortages