Prescription medication · Thyroid Hormone (T3)

liothyronine

Also sold as Cytomel. This medicine treats hypothyroidism, a condition where your thyroid gland doesn't make enough thyroid hormone.

Data updated 2026-05-15

8,408
FDA reportsLightly reported
17
InteractionsSeveral interactions
47% less
Generic vs brandReal savings
$0.51
Brand price (NADAC)

What the data shows

liothyronine (Cytomel) is a prescription Thyroid Hormone (T3), reported less often than most tracked drugs (8,408 FDA reports), with a lower-cost generic available (47% less than brand).

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.

liothyronine (Cytomel) is a prescription Thyroid Hormone (T3). This medicine treats hypothyroidism, a condition where your thyroid gland doesn't make enough thyroid hormone.

Liothyronine (Cytomel) is a medicine that replaces a thyroid hormone called T3. It helps your body work properly if you don't make enough thyroid hormone on your own.

Drug Pricing (NADAC)

Brand Price

$0.51/unit

Generic Price

$0.27/unit

Generic Savings

47%

Generic Available

Yes (7 manufacturers)

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

Compare with Another Drug → Full Side Effects Report →

What it does

This medicine treats hypothyroidism, a condition where your thyroid gland doesn't make enough thyroid hormone.

Common side effects

Fatigue, Increased appetite, Weight loss

Key warnings

This medicine should not be used for weight loss or to treat obesity.

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

How It Works

Liothyronine is a synthetic form of the T3 thyroid hormone. It works by increasing thyroid hormone levels in your body. This helps to regulate your body's metabolism and energy levels.

Side Effects (from patient reports)

Based on 8,408 FDA adverse event reports.

Most-reported reactions

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

02004006008001,000 20042007201020132016201920222025 414

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

Where liothyronine sits

liothyronine has more FDA adverse-event reports than 35% 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 liothyronine; the line is the median (50th percentile).

FDA Adverse Event Report Analysis

Detailed analysis of 8,408 reports from the FDA Adverse Event Reporting System (FAERS). Reports span 2004–2025.

Total Reports

8,408

Reports Mentioning Death

195

2.3% of reports — not proof of cause

Hospitalization Reports

1,457

Top Indication

Product Used For Unknown Indication

Gender Distribution

Female 6,866 (89%)
Male 852 (11%)

Age Distribution

0–17 62
18–44 827
45–64 2,556
65–74 868
75+ 393

Most Reported Adverse Reactions (FAERS)

# Reaction Reports
2 HEADACHE 859
3 FATIGUE 816
4 NAUSEA 569
5 DYSPNOEA 549
6 PAIN 469
7 HYPERTENSION 461
8 MALAISE 431
9 WEIGHT INCREASED 431
10 HYPOTHYROIDISM 426
11 FEELING ABNORMAL 411
12 DIZZINESS 385
13 DIARRHOEA 374
15 ASTHMA 354
16 INSOMNIA 351
17 GASTROOESOPHAGEAL REFLUX DISEASE 350

Reactions in Death Reports

DEATH 92
COMPLETED SUICIDE 23
DYSPNOEA 15
FALL 13
TOXICITY TO VARIOUS AGENTS 12
NAUSEA 10
PYREXIA 9
SEPSIS 9
CARDIAC ARREST 8
ATRIAL FIBRILLATION 7

Reactions in Hospitalization Reports

HEADACHE 317
HYPERTENSION 281
DYSPNOEA 268
HYPOTHYROIDISM 243
ASTHMA 240
CARDIAC DISORDER 238
GASTROOESOPHAGEAL REFLUX DISEASE 227
BURNING SENSATION 222
THERAPEUTIC PRODUCT EFFECT INCOMPLETE 222
FIBROMYALGIA 219

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

Serious Warnings

This medicine should not be used for weight loss or to treat obesity. Taking high doses of thyroid hormone for weight loss can cause serious and life-threatening side effects, especially when taken with stimulant medicines.

Known Drug Interactions

Other drugs: Amiodarone Amiodarone inhibits peripheral conversion of levothyroxine (T4) to triiodothyronine (T3) and may cause isolated biochemical changes (increase in serum free-T4, and decreased or normal free-T3) in clinically euthyroid patients.

Mechanism: This interaction can stop your body from turning one type of thyroid hormone into another, which can change your blood test results.

Administration of sertraline in patients stabilized on liothyronine sodium tablets may result in increased liothyronine sodium tablets requirements.

Mechanism: This antidepressant can lower the effectiveness of your thyroid medicine, meaning your body might need a higher dose.

Other drugs: Carbamazepine Furosemide (>80 mg IV) Heparin Hydantoins Non-Steroidal Anti-inflammatory Drugs - Fenamates These drugs may cause protein binding site displacement. Furosemide has been shown to inhibit the protein binding of T4 to TBG and albumin, causing an increased free-T4 fraction in serum. Furosemide competes for T4-binding sites on TBG, prealbumin, and albumin, so that a single high dose can acutely lower the total T4 level.

Mechanism: This water pill can knock thyroid hormones off the proteins they usually ride on in your blood, which changes the amount of active hormone in your body.

Drug or Drug Class Effect Beta-adrenergic antagonists (e.g., Propranolol >160 mg/day) In patients treated with large doses of propranolol (>160 mg/day), T3 and T4 levels change, TSH levels remain normal, and patients are clinically euthyroid.

Mechanism: Taking high doses of this blood pressure medicine can change the amount of thyroid hormones found in your blood.

7.5 Antidepressant Therapy Concurrent use of tricyclic (e.g., amitriptyline) or tetracyclic (e.g., maprotiline) antidepressants and liothyronine sodium tablets may increase the therapeutic and toxic effects of both drugs, possibly due to increased receptor sensitivity to catecholamines.

Mechanism: Using these two drugs together can make both of them more powerful and increase the risk of side effects.

Check all your medications →

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

Common Questions

Can I use this medicine for weight loss?
No, this medicine should not be used for weight loss.
What should I do if I experience chest pain?
Tell your doctor right away if you experience chest pain or other heart problems.
How often will my doctor check my thyroid levels?
Your doctor will check your thyroid levels regularly to make sure you are on the right dose.
Can this medicine affect my blood sugar if I have diabetes?
Yes, this medicine can affect your blood sugar. If you have diabetes, monitor your blood sugar levels closely.
What are the symptoms of taking too much of this medicine?
Symptoms of taking too much include fast heartbeat, nervousness, and weight loss.
Can I take this medicine with other medications?
Tell your doctor about all the medicines you take, including over-the-counter medicines and supplements.
What if I have heart disease?
If you have heart disease, your doctor will start you on a lower dose and monitor you closely.
Can this medicine cause bone loss?
Taking too much of this medicine can cause bone loss.
Is it safe to take this medicine during breastfeeding?
This medicine passes into breast milk, but it is not expected to harm your baby.
What happens if I stop taking this medicine?
Stopping this medicine without talking to your doctor can cause your thyroid levels to drop.
What are the common side effects of liothyronine?
The registry lists Fatigue, Increased appetite, Weight loss, Feeling hot, Fever among the most-reported FAERS reaction terms for liothyronine. The compiled record contains 8,408 FDA adverse-event reports. These counts are not an individual symptom assessment.
Does liothyronine interact with other medications?
The registry has 17 documented interaction rows for liothyronine. Notable source-record pairings include levothyroxine, sertraline, furosemide. These rows are not a complete medication review.
What drug class is liothyronine?
liothyronine belongs to the Thyroid Hormone (T3) drug class. It requires a prescription (Rx). This medicine treats hypothyroidism, a condition where your thyroid gland doesn't make enough thyroid hormone.
Is there a generic version of liothyronine?
Yes, generic liothyronine is available from 7 manufacturers. The generic costs $0.27 per unit compared to $0.51 for the brand version, saving approximately 47%. Pricing is based on NADAC (National Average Drug Acquisition Cost) data from CMS.
What pregnancy or breastfeeding source fields are listed for liothyronine?
The FDA label for liothyronine contains product-specific pregnancy or breastfeeding language. PlainMeds does not apply that source text to an individual.

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

Compare liothyronine vs levothyroxine side-by-side →

Compare beyond drug class

Nationwide peers by FAERS volume & death-report share

Two PlainMeds-derived comparison paths for liothyronine: 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.

Medication Guides

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What the FDA Data Shows for liothyronine

The FDA label for liothyronine (sold under brand names such as Cytomel) classifies it as a prescription-only medication in the Thyroid Hormone (T3) class. This medicine treats hypothyroidism, a condition where your thyroid gland doesn't make enough thyroid hormone. Official labeling lists 18 commonly reported side effects, including Fatigue, Increased appetite, Weight loss.

Post-market surveillance from the FDA Adverse Event Reporting System (FAERS) captures real-world experience. For this drug, FAERS contains 8,408 voluntary reports. The database also lists 17 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 $0.27 versus $0.51 for the brand - a 47% generic savings.

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).

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: March 15, 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