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Liothyronine (T3)

Synthetic T3. Short half-life, so it is often split across the day rather than taken once.

Medications & hormones

Research records

Historical source snapshot. Not freshly verified, not a recommendation. Study findings, community accounts and app defaults are not interchangeable.

Publication suitability · 2026-10-15: Historical reference only; not a clinical verification. Clinical, regulatory, efficacy, safety and dose claims are not independently established by this review.

Liothyronine (T3)

Synthetic T3. Short half-life, so it is often split across the day rather than taken once.

Evidence category: Regulator / guideline. This describes the source category, not approval or certainty.

Regulatory statement in source: FDA-approved.

Liothyronine is synthetic T3 with an FDA-approved label (Cytomel). It is approved as replacement in hypothyroidism, as an adjunct in managing well-differentiated thyroid cancer by suppressing TSH, and as a diagnostic agent in thyroid suppression tests. The label carries a boxed warning that thyroid hormones must not be used for obesity or weight loss, and that amounts beyond hormonal needs can cause serious toxicity.

Benefits reported in the imported source

  • Replacement therapy in hypothyroidism.
  • An adjunct in well-differentiated thyroid cancer, by suppressing TSH.
  • A diagnostic agent in thyroid suppression tests.

Risks and limits

  • A boxed warning states thyroid hormones must not be used for obesity or weight loss.
  • The label warns that amounts beyond hormonal needs can cause serious toxicity.

Source bottom line: Liothyronine is FDA-approved thyroid hormone replacement, with a boxed warning against use for weight loss.

Uncertainty: Reference information only. Not medical advice.

Study protocols — reports, not instructions

Adults with hypothyroidism, per the US label

Reported regimen
25 mcg orally once daily to start, increased by 25 mcg daily every 1 or 2 weeks; usual maintenance 25 mcg to 75 mcg once daily
Duration
Ongoing, per the label
Reported outcome
Approved as replacement therapy in hypothyroidism; the label's boxed warning states thyroid hormones must not be used for obesity or weight loss.
Source
Liothyronine sodium tablets FDA prescribing information
Claim provenance

evidence.json#/catalog:hormone:liothyronine/protocols/0

People with well-differentiated thyroid cancer needing TSH suppression, per the US label

Reported regimen
Dose targeted to keep TSH within the desired therapeutic range, which the label says may require higher doses
Duration
Ongoing, per the label
Reported outcome
Approved as an adjunct to surgery and radioiodine in managing well-differentiated thyroid cancer.
Source
Liothyronine sodium tablets FDA prescribing information
Claim provenance

evidence.json#/catalog:hormone:liothyronine/protocols/1

People undergoing a thyroid suppression test, per the US label

Reported regimen
75 mcg to 100 mcg daily, with radioactive iodine uptake measured before and after the administration
Duration
7 days
Reported outcome
Approved as a diagnostic agent in thyroid suppression tests.
Source
Liothyronine sodium tablets FDA prescribing information
Claim provenance

evidence.json#/catalog:hormone:liothyronine/protocols/2

Community and practice descriptions

Accounts of a practice are not evidence of safety or effectiveness. Words such as “standard”, “safe” or “recommended” describe the source account, not verified consensus or this wiki’s advice. Commercial and self-published citations are retained for traceability, not vendor endorsement or independent clinical corroboration.

Pharmacokinetic context

Historical half-life estimate: 60 hours. FDA label, Cytomel: biological half-life about 2 1/2 days Population/route context and estimates may differ. This is not a schedule or a verified human dosing rule.

Source references

Snapshot provenance

Source ID: catalog:hormone:liothyronine. Commit: adc7684614f9439b41d91a3312b62e7982c7e20e. Review state: historical-not-reverified. Authored links are retained separately from the canonical evidence links in the public data. App templates/defaults and rejected drafts are archived, not deployed.

Related entries and components

None listed.