Tamoxifen
An FDA-approved selective estrogen receptor modulator used to treat hormone receptor-positive breast cancer.
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Publication suitability · 2026-10-15: Historical reference only; not a clinical verification.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.
Tamoxifen
An FDA-approved selective estrogen receptor modulator used to treat hormone receptor-positive breast cancer.
Evidence category: Regulator / guideline. This describes the source category, not approval or certainty.
Regulatory statement in source: FDA-approved.
Tamoxifen was the first selective estrogen receptor modulator (SERM) approved by the FDA in 1977. It reduces cancer recurrence risk by 50% during the first 5 years and 33% during years 5-9 in estrogen receptor-positive early breast cancer. FDA-approved for early breast cancer, ductal carcinoma in situ, and risk reduction in high-risk women.
Benefits reported in the imported source
- Reducing recurrence and death in early-stage ER+ breast cancer.
- DCIS and risk reduction in high-risk women.
Risks and limits
- Endometrial cancer risk
- Thromboembolic events
- Hot flashes
- Sexual dysfunction
Source bottom line: First SARM approved by FDA with robust evidence of benefit in hormone receptor-positive breast cancer.
Uncertainty: Reference information only. Not medical advice.
Study protocols — reports, not instructions
Women with estrogen receptor-positive early breast cancer
- Reported regimen
- Median 5 years of tamoxifen therapy
- Duration
- 5 years; extended therapy studied
- Reported outcome
- 50% reduction in recurrence risk during years 1-5; 33% reduction during years 5-9
- Source
- Treating ER-positive breast cancer: SERMs and SERDs review (availability check 2026-10-15: possible access barrier; not independently inspected; HTTP 200)
Claim provenance
evidence.json#/catalog:hormone:tamoxifen/protocols/0
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.
Unverified imported account — Nolvadex (Tamoxifen Citrate) - EliteFitness Steroid Profiles
An imported authored paraphrase, not a quotation or a recommended protocol.
Review: unverified historical account. The imported wording is preserved for attribution; its full clinical, dosing, efficacy or consensus claims have not been independently established. Unvalidated source account; no validated human dosing population or animal-to-human equivalence is inferred.
Imported wording: A steroid community profile documents post-cycle use at 10 mg daily for males (sufficient to prevent estrogenic side effects) and 25 mg daily for females, with initiation 3-4 weeks after anabolic steroid use, with general dosing at 10-30 mg daily.
Nolvadex (Tamoxifen Citrate) - EliteFitness Steroid Profiles
Pharmacokinetic context
Historical half-life estimate: 120–168 hours. FDA label, tamoxifen citrate: terminal elimination half-life 5 to 7 days Population/route context and estimates may differ. This is not a schedule or a verified human dosing rule.
Source references
- DailyMed: tamoxifen
- Use of SERMs for Adjuvant Therapy - Johns Hopkins University
- Tamoxifen - StatPearls (availability check 2026-10-15: possible access barrier; not independently inspected; HTTP 200)
- Treating ER-positive breast cancer: SERMs and SERDs review (availability check 2026-10-15: possible access barrier; not independently inspected; HTTP 200)
Snapshot provenance
Source ID: catalog:hormone:tamoxifen. 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.