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Oestradiol

Oestrogen used in feminising HRT and menopausal HRT. Available as tablets, patches, gel and injectable esters.

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Publication suitability · 2026-10-15: Historical reference only; not a clinical verification.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.

Oestradiol

Oestrogen used in feminising HRT and menopausal HRT. Available as tablets, patches, gel and injectable esters.

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

Regulatory statement in source: FDA-approved.

Oestradiol is an approved oestrogen medicine with an FDA prescribing label. The label covers menopausal symptoms and other conditions linked to low oestrogen. In February 2026 the FDA approved labelling changes for six menopausal hormone therapy products, removing boxed-warning statements about cardiovascular disease, breast cancer and probable dementia. This is regulator-level information rather than new trial evidence.

Benefits reported in the imported source

  • Treats menopausal symptoms.
  • Labelled as replacement in female hypoestrogenism due to hypogonadism.
  • In February 2026 the FDA removed boxed warnings on heart disease, cancer and dementia from six products.

Risks and limits

  • The label still carries boxed warnings on endometrial cancer and cardiovascular risk.
  • The 2026 change is a regulatory labelling decision, not new trial evidence.

Source bottom line: Oestradiol is an FDA-approved oestrogen for menopausal and low-oestrogen conditions, with boxed warnings.

Uncertainty: Reference information only. Not medical advice.

Study protocols — reports, not instructions

women with moderate to severe vasomotor symptoms of the menopause, per the US Depo-Estradiol label

Reported regimen
1 to 5 mg estradiol cypionate injected intramuscularly every 3 to 4 weeks
Duration
short-term cyclic use, with attempts to stop or taper at 3- to 6-month intervals
Reported outcome
The label lists this as the approved regimen for menopausal vasomotor symptoms and carries boxed warnings on endometrial cancer and cardiovascular risk.
Source
Depo-Estradiol (estradiol cypionate injection) FDA Label
Claim provenance

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

women with hypoestrogenism due to hypogonadism, per the US Depo-Estradiol label

Reported regimen
1.5 to 2 mg estradiol cypionate injected intramuscularly at monthly intervals
Duration
ongoing, per the label, with reassessment at 3- to 6-month intervals
Reported outcome
The label lists this as the approved regimen for female hypoestrogenism due to hypogonadism.
Source
Depo-Estradiol (estradiol cypionate injection) FDA Label
Claim provenance

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

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

No half-life recorded in this source snapshot. No value has been inferred.

Source references

Snapshot provenance

Source ID: catalog:hormone:estradiol. 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.