Progesterone (Oral)
Prometrium
Half-life
16 hr
Time to Peak
3 hr
Steady State
~4 days
Bioavailability
10%
Dose Range
100–200 mg
Frequency
Daily
Overview
Micronized bioidentical progesterone taken orally. Extensively metabolized by first-pass effect (oral bioavailability ~10%). Major metabolite allopregnanolone is sedating, which is why bedtime dosing is recommended. Used in transfem HRT for breast development (Tanner stage 4-5 progression), mood regulation, and sleep improvement.
Mechanism of Action
Natural progesterone receptor agonist. Oral administration produces significant first-pass metabolism to allopregnanolone (sedating neurosteroid) and other metabolites.
Dosing Information
| Route | Dose Range | Half-life | Tmax | Frequency |
|---|---|---|---|---|
| Oral | 100–200 mg | 16 hr | 3 hr | Daily |
Used in Regimens
10 regimensEV + Bicalutamide Pathway
Estradiol valerate with bicalutamide non-steroidal anti-androgen. Bicalutamide blocks androgen receptors without affecting LH/FSH or testosterone production — testosterone remains high but its effects are blocked. Liver monitoring required. Growing in popularity as a spironolactone and CPA alternative.
Progesterone oral after 3 months.
EV + CPA (European Pathway)
Estradiol valerate injections with low-dose cyproterone acetate (CPA) anti-androgen. Standard in Germany, Netherlands, and much of Europe. CPA at low dose (6.25–12.5mg/day alternate days) provides potent androgen suppression with significantly lower meningioma risk than legacy high doses.
Progesterone oral after 3 months.
EV Injection Monotherapy — DIY Community
Estradiol Valerate injection monotherapy per community consensus: 4–7mg every 5 days (IM) targeting trough E2 >200 pg/mL to suppress testosterone without an anti-androgen. The community-driven approach to transfeminine HRT — higher estradiol targets than clinical guidelines. Every-5-day schedule is community standard; clinical biweekly schedule causes unacceptable level swings.
Add progesterone at Tanner stage 3–4 per Dr Powers recommendation.
EV Monotherapy (High-Dose Clinical)
High-dose estradiol valerate monotherapy targeting oestradiol levels high enough to suppress testosterone without any anti-androgen. Clinical version — biweekly schedule as prescribed. See community regimen C4 for DIY every-5-day variant.
Progesterone oral after 3 months.
Menopause — Combined HRT (Patches + Progesterone)
Standard combined menopausal HRT: oestradiol patches for symptom relief with cyclical or continuous progesterone for endometrial protection. The NICE 2024 menopause guideline recommends transdermal oestradiol as first-line for lower VTE risk vs oral.
Progesterone 100–200mg at bedtime. Continuous or sequential.
NHS Pathway — Patches + GnRH Analogue
NHS Gender Dysphoria Clinic standard pathway: oestradiol patches with goserelin (Zoladex) GnRH analogue for testosterone suppression. Safest VTE risk profile. Goserelin implant every 1 or 3 months administered by GP or GIC nurse.
Progesterone oral after 3 months once E2 stable.
Data Sources
- FDA Label Prometrium (progesterone) FDA Prescribing Information
- Peer-reviewed Kuhl H. Pharmacology of estrogens and progestogens
Related Tools
Track Progesterone (Oral) with Doseline
Reminders, medication level charts, injection site rotation, and protocol tracking — all free, all private.
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