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Pharmaceuticals/Chemicals Human RCT evidence

Progesterone (Oral)

Prometrium · Oral P4

22.8 hours
Half-life
100–300 mg
Typical dose
Chronic or cyclic (HRT); luteal phase (fertility)
Cycle length

Micronized oral progesterone; short half-life with high first-pass metabolism.

Key takeaways

  • FDA-approved for endometrial protection on estrogen therapy; off-label in fertility and feminizing HRT.
  • Heavy first-pass metabolism: only ~10% of the dose reaches blood as progesterone itself.
  • Sedating metabolite allopregnanolone makes bedtime dosing the standard reported pattern.
  • Serum levels stay low even at 200–300 mg, so bloodwork under-represents the clinical effect.
🚧 Expanded guide coming soon. This compound has PK data and a source — a full overview, mechanism, and dosing guide is pending editorial review.

Reported dosing protocols

Protocols reported in research literature and clinic/community use — informational context, not a dosing recommendation.

Use case Dose Route Frequency Duration
Endometrial protection (label) 200 mg Oral Once daily at bedtime 12 days per 28-day cycle
Continuous HRT (off-label) 100 mg Oral Once daily at bedtime Ongoing

Pharmacokinetic summary

Model tier
Advanced (t½ + Cmax + Tmax + F)
Half-life
22.8 hours
Cmax
169.53 ng/mL
Tmax
0.1 days
Bioavailability
10%
Typical dose
100–300 mg

Frequently asked questions

Why is oral progesterone taken at bedtime?

First-pass metabolism converts a large share of the dose into allopregnanolone, a sedating neurosteroid. Bedtime dosing turns that drowsiness into a sleep benefit instead of a daytime problem.

Does oral progesterone raise blood progesterone much?

Not much. Only about 10% survives first-pass metabolism, so serum progesterone stays low even at 200–300 mg. Endometrial protection is still achieved, but uses chasing high serum levels usually switch routes.

Is micronized progesterone the same as medroxyprogesterone?

No. Micronized progesterone is bioidentical to human progesterone; medroxyprogesterone acetate (Provera) is a synthetic progestin with a different risk and side-effect profile. The two are not interchangeable.

References

Related compounds

Protocols featuring Progesterone (Oral)

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