What dose of oral progesterone (micronized progesterone) is recommended for the treatment of menopausal symptoms?

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Oral Micronized Progesterone Dosing for Menopausal Symptoms

For treatment of menopausal symptoms, oral micronized progesterone 300 mg at bedtime is the recommended dose, which effectively reduces vasomotor symptoms by approximately 55% and improves sleep quality. 1

Primary Treatment Regimen

Oral micronized progesterone 300 mg taken at bedtime is the evidence-based dose for treating hot flashes and night sweats in postmenopausal women. 1, 2 This dose demonstrated:

  • 55% overall reduction in vasomotor symptoms in a 3-month randomized controlled trial 1
  • 58.9% improvement in vasomotor symptoms compared to 23.5% with placebo 2
  • Greater effectiveness in women with ≥50 moderate-to-severe vasomotor symptoms per week 1
  • No withdrawal-related vasomotor symptom rebound 1
  • Improved deep sleep without causing depression 1

When Combined with Estrogen Therapy

If progesterone is being used for endometrial protection in women taking estrogen (rather than as monotherapy for symptoms), the dosing differs:

Sequential Regimen

  • 200 mg oral micronized progesterone daily for 12-14 days per 28-day cycle 3, 4
  • This provides proven endometrial protection when combined with estradiol 3
  • The 12-14 day duration is critical—shorter durations provide inadequate endometrial protection 3

Continuous Regimen

  • 100 mg oral micronized progesterone daily without interruption 3, 4
  • This regimen avoids withdrawal bleeding for women preferring amenorrhea 3

Pharmacokinetic Considerations

The FDA label confirms that oral micronized progesterone demonstrates dose-proportional pharmacokinetics across the therapeutic range 5:

  • Maximum serum concentrations occur within 1.5-2.3 hours 5
  • Food increases bioavailability, supporting bedtime dosing after an evening meal 5
  • Progesterone is 96-99% protein-bound and metabolized primarily by the liver 5

Critical Clinical Advantages

Micronized progesterone is strongly preferred over synthetic progestins due to superior safety profiles: 3, 4

  • Lower cardiovascular disease risk compared to synthetic progestins 3, 4
  • Lower venous thromboembolism risk 3, 4
  • An 8-year prospective cohort study in over 80,000 menopausal women showed progesterone prevented breast cancer in estrogen-treated women 1
  • Equally or more effective than estradiol in improving cardiovascular endothelial function 1

Common Pitfalls to Avoid

Never use progesterone for fewer than 12 days per cycle in sequential regimens when providing endometrial protection—this is inadequate. 3 The only exception is when using progesterone as monotherapy for vasomotor symptoms (300 mg at bedtime), where endometrial protection is not the primary goal.

Do not start with lower doses (100-200 mg) when treating vasomotor symptoms as monotherapy. 1, 2 The evidence specifically supports 300 mg for symptom relief, with lower doses showing less consistent efficacy 2, 6.

Side Effects and Tolerability

The primary side effect is mild, transient drowsiness, which is minimized by bedtime administration 7. In clinical trials:

  • Side effects (headaches, vaginal bleeding) led to discontinuation in only 6-21% of patients 2
  • The therapy is generally well-tolerated with no significant changes in blood pressure or weight 6
  • No depression or mood worsening occurs at therapeutic doses 1

Monitoring

Annual clinical review focusing on compliance, bleeding patterns, and symptom control is recommended, with no routine laboratory monitoring required unless specific symptoms arise 3.

References

Research

Progesterone for treatment of symptomatic menopausal women.

Climacteric : the journal of the International Menopause Society, 2018

Guideline

Lowest Dose of Progesterone for Hormone Replacement Therapy

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Hormone Replacement Therapy in Females

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Oral micronized progesterone.

Clinical therapeutics, 1999

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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