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FAQs and support tools

Ensure the women in your care get the most from their treatment
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Utrogestan Product Packshot
Menopause Product Packshot
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Frequently asked questions

We have compiled responses to patient queries to help the women in your care feel informed, confident and ready to ‘Own It’.

Can Utrogestan 100mg (micronised progesterone) be given continuously?

The recommended dosing regime is 200mg daily at bedtime, for 12 days in the last half of each therapeutic cycle (beginning on Day 15 of the cycle and ending on Day 26). Withdrawal bleeding may occur in the following week.2 

Alternatively, 100mg can be given at bedtime from Day 1 to Day 25 of each therapeutic cycle, withdrawal bleeding being less with this treatment schedule. These two dosing regimens are based on the comprehensive licensing studies for Utrogestan 100mg.2

Is Utrogestan 100mg body-identical?

Utrogestan 100mg is a body-identical hormone replacement therapy (HRT) containing progesterone, which is identical in molecular structure to the hormone progesterone made in the body.2,3

Can Utrogestan 100mg be used vaginally?

Utrogestan 100mg capsules are not indicated for vaginal use. Utrogestan 100mg capsules are licensed for oral use as an adjunctive treatment with oestrogen HRT in postmenopausal women with an intact uterus.2

Do you have specific questions on Utrogestan 100mg?

Support Tools  
   Information for healthcare professionals

We have developed a range of resources to support your conversations with women who are seeking menopause care and to give you clear and comprehensive information about prescribing Utrogestan.

Information to support your patients

Visit the patient support site which provides information for patients who have been prescribed Utrogestan.

Looking for further support?

Abbreviations

HRT, hormone replacement therapy.

References

  1. Data on file. REF-UTO-00078 July 2025
  2. Utrogestan 100mg (micronised progesterone) Summary of Product Characteristics.
    https://www.medicines.org.uk/emc/product/352/smpc.Accessed June 2026
  3. Panay N. Post Reprod Health 2014;20(2):69-72.
June 2026 | MAT-PROMO-UTO-0028

Adverse event reporting

Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to Besins Healthcare (UK) Ltd Drug Safety on 0203 862 0920 or Email: drugsafety@besins-healthcare.com