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This website includes promotional information and is intended for UK healthcare professionals only. This website has been developed and funded by Exeltis UK.

Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App store. Adverse events should also be reported to Exeltis UK Limited by email to pharmacovigilance.uk@exeltis.com

Life is busy…
…HRT doesn’t have to be

Women and their doctors can rely on Femoston® for a reliable, consistent bleeding profile and well-established safety profile. 1

Femoston® & postmenopause bleeding profile

Femoston® 1mg /10mg

Estradiol / Dydrogesterone

Femoston® 2mg /10mg

Estradiol / Dydrogesterone

Demostrated bleeding control with 75% – 80% and 90% achieving regular withdrawal bleeds respectively. 2-4

Femoston® & vasomotor symptom control

Compared to the placebo, Femoston®-conti 0.5/2.5mg and 1/5mg resulted in a statistically significant greater reduction in the number of daily hot flushes by Week 4, Week 8 and Week 13.

Femoston® & endometrial protection

Across all doses, Femoston® has demonstrated endometrial protection of ≥ 98% of women using Femoston®. 1-5-6

  • An adequate progestational response was confirmed by biopsy in 98% of postmenopausal women (n=275) following 26 cycles of oral HRT treatment with a range of Femoston® doses in a randomised, placebo-controlled trial: 1/5mg, 97.7% (n=96); 1/10mg, 98.9% (n=93); 2/10mg, 98.8% (n=84). Placebo, 100% (n=55).5
    Study definition of adequate progestational response: histological (microscopic) appearance after treatment showing secretory changes typical of exposure to pregestogen, plus no evidence of hyperplasia or malignancy in biopsy. 5

     

  • Femoston®-conti 0.5/2.5mg was assessed for endometrial safety in an open, multi-centre study of 290 healthy, non-hysterectomised postmenopausal women. 289 of 290 (99.7%) achieved an adequate progestational response following 1 year of treatment. 1

Reduced risk of endometrial cancer with fixed-dose combination HRT

Compared to separate oestradiol/progesterone HRT

Study conducted in the EPIC cohort concluded that there was a significant reduction in endometrial cancer risk in continuous combined HRT users compared with sequential combined HRT and oestradiol/micronised progesterone users7.

A possible explanation is that there was less compliance in oestradiol (transdermal)/ micronised progesterone (oral) users because there were two separate components to their HRT which had to be complied with7

*Oestradiol was administered transdermally while micronised progesterone was administered orally

This is a promotional website developed and funded by Exeltis UK and it is intended for UK healthcare professionals only.

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