Sequential combined (oral)
Choice | Drug | Dosage |
---|---|---|
1st choice | Elleste-Duet® 1mg, 2mg tablets (estradiol and norethisterone) | Dose: Elleste-Duet® 2mg tablets – menopausal symptoms and osteoporosis prophylaxis (see section 6.6), 1 orange tablet daily for 16 days, starting on day 1 of menstruation (or at any time if cycles have ceased or are infrequent) then 1 grey tablet daily for 12 days; subsequent courses are repeated without interval |
Or | ||
Femoston® 1/10, 2/10 tablets (estradiol and dydrogesterone) | Dose: Femoston® 2/10 tablets - menopausal symptoms and osteoporosis prophylaxis (see section 6.6), in women with a uterus, 1 red tablet daily for 14 days, starting within 5 days of onset of menstruation (or any time if cycles have ceased or are infrequent) then 1 yellow tablet daily for 14 days; subsequent courses repeated without interval; Where therapy required for menopausal symptoms alone, Femoston® 1/10 given initially and Femoston® 2/10 substituted if symptoms not controlled |
Sequential combined (transdermal)
Choice | Drug | Dosage |
---|---|---|
1st choice | Evorel® Sequi patches: combination pack of 4 Evorel® 50 patches (estradiol 50micrograms/24hours) and 4 Evorel® Conti patches (estradiol 50micrograms/24hours) and norethisterone acetate 170micrograms/24hours | Dose: |
2nd choice | FemSeven Sequi® patches: providing estradiol 50micrograms per 24 hours (phase 1); estradiol 50micrograms and levonorgestrel 10micrograms per 24 hours (phase 2) | Dose: |
Continuous combined (oral)
Choice | Drug | Dosage |
---|---|---|
1st choice | Kliovance® tablets (estradiol 1mg and norethisterone 500micrograms) | Dose: Menopausal symptoms in women with a uterus whose last menstrual period occurred over 12 months previously, Osteoporosis prophylaxis in women with a uterus (see section 6.6), 1 tablet daily continuously, to be started at end of scheduled bleed if changing from cyclical HRT |
or | ||
Kliofem® tablets (estradiol 2mg and norethisterone 1mg) | Dose: Menopausal symptoms in women with a uterus whose last menstrual period occurred over 12 months previously , Osteoporosis prophylaxis in women with a uterus (see section 6.6), 1 tablet daily continuously, to be started at end of scheduled bleed if changing from cyclical HRT | |
2nd choice | Bijuve® 1mg/100mg capsules (estradiol 1 mg, progesterone 100mg) | Dose: Menopausal symptoms in women with a uterus whose last menstrual period occurred over 12 months previously, 1 capsule daily continuously, dose to be taken in the evening with food, if changing from continuous sequential or cyclical HRT, start treatment the day after finishing the 28-day cycle. Treatment may start immediately after surgical menopause or if changing from another continuous combined HRT |
or | ||
Femoston® - conti 0.5mg/2.5mg tablets; 1mg/5mg tablets (estradiol and dydrogesterone) | Dose: Femoston®-conti 0.5mg/2.5mg tablets: Menopausal symptoms in women with a uterus whose last menstrual period occurred over 12 months previously, 1 tablet daily continuously, if changing from cyclical HRT begin treatment the day after finishing oestrogen plus progestogen phase. Femoston®-conti 1 mg/5 mg tablets: Menopausal symptoms and osteoporosis prophylaxis (see section 6.6) in women with a uterus whose last menstrual period occurred over 12 months previously, 1 tablet daily continuously (if changing from cyclical HRT begin treatment the day after finishing oestrogen plus progestogen phase) |
Continuous combined (transdermal)
Choice | Drug | Dosage |
---|---|---|
1st choice | Evorel® Conti patches (estradiol 50micrograms/24hours and norethisterone 170micrograms/24hours (matrix patch)) | Dose: |
Prescribing Notes
- HRT preparations should be brand prescribed to aid product identification
- It is recommended that the lowest dose of HRT based on relieving menopausal symptoms should be prescribed
- Women with an early menopause (<45 years), especially if surgically induced, require the higher dose of oestrogen to control their vasomotor symptoms and for bone protection
- Women with irregular or heavy bleeding with HRT which persists for more than 3 months should be referred to a gynaecology or menopause service
- Amenorrhoea with HRT is not a risk for endometrial cancer and does not require investigation
- Progestogenic side effects (women typically describe symptoms similar to PMS) may resolve within a few months. For persistent or troublesome symptoms consider:
- Changing the progestogen type, e.g. to a less androgenic one such as dydrogesterone
- Changing the route of delivery e.g. oral to transdermal
- 3 monthly bleed preparation (Tridestra®)
- Using a Mirena® IUS as the progestogen component of HRT