▶ Risk of endometrial cancer The increased risk of endometrial

cancer depends on the dose and duration of oestrogenonly HRT.

In women with a uterus, the addition of a progestogen

cyclically (for at least 10 days per 28-day cycle) reduces the

additional risk of endometrial cancer; this additional risk is

eliminated if a progestogen is given continuously.

However, this should be weighed against the increased risk

of breast cancer.

▶ Risk of ovarian cancer Long-term use of combined HRT or

oestrogen-only HRT is associated with a small increased

risk of ovarian cancer. This excess risk disappears within a

few years of stopping.

▶ Risk of venous thromboembolism Women using combined or

oestrogen-only HRT are at an increased risk of deep vein

thrombosis and of pulmonary embolism especially in the

first year of use.

In women who have predisposing factors (such as a

personal or family history of deep vein thrombosis or

pulmonary embolism, severe varicose veins, obesity,

trauma, or prolonged bed-rest) it is prudent to review the

need for HRT, as in some cases the risks of HRT may

exceed the benefits.

Travel involving prolonged immobility further increases

the risk of deep vein thrombosis.

▶ Risk of stroke Risk of stroke increases with age, therefore

older women have a greater absolute risk of stroke.

Combined HRT or oestrogen-only HRT slightly increases

the risk of stroke.

▶ Risk of coronary heart disease HRT does not prevent coronary

heart disease and should not be prescribed for this

purpose. There is an increased risk of coronary heart

disease in women who start combined HRT more than

10 years after menopause. Although very little information

is available on the risk of coronary heart disease in

younger women who start HRT close to the menopause,

studies suggest a lower relative risk compared with older

women.

▶ Other conditions The product literature advises caution in

other conditions including hypertension, renal disease,

asthma, epilepsy, sickle-cell disease, melanoma,

otosclerosis, multiple sclerosis, and systemic lupus

erythematosus (but care required if antiphospholipid

antibodies present). Evidence for caution in these

conditions is unsatisfactory and many women with these

conditions may stand to benefit from HRT.

l INTERACTIONS → Appendix 1: hormone replacement

therapy

l SIDE-EFFECTS

▶ Common or very common Alopecia . arthralgia . breast

abnormalities . depression . leg cramps . menstrual cycle

irregularities . vaginal discharge . weight changes

▶ Uncommon Anxiety . cervical abnormalities . contact lens

intolerance . dizziness . embolism and thrombosis . gallbladder disorder. gastrointestinal discomfort. headaches . hirsutism . libido disorder. mood altered . nausea . oedema . skin reactions . vulvovaginal candidiasis

▶ Rare or very rare Angioedema . asthma exacerbated . cerebrovascular insufficiency . chorea exacerbated . colitis

ischaemic . epilepsy exacerbated . galactorrhoea . glucose

tolerance impaired . hypocalcaemia . jaundice cholestatic . myocardial infarction . neoplasms . pancreatitis . pelvic

pain . vomiting

▶ Frequency not known Endometrial hyperplasia . erythema

nodosum

SIDE-EFFECTS, FURTHER INFORMATION Cyclical HRT

(where a progestogen is taken for 12–14 days of each

28-day oestrogen treatment cycle) usually results in

regular withdrawal bleeding towards the end of the

progestogen. Continuous combined HRT commonly

produces irregular breakthrough bleeding in the first

4–6 months of treatment. Bleeding beyond 6 months or

after a spell of amenorrhoea requires further investigation

to exclude serious gynaecological pathology.

l CONCEPTION AND CONTRACEPTION HRT does not provide

contraception and a woman is considered potentially

fertile for 2 years after her last menstrual period if she is

under 50 years, and for 1 year if she is over 50 years. A

woman who is under 50 years and free of all risk factors for

venous and arterial disease can use a low-oestrogen

combined oral contraceptive pill to provide both relief of

menopausal symptoms and contraception; it is

recommended that the oral contraceptive be stopped at

50 years of age since there are more suitable alternatives.

If any potentially fertile woman needs HRT, non-hormonal

contraceptive measures (such as condoms) are necessary.

Measurement of follicle-stimulating hormone can help to

determine fertility, but high measurements alone

(particularly in women aged under 50 years) do not

necessarily preclude the possibility of becoming pregnant.

l PREGNANCY Manufacturer advises avoid—not indicated

during pregnancy.

l BREAST FEEDING Avoid until weaning or for 6 months

after birth (adverse effects on lactation).

l HEPATIC IMPAIRMENT Avoid in active liver disease

including disorders of hepatic excretion (e.g. DubinJohnson or Rotor syndromes), infective hepatitis (until

liver function returns to normal), and liver tumours.

l MEDICINAL FORMS There can be variation in the licensing of

different medicines containing the same drug.

Tablet

▶ Premarin (Pfizer Ltd)

Conjugated oestrogens 300 microgram Premarin 0.3mg tablets | 84 tablet P £6.07 DT = £6.07

Conjugated oestrogens 625 microgram Premarin 0.625mg tablets

| 84 tablet P £4.02 DT = £4.02

Conjugated oestrogens 1.25 mg Premarin 1.25mg tablets | 84 tablet P £3.58 DT = £3.58

Combinations available: Conjugated oestrogens with

medroxyprogesterone, p. 761

Conjugated oestrogens with

bazedoxifene acetate 28-Mar-2017

The properties listed below are those particular to the

combination only. For the properties of the components

please consider, conjugated oestrogens (equine) p. 754.

l INDICATIONS AND DOSE

Menopausal symptoms (in women with at least 12 months

since last menses for whom treatment with progestogencontaining therapy is not appropriate)

▶ BY MOUTH

▶ Adult: 0.45/20 mg daily continuously

DOSE EQUIVALENCE AND CONVERSION

▶ Dose expressed as x/y mg conjugated

oestrogens/bazedoxifene.

l INTERACTIONS → Appendix 1: hormone replacement

therapy

l SIDE-EFFECTS

▶ Common or very common Abdominal pain . constipation . diarrhoea . drowsiness . dry mouth . hot flush . muscle

complaints . nausea . peripheral oedema . skin reactions . vulvovaginal candidiasis

▶ Uncommon Cholecystitis

▶ Rare or very rare Embolism and thrombosis

▶ Frequency not known Dry eye . eye disorders . eye

inflammation . eye pain . palpitations . vision disorders

BNF 78 Female sex hormone responsive conditions 755

Endocrine system

6

l MEDICINAL FORMS There can be variation in the licensing of

different medicines containing the same drug.

Modified-release tablet

CAUTIONARY AND ADVISORY LABELS 3, 25

▶ Duavive (Pfizer Ltd)

Conjugated oestrogens 450 microgram, Bazedoxifene (as

Bazedoxifene acetate) 20 mg Duavive 0.45mg/20mg modifiedrelease tablets | 28 tablet P £15.00 DT = £15.00

Estradiol

l INDICATIONS AND DOSE

BEDOL ®

Menopausal symptoms | Osteoporosis prophylaxis

▶ BY MOUTH

▶ Adult: 2 mg daily, started on day 1–5 of menstruation

(or at any time if cycles have ceased or are infrequent),

to be taken with cyclical progestogen for 12–14 days of

each cycle in women with a uterus

ELLESTE SOLO ® MX

Menopausal symptoms

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch twice weekly continuously,

started within 5 days of onset of menstruation (or at

any time if cycles have ceased or are infrequent), to be

used with cyclical progestogen for 12–14 days of each

cycle in women with a uterus, initiate therapy with MX

40, subsequently adjust according to response

Osteoporosis prophylaxis

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch twice weekly continuously,

started within 5 days of onset of menstruation (or at

any time if cycles have ceased or are infrequent), to be

used with cyclical progestogen for 12–14 days of each

cycle in women with a uterus, initiate therapy with MX

80, subsequently adjust according to response

ELLESTE-SOLO ® 1-MG

Menopausal symptoms

▶ BY MOUTH

▶ Adult: 1 mg daily, starting on day 1 of menstruation (or

at any time if cycles have ceased or are infrequent), to

be taken with cyclical progestogen for 12–14 days of

each cycle in women with a uterus

ELLESTE-SOLO ® 2-MG

Menopausal symptoms not controlled with lower strength

| Osteoporosis prophylaxis

▶ BY MOUTH

▶ Adult: 2 mg daily, started on day 1 of menstruation (or

at any time if cycles have ceased or are infrequent), to

be given with cyclical progestogen for 12–14 days of

each cycle in women with a uterus

ESTRADERM MX ®

Menopausal symptoms

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch twice weekly continuously,

started within 5 days of onset of menstruation (or at

any time if cycles have ceased or are infrequent), to be

used with cyclical progestogen for at least 12 days of

each cycle in women with a uterus, initiate therapy

with MX25 for first 3 months; subsequently adjust

according to response

Osteoporosis prophylaxis

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch twice weekly continuously,

started within 5 days of onset of menstruation (or at

any time if cycles have ceased or are infrequent), to be

used with cyclical progestogen for at least 12 days of

each cycle in women with a uterus, initiate therapy

with MX50; subsequently adjust according to response

ESTRADOT ®

Menopausal symptoms

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch twice weekly continuously, to be

used with cyclical progestogen for 12–14 days of each

cycle in women with a uterus, initiate therapy with

25 patch for 3 months; subsequently adjust according

to response

Osteoporosis prophylaxis

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch twice weekly continuously, to be

used with cyclical progestogen for 12–14 days of each

cycle in women with a uterus, initiate therapy with

50 patch; subsequently adjust according to response

EVOREL ®

Menopausal symptoms | Osteoporosis prophylaxis

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch twice weekly continuously,

started within 5 days of onset of menstruation (or at

any time if cycles have ceased or are infrequent), to be

used with cyclical progestogen for 12–14 days of each

cycle in women with a uterus, therapy should be

initiated with Evorel 50 patch; subsequently adjust

according to response; dose may be reduced to Evorel

25 patch after first month if necessary for menopausal

symptoms only

FEMSEVEN ®

Menopausal symptoms | Osteoporosis prophylaxis

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch once weekly continuously, to be

used with cyclical progestogen for 12–14 days of each

cycle in women with a uterus, initiate therapy with

FemSeven 50 patches for the first few months,

subsequently adjust according to response

OESTROGEL ®

Menopausal symptoms

▶ TO THE SKIN

▶ Adult: Apply 1.5 mg once daily continuously, increased

if necessary up to 3 mg after 1 month continuously, to

be applied over an area twice that of the template

provided, starting within 5 days of menstruation (or

anytime if cycles have ceased or are infrequent), to be

used with cyclical progestogen for at least 12 days of

each cycle in women with a uterus

Osteoporosis prophylaxis

▶ TO THE SKIN

▶ Adult: Apply 1.5 mg once daily continuously, to be

applied over an area twice that of the template

provided, starting within 5 days of menstruation (or

anytime if cycles have ceased or are infrequent), to be

used with cyclical progestogen for at least 12 days of

each cycle in women with a uterus

DOSE EQUIVALENCE AND CONVERSION

▶ With topical use

▶ For Oestrogel ®: 2 measures is equivalent to estradiol

1.5 mg.

PROGYNOVA ®

Menopausal symptoms

▶ BY MOUTH

▶ Adult: 1–2 mg daily continuously, to be started on day

1 of menstruation (or at any time if cycles have ceased

or are infrequent), to be taken with cyclical

progestogen for 12–14 days of each cycle in women

with a uterus

756 Sex hormone responsive conditions BNF 78

Endocrine system

6

Osteoporosis prophylaxis

▶ BY MOUTH

▶ Adult: 2 mg daily continuously, to be taken with

cyclical progestogen for 12–14 days of each cycle in

women with a uterus

PROGYNOVA ® TS

Menopausal symptoms | Osteoporosis prophylaxis

▶ BY TRANSDERMAL APPLICATION

▶ Adult: Apply 1 patch once weekly continuously,

alternatively apply 1 patch once weekly for 3 weeks,

followed by a 7-day patch-free interval (cyclical), to be

used with cyclical progestogen for 12–14 days of each

cycle in women with a uterus, initiate therapy with

Progynova TS 50, subsequently adjust according to

response, women receiving Progynova TS 100 patches

for menopausal symptoms may continue with this

strength for osteoporosis prophylaxis

SANDRENA ®

Menopausal symptoms

▶ TO THE SKIN

▶ Adult: Apply 1 mg once daily, to be applied over area

1–2 times size of hand; with cyclical progestogen for

12–14 days of each cycle in women with a uterus, dose

may be adjusted after 2–3 cycles to lowest effective

dose; usual dose 0.5–1.5 mg daily

ZUMENON ®

Menopausal symptoms

▶ BY MOUTH

▶ Adult: Initially 1 mg daily, to be started within 5 days of

onset of menstruation (or any time if cycles have

ceased or are infrequent), increased if necessary to

2 mg daily, to be taken with a cyclical progestogen for

12–14 days of each cycle in women with a uterus

Osteoporosis prophylaxis

▶ BY MOUTH

▶ Adult: 2 mg daily, to be taken with a cyclical

progestogen for 12–14 days of each cycle in women

with a uterus

l CONTRA-INDICATIONS Active arterial thromboembolic

disease (e.g. angina or myocardial infarction). active

thrombophlebitis .Dubin-Johnson syndrome (or monitor

closely). history of breast cancer. history of recurrent

venous thromboembolism (unless already on

anticoagulant treatment). oestrogen-dependent cancer. recent arterial thromboembolic disease (e.g. angina or

myocardial infarction). Rotor syndrome (or monitor

closely).thrombophilic disorder. undiagnosed vaginal

bleeding . untreated endometrial hyperplasia . venous

thromboembolism

l CAUTIONS Acute porphyrias p. 1058 . diabetes (increased

risk of heart disease). history of breast nodules—closely

monitor breast status (risk of breast cancer). history of

endometrial hyperplasia; factors predisposing to

thromboembolism . history of fibrocystic disease—closely

monitor breast status (risk of breast cancer). hypophyseal

tumours . increased risk of gall-bladder disease . migraine

(or migraine-like headaches). presence of

antiphospholipid antibodies (increased risk of thrombotic

events). prolonged exposure to unopposed oestrogens

may increase risk of developing endometrial cancer.risk

factors for oestrogen-dependent tumours (e.g. breast

cancer in first-degree relative). symptoms of

endometriosis may be exacerbated . uterine fibroids may

increase in size

CAUTIONS, FURTHER INFORMATION

▶ Risk of breast cancer It is estimated that using all types of

HRT increases the risk of breast cancer within 1–2 years of

initiating treatment. The increased risk is related to the

duration of HRT use (but not to the age at which HRT is

started) and this excess risk disappears within 5 years of

stopping.

Radiological detection of breast cancer can be made

more difficult as mammographic density can increase with

HRT use.

▶ Risk of endometrial cancer The increased risk of endometrial

cancer depends on the dose and duration of oestrogenonly HRT.

In women with a uterus, the addition of a progestogen

cyclically (for at least 10 days per 28-day cycle) reduces the

additional risk of endometrial cancer; this additional risk is

eliminated if a progestogen is given continuously.

However, this should be weighed against the increased risk

of breast cancer.

▶ Risk of ovarian cancer Long-term use of combined HRT or

oestrogen-only HRT is associated with a small increased

risk of ovarian cancer. This excess risk disappears within a

few years of stopping.

▶ Risk of venous thromboembolism Women using combined or

oestrogen-only HRT are at an increased risk of deep vein

thrombosis and of pulmonary embolism especially in the

first year of use.

In women who have predisposing factors (such as a

personal or family history of deep vein thrombosis or

pulmonary embolism, severe varicose veins, obesity,

trauma, or prolonged bed-rest) it is prudent to review the

need for HRT, as in some cases the risks of HRT may

exceed the benefits.

Travel involving prolonged immobility further increases

the risk of deep vein thrombosis.

▶ Risk of stroke Risk of stroke increases with age, therefore

older women have a greater absolute risk of stroke.

Combined HRT or oestrogen-only HRT slightly increases

the risk of stroke.

▶ Risk of coronary heart disease HRT does not prevent coronary

heart disease and should not be prescribed for this

purpose. There is an increased risk of coronary heart

disease in women who start combined HRT more than

10 years after menopause. Although very little information

is available on the risk of coronary heart disease in

younger women who start HRT close to the menopause,

studies suggest a lower relative risk compared with older

women.

▶ Other conditions The product literature advises caution in

other conditions including hypertension, renal disease,

asthma, epilepsy, sickle-cell disease, melanoma,

otosclerosis, multiple sclerosis, and systemic lupus

erythematosus (but care required if antiphospholipid

antibodies present). Evidence for caution in these

conditions is unsatisfactory and many women with these

conditions may stand to benefit from HRT.

l INTERACTIONS → Appendix 1: hormone replacement

therapy

l SIDE-EFFECTS

GENERAL SIDE-EFFECTS

▶ Common or very common Headaches . nausea . skin

reactions

▶ Uncommon Hypertension

SPECIFIC SIDE-EFFECTS

▶ Common or very common

▶ With oral use Asthenia . gastrointestinal discomfort. gastrointestinal disorders . haemorrhage . menstrual cycle

irregularities . muscle complaints . pelvic pain . weight

changes

▶ With transdermal use Abdominal pain . breast abnormalities . menstrual cycle irregularities . uterine disorders . vaginal

discharge . weight changes

▶ Uncommon

▶ With oral use Anxiety . back pain . breast abnormalities . cervical abnormalities . cystitis-like symptom . depression . dizziness . embolism and thrombosis . erythema nodosum . gallbladder disorder. oedema . palpitations . peripheral

BNF 78 Female sex hormone responsive conditions 757

Endocrine system

6

vascular disease .tumour growth . visual impairment. vulvovaginal candidiasis

▶ With transdermal use Asthenia . breast neoplasm benign . depression . flatulence . increased risk of infection . leiomyoma . mood swings . venous thromboembolism . vertigo . vomiting

▶ Rare or very rare

▶ With oral use Angioedema . cerebrovascular insufficiency . chorea . contact lens intolerance . haemolytic anaemia . hepatic disorders . hirsutism . malaise . myocardial

infarction . sexual dysfunction . steepening of corneal

curvature . vaginal discharge . vomiting

▶ With transdermal use Epilepsy exacerbated . galactorrhoea . glucose tolerance impaired . libido disorder

▶ Frequency not known

▶ With oral use Carbohydrate metabolism change . epilepsy

exacerbated . hypertriglyceridaemia . increased risk of

coronary artery disease . neoplasms . pancreatitis . systemic lupus erythematosus (SLE)

SIDE-EFFECTS, FURTHER INFORMATION Cyclical HRT

(where a progestogen is taken for 12–14 days of each

28-day oestrogen treatment cycle) usually results in

regular withdrawal bleeding towards the end of the

progestogen. Continuous combined HRT commonly

produces irregular breakthrough bleeding in the first

4–6 months of treatment. Bleeding beyond 6 months or

after a spell of amenorrhoea requires further investigation

to exclude serious gynaecological pathology.

l CONCEPTION AND CONTRACEPTION HRT does not provide

contraception and a woman is considered potentially

fertile for 2 years after her last menstrual period if she is

under 50 years, and for 1 year if she is over 50 years. A

woman who is under 50 years and free of all risk factors for

venous and arterial disease can use a low-oestrogen

combined oral contraceptive pill to provide both relief of

menopausal symptoms and contraception; it is

recommended that the oral contraceptive be stopped at

50 years of age since there are more suitable alternatives.

If any potentially fertile woman needs HRT, non-hormonal

contraceptive measures (such as condoms) are necessary.

Measurement of follicle-stimulating hormone can help to

determine fertility, but high measurements alone

(particularly in women aged under 50 years) do not

necessarily preclude the possibility of becoming pregnant.

l PREGNANCY Not known to be harmful.

l BREAST FEEDING Avoid; adverse effects on lactation.

l HEPATIC IMPAIRMENT Avoid in active liver disease

including disorders of hepatic excretion (e.g. DubinJohnson or Rotor syndromes), infective hepatitis (until

liver function returns to normal), and liver tumours.

l MONITORING REQUIREMENTS

▶ History of breast nodules or fibrocystic disease—closely

monitor breast status (risk of breast cancer).

▶ The endometrial safety of long-term or repeated use of

topical vaginal oestrogens is uncertain; treatment should

be reviewed at least annually, with special consideration

given to any symptoms of endometrial hyperplasia or

carcinoma.

l DIRECTIONS FOR ADMINISTRATION

▶ With transdermal use Patch should be removed after

3–4 days (or once a week in case of 7-day patch) and

replaced with fresh patch on slightly different site;

recommended sites: clean, dry, unbroken areas of skin on

trunk below waistline; not to be applied on or near breasts

or under waistband. If patch falls off in bath allow skin to

cool before applying new patch.

l PATIENT AND CARER ADVICE

▶ With transdermal use Patient counselling is advised for

estradiol patches (administration).

▶ With topical use Patient counselling is advised for estradiol

gels (administration).

OESTROGEL ® ▶ With topical use Apply gel to clean, dry,

intact skin such as arms, shoulders or inner thighs and

allow to dry for 5 minutes before covering with clothing.

Not to be applied on or near breasts or on vulval region.

Avoid skin contact with another person (particularly male)

and avoid other skin products or washing the area for at

least 1 hour after application.

SANDRENA ® ▶ With topical use Apply gel to intact areas of

skin such as lower trunk or thighs, using right and left

sides on alternate days. Wash hands after application. Not

to be applied on the breasts or face and avoid contact with

eyes. Allow area of application to dry for 5 minutes and do

not wash area for at least 1 hour.

l MEDICINAL FORMS There can be variation in the licensing of

different medicines containing the same drug.

Tablet

▶ Bedol (ReSource Medical UK Ltd)

Estradiol 2 mg Bedol 2mg tablets | 84 tablet P £5.07 DT = £5.06

▶ Elleste Solo (Meda Pharmaceuticals Ltd)

Estradiol 1 mg Elleste Solo 1mg tablets | 84 tablet P £5.06 DT =

£5.06

Estradiol 2 mg Elleste Solo 2mg tablets | 84 tablet P £5.06 DT =

£5.06

▶ Progynova (Bayer Plc)

Estradiol valerate 1 mg Progynova 1mg tablets | 84 tablet P £7.30 DT = £7.30

Estradiol valerate 2 mg Progynova 2mg tablets | 84 tablet P £7.30 DT = £7.30

▶ Zumenon (Mylan)

Estradiol 1 mg Zumenon 1mg tablets | 84 tablet P £6.89 DT =

£5.06

Estradiol 2 mg Zumenon 2mg tablets | 84 tablet P £6.89 DT =

£5.06

Transdermal patch

▶ Elleste Solo MX (Meda Pharmaceuticals Ltd)

Estradiol 40 microgram per 24 hour Elleste Solo MX 40

transdermal patches | 8 patch P £5.19 DT = £5.19

Estradiol 80 microgram per 24 hour Elleste Solo MX 80

transdermal patches | 8 patch P £5.99 DT = £5.99

▶ Estraderm MX (Merus Labs Luxco S.a R.L.)

Estradiol 25 microgram per 24 hour Estraderm MX 25 patches | 8 patch P £5.50 DT = £3.42 | 24 patch P £16.46 DT = £16.46

Estradiol 50 microgram per 24 hour Estraderm MX 50 patches |

8 patch P £5.51 DT = £3.88 | 24 patch P £16.46 DT = £11.66

Estradiol 75 microgram per 24 hour Estraderm MX 75 patches | 8 patch P £6.42 DT = £4.12 | 24 patch P £19.27

Estradiol 100 microgram per 24 hour Estraderm MX 100 patches | 8 patch P £6.66 DT = £4.28 | 24 patch P £19.99 DT = £19.99

▶ Estradot (Novartis Pharmaceuticals UK Ltd)

Estradiol 25 microgram per 24 hour Estradot

25micrograms/24hours patches | 8 patch P £5.99 DT = £3.42

Estradiol 37.5 microgram per 24 hour Estradot

37.5micrograms/24hours patches | 8 patch P £6.00 DT = £6.00

Estradiol 50 microgram per 24 hour Estradot

50micrograms/24hours patches | 8 patch P £6.02 DT = £3.88

Estradiol 75 microgram per 24 hour Estradot

75micrograms/24hours patches | 8 patch P £7.00 DT = £4.12

Estradiol 100 microgram per 24 hour Estradot

100micrograms/24hours patches | 8 patch P £7.27 DT = £4.28

▶ Evorel (Janssen-Cilag Ltd)

Estradiol 25 microgram per 24 hour Evorel 25 patches |

8 patch P £3.42 DT = £3.42

Estradiol 50 microgram per 24 hour Evorel 50 patches | 4 patch P s DT = £6.04 | 8 patch P £3.88 DT = £3.88 | 24 patch P £11.66 DT = £11.66

Estradiol 75 microgram per 24 hour Evorel 75 patches | 8 patch P £4.12 DT = £4.12

Estradiol 100 microgram per 24 hour Evorel 100 patches | 8 patch P £4.28 DT = £4.28

▶ FemSeven (Theramex HQ UK Ltd)

Estradiol 50 microgram per 24 hour FemSeven 50 patches |

4 patch P £6.04 DT = £6.04 | 12 patch P £18.02 DT = £18.02

Estradiol 75 microgram per 24 hour FemSeven 75 patches | 4 patch P £6.98

Estradiol 100 microgram per 24 hour FemSeven 100 patches | 4 patch P £7.28 DT = £7.28

758 Sex hormone responsive conditions BNF 78

Endocrine system

6

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