• FCMS
  • Doncaster and Bassetlaw Teaching Hospitals NHS Foundation Trust
  • Rotherham Doncaster and South Humber NHS Foundation Trust
  • Nottingham and Nottinghamshire
  • South Yorkshire ICB

Shared care Protocol for Relugolix-estradiol-norethisterone acetate(Ryeqo®) for moderate to severe symptoms of uterine fibroids in adult patients linked to IMOC website Click Here

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Relugolix 1 mg, estradiol (as hemihydrate), and 0.5 mg norethisterone acetate

Uterine fibroids

NICE Guidance 

Follow Shared Care protocol 

Pack Price
28 tablet
84 tablet

Endometriosis or fibroids

Prescribing for gynaecological conditions:

Licensed status:
All GnRH analogues are licensed to treat endometriosis, however only goserelin, leuprorelin and triptorelin are licensed to treat fibroids.

Duration of treatment:
Maximum duration of treatment will be 6 months as per product licence.

Monitoring requirements:
No specific biochemical monitoring is required by Secondary or Primary Care

Secondary care review process:
Most patients will be reviewed after a 3 month period to evaluate response to treatment and review side effects. Benefit is unlikely to be seen before the 3rd injection.

Transfer of prescribing:
Secondary Care will administer the initial injection, thereafter prescribing responsibility will be passed to Primary Care. GP’s are advised to contact the Gynaecology department for further advice if they have enquiries regarding prescribing or the clinical management of these patients

Verbal communication Mr Alloub, Consultant Gynaecologist, DBH FT
January 2013

For treatment of endometriosis: Suitable for restricted prescribing under defined conditions

The gonadorelin analogues (buserelin, goserelin, leuprorelin, nafarelin and triptorelin) are suitable for prescribing in primary care upon the advice of a specialist (or a primary care prescriber with a special interest in womens health).

Gonadorelin analogues for the treatment of endometriosis
MTRAC Verdict & Summary November 2010

Pack Price
1 pre-filled disposable injection £235.00
Pack Price
1 pre-filled disposable injection £94.50

Prescribing for gynaecological conditions:
Licensed status:
All GnRH analogues are licensed to treat endometriosis, however only goserelin, leuprorelin and triptorelin are licensed to treat fibroids.

Drug choice:
Goserelin 3.6mg preparation is the first line choice.
Leuprorelin is the second line choice

Duration of treatment:
Maximum duration of treatment will be 6 months as per product licence.

Monitoring requirements:
No specific biochemical monitoring is required by Secondary or Primary Care

Secondary care review process:
Most patients will be reviewed after a 3 month period to evaluate response to treatment and review side effects.
Benefit is unlikely to be seen before the 3rd injection.

Transfer of prescribing:
Secondary Care will administer the initial injection, thereafter prescribing responsibility will be passed to Primary Care.
GP's are advised to contact the Gynaecology department for further advice if they have enquiries regarding prescribing or the clinical management of these patients
Verbal communication Mr Alloub, Consultant Gynaecologist, DBH FT
January 2013
-----------------------
For treatment of endometriosis: Suitable for restricted prescribing under defined conditions
The gonadorelin analogues (buserelin, goserelin, leuprorelin, nafarelin and triptorelin) are suitable for prescribing in primary care upon the advice of a specialist (or a primary care prescriber with a special interest in womens health).
Gonadorelin analogues for the treatment of endometriosis
MTRAC Verdict & Summary November 2010

Endometriosis

For treatment of endometriosis: Suitable for restricted prescribing under defined conditions

The gonadorelin analogues (buserelin, goserelin, leuprorelin, nafarelin and triptorelin) are suitable for prescribing in primary care upon the advice of a specialist (or a primary care prescriber with a special interest in womens health).

Gonadorelin analogues for the treatment of endometriosis
MTRAC Verdict & Summary November 2010

The recommended duration of therapy is six months; only one 6-month course is advised.

Nafarelin Acetate (Synarel nasal spray) Summary of Product Characteristics (9/8/2007)

Central precocious puberty in children

Rationale: 1,2,3

 

Ovarian function (preservation) in pre-menopausal women with neoplastic disease undergoing chemotherapy treatment that can cause premature ovarian insufficiency

Rationale: 1,2,3

 

Treatment of moderate to severe symptoms of uterine fibroids in adult women of reproductive age

For treating symptoms of endometriosis

Rationale 1

NICE Guidance 

IVF

Rationale 1,2

The recommended duration of therapy is six months; only one 6-month course is advised.

Nafarelin Acetate (Synarel nasal spray) Summary of Product Characteristics (9/8/2007)

Used to suppress puberty as part of treating gender incongruence or gender dysphoria in children and young people who are under 18 years of age

MHRA New restrictions on puberty blockers Click here

New regulations restrict the prescribing and supply of puberty-suppressing hormones to children and young people under 18.