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hydrocortisone MR (Efmody®)

 

Following a full submission

AWMSG advice

Status: Recommended with restrictions

Hydrocortisone (Efmody®) is recommended as an option for restricted use within NHS Wales.

Hydrocortisone (Efmody®) is licensed for the treatment of congenital adrenal hyperplasia in adolescents aged 12 years and older and in adults.

Hydrocortisone (Efmody®) is restricted for use as a second-line treatment option in adolescents not adequately controlled on maximum guideline doses of immediate-release hydrocortisone; and as a third-line treatment in adults not adequately controlled on maximum guideline doses of immediate-release hydrocortisone and/or prednisolone.

Hydrocortisone (Efmody®) is not recommended for use within NHS Wales outside of this subpopulation.

This recommendation applies only in circumstances where the approved Wales Patient Access Scheme (WPAS) is utilised or where the list/contract price is equivalent or lower than the WPAS price.

 Final Recommendation: hydrocortisone (Efmody) 3017 (PDF, 336Kb)
 Appraisal Report: hydrocortisone (Efmody) 3017 (PDF, 295Kb)

Medicine details

Medicine name hydrocortisone MR (Efmody®)
Formulation 5 mg, 10 mg, 20 mg modified-release hard capsules
Reference number 3017
Indication

Treatment of congenital adrenal hyperplasia (CAH) in adolescents aged 12 years and over and adults

Company Diurnal Limited
BNF chapter Endocrine system
Submission type Full
Status Recommended with restrictions
NMG meeting date 06/07/2022
AWMSG meeting date 14/09/2022
Date of issue 03/10/2022
Commercial arrangement WPAS
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