Estradiol 2mg / Norethisterone 1mg tablets
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MHRA alerts for Estradiol + Norethisterone
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Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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2 branded products available
Part of the Evorel brand family (generic: Estradiol + Norethisterone)
MHRA licensed products
View all licensed products for Estradiol + Norethisterone on the MHRA register
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(6)
Linzagolix for treating symptoms of endometriosis (TA1067)
Relugolix–estradiol–norethisterone acetate for treating moderate to severe symptoms of uterine fibroids (TA832)
Relugolix–estradiol–norethisterone for treating symptoms of endometriosis (TA1057)
Linzagolix for treating moderate to severe symptoms of uterine fibroids (TA996)
Heavy menstrual bleeding: assessment and management (NG88)
Endometriosis: diagnosis and management (NG73)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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Codes for healthcare professionals and prescribing systems
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NHS UK identifiers
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 22 · Randomised trials: 11 · 1986–2026
Showing the 50 most relevant studies, sorted by most relevant.
Weijuan Cui, Ling-Zhi Zhao
Frontiers in Endocrinology, 2023
Carballo García A, Fernández Rísquez AC, Delgado García S, et al.
2025
Background: Uterine fibroids (UFs) and endometriosis are gynecological conditions that significantly increase morbidity among women of reproductive age. Relugolix, a novel gonadotropin-releasing hormone receptor antagonist, is approved in combined therapy for the management of symptoms related to these disorders. However, its potential impact on bone mineral density (BMD) and osteoporosis risk should be considered when using a gonadotropin-releasing hormone (GnRH) antagonist. This systematic review aims to evaluate the effects of daily relugolix intake in monotherapy and combination therapy on BMD, ensuring safe long-term management. Methods: A systematic literature review was conducted following PRISMA 2020 guidelines. Searches were performed in PubMed, Medline, and the Cochrane Library. Relevant clinical guidelines from international societies were also reviewed. Studies assessing the impact of relugolix on BMD were selected, and data on treatment efficacy, adverse effects, and bone health outcomes were synthesized. Results: Relugolix monotherapy has been associated with significant BMD loss due to its potent estrogen-suppressing effect. To mitigate this, combination therapy with estradiol and norethisterone acetate has been developed. Although initial monotherapy before transitioning to combination therapy results in transient BMD reduction, clinical trials have demonstrated that relugolix combination therapy maintains BMD over two years while effectively reducing endometriosis- and UF-related symptoms. Conclusions: Relugolix combination therapy is an effective and well-tolerated treatment for UFs and endometriosis, minimizing the risk of hypoestrogenism-related bone loss while maintaining clinical benefits. Although monotherapy may lead to transient BMD reduction, combination therapy appears to stabilize bone health.
Abstract licence: CC BY
Ling Zhao (111365), Weijuan Cui (15536306)
2023
Ling Zhao (111365), Weijuan Cui (15536306), Weijuan Cui, et al.
Frontiers Media SA, 2023
Ling Zhao (111365), Weijuan Cui (15536306)
2023
Ling Zhao (111365), Weijuan Cui (15536306)
2023
Qian Z, Velu P, Prabahar K, et al.
2025
- Testosterone
- Estradiol
- Norethindrone
A. D. Makatsariya, V. O. Bitsadze, D. V. Blinov, et al.
IRBIS LLC, 2019
M. Singata-Madliki, J. Smit, M. Beksinska, et al.
PLOS ONE, 2024
Bedair NI, El-Komy MHM, Mohamed RE, et al.
2025
- Alopecia
- Minoxidil
- Estradiol
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.