Co-cyprindiol 2000microgram/35microgram tablets
Requires a prescription from a doctor or prescriber
Combination drug
Official documents, adverse reaction reporting, and safety monitoring
Report a side effect
Submit a Yellow Card report to the MHRA
Official medicine documents
Safety monitoring data
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.
View Drug Analysis Profile
Browse all Drug Analysis Profiles A–Z
Browse all iDAP reports
Interactive Drug Analysis Profiles for all medicines
Report a side effect
Submit a Yellow Card report to the MHRA
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.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
Search EudraVigilance database
Browse substances A–Z in the European adverse reaction database
About EudraVigilance
Learn about EU pharmacovigilance and safety monitoring
EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
31 branded products available
MHRA licensed products
View all licensed products for Co-cyprindiol on the MHRA register
Clairette 2000/35 tablets
Dianette tablets
Dianette tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
Co-cyprindiol 2000microgram/35microgram tablets
This is the NHS Drug Tariff indicative price used for reimbursement purposes. It may not reflect the price paid by patients or pharmacies.
View full Drug TariffSource: NHS Drug Tariff via NHSBSA. Derived from dm+d VMPP (Virtual Medicinal Product Pack) pricing data. Contains public sector information licensed under the Open Government Licence v3.0.
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(2)
Polycystic ovary syndrome: metformin in women not planning pregnancy (ESUOM6)
Acne vulgaris: management (NG198)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. 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: 6 · Randomised trials: 20 · 1975–2026
Showing the 50 most relevant studies, sorted by most relevant.
Heather Green, Kenneth I. Pakenham, B.C. Headley, et al.
British Journal of Urology, 2002
- Analysis of Variance
- Androgen Antagonists
- Cognition Disorders
M. Pavone‐Macaluso, H. J. de Voogt, G. Viggiano, et al.
The Journal of Urology, 1986
- Bone Neoplasms
- Carcinoma
- Cardiovascular Diseases
P Vexiau, C Chaspoux, Philippe Boudou, et al.
British Journal of Dermatology, 2002
- Administration, Topical
- Alopecia
- Androgen Antagonists
Vercellini P, Vercellini P, Buffo C, et al.
2025
- Endometriosis
- Contraceptives, Oral, Combined
BackgroundNo conceptually new drugs for the safe and successful cure of endometriosis are likely to become available soon. Hormonal modulation of ovarian function and suppression of menstruation remain the pillars of disease control. However, existing drugs may be used following novel modalities to limit the consequences of endometriosis progression.ObjectivesThe aims of this review were to propose a pharmacological approach aimed at limiting the potential detrimental effects of the recent dramatic increase in postmenarcheal repetitive ovulatory menses and to define the type of hormones and the routes of administration that can be used to maximize safety and tolerability in the medical treatment of endometriosis.MethodsFor this narrative review, we selected the best quality evidence, prioritizing RCTs, systematic reviews, meta-analyses, network meta-analyses, and international guidelines, preferably published in the last decade.OutcomeMedical treatment of endometriosis should be included into all aspects of prevention. Very-low-dose combined oral contraceptives can be used for years to counteract the increased risk of ovarian cancer observed in patients with endometriosis. This primary prevention measure saves lives and can effectively integrate targeted risk-reducing surgery. Secondary pharmacological prevention, based on a working diagnosis of early onset adenomyosis-endometriosis selectively in adolescents with severe dysmenorrhea and heavy menstrual bleeding, can potentially impede the development of advanced disease forms, and reduce the need for management of complications due to a delay in diagnosis and treatment. Tertiary prevention, i.e., medical therapy of established disease, is based initially on the safest available estrogen-progestogen combinations and progestogen monotherapies. Whenever possible, ethinyl estradiol and cyproterone acetate should be avoided because of thromboembolic and meningioma risks, respectively. Estradiol can be administered transdermally. Switching to gonadotropin-releasing hormone agonists and antagonists should not be delayed when the first-line agents fail.Conclusions and outlookTwo-thirds of symptomatic endometriosis patients can be managed satisfactorily for many years using, with the right modality, the existing safe, effective, and well-tolerated medications. Despite the constant plea for new drugs, this already appears to be an excellent clinical outcome, unsurpassed when managing other human chronic inflammatory diseases. Cohort studies are needed to verify whether turning off the recurrent inflammation caused by repeated ovulation and menstruation could also affect the risk of systemic conditions associated with endometriosis.
Abstract licence: CC BY
Jacques Irani, Laurent Salomon, Rostand Oba, et al.
The Lancet Oncology, 2009
- Venlafaxine Hydrochloride
- Adenocarcinoma
- Androgen Antagonists
M. Amiri, F. Ramezani Tehrani, F. Nahidi, et al.
Metabolism: clinical and experimental, 2017
Stefano Venturoli, O. Marescalchi, F. M. Colombo, et al.
The Journal of Clinical Endocrinology & Metabolism, 1999
- Ethinyl Estradiol
- Flutamide
- Hirsutism
K. Lee, John J. Y. Zhang, R. Kirollos, et al.
Scientific Reports, 2022
T. Harada, Saori Kosaka, J. Elliesen, et al.
Fertility and sterility, 2017
JJ Keating, PJ Johnson, AMG Cochrane, et al.
British Journal of Cancer, 1989
- Adenocarcinoma
- Androgen Antagonists
- Antineoplastic Agents
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.
Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q16628711), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.