Ethinylestradiol 35microgram / Norgestimate 250microgram tablets
Requires a prescription from a doctor or prescriber
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MHRA alerts for Ethinylestradiol + Norgestimate
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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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9 branded products available
MHRA licensed products
View all licensed products for Ethinylestradiol + Norgestimate on the MHRA register
Cilique 250microgram/35microgram tablets
Lizinna 250microgram/35microgram tablets
Ethinylestradiol 35microgram / Norgestimate 250microgram tablets
Ethinylestradiol 35microgram / Norgestimate 250microgram tablets
AM Distributions (Yorkshire) Ltd
Ethinylestradiol 35microgram / Norgestimate 250microgram 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.
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NICE clinical guidance(1)
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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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: 8 · Randomised trials: 6 · 1995–2026
Showing the 50 most relevant studies, sorted by most relevant.
T. Harada, Saori Kosaka, J. Elliesen, et al.
Fertility and sterility, 2017
Diane Thiboutot, David F. Archer, André Lemay, et al.
Fertility and Sterility, 2001
J. Dinger
2020
L. Barreiros, J. Queiroz, Luís M. Magalhães, et al.
Microchemical Journal, 2016
M. Kangasniemi, R. Arffman, S. Joenväärä, et al.
Human Reproduction (Oxford, England), 2022
T. Harada, M. Momoeda
Reproductive Medicine and Biology, 2021
Susan S. Jick, James A. Kaye, Stefan Russmann, et al.
Contraception, 2006
- Administration, Cutaneous
- Contraceptives, Oral, Combined
- Contraceptives, Oral, Synthetic
Stanczyk FZ, Archer DF, Lohmer LRL, et al.
2022
- Ethinyl Estradiol
- Levonorgestrel
- Estradiol
ObjectiveThis study employed population pharmacokinetic (popPK) models to predict levonorgestrel (LNG) and ethinyl estradiol (EE) exposure after dosing with the transdermal contraceptive TWIRLA® (LNG/EE TDS) as a 12-week extended regimen in a healthy female population.MethodsPopPK models were developed using data from a previously published phase 1, open-label, randomized clinical trial, ATI-CL14 (NCT01243580), in 36 healthy individuals. Models used cycle 2 data from 18 individuals who received the LNG/EE TDS, delivering LNG 120 μg/day and EE 30 μg/day, followed by a 1-week TDS-free period. Noncompartmental PK analyses were performed on simulated concentration-time profiles of 12 consecutive weeks of LNG/EE TDS use.ResultsThe simulated concentration-time profiles and PK parameters for the simulated extended regimen indicated that predicted LNG and EE exposures at week 12 were similar to week 3 (predicted geometric mean EE area under the concentration-time curve from time 0 to 168 h [AUC0-168] on week 3 was 0.2% lower than week 12 and LNG AUC0-168 on week 3 was 0.9% lower than week 12), suggesting both were at steady state by week 3. Therefore, no notable accumulation beyond that at week 3 is predicted for LNG and EE following a 12-week extended regimen. The results are supported by the accumulation ratios based on maximum concentration and the area under the curve being similar at weeks 3 and 12 for LNG and EE.ConclusionThese results indicate that a 12-week extended LNG/EE regimen would provide similar systemic hormonal exposure as that seen by week 3 in a standard 28-day regimen, without further hormonal accumulation. The data support the safe use of a non-daily, low-dose hormonal contraceptive in an extended regimen but should be confirmed in a clinical PK study.
Abstract licence: CC BY
Â. Almeida, Mónica G. Silva, A. Soares, et al.
Environmental research, 2020
N. Torres, Géssica O. S. Santos, L. F. Romanholo Ferreira, et al.
Chemosphere, 2020
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.