Betamethasone dipropionate 0.064% / Clotrimazole 1% cream
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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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7 branded products available
MHRA licensed products
View all licensed products for Betamethasone + Clotrimazole on the MHRA register
Lotriderm cream
Lotriderm cream
Lotriderm cream
Lotriderm cream
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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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).
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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: 5 · Randomised trials: 6 · 2002–2026
Showing the 50 most relevant studies, sorted by most relevant.
C. Crowther, P. Ashwood, C. Andersen, et al.
The Lancet. Child & adolescent health, 2019
Pratima Soni, Komali Garlapati, Pedada Divya Harika, et al.
Cureus, 2025
ContextOral lichen planus (OLP) is a chronic inflammatory mucocutaneous disease characterized by pain and burning sensation. As etiology remains unclear, the treatment of OLP is focused mainly on reducing symptoms through modulation of local immune response.AimsThe aim of this study is to evaluate and compare the clinical efficacy of Clobetasol 0.05% orabase and Betamethasone 0.05% orabase, both combined with Clotrimazole 1%, in managing symptomatic OLP.MethodologyA double-blind, randomized clinical trial was conducted on 30 patients diagnosed with OLP at a tertiary dental hospital. Patients were randomly divided into two groups: Group A (Clobetasol + Clotrimazole) and Group B (Betamethasone + Clotrimazole). Clinical response was assessed at two and four weeks using the Global Assessment Scale for lesion size and the visual analogue scale (VAS) for burning sensation. The collected data were analyzed using IBM SPSS Statistics for Windows, Version 17 (Released 2009; IBM Corp., Armonk, New York, United States).ResultsAt the end of four weeks, the change in mean size obtained was score 2.0±0.95 in Group A and 1.66±1.4 in Group B (p-value = 0.51), indicating that both the study drugs had a similar decrease in the global assessment of efficacy scores with no significant statistical difference. Mean change in the VAS score at the end of four weeks revealed a decrease in the mean score of 4.66±2.30 in Group A and a decrease by 4.00±1.80 score in Group B (p-value=0.44), indicating no statistical significance.ConclusionsBoth clobetasol and betamethasone demonstrated comparable efficacy in reducing pain and lesion size among patients with OLP. This finding suggests that either regimen can serve as a viable therapeutic option in the management of OLP. Considering their similar clinical outcomes, the choice between these corticosteroids may depend on factors such as drug availability, patient tolerance, cost, and physician preference.
Abstract licence: CC BY
Lesly Jimenez-Garcia, E. Celis-Aguilar, G. Diaz-Pavon, et al.
Brazilian Journal of Otorhinolaryngology, 2019
Fatemeh Ahangari, A. Farshbaf-khalili, Y. Javadzadeh, et al.
Journal of Obstetrics and Gynaecology Research, 2019
A. Asilian, F. Fatemi, Zakiye Ganjei, et al.
Iranian Journal of Pharmaceutical Research : IJPR, 2021
Masoumeh Mirzamoradi, Fatemeh Hasani Nejhad, R. Jamali, et al.
The Journal of Maternal-Fetal & Neonatal Medicine, 2020
Manisha Pandey, H. Choudhury, Tarakini A. P. Gunasegaran, et al.
Drug Delivery and Translational Research, 2019
Seda Rençber, S. Karavana, Z. Senyigit, et al.
Pharmaceutical Development and Technology, 2017
W. Mendling, Maged Atef El Shazly, Lei Zhang
Pharmaceuticals, 2020
Manar Adel Abdelbari, S. El-Mancy, A. Elshafeey, et al.
International Journal of Nanomedicine, 2021
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.