Betamethasone valerate 0.1% ointment 25% / Coal tar solution 5% in Generic Unguentum M cream
Requires a prescription from a doctor or prescriber
Chemical compound: steroid medication
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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.
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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.
EudraVigilance
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
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View all licensed products for Coal tar + Betamethasone on the MHRA register
Betamethasone valerate 0.1% ointment 25% / Coal tar solution 5% in Unguentum M cream
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(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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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
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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. 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: 9 · Randomised trials: 3 · 2014–2025
Showing the 50 most relevant studies, sorted by most relevant.
Totté JEE, van Doorn MB, Pasmans SGMA
2017
Staphylococcus aureus plays an important role in skin and soft tissue infections and contributes to the pathophysiology of complex skin disorders such as atopic dermatitis. Bacterial resistance against commonly used antibiotics has increased considerably in the last decades demanding alternative treatment approaches. We present 3 cases where patients with chronic and recurrent S. aureus-related dermatoses were successfully treated with Staphefekt SA.100. Staphefekt SA.100 is a recombinant phage endolysin for topical skin application that specifically targets both methicillin-sensitive and methicillin-resistant S. aureus. As a consequence of its specific mechanism of action, bacterial resistance is unlikely to develop. In our 3 cases, resistance induction was not observed. Our results indicate that targeted treatment with Staphefekt might be an attractive alternative for (long-term) classical antibiotic therapy, and confirmatory randomized controlled trials are warranted to evaluate its clinical efficacy and safety.
Abstract licence: CC BY-NC
Jia Guo, H. Zhang, Wenrui Lin, et al.
Signal Transduction and Targeted Therapy, 2023
- Psoriasis
- Signal Transduction
- Cytokines
Xiaojun He, Xiaojing Li, Hao Ma, et al.
Journal of Power Sources, 2017
Qian Liu, Dongling Wu, Tao Wang, et al.
Advanced Functional Materials, 2024
Zhi-Hao Ma, Xianyong Wei, Guang-Hui Liu, et al.
Fuel, 2021
Xiaojun He, Hao Ma, Jingxian Wang, et al.
Journal of Power Sources, 2017
Weidan Geng, Fangwei Ma, Guang Wu, et al.
Electrochimica Acta, 2016
Chandrachur Banerjee, V. K. Chandaliya, P. S. Dash
Journal of Analytical and Applied Pyrolysis, 2021
Y. Ju, Zhu Yan, Hongwei Zhou, et al.
Energy Reports, 2021
Yuwei Wang, Nan Xiao, Zhiyu Wang, et al.
Chemical Engineering Journal, 2018
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 (Q416132), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.
Scientific data (pharmacology, interactions, ADME) is not yet available for this medicine. Clinical sections are sourced from the NHS dm+d database.