Povidone-Iodine 10% alcoholic solution
Available from a pharmacy with pharmacist advice
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2 branded products available
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View all licensed products for Industrial methylated spirit + Povidone-Iodine on the MHRA register
Videne 10% alcoholic tincture
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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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.
1970–2020
Showing the 50 most relevant studies, sorted by most relevant.
Lepelletier D, Maillard JY, Pozzetto B, et al.
2020
- Staphylococcal Infections
- Anti-Infective Agents, Local
- Methicillin-Resistant Staphylococcus aureus
Nasal decolonization is an integral part of the strategies used to control and prevent the spread of methicillin-resistant Staphylococcus aureus (MRSA) infections. The two most commonly used agents for decolonization are intranasal mupirocin 2% ointment and chlorhexidine wash, but the increasing emergence of resistance and treatment failure has underscored the need for alternative therapies. This article discusses povidone iodine (PVP-I) as an alternative decolonization agent and is based on literature reviewed during an expert's workshop on resistance and MRSA decolonization. Compared to chlorhexidine and mupirocin, respectively, PVP-I 10 and 7.5% solutions demonstrated rapid and superior bactericidal activity against MRSA in in vitro and ex vivo studies. Notably, PVP-I 10 and 5% solutions were also active against both chlorhexidine-resistant and mupirocin-resistant strains, respectively. Unlike chlorhexidine and mupirocin, available reports have not observed a link between PVP-I and the induction of bacterial resistance or cross-resistance to antiseptics and antibiotics. These preclinical findings also translate into clinical decolonization, where intranasal PVP-I significantly improved the efficacy of chlorhexidine wash and was as effective as mupirocin in reducing surgical site infection in orthopedic surgery. Overall, these qualities of PVP-I make it a useful alternative decolonizing agent for the prevention of S. aureus infections, but additional experimental and clinical data are required to further evaluate the use of PVP-I in this setting.
Abstract licence: CC BY
Chang-Min Lee, Eun-Hee Jeong, Andris Freivalds
International Journal of Industrial Ergonomics, 2001
A. Anderson, T.S. Sun
Chemical Physics Letters, 1970
D.P. Joshi, Y.L. Lan-Chun-Fung, J.G. Pritchard
Analytica Chimica Acta, 1979
R.G. Derwent, B.A. Thrush
Chemical Physics Letters, 1971
Bas Hillebrand, Robert A.W. Kok, Wim G. Biemans
Industrial Marketing Management, 2001
M.D. Danyluk, G.W. King
Chemical Physics, 1977
André A Neves, Dora A Pereira, Luı́s M Vieira, et al.
Journal of Biotechnology, 2000
Y Tamura, H Kikuchi, K Hibi
Journal of Wind Engineering and Industrial Aerodynamics, 2001
B.R. Higginson, D.R. Lloyd, P.J. Roberts
Chemical Physics Letters, 1973
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.