Ciprofloxacin 0.3% / Dexamethasone 0.1% ear drops
Requires a prescription from a doctor or prescriber
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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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6 branded products available
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View all licensed products for Ciprofloxacin + Dexamethasone on the MHRA register
Ciprofloxacin 0.3% / Dexamethasone 0.1% ear drops
Ciprofloxacin 0.3% / Dexamethasone 0.1% ear drops
Ciprofloxacin 0.3% / Dexamethasone 0.1% ear drops
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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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: 5 · 2001–2026
Showing the 50 most relevant studies, sorted by most relevant.
A. Leach, Y. Wood, Edna Gadil, et al.
The Pediatric Infectious Disease Journal, 2008
Yasser fouad, mohamed rabea, mohamed El-Anwar, et al.
Kasr Al Ainy Medical Journal, 2022
N. Mohan, V. Gupta, R. Tandon, et al.
Journal of Cataract and Refractive Surgery, 2001
Abrahamson CW, Landini AL, Stewart J, et al.
2025
- Laryngostenosis
- Tracheal Stenosis
- Ciprofloxacin
ObjectiveMultiple medical therapies exist to improve outcomes following surgical management of laryngotracheal stenosis. One method involves ciprofloxacin-dexamethasone (CPD) administration into the airway, although minimal information exists on this treatment. This scoping review evaluates the current literature to understand the potential utility of CPD after airway surgery.Data sourcesPubMed, EMBASE, Cochrane Library, Scopus, Web of Science.Review methodsDatabases were searched according to PRISMA guidelines. Studies were excluded if they did not administer CPD in the airway, were solely in vitro or animal studies, or lacked full text availability.ResultsFrom 1340 studies identified, seven met inclusion criteria, and one was added from manual searching. All eight articles were published between 2008 and 2025. Four described nebulized CPD, one discussed intratracheal drops, and three evaluated both. Four studies carefully evaluated CPD to assess efficacy and side effects across an aggregate of 167 pediatric and 53 adult patients. One group demonstrated fewer postoperative bronchoscopies and a shorter hospital stay after pediatric open airway surgery. Another study showed fewer granulation tissue events and earlier decannulation for pediatric tracheostomy patients. Side effects were infrequent, and three of the four groups reported no adverse events. In the fourth study, 4.5% of surveyed pediatric otolaryngologists observed a side effect from CPD.ConclusionAlthough there is a paucity of literature regarding the safety and efficacy of CPD use in the airway, the available data suggest low risks and potential benefits. Further research is needed to assess safety, optimal treatment regimens, and efficacy of this off-label therapy.
Abstract licence: CC BY-NC 4.0
Li T, Wang J, Zhang Z, et al.
2025
- Gordonia Bacterium
- Actinomycetales Infections
- Communicable Diseases, Emerging
BACKGROUND: Gordonia bronchialis (G. bronchialis) is an emerging opportunistic pathogen that primarily affects immunocompromised individuals and is often associated with indwelling catheters. CASE PRESENTATION: This paper presents a case of central line-associated bloodstream infection caused by G. bronchialis in a 15-year-old male with acute myeloid leukemia (AML), highlighting diagnostic challenges and successful treatment with antimicrobial therapy. The isolate was identified as G. bronchialis using matrix-assisted laser desorption/ionization-time of flight mass spectrometry (MALDI-TOF MS). Subsequent antimicrobial susceptibility testing revealed it to be susceptible to amikacin, amoxicillin-clavulanate, ceftriaxone, ciprofloxacin, clarithromycin, imipenem, linezolid, minocycline, moxifloxacin, trimethoprim-sulfamethoxazole, tobramycin, cefepime, cefotaxime and doxycycline. A comprehensive literature review of 41 reported cases underscores the diverse clinical manifestations of G. bronchialis infections, including bacteremia, sternal wound infections, and osteomyelitis, with a 95.1% cure rate. Diagnostic limitations and the need for advanced microbiological techniques are discussed, emphasizing the importance of clinical awareness in immunocompromised patients. CONCLUSIONS: This review advocates for standardized treatment guidelines and further research into virulence mechanisms and biofilm-disrupting agents to combat this pathogen effectively.
Abstract licence: CC BY
Katherine R. Kavanagh, Kourosh Parham, Scott R. Schoem
Archives of Otolaryngology–Head & Neck Surgery, 2009
- Ear, Middle
- Tympanic Membrane
- Mice, Inbred CBA
H. Khan, A. Amitava
Indian journal of ophthalmology, 2007
Michael Wall, D. Stroman, P. Roland, et al.
The Pediatric infectious disease journal, 2009
Tom Ben-Dov, Jackie Yang, Max M. April
Annals of Otology, Rhinology & Laryngology, 2022
- Diabetes Mellitus, Type 1
- Hyperglycemia
- Drug-Related Side Effects and Adverse Reactions
J. Dohar, W. Giles, P. Roland, et al.
Pediatrics, 2006
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.