Econazole 1% eye drops preservative free
Requires a prescription from a doctor or prescriber
A broad spectrum antimycotic with some action against Gram positive bacteria.
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
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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Suspected adverse reactions reported for Econazole
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Report a side effect
Submit a Yellow Card report to the MHRA
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
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Econazole
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Learn about EU pharmacovigilance and safety monitoring
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
Part of the Ecostatin brand family (generic: Econazole)
MHRA licensed products
View all licensed products for Econazole on the MHRA register
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.
Check stock at pharmacies and supply information
Pharmacy stock checkers
Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
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
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
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.
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: 3 · Randomised trials: 2 · 1978–2026
Showing the 50 most relevant studies, sorted by most relevant.
Ahmed B, Saini N, Barathi VA, et al.
2025
- Eye Diseases
- Lipids
- Drug Delivery Systems
TopicThis systematic review explores solid lipid nanoparticles (SLNs) as innovative drug delivery systems for ocular applications. It evaluates their ability to improve bioavailability, sustain drug release, and overcome ocular barriers in treating anterior and posterior segment disorders such as dry eye syndrome, glaucoma, infections, and retinal diseases. Comparisons with traditional delivery systems and other nanoparticle platforms are also addressed.Clinical relevanceOcular diseases often face challenges in effective drug delivery due to the eye's unique anatomy and physiological barriers. Current treatments, including eye drops and intravitreal injections, are limited by rapid clearance, invasiveness, and systemic side effects. SLNs offer a next-generation alternative, addressing these limitations with enhanced corneal permeability, drug retention, and targeted delivery.MethodsA comprehensive search was conducted across PubMed, Scopus, Web of Science, and Google Scholar, focusing on studies and patents published from 2010 to 2024. Inclusion criteria targeted original studies using SLNs for ocular applications, excluding studies describing only liposomes and micelles. The PRISMA 2020 guidelines were followed, and data extraction included active pharmaceutical ingredients (APIs), particle size, zeta potential, and therapeutic outcomes. Risk of bias was evaluated using appropriate frameworks.ResultsTwenty-eight (28) studies and twenty (20) patents met inclusion criteria, covering SLNs encapsulating APIs such as econazole, atorvastatin, and cannabinoids. Key findings highlighted enhanced bioavailability (up to 12-fold in vitreous humour for atorvastatin-SLNs), sustained release (24-96 h), and improved corneal permeability (up to 287 % higher than controls). Patented formulations incorporated cationic SLNs, PEGylated lipid nanoparticles, and bioactive-loaded SLNs, demonstrating superior stability and therapeutic efficacy. No significant ocular toxicity was observed across in vitro and in vivo studies.ConclusionSLNs represent a transformative approach for ocular drug delivery, combining safety, scalability, commercial viability, and enhanced therapeutic outcomes due to higher permeability and controlled release. However, challenges remain in industrial translation and regulatory approvals. Future research should focus on quality by design (QbD) formulation development; simple, viable, energy-efficient, and preferably organic solvent-free methods of preparation; and leveraging advanced characterization techniques like SAXS and molecular simulations to refine and define SLNs design, molecular structure, and function.
Abstract licence: CC BY
Ye C, Hong Y, Cai Y
2025
N. Prajna, R. John, P. Nirmalan, et al.
British Journal of Ophthalmology, 2003
- Antifungal Agents
- Econazole
- Keratitis
R.C. Heel, Rex N. Brogden, T.M. Speight, et al.
Drugs, 1978
- Haplorhini
- Bacterial Infections
- Candidiasis, Vulvovaginal
Poonam Verma, Kamla Pathak
Nanomedicine Nanotechnology Biology and Medicine, 2011
- Acrylates
- Antifungal Agents
- Drug Carriers
Taylor Hughes, David T. Lodowski, Kevin W. Huynh, et al.
Nature Structural & Molecular Biology, 2017
- Cryoelectron Microscopy
- Epitopes
- Calcium
Kerstin Hill, Shaun McNulty, Andrew D. Randall
Naunyn-Schmiedeberg s Archives of Pharmacology, 2004
- Antifungal Agents
- Cell Line
- Clotrimazole
Alireza Firooz, Shohreh Nafisi, Howard I. Maïbach
International Journal of Pharmaceutics, 2015
- Antifungal Agents
- Chemistry, Pharmaceutical
- Drug Carriers
Abhay Thakur
African Journal OF Biomedical Research, 2024
Renuka Sharma, K. Pathak
Pharmaceutical development and technology, 2011
- Acrylates
- Administration, Cutaneous
- Diffusion
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.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
1 found
Half-life
Not available
Mechanism
Econazole interacts with 14-α demethylase, a cytochrome P-450 enzyme neces…
Food interactions
None known
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Metabolism
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 120 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
Response to specific ligands is species-specific. Activated by naturally occurring steroids, such as pregnenolone and progesterone. Binds to a response element in the promoters of the CYP3A4 and ABCB1/MDR1 genes
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC G01AF05
ATC D01AC03
ATC G01AF20
ATC G01AF55
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Econazole
Additional database identifiers
Drugs Product Database (DPD)
2110
ChemSpider
3086
BindingDB
31773
Guide to Pharmacology
2446
GenBank Gene Database
X13296
GenBank Protein Database
578119
UniProt Accession
CP51_CANAL
HUGO Gene Nomenclature Committee (HGNC)
HGNC:7968
GenAtlas
NR1I2
GeneCards
NR1I2
GenBank Gene Database
AF061056
GenBank Protein Database
3511138
Guide to Pharmacology
606
UniProt Accession
NR1I2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2594
GenAtlas
CYP19A1
GeneCards
CYP19A1
GenBank Gene Database
M22246
GenBank Protein Database
179002
Guide to Pharmacology
1362
UniProt Accession
CP19A_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2631
GeneCards
CYP2E1
GenBank Gene Database
J02625
GenBank Protein Database
181360
Guide to Pharmacology
1330
UniProt Accession
CP2E1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2637
GenAtlas
CYP3A4
GeneCards
CYP3A4
GenBank Gene Database
M18907
Guide to Pharmacology
1337
UniProt Accession
CP3A4_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q417141), 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.