Naphazoline 0.012% eye drops
Available from a pharmacy with pharmacist advice
Naphazoline is a rapid acting imidazoline sympathomimetic vasoconstrictor of ocular or nasal artierioles[L5804,L5807].
Safety information for pregnancy and breastfeeding
Pregnancy
Breastfeeding
Always consult your doctor or midwife before taking any medicine during pregnancy or while breastfeeding. Source: DrugBank (CC BY-NC 4.0).
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Yellow Card
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Drug safety updates
MHRA alerts for Naphazoline
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 Naphazoline
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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 Naphazoline
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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
Part of the Murine brand family (generic: Naphazoline)
MHRA licensed products
View all licensed products for Naphazoline on the MHRA register
Murine irritation & redness relief 0.012% eye 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.
NHS prescribing volume and spending trends
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
Browse tools
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: 3 · Randomised trials: 1 · Trials: 1 · 1975–2027
Showing the 50 most relevant studies, sorted by most relevant.
de Carvalho WF, Junior LCV, Junior HFB, et al.
2021
- Naphazoline
- Gingival Retraction Techniques
- Gingiva
Letícia Apolinário Carlos da Silva, Mirella Camargo do Nascimento, Thais Ranielle Souza de Oliveira
Scientific Electronic Archives, 2024
This study examines the risks and harms associated with the use of naphazoline hydrochloride (NHC). The methodology involved a narrative literature review from 2013 to 2023 in Portuguese, English, and Spanish, which identified eleven relevant articles from Scielo, Medline Complete, PubMed, and Google Scholar. The guiding question was: What are the risks and potential adverse effects associated with the use of NHC? Results and Discussion: Pharmacists play a crucial role in educating against misuse and promoting responsible medication use. However, challenges arise due to the prevalence of self-medication and limited pharmacist involvement in prescribing. The Role of Pharmacists: Harms of Misuse: Key concerns identified include systemic effects, drug-induced rhinitis, and dependence. Overuse of NHC during pregnancy and in children can lead to serious consequences such as hypothermia, bradycardia, and nervous system depression. The abuse hazards of NHC include rebound effects, drug-induced rhinitis, and long-term health risks such as hypertension and heart problems. Conclusion: The study emphasizes the pressing need for enhanced pharmacist training to equip them to effectively counsel and prevent misuse. Additionally, increased public awareness campaigns should be implemented to promote responsible non-prescription healthcare (NHC) use. Stricter dispensing measures, such as regulations to restrict over-the-counter access, should also be put in place. It is essential to promote responsible NHC use. Pharmacists play a critical role in mitigating the risks associated with this widely used medication as public health educators and patient guides.
Abstract licence: CC BY 4.0
Robert Skopec
Journal of Bio Innovation, 2020
Haixia He, Yameng Wan, Fanfan Li, et al.
Journal of Molecular Liquids, 2024
Chou AK, Chiu CC, Zhu GC, et al.
2023
- Lidocaine
- Analgesia
- Rats
Oishi T, Kashiura M, Yasuda H, et al.
2024
- Naphazoline
- Nicardipine
- Phentolamine
Uehara H, Taguchi D, Osanai T, et al.
2024
Karolina Lejwoda, Anna Gumieniczek, Agata Filip, et al.
Molecules, 2024
- Naphazoline
- Photolysis
- Mice
Because of their topical application in patients and meaningful UV/VIS absorptive properties, the degradation and potential toxicity under irradiation of diflunisal (DIF) and naphazoline (NAF) were studied. In addition, the impact of pH on their photostability was examined, showing the highest degradation of acidic DIF at pH 1 and 13 and the highest degradation of basic NAF at pH below 7. An LC–UV analysis and chemical tests showed the first-order kinetics for their degradation and generation of reactive oxygen species (ROS). A UPLC-HRMS/MS analysis allowed us to identify four degradants of DIF (from DD-1 to DD-4) and six degradants of NAF (from ND-1 to ND-6). When Toxtree software was used, a high class III of toxicity was observed for DD-2, DD-3, and DD-4, and for all the NAF degradants. Furthermore, the ND-2 product, i.e., 2-[(1-methylnaphthalen-2-yl)methyl]-4,5-dihydro-1H-imidazole, was shown to present medium mutagenic and high tumorigenic effects according to OSIRIS Property Explorer. In addition, two in vitro tests on BALB/c 3T3 mouse fibroblasts showed a phototoxic effect of DIF and NAF at the lowest concentrations tested, i.e., 5 µg/mL. Thus, our present results could be useful to design further phototoxicity studies for DIF and NAF to minimize the risk of phototoxicity due to their photodegradation.
Abstract licence: CC BY 4.0
M Galasso
European Heart Journal Supplements, 2024
Rehab M Abdelfatah, Maimana A Magdy
Journal of AOAC International, 2023
- Ephedrine
- Naphazoline
- Parabens
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
4 to 8 hours
Mechanism
Naphazoline is a vasoconstrictor that functions by stimulating alpha adrenergic…
Food interactions
None known
Human targets
3 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
4 to 8 hours
[L5807]
…
Protein binding
Volume of distribution
Metabolism
Elimination
Clearance
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Naphazoline was first developed in 1942 as a nasal formulation for congestion[A176609].
[A176558][L5804][L5807]
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 935 interactions
[A176558]
This effect is especially pronounced in children under 6 years.
[A176558][A176564]
Long term use of naphazoline can lead to rhinitis medicamentosa once naphazoline is stopped.
[A176567]
This condition is a result of norepinephrine release by naphazoline triggering a negative feedback loop.
[A176567]
Safety and effectiveness in children under 12 has not been established[F4214]. Studies in elderly patients have yet to be performed[F4214]. Risk in pregnancy, breast feeding, and on overall fertility have not been established, though pregnant and breast feeding patients should consider the risk and benefit before starting naphazoline treatment[F4214].
Naphazoline causes the release of norepinephrine in sympathetic nerves[A176567]. Norepinephrine binds to alpha adrenergic receptors and causes vasoconstriction[A176567]. Naphazoline is also a mild beta adrenergic receptor agonist, which can cause rebound vasodilation after the alpha adrenergic stimulation has ended[A176567]. Naphazoline's release of norepinephrine also triggers a negative feedback loop which decreases production of norepinephrine, which can lead to rhinitis medicamentosa after long term use when naphazoline is stopped[A176567].
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L5807]
Other imidazoline compounds have half lives varying from 2 to 12 hours[T530].
Proteins and enzymes this drug interacts with in the body
PMID:21645528
Positively regulates postnatal regression of retinal hyaloid vessels via suppression of VEGFR2/KDR activity, downstream of OPN5 (By similarity)
ATC R01AB02
ATC S01GA01
ATC S01GA51
ATC R01AA08
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Show
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Naphazoline
Additional database identifiers
Drugs Product Database (DPD)
9542
Drugs Product Database (DPD)
5642
ChemSpider
4283
BindingDB
50001922
ZINC
ZINC000000119717
HUGO Gene Nomenclature Committee (HGNC)
HGNC:281
GenAtlas
ADRA2A
GeneCards
ADRA2A
GenBank Gene Database
M23533
GenBank Protein Database
178196
Guide to Pharmacology
25
UniProt Accession
ADA2A_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:277
GenAtlas
ADRA1A
GeneCards
ADRA1A
GenBank Gene Database
D25235
GenBank Protein Database
433201
Guide to Pharmacology
22
UniProt Accession
ADA1A_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:3023
GenAtlas
DRD2
GeneCards
DRD2
GenBank Gene Database
M30625
GenBank Protein Database
181432
Guide to Pharmacology
215
UniProt Accession
DRD2_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72