Netilmicin 100mg/1ml solution for injection ampoules
Netilmicin is a semisynthetic 1-N-ethyl derivative of sisomycin, an aminoglycoside antibiotic with action similar to gentamicin, but less ear and kidney toxicity.
Official documents, adverse reaction reporting, and safety monitoring
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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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Suspected adverse reactions reported for Netilmicin
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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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Suspected adverse reactions reported for Netilmicin
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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
WHO defined daily dose (DDD)
350 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary BNF/ATC mapping files (NHSBSA). 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
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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
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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: 2 · Randomised trials: 10 · 1976–2026
Showing the 50 most relevant studies, sorted by most relevant.
Petkani F, Lamprogiannis L, Tsinopoulos I, et al.
2025
Antisepsis is a critical aspect of ocular surgery, particularly in intraocular procedures, due to the high risk of postoperative infections. Povidone-iodine is widely recognized for its broad-spectrum antimicrobial properties. This systematic review evaluates the intraoperative use of povidone-iodine applied to the conjunctiva in ocular surgeries. A systematic literature search was conducted using PubMed, Scopus, and Google Scholar for randomized controlled trials (RCTs) published between 2009 and 2023 in English that involved individuals who had undergone an ophthalmological intervention. The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines were followed, and a PRISMA flow diagram was used to illustrate the study selection process. Keywords used included the following: ("Povidone-iodine" OR "Betadine") AND ("Conjunctiva" OR "Ocular surgery"). Studies were selected based on predefined inclusion criteria focusing on the intraoperative antiseptic application of povidone-iodine in human ocular procedures, omitting conference abstracts or unpublished studies. Four RCTs met the inclusion criteria. The evidence base is limited by the small number of included RCTs, which restricts the statistical power and generalizability of the findings. This small sample increases susceptibility to methodological bias, reduces the reliability of pooled estimates, and limits the ability to explore heterogeneity. Furthermore, the potential for publication bias cannot be excluded, particularly given the limited number of studies, which may overestimate treatment effects. These studies compared povidone-iodine 5% to other concentrations or antibiotic agents such as povidone-iodine 1%, chloramphenicol 5%, netilmicin, commercial ozonized antiseptic solution (ozone), moxifloxacin 0.5%, and gatifloxacin. The application of all agents was topically on the conjunctiva just before the ophthalmological procedure started, and only gatifloxacin was applied for three days prior to the procedure. Across all included trials, povidone-iodine demonstrated superior antiseptic efficacy, significantly reducing conjunctival bacterial flora before surgery. The comparative agents showed minimal or less consistent antimicrobial effects. No serious or minor adverse effects related to povidone-iodine use were reported in any of the trials. Povidone-iodine remains a highly effective and safe antiseptic agent for intraoperative use in ocular surgery, while a need exists for additional high-quality independently conducted RCTs to confirm the observed effects and expand the evidence base. Its broad antimicrobial spectrum and favorable safety profile support its continued and widespread application for conjunctival antisepsis, outperforming several commonly used alternatives.
Abstract licence: CC BY
A. Martin Lerner, LawrenceA Cone, Winfried Jansen, et al.
The Lancet, 1983
- Vestibulocochlear Nerve
- Anti-Bacterial Agents
- Bacterial Infections
Lillian J. Love, Stephen C. Schimpff, Davis M. Hahn, et al.
The American Journal of Medicine, 1979
- Agranulocytosis
- Amikacin
- Bacterial Infections
J. Blaser, B. Stone, Michael C. Groner, et al.
Antimicrobial Agents and Chemotherapy, 1987
- Anti-Bacterial Agents
- Bacteria
- Drug Resistance, Microbial
Stephen H. Powell, W. Leigh Thompson, M. A. Luthe, et al.
The Journal of Infectious Diseases, 1983
- Anti-Bacterial Agents
- Cystic Fibrosis
- Dogs
Alain Cometta, J. D. Baumgartner, Daniel Lew, et al.
Antimicrobial Agents and Chemotherapy, 1994
- Bacterial Infections
- Cross Infection
- Netilmicin
Gert A. Verpooten, Rubén A. Giuliano, L. Verbist, et al.
Clinical Pharmacology & Therapeutics, 1989
- Gentamicins
- Kidney
- Netilmicin
Clara C. Chan, B. Oppenheim, Heather Anderson, et al.
Antimicrobial Agents and Chemotherapy, 1989
- Agranulocytosis
- Bacterial Infections
- Ciprofloxacin
P. Mccormick, L. Greenslade, C. Kibbler, et al.
Hepatology, 1997
- Ceftazidime
- Cephalosporins
- Gentamicins
George Samonis, Sofia Maraki, Drosos E. Karageorgopoulos, et al.
European Journal of Clinical Microbiology & Infectious Diseases, 2011
- Drug Synergism
- Drug Resistance, Multiple, Bacterial
- Anti-Bacterial Agents
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
23 found
Half-life
2.5 hours
Mechanism
Aminoglycosides like netilmicin "irreversibly" bind to specific 30S-subunit proteins and 16S rRNA.
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
30-60 minutes
Half-life
2.5 hours
Protein binding
Metabolism
80%
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 874 interactions
Netilmicin is less nephrotoxic than neomycin, gentamicin, tobramycin, and amikacin, likely due to a reduced number of cationic amino groups in its structure. Otoxicity occurs as a result of irreversible damage to hair cells of the cochlea and/or summit of the ampullar cristae in the vestibular complex caused drug accumulation in the endolymph and perilymph of the inner ear. Otoxicity appears to be correlated to total exposure and may be cumulative with further doses of aminoglycosides or other ototoxic drugs (e.g. cisplatin, furosemide).
High frequency hearing loss is followed by low frequency hearing loss, which may be followed by retrograde degeneration of the auditory nerve. Vestibular toxicity may cause vertigo, nausea and vomiting, dizziness and loss of balance.
How the body processes this drug — absorption, distribution, metabolism, and elimination
ATC S01AA23
ATC J01GB07
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)
Netilmicin
Additional database identifiers
Drugs Product Database (DPD)
8353
Drugs Product Database (DPD)
23381
ChemSpider
20152952
BindingDB
50470664
ZINC
ZINC000052981502
GenBank Gene Database
V00355
GenBank Protein Database
43010
UniProt Accession
RS12_ECOLI
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 (Q2553496), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.