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Description
Curator's Comment: description was created based on several sources, including http://reference.medscape.com/drug/neo-fradin-myciguent-neomycin-po-342515

Neomycin is an aminoglycoside antibiotic found in many topical medications such as creams, ointments, and eye drops. In vitro tests have demonstrated that neomycin is bactericidal and acts by inhibiting the synthesis of protein in susceptible bacterial cells. It is effective primarily against gram-negative bacilli but does have some activity against gram-positive organisms. Neomycin is active in vitro against Escherichia coli and the Klebsiella-Entero. Topical uses include treatment for superficial eye infections caused by susceptible bacteria (used in combination with other anti-infective), treatment of otitis externa caused by susceptible bacteria, treatment or prevention of bacterial infections in skin lesions, and use as a continuous short-term irrigant or rinse to prevent bacteriuria and gram negative rod bacteremia in bacteriuria patients with indwelling catheters. May be used orally to treat hepatic encephalopathy, as a perioperative prophylactic agent, and as an adjunct to fluid and electrolyte replacement in the treatment of diarrhea caused to enter pathogenic E. coli (EPEC). Neomycin sulfate has been shown to be effective adjunctive therapy in hepatic coma by reduction of the ammonia forming bacteria in the intestinal tract. The subsequent reduction in blood ammonia has resulted in neurologic improvement. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Neomycin Sulfate Oral Solution and other antibacterial drugs, susceptible bacteria should use Neomycin Sulfate Oral Solution only to treat or prevent infections that are proven or strongly suspected to be caused. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy. Neomycin binds to four nucleotides of 16S rRNA and a single amino acid of protein S12. This interferes with decoding site near nucleotide 1400 in 16S rRNA of 30S subunit. This region interacts with the wobble base in the anticodon of tRNA. This leads to interference with the initiation complex, misreading of mRNA so incorrect amino acids are inserted into the polypeptide leading to nonfunctional or toxic peptides and the breakup of polysomes into nonfunctional monosomes

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
CVP TRIPLE ANTIBIOTIC

Approved Use

Uses: first aid to help prevent infection in minor: cuts, scrapes, burns

Launch Date

1995
Palliative
NEO-FRADIN

Approved Use

Hepatic coma (portal-systemic encephalopathy): Neomycin sulfate has been shown to be effective adjunctive therapy in hepatic coma by reduction of the ammonia forming bacteria in the intestinal tract. The subsequent reduction in blood ammonia has resulted in neurologic improvement. To reduce the development of drug-resistant bacteria and maintain the effectiveness of Neomycin Sulfate Oral Solution and other antibacterial drugs, Neomycin Sulfate Oral Solution should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria. When culture and susceptibility information are available, they should be considered in selecting or modifying antibacterial therapy. In the absence of such data, local epidemiology and susceptibility patterns may contribute to the empiric selection of therapy.

Launch Date

2001
PubMed

PubMed

TitleDatePubMed
The evaluation of neomycin and other antimicrobial agents of bacterial and fungal origin, and substances from higher plants.
1949 Dec 14
[Acute renal failure in neomycin-treated pancreatitis patients].
1975 Dec
A hole in the drum. An overview of tympanic membrane perforations.
2002 Aug
Are topical antibiotics necessary in the management of otitis externa?
2002 Aug
Stereospecificity of aminoglycoside-ribosomal interactions.
2002 Aug 20
Inhibition of protein synthesis by aminoglycoside-arginine conjugates.
2002 Oct
Delayed hypersensitivity reaction to topical aminoglycosides in patients undergoing middle ear surgery.
2002 Oct
Reexamination of neomycin B degradation: efficient preparation of its CD and D rings as protected glycosyl donors.
2002 Oct 3
Experimental evidence for the existence of non-exo-anomeric conformations in branched oligosaccharides: the neomycin-B case.
2002 Oct 7
Mutations in gp41 and gp120 of HIV-1 isolates resistant to hexa-arginine neomycin B conjugate.
2003 Dec 26
Effect of neomycin B on rotavirus plus- and minus-strand RNA synthesis.
2003 Jun
Aminoglycoside antibiotics reduce glucose reabsorption in kidney through down-regulation of SGLT1.
2003 Sep 5
Changing patterns of contact allergy in chronic inflammatory ear disease.
2004 Feb
An approach to enhance specificity against RNA targets using heteroconjugates of aminoglycosides and chloramphenicol (or linezolid).
2004 Feb 25
New agents active against Mycobacterium avium complex selected by molecular topology: a virtual screening method.
2004 Jan
Interactions of the antibiotics neomycin B and chlortetracycline with the hammerhead ribozyme as studied by Zn2+-dependent RNA cleavage.
2004 Mar 1
Randomized, double-blind trial comparing topical nitroglycerine with xylocaine and Proctosedyl in idiopathic chronic anal fissure.
2004 May-Jun
Molecular evaluation of residual endodontic microorganisms after instrumentation, irrigation and medication with either calcium hydroxide or Septomixine.
2004 Nov
Lipoprotein lipase in hemodialysis patients: indications that low molecular weight heparin depletes functional stores, despite low plasma levels of the enzyme.
2004 Nov 3
The efficacies of affected-limb care with penicillin diethylcarbamazine, the combination of both drugs or antibiotic ointment, in the prevention of acute adenolymphangitis during bancroftian filariasis.
2004 Oct
Delayed neurotrophic treatment preserves nerve survival and electrophysiological responsiveness in neomycin-deafened guinea pigs.
2004 Oct 1
Chemoenzymatic synthesis and high-throughput screening of an aminoglycoside-polyamine library: identification of high-affinity displacers and DNA-binding ligands.
2004 Oct 6
Disaccharide mimetics of the aminoglycoside antibiotic neamine.
2004 Sep 6
[The effectiveness of some methods in eliminating bacteria from the root canal of a tooth with chronic apical periodontitis].
2005
Neamine inhibits xenografic human tumor growth and angiogenesis in athymic mice.
2005 Dec 15
Targeted infection of HIV-1 Env expressing cells by HIV(CD4/CXCR4) vectors reveals a potential new rationale for HIV-1 mediated down-modulation of CD4.
2005 Dec 21
Prescription pattern for treatment of hemorrhoids under the universal coverage policy of Thailand.
2005 Jul
Disruption and restoration of cell-cell junctions in mouse vestibular epithelia following aminoglycoside treatment.
2005 Jul
A simple structural-based approach to prevent aminoglycoside inactivation by bacterial defense proteins. Conformational restriction provides effective protection against neomycin-B nucleotidylation by ANT4.
2005 Jun 15
Introduction of a substituent at the 5"-position of N-Boc neomycin B under Mitsunobu reaction conditions.
2005 Jun 7
Aminoglycosides induce acute cell signaling and chronic cell death in renal cells that express the calcium-sensing receptor.
2005 May
tRNAPhe cleavage by aminoglycosides is triggered off by formation of an abasic site.
2005 May 27
Quantitative analysis of shape-specific interactions of Rev response element with a positively charged Rev peptide by capillary electrophoresis.
2005 Nov
Neamine dimers targeting the HIV-1 TAR RNA.
2005 Nov 1
Contact allergy to neomycin sulfate: results of a multifactorial analysis.
2005 Oct
Branched aminoglycosides: biochemical studies and antibacterial activity of neomycin B derivatives.
2005 Oct 15
Analysis of neomycin sulfate and framycetin sulfate by high-performance liquid chromatography using evaporative light scattering detection.
2005 Sep 16
Identification and quantitation of polymyxin B, framycetin, and dexamethasone in an ointment by using thin-layer chromatography with densitometry.
2005 Sep-Oct
Neamine derivatives having a nucleobase with a lysine or an arginine as a linker, their synthesis and evaluation as potential inhibitors for HIV TAR-Tat.
2006 Apr 15
Trisaccharide mimetics of the aminoglycoside antibiotic neomycin.
2006 Apr 7
Rapid analysis of native neomycin components on a portable capillary electrophoresis system with potential gradient detection.
2006 Aug
Synthesis and antibacterial activity of novel neamine derivatives.
2006 Dec 15
Elucidation of ATP-stimulated stress protein expression of RBA-2 type-2 astrocytes: ATP potentiate HSP60 and Cu/Zn SOD expression and stimulates pI shift of peroxiredoxin II.
2006 Feb 1
Exploring the use of conformationally locked aminoglycosides as a new strategy to overcome bacterial resistance.
2006 Jan 11
Mitsunobu dehydration of N-Boc neomycin B.
2006 Jan 7
Neonatal deafness results in degraded topographic specificity of auditory nerve projections to the cochlear nucleus in cats.
2006 Jul 1
Biosolids from two-stage bioleaching could produce compost for unrestricted use.
2006 Jun
The role of phospholipase D and phosphatidic acid in the mechanical activation of mTOR signaling in skeletal muscle.
2006 Mar 21
Removal of p-xylene with Pseudomonas sp. NBM21 in biofilter.
2006 Oct
Selectively guanidinylated derivatives of neamine. Syntheses and inhibition of anthrax lethal factor protease.
2006 Oct 1
Patents

Sample Use Guides

Hepatic coma: 4-12 grams per day given in the following regimen: 1. Withdraw protein from diet. Avoid use of diuretic agents. 2. Give supportive therapy including blood products, as indicated. 3. Give NEO-FRADIN Oral Solution in doses of four to twelve grams of neomycin sulfate per day in divided doses. Treatment should be continued over a period of five to six days during which time protein should be returned incrementally to the diet.
Route of Administration: Oral
In Vitro Use Guide
Curator's Comment: TRMU, tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase, is expressed in both hair cells and HEI-OC-1 cells, and its expression is significantly decreased after 24 h neomycin treatment. Downregulated TRMU expression with siRNA and found that cell death and apoptosis were significantly increased after neomycin injury.
Unknown
Substance Class Mixture
Created
by admin
on Mon Mar 31 18:33:59 GMT 2025
Edited
by admin
on Mon Mar 31 18:33:59 GMT 2025
Record UNII
I16QD7X297
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEOMYCIN
HSDB   INN   MI   VANDF   WHO-DD  
INN  
Official Name English
KAOMYCINE
Preferred Name English
NEOMIN
Brand Name English
NEOMYCIN [HSDB]
Common Name English
PIMAVECORT
Brand Name English
NEOMYCIN [VANDF]
Common Name English
Neomycin [WHO-DD]
Common Name English
ANTIBIOTIC COMPLEX COMPOSED OF NEOMYCINS A, B AND C PRODUCED BY STREPTOMYCES FRADIAE
Common Name English
NEOMYCIN [MI]
Common Name English
NEOMAS
Brand Name English
neomycin [INN]
Common Name English
NEOLATE
Brand Name English
VONAMYCIN
Brand Name English
FRADIOMYCIN
Common Name English
Classification Tree Code System Code
CFR 21 CFR 524.154
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
WHO-VATC QD06AX04
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
NDF-RT N0000007853
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WHO-VATC QS03AA01
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
CFR 21 CFR 520.1921
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
WHO-VATC QB05CA09
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
CFR 21 CFR 524.1484E
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
NCI_THESAURUS C2363
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
CFR 21 CFR 333.120
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
CFR 21 CFR 524.1484
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
CFR 21 CFR 524.1484K
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WHO-VATC QG51AG03
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
WHO-ATC D06AX04
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
EPA PESTICIDE CODE 6303
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
WHO-ATC A07AA01
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WHO-VATC QA01AB08
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WHO-ATC A07AA51
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WHO-VATC QG51AG06
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WHO-VATC QJ51RG01
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WHO-VATC QA07AA51
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WHO-ATC S01AA03
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LIVERTOX NBK547874
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WHO-ATC A01AB08
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CFR 21 CFR 524.1484J
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
CFR 21 CFR 524.155
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CFR 21 CFR 524.1484H
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WHO-ATC S02AA07
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CFR 21 CFR 524.960
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WHO-VATC QJ01GB05
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CFR 21 CFR 520.1484
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
WHO-VATC QS02AA07
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
CFR 21 CFR 524.1484D
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WHO-ATC R02AB01
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WHO-VATC QS01AA03
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WHO-ATC J01GB05
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WHO-VATC QS02AA57
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CFR 21 CFR 524.1484F
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CFR 21 CFR 524.1484I
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
WHO-ATC S03AA01
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WHO-VATC QA07AA01
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CFR 21 CFR 524.1484B
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CFR 21 CFR 556.430
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CFR 21 CFR 524.1600A
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CFR 21 CFR 558.455
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NDF-RT N0000175477
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CFR 21 CFR 520.82B
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WHO-ATC B05CA09
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CFR 21 CFR 524.1484C
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CFR 21 CFR 524.981C
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CFR 21 CFR 524.1484G
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CFR 21 CFR 524.1600B
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WHO-VATC QR02AB01
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
Code System Code Type Description
SMS_ID
100000090456
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
MESH
D009355
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
DRUG CENTRAL
4247
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
WIKIPEDIA
NEOMYCIN
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
LACTMED
Neomycin
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
EVMPD
SUB03406MIG
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
ECHA (EC/EINECS)
215-766-3
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
NCI_THESAURUS
C683
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
DAILYMED
I16QD7X297
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
MERCK INDEX
m7809
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID9041073
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
INN
232
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
HSDB
3242
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
ChEMBL
CHEMBL184618
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
RXCUI
7299
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY RxNorm
CHEBI
7507
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PRIMARY
IUPHAR
709
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
CAS
1404-04-2
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
DRUG BANK
DB00994
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
FDA UNII
I16QD7X297
Created by admin on Mon Mar 31 18:33:59 GMT 2025 , Edited by admin on Mon Mar 31 18:33:59 GMT 2025
PRIMARY
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