DescriptionCurator's Comment: Description was created based on several sources, including:
http://www.drugs.com/cdi/kanamycin.html
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d4865638-1259-4eef-a73c-fe919af6e850
Curator's Comment: Description was created based on several sources, including:
http://www.drugs.com/cdi/kanamycin.html
https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d4865638-1259-4eef-a73c-fe919af6e850
Kanamycin (a mixture of kanamycin A, B and C) is an aminoglycoside bacteriocidal antibiotic, available in oral, intravenous, and intramuscular forms, and used to treat a wide variety of infections. It is effective against Gram-negative bacteria and certain Gram-positive bacteria. Aminoglycosides work by binding to the bacterial 30S ribosomal subunit, causing misreading of t-RNA, leaving the bacterium unable to synthesize proteins vital to its growth. Serious side effects include tinnitus or loss of hearing, toxicity to kidneys, and allergic reactions to the drug. Mixing of an aminoglycoside with beta-lactam-type antibiotics (penicillins or cephalosporins) may result in a significant mutual inactivation. Even when an aminoglycoside and a penicillin-type drug are administered separately by different routes, a reduction in aminoglycoside serum half-life or serum levels has been reported in patients with impaired renal function and in some patients with normal renal function.
CNS Activity
Curator's Comment: In adults, does not cross the blood-brain barrier (BBB) in therapeutically adequate concentrations. Small improvement in penetration with inflamed meninges.
http://www.nikapharm.uz/en/products/kanamycin
https://www.google.ru/url?sa=t&rct=j&q=&esrc=s&source=web&cd=6&ved=0ahUKEwi7rPuFzZ3MAhWnYZoKHT49B1gQFghCMAU&url=http%3A%2F%2Fwww.kurgansintez.ru%2Fen%2Fcatalog%2Fdoc_en%2F%25D0%259A%25D0%25B0%25D0%25BD%25D0%25B0%25D0%25BC%25D0%25B8%25D1%2586%25D0%25B8%25D0%25BD%2520%25D0%25B8%25D0%25BD%25D1%2581%25D1%2582%25D1%2580%25D1%2583%25D0%25BA%25D1%2586%25D0%25B8%25D1%258F_ENG.doc&usg=AFQjCNEbniX1AkdM3gQf_NmUv6xsx7rMOA&sig2=WDq4GgcENoEZxCI1BLyvUw&bvm=bv.119745492,d.bGs
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: CHEMBL2363135 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Curative | KANAMYCIN SULFATE Approved UseKanamycin may be considered as initial therapy in the treatment of infections where one or more of the following are the known or suspected pathogens: E. coli, Proteus species (both indole-positive and indole-negative), Enterobacter aerogenes, Klebsiella pneumoniae, Serratia marcescens, Acinetobacter species.
Although kanamycin is not the drug of choice for staphylococcal infections, it may be indicated under certain conditions for the treatment of known or suspected staphylococcal disease. Launch Date2002 |
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Curative | KANAMYCIN SULFATE Approved UseKanamycin may be considered as initial therapy in the treatment of infections where one or more of the following are the known or suspected pathogens: E. coli, Proteus species (both indole-positive and indole-negative), Enterobacter aerogenes, Klebsiella pneumoniae, Serratia marcescens, Acinetobacter species.
Although kanamycin is not the drug of choice for staphylococcal infections, it may be indicated under certain conditions for the treatment of known or suspected staphylococcal disease. Launch Date2002 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
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11.9 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/4790604/ |
250 mg single, intramuscular dose: 250 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
KANAMYCIN A plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
Value | Dose | Co-administered | Analyte | Population |
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44.2 μg × h/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/4790604/ |
250 mg single, intramuscular dose: 250 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
KANAMYCIN A plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
2.1 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/4790604/ |
250 mg single, intramuscular dose: 250 mg route of administration: Intramuscular experiment type: SINGLE co-administered: |
KANAMYCIN A plasma | Homo sapiens population: HEALTHY age: ADULT sex: MALE food status: UNKNOWN |
PubMed
Title | Date | PubMed |
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[Clinical studies of cochleotoxicosis due to viomycin and kanamycin during tuberculostatic treatment (a prophylactic attempt)]. | 1968 |
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Acute renal failure in general surgical patients. | 1971 Jun |
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Proceedings: The use of conditioned tone discrimination to study kanamycin ototoxicity in the rat. | 1975 Dec |
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Treatment of meningitis and septicemia in infancy with a sulphamethoxazole/trimethorpim combination. | 1975 Jan |
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Further studies on effects of irrigation solutions on rat bladders. | 1976 Dec |
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Auditory thresholds and kanamycin-induced hearing loss in the guinea pig assessed by a positive reinforcement procedure. | 1978 Feb |
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Reflex modification as a test for sensory function. | 1985 Nov-Dec |
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Furosemide ototoxicity: clinical and experimental aspects. | 1985 Sep |
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[Acute renal failure caused by ceporin, kanamycin and gentamicin]. | 1989 Mar-Apr |
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Spectrum of drugs against atypical mycobacteria: how valid is the current practice of drug susceptibility testing and the choice of drugs? | 1992 Dec |
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[The role of mtDNA deletion in the sensitivity to aminoglycoside antibiotic induced deafness]. | 2000 Apr |
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Use of genomics and combinatorial chemistry in the development of new antimycobacterial drugs. | 2000 Feb 1 |
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Temporal bone studies of the human peripheral vestibular system. Aminoglycoside ototoxicity. | 2000 May |
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Mutant prevention concentration as a measure of antibiotic potency: studies with clinical isolates of Mycobacterium tuberculosis. | 2000 Sep |
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Inhibition of the HIV-1 rev-RRE complex formation by unfused aromatic cations. | 2001 May |
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Overexpression of copper/zinc-superoxide dismutase protects from kanamycin-induced hearing loss. | 2001 May-Jun |
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Rapamycin and less immunosuppressive analogs are toxic to Candida albicans and Cryptococcus neoformans via FKBP12-dependent inhibition of TOR. | 2001 Nov |
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Bactericidal activities of commonly used antiseptics against multidrug-resistant mycobacterium tuberculosis. | 2002 |
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New agents active against Mycobacterium avium complex selected by molecular topology: a virtual screening method. | 2004 Jan |
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Adeno-associated virus-mediated Bcl-xL prevents aminoglycoside-induced hearing loss in mice. | 2007 Jul 20 |
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Deafferentation-associated changes in afferent and efferent processes in the guinea pig cochlea and afferent regeneration with chronic intrascalar brain-derived neurotrophic factor and acidic fibroblast growth factor. | 2008 Apr 1 |
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Antimycobacterial activity of cinnamate-based esters of the triterpenes betulinic, oleanolic and ursolic acids. | 2008 Feb |
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Enhanced survival of spiral ganglion cells after cessation of treatment with brain-derived neurotrophic factor in deafened guinea pigs. | 2009 Sep |
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Novel cathelicidin-derived antimicrobial peptides from Equus asinus. | 2010 May |
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Isoxazole analogs of curcuminoids with highly potent multidrug-resistant antimycobacterial activity. | 2010 Oct |
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Chlorinated coumarins from the polypore mushroom Fomitopsis officinalis and their activity against Mycobacterium tuberculosis. | 2013 Oct 25 |
Sample Use Guides
Intramuscular and intravenous: 15 mg/kg/day in two equally divided dosages. Intraperitoneal: 500 mg diluted in 20 mL sterile distilled water may be instilled through a polyethylene catheter sutured into the wound at closure.
Aerosol treatment: 250 mg two to four times a day.
Irrigation: injection in concentrations of 0.25 percent (2.5 mg/mL).
Route of Administration:
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CFR |
21 CFR 524.1204
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WHO-ATC |
S01AA24
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WHO-ESSENTIAL MEDICINES LIST |
6.2.4
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CFR |
21 CFR 524.1200
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NDF-RT |
N0000007853
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CFR |
21 CFR 862.3520
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WHO-VATC |
QA07AA08
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NDF-RT |
N0000175477
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WHO-ATC |
J01GB04
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QS01AA24
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WHO-ATC |
A07AA08
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WHO-VATC |
QJ01GB04
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CFR |
21 CFR 524.1200B
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CFR |
21 CFR 520.1204
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CFR |
21 CFR 524.1200A
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NCI_THESAURUS |
C2363
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6104
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6099
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D007612
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KANAMYCIN
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870
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DB01172
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m6599
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RUC37XUP2P
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C65997
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Kanamycin
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All of the following components must be present:
ACTIVE MOIETY