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Description

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

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
KANAMYCIN SULFATE
Curative
KANAMYCIN SULFATE

Cmax

ValueDoseCo-administeredAnalytePopulation
11.9 μg/mL
250 mg single, intramuscular
KANAMYCIN A plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
44.2 μg × h/mL
250 mg single, intramuscular
KANAMYCIN A plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
2.1 h
250 mg single, intramuscular
KANAMYCIN A plasma
Homo sapiens

PubMed

Sample Use Guides

In Vivo Use Guide
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: Other
In Vitro Use Guide
The minimum inhibitory concentration (MIC), determined by the microdilution method, of E. coli and S. aureus were 4.5 and 3.5 mg/L, respectively. The MIC was 5.0 mg/L for the dual species scenario.
Substance Class Mixture
Record UNII
RUC37XUP2P
Record Status Validated (UNII)
Record Version
All of the following components must be present:
Definition References