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Amikacin

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Amikacin
Clinical data
Pregnancy
category
  • AU: D
Routes of
administration
Intramuscular, intravenous
ATC code
Legal status
Legal status
Pharmacokinetic data
Protein binding0-11%
Elimination half-life2-3 hours
ExcretionRenal
Identifiers
  • (2S)-4-amino-N-[(2S,3S,4R,5S)-5-amino-2-
    [(2S,3R,4S,5S,6R)-4-amino-3,5-dihydroxy-
    6-(hydroxymethyl)oxan-2-yl]oxy-4-[(2R,3R,
    4S,5R,6R)-6-(aminomethyl)-3,4,5-trihydroxy-
    oxan-2-yl]oxy-3-hydroxy-cyclohexyl]-2-hydroxy-
    butanamide
CAS Number
PubChem CID
DrugBank
CompTox Dashboard (EPA)
ECHA InfoCard100.048.653 Edit this at Wikidata
Chemical and physical data
FormulaC22H43N5O13
Molar mass585.603 g/mol g·mol−1

Amikacin is an aminoglycoside antibiotic used to treat different types of bacterial infections. Amikacin works by binding to the bacterial 30S ribosomal subunit, causing misreading of mRNA and leaving the bacterium unable to synthesize proteins vital to its growth.

Amikacin may be administered once or twice a day but must be given by the intravenous or intramuscular route. There is no oral form available. Dosage must be adjusted in people with kidney failure.

Amikacin is most often used for treating severe, hospital-acquired infections with multidrug resistant Gram negative bacteria such as Pseudomonas aeruginosa, Acinetobacter, and Enterobacter. Amikacin may be combined with a beta-lactam antibiotic for empiric therapy for people with neutropenia and fever.

Side effects of amikacin are similar to other aminoglycosides. Kidney damage and hearing loss are the most important effects. Because of this potential, blood levels of the drug and markers of kidney function (creatinine) may be monitored.

References

  • Edson RS, Terrell CL. The aminoglycosides. Mayo Clin Proc. 1999 May;74(5):519-28. Review. PMID 10319086
  1. ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 Oct 2023.