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Amikacin has the same spectrum of activity as gentamicin and tobramycin, but it is less susceptible to enzymatic inactivation. This makes amikacin valuable in managing infections caused by Gram-negative bacilli resistant to gentamicin and tobramycin.
Amikacin’s use can include coverage against some aerobic Gram-positive bacteria,which include E.coli, klebsiella, proteus, pseudomonas, salmonella, enterobacter, serratia and mycoplasma.
The drug is almost exclusively eliminated by way of glomerular filtration when given in parenteral form.
Aminoglycosides do not readily cross the blood-brain barrier. However, they are able to cross placental barrier, and may cause nerve or nephrotoxic effects to the fetus. It is not recommended that these drugs be used in pregnant rats.
Per the manufacturer it is not a recommendation to mix amikacin in with other drug compounds. Give separately.
For other interactions and contraindications check with a pharmacist.
CNS: lethargy, neuromuscular blockade, facial edema, tremors, pain/inflammation at injection site.
Resp: bronchoconstriction and/or bronchospasm can occur when nebulizing, but are reportedly rare
GI: Affects GI flora
GU: nephrotoxicity (oliguria,proteinuria)
Skin: itching, swelling
Other: loss of coordination
*Note:
All aminoglycosides have the potential for causing ototoxicity, nephrotoxicity and neuromuscular blockade due to high serum and tissue concentrations, as well as prolonged use. This is especially prevalent when given by parenteral administration (e.g. IM, IV, SQ) due to systemic absorption. Studies have shown no evidence of toxicity when nebulized in therapeutic doses even with prolonged use. The lack of toxicity seen with nebulized aminoglycosides may be due to minimal or no systemic absorption, having lower unsustained serum concentrations due to a lower dosage used, and being directly delivered to the area of infection. A noted concern of prolonged or repetitive nebulizing of antimicrobials, such as the aminoglycosides, is the potential for the overgrowth of resistant organisms.1, 2, 3
or
10 mg/kg to 20 mg/kg total per day divided q8hrs to q24hrs; SQ or IM 2
or
10 mg/kg to 20 mg/kg per day 11
or
5 mg/lb , SQ or IM , BID or TID, for 7 to 14 days(as recommended on RMCA Drug Chart)
or
2 mg/kg to 5 mg/kg , SQ or IM , q8hrs to q12hrs 1
Posted on June 17, 2003, 15:34,
Last updated on October 6, 2010, 12:53
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