Kanamycin Sulfate
Action
Indications
Contraindications
Route/Dosage
Interactions
Lab Test Interferences
Adverse Reactions
Precautions
Patient Care Considerations
Administration/Storage
Assessment/Interventions
Patient/Family Education
(kan-uh-MY-sin SULL-fate)
Kantrex
Class: Antibiotic/aminoglycoside
Action Inhibits production of bacterial protein, causing cell death.
Indications
Parenteral: Short-term treatment of serious infections caused by susceptible strains of microorganisms, especially gram-negative bacteria. Oral: Short-term adjunctive therapy for suppression of intestinal bacteria; treatment of hepatic coma.
Contraindications Hypersensitivity to aminoglycosides; intestinal obstruction (oral). Generally not indicated for long-term therapy (> 14 days) because of ototoxicity and nephrotoxicity.
Route/Dosage
Infection
ADULTS & CHILDREN: IM/IV 15 mg/kg/day in 24 divided doses. Do not exceed 1.5 g/day.
Suppression of Intestinal Bacteria
Adults: PO 1 g qh for 4 hr, then 1 g q 6 hr for 3672 hr.
Hepatic Coma
Adults: PO 812 g/day in divided doses.
Interactions
Digoxin, methotrexate, vitamin A, vitamin K: Oral kanamycin may decrease absorption of these drugs. Beta-lactam antibiotics (eg, cephalosporins, penicillins): Do not mix in IV solutions. Drugs with nephrotoxic potential (eg, amphotericin, cephalosporins, enflurane, methoxyflurane, vancomycin): Increased risk of nephrotoxicity. Loop diuretics: Increased auditory toxicity. Neuromuscular blocking agents: Enhanced effects of these agents. Polypeptide antibiotics: Increased risk of respiratory paralysis and renal dysfunction.
Lab Test Interferences None well documented.
Adverse Reactions
CNS: Neuromuscular blockade. EENT: Hearing loss, deafness, loss of balance. GI: Malabsorption syndrome (eg, increased fecal fat, decreased serum carotene, fall in xylose absorption), nausea, vomiting, diarrhea. GU: Oliguria, proteinuria, elevated serum creatinine and BUN, granular casts, red and white cells in urine, decreased creatinine clearance. RESP: Apnea. OTHER: Pain and irritation at injection site, acute muscular paralysis; hypomagnesemia.
Precautions
Pregnancy: Category D. Lactation: Excreted in breast milk. Children: Use cautiously in premature infants and neonates because of renal immaturity. Neuromuscular blockade: Use with caution in patients with neuromuscular disorders, those receiving anesthesia or muscle relaxants, hypomagnesemia, hypocalcemia, hypokalemia or in neonates whose mothers received magnesium sulfate. Oral absorption: Increased absorption (and potential for toxicity) when intestinal mucosa is ulcerated or denuded. Toxicity: Can cause ototoxicity, both auditory and vestibular. Nephrotoxicity may occur; greater risk factors in the elderly, patients with renal impairment, high or frequent doses, long duration of therapy, other nephrotoxic drugs, potassium depletion and decreased intravascular volume.
PATIENT CARE CONSIDERATIONS
Administration/Storage
- Do not mix with other antibacterial agents; administer separately.
- For IV administration, dilute each 500 mg with at least 100200 ml of 0.9% Sodium Chloride or D5W. Give slowly over 3060 min.
- Give IM injection deeply into upper outer quadrant of gluteal muscle.
- Store at room temperature. Darkening of vials during shelf life does not indicate loss of potency.
Assessment/Interventions
- Obtain patient history, including drug history and any known allergies. Note hypersensitivity to aminoglycosides.
- Ensure that culture and sensitivity, renal function tests and serum electrolytes have been performed before beginning therapy and repeat periodically.
- Assess for superinfection (bacterial or fungal overgrowth).
- Assess for allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in susceptible persons (more frequent in asthmatic or atopic nonasthmatic persons).
- Keep patient well hydrated (especially important in elderly).
- Assess auditory function regularly.
- Monitor drug serum concentrations periodically.
- Monitor I&O.
OVERDOSAGE: SIGNS & SYMPTOMS
Nephrotoxicity, auditory toxicity, vestibular toxicity, neuromuscular blockade, respiratory paralysis
Patient/Family Education
- Advise patient that drug may cause nausea, vomiting or diarrhea.
- Instruct patient to drink plenty of fluids while taking medication.
- Emphasize importance of follow-up visits and serial audiograms, because ototoxicity may be asymptomatic.
- Instruct patient to report these symptoms to physician: ringing in ears, hearing impairment, rash, difficulty urinating or dizziness.
Справочник препаратов (англ.) / K
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