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Pronunciation |
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(bas
i TRAY
sin) |
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U.S. Brand
Names |
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AK-Tracin® Ophthalmic; Baciguent®
Topical [OTC]; Baci-IM®
Injection |
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Generic
Available |
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Yes |
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Canadian Brand
Names |
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Bacigvent; Bacitin |
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Pharmacological Index |
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Antibiotic, Ophthalmic; Antibiotic, Topical; Antibiotic,
Miscellaneous |
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Use |
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Treatment of susceptible bacterial infections mainly has activity against
gram-positive bacilli; due to toxicity risks, systemic and irrigant uses of
bacitracin should be limited to situations where less toxic alternatives would
not be effective; oral administration has been successful in
antibiotic-associated colitis and has been used for enteric eradication of
vancomycin-resistant enterococci (VRE) |
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Pregnancy Risk
Factor |
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C |
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Contraindications |
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Hypersensitivity to bacitracin or any component; I.M. use is contraindicated
in patients with renal impairment |
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Warnings/Precautions |
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Prolonged use may result in overgrowth of nonsusceptible organisms; I.M. use
may cause renal failure due to tubular and glomerular necrosis; do not
administer intravenously because severe thrombophlebitis
occurs |
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Adverse
Reactions |
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1% to 10%:
Central nervous system: Pain
Dermatologic: Rash, itching
Gastrointestinal: Anorexia, nausea, vomiting, diarrhea, rectal itching
Hematologic: Blood dyscrasias
Miscellaneous: Diaphoresis |
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Overdosage/Toxicology |
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Symptoms of overdose include nephrotoxicity (parenteral), nausea, vomiting
(oral) |
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Drug
Interactions |
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Increased toxicity: Nephrotoxic drugs, neuromuscular blocking agents, and
anesthetics ( neuromuscular
blockade) |
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Stability |
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For I.M. use; bacitracin sterile powder should be dissolved in 0.9% sodium
chloride injection containing 2% procaine hydrochloride; once reconstituted,
bacitracin is stable for 1 week under refrigeration (2°C
to 8°C); sterile powder should be stored in the
refrigerator; do not use diluents containing parabens |
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Mechanism of
Action |
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Inhibits bacterial cell wall synthesis by preventing transfer of mucopeptides
into the growing cell wall |
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Pharmacodynamics/Kinetics |
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Duration of action: 6-8 hours
Absorption: Poor from mucous membranes and intact or denuded skin; rapidly
absorbed following I.M. administration; not absorbed by bladder irrigation, but
absorption can occur from peritoneal or mediastinal lavage
Distribution: Relative diffusion of antimicrobial agents from blood into
cerebrospinal fluid (CSF): Nil even with inflammation
Protein binding: Minimally bound to plasma proteins
Time to peak serum concentration: I.M.: Within 1-2 hours
Elimination: Slow elimination into urine with 10% to 40% of dose excreted
within 24 hours |
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Usual Dosage |
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Children and Adults ( do not administer I.V.):
less than or equal to 2.5 kg: 900 units/kg/day in 2-3 divided doses
>2.5 kg: 1000 units/kg/day in 2-3 divided doses
Children: I.M.: 800-1200 units/kg/day divided every 8 hours
Adults: Antibiotic-associated colitis: Oral: 25,000 units 4 times/day for
7-10 days
Topical: Apply 1-5 times/day
Ophthalmic, ointment: Instill
1/4
" to 1/2
" ribbon every 3-4 hours into conjunctival sac for acute infections, or 2-3
times/day for mild to moderate infections for 7-10 days
Irrigation, solution: 50-100 units/mL in normal saline, lactated Ringer's, or
sterile water for irrigation; soak sponges in solution for topical compresses
1-5 times/day or as needed during surgical procedures |
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Monitoring
Parameters |
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I.M.: Urinalysis, renal function tests |
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Mental Health: Effects
on Mental Status |
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None reported |
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Mental Health:
Effects on Psychiatric
Treatment |
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None reported |
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Dental Health: Local
Anesthetic/Vasoconstrictor
Precautions |
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No information available to require special precautions |
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Dental Health:
Effects on Dental Treatment |
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No effects or complications reported |
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Patient
Information |
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Oral, I.M.: Maintain adequate hydration (2-3 L/day of fluids unless
instructed to restrict fluid intake). Report rash, redness, or itching; change
in urinary pattern; acute dizziness; swelling of face or lips; chest pain or
tightness; acute nausea or vomiting; or loss of appetite (small frequent meals
or frequent mouth care may help).
Ophthalmic: Instill as many times per day as directed. Wash hands before
using. Gently pull lower eyelid forward, instill prescribed amount of ointment
into lower eyelid. Close eye and roll eyeball in all directions. May cause
blurred vision; use caution when driving or engaging in tasks that require clear
vision. Report any adverse reactions such as rash or itching, swelling of face
or lips, burning or pain in eye, worsening of condition, or if condition does
not improve.
Topical: Apply a thin film as many times as day as prescribed to the affected
area. May cover with porous sterile bandage (avoid occlusive dressings). Do not
use longer than 1 week unless advised by healthcare provider.
Pregnancy/breast-feeding precautions: Inform prescriber if you are or
intend to be pregnant. Consult prescriber if breast-feeding.
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Nursing
Implications |
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For I.M. administration, pH of urine should be kept above 6 by using sodium
bicarbonate |
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Dosage Forms |
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Injection: 50,000 units
Ointment:
Ophthalmic: 500 units/g (1 g, 3.5 g, 3.75 g)
Topical: 500 units/g (1.5 g, 3.75 g, 15 g, 30 g, 120 g, 454 g)
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References |
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Katz BE and Fisher AA,
"Bacitracin: A Unique Topical Antibiotic Sensitizer," J Am Acad Dermatol,
1987, 17(6):1016-24.
Kelly CP, Pothoulakis C, and LaMont JT,
" Clostridium difficile Colitis," N Engl J Med, 1994,
330(4):257-62.
Vale MA, Connolly A, Epstein AM, et al, "Bacitracin-Induced Anaphylaxis,"
Arch Dermatol, 1978, 114(5):800.
Westerman EL, "Toxicity of Mediastinal Irrigation With Bacitracin,"
JAMA, 1983, 250(7):899. |
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