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neomycin sulfate |
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neomycin sulfate [ne′ō-mī′sin] an aminoglycoside antibiotic. indications It is prescribed orally to treat hepatic coma and infections of the intestine and to prepare the gastrointestinal tract for surgery. It is prescribed topically to treat skin infections. contraindications Renal dysfunction, intestinal obstruction, or known hypersensitivity to this drug or to any aminoglycoside medication prohibits its use. Neomycin is not administered parenterally. adverse effects Among the more serious adverse effects are nausea, vomiting, diarrhea, malabsorption, or superinfection. Prolonged treatment in patients with impaired renal function may result in the toxicities of systemic aminoglycosides (e.g., ototoxicity, nephrotoxicity, neuromuscular toxicity). Hypersensitivity reactions may occur with topical administration of this drug. neomycin sulfate (topical), n brand name: Myciguent;
drug class: local antibacterial; action: interferes with bacterial protein synthesis; use: skin infections. neomycin
sulfate A broad-spectrum antibiotic agent effective against gram-negative and gram-positive organisms, although it is not effective against Pseudomonas aeruginosa. It may be applied topically as eyedrops or eye ointment, but it is most commonly combined with bacitracin and polymyxin B. Syn. framycetin (a mixture of neomycin A, neomycin B and neomycin C).
neomycin sulfate Neo-Fradin, Nivemycin (UK) Pharmacologic class: Aminoglycoside Therapeutic class: Anti-infective Pregnancy risk category D FDA Boxed Warning• Systemic absorption follows oral use and may lead to toxic reactions. Observe patient closely for indications of toxicity. Neurotoxicity (including ototoxicity) and nephrotoxicity have occurred, even at recommended doses. Perform serial, vestibular, and audiometric tests as well as renal function tests, especially in high-risk patients. Risk of nephrotoxicity and ototoxicity is greater in patients with renal impairment. Ototoxicity may be delayed, and patients developing cochlear damage won't have symptoms during therapy; total or partial deafness may occur long after drug is stopped ActionInterferes with bacterial protein synthesis by binding to 30S ribosomal subunit, causing misreading of genetic code. Inaccurate peptide sequence then forms in protein chain, causing bacterial death. AvailabilityOintment: 0.5% Oral solution: 125 mg/5 ml Tablets: 500 mg ⊘Indications and dosages ➣ Preoperative intestinal antisepsis Adults: 1 g P.O. q hour for four doses, then 1 g q 4 hours for 24 hours or 1 g at 19 hours, 18 hours, and 9 hours before surgery ➣ Hepatic encephalopathy Adults: 4 to 12 g/day P.O. in divided doses ➣ Superficial bacterial infections Adults: Apply ointment topically one to five times daily. Contraindications• Hypersensitivity to drug or other aminoglycosides PrecautionsUse cautiously in: Administration• Give preoperative dose before bowel surgery, after cathartic administration, as ordered.
Adverse reactionsCNS: neuromuscular blockade EENT: ototoxicity (with prolonged, high-dose use) GI: nausea, vomiting, diarrhea, malabsorption syndrome GU: nephrotoxicity (with prolonged, high-dose use) Other: superinfection InteractionsDrug-drug. Acyclovir, amphotericin B, cephalosporin, cisplatin, other aminoglycosides, vancomycin: increased risk of ototoxicity and nephrotoxicity Digoxin: decreased digoxin absorption Dimenhydrinate: masking of ototoxicity symptoms Oral anticoagulants: increased anticoagulant effect Potent loop diuretics: increased risk of ototoxicity Patient monitoring• Assess for neuromuscular blockade, ototoxicity, and nephrotoxicity. Patient teaching• Instruct patient to drink plenty of water. How to thank TFD for its existence? Tell a friend about us, add a link to this page, add the site to iGoogle, or visit webmaster's page for free fun content. |
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