NEOMYCIN SULFATE
(nee-oh-mye'sin)
Mycifradin, Myciguent, Neo-Tabs, Neo-fradin
Classifications: antiinfective; aminoglycoside antibiotic
Prototype: Gentamicin
Pregnancy Category: D

Availability

500 mg tablet; 125 mg/5 mL oral solution; 3.5 mg/g ointment, cream

Actions

Aminoglycoside antibiotic obtained from Streptomyces fradiae; reported to be the most potent in neuromuscular blocking action and the most toxic of this group.

Therapeutic Effects

Active against a wide variety of gram-negative bacteria, including Citrobacter, Escherichia coli, Enterobacter, Klebsiella, Proteus (including indole-positive and indole-negative strains), Pseudomonas aeruginosa, and Serratia sp. Also effective against certain gram-positive organisms, particularly, penicillin-sensitive and some methicillin-resistant strains of Staphylococcus aureus (MRSA).

Uses

Severe diarrhea caused by enteropathogenic Escherichia coli; preoperative intestinal antisepsis; to inhibit nitrogen-forming bacteria of GI tract in patients with cirrhosis or hepatic coma and for urinary tract infections caused by susceptible organisms. Also topically for short-term treatment of eye, ear, and skin infections. Available in a variety of creams, ointments, and sprays in combination with other antibiotics and corticosteroids.

Contraindications

Use of oral drug in patients with intestinal obstruction; ulcerative bowel lesions; topical applications over large skin areas; parenteral use in patients with kidney disease or impaired hearing; parkinsonism; myasthenia gravis; pregnancy (category D), lactation.

Cautious Use

Topical otic applications in patients with perforated eardrum, children.

Route & Dosage

Intestinal Antisepsis
Adult: PO 1 g q1h times 4 doses, then 1 g q4h times 5 doses
Child: PO 10.3 mg/kg q4–6h for 3 d

Hepatic Coma
Adult: PO 4–12 g/d in 4 divided doses for 5–6 d
Child: PO 437.5–1225 mg/m2 q6h for 5–6 d

Diarrhea
Adult: PO 50 mg/kg in 4 divided doses for 2–3 d IM 1.3–2.6 mg/kg q6h
Child: PO 8.75 mg/kg q6h for 2–3 d

Cutaneous Infections
Adult: Topical Apply 1–3 times/d

Administration

Oral
Topical

Adverse Effects (1%)

Body as a Whole: Neuromuscular blockade with muscular and respiratory paralysis; hypersensitivity reactions. GI: Mild laxative effect, diarrhea, nausea, vomiting; prolonged therapy: malabsorption-like syndrome including cyanocobalamin (vitamin B12) deficiency, low serum cholesterol. Urogenital: Nephrotoxicity. Special Senses: Ototoxicity. Skin: Redness, scaling, pruritus, dermatitis.

Interactions

Drug: May decrease absorption of cyanocobalamin.

Pharmacokinetics

Absorption: 3% absorbed from GI tract in adults; up to 10% absorbed in neonates. Peak: 1–4 h. Elimination: 97% excreted unchanged in feces. Half-Life: 3 h.

Nursing Implications

Assessment & Drug Effects

Patient & Family Education


Common adverse effects in italic, life-threatening effects underlined; generic names in bold; classifications in SMALL CAPS; Canadian drug name; Prototype drug