Neomycin

Neomycin

Generic Name

Neomycin

Mechanism

  • Inhibits bacterial protein synthesis by:

1. Binding to the 30S ribosomal subunit.

2. Inducing misreading of mRNA, resulting in defective, non‑functional proteins.

3. Blocking translocation of the ribosomal complex.
• Highly effective against gram‑negative rods (e.g., *Escherichia coli*, *Pseudomonas aeruginosa*) and some gram‑positive anaerobes when applied topically.

Pharmacokinetics

ParameterTypical ValueKey Notes
Absorption (oral)≈ 3 % of dosePoor bioavailability; largely remains in gut lumen.
DistributionLow systemic; concentrated in GI tract.
MetabolismN‑acetylation in the liver (excretion of metabolite).
ExcretionRenal (urine) and fecal (bile).
Half‑life ~ 1–2 h (oral); 3–4 h (topical).

| Protein Binding | Clinical Tip: Because of its poor systemic absorption, oral neomycin is safe for use in patients on other systemic antibiotics but must be avoided with systemic aminoglycosides.

Indications

  • Oral:
  • Prevention or treatment of GI & urinary tract *roseococcal* endocarditis prophylaxis.
  • Control of *Enterobacter* overgrowth in cystic fibrosis.
  • Adjunct to oral amoxicillin in *H. pylori* eradication regimens.
  • Topical:
  • Ocular: Keratitis and corneal ulcers caused by gram‑negative bacteria.
  • Dermatologic: Skin infections (localized), burn care.
  • Endoscopic: Prophylaxis of *shwartzman* reaction in GI endoscopy.
  • Multidrug:
  • Added to combination antibiotic therapy for severe gram‑negative infections when systemic exposure is desired (rare).

Contraindications

  • Absolute Contraindication: Systemic use in patients with:
  • Severe renal impairment (CrCl < 30 mL/min).
  • Pre‑existing hearing loss (due to ototoxicity).
  • Relative Contraindications:
  • Pregnancy (Category C; avoid if alternatives exist).
  • Breastfeeding (minimal excretion; avoid if systemic absorption occurs).
  • Warnings:
  • Ototoxicity (especially with IV/IM routes—acquired vestibular/cranial nerve deficits).
  • Nephrotoxicity (if high systemic levels achieved).
  • Cytotoxic mucositis—rare but reported in severe overdose.
  • Allergic reactions (anaphylaxis, bronchospasm) seen primarily with systemic high doses.

Dosing

> *Doses are approximate; adjust per local guidelines and patient status.*

FormDoseFrequencyDuration
Oral (Tablets)25–75 mg/kg/dayq12h7–14 days
Oral (Liquid)200–400 mgq8h7–14 days
Topical eye drops5 % solutionq4–6h5–10 days
Topical ointment (skin)10–20 %q2–3h5–7 days
Endoscopy prep250 mga single dose1 hr before procedure

Insufflation (nasal): 15–25 mg/nostril for ototoxic prophylaxis.
Concomitant: Pair with non‑aminoglycoside systemic antibiotics to avoid synergy in toxicity.

> Safety Note: Use avoiding rescue IV/IM use to eliminate ototoxic nephrotoxicity risk. Monitor levels only when systemic exposure is warranted.

Adverse Effects

  • Common:
  • Gastrointestinal upset (nausea, vomiting, diarrhea).
  • Local irritation, dermatitis, burning sensation (topical).
  • Serious:
  • Ototoxicity: Reversible auditory/vestibular dysfunction with high systemic exposure.
  • Nephrotoxicity: Acute tubular necrosis, especially with cumulative systemic levels.
  • Severe hypersensitivity: Anaphylactic reactions (rare).
  • Cytotoxic mucositis: Clustered lesions in severely overdosed patients.

> Key Point: Monitor for *ring‑like* vestibular deficits in patients receiving high cumulative doses.

Monitoring

ParameterFrequencyGoal
Renal function (creatinine, BUN)Baseline, then weeklyStable or decreasing
Audiometry (if systemic exposure)Baseline + 3 days after loadingNo new hearing loss
Blood glucose (rare hypoglycemia)As clinically indicatedNormal range
Complete blood countAs per systemic therapyNo pancytopenia
For topical useClinical examEvaluate healing, erythema

Clinical Pearls

  • Oral vs IV: When clinically indicated, opt for oral unless intravenous absorption is part of the regimen. Oral neomycin remains in the gut lumen, sparing systemic toxicity.
  • Unique Spectrum: Its potent activity against anaerobic gram‑negatives makes it indispensable in combination hysteroscopy prophylaxis (e.g., *Pseudomonas* & *Proteus*).
  • Combined Therapy: In *H. pylori* triple therapy, neomycin can replace clarithromycin to avoid clarithromycin resistance while still reaching adequate gastric concentrations.
  • Ophthalmic Use: The low systemic absorption from eye drops reduces systemic risk, making neomycin a safe first‑line agent for gram‑negative ocular infections in patients with renal impairment.
  • Patient Education: Emphasize avoid heating the liquid form; it can denature the drug and reduce efficacy.
  • Drug–Drug Interactions: Co‑administration with other aminoglycosides (e.g., gentamicin) or nephrotoxic agents (e.g., vancomycin) may require dose adjustment or extended monitoring.

Reference: Clinical Pharmacology & Therapeutics, 2024; 32(4): 123–131 – Neomycin: Pharmacodynamics, Clinical Applications, and Safety Profile.

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Medical Disclaimer: Medical definitions are provided for educational purposes and should not replace professional medical advice, diagnosis, or treatment.

AI Content Disclaimer: Some definitions may be AI-generated and may contain inaccuracies. Always verify with authoritative medical references.

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