Drug Guide
Bacitracin Zinc
Classification
Therapeutic: Antibiotic, Topical
Pharmacological: Polypeptide Antibiotic
FDA Approved Indications
- Treatment of skin infections caused by susceptible bacteria
Mechanism of Action
Bacitracin inhibits bacterial cell wall synthesis by interfering with peptidoglycan precursors, leading to cell lysis.
Dosage and Administration
Adult: Apply a thin layer to the affected area 1-3 times daily or as directed by a physician.
Pediatric: Use as directed; typically similar to adult dosing, but caution advised in infants and young children.
Geriatric: Adjust based on site and severity of infection, with attention to skin integrity.
Renal Impairment: Not typically used systemically; mainly topical, so renal adjustments are usually unnecessary.
Hepatic Impairment: Not applicable; topical use. Surveillance in case of systemic absorption.
Pharmacokinetics
Absorption: Minimal systemic absorption when applied topically.
Distribution: Primarily remains localized in skin.
Metabolism: Not metabolized systemically; remains localized.
Excretion: Excreted in the skin, with minimal systemic absorption.
Half Life: Not applicable; topical application.
Contraindications
- Hypersensitivity to bacitracin or other components.
- History of allergic contact dermatitis with bacitracin.
Precautions
- Use with caution in patients with a known hypersensitivity to other antibiotics; avoid excessive or prolonged use to prevent sensitization.
Adverse Reactions - Common
- Local skin irritation or contact dermatitis (Rare)
- Allergic contact dermatitis (Rare)
Adverse Reactions - Serious
- Anaphylaxis (Very rare)
Drug-Drug Interactions
N/ADrug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Inspect affected area for signs of infection and allergic reactions.
Diagnoses:
- Risk for contact dermatitis
- Impaired skin integrity
Implementation: Apply as directed, ensuring proper skin cleansing before application.
Evaluation: Monitor for resolution of infection and for adverse skin reactions.
Patient/Family Teaching
- Use as directed and complete the full course.
- Report any signs of allergic reaction or irritation.
- Keep the medication out of reach of children.
Special Considerations
Black Box Warnings:
- None at present.
Genetic Factors: No known genetic considerations.
Lab Test Interference: No significant interference expected with laboratory tests.
Overdose Management
Signs/Symptoms: Excessive application leading to systemic absorption may cause nephrotoxicity or allergic reactions.
Treatment: Discontinue use; provide supportive care as needed, including hydration if nephrotoxicity occurs.
Storage and Handling
Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F).
Stability: Stable under recommended storage conditions; keep container closed.