Drug Guide
Natamycin
Classification
Therapeutic: Antifungal
Pharmacological: Polyene macrolide antifungal
FDA Approved Indications
- Ocular fungal infections, such as fungal keratitis
Mechanism of Action
Natamycin binds to ergosterol in fungal cell membranes, disrupting membrane integrity and causing cell death.
Dosage and Administration
Adult: Apply as a 5% ophthalmic suspension to affected eye(s) as directed by the physician, typically every 1-2 hours initially.
Pediatric: Use as prescribed by a healthcare provider; dosing may be similar to adults, but specific guidelines should be followed.
Geriatric: No specific adjustments required, but caution in elderly with other ocular conditions.
Renal Impairment: No specific dosage adjustment; systemic absorption is minimal.
Hepatic Impairment: No specific dosage adjustment; primarily used topically. Systemic effects are rare.
Pharmacokinetics
Absorption: Minimal systemic absorption when used topically.
Distribution: Primarily localized to ocular tissues.
Metabolism: Not extensively metabolized; primarily remains unmetabolized topical form.
Excretion: Minor systemic absorption; excreted via tear drainage and local ocular tissues.
Half Life: Not well-defined; topical application with local action.
Contraindications
- Hypersensitivity to natamycin or other components of the formulation.
Precautions
- Monitor for allergic reactions; use with caution in patients with known hypersensitivity to polyene antifungals.
Adverse Reactions - Common
- Transient stinging or burning upon application. (Common)
- Eyedrops irritation or redness. (Uncommon)
Adverse Reactions - Serious
- Allergic reactions, including swelling or rash. (Rare)
- Corneal edema or epithelial defect. (Rare)
Drug-Drug Interactions
N/ADrug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Assess for signs of ocular infection, allergy, or irritation.
Diagnoses:
- Risk for infection progression
- Knowledge deficit regarding medication use
Implementation: Administer as prescribed; educate patient on proper application and hygiene.
Evaluation: Monitor improvement in infection, resolution of symptoms, and absence of adverse reactions.
Patient/Family Teaching
- Apply medication exactly as prescribed.
- Avoid touching the tip of the dropper to any surface.
- Report any worsening symptoms, side effects, or signs of allergic reaction.
- Use medication for the full prescribed duration, even if symptoms improve.
Special Considerations
Black Box Warnings:
- None currently issued.
Genetic Factors: None relevant.
Lab Test Interference: Not known to interfere with laboratory tests.
Overdose Management
Signs/Symptoms: Rare, but excessive application may cause increased irritation or adverse effects.
Treatment: Supportive care; discontinue medication and provide symptomatic relief.
Storage and Handling
Storage: Store at room temperature, protected from light.
Stability: Stable until the expiration date on the packaging.