Drug Guide

Generic Name

Nystatin and Triamcinolone Acetonide

Brand Names Mycolog-II, Myco-triacet II, Nystatin And Triamcinolone Acetonide, Mykacet, Nystatin Triamcinolone Acetonide, Mytrex F, Nystatin-triamcinolone Acetonide

Classification

Therapeutic: Topical antifungal and corticosteroid combination

Pharmacological: Antifungal (Nystatin), Corticosteroid (Triamcinolone Acetonide)

FDA Approved Indications

  • Treatment of Cutaneous Candidiasis with inflammation
  • Adjunctive treatment of inflammatory dermatoses prone to fungal superinfection

Mechanism of Action

Nystatin binds to ergosterol in fungal cell membranes, creating pores that cause cell contents to leak, leading to fungal cell death. Triamcinolone acetonide suppresses inflammation, reducing swelling, redness, and itching by inhibiting multiple inflammatory cytokines.

Dosage and Administration

Adult: Apply a thin layer to affected area 2-4 times daily as advised by healthcare provider.

Pediatric: As directed by a healthcare provider, usually similar to adult dosing but with careful monitoring.

Geriatric: Use with caution; consider reduced frequency and dose due to increased skin fragility.

Renal Impairment: No dose adjustment needed for topical use.

Hepatic Impairment: No specific adjustment for topical use.

Pharmacokinetics

Absorption: Minimal systemic absorption from topical application.

Distribution: Primarily localized at the application site.

Metabolism: Nystatin is not significantly metabolized; Triamcinolone undergoes hepatic metabolism.

Excretion: Elimination via feces and urine depending on systemic absorption.

Half Life: Nystatin: primarily local action, not applicable; Triamcinolone: approximately 2 hours systemically.

Contraindications

  • Hypersensitivity to any component.
  • Viral, bacterial, or fungal infections not susceptible to the antifungal.
  • Untreated cutaneous infections.

Precautions

  • Use cautiously in broken or raw skin; avoid extensive or occlusive dressings; monitor for signs of secondary infection.

Adverse Reactions - Common

  • Skin irritation or burning sensation (Common)
  • Itching (Common)

Adverse Reactions - Serious

  • Allergic contact dermatitis (Rare)
  • Secondary bacterial or fungal infections at application site (Rare)

Drug-Drug Interactions

  • None specifically identified for topical use; systemic interactions are unlikely.

Drug-Food Interactions

  • None

Drug-Herb Interactions

  • None

Nursing Implications

Assessment: Assess skin condition and signs of infection or hypersensitivity before application.

Diagnoses:

  • Impaired skin integrity related to topical application.

Implementation: Apply as prescribed, clean affected area before application, avoid contact with eyes.

Evaluation: Monitor skin response; assess for adverse reactions or signs of systemic absorption.

Patient/Family Teaching

  • Use as directed; do not cover the area with occlusive dressings unless instructed.
  • Wash hands before and after applying medication.
  • Report any signs of allergic reaction or worsening skin condition.

Special Considerations

Black Box Warnings:

  • None

Genetic Factors: None specific.

Lab Test Interference: None expected from topical use.

Overdose Management

Signs/Symptoms: Excessive absorption may lead to systemic corticosteroid effects such as adrenal suppression, hyperglycemia, or Cushingoid appearance.

Treatment: Discontinue use; manage symptoms supportively; consider systemic corticosteroid if needed.

Storage and Handling

Storage: Store at room temperature away from moisture and heat.

Stability: Stable for up to the expiration date when stored properly.

This guide is for educational purposes only and is not intended for clinical use.