Drug Guide

Generic Name

Azelastine Hydrochloride and Fluticasone Propionate

Brand Names Dymista

Classification

Therapeutic: Allergic Rhinitis, Nasal corticosteroid/antihistamine combination

Pharmacological: Antihistamine (Azelastine), Corticosteroid (Fluticasone)

FDA Approved Indications

Mechanism of Action

Azelastine works as a selective antihistamine that blocks H1 receptors, reducing allergy symptoms. Fluticasone is a corticosteroid that reduces inflammation by suppressing multiple inflammatory genes.

Dosage and Administration

Adult: One spray in each nostril twice daily for adults.

Pediatric: Not established for children under 12; dosing should be determined by physician.

Geriatric: No specific dosage adjustment necessary but monitor for increased sensitivity.

Renal Impairment: No specific adjustments recommended.

Hepatic Impairment: Use with caution; no specific dose adjustment established.

Pharmacokinetics

Absorption: Rapid absorption after intranasal administration.

Distribution: Systemic distribution, primary localized effect in nasal tissues.

Metabolism: Azelastine is metabolized in the liver; Fluticasone extensively metabolized by CYP3A4.

Excretion: Metabolites are excreted primarily via urine and feces.

Half Life: Azelastine: approximately 22 hours; Fluticasone: approximately 7 hours.

Contraindications

Precautions

Adverse Reactions - Common

Adverse Reactions - Serious

Drug-Drug Interactions

Drug-Food Interactions

N/A

Drug-Herb Interactions

N/A

Nursing Implications

Assessment: Monitor nasal symptoms and for adverse reactions like nasal irritation or bleeding.

Diagnoses:

  • Risk for nasal mucosal injury
  • Risk for systemic corticosteroid effects

Implementation: Administer intranasally as directed, instruct patient on proper spray technique.

Evaluation: Assess reduction in allergy symptoms and monitor for adverse effects.

Patient/Family Teaching

Special Considerations

Black Box Warnings:

Genetic Factors: No specific genetic considerations known.

Lab Test Interference: May affect adrenal function tests.

Overdose Management

Signs/Symptoms: Drowsiness, increased adrenergic effects, nasal mucosal irritation.

Treatment: Supportive care, symptomatic treatment, consult poison control.

Storage and Handling

Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F).

Stability: Stable for the duration of the shelf life indicated by the manufacturer.

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