Ryaltris (Azelastine and Fluticasone) for Allergic Rhinitis Treatment
For moderate to severe allergic rhinitis in patients 12 years and older, Ryaltris (azelastine and fluticasone combination) is recommended at a dosage of 1 spray per nostril twice daily. 1
Dosage and Administration
- Recommended dosage: 1 spray per nostril twice daily for adults and adolescents ≥12 years 1
- For optimal efficacy:
- Gently blow nose before administration
- Shake bottle well before use
- Tilt head slightly forward
- Insert spray tip into nostril
- Breathe in gently while spraying 1
Efficacy
The combination of azelastine and fluticasone in Ryaltris provides superior efficacy compared to either component alone:
- 37-40% relative improvement with combination therapy versus 24-29% for individual components 1
- Greater reduction in Total Nasal Symptom Score (TNSS) compared to monotherapy 1, 2
- Studies show that the combination therapy reduced TNSS by -5.31 to -5.7 points compared to -3.84 to -5.1 for fluticasone alone and -3.25 to -4.54 for azelastine alone 3
- Improvement in both nasal and ocular symptoms 3, 1
Treatment Algorithm
- First-line for mild symptoms: Intranasal corticosteroid alone (e.g., fluticasone)
- For moderate to severe symptoms: Combination therapy with azelastine/fluticasone (Ryaltris) 1
- For patients who cannot tolerate intranasal corticosteroids: Consider oral antihistamines or leukotriene receptor antagonists (e.g., montelukast), though these are less effective 3
- For patients with concurrent asthma: Consider adding a leukotriene receptor antagonist 3, 1
Side Effects and Safety
- Most common side effect: Bitter taste (dysgeusia) in 2.1-13.5% of patients 3, 1
- Other potential side effects:
- Epistaxis (nosebleed)
- Headache
- Somnolence (0.4-1.1% of patients) 1
- Recent studies show somnolence rates with intranasal antihistamines are similar to placebo (0.4-3%) 1
- Overall excellent safety profile 4
Clinical Considerations
- Combination therapy is particularly beneficial for patients with moderate to severe symptoms not adequately controlled with monotherapy 3, 2
- The 2017 Joint Task Force on Practice Parameters provides a weak recommendation for combination therapy as initial treatment for moderate to severe seasonal allergic rhinitis 3
- Patient satisfaction studies suggest that sensory attributes (taste, smell, irritation) are important factors in treatment adherence 5
Pitfalls and Caveats
- Exceeding the recommended dose does not provide additional efficacy 6
- Individual response to treatment may vary, with onset of action occurring as soon as 12 hours but maximum effect taking several days 6
- Quality of life improvements with combination therapy do not consistently exceed the minimal clinically important difference compared to monotherapies 3
- For pediatric patients (4-11 years), treatment should be initiated with lower doses and increased only if inadequate response is observed 6