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Table 2 Incidence of Treatment-Related AEs Reported by ≥1% of Patients

From: Improved adherence with once-daily versus twice-daily dosing of mometasone furoate administered via a dry powder inhaler: a randomized open-label study

 

MF-DPI 400 μg QD PM

(n = 611)

MF-DPI 200 μg BID

(n = 622)

Patients reporting any AE, n (%)

85 (14)

109 (18)

   Headache

10 (2)

12 (2)

   Dysphonia

3 (<1)

9 (1)

   Mouth dry

12 (2)

11 (2)

   Mouth ulceration

5 (1)

1 (<1)

   Candidiasis, oral

9 (1)

16(3)

   Pharyngitis

16 (3)

15 (2)

   Upper respiratory tract infection

5 (1)

0

   Cough

2 (<1)

6 (1)

   Hoarseness

4 (1)

5 (1)

   Throat dry

11 (2)

3 (<1)

   Rash

0

4 (1)

  1. AE = adverse event; BID = twice-daily; MF-DPI = mometasone furoate administered via a dry powder inhaler; QD PM = once-daily in the evening.