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Table 3 Frequency of TEAEs Overall and Occurring in ≥2 Patients, by MedDRAa Preferred Term (Safety Population)

From: Navafenterol (AZD8871) in patients with COPD: a randomized, double-blind, phase I study evaluating safety and pharmacodynamics of single doses of this novel, inhaled, long-acting, dual-pharmacology bronchodilator

TEAE (Preferred Terma)

Placebo (n = 32)

navafenterol 400 μg (n = 34)

navafenterol 1800 μg (n = 31)

Indacaterol 150 μg (n = 32)

Tiotropium 18 μg (n = 30)

All (N = 38)

Any event, n (%)

11 (34.4)

18 (52.9)

7 (22.6)

12 (37.5)

11 (36.7)

31 (81.6)

Headache

7 (21.9)

5 (14.7)

3 (9.7)

4 (12.5)

7 (23.3)

12 (31.6)

Nasopharyngitis

1 (3.1)

1 (2.9)

1 (3.2)

2 (6.3)

1 (3.3)

5 (13.2)

COPD

0

2 (5.9)

1 (3.2)

1 (3.1)

0

4 (10.5)

Erythema

1 (3.1)

1 (2.9)

0

1 (3.1)

0

3 (7.9)

Medical device site reaction

1 (3.1)

0

1 (3.2)

1 (3.1)

0

3 (7.9)

Constipation

1 (3.1)

1 (2.9)

1 (3.2)

0

0

2 (5.3)

Nausea

1 (3.1)

1 (2.9)

0

0

0

2 (5.3)

Rhinitis

0

1 (2.9)

0

1 (3.1)

0

2 (5.3)

  1. COPD chronic obstructive pulmonary disease, MedDRA Medical Dictionary for Regulatory Activities, TEAE treatment emergent adverse event.
  2. aMedDRA version 18.1