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. 2016 Sep;6(3):329–337. doi: 10.1086/688059

Table 5.

Respiratory-related adverse events reported in ≥5% of patients in either treatment group with a medical history of parenchymal lung disease

Inhaled treprostinil (N = 420; 568.6 pt-yr) Control (N = 403; 663.4 pt-yr)
Patients, no. (%) Events, no. (per pt-yr) Patients, no. (%) Events, no. (per pt-yr)
Any event 265 (63) 876 (1.541)a 252 (63) 899 (1.355)a
Cough 80 (19) 96 (0.169)a 71 (18) 80 (0.121)a
Upper respiratory tract infection 63 (15) 85 (0.149) 77 (19) 100 (0.151)
Epistaxis 63 (15) 84 (0.148)a 50 (12) 70 (0.106)a
Pneumonia 43 (10) 47 (0.083) 40 (10) 55 (0.083)
Bronchitis 40 (10) 53 (0.093) 40 (10) 52 (0.078)
Dyspnea 37 (9) 43 (0.076) 51 (13) 68 (0.103)
Wheezing 35 (8) 46 (0.081) 42 (10) 58 (0.087)
Sinusitis 28 (7)a 35 (0.062) 45 (11)a 51 (0.077)
Nasopharyngitis 27 (6) 32 (0.056) 30 (7) 41 (0.062)
Oropharyngeal pain 24 (6) 28 (0.049) 18 (4) 20 (0.030)
Throat irritation 21 (5)a 21 (0.037)a 6 (1)a 7 (0.011)a
COPD 20 (5) 27 (0.047)a 11 (3) 14 (0.021)a
Nasal congestion 17 (4) 20 (0.035) 26 (6) 26 (0.039)
Note

Listed events use preferred terms from the Medical Dictionary for Regulatory Activities (MedDRA), version 13.1. COPD: chronic obstructive pulmonary disease; pt-yr: patient-years of exposure.

a

The 95% confidence interval on the ratio of frequencies or incidence rates excludes 1.00.