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. 2019 Dec 2;9(3):411–421. doi: 10.1002/cpdd.756

Table 4.

Participants Experiencing at Least 1 Adverse Event

AZD5718 200 mg
Fasted Fed
Participants With Rosuvastatin 10 mg (n = 12) Tablet Plus Rosuvastatin 10 mg (n = 12) Tablet (n = 12) Suspension (n = 12) Tablet (n = 12) All (n = 12)
Any AE, n (%) 1 (8.3) 1 (8.3) 3 (25.0) 2 (16.7) 1 (8.3) 6 (50.0)
AEs
Headache, n (%) 1 (8.3) 0 0 1 (8.3)a 0 2 (16.7)
Poor‐quality sleep, n (%) 0 0 1 (8.3)b 0 0 1 (8.3)
Nausea, n (%) 0 0 0 1 (8.3)a 0 1 (8.3)
Influenza‐like illness, n (%) 0 0 0 1 (8.3)b 0 1 (8.3)
Nasopharyngitis, n (%) 0 0 0 0 1 (8.3) 1 (8.3)
Musculoskeletal pain, n (%) 0 1 (8.3) 0 0 0 1 (8.3)
Nasal congestion, n (%) 0 0 1 (8.3)a 0 0 1 (8.3)
Oropharyngeal pain, n (%) 0 0 1 (8.3)a 0 0 1 (8.3)
Dry skin, n (%) 0 0 1 (8.3) 0 0 1 (8.3)
Hot flush, n (%) 0 0 0 1 (8.3)a 0 1 (8.3)

AE, adverse event.

AEs were coded using Medical Dictionary for Regulatory Activities (MedDRA) version 19.1 vocabulary.

a

Considered possibly related to AZD5718 by the investigator (all other AEs were unrelated).

b

Moderate intensity (all other AEs were mild).