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